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MULTIPLE SCLEROSIS TESTIMONIALS
FRIEDREICH'S ATAXIA TESTIMONIALS
MOTOR NEURONE DISEASE/ALS TESTIMONIALS
OPCA TESTIMONIALS
PRIMARY LATERAL SCLEROSIS TESTIMONIALS
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Multiple Sclerosis Testimonial 1:
Patient Into His 20th Year On Treatment
 Hello, my name is Eddie Cardinal and I am into my 20th year on the Esperanza Homeopathic NeuroPeptide treatment. I became the first human being with Multiple Sclerosis (MS) to go on the Esperanza Homeopathic NeuroPeptide and I am so glad that I was given the opportunity to do so. Before going on the Esperanza Homeopathic NeuroPeptide my body was ravaged by the symptoms of Multiple Sclerosis (MS) including loss of balance, dizziness, muscle pain, spasms, and problems with regards to walking, eye site and chronic fatigue. After going on the peptide, I am happy to say that all of the symptoms disappeared and I was able to function normally once again without these horribly disabling symptoms. I can honestly say that I owe the fantastic quality of life that I have experienced the past 20 years to the peptide and the treatment offered to me through The Esperanza Research Foundation. I start each day by spraying the peptide under my tongue (sublingual) and it lasts for at least 24 hours until I have to spray again the next morning ... simple as that. Again, I am now in my 20th year on the peptide and I live and look forward to each day because of the peptide and the work of the Esperanza Research Foundation to reach out around the world and make this fantastic treatment available to all those afflicted with MS like myself. The best tribute and testimonial to the Esperanza Homeopathic NeuroPeptide treatment is the fact that I have had an exceptional quality of life for the past 20 years when all seemed very bleak at the onset of my initial diagnosis for MS. I have lived an excellent and symptoms-free life the past 20 years, however without the peptide I would revert immediately back to the horrible symptoms that all of us with MS know and dread all too well. I hear the word "HOPE" often associated with Multiple Sclerosis and it is quite appropriate that ESPERANZA in Spanish means "HOPE". I actually see "hope" in action at The Esperanza Research Foundation as they offer hope through actual treatments that work for neurological diseases in my case Multiple Sclerosis. I can only say a huge and heartfelt thank you to all the fine doctors, scientists, researchers and all the others associated with The Esperanza Research Foundation and the development of the Esperanza Homeopathic NeuroPeptide that is now an integral part of my everyday life. I hope one day to see the peptide treatment available to all MS patients worldwide and being able to hear the stories of their change in life quality as I have experienced these past 20 years.
Eddie Cardinal
Canada
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Multiple Sclerosis Testimonial 2:
From Wheelchair To Walking
 My name is Sandy Williams. In 1983 I was diagnosed with M.S. at the Cleveland Clinic in Cleveland, Ohio. The symptoms I had that sent me there for answers were weakness on the right side of my body and double vision. Diagnosis came from having a CT scan and then a spinal tap. In 1983 there was no treatment or cure known by the doctors at the Cleveland Clinic, so I went back to my life hoping the symptoms would go away, and stay away. They came and went over the next decade and the weakness that was slight and intermittent came more often, stayed longer, and was more pronounced each time. In the years between 1996 and 2002 I began to admit to myself that I was going to have to use a wheel chair. That meant that I would have to sell my house and buy one that was more fitted to suit my disabilities. In January of 2002 I learned about the Esperanza Homeopathic NeuroPeptide that was being developed and manufactured in Freeport in The Bahamas. A trusted doctor friend of mine was the one that got the message to me about the peptide and as I knew I could trust what he said to be true, I was on a plane three weeks later to try the stuff out! In February of 2002 my mother had to push me in a wheel chair to the gate at the airport since it was such a long walk. Three days later, after taking "puffs" of the peptide, I felt that I could walk through 10 airports! In fact, I could and did walk the same distances that I was unable to three days before. Mom picked me up at the curb instead of having a wheel chair ready. After four years of Esperanza Homeopathic NeuroPeptide use, the quality of my life is not only more dependable, it is MORE! I can usually walk through most of the activities that I would like to. I can usually write legibly (which I could not do by the year 2002), I can put mascara on without the incredibly shaky right hand I used to have, and my speech was no longer slurred. One of the first things I noticed those first three days on the Esperanza Homeopathic NeuroPeptide was being able to sit and read a book for an extended period of time without getting so tired I felt I had to close the book. I have virtually lost all signs of fatigue and often, my balance is nearly perfect. There has never been one single side-effect on me from using the peptide. As all M.S. patients know, every day is different, even on the peptide. The difference that the Esperanza Homeopathic NeuroPeptide has made to my life, therefore my daughter's, is absolute. Before I started on it I would have been happy to have one "normal" day in a year. Today I can expect to have "normal" days EVERY day and am surprised and upset when I have a bad day in a week! I don't see a wheel chair in my future because of the peptide and my house is NOT for sale.
UPDATE:
AFTER FOUR YEARS ESPERANZA NEUROPEPTIDE IS STILL A LIFE SAVER
After 4 plus year on the Esperanza NeuroPeptide it has been ... a life saver. Without it I would probably have to use a walker or a wheelchair.
FURTHER UPDATE:
Eddie Cardinal (21 years on NeuroPeptide) and Sandy Williams (6 years on NeuroPeptide)
June 16, 2008
Since the NeuroPeptide is still doing what it is supposed to, and has done for over 6 years now, I had to think of a new twist to "up-date" my testimonial on the Esperanza NeuroPeptide website, so I have decided to focus on the areas that may have stopped or prevented the NeuroPeptide from working on me a points over the past 6 years!
If there is one thing everyone who is thinking of trying the peptide or is using it needs to know, it is the following:
I have had to "re-boot" the peptide into action several times over the years. I will give you some bullet points to list what I know to be the reasons:
- I tried smoking cigarettes which of course we all no is a complete "no-no" any nicotine will stop the NeuroPeptide from working!
- I tried to use Vinpocetine in addition to the NeuroPeptide.
- I tried natural hormone replacement in addition to the NeuroPeptide.
- I tried to use Holosync in addition to the NeuroPeptide.
- I have had my fair share of viruses that also have impacted the NeuroPeptide.
Everything noted above are things I have done over the years in conjunction with the Esperanza NeuroPeptide that have actually STOPPED THE NEUROPEPTIDE FROM WORKING ... and that is what we do not want! So in order to re-boot the Esperanza NeuroPeptide back into action I have had to do a short round of oral steroid called Dexamethasone each time. Now, as in all medication, this may not work for everyone, but I wanted to share what did and does work for me. I also wanted to point out that viruses and what we take in conjunction with the Esperanza NeuroPeptide can diminish and combat the effectiveness of this wonderful daily spray that myself and thousands worldwide have made part of our daily life ... AND IT WORKS!
Aside from those instances where I have needed to re-boot my Esperanza experience, the past 6 years have been amazing for me! I was close to needing a full time wheel chair in 2002 when I heard about the Esperanza NeuroPeptide and I have still not needed to come close to that wheel chair, nor do I intend to!
I wish you all the best and I thank all at Esperanza for giving me my life back these past 6 wonderful years!
Sandy Williams
North Carolina, USA
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Multiple Sclerosis Testimonial 3:
It Was Peptide Or Nothing - First Peptide Birth!
 I was diagnosed with Multiple Sclerosis in 2001 at age 27. I was a dancer and a theatre actress. I ,unknowingly, started having MS symptoms at age 19. I was so physical with theatre and dance, that would be symptoms got blown off as pulled muscles, ligaments, nerves, etc. I would be at the top of my game and would become completely exhausted. I would take about three weeks off from life, and would go and see psychiatrists and counselors. I felt something was going on in my head. To my dismay, they would agree with me and tell me that I was bipolar, schitzo, and manic. MS had just not manifested physically yet. From this point my journey became ever so slowly worse. I finally got properly diagnosed and treated. The medications that were to make me better, made what I considered worse. My hair fell out. I hallucinated, insanity actually started to set in, and I could not understand why the meds did not protect me from exacerbations. By the time I made it to Freeport, I was walking with a cane and human assistance, and a wheel chair if there was one around. It was Esperanza Homeopathic NeuroPeptide or nothing. I had tried everything; I was so desperate I even tried some unconventional tactics. The first time that David dosed me was with the puffer, no injection. He told me to get up and walk to the wall. I did! Now, I have to give an explanation of what this means. For me to even stand up from a sitting position, I would first have to mentally tell my body piece by piece what to expect and what to do. After I had made it through the instruction, then I would have to wait for the uncontrollable shaking in my legs to stop, then I would have to scout out things that I could reach out and fall into. Go through the whole process again to reach the next point just to get across a room. Now let me say it again. David said "Get up & walk to the wall." Instantly, without thinking, I did! Then, since I was so good at standing AND walking without thinking, he wanted me to again stand with my feet together and my eyes closed. The first time, prior peptide, I could do it for about 3 seconds. This time I did it for 3 minutes plus. For as long as I live, I will never forget David saying, "Welcome Back!" It was as if I had been in a semi-state of unconsciousness for years. Suzanne asked me how did it feel. It was if someone had taken off huge chains that had been wrapped around my feet, legs, arms, hands, and shoulders. It was almost like sighing after holding my breath for years. Even more remarkable, I had a Esperanza Homeopathic NeuroPeptide baby. Before, any other medications that I was taking to treat my MS, I was told not to conceive a child without being off the medication for at least a year. I took my peptide through my whole pregnancy and while I was nursing. I also did not or have not had even a whisper of MS before, during, or after. To be quite honest, since I have been on Esperanza Homeopathic NeuroPeptide, I have not had an exacerbation in over two years, which is over half of my MS life.
UPDATE:
Maybe someday they will award Esperanza a NOBEL PRIZE
Just a quick update to say that I am doing great! I went to visit friends in NY! I had lay over in Cincinnati all day, and still made it to the Birthday Party! (It was a surprise for my friend ... and I was the present). I ran all over the airport, all day long, and partied all night! 6 months ago, not to mention 1, 2 or 3 years ago that would not have been an utter impossibility without my NeuroPeptide.
I am also a happy substitute teacher now, as well as being a full time Mommy. Speaking of which ... my lovely son Jude is going to be 2 on the 8th of October. So, I am doing pretty great all thanks to the Esperanza NeuroPeptide!
I hope all is well with you! I know you and all at Esperanza are busy! busy! busy! It is so exciting to read the updates and see that clinics are being opened in other countries. Maybe someday they will award Esperanza a NOBEL PRIZE ... you sure deserve it and my son and I will be there in person when that day comes to stand up and cheer!
Thanks Again! God Bless You! and Much Love!
FURTHER UPDATE:
My Life Could Not Be Without Esperanza NeuroPeptide.
I am happy to report that I am now going back to school to obtain my Masters Degree. I tried once before without my NeuroPeptide spray, and it was impossible. At 29 years old, my neurologist told me that I was experiencing cognitive dysfunction due to demyelination. There was not a drug for M.S. that stopped and reversed the effects of this debilitating disease. Esperanza NeuroPeptide did just that. Now, I will be able to get my Masters Degree, raise my son, and show him, when he is old enough to understand, that anything is possible.
I can't thank God and the Esperanza team enough for giving me a second chance at life!
My life could not be without Esperanza Peptide.
Gillie Daugherty
Kentucky, USA
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Multiple Sclerosis Testimonial 4:
Much Needed Hope
 I am still on the Esperanza Homeopathic NeuroPeptide (since March 2005) and it has slowed the disease down. Every day is different. The peptide has given me much needed hope! When I came home from the Bahamas, I started going swimming at the Y twice a week which I am still doing. A great advantage to me now, is that instead of sliding from my chair at work to my wheelchair I stand and transfer myself under my own control (which I could not do prior to going on the peptide). I also try to do standing exercises at least 3 times a day.
UPDATE:
I REALLY FEEL THAT THE ESPERANZA NEUROPEPTIDE IS KEEPING THE DISEASE FROM PROGRESSING!
My upper body is fine and still working full time for me. I really feel the peptide is keeping the disease from progressing to my upper body and I take the Esperanza NeuroPeptide daily.
Debbie Hicken
Canada
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Multiple Sclerosis Testimonial 5:
I Am So Lucky To Have Found Esperanza Homeopathic NeuroPeptide
 In 1993, my wife of 22 years died of breast cancer. I took this very hard and two years later in 1995, I was diagnosed with a debilitating disease called Multiple Sclerosis (MS). This disease affected the right side of my body disabling my muscles in the arm and leg but not my face or my ability to think or to speak. There is absolutely no pain, but I experience fatigue, lethargy and heat frustration especially when temperatures are humid. My treatments were injections of Interferon Avenox once a week for one year along with physical therapy but after each injection and therapy, I was unable to do anything but rest or sleep. After the year was up I discontinued the treatment and was able to do my own hygiene, fix my bed each morning, drive my car to take my daughter to and from school and do my shopping with occasional help from people who would allow me to hold on to their shoulders and assist me up and down stairs. Since the discontinuation of the Interferon Avenox, I have been taking no other drugs but used multi-purpose mineral supplements along with other natural herbal agents such as seaweed and Goji juice, none of which has had the positive affects that I have experienced just recently with the Esperanza Homeopathic NeuroPeptide treatment. In May, 2006, I was introduced to the Peptide treatment through a Good Samaritan named Bill who told me about David Mundschenk and Peptide. Immediately I started the treatment which is now ongoing. I must say that I am very hopeful, I am feeling stronger, more alert and I am able to exercise early in the morning at 9:00 am and again between 12 noon and 1:00pm. My gait is more balanced and I am able to stay awake longer in the evenings. I am now walking with little or no help especially when I am making turns or curves (which I could not do prior to the Peptide). My intention is to continue the treatment as an aid in my complete recovery along with my total hope and trust in the Lord. I want to say thanks to Bill for introducing me to Dave, and for their assistance with the Peptide treatment. Thanks guys!
Paul Henry Thompson
Freeport, Bahamas.
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Multiple Sclerosis Testimonial 6:
PPMS Patient On Peptide For Four Years
My name is Raye Duthie, and I was diagnosed with MS in 2002 when I was having trouble with my right leg, and my foot was dragging, resulting in several falls. I heard about the peptide treatment in the spring of 2003, and we immediately made arrangements to travel to the Bahamas to meet David, and to see if the Esperanza Homeopathic NeuroPeptide could help me. Within 24 hours I was able to walk up stairs normally instead of one step at a time, and found that there was a steady improvement over the following 6 months. I have been taking the Esperanza Homeopathic NeuroPeptide for 4 years now, and although it is estimated that I have had Primary Progressive MS for around 10 years, I am able to live a fairly normal life although my right knee was damaged by the initial symptoms and does restrict my walking. If for any reason I have not taken my dose of Peptide, the deterioration in my mobility is very noticeable. Luckily I was diagnosed early in the progression, and was able to start the Peptide treatment before any of the more obvious symptoms occurred, and as yet I have had no speech problems. I did have eyesight problems early on but these have virtually disappeared. The Esperanza Homeopathic NeuroPeptide, coupled with a programme of diet and vitamins has significantly slowed the progression of the illness.
Raye Duthie
England.
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Multiple Sclerosis Testimonial 7:
I Can Confidently Say That I Have Experienced Only Benefits On Esperanza Homeopathic NeuroPeptide
"I am a 61 year old Englishman. I was dx'd with MS about 14 years ago by evoked potential and MRI scan. My only symptom, which came on over 10 or 15 years, was a slight weakness in my right ankle and slight foot drop. When first dx'd in a UK hospital, in 1992 (it took them a year to dx!!), they said they had no idea what causes MS and there was no cure or treatment. I bought a load of books and started a strict diet and then discovered that symptoms I hadn't even noticed disappeared, such as slight loss of balance, slight speech slur and some fatigue. I stayed on this diet until about 2004. (McDougall's I think) During that period I searched high and low for a cure, treatment, anything to no avail. I was refused interferon and any other treatment by the UK NHS. One day I found the Esperanza Homeopathic NeuroPeptide website while looking into "improved nerve conduction". I did have some doubt initially at the possible effectiveness of the Esperanza Homeopathic NeuroPeptide as I had read so much about "cures" and "treatments" and tried a few as well, that I was naturally sceptical. I eventually arranged to visit Esperanza Peptide's clinic in the Bahamas and in May 2004 took a week off, with my wife and made it a holiday as well, staying in Grand Bahama's top Hotel, The Westin at Our Lucaya ... a treat in itself! The treatment started as soon as I arrived with the clinic recording my progress before and after with a number of tests and videos. Immediately I had my first sublingual puff of the Esperanza Homeopathic NeuroPeptide, I felt a tingle through my right arm to my hand. I didn't even realise that I had a slight problem with my right hand but I have since discovered that I did! My walking and gait improved over the week after going onto the Peptide and it was the first real gain for me in 12 years. I stopped my specialised diet (which to be frank was a nuisance and was destroying my quality of life). My progress at first with the Esperanza Homeopathic NeuroPeptide was gradual although many very minor symptoms I was hardly aware of disappeared. I found that my dosing of the Peptide originally lasted 4 or 5 hours or so and then I felt the tingles and slight ache and loss of coordination and knew it was time for further dosing. I have now been on the Esperanza Homeopathic NeuroPeptide for over two years and have experienced no side effects whatsoever ... indeed I can confidently say that I have experienced only benefits. I have had no further worsening of symptoms nor any new symptoms develop in the time I have been on the Esperanza Homeopathic NeuroPeptide and my older symptoms are well controlled by using the Peptide (during my diet only period, I was getting some ). Although the Esperanza Homeopathic NeuroPeptide is not a cure it does seem to control my symptoms and thus far prevents them worsening and any new ones developing. It also makes me feel much better and I hardly notice the original slight leg problem which was my original symptom.
CC
England.
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Multiple Sclerosis Testimonial 9:
I Am Experiencing A Truly Amazing Quality Of Life Now With My Daily Esperanza Homeopathic NeuroPeptide Sublingual Spray Treatment
 My Name is Nelun Jayasuriya, now living in Australia I was a doctor working in Sri Lanka when I began to expect that I had MS. I started having symptoms of Multiple Sclerosis after the birth of my third child. Since MS is rare in the tropics it was never diagnosed in Sri Lanka. One of my colleagues jokingly called me a pain in the neck when I was trying to unravel the bizarre symptoms of MS. MS was diagnosed 12 years later in Australia. I had Betaferon, Avonex, and Copaxone injections for years for which I had side effects. I stopped these drugs in 2004. When I heard of the Esperanza Homeopathic NeuroPeptide I was really excited. Two members of my family being doctors there was no encouragement to go for the treatment. Only statistically significant results were believed after clinical trials. Statistically proven drugs did not help me. As I am unemployed, the cost of the Esperanza Homeopathic NeuroPeptide was beyond me. It was a stroke of luck that my brother wanted me to have a try. I had balance problems dizziness muscle pains problem in walking (dragging my right leg) as well as strength problems in my right arm. After I had the Esperanza Homeopathic NeuroPeptide sublingual spray everything changed so much so I broke the screen door in Gerry's house in the Bahamas under-estimating the strength in my right arm! I am very resistant to heat so can not go to my home country (Sri Lanka) much anymore. I am still affected by heat but managed to stay one month in Sri Lanka recently on holiday. I had two falls before I went to Bahamas but none since I returned. Even if my balance is affected I can correct myself , before I fall. I continue the exercises that I learned in The Bahamas, in the pool and on land and I take a healthy diet take vitamins do alternate therapies such as meditation, hypnotherapy and yoga. I used to get very fatigued quickly. Now my recovery time is much faster. I am learning to swim better and I am stronger. I am getting my life back slowly but very surely. My only regret is I can't convince everyone to take up this treatment as it works and I am living proof of that fact. I thank Gerry Gallagher (CEO of Esperanza) and David (who treated me in The Bahamas) and all who helped me from the bottom of my heart. I also have a very big thank you for my friend Suroo who accompanied me to Bahamas and helped me to keep a positive attitude and kept me happy throughout the trip ... Thank You All!
Nelun Jayasuriya
Australia
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Multiple Sclerosis Testimonial 10:
Esperanza Homeopathic Sublingual Spray has returned my sense of "Joy of Life".
 Like many people who have experienced a M.S diagnosis, for me it ended a history of being doggedly followed by mysterious symptoms that came and went. I thought I finally knew what was going on back in 1994, and I was relieved when my doctors were confident that in 2 years they would have a cure. I was misinformed, and I learned a lot in the years ahead, mostly from personal experiences. During the next twelve years I searched for and tried everything I could to return the intuitive sense of 'Joy of Life' I had previously always had. I had been a creative professional who dedicated my life to the idea that "if I intuitively looked for something long enough, it would somehow appear." This intuitive feeling NEVER failed me. That is, until shortly before my M.S. diagnosis at age 42 (in 1994), when I first noticed the intuitive feelings disappearing. At that time I asked one of my doctors why something I had tried seemed to help. He said, "it doesn't matter as long as it does no harm' if it works for you, IT WORKS!" All I can say is that Esperanza Homeopathic NeuroPeptide sublingual spray has returned my sense of "Joy of Life". IT REALLY WORKS! Allen Ainsworth, California, Feel free to visit our MS Warrior Website at www.mswarrior.org
UPDATE:
FIRST FULL YEAR ON THE ESPERANZA NEUROPEPTIDE AND IT HAS
BEEN A VERY ENCOURAGING YEAR!
It has been almost 1 year since I started dosing with Esperanza NeuroPeptide ... It has been an encouraging year! I first experienced M.S. symptoms at around age 15 (1967), without then knowing what the symptoms meant. It was not until I started limping around at age 42 that I was diagnosed as having M.S. (in 1994). This illustrates my point, which is that people with M.S. know a lot more about living with it from the inside/out, than anybody else! I feel Esperanza NeuroPeptide has enabled my body to transmit impulses across damaged nerves. To what extent my body is able to recover neuromuscular connections remains to be seen. So, thank you for developing this treatment. I assure you that I am along for the ride for the duration!
FURTHER UPDATE
Due to the miracle for me of Esperanza NeuroPeptide, my energy has greatly improved! I am currently rebuilding my creative life, centered around part-time creative writing. Currently I have rewritten my website explaining the non-profit M.S. Organization I have developed. I am presently preparing a step-outline for my story (a book/screenplay) which I hope to sell to a publisher.
FURTHER UPDATE
AFTER A YEAR AND A HALF ON ESPERANZA NEUROPEPTIDE UPDATE - "MAKING GREAT STRIDES"
A brief note to let you know that from my point of view here in San Francisco (S.F.), all the Esperanza Public Relations pieces issued that bear your signature keep getting more on target!
Keep up the good work, and every day I thank my lucky stars that I found the Esperanza Homeopathic NeuroPeptide sublingual spray treatment for my M.S..
I can see you are fighting an uphill P.R. battle, against the established vested interests here in the U.S.A. from the $3.5 billion M.S. treatment industry.
It appears, from my point of view in S.F., that you are making great strides!
Best Wishes, and keep up the good work!
Allen Ainsworth
San Francisco, USA
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Multiple Sclerosis Testimonial 12:
I Am Beating MS With The Esperanza Peptide Sublingual Spray
 I have had MS since 1994. In 2002 my health really began to decline. I had to use a walker or wheelchair to get where I wanted to go. I decided to look for Alternative Medicine for help. I had received an e-mail from Gerry Gallagher (the CEO of Esperanza Peptide) about a peptide spray and treatment for MS being offered in the Bahamas called the Esperanza Homeopathic NeuroPeptide . I researched their information and testimonials and decided I HAD to go and find out for myself if it could help me. I can only say great thing about going to the Bahamas and starting the peptide spray. Because of drop foot in my right leg and stiffness in my neck due to the auto accident I had not driven in 2 ' years. After starting peptide spray and doing Physical Therapy I was able to get my Drivers License back on 9-28-06. 50 days after starting peptide spray. I also don't use my walker anymore, just a cane. I have my independence back and I thank God everyday. I went to the Bahamas 8-8 thru 8-11-06. David Mundschenk (Esperanza Research Foundation's Scientific Director) evaluated me and saw how I had no balance at all. He sat me down and gave me 3 sprays under my tongue, waited 5 minutes and administered another 3 sprays. After 5 minutes again he asked me to stand and hold my balance. I held my balance for 2 1/2minutes 30 seconds with my eyes closed. Amazing. Kellie Mannen, a Bio Medical Engineer is one of my best friend's who helped me get to the Bahamas claimed that if she had not seen the results with her own eyes she never would have believed how quickly my balance had improved. David taught me exercises to do in the swimming pool to get my right leg working again and stronger. After 2 days of working out in the gym and the swimming pool, 2 hours every day. I felt confident enough to go Parasailing. I needed help walking through the sand and was caught on the landing in the boat. Bahamas was absolutely beautiful when you are up in the air being pulled by a boat ... and getting your life back with the Esperanza peptide spray. I am doing Physical Therapy 2 days a week and will start using the Power Plate. I believe with peptide spray and hard work we can improve our lives. I am beating MS and a bad Spine Injury; it just takes hard work, determination and faith. MS brings us all down even if you were superman it will. The Esperanza Homeopathic NeuroPeptide sublingual spray helps our brain command our nerves to walk or move our arms etc. The opportunity is there, P. T. and the Esperanza Homeopathic NeuroPeptide sublingual spray open the door for you to have a manageable life again. If you work hard you can improve your life. I am only 44 and was refusing to get worse. I thank God and all the people at Esperanza Research Foundation for giving me the opportunity to get stronger and regain my self confidence plus making my life more manageable.
Cheri Bacon
Illinois, USA
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Multiple Sclerosis Testimonial 13:
I feel better and have more energy with Esperanza Peptide!
In 1990, at the age of 26 and only 6 months after my wedding, I was diagnosed with MS (secondary progressive form). One year later I was stuck in a wheel chair. Since then my condition has slowly stabilized however none of the traditional treatments can be applied for the secondary form of MS. In the Summer of 2006, I heard about Esperanza Peptide sublingual spray therapy and rapidly got my act together and in November 2006, I went to Esperanza Peptide's Bahamas Clinic for the Esperanza Homeopathic NeuroPeptide sublingual treatment. The immediate result was not the immediate miracle I was hoping for; BUT soon enough I experienced the following improvements:
- my speech became better,
- the tremors of my hands lessen,
- my leg's blood circulation got better and thus thee oedema diminished.
Since then, I have been rehabilitating my brain and my body to do their job again with the help of renewed connectivity as a result of the Esperanza Homeopathic NeuroPeptide sublingual spray. I also exercise daily in my home gym and with the help of my physio (2 visits per week) I have been:
- working out my stomach muscles,
- walking with the help of parallel bars
- doing exercises with the "Powerplate" device which allows me to activate the muscles by stretching them.
I feel better and have much more energy to cope with my everyday activities. Please do not hesitate to consider the Esperanza Homeopathic NeuroPeptide sublingual treatment as I did!
Frederique Tardif
Canada
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Multiple Sclerosis Testimonial 14:
No miracles as yet but a few interesting developments have occurred :
- The right hand is much stronger and not so "claw like". Able to grip better but there is some way to go before a semblance of normal use is achieved.
- With husband Rex's help Anita can stand for up to 1 minute without the legs buckling. Rex has to hold Anita all the time but at least it is some small progress.
- The bowel problem is not so acute and seems to be more controlled in that warning is given
- Ability to speak clearly again is perhaps the most significant development. Before treatment she tended to slur some words, now her speech is very clear, precise and logical.
- Generally speaking she seems to be more cheerful but is not getting carried away. It will be very interesting to see if other improvements take place in the period ahead.
Anita Stone
Derbyshire
England
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Multiple Sclerosis Testimonial 15:
A genuine medication that has and will continue to give me a new lease on life!
 My name is Karen Kristensen. I live in Mt.Morelamd, Durban. I have Multiple Sclerosis. I was diagnosed in June 2003, although I have had the symptoms for many years. I am 46 years old, and am in the relapsing /remitting stage. My most debilitating symptoms are difficulty in walking, and chronic fatigue. I have been on a fairly effective range of medication which has helped to a degree. I have just recently had a relapse, and was treated with IV Cortisone for 5 days. This relapse has been particularly difficult, and my walking ability has deteriorated and my balance has been affected. Have also had increased fatigue, and the sensation of a tight band around my Thoracic area, making it difficult to breath.
Dr Gardner has just returned from the Bahamas, where he has been trained to administer Esperanza Peptide treatment. I came up to Ixopo on Sunday and was prepared for my first Peptide treatment. A series of tests were done and at 2.30pm, I received my first treatment. within approximately 20 minutes, I felt a sensation of weights being removed from my legs, and an amazing sensation of being able to breathe with ease. 1 hour later I got up to go to the toilet and to my absolute amazement was able to walk with much greater ease. I also noticed that I was able to pass urine easily, as had been experiencing bladder retention. Dr Gardner then requested that I repeat the entire test. Well, the results were incredible. My walking and my balance has improved by 50%. I then attempted to walk up and down a flight of stairs, and was able to do so with ease. I felt as though my body was in water, light and buoyant. We all witnessed a miracle. Truly Esperanza Peptide has been the most incredible blessing, and I give all thanks and glory to God. I am to have my second treatment today, and can't wait to experience the results. I want to share this wonderful news with all MS sufferers in South Africa, and pray that many people will be greatly blessed, and enjoy this wonderful, genuine medication that has and will continue to give me a new lease of life. Thank you Esperanza Peptide!!!
UPDATE
AFTER 1 YEAR ON THE ESPERANZA NEUROPEPTIDE
I am still amazed at the incredible improvement that the Esperanza Neuropeptide has made and I really love to share that news with everyone I can.
Hi Everyone at Esperanza, Just a quick update for you with regards my progress on the Esperanza Peptide. I shall draft a full updated testimonial with photo, and email this to you soon. I just wanted to let you know that I am still amazed, as there are days when I wake up with difficulty to walk. I take my Esperanza, and within 20mins, I can walk with ease. I am still able to stand, eyes closed without falling, and I am leading a pretty full life, working full day, and fetching and taking care of my Grandson in the afternoons, as well as cooking the evening meal for my husband and children. I do watch my diet and exercise, and this does help. I am still amazed at the incredible improvement that the Esperanza Neuropeptide has made and I really love to share that news with everyone I can.
FURTHER UPDATE:
AFTER A YEAR AND A HALF ON THE ESPERANZA NEUROPEPTIDE
My Stability Remains Excellent
My name is Karen Kristensen, and I was blessed in May 2007, by experiencing the wonderful benefits of Esperanza NeuroPeptide. I was the first MS patient in South Africa to receive this treatment. It is now almost a year and a half that I have been on Esperanza, and I can honestly say that I have not deteriorated , and have not had one cortisone treatment in hospital. Prior to this, I had at least two hospital visits a year. Without realizing it, my day to day living has become fairly normal, in that I am now able to work for at least 5 hours a day, collect my Grandson from school and take care of him, as well as prepare the evening meal for the rest of the family. My stability has remained excellent, and only when I am tired, does my walking become difficult, and even then , I walk without aid. My friends and family are always amazed at how well I look, and find it hard to believe that I have MS. I do stress the fact that I remain on a strict healthy diet, of mostly raw fresh foods, and take all the recommended supplements, and I am working on an exercise program. Grateful thanks to Dr. Ian Gardner, and to all the Doctors, Practitioners and Staff at Esperanza.
Karen Kristensen
Durban, South Africa
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Multiple Sclerosis Testimonial 16:
It has been truly amazing journey for me and I have been spreading the word!
 I was diagnosed with Relapsing/Remitting MS in 1992 after the birth of my third daughter although I first went to my GP 3 years before that as I had suspected it then.
I first read about Esperanza Peptide in New Pathways Magazine a few months ago but at that time it was only available in the Bahamas. I was delighted when I realised that Jan de Vries was setting up a clinic in Scotland to treat patients there so I made contact with Gerry Gallagher (Esperanza Peptide CEO) and arranged for an appointment.
I was treated in Troon on 20th June. I live in Aberdeen so it was only a 3 hour car journey to Jan de Vries' Clinic in Troon. I was delighted that David Mundschenk and Gerry Gallagher were in attendance at my treatment. There were also another 3 MS patients being treated along with me.
We were asked to perform a series of tasks before we were sprayed with the peptide. This was to test for fine motor skills, cognitive ability, upper body strength, balance and ability to walk with or without aids. The various tests were videoed and timed. After we had all completed the tests we each received 3 sprays under the tongue of the peptide and after 5 minutes we received another 3 sprays. We waited for 15 minutes and then went to have something to eat. After an hour we came back to the treatment room and performed the same tasks ' writing 3 sentences about ourselves, testing for balance and were videoed walking and the speed was noted. All participants did better in all the tests. My husband helped with timing the walks and was truly amazed to see the difference from before and after in all patients.
The strength in my left arm was double what it had been prior to the peptide, my balance had improved from being able to stand with eyes closed for 23 seconds to 3 minutes and I was able to walk faster with taking longer steps to cover the same distance. The results were truly amazing and if I had not been there to witness it for myself I would not have believed it ' it was so inspiring to witness the friends I had made getting function back and now able to do things that they had been unable to do for such a long time!!
I came back to Aberdeen and have definitely noticed an improvement in a lot of things. I don't tend to get so fatigued in the afternoons and after I left work on Friday I had a real spring in my step and was definitely walking much faster. My balance also seems to be so much better. People at work have commented on how well I look now.
It was a truly amazing journey for me and I have been spreading the word to everybody I know who has MS or knows of somebody who has MS. David and Gerry were truly dedicated to treating us all and were so knowledgeable about the product and able to answer the many questions we had.
UPDATE:
Just to give you an update since my initial treatment on the Esperanza NeuroPeptide in June 2007. I had a fantastic day on Friday - the best I had felt in a long time. I had a real spring in my step and was walking really well and really fast. I have had a lot of good days now and seem to be using my calf muscles more when I am walking. I am also taking supplements and have started on the gluten-free diet so I think this will really go a long way to improving my situation.
Janice Kirkbride
Scotland
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Multiple Sclerosis Testimonial 17:
I am so grateful! May I go from strength to strength, little by little, in the knowledge that all is not lost! Viva l'Esperanza!!
Well, what can I say!! MS is a disease that is progressive and everywhere I turned the medical profession said, "Sorry, we have no cure or even an 'arresting' medication. We cannot help you, but we can try to make your life more bearable". This, to me, is like a red rag to a bull. I find the disease extremely hard to live with and it has made dramatic inroads into every aspect of my life.
I am now wheelchair bound and was feeling that the prognosis was very bleak indeed. The worst symptom was the rapid deterioration in my speech. It cut me off from the world, and talking on the phone was a nightmare. I have so much to say to everyone and no way of being able to express myself. Very recently I have become a grandma for the first time, and the joy was replaced by a feeling of frustration at not being able to do my 'job' properly.
All this makes it sound as though my cup is always 'half-empty'. Now it is 'half-full' due to the Esperanza Peptide treatment. My despair has now been replaced with hope. The change in my mental outlook has been dramatic and I now look forward with anticipation of further improvement.
I read about the treatment and came to the conclusion "Nothing ventured, nothing gained". It seemed as though everyone was saying, "You're on your own". However, I thought that I would just try to make sure. I left a message on the email address of someone who had already been over to the Bahamas, and, bless her, she rang me back! That tipped the balance and I decided that this was for me. The prospect of going over to the West Indies was daunting and with relief I found out from Gerry Gallagher (CEO) that there was the possibility of treatment in Scotland, in Troon. Whoopie!!
The whole set of arrangements took about two months and I couldn't wait. I was extremely lucky to have David Mundschenk, the Scientific Director of Esperanza in the Bahamas, administer the spray on 20th June. He is such a lovely man who made me very relaxed about it all. I got the feeling that they both care very much about MS sufferers.
The effects on some parts of my body were almost immediate, but my lack of muscle tone does hamper me somewhat. (I will have to exercise to improve this). Within five minutes there was a distinct lessening of the blurring in my speech. Within an hour (and a second dose of peptide) my balance, which was non-existent, made a miraculous improvement so that I could stand unaided, albeit for only a few seconds. The strength of my hands and arms increased somewhat dramatically and I had better movement in them.
Oh, I am grateful! May I go from strength to strength, little by little, in the knowledge that all is not lost. Viva l'Esperanza!!
Barbara Bentley
Oxfordshire, England
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Multiple Sclerosis Testimonial 18:
I have absolutely no doubts that the Esperanza NeuroPeptide treatment is the right thing for my MS.
My name is Trevor Crabtree from England. It is seven years since I was diagnosed with PPMS. Ironically, my diagnosis was approximately six months after my sister who is 12 months younger than I was also diagnosed with MS herself. I am now 60.
I had never even heard of MS up to that point, but I certainly know about it now ... and what it can do to the body. I also see that it is different but similar in many ways! No two individuals seem to be exactly the same with the disease, but similar symptoms do prevail such as fatigue, balance, no feeling of well being, pain, eyesight and speech problems etc. Each MS sufferer is thus the same in that we have the disease, but with small or big differences as individual sufferers.
I chose from the beginning to try and pursue the things I thought were going to help my sister and myself. I have to say that from that day until now what helped me did not necessarily help her!
What is the guideline or data that we can use as a measure to see how bad we have become and how any treatments are improving our conditions other than a daily diary when we really do not want to be reminded? Well, some of us will become bad almost overnight while others it slowly creeps forward. I never kept a record I really do not think I wanted to be reminded of how bad it was becoming! I just kept hoping for something to happen that would treat me and all would be a bad experience then behind me and I would be well and a better person because I really did start to appreciate what I always took for granted,my health! I have tried Aimspro, stemcells (cord and bone marrow), I have changed my diet and I exercise, I have tried energy balancing, reflexology and even a healer and everything I honestly believe helped in some way or other but I still have MS!
I recently was treated in The Bahamas with the Esperanza NeuroPeptide treatment in April of this year and met some genuine people and was treated. I have indeed noticed a change within my daily routine and because my MS is primarily "within", great discomfort, fatigue, frustration, back ache and the well being feeling at zero are my major symptoms, no one really notices much. I am lucky that I can continue in my work in the business I have built up over 35 years but I have to be always (while in that work mode environment) aware that no one will be making allowances for my disease! Leg drag is seen and passed of as old age and balance is something I try hard to control but is ... old age also and my temperament or short fuse is perceived as ...old age and my fatigue a constant inner companion.
After undergoing the Esperanza NeuroPeptide treatment I am happy to say that my walking is now much better I do not have to think and judge as to "do I really want to walk over there" the same as before but I still have my limitation to consider but progress is certainly there! My balance is much better without doubt but I still do have a little wobble from time to time! Spasms first thing in the morning are less but they still do greet me but much less and my feeling of well being is without question improved! It is another treatment unfortunately costing money but most things do! It is something that will help some and maybe not others but it is at least something that is our choice to take and the way I feel right now is it is a definite reason to have hope .. that's a treatment in itself!
I have absolutely no doubts it was the right thing to have done. I am arranging for my sister to start soon and I am hoping that this will give her a chance to start to also have hope! Maybe we will both be around much fitter, healthier, positive and ready for the cure future cure for MS! That's my plan and most of all my choice!
Trevor Crabtree, England
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Multiple Sclerosis Testimonial 21:
The whole thing has been the most amazing experience and I am so excited to be among the lucky few who have been treated in the UK to date!
 Thank you so much for seeing Graham Louch and myself for treatment on Tuesday 19th June. This is the email I have sent to all my friends and fellow MS sufferers who want to know about the Esperanza Peptide! Just back from Troon and meeting the amazing David Mundschenk and Gerry Gallagher from Esperanza Peptide, who are bringing the treatment to the UK. The peptide results were in a word brilliant! My worst fear was that it might not work on me, but after being dosed with the spray all tests performed showed an improvement in every area, especially in balance and strength. It was very strange, as Graham Louch (who was treated with me) and I felt so tired after the treatment ' and the next day too! Which was quite frightening as I expected to be bouncing around! But that was due to using muscles and doing things we hadn't done in such a long time. However, today ' which is my 3rd day on the treatment, I feel absolutely fantastic and much more energy and zip! I was also pleased to meet another patients due to see David and Gerry named Janice Kirkbride from Aberdeen (who I had been emailing before we got for treatment in Troon) came to our hotel the same day as our appointment with her husband and asked us how we were feeling. David (my husband), who is an osteopath came along and witnessed first-hand my treatment given to Graham and I and he was thoroughly impressed by all that he saw, as he understands all the science behind the treatments and could explain it to Graham and I later! He said it was so good and refreshing to meet people like David and Gerry who are not trying to make money out of us MS'ers by selling all kinds of supplements and special gadgets except for the peptide, which we had already paid for, and we got a whole years supply when we left! They are really caring people and it comes through in the way they treat you and explain what they are doing. On day 3 I was seeing small improvement all the time, I can now walk along the corridor carrying 2 cups of tea without spilling half the contents on route!! - I must start keeping the dairy, which David and Gerry told us to do, in case I forget how much improvement I am making everyday!! Still not good at the leg crossing with the left leg ' its good after dosing but wears out as the day goes on! I'm still lifting my leg into the car when I get in, but my balance and walking gait are SO MUCH better and my left foot has stopped slapping when I walk! I went out to dinner this evening in sleeveless T-shirt and when it got cool I ended up lending my cardigan to my friend, as I was so warm, including my usually freezing cold fingers! This is absolutely a first for me as I am always cold including my feet, which are now warm ' this has too be due to the peptide! I wrote my Mum a thank you card on first day of treatment, as she paid for me and my writing was much smaller, I filled 2 sides of the card with about 20 lines of neat writing instead of my usual 8 lines of flamboyant scrawl, I hadn't realised I had a problem with my writing until then!! The whole thing has been the most amazing experience and I am so excited to be among the lucky few who have been treated in the UK to date !!!!!
UPDATE:
LDN/PEPTIDE COMBINATION UPDATE
I started the Esperanza peptide in June 2007. Gerry Gallagher and David Mundschenk recommended that I stop taking the LDN (Low Dose Naltrexone) as soon as I started the peptide. I had been on the LDN for 18 months, during which time I found I had a marked increase in energy.
I experienced a drop in my energy after I started taking the Esperanza peptide, which I found frustrating, this has lasted for the 3 months I have been on it. So I thought I would experiment and try a combination of LDN and the peptide to see if I regained my previous energy.
The results after 10 days on LDN with the peptide were as follows:
From Day 1 of taking LDN I did actually have an increase in energy, which at first I thought was brilliant! However, by Day 10, the positive results from the peptide started to decrease as a result of the LDN, I found I had a decrease in leg lifting power, I could no longer cross my weaker leg over the stronger, a return of stiffness in my body when standing up from sitting, or getting out of bed in the morning. Also I had a return of my restless leg symptoms and calf muscle cramp.
Therefore I have decided that to mix the two treatments causes me to lose more than the many positives that I have gained on the peptide. To me the energy is well outweighed by the loss of function that I experience from the peptide and I have therefore decided to stop taking the LDN and continuing on the peptide alone.
19 Sept 2007
Love and best wishes,
"Charlie"
Charlotte Sercombe
England
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Multiple Sclerosis Testimonial 22:
I deliberately havent been in touch as I wanted to let the euphoria calm down and then look at myself objectively.
 I would like to thank Gerry Gallagher and David Mundschenk for everything they have done for us and to say how good it was to meet you both ... so, thank you so much !!
As regards to my progress with the peptide, its been six days now and im a little disappointed I can't run the 100m yet (joking of course)! However:
- My balance has been terrific
- I'm crossing my legs without even thinking about it
- I have greater strength to my weaker right hand side
- I no longer use my stick walking around the house
- I find myself laughing sometimes as im doing things without thinking
- Stepping into the shower not dragging my right foot over the threshold
- Getting into the car without lifting my legs
- My best times are in the mornings as I can lift my feet as I walk and really feel the progress made
- Later in the day I do feel physically tired (granted because I am using muscels and doing things I haven't done in years) and my legs return to being heavy and I drag my feet again
All the above said, I am doing my daily exercises as advised and my vibe trainer every other day so I hope I will be able to increase my muscle stamina and enjoy longer times of walking well over greater distances.
I know a friend with MS has been in touch and is coming to see you but charlotte and I are going to the Portsmouth ms centre on wednesday to spread the word so beware!
On Saturday I went to the theatre and had front row circle seats, there was no lift to the circle so after a 400 yard walk from the car I faced three flights of stairs going up a landing area 1/2 flight going down another 1/2 flight going up and a full flight going down to get to the seat (great show ) then repeated to go home I was really tired at the end but managed it all and went out to dinner afterwards following a very short rest!
Theres my proof peptide is working for me I just want to continue improving so I can run that 100m! ... Thank you all so much ... this gives me hope for the future.
Yours,
Graham Louch
England
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Multiple Sclerosis Testimonial 23:
I raise my glass of fruit juice to you and the cobra!
As far as I'm concerned the spray is definitely doing something! Perhaps not a miracle of Biblical proportions but the pain has gone from my legs even though my left leg remains a bit weak. I also seem to have slightly more feeling in my left hand but this varies. Fatigue is better and I have started taking some short walks which I couldn't do previously. I tend to find that I am now watering the greenhouse and this does tire me out, this also applies to my physiotherapy, but perhaps I'm doing too much too soon. My wife tested my balance this morning and got bored after 3 min (I could only stand for a few seconds in Troon)! My daughter has noticed that my voice is much stronger on the telephone and that I sound much more positive. Thank you again for your hard work in tackling this terrible disease and for giving me hope. After 20 days of spraying I raise my glass of fruit juice to you and the cobra!
UPDATE:
Update from Keith George after his treatment in June of 2007.
"My physiotherapist was completely baffled"
Keith George here with an update to let you know that I'm feeling a lot better since my treatment in June of 2007. My left leg is still a bit weak but I'm exercising daily in the hope that it will get stronger. My physiotherapist was completely baffled when she did her last assessment as there was so much improvement in my strength and balance after the Esperanza NeuroPeptide treatment!
FURTHER UPDATE:
"Since starting the treatment the quality of my life has improved greatly"
I have only positive comments to make! Since starting treatment in June 2007 noticeable progress has been made in all areas with a marked increase in self esteem and confidence. My wife remarked the other day that the old Keith had returned! Members of the family often more aware of certain improvements!
BALANCE: Much improved although left leg still the weaker of the two.
MOTOR FUNCTION: Able to do the following (that i previously could not do) ... lift and cross bad leg over good leg, lift both knees up to 90 degrees, rub back of calf using opposite leg , step in and out of bath. WALKING ... a gradual improvement, increasing distance daily and today managed 400 metres without using a stick!! Left foot was tired and dragging by the time I arrived back home after the 400 metres and was I glad to reach home - but what an achievement! Also able to read in bed without aching arms.
ENERGY LEVELS: A marked improvement but I have to be careful that I pace myself and not to get overtired and fatigued. It's important to know one's limitations. I still find it tiring to carry certain objects.
PAIN: Far less pain in legs and calves after taking the NeuroPeptide, but get burning sensation now and again in calves, a massage with Chinese liniment usually eases this.
BLADDER FUNCTION: Much better despite great urgency at times!
I do daily physio exercises and take supplements. I also try to stick to a sensible healthy gluten free, dairy free diet with no alcohol.
In short, since starting the treatment the quality of my life has improved greatly and I find that I am able to socialise much more. I actually went to the theatre last week with no ill effects the following day.
I would advise anyone contemplating starting the treatment to persevere as some symptoms take more time to improve than others.It has also been worthwhile keeping a daily journal. After all it is only just over three months since I took the first spray.I look forward to continued improvement and would appreciate any additional advice and guidance to help me maximize the wonderful results that I am experiencing from the Esperanza treatment.
Keith George
Keith the Welshman!
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Multiple Sclerosis Testimonial 24:
 Remarkable! Amazing! Wonderful!
I recently had the Esperanza Neuropeptide treatment for my MS at the Troon clinic in Scotland and the treatment has impacted my life with incredible results!
I found out that I had MS in 1981 and have lived with many unpleasant, uncomfortable, life shattering and debilitating symptoms since then ... but that is unfortunately what MS is all about!
I decided to go for the Esperanza NeuroPeptide treatment after reading about it in New Pathways Magazine and I will honestly admit that I was very sceptical at first! However, I will say now that I really can't believe what I am experiencing ... it is truly remarkable, amazing and wonderful! My whole body loves the signals that are getting transferred through so easily now. It is so strange to feel and react to feelings as they were initially intended and not blocked by the MS! I am still basically in a very pleasant state of disbelief and quite frankly ... I forgot that I could feel this well again! The Esperanza Neuropeptide spray is liquid magic to my body!
I now look forward to physiotherapy and it will now be more useful than ever! The Esperanza treatment may not be the cure for my MS but what it offers me now is unimaginable relief from what I have experienced over the past 26 years! I say again ... Remarkable! Amazing! Wonderful!
UPDATE:
AMAZED ... actually BLOWN AWAY!
I just wanted to let you know that after a slow start, my Esperanza peptide has become THE MOST IMPORTANT thing in my life over the past 2 months! For me, it's the fluidity of movement. no stiffness, no pain. I am getting on fine now, progressing and still AMAZED, actually BLOWN AWAY by the treatment and what it has done for me!
Thank you so much!
FURTHER UPDATE:
Approaching a year on the Esperanza Neuropeptide and what more can I say ... YES, I am progressing and all is good with Esperanza !!
All is well on the Esperanza NeuroPeptide as well as the Esperanza vitamin D3 is wonderful, really makes a difference!
Everything is good! An amazing thing happened for me 3 days ago, suddenly I was able to write again ... exciting, and another small physical but very positive thing happening because of the Esperanza NeuroPeptide!
The whole Esperanza experience feels great.
I live in the Northern Hemisphere where I feel the climate and lack of sunlight is against me, by now I rely totally on my Esperanza NeuroPeptide and Esperanza D3 Vitamins to deal with my MS and I am getting great response!
People really don't realise the Esperanza special qualities and what it has done for so many like myself ... I could go on and on regarding my treatment as I am getting ongoing benefit from the Esperanza NeuroPeptide treatment and want to tell anyone with MS to seriously look into and to consider this wonderful treatment, attention and follow-up!
In September I will have been on the Esperanza NeuroPeptide treatment for an entire year and I can honestly say that I am emphatically pleased with Esperanza and all that they have done for me!
What more can I say ... YES, I'm progressing and it's all good with Esperanza !!
Julie Boocock
England
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Multiple Sclerosis Testimonial 26:
Improvement since I began taking the Esperanza NeuroPeptide
This is to let you know that there is an improvement regarding the tremor of my hands and general condition since I began taking the Esperanza NeuroPeptide.
* I have noticed that my spasticity has substantially been reduced.
* Spasticity goes away when the weather is not hot.
* Speech is back to normal.
* Hands are better.
* Also do reflexology 3 times a week.
Costas Styliano
Nicosia
Cyprus
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Multiple Sclerosis Testimonial 27:
OSTEOPATHIC DOCTOR SUBMITS A REVIEW OF
ESPERANZA NEUROPEPTIDE PATIENT CHARLOTTE
Since Charlotte's first dose of the neuropeptide in Troon on 19th June 2007, I have noticed a strengthening of the left hip flexors along with an improved dorsi-flexion of her left foot. Charlotte has herself reported a more balanced leg kick when swimming front crawl.
This has led to an improved balance in her low thoracic, upper lumber para-spinal muscle balance. Note that before she was using her right para-spinal muscle group to help lift her left leg mechanically. I have always made sure that her low thoracic/upper lumbar spines have been kept mobile. Recently there has been less of a need for me to treat these areas.
Charlotte's cranio-sacral rhythm has strengthened in depth and vitality and it is not diminished even when she feels tired. The persistent sub-occipital (upper neck) pressure is still evident. But I know she is doing more than before and the resultant tiredness reflects in an over-strain of this area. I find that all MS sufferers are prone to pressure in the base of the spine and benefit from having it decompressed on a regular basis.
Charlotte is able to cross her left leg over her right when sitting but not repeatedly. She now moves in a more positive fashion from resting and walks with her left heel down when not tired. She still tires late in the day, but her horizons are farther i.e. she is doing more than she was. If she strays from her diet she still suffers the following day, but a recent short course of antibiotics did not appear to affect her adversely, this is unusual for MS sufferers in my experience.
In summary the situation so far is a case of fluctuation in symptom pattern with an overall slow improvement. Charlotte's MS is secondary progressive and I wonder how much of her improvement is stabilised by my treatment. I.e. The changes in her musculo-orthopaedic balance are kept in check by the releasing of spinal restrictions as they occur. I check her on a weekly basis and will update her review periodically.
Charlotte's MS is secondary progressive multiple sclerosis with left side weakness and balance problems, she is able to walk unaided. She also follows the Roger McDougall diet plan that is endorsed by Jan de Vries.
David Sercombe BsC Hons (Ost)
Doctor of Osteopathy
Member of the Register of Osteopaths.
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Multiple Sclerosis Testimonial 29:
I am improving and my aim is to walk one day and do the lambrini dance!
 Hi, I just wanted to send on a few words of my progress on my recent Esperanza treatment. I had just came out of hospital suffering from a serious MS attack right before going on the Esperanza NeuroPeptide.
I came out of hospital with no balance, not being able to stand and my head felt like it was going to explode. The hospital decided no treatment was to be given to me, not even steroids which I asked for ... but they refused! When I came home from the hospital I needed 2 carers in the morning and 2 at night to hoist me in & out of bed. I decided to contact Gerry Gallagher and the Esperanza treatment and Gerry booked me in for treatment in July with the Esperanza NeuroPeptide treatment. NOW, I am delighted to give you my update and to report that I can now stand and my balance is 50 to 75% better! My head now feels so much better and I have only 1 carer in the morning and 1 at night now! All of this thanks to the Esperanza NeuroPeptide treatment.
I strongly urge anyone with MS to seriously consider the Esperanza treatment! In my case, things are slowly improving, my aim is to walk one day and do the lambrini dance ...
THANK YOU SO MUCH ESPERANZA!
UPDATE:
Still doing well and I strongly believe that the Esperanza NeuroPeptide is helping as it gives me the weapons to fight MS. I don't want to go back to the way I was before going on the Esperanza treatment!
Again, thank you so much Esperanza Peptide!
Michael Hughes
England
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Multiple Sclerosis Testimonial 30:
AFTER ABOUT SIX WEEKS I WAS ABLE TO TAKE A FEW STEPS - I WAS UNABLE TO DO THIS PRIOR TO THE ESPERANZA NEUROPEPTIDE TREATMENT
I have felt generally better since my Esperanza NeuroPeptide treatement on June 21, 2007. I would like to update you with my positives as well as negatives as I see them.
POSITIVES:-
- Generally feeling better!
- Waterworks and bladder control much improved.
- Circulation to my feet is better giving them a human look (eliminating dark discolouration)!
- I do not suffer from fatigue as I used to!
- After about 6 weeks I was able to take a few steps, assisted by my husband and a table - I was definately unable to do this prior to the Esperanza treatment!
NEGATIVES:-
- My feet are often swollen.
- Although able to take steps as noted above, progress is slow, which is disappointing.
UPDATE:
UPDATE REPORT AFTER 6 MONTHS ON THE ESPERANZA NEUROPEPTIDE
I CONTINUE TO IMPROVE!
Hi, 3 update comments
- bladder is retaining improvement.
- circulation continues to improve.
- my overall "feel good" factor seems to be dependent on 2 extra sprays at the end of the afternoon/early evening.
I have great faith in the Esperanza NeuroPeptpide treatment and I remain optimistic!
Regards,
Pam Adams
England
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Multiple Sclerosis Testimonial 31:
The Esperanza NeuroPeptide has brought back HOPE to our lives!
My husband and I came up to Troon for the Esperanza NeuroPeptide treatment on the 25th July. When we came home my husband was disappointed that he could not walk across the room, but after not walking for 3 to 4 years it would be like expecting a miracle. However, like you have said everyone is different and the wonderful thing is that his balance has improved, he can now sit up on the bed on his own without falling back. Also, we have not had to use a hoist since a week after we came back. With a bit of help from me he can transfer from wheelchair to stair rider and on to the bed, he has not done that for 18 months, so his standing has definitely improved. Also he has had a wet shave which he could not do but the most significant change is in his energy levels, he is nowhere near as fatigued as he was and we think this has increased by 75% already and he also feels much more with it.
We are both delighted and are so pleased that we have had the opportunity to try the peptide which has brought hope back to our life.
UPDATE:
Hope you had a good Christmas and a very happy New Year to you! You cannot imagine what a difference meeting you had made to our lives.
Regards,
Ann & John (William) Down
England
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Multiple Sclerosis Testimonial 32:
FATIGUE IS IMPROVED, WALKING IS PROGRESSING SPORADICALLY
 Fatigue is improved walking is progressing sporadically.
My outlook is so much more positive now and my "head fog" is much improved since the Esperanza treatment.
My balance is much improved since the treatment and is still good!
I am away in France until April and would like to arrange for another years supply of the peptide. Can you please advise and what the cost will be?
UPDATE
LOOKING FORWARD TO YEAR TWO ON ESPERANZA NEUROPEPTIDE
In general my co-ordination is better particularly with my hands and I can get to grips with a knife and fork much better, so at least I can enjoy the French cuisine here in the South of France, within moderation of course. Since starting with the Peptide my outlook is much brighter and even if I can't run a marathon my foot doesn't drop as dramatically as before and my balance is much improved. I'm hoping that through the springtime without the exertion of a double move (from the north of Scotland, to Edinburgh and then on to the South of France), I can consolidate this progress and I very much look forward to year 2 of my Esperanza NeuroPeptide spray.
Wishing you a Very Happy New Year!
Regards,
Izabela Eliasinska
South Of France
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Multiple Sclerosis Testimonial 33:
MY PROGRESS HAS BEEN PRETTY GOOD SINCE MY ESPERANZA NEUROPEPTIDE TREATMENT
My progress has been pretty good since my Esperanza NeuroPeptide treatment. Before my treatment my speech was very bad indeed and almost inaudible. My speech is now coming back very nicely. Many people have said (on hearing me after the treatment) how much clearer I am and easier to understand.
My other main problem prior to the treatment was that I could barely stand without holding onto something and my body was fixed and rigid ... I was like a "wooden pole". Any movement and I would fall as I had no balance or mobility! Now (after the treatment) I find that I can stand much easier and I am delighted that I can move my arms, rotate my trunk and I have mobility in my body ... I am no longer that "wooden pole" and I have balance again. I cannot yet stand on one leg, but I will accomplish that in due course I am sure if that!
I also had bad bladder problems and I now find my bladder functioning much better. I feel that the overall strength return in my body after the treatment has also brought back strength to my bladder control. I used to have to relieve my bladder every hour and now I am happy to say that it is every 4 hours or so and that is a great relief to me!
My right hand was dexterity has improved a bit but it has only been going on 3 months and I look forward to getting more mobility in my hands as well.
In all I could not ask for more!
I hope you are doing well!
Regards,
Marc Eaton
Portsmouth
England
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Multiple Sclerosis Testimonial 34:
I HAVE EXPERIENCED REAL BENEFITS
I have no real dramatic updates to report, however I see myself slowly improving over the past 4 months. I see improvement in balance, physical strength, I am also now using a physiotherapist on a monthly basis.
The best example of the treatment working for me is that I can now stand up straight out of a chair and have worked up to 20 of these daily when I could not do that before the Esperanza treatment. So, I do feel that I am making steady progress and I feel that my strength and energy levels are much better now than before the treatment. I will be contacting you for a follow-up appointment at the Southampton clinic.
My conclusion is that after 4 months on the Esperanza NeuroPeptide that I have experienced real benefits and hope that in the years to come I can add to these comments of progress,
Yours Sincerely,
Christine Watkinson
Romsey
England
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Multiple Sclerosis Testimonial 35:
I started treatment on August 22, 2007 and my progress thus far has been as follows:
- My hands do not shake anywhere near as much as before going on the Esperanza Neuropeptide treatment.
- I am certainly more mentally alert and my speech is not as slurred as it was before the treatment.
- My memory is certainly much better.
- My eyesight is not so blurred
- My legs are much less stiff and I can straighten them out in much more comfortable positions while in bed.
Yours Sincerely,
Lorna Rees,
Port Albert
South Wales
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Multiple Sclerosis Testimonial 36:
JUST ONE APPLICATION OF THE SUBLINGUAL SPRAY APPEARS TO PROVE THE EFFICACIOUSNESS OF THE PRODUCT
 My name is Peter McCann and I am a Doctor of Chiropractic (BSc Hons) registered in the UK with the General Chiropractic Council.
My experience of the Esperanza Homeopathic NeuroPeptide is one of extreme and positive optimism. Just one application of the sublingual spray appears to prove the efficaciousness of the product. Tests that I have witnessed and was involved in showed marked improvement in strength and balance post NeuroPeptide dosing compared to pre NeuroPeptide dosing results. I was so impressed with what I had observed that I am getting involved with Esperanza Peptide to assist in the regional clinics in the U.K. to better provide Esperanza NeuroPeptide access and monitoring and follow-up of patient progress.
Peter McCann
BSc (Hons) Chiropractic
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Multiple Sclerosis Testimonial 37:
I FEEL SO POSITIVE SINCE THE ESPERANZA TREATMENT ... IT IS GREAT
WOW! What a difference! This is more than I dared to hope for!
After just a week - here is a list of improvements!
Balance - I can walk without bouncing off walls and I'm not using my stick at all in the house neither am I holding on to the furniture to get around
Muscle strength - I can now stand up in the shower without holding the grab rails and without my legs sinking. My standing up is much improved - I'm more upright, and I don't keep buckling at the knees.
Bladder control - definitely improved- frequency has also slowed down
Stamina - What a difference! I can now get throughout the whole day without taking a nap after lunch, and I have much more energy than I've had in years.
Sleep - I am sleeping without the aid of Diazepam - which I've relied on for 10 years. I'm sleeping like a top! and waking feeling refreshed.
General comments - I feel as if a slightly hazy picture has suddenly come into focus - everything appears clearer - I'm moving more purposefully, I feel more in control and more focused. As if a fog has cleared. I feel so positive! It's great!
I'm now beginning to work on my VibroGym and take exercise (yoga and pilates) to improve my core strength and increase the leg strength especially. My aim now is to try to manage without walking sticks/elbow crutches when I'm actually outside of my home - it may take a while, but I will achieve it!
My verdict on Esperanza - It really does feel like a miracle.
UPDATE:
I am now in control of my own destiny, capable,worthwhile and HAPPY
A very happy New Year to you a your family!
Haven't given you a progress report since the beginning of December - I think that a monthly report is about all I'm going to manage because I'm doing so much more than I was - I will just about have the time and space to stay in touch once a month!
It's very easy to take things for granted isn't it? I can sit down, stand up and move around with such ease now that it very quickly becomes the norm, and one forgets how hard those simple tasks used to be! My balance is so much better than it was, I haven't fallen once since starting the treatment - I used to fall at least every week.
As other people have reported, I'm getting quite a few aches and pains where I'm using muscles that I haven't used in years, I use my VibroGym every other day for half hour, and my personal trainer is with me weekly for an hour's workout. I am planning on increasing the VibroGym to 3/4 hour every other day as my stamina is improving.
My right leg is still weaker than my left, but is now clearing the ground when I walk, rather than dragging and i could not do this before the treatment.
My GP has remarked that my general muscle tone has improved, and this year I put up all the Christmas decorations, and wrote all the Christmas cards for the first time in 8 years!
Most important of all aspects of my progress is my mental state - I am not suggesting that Esperanza is an anti-depressant! It's just that I now wake in the morning (after a good night's sleep since starting the NeuroPeptide) and I feel rested, energised, ready to cope with the day and NOT AT ALL LIKE AN INVALID. I still have my limitations but they are so much less significant than they were - I am no longer overwhelmed by my condition. How does that make me feel? I am now in control of my own destiny, capable, worthwhile and HAPPY
Sally Brown
South Warwickshire
England
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Multiple Sclerosis Testimonial 39:
I AM DELIGHTED WITH THE ESPERANZA NEUROPEPTIDE
AND LOOKING SO MUCH MORE FORWARD TO THE FUTURE NOW!
After Esperanza NeuroPeptide Treatment Mark Scott reports the following:
- Balance Much Better
- Walking Measurably Better
- Diet Better and Eating Much More Regularly
- Much More Energy
- Less Fatigue
- Standing Taller & More Confidently
- Circulation In Feet Much Better
- Strength is Much Improved
- Bladder control much improved
In short, I feel amazing. I was diagnosed with MS in 2001 but I can trace symptoms and I know have been battling MS for more than 20 years now! I feel so many differences since going on the NeuroPeptide. I know my body better than anyone and I can certainly feel, see and experience many differences! My partner Denise, my brothers, my Uncle, and my friends have all seen the differences in me and are amazed! I simply feel completely different and very good inside as well as experiencing the differences in my body that I have noted above. I am looking forward to going back to my hobby of photography and I can actually see that happening now with the help of the Esperanza NeuroPeptide and I am delighted and looking so much more forward to the future now!
Denise (Mark's partner) reports the following observations:
Mark is much different since going on the NeuroPeptide and I have observed the following and am noting all the changes we experience in a daily journal as advised to do so:
- Mark is much brighter and more alert
- His Energy is very much improved
- His fatigue is considerably less than pre NeuroPeptide
- He is standing and walking much steadier, straighter and more upright
- His speech is much better and more defined
- When walking he is not grabbing for support and walking much more under his own control
- He is doing so much more for himself now
- He is dressing and undressing with ease now and that is a huge plus
- Mark is not having to get up at night as much as before in order to go to the bathroom
- His shakes and spasms are much improved
Mark and I are both so very glad that he went on the NeuroPeptide and we look forward to his ongoing improvement.
UPDATE:
I walked 600-800 feet after the Esperanza NeuroPeptide ... a fairly major achievement for me.
Previously you will recall that my right leg tremored a lot and I could not control it most of the time. Now after 4 months of using the Esperanza NeuroPeptide I can control my right leg and the spasms are almost non-existent. The leg and foot are warm all the time. I can also say the same for my right arm. Before the Esperanza treatment I could hardly hold a cup of tea without pouring it all over myself. Now I can happily drink without even thinking about it.
My body does still spasm a lot when I first stand up and walk but, I'm hopeful that the NeuroPeptide will help this too, in time. After all, I did walk with my walker from the bus to my Esperanza clinic appointment in Edinburgh with help from my partner Denise (a good 600-800 feet and a fairly major achievement for me). I am continuing to use the exercise bike and now that the better weather is almost here I hope to start doing some short walks outside. I'm sure the exercise will help to as long as I don't over do it and continue on my daily Esperanza NeuroPeptide sublingual spray treatment.
Mark Scott
Scotland
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Multiple Sclerosis Testimonial 40:
DEEP DOWN I KNOW I AM LUCKY TO HAVE RENEWED ABILITIES
DUE TO THE ESPERANZA NEUROPEPTIDE TREATMENT
- Energy levels improved dramatically.
- Warmer feet.
- More feeling in toes.
- Confidence has increased enabling me do so much more.
- I am pleased that I can do so much more for Jasmine my 2 1/2 year old daughter and most of all I am able to look after my fiance Tony again.
- Deep down I know I am lucky to have the renewed abilities noted above and I hold true that the Esperanza NeuroPeptide will continue to halt the progression on my MS.
Paula Odey
Hampshire
England
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Multiple Sclerosis Testimonial 41:
THESE RESULTS HAVE BEEN SIGNIFICANT ENOUGH TO GIVE US HOPE
Eager to enter year two on the Esperanza NeuroPeptide Nova Ronayette reports the following in regards to her husband Bernard Ronayette.
Bernard is very disabled and was diagnosed with MS 14 1/2 years ago. We were very realistic starting the treatment based upon the severity of Bernard's condition and we have been very pleased to get many favourable results from the Esperanza NeuroPeptide. These results have been significant enough to give us hope and to encourage us to continue treatment into year number 2.
The results we have seen significant response in are as follows:
- Improved balance
- Less fatigue
- Improved responses & alertness
- Small movement in fingers, left hand and arm which was not there before treatment
- Much more smiles now
- More facial expressions
- Quicker responses
- New feeling in feet which was not there before treatment
- Much more relaxed muscles
Bernard Ronayette
Newcastle-upon-Tyne
England
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Multiple Sclerosis Testimonial 42:
I LOOK FORWARD TO MY PROGRESS AND CONTINUING TO TAKE THE ESPERANZA NEUROPEPTIDE
I have experienced the following since starting the Esperanza NeuroPeptide treatment:
- I am having good results in balance when walking
- Lessening in the heaviness in legs and feet
- Softer leg muscles
- Generally feeling better and brighter in myself
I look forward to my progress and would like to keep taking the peptide as it is working for me!
Thank You.
Linda Beavis
Cumbria
England
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Multiple Sclerosis Testimonial 43:
THANKS ESPERANZA NEUROPEPTIDE
Update after going on the Esperanza NeuroPeptide treatment.
Since I started on the Esperanza NeuropPeptide treatment I have experienced the following:
- I am definitely getting stronger
- My speech has improved dramatically
- I am not getting as tired during the day
- I am beginning to move my hips and look forward to eventually moving my legs!
- Now don't laugh as it is important to me, but I can now blow my nose which I couldn't before.
Thanks Esperanza NeuroPeptide!
Jackie Clarke
London
England
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Multiple Sclerosis Testimonial 44:
It is three months since my last update to you. I am very pleased with my progress. I have increased energy, improved balance and much reduced brain fog. I continue with enthusiasm for exercise regimes. Swim Monday, Wednesday and Friday, pilates Tuesday and yoga Thursday. Rest Saturday and Sunday. Sleep is greatly improved, bladder and bowel function also under better control.
All in all things are on the up and I am looking forward to my next appointment in March/April to see if any of your recorded data sets show measurable improvement over time.
Regards
Janice Thomson
East Lothian,
Scotland
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Multiple Sclerosis Testimonial 45:
3 Month Update on the Esperanza NeuroPeptide
I am walking to the alter rail at church each Sunday!
After 3 months on the Esperanza NeuroPeptide I can report the following:
I am walking to the alter rail at church each Sunday and also walking down the aisle to my pew for the services (which I was unable to do so prior to the Esperanza NeuroPeptide treatment).I have ordered a treadmill so that I can improve my walking and walk with purpose again rather than using my frame with wheels. My sister says that I seem to be much more alert and more able to assimilate. My right arm no longer feels heavy in the evenings. My energy levels are overall much better. Fatigue is improved as I don't seem to lie down and sleep in the afternoons anymore.
Christine Skidmore
West Bromwich,
England
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Multiple Sclerosis Testimonial 46:
Better balance, more energy, less fatigue, better posture, pink feet!
As I write I can honestly say that I have only positives from the Esperanza NeuroPeptide treatment and I actually look forward to taking it each and every day! From day one I have experienced the following:
* Better balance
* More energy, less fatigue and I can do much more
* Much better posture (that is the first thing that others notice about me now)
* My feet were blue all the time but from day one they have been and are now pink (or normal)
* My writing and holding of a pen is so much better
* Getting out of a chair and also crossing my legs when sitting is so much easier
* Finally, I often leave my walking frame behind and go off walking on my own ... unaided!
Maggie Dimmock,
England
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Multiple Sclerosis Testimonial 47:
I do not want to go without the Esperanza NeuroPeptide each and every day!
Generally my walking is better, my legs feel lighter and much more free.
Before I went for the Esperanza NeuroPeptide treatment in June of 2007 I could barely move and really struggled to lift my feet off the ground!
My balance is now better, I don't even think about it any more. I am certainly doing a lot more than I used to! I also have less pain in my legs. Friends have noticed and remarked that I am moving differently.
I joined a gym and now go three times a week. I like using the PowerPlate machine as it does most of the work for me.
The muscle tone in my arms is much better.
The results are positive and when my 12 months is up in June I would be very frightened not to go on with the Esperanza NeuroPeptide each and every day!
Sara Wrigley,
Cheshire
England
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Multiple Sclerosis Testimonial 48:
Experiencing many improvements in the past year and is continuing to improve!
One year has passed since Barry started on the Esperanza NeuroPeptide. We are out of the peptide spray and would like to renew for another year.
Barry has experienced many improvements in the past year and is continuing to improve. Best of all, there has been no progression in the Multiple Sclerosis! So we are anxious to continue.
Hope this message finds you healthy and happy.
Best Wishes,
Barry and Carol Ralbag
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Multiple Sclerosis Testimonial 49:
I feel that my life has suddenly got much better for me!
Following are things that I see improved since going on the Esperanza NeuroPeptide:
- Ability to pick my right leg up when walking, feel so much more normal
- Feel much more stable when walking
- Can turn round in the shower much more easily
- Can lift and bend my leg when getting into the car
- No longer have such a feeling of "heaviness"
- My family have noticed much improvement in me
- I do feel that my life has suddenly got much better for me.
Thank You!
Diana Cross
Oxon,
England
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Multiple Sclerosis Testimonial 50:
I am pleased about Esperanza - its fantastic!
My very sceptical Father telephoned me the night before my first Esperanza NeuroPeptide appointment and wanted to "manage my expectations'"and said "do not expect to be touched by the hand of God"! Not being a religious man he was politely telling me miracles do not happen! He has eaten his words and is telling everyone how well I am now doing after the Esperanza NeuroPeptide treatment. I will tell you my story, it goes on a bit, but I want to give you the full picture, and not just say "go for it".
THE UPSIDE
I am 39 (40) in October and I have had MS since I was 24, I was doing well but the last 4-5 years its gone wrong, especially the last 2 years when I have started to use a stick to walk or rather shuffle. Stairs were very difficult and often required my boyfriend to lift one leg at a time for me. I also had a chair in the shower as I was unable to stand for very long, let alone with my eyes closed!
On Monday 4 February 2008 I visited the hospital for my neuro-physiotherapy appointment. She was aware that I was about to trial Esperanza. We did a test that involves turning, walking with and without stick, sitting and standing up off chair, standing with eyes closed etc. This is a test that I have done many times over the past 4 years. We wanted a clear medical comparison.
On Monday 11 February my boyfriend Neil and I went to Heathrow and met Gerry Gallagher (who is a wonderful man). Everything is clearly explained and then you do tests, crossing legs, lifting legs, arm strength, hand strength, vibration on hands and feet, balance.
Did the sprays and after 45 minutes we re-did the tests - AMAZING DIFFERENCE for me, even then. Standing with my legs together and eyes closed before was 1.8 seconds before I lost balance, after the Esperanza we stopped the clock after 2 minutes!!
It was very surreal and still is:
On Wednesday 13 February I returned to neuro-physio and did the same test the results were nearly as good as they were 4 years ago! My NHS Neuro-physio is telling all her MS patients about Esperanza as she was completely stunned.
- I got home and I could sit down and cross my legs - not done for 4 years without lifting.
- I can stand up from sitting, first attempt, not 3,4 or 5!
- I do not use my stick around the house ever. I still use it outdoors, but intend to loose that eventually.
- If I see something on the floor I can bend down and pick it up.
- Stairs I now walk one at a time - normally.
- The chair has gone in the shower
- Getting dressed is now much easier - not an event in itself, I can bend down and tie shoelaces without falling over!
- I am much happier, I am sleeping better, I am laughing again - you don't notice how much you have changed until you return (I hope that makes sense).
The best thing was dancing at a nightclub on my best friends birthday, OK my feet were not moving but the balance and confidence allowed a good stable wiggle - had my mate and Neil in tears! This weekend I was at another party and friends wanted to test my balance and stability so a I had a plate and then a glass of red wine placed on my head - I just stood there grinning at them, AMAZING.
THE DOWN SIDE
I have over fatigued myself, suddenly I had my life back and I wanted to use it! Even though warned and advised not to overdo it by Gerry Gallagher, I took advantage of the ability to be partying, decorated my bedroom, showing off my newly returned functions and then ... as warned ... I crashed and burnt out. I have slept pretty much for 3 weeks, remembered that I do still have MS, got a bit wobbly on the walking and slow on the stairs. However, normally with a relapse I am hospital and steroids. This time, rest and fresh air, water and Esperanza and I am getting better and I have no doubt that I am continuing to get better daily and soon I will be able to do everything again - and more, just at a more manageable pace - HOWEVER, I DO STILL HAVE MS!
I hope you have found this interesting and you have not fallen asleep, this is my experience and it is different for everyone. All I know is that it is right for me!
Regards,
Susan Fitzgibbon
England
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Multiple Sclerosis Testimonial 51:
I Intend To Continue With The Esperanza NeuroPeptide Treatment
Since my visit to Edinburgh on 11th March 2008 and beginning a trial of the Esperanza NeuroPeptide I have noticed I have much more strength in my upper body and an improvement in strength in my right arm. I also have some feeling in my feet that was not there before the NeuroPeptide.
I had been taking the spray at 1.45pm and today changed to taking it after breakfast.
I look forward to my appointment on 9th June in Edinburgh and I intend to continue with the Esperanza NeuroPeptide treatment.
Margaret Drummond
Isle Of Skye
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Multiple Sclerosis Testimonial 52:
I HAVE BEEN TAKING THE ESPERANZA NEUROPEPTIDE FOR 2 YEARS ... AND I CONTINUE TO FEEL GOOD!
From 2004 through August of 2006 my health was deteriorating. In 1994, my neurologist, who was then the head neurologist at Kaiser in San Francisco, changed my diagnosis from relapsing/remitting ms to progressive ms. From then until 2004 I went through periods of stability and periods of decline. In 2004 I was alarmed to discover that my symptoms were becoming scarier. I felt as though I was "drifting away." These sensations increased in frequency until around the holidays in 2005 I gathered my husband and daughter, who was at that time home for a visit from college, and told them that I did not know how much longer I would be alive. They were quite upset, but I did not know what else to do. In 2006 I began researching on the internet and discovered the Esperanza NeuroPeptide information. At first I could not believe that there was anything for progressive MS besides chemotherapy or other drugs with potentially lethal side-effects. I researched further. I was able to contact the people at Esperanza NeuroPeptide. They were coming to San Francisco and they agreed to see me. Prior to this I had some previous positive experiences with homeopathy.
I met them and received my first NeuroPeptide treatment. Within minutes I felt much better than I had been feeling. For me the treatment had the following benefits:
- I experienced a profound feeling of well-being. I no longer felt as though I was dying. The peptide has given me a life back. I feel like myself again.
- I experienced mental clarity. Prior to taking the peptide, it was difficult to think clearly.
- I experienced an increase in my ability to concentrate - longer and longer. Prior to the treatments my thoughts were often scattered and I was not able to focus very long.
- I had a dramatic increase in energy. I was able to work on writing projects once again, without becoming exhausted.
- I am quadriplegic. The peptide did not reverse this but I do have an increase in involuntary muscle spasms and I feel physically stronger. In fact, I felt well enough to take a trip to Portland, as well as going sky diving. These were things I would never have done before starting the Esperanza NeuroPeptide!
- Instead of having, say, five bad days in a row followed by one good day followed by five more bad days, my days are invariably all good. I can count on having good days.
In addition to the aforementioned benefits, the effects of the Esperanza NeuroPeptide seemed to be cumulative. I have been taking it for almost two years and I continue to feel good. And my abilities and energy are still increasing. I don't always need to take a nap midday as I used to.
The Esperanza NeuroPeptide makes being disabled bearable. It is helping me to live life, the only life I have, to the fullest.
Further Update:
I was on CBS radio yesterday because I have a connection to the 2009 Naked Clown Calendar. They asked me if I took anything for my MS and I told them I took homeopathic neuropeptides. They did not want me to mention brand names but they did ask me if it helped, and I told them it did and how pleased I was with my progress on the Esperanza Neuropeptide treatment.
Judy Finelli
San Francisco
California, USA
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Multiple Sclerosis Testimonial 53:
I am Getting Much Stronger
I am getting more strength! The problem with me is that I tend to overdo things and I must regulate myself in regards to exercising! By the way, I stopped smoking since that day I have met Gerry in Brussels and feeling much stronger on the Esperanza NeuroPeptide.
Peter DeSmet
Belgium
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Multiple Sclerosis Testimonial 54:
I Look Forward To Things Getting Better And Better With Esperanza NeuroPeptide
Concerning the NeuroPeptide, things are going great. But I wish I had headed Gerry's instructions at the clinic and I'm happy that you reminded me not to overdo my activity as I felt so good after the NeuroPeptide that I did overdo my activities. The second day (Tuesday) on the NeuroPeptide was the best thus far and I was a little too enthusiastic as I walked plus or minus about 3 miles doing some shopping which was something that I was unable to do prior to the Esperanza NeuroPeptide treatment. As such, the next days I had to recuperate, and as a result I have to work my strength back up to the after-treatment results. However, I will (from now on) keep in mind not to overdo things, and I look forward to things getting better and better into the future with Esperanza NeuroPeptide.
Many Thanks & Regards,
Eric Delpierre
Belgium
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Multiple Sclerosis Testimonial 55:
I am feeling lighter on my feet and using my walking sticks less
Since starting on the Esperanza NeuroPeptide things appear to be looking up in terms of my MS symptoms. I am feeling lighter on my feet and use my walking stick less and less around the house and I feel that I have much more energy. I have been taking your vitamin D at 5000 iu for about three months now and wonder how much it may facilitate the effectiveness of the peptide.
With Thanks
Steve Roberts
England
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Multiple Sclerosis Testimonial 56:
Things have changed dramatically for the better with the Esperanza NeuroPeptide!
I am Carolyn Phimister from Buckie, I started my treatment at the end of February and have been feeling very good since starting the treatment.
I feel my legs are not so stiff and generally feel so much better.
Before I started I was feeling quite low, couldn't be bothered with much, had very low energy, didn't sleep well and therefore during the day I was weary. Things has changed dramatically better now with the Esperanza NeuroPeptide!
Now I've started a hobby, card making, I love it, I have to cut, use tweezers etc, and I don't think I could have been so enthused about anything. I've been given orders which really pleased me.
My walking seems a bit easier and I am definitely not so tired, My general day to day life seems much more enjoyable. Some days I am a bit stiffer but it all goes with the illness and I am not so tense when I am a bit wearier.
Hopefully I'll continue to feel this way.
I'll keep in touch with any progress.
Thank You!!
Carolyn Phimister
Buckie, Scotland
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Multiple Sclerosis Testimonial 57:
Although Severely Handicapped By MS I Am Making Steady Progress
Although severely handicapped as a result of MS, I am making steady progress since starting on the Esperanza NeuroPeptide.
My hands are stronger and I am capable of holding the bars of my bed and have more control of my upper body.
I am slowly getting more feeling and motion in my hands and managing to use them more and I am now able to control them and shake hands with others now.
Anita Bahl
Aberdeen, Scotland
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Multiple Sclerosis Testimonial 58:
I have been consistently amazed at the benefitis of the Esperanza NeuroPeptide
I have been involved with Esperanza since early 2005 and I have been consistently amazed at the benefits of the Esperanza NeuroPeptide, even from day one! Meeting Eddie Cardinal our longest standing patient of 20 years was a real "eye opener" as to what is possible with Esperanza NeuroPeptide.
Having now attended many of the UK clinics from 2007 to date I am delighted to state that I am yet to be at a clinic where the clinical tests and results do not show a significant improvement in one or more of the areas analysed.
I consider it a privilege to be associated with Esperanza due to the high principles to which the company operate and the effort put in to do the best for each patient. By striving to always do even better, new ideas are often quickly adopted to the benefit of Esperanza's patients worldwide.
Brian Campbell - BA MIB
Northern Ireland
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Multiple Sclerosis Testimonial 59:
I Am Very Happy To Be Part Of The Esperanza Team
Dr. Peter Livesey
My name is Peter Livesey and I am a Doctor of Chiropractic (BSc Hons) registered in the UK with the General Chiropractic Council. I am married with two children and I live and work in Poole, Dorset. I have recently been invited to join Esperanza Peptide to assist with the regional clinics in the U.K.
I have been very impressed with the objective positive strength and balance changes that I have observed following the administration of the Esperanza NeuroPeptide sub-lingual spray. As a health practitioner who very much believes in a homeopathic approach to healing I am very happy to be part of the Esperanza team and I am looking forward to helping support its increased availability and uptake throughout the area.
Peter Livesey
BSc (Hons) Chiropractic
Poole, England
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Multiple Sclerosis Testimonial 60:
Dr. Peter Livesey
I am looking Forward To The Future With The Esperanza NeuroPeptide Team
Esperanza peptide is proud to announce that Dr. Peter Livesey has completed his training and will be administering the Esperanza NeuroPeptide in the southwest coast region of the UK.
Peter was born and raised in Accrington, Lancashire in 1949 and in 2005 he qualified as a Doctor of Chiropractic and now lives in the Poole area of Dorset with his wife and two sons.
Peter is extremely interested in all aspects of health and fitness and he is also a qualified Reflexologist and Reiki Therapist and looks forward to his ongoing association with Esperanza NeuroPeptide. Peter said: "I very much appreciate the opportunity that has come my way and am looking forward to being a part of the Esperanza NeuroPeptide team"
Peter Livesey
BSc (Hons) Chiropractic
Poole, England
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Multiple Sclerosis Testimonial 61:
Eleven Years On Esperanza NeuroPeptide
Thanks to Esperanza and their fabulous NeuroPeptide as I am able to live a fulfilled life without limitations!
After experiencing double vision and eventually having an MRI done, I was diagnosed with MS in 1995. Due to my MS, I was told by my doctors not to have another child. However, I became pregnant one month after my diagnosis. My pregnancy and delivery went very well. When my son was about 3 months old I had weakness on my right side, sharp pains in my feet and a heavy limp in my right foot. I was very tired and fatigued all the time. These feelings persisted for approximately 3 years. During that time I searched for an alternative to the drugs the doctors suggested I take. I just did not want to feel bad using drugs administered to my body that would have other side effects and would at best slow the progression of this disease. A friend of mine told me about promising news about Esperanza NeuroPeptide. I started on the Esperanza NeuroPeptide 11 years ago. When I started with I was truly amazed at how quickly the heavy limp and drag in my foot disappeared. I now use puff once a day. At times when I am overheated or stressed - just no feeling "right" I will take an extra puff to bring me back to my base. My energy level has improved over the years incredibly. I wake at 5:30am and don't take a rest until bed at around 11:00pm. I have a family, horses,dogs and pigs to care for. I have recently started a candle business - manufacturing and retailing. I also am vice president of a family forklift company. Thanks to Esperanza and their fabulous NeuroPeptide as I am able to live a fulfilled life without limitations!
Tish Accardi
Jupiter, FL USA
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Multiple Sclerosis Testimonial 62:
I FEEL IN CONTROL OF MY LIFE AGAIN!
What can I say as I don't know where to begin and so many positive results have been experienced on the Esperanza NeuroPeptide!
I started on the Esperanza NeuroPeptide in February 2008 and it has been amazing the amount of positive changes that I have experienced! I just wish I had received £1 from every person that says to me "wow, you look so well" or "you look so different" since I have been on the NeuroPeptide as I will have covered next years renewal!
Vision, Balance, Hands & Feet Improved
I have had to get new glasses and contacts as my vision has improved. I no longer get double vision or a wandering left eye when I get tired. The sensation in my feet and hands have improved and are not as cold. My balance is fantastic and I have been able to take the chair out of the shower which has been wonderful.
Helping Me Rebuild My Strength
Having completed a hydrotherapy course at the hospital I am now continuing the exercises in my local pool. I have not had the confidence to go to the swimming pool on my own for over three years, this is helping me rebuild the strength in my legs which I hope will eventually mean that I can say goodbye to my walking stick.
Appear To Have My MS Under Control With Esperanza NeuroPeptide
Last year before I started Esperanza, I saw my MS nurse. We changed my medication to Copaxone and had a very depressing conversation about the reality of entering secondary progressive MS after 14 years. At the beginning of August we discussed how I am getting stronger and not entering secondary progressive and appear to have my MS well and truly under control, and whilst she could not officially 'recognise' Esperanza things have definitely changed in me.
More Energy & Much Happier With Life
I have much more energy and I am much happier and feel in control of my life again. Thank you Esperanza.
Susan FitzGibbon
UK
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Multiple Sclerosis Testimonial 63:
I HAVE ALREADY NOTICED SUCH A SIGNIFICANT DIFFERENCE!
Hi, I had my first treatment with Brian on the 20th August at Southampton and acquired my 6 month supply of Esperanza NeuroPeptide.
My spasms have lessened and reduced in frequency. My 'helper' who does physio with me every day has noticed less resistence when bending my legs - so that is good.
I have been able to go back to a 'normal' way of getting myself into bed, rather than sitting on the side and trying to swing my legs round and up, which often needed my husbands help. I'm also lifting my feet a little when walking rather than 'scuffing' along the floor.
I'm very pleased to say that I have already noticed such a significant difference that I wish to upgrade to a full year supply right away!
Many thanks,
Karen Silman
England
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Multiple Sclerosis Testimonial 64:
MY LIFE HAS TRULY TRANSFORMED WITH ESPERANZA NEUROPEPTIDE
Six Years On Esperanza NeuroPeptide
I have had MS since 2000. I actually progressed to where I was using a wheelchair and having all kinds of other problems. My boyfriend through extensive research found me a treatment called Esperanza NeuroPeptide and I have been on the NeuroPeptide sublingual spray now since 2002. My life has truly transformed with Esperanza NeuroPeptide.
Thank You Esperanza!
Stella Zaffarano
Florida
USA
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Multiple Sclerosis Testimonial 65:
NEW MOTTO NOW THAT I AM ON THE ESPERANZA NEUROPEPTIDE - "REACH FOR THE STAR" ONWARDS AND UPWARDS.
Kia Ora (which is Maori for "be well and healthy"), "Climb every mountain" has always been my philosophy and I could always achieve my mountains until 1992 when M.S. struck me and buried me under its avalanche.
My name is Maureen Wood. I am a pharmacist from New Zealand and I have MS!
I was born in Wellington but now live between two beautiful cities Tauranga and Auckland. I make the most of my life with the limitations of M.S. and using my little red scooter to go everywhere.
1992 - I was working fulltime in my newly established pharmacy in Papamoa Beach, New Zealand. I had two young teenagers and twins of 11years so when my calf muscles tightened I presumed I was just a bit burnt out so reduced my working hours, saw a neurologist, had an MRI, thinking all would be O.K. But what a shock awaited me -Multiple Sclerosis!!
I remember crying all the way home driving my Chemist Maureen van. My life as I knew it collapsed overnight.
Firstly I decided to sell my pharmacy to minimize stress. I then read and read all I could about M.S., tried every possible recommended remedy, started Beta-interferon in 2000 and although I think it slowed progression, I was disappointed with it. I did find help from exercising in a gym three days a week and have set up the home garage as a gym (no cars allowed).
In June this year I was surfing the net and found the Esperanza website. What a blessing!! I have taken my Esperanza Neuropeptide for 3 weeks now and already have more energy, better balance for standing, and a much improved mental attitude - no more hopelessness. I am going through the de-toxification stage which is when homeopathy rids the body of toxins. I have studied homeopathy so I expected a good clean out.
New Motto Now That I Am On The Esperanza NeuroPeptide-"Reach For The Star" Onwards and upwards.
Deo Gratias,
Maureen Wood.
New Zealand
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Multiple Sclerosis Testimonial 66:
MY MS HAS SLOWED DOWN AND MY BLADDER FUNCTION HAS IMPROVED IMMENSELY
I would like to let you all know that since I have been taking the Esperanza NeuroPeptide the progression of my MS has slowed down and my bladder function has improved immensely. I feel much more in control of my bladder and my body for that matter. The circulation in my legs and feet has improved and they stay warmer for longer periods of time! Thanks Esperanza, I look forward to the continuation of these significant improvements!
June Preston
England
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Multiple Sclerosis Testimonial 67:
16 MONTHS ON ESPERANZA NEUROPEPTIDE
For the first time in years, I raked all the fall leaves in my backyard thanks to Esperanza NeuroPeptide
Sixteen months ago I found out about Esperanza Homeopathic Neuropeptide.At that time I had terrible spasms in my legs and unbearable pain. Since the traditional medications didn't seem to help I felt I had to try the Esperanza NeuroPeptide sublingual spray. As the year went by, faithfully spraying under my tongue daily, I noticed various changes in my abilities.
Some of the changes:
No jumpy spastic legs - although still tight
No more pain
More energy - feel up to physiotherapy twice a week
Better bladder control
Hand writing is now legible
Feel good overall with a positive attitude
For the first time in years, I raked all the fall leaves in my backyard.
This may sound small but to me it was a huge accomplishment.
Thank you Esperanza
Gail Weber
Canada
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Multiple Sclerosis Testimonial 68:
Esperanza NeuroPeptide - The Difference Is Amazing
I have been taking the peptide since September 2008.
The differences in my physical and mental abilities after going on the Esperanza NeuroPeptide are truly amazing!
Since going on the Esperanza NeuroPeptide I hardly ever have a nap in the middle of the day.
I am now able to spend quality time with my eight year old daughter.
Although I cant walk, I am able to enjoy activities like card making and latch hook rug making.
The strength I now have in my arms is incredible.
My legs are also a bit stronger,I have taken 15 steps holding onto my walking frame, which I could not do before the Esperanza NeuroPeptide.
My parents have noticed a huge difference in my speech,it is very clear and a lot quicker since going on the Esperanza spray.
Susan Crook
Scotland
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Multiple Sclerosis Testimonial 69:
I Am Delighted With The Improvement I Continue To Feel
I started my journey with the Esperanza NeuroPeptide on the 14 March 2008 and since the first spray I have been pleasantly surprised and utterly delighted at the improvement I continue to feel.
I think of myself as a work in progress. I have kept a diary to jot down improvements.The biggest for me has been the reduction in fatigue. I used to wake up feeling worn out but that is not the case any longer. Since starting on the Esperanza NeuroPeptide I am out of bed and eagerly looking forward to the day in front of me. The fog in my brain has cleared and my feeling of well being is wonderful. My speech is much better I now no longer slur my speech.
The improvement in my fatigue levels have led to me being able to socialise which is wonderful! My husband recently brought me a Bengal kitten for company (See photo) and it was suggested I might enjoy showing him at cat shows but that cat shows are a very long day and may test my fatigue levels. At these shows you are not allowed to leave early and indeed the days are long and demanding. I decided that I would like to try and so glad I did because I love the cat shows and I meet new, interesting and wonderful people! I go to as many different venues as i can and thanks to my Esperanza NeuroPeptide I survive all day with out an afternoon rest.
I feel my life has just started for me. I continue to do light exercises and I drink plenty of water as advised and most importantly ... I continue to experience the ongoing benefits that the Esperanza NeuroPeptide provides for me.
Kind regards
Petula B.
England
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Multiple Sclerosis Testimonial 70:
Trisha Started On The Esperanza NeuroPeptide In 2003
I have been on the Esperanza NeuroPeptide since May 2003 and my symptoms, (especially fatigue and pain) have greatly improved.
I am still on the NeuroPeptide in 2008, five years later.
Trisha
USA
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Multiple Sclerosis Testimonial 71:
TANIA ROSE ON ESPERANZA NEUROPEPTIDE FOR ONE YEAR
I Feel That My Life Has Been Considerably Improved
Through Taking Esperanza NeuroPeptide
I would just like to give you a short update on my progress since I have started taking Esperanza NeuroPeptide for use as a testimonial. I have far more energy than I had before. I can walk further than I have been able to in a long time. I am even able to go to the gym which enables me to keep mobile. I also have more strength in my upper body. It has even made a difference to the amount of times that I need to use the bathroom during the night.
I have nothing but good to say about the Esperanza NeuroPeptide.
I feel that my life has been considerably improved through taking Esperanza NeuroPeptide and I have had no negative side effect what so ever.
Thank you!
Tania Rose
England
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Multiple Sclerosis Testimonial 73:
SIGNIFICANT RESULTS IN FIRST MONTH
"I did spend many years considering and researching this treatment before making this commitment."
Stephen Walker
Hello, my name is Stephen Walker. I am, at the time of writing, 51 years old and I live in Fife, Scotland. I started the Esperanza NeuroPeptide homeopathic treatment only one month ago, May 2009.
I did spend many years considering and researching this treatment before making this commitment. I must be honest and say that at least some of my hesitation was a financial consideration; it is only recently that I have been in a position to afford this rather expensive treatment.
However having made the decision and begun this remarkable sublingual spray, I wish I had started much earlier. Within an hour of my initial dose, administered at the Esperanza clinic in Edinburgh, it became apparent the treatment was being beneficial.
Perhaps not the miraculous transformation I may have hoped for, but a significant improvement nonetheless. My balance was improved my legs felt steadier and my eyesight was more focussed. By the following day I was walking strongly and steadily.
It has been only a month so I am still hopeful of further improvement.
Stephen Walker
Edinburgh, Scotland
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Multiple Sclerosis Testimonial 74:
"YES it works, for me, and yes it's expensive - it's PRICELESS"!
Susan Fitzgibbon
I have been on Esperanza NeuroPeptide for a year and the time had come to purchase my next annual supply. The question I had to ask myself was "do you think it works, it is a lot of money"? My answer was, "I don't really know, I had an initial response that was amazing, I was obviously better but I still wobbled, I still had to use my stick, and of course I still have MS so who knows"!
That answer made me decide to try a few days without my NeuroPeptide and see what would happen. OH MY.... after just three days my Mum had to help me put one foot in front of the other to shuffle a few paces, my legs hurt, I was so tired, I was very weak, I had trouble sitting up and moving without help. I was struggling in a big way with my MS now that I had been off the Esperanza NeuroPeptide for 3 days. The situation became so bad that I thought for sure that it was going to be a trip to the hospital for me!
I sat there with my last bottle of Esperanza NeuroPeptide in my hands! In deep thought I had to ask "was it just a coincidence that I was now doing so poorly after I stopped taking my daily sublingual spray"? Well, I decided not to take any chances and I did my sprays, slept for an hour and when I woke I sat up and crossed my legs and realised that Mum and Dad were staring at me in amazement, then we all burst out laughing with joy as I had begun to regain function and strength that just hours ago had been lost!
Back to the answer to my question...."do you think it works, it is a lot of money"? and my answer is an emphatic.... "YES it works, for me, and yes it's expensive - it's PRICELESS"!
I am now back to where I was before stopping my Esperanza NeuroPeptide! Granted, it took a couple of months to get back to where I was but I am happy and taking my Esperanza NeuroPeptide sublingual spray each and every day!
Thanks to all at Esperanza!
Regards
Susan Fitzgibbon
England
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Multiple Sclerosis Testimonial 76:
Shirley Upton
TESTIMONIAL UPDATE:
After Two Years I Am Still Very Pleased With My Results!
I have now been taking Esperanza NeuroPeptide for two years and am very pleased with the results that I have had with it. Like many of us with MS, I have tried a number of different treatments to help my symptoms, but feel that I have benefited most over the last few years from a combination of the NeuroPeptide and regular Bowen treatment, which helps relieve stiffness and increase mobility in my legs.
During this time I have periodically elected to stop using the NeuroPeptide just to see if I felt any different when not taking it and YES, I have each time realised that my energy levels have fallen drastically. I also realised and experienced that awful overwhelming feeling of fatigue that I used to have had returned, making it totally impossible for me to maintain my usual activity levels. The Esperanza NeuroPeptide is now part of my daily routine and I am convinced that it works for me!
For me, the Esperanza NeuroPeptide has allowed me to return to much higher levels of energy day-to-day, letting me run the home better, go out more frequently and generally enjoy life more.
+++++++++++++++++++++++++++++++++++++++++
Below is Shirley's Testimonial from a year ago
The Esperanza NeuroPeptide Has Really Made A Difference In My Balance!
I am very pleased with the effects of the Esperanza NeuroPeptide. It has really made a difference to my balance and I know I can now stand for longer periods of time. My family have noted me being more active and I have found that I can generally get more done in a day. One thing, however, has been an increase in the number of aches and pains that I am suffering, but I believe that it is a direct consequence of higher activity levels and using muscles that have been stagnant for a long period of time. I have decided to see a physiotherapist to help me with that and I look forward to continued progress.
Many thanks for all your help!
Kind Regards
Shirley Upton
England
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Multiple Sclerosis Testimonial 77:
Sheila Laird
After 3 months of taking the peptide I am now back at work part-time.
Thanks to Esperanza NeuroPeptide my life has changed for the better.
I was diagnosed with MS in 1987 and my illness has progressed over the years. In the last year my health has rapidly been declining and I had been unable work for seven months due this. My walking had been getting much poorer and my balance worse. Fatigue being one of the most prominent symptoms, until I discovered the Esperanza NeuroPeptide.
Shortly after taking the Esperanza NeuroPeptide my husband and I were sitting talking in the living room when I crossed my legs for the first time in years. A few days later I was able to stand and put my make up on without my legs giving way.
After 3 months of taking the Esperanza NeuroPeptide I am now back at work part-time. I am less fatigued and have no need for a sleep during the day, and I now sleep much better at night. Thanks to Esperanza NeuroPeptide my life has changed for the better. I no longer need walking aids and my balance has improved. Hopefully my strength will increase. Taking the Esperanza NeuroPeptide has given me great hope for the future as I truly believe that I had none before.
Sheila Laird
Inverness
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Multiple Sclerosis Testimonial 78:
Susan Fitzgibbon
I HAD A RECENT MRI SCAN AND THERE WAS NO NEW LESION ACTIVITY!
I feel "On Top Of The World" ... Thanks to the Esperanza NeuroPeptide!
I have now been on the Esperanza NeuroPeptide for about two years now and my improvement continues!
I have had a recent MRI scan and there is no new lesion activity!
Therefore the neurologist does not want to see me for 6 months (unless I have a relapse in the meantime). I now feel that I am in a good place and I am slowly coming off various pills I have been on for 15 years - so I feel fantastic, and really allowing the Esperanza NeuroPeptide to do its thing without any interruptions.
A journalist read a story about me in the local magazine "South Downs Living" and felt so inspired by my positive attitude that she had to contact me. I have now been interviewed and I am waiting for the photographer and there is going to be a full page feature on me in "The Daily Express"!
I feel "On Top Of The World" ... Thanks to the Esperanza NeuroPeptide!
Regards
Susan
England
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Multiple Sclerosis Testimonial 79:
Two Years On The Esperanza NeuroPeptide
I am pleased to let others know of my positive changes with the Esperanza NeuroPeptide.
I have been taking the Esperanza NeuroPeptide for over 2 years now. The initial visit to the clinic got me moving more. I started a vigorous exercise program with a physiotherapist and changes slowly began. Thanks to the Esperanza NeuroPeptide I have energy to get to therapy, work out and keep stretching and strengthening at home. I have pretty good strength even though I'm in a wheelchair full time, my transfering is problem free. Another problem that has improved is bladder control and bathroom frequency. I'm not sure if this is a NeuroPeptide connection but I have had no attacks at all since I started the Esperanza NeuroPeptide sublingual (under my tongue) spray.
Regards
Gail Weber
England
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Friedreich's Ataxia/Testimonial 1
 Hi Esperanza NeuroPeptide, here is an update testimonial on my recent treatment in Freeport, The Bahamas.
I went in pool, stood holding my 15-month old son and walked holding him in pool ... I have never been able to do this.
While washing dishes knees were not aching as they normally do after 5 minutes.
Grocery shopping - no pain in knees could walk further than the 'milk' section. I am usually in agony by that stage. Although I still lock my knees when I walk, they are no longer aching. Strange hey!!
Stairs - brain seems more connected with knees bending, down the stairs.
I always say 'bend, bend, bend,' when I walk down the stairs. My knees were still hesitant to bend before the Peptide. But now they seem to listen to my instruction immediately.
I ordered the SCENAR machine from USA this week. Hopefully this will help to loosen up my rigid knees. I will of course use the machine on all the points on my face and up and down my legs.
I also ordered a Power Plate. I'm hoping that this machine will strengthen those unused muscles. They are the muscles that I can feel are still very tired. This machine will also help my poor circulation as well as make me feel extremely good in myself. A 10-minute session will be equivalent to a 60-minute workout. Something I am not able to do, but who knows, after 2 months I might find myself a lot more active as those weak muscles will be stronger.
I was quite active today my as knees are not aching (still locking though). I feel a slight increase in energy. My balance is still bad, but it feels so good to get things done with less effort. I hope the pain stays away as I don't feel 80 anymore but 35 again. Not getting too excited, just in case it doesn't last, but totally positive still. Legs do not feel as heavy anymore.
Still have no aching in my knees. What a pleasure ... therefore standing longer periods (cooking and washing dishes has actually become a pleasure). No real improvement on the balance and walking as yet. I am using walking stick when there is not something to hold onto. I am also doing exercises on land - quite tiring, especially marching as lifting legs high and walking 3 metres along sideboard and back.
I am delighted that I was able to take my son to the funfair and was able to walk around for a long time pushing my baby in his pram.
Luzan Murphy
England
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Friedreich's Ataxia/Testimonial 2
Since going on the Esperanza NeuroPeptide the disease progression in my brother Renato has nearly stopped.
Friedreich's Ataxia Patients, Brothers Renato di Capitani (left)
and Sandro di Capitani (right)
A friend of ours who lives in Freeport The Bahamas told us in Spring 2004 about the Esperanza NeuroPeptide. In the Autumn of 2004 we went to Freeport (The Bahamas) and we were given the NeuroPeptide (at that time it was injectable) and we had to inject the NeuroPeptide once a day for about one year.
Esperanza introduced the easier to use sublingual spray and we then received these new sprays that we are still on to this day. Although the Esperanza sublingual NeuroPeptide was designed to combat MS, we took the chance to see if it worked on our problem disease Friedreich's Ataxia (FA) and I am happy to say it worked for us and especially my brother who is getting even better results that even I am.
Since going on the Esperanza NeuroPeptide the disease progression in my brother Renato has nearly stopped. For myself unfortunately it is working, but slower than on Renato, however I live in hope that the Esperanza Neuropeptide will continue to work for both of us and we both look forward to continuing the Esperanza NeuroPeptide in our campaign to battle FA ... so much so we have both just recently renewed new 18 month supplies each!
Kind Regards
Sandro and Renato di Capitani
Switzerland
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Motor Neurone Disease/ALS Testimonial 1
In 2002 I Was Told I'd 15 Months To Live - Now I'm Looking Forward To 2007!
A BRAVE mum, given only months to live, is celebrating seeing another year with her family.
 Debbie Christie, 34, was diagnosed with Motor Neurone Disease (MND/ALS) in December 2002 and given a maximum of 15 months to live. By June 2004 she was in constant pain and could barely talk. Her husband Colin and their children Lauren, 13, and Colin, 17, began preparing themselves for her death. But in July Debbie flew to The Bahamas for an experimental drug treatment that has transformed her life. Now she's no longer in pain and can do most things for herself. And, above all, she is looking forward to the future with her family. Debbie said: "I didn't think I would see 2005 and I know I was not expected to be here at Christmas, but in the last six months I've felt better than I have in years. "I know this drug is not going to stop my illness, but it's slowing it down. "It's giving me more time with my family and every extra day is fantastic. "I'm taking it day by day, but I do hope I'll be celebrating Hogmanay in 2006."Debbie, of Girdle Toll in Irvine, Scotland, flew to The Bahamas in July after generous Evening Times readers helped raise '8000 for the trip and treatment. She spent a week being injected three times daily with peptide, a drug derived from cobra venom and not yet licensed in the UK. After just one day of treatment Debbie's pain lessened and she was able to move her hips for the first time in months. By the last day of the course she could walk without any help. Debbie said: "For almost two years every month brought some new problem. I was just getting worse and worse. "I would just stay in bed all day because I was so ill. "Now I only go to bed at night. The last six months are the best I've experienced for years. "It was my daughter's birthday in December and my son's on January 1, and I was really glad to be here with them. Last year there was a good chance that I wouldn't have been. "Although Debbie is feeling much better, she still has health problems. She said: "I've gone downhill a bit recently - but that's not because of the disease. "I'm finding it hard to eat and my immune system is low, so I'm going into hospital soon to have a tube fitted into my stomach. "The doctors will give me nutrients through that and I'll have to stay on for a couple of days. But once that's over I should be okay. "I'm just taking life one day at a time. Every extra day I spend with my family is FANTASTIC! "Motor Neurone Disease (MND/ALS) is a progressive fatal condition that causes weakness and muscle wastage.
To see Debbie's Story in the press please click here
Debbie Christie
Scotland
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Motor Neurone Disease/ALS Testimonial 2
I Now Celebrate Life, My Future Looks Bright And I'm Also A Proud New Father!
Alastair Purple is a Trustee with the North East Motor Neurone Disease Trust (NEMNDT).
 My name is Alastair Purple from Newcastle-upon-Tyne in England. I was diagnosed in October 2003 with Motor Neurone Disease, I was told to expect to live for 3 years, I was given the only drug available to MND/ALS sufferers; this was expected to extend life by a few months. I had terrible side effects from the drug, and took to my bed unable to move my limbs without help. This was the only treatment available (Rilutek'/Riluzol'), and I decided that this was not how I wanted to end my days and ceased the treatment. In 2005 my luck began to change, by chance I met Gerry Gallagher of the Esperanza Research Foundation, he told me about his research program and the Peptide formula. Gerry offered me about the Esperanza Homeopathic NeuroPeptide sublingual spray treatment and I gladly tried it. Immediately after taking the Esperanza Homeopathic NeuroPeptide, muscle cramps and fasciculations stopped, especially at night I could feel a difference as I could stretch out in bed without my muscles going into a spasm. I also regained some of my finer motor skills, I could do my own buttons, tie laces, hold a knife and fork again without my hands cramping up. I couldn't believe it. I had no adverse side effects from the Peptide. Since I have been taking the Esperanza Homeopathic NeuroPeptide the motor skills I regained remain unchanged, and I rarely get any muscle cramps. Throughout my body muscle wasting has slowed down if not stopped, I don't feel any worse than I did before I started the treatment, as matter of fact I feel, and I am doing much better ' which is a significant statement when you are talking about a disease like MND/ALS because time is an enemy of the disease and I should (by all traditional accounts) have deteriorated healthwise during that timeframe. The Peptide has most certainly halted the progression of my disease which usually progresses at an alarmingly ravaging pace. I now celebrate life, my future looks bright and I'm also the proud father of Lucy, my newborn daughter, something that would never of happened if I had listened to the my Neurologist... according to the Neurologist... I should be dead this year. On the contrary I am feeling better than I have in years. Thanks to the Esperanza Homeopathic NeuroPeptide sublingual spray treatment, I have a positive, hopeful and productive future again.
Alastair Purple is a Trustee with the North East Motor Neurone Disease Trust (NEMNDT). Feel free to visit their website at: http://www.nemndt.co.uk/
Alastair Purple
England
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Motor Neurone Disease/ALS Testimonial 3
I do find the strength I received from taking it helps me immensely.
I have been taking Esperanza NeuroPeptide for almost a year now after being diagnosed with Motor Neurone Disease/ALS. I do find the strength I receive from taking it helps me immensely. I do have an arthritic spine in addition to my diagnosed disease, so the added strength that I derive from the daily sublingual treatment helps me very much.
Gerry Gallagher (CEO of Esperanza) and his staff of professionals are such a help with any questions you might have in regards to the NeuroPeptide and the treatment procedures. You will never feel on your own dealing with Esperanza.
I can tell an immediate difference if I forget or miss my regular daily dosing time, so the Esperanza NeuroPeptide is truly an integral part of my daily routine!
Marion Bowdler
England
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Motor Neurone Disease/ALS Testimonial 4
No ALS-Motor Neurone Disease Deterioration For Over A Year On The Esperanza NeuroPeptide
My wife Lana Murad Bataineh has been using the NeuroPeptide for over a year now, and I am pleased to tell you that her ALS condition is not deteriorating any further.
L M
Bahrain
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OPCA (Olivopontocerebellar Atrophy) Testimonial - 1
We Have Been Searching For Years... We Found It With Esperanza Peptide
 If you are reading this, you are probably at a point of needing help for yourself or someone you love which you have been unable to find thus far. Well, look no further. I will tell you our story of my husband's neurological disease that left us hopeless until several weeks ago. We have been searching for several years all over the nation trying to find some answers for his degenerative cerebellar disease, labelled as OPCA (olivopontocerebellar atrophy). This condition resulted in his early retirement as an orthodontist. It is very difficult to accept that there are really no concrete answers, especially in neurology. So many of the same symptoms are present in different neurological diseases making it hard at first to even get a diagnosis. Around 1998, he first noticed a slurring of his speech, a mild balance problem and a deterioration of his handwriting. He thought for sure that he had MS. Over the last two years this progressed into a total loss of balance, an inability to walk, weakness in all of the body, speech that was very difficult to understand, and the ability to write was lost. In April 2006, we decided to visit the Mayo Clinic in hopes of finding something that we may have missed along the way. Unfortunately, there was no new diagnosis or treatment available. My husband was so weak at this point that we needed help. He was unable to dress, shower, or shave, much less stand with any balance. It was very difficult for me to even get him out of the wheelchair. He was unable turn in bed at all. We were both desperate and determined to find something in this world that could make a real difference in his condition. We never gave up hope. We had to continue to take charge and investigate everything we could find and talk to everyone we knew. We were introduced to Dr. David Mundschenk through a mutual friend of my sister and brother-in-law who live in New York. I was told to call him and get information on his peptide treatment. I reached him right away and he explained what he researched and developed. After hearing what he said, it made sense to us, but most of all it was the hope that David had to offer. After all, what did we have to lose, a nice trip to Freeport! We left the next day and our son had to come with us because I could not handle my husband anymore. The pilot and our son literally had to carry him up the stairs to get him into the small plane from Fort Lauderdale to Freeport. The next day we started with the routine David had explained to us. Every test was timed and documented on video. He asked him to speak, stand, walk, do certain types of movements, etc. Of course he was unable to stand or walk, and his speaking and writing were very poor. His movements were limited and slow, and others were just not there at all. After this was done, the peptide was sprayed under his tongue and we waited for about 45 minutes. David then told us that we would do all of the same things again and see what effect the peptide had on his neuromuscular system. I can tell you what happened next was truly a miracle. Bob was able to stand up from his wheelchair on his own, he stood balanced for at least 30 seconds. David then asked him if he could take a step. Well, to our total amazement not only did he take a step he took about 10 steps, totally on his own and stood for another 2 minutes!!!!!! Totally balanced with no help!!!!!!!!! Then he sat down. We were all in shock! He had not done this in almost 2 years!!!!! The very next day he was able to stand with his eyes closed, feet together for over 2 minutes. It's been at least 3 years since he did that. His strength was returning and from this point on I had to be careful not to use as much force handling him because I would throw him across the room! The second night, he turned in bed twice. He was able to cross his legs. He could sit and stand much easier. The change in his body was tremendous. We left Freeport with so much hope thanks to David and his research. On the way back home my husband actually walked with assistance up the stairs into the plane. What a difference. In the past three weeks, his voice is better, along with his handwriting. He is walking short distances everyday, making further progress. He can get up and sit on the side of the bed. He is much, much stronger. This week he started on a physical, occupational and speech therapy program. After 2 sessions the therapists cannot believe his progress. They say that usually it takes much longer for a patient to obtain the progress that he has made. We have told them about the peptide and no one can believe it. We are so grateful that we have met David and his team who have dedicated themselves to helping people all over the world. It has only been one month for us and we are so excited with what has happened thus far. We will keep everyone posted on our progress and are definitely interested in helping anyone who wishes to contact us. We hope that our story will give others the support and encouragement that they need. Again, our many, many thanks!
Bob & Debbie Morley
Louisiana, USA
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OPCA (Olivopontocerebellar Atrophy) Testimonial - 2
I took a chance coming to the Bahamas and I've been greatly rewarded
I was diagnosed with a neurodegenerative disease in 2006. This was after four neurologists, two movement experts, and a neurosurgeon have examined me. My cerebellum was shrinking! The cause was unknown. I was tested for hereditary ataxia and muscle diseases through the Athena laboratory. All came back negative. My grandmother died of heart failure with cerebellar complications in 1972. She could not speak clearly, her arms and legs were ataxic. She died in a nursing home. Just before she died she had a broken arm which no one knew about. When I arrived at the Bahamas I was in my pyjamas 24/7. I was in a wheelchair, the few times I used my walker I would lean heavily on my left side (my bad side) and literally drag my left leg. I was having difficulty talking, my tremors (whole body) would make it difficult for me to sit down (I didn't know if I would reach my target without falling). I was 5'51/2" tall and weighed 92 pounds. I smoked 2 packs a day (I had quit for 18 years but when things were getting worse for me, I picked up the habit again). I quit fixing my hair and putting on make up. I had literally given up! Thank goodness I had a wonderful family to support me. My husband was so worried about me that he threw a lavish Christmas, thinking it would be the last I would see. Then purely by accident (none of my regular doctors told me about it) I came across the Esperanza Clinic while surfing the internet. I contacted them and the next day they replied. What a difference from regular neurologists who make you wait for months to see them! My husband and I arranged for our passports, airline tickets, and motel reservations. Within 2 months we were headed towards the Bahamas. We were privileged to meet Dr. David Mundschenk (PhD) inventor of this unique spray, Dr. Bethel (MD), Jacob, who does the videotaping (yes you will be video taped) and Carrington, hotel aquatics team (Sheraton). I did not meet Gerry Gallagher (the CEO of Esperanza Peptide) as he was in the states on business when we arrived but have corresponded with him several times via email. The most noticeable difference I recall after taking the spray was my talking. Instead of slurring and scanning to find words, my words came out fluently. I had trouble with standing still with my eyes closed and feet together, only could do it for 8 seconds. Also had trouble walking unaided, even though I stood straighter and did not lean heavily on my left side. Exercise in the pool was something else, I found out I could swim! I avoided water for years (after a near drowning when I was small). Heck of a thing to find out you can swim and you're 53 years old. Dr. Bethel made a determination that my cerebellum was being destroyed because of aspartame poisoning (artificial sweeteners). It appears my grandmother was a "red herring" since no one else in our family showed signs of this disease.
Today:
I am only in my pyjamas at night. I am never in my wheelchair even in public, I use my walker. I no longer lean to my left or drag my left leg, I stand straight and tall. My talking has improved by 80%, my body tremors have lessened by 80%. I weigh now 108 pounds and don't look like a walking skeleton anymore! I quit smoking, yes cold turkey. I now put on makeup and fix my hair. I swim 5 days a week, trike whenever I can and planning to buy a horse (I use to show western pleasure horses). I can now stand with feet 2 inches apart and eyes closed for 3 minutes. I also can walk with a cane. I now have a future. Just because you don't show immediate improvement doesn't mean you won't show improvement down the road! I took a chance coming to the Bahamas and I've been greatly rewarded. Thank you wonderful people for giving me hope and my life back.
UPDATE:
Here's an update to my testimony: 22 June 2007
I continue to improve. My speech is normal. I'm involved in a rigorous exercise program. Still swimming 5 times a week, and I do home exercises for 45 minutes everyday. There are several profound improvements. I can stand with heels together and the rest of my feet about 2 inches apart for 10 minutes. In the pool or at my home. I also can walk unaided for 7 minutes. It's not a pretty walk but I can do it! Hard to believe just 6 months ago I was in a motorized wheelchair. I also can read again! I haven't been able to for four years. My energy level is at an all time high. I literally can go all day long. I have no regrets on taking this venture. It's given me my life back!
Sara McArthur
Sara McArthur
Oklahoma, USA
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Primary Lateral Sclerosis Testimonial - 1
The peptide helped me from the very fist dose
 My name is Loretta. I am 72 years old and I have had PLS (Primary Lateral Sclerosis) for about 7 years now. It is a progressive disease involving the upper neurons. The Esperanza Peptide treatment helped me from the very first dose. It helps balance, strength and coordination. I have been on it for 4 years now. My new neurologist said, "There is no proof this works". HOWEVER, as I left his office, he readily admitted that I was in much better shape than he ever expected for having had the disease for seven years..... 4 of those years on the peptide, and as I said.... "it has helped me from the very first dose"!
Loretta Johnston
Massachusetts, USA
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