Multiple Sclerosis Testimonial 1

Multiple Sclerosis Testimonial 2

Multiple Sclerosis Testimonial 3

Multiple Sclerosis Testimonial 4

Multiple Sclerosis Testimonial 5

Multiple Sclerosis Testimonial 6

Multiple Sclerosis Testimonial 7

Multiple Sclerosis Testimonial 8

Multiple Sclerosis Testimonial 9

Multiple Sclerosis Testimonial 10

Multiple Sclerosis Testimonial 11

Multiple Sclerosis Testimonial 12

Multiple Sclerosis Testimonial 13

Multiple Sclerosis Testimonial 14

Multiple Sclerosis Testimonial 15

Multiple Sclerosis Testimonial 16

Multiple Sclerosis Testimonial 17

Multiple Sclerosis Testimonial 18

Multiple Sclerosis Testimonial 20

Multiple Sclerosis Testimonial 21

Multiple Sclerosis Testimonial 22

Multiple Sclerosis Testimonial 23

Multiple Sclerosis Testimonial 24

Multiple Sclerosis Testimonial 25

Multiple Sclerosis Testimonial 26

Multiple Sclerosis Testimonial 27

Multiple Sclerosis Testimonial 29

Multiple Sclerosis Testimonial 30

Multiple Sclerosis Testimonial 31

Multiple Sclerosis Testimonial 32

Multiple Sclerosis Testimonial 33

Multiple Sclerosis Testimonial 34

Multiple Sclerosis Testimonial 35

Multiple Sclerosis Testimonial 36

Multiple Sclerosis Testimonial 37

Multiple Sclerosis Testimonial 39

Multiple Sclerosis Testimonial 40

Multiple Sclerosis Testimonial 41

Multiple Sclerosis Testimonial 42

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Multiple Sclerosis Testimonial 59

Freidreich's Ataxia/Testimonial 1

Motor Neurone Disease/ALS Testimonial 1

Motor Neurone Disease/ALS Testimonial 2

OPCA (Olivopontocerebellar Atrophy) Testimonial - 1

OPCA (Olivopontocerebellar Atrophy) Testimonial - 2

Primary Lateral Sclerosis Testimonial - 1

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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.

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!

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 8:

The Best Decision I Ever Made ... Regarding My Health!

As you can see below, I have changed my name to "Bahama Mama", because of the glorious success of going to the Bahamas for the Esperanza Peptide Treatment for my MS. I had been deleting the Esperanza Homeopathic NeuroPeptide emails and ignoring the Esperanza Homeopathic NeuroPeptide site for quite some time, because I saw the cost and thought it was another one of those scams preying on desperate people suffering from MS. I then took the information seriously and decided to look into this treatment and contacted and relied on Debbie in N.O. and Cheri in Chicago who had told me of their experiences with the Esperanza Homeopathic NeuroPeptide and the results of their visit to the clinic in The Bahamas, and I was sold immediately. I had to retire from teaching school after 21 years because of MS, which wasn't diagnosed for another two years. I was very athletic all my life: water skiing, scuba diving, snow skiing, all sports but golf, but I have 2 golf pro sons, so does that count. I finally got a diagnosis the day the shuttle blew up in January of l986 for MS. I started having difficulty walking and ended up walking with a cane in l987, and finally using a wheelchair in late 1988. I vacationed in Hawaii with my wheelchair in Nov., 1988, came home and ordered a motorized scooter in January of 1989, and that has been my MS life for the past 18 years, just totally no balance at all and not lifting of my right leg. From day one, spraying the sublingual peptide (under the tongue), I could stand without holding on for well over a minute (which was a huge accomplishment for me and it was only day one). Later that day, my husband timed me and the balancing increased to at least 3 minutes (on that same first day) and with eyes closed and touching my nose. Walked on the 4th day, 15 feet, running a few feet of that. I was so excited, that I felt ... "LIKE A REAL PERSON AGAIN", for the first time in almost 18 years. This was truly the most remarkable feeling being really "REAL". Just being able to stand in the kitchen and cook is "REAL". I am so glad that I decided to open up the Esperanza Peptide email, and this time really read and researched the Esperanza Peptide Website. I am equally glad that I took the next step to make contact, scheduled treatment, made my reservations and flew to the Bahamas less than a month later on Nov. 25, 2006 and stayed till Nov. 30, 2006 ... "THE BEST DECISION I EVER MADE" regarding my health. I am taking the peptide faithfully and doing the exercises that the Esperanza Clinic gave me, and feel more ability every day, that I feel sure that I will be back to my NORMAL self in no time. PLEASE, do as I did, research and study all that is on the Esperanza Website or contact the site and ask them to pass on my phone number and email address and I will certainly help you with any questions you may have.

Fran Lorant-Moore
"Bahama Mama"
Shreveport, Louisiana, USA

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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 11:

Bless the pioneers at Esperanza Peptide for developing this remarkable treatment for MS!

January of 2007 was the 17th anniversary of my MS diagnosis. I'd been diagnosed with MS and it turned progressive in 1999 and I'd lost much of my ability, including to lift my legs, and much sensation in my legs and palms. A friend told me about Esperanza Homeopathic NeuroPeptide and I knew I had to try it. I borrowed the money and flew to Freeport, in The Bahamas. Two days later I took my first "puffs" of the sublingual neuropeptide spray. In 45 minutes I could lift my right leg off the floor, feel vibration in my right foot and most significant, feel heat in my left leg for the first time in 17 years! I've been taking the peptide regularly now and seem to be improving each and every day. I can now roll over in bed, sit up without leaning on my arm, and shake hands with my right hand, none of which I could even think about doing prior to the taking the Esperanza Homeopathic NeuroPeptide sublingual spray. I have experienced no side effects at all, just improvement after improvement. Bless the pioneers at Esperanza Peptide for developing this remarkable treatment for MS!

UPDATE:

Slowly but surely I am headed in the right direction in my battle with MS. I haven't been able to do as much physical therapy as I want, especially the aquatherapy. But I'm improving with diet and supplements and of course my daily Esperanza NeuroPeptide!

James Hamp
Michigan, 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 :

1. 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.
2. 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.
3. The bowel problem is not so acute and seems to be more controlled in that warning is given
4. 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.
5. 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!!!

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 20:

There are no words sufficient to express the depth of my gratitude and admiration toward Gerry Gallagher, David Mundschenk and the Esperanza NeuroPeptide

Not too sure quite where to start? Having travelled to Troon on 20th June - full of hope but also dread. As ever a triumph of optimism over experience my husband and I arrived complete with wheelchair and crutches. I'm so lucky - I can walk - not terribly well - but I can walk. Even after 21 years of living with this wretched illness.Then Pam and Chris arrived with their respective husband and wife - both Pam and Chris were confined to wheelchairs and obviously much less mobile than me. There we met with Gerry Gallagher and David Mundschenck - the "Main Men". They filmed us three doing various tests. First we had to use left and right hands to take pegs out of a pot and put them into a holder - one at a time - "No cheating Bev just cos you're a lawyer!". Then we had to take them out again. Strength tests on both right and left hands - and thumbs. Then conductivity tests - how long could we feel the vibrations in our hands and feet. Could we lift our left and right legs - up - out and down again - and could we shine our shoes on the rear of our calves - right great - left No Way!!! Arms up and over your head - out to the side and down on to your lap. And then the killer test - standing still with your feet together and shut your eyes (don't try it unless you've got someone to catch you when you fall). I lasted 3 seconds before I fell into my husband's arms. And the 15 metre walk? I wear a splint on my left leg, so off with that. Put the crutches down, get the sensible concentrating head on and DO IT - well I did, but I felt as if I was bouncing off the walls! As Pam's husband said to me as he watched me stagger drunkenly past the door in the corridor "that's a typical MS walk". Now we took the peptide spray - under the tongue - 1, 2, 3 sprays, wait 5 minutes and do it again. Was this the moment I had hoped for and longed for ever since I read the article in New Pathways on Saturday May 13th? I felt no different - no different at all. And then we repeated all the tests. I didn't think there was any difference at all but Stedders, my husband, watching with baited breath, said my left hand was very much quicker with the pegs. Gerry and David filmed and timed everything and my results were, on average 20 - 25% improved after the spray. But I felt no different. . . . Until it came to crossing my left leg over my right - oh My word I did it without heaving it over using my right hand. And the killer test - standing feet together, eyes shut - Stedders at the ready to catch me should I fall again - being timed and filmed - and I passed a minute - and then David asked could I do 2 - and I did - and then he said I didn't have to but could I keep going - well set me a challenge . . . . I think Gerry said we stopped filming and timing at beyond 3 minutes. It was difficult - I was using muscles I'd forgotten I had - especially in my backside! And I cried - I still blub now when I think of it. And the 15 metre walk? Well, just try stopping me now - no staggering or furniture grabbing or bouncing off walls. I didn't even notice but Stedders said that for the first time since he can remember that I didn't look at my feet but just walked down the corridor. Even I noticed that I could stand up from a chair so much more easily - and walk across the room to sit on another one - and I could sit down slowly and elegantly - not "flumping" into it. In the pub that night with friends, Pat remarked that we were sitting about as far away from the Ladies' restroom as possible. When we'd been to that pub before we sat right next to the facilities!! They were staggered at the difference in my posture and ability to get up out of my chair. And here I am on Saturday - 2 days since that first spray. I want to go to the supermarket - I haven't been for 2 years now - but Stedders says wait until tomorrow and we'll go together. I can walk around my house without grabbing all the grab rails we had put it - I carried a tray last night with my supper on it - including a glass of wine - without spilling a drop. And I talked to my sister on the phone this morning walking with a cup of coffee!! There are no words sufficient to express the depth of my gratitude and admiration toward Gerry Gallagher, David Mundschenk and the Esperanza NeuroPeptide. David told us that it has taken him 23 years to develop this peptide spray. Thank you Esperanza NeuroPeptide for not giving up - and thank you for the beginning of the rest of my life.

GOING ON 6 MONTHS UPDATE:

The POSITIVE benefits remain going on 6 months with Esperanza NeuroPeptide!

* I can stand for much longer periods - long enough now to cook a Sunday lunch!

* I can now cross my left leg over my right, which I could not do pre Esperanza!

* I can feel the bed sheets beneath my feet, which I could not do pre Esperanza!

* I can climb my front steps one at a time, which I could not do pre Esperanza!

* I still walk with one crutch - pre Esperanza it was two!

* When I forgot to spray one Monday for 3 days I went back to jelly legs with no strength, wobbles, shakiness and much fatigue, needless to say, I will not miss my Esperanza NeuroPeptide ever again!

* My physiotherapist is helping me to lift my dropping left foot and I am learning how to walk with legs that bend again rather than rigid legs again. The physiotherapist simply cannot believe the change sin me and that the Esperanza treatment can render such a change in a person !!!

* I still am constantly being contacted by others and recommend Esperanza to all!

Beverley Rockliff
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 25:

ESPERANZA NEUROPEPTIDE TREATMENT ... It Has Made A Real Difference!

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 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:-

1. Generally feeling better!
2. Waterworks and bladder control much improved.
3. Circulation to my feet is better giving them a human look (eliminating dark discolouration)!
4. I do not suffer from fatigue as I used to!
5. 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:-

1. My feet are often swollen.
2. 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

1. bladder is retaining improvement.
2. circulation continues to improve.
3. 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 UPSI