Esperanza Research Foundation

Long Term Esperanza NeuroPeptide Patients Speak Out On The Ongoing And Accumulative Effects Of Their Treatment Over Many Years!

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.

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.

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.

Eddie Cardinal (21 years on NeuroPeptide) and Sandy Williams (6 years on NeuroPeptide)

Since the NeuroPeptide is still doing what it is supposed to, and has done for over 6 years now, I had to think of a new twist to "up-date" my testimonial on the Esperanza NeuroPeptide website, so I have decided to focus on the areas that may have stopped or prevented the NeuroPeptide from working on me a points over the past 6 years!

If there is one thing everyone who is thinking of trying the peptide or is using it needs to know, it is the following:

I have had to "re-boot" the peptide into action several times over the years. I will give you some bullet points to list what I know to be the reasons:

Everything noted above are things I have done over the years in conjunction with the Esperanza NeuroPeptide that have actually STOPPED THE NEUROPEPTIDE FROM WORKING ... and that is what we do not want! So in order to re-boot the Esperanza NeuroPeptide back into action I have had to do a short round of oral steroid called Dexamethasone each time. Now, as in all medication, this may not work for everyone, but I wanted to share what did and does work for me. I also wanted to point out that viruses and what we take in conjunction with the Esperanza NeuroPeptide can diminish and combat the effectiveness of this wonderful daily spray that myself and thousands worldwide have made part of our daily life ... AND IT WORKS!

Aside from those instances where I have needed to re-boot my Esperanza experience, the past 6 years have been amazing for me! I was close to needing a full time wheel chair in 2002 when I heard about the Esperanza NeuroPeptide and I have still not needed to come close to that wheel chair, nor do I intend to!

I wish you all the best and I thank all at Esperanza for giving me my life back these past 6 wonderful years!