Sign & Support the campaign for Research & Trials in 'Low Dose Naltrexone for Multiple Scler
Target:
Linda Elsegood, Campaign Team Low Dose Naltrexone, LDN Campaign Team
Sponsored by:
This petition is in support of the campaign to get Low Dose Naltrexone (LDN) into clinical trials as soon as possible.
At the moment there are very few Neurologists and GP's willing to prescribe LDN. We need it trialed urgently for the benefit of all those with Multiple Sclerosis.
For more LDN information pleae visit the following sites:
http://www.ldninfo.org
http://www.ldnresearchtrust.org
At the moment there are very few Neurologists and GP's willing to prescribe LDN. We need it trialed urgently for the benefit of all those with Multiple Sclerosis.
For more LDN information pleae visit the following sites:
http://www.ldninfo.org
http://www.ldnresearchtrust.org
This petition is in support of the campaign to get Low Dose Naltrexone (LDN) into clinical trials as soon as possible.
At the moment there are very few Neurologists and GP's willing to prescribe LDN. We need it trialed urgently for the benefit of all those with Multiple Sclerosis.
For more LDN information pleae visit the following sites:
http://www.ldninfo.org
http://www.ldnresearchtrust.org
At the moment there are very few Neurologists and GP's willing to prescribe LDN. We need it trialed urgently for the benefit of all those with Multiple Sclerosis.
For more LDN information pleae visit the following sites:
http://www.ldninfo.org
http://www.ldnresearchtrust.org
This petition is in support of the campaign to get Low Dose Naltrexone (LDN) into clinical trials. Many drugs used for MS on a daily basis have not been in clinical trials and yet Doctors still prescribe them to MS patients. Some drugs used in the treatment of MS have serious side effects. Low Dose Naltrexone is prescribed at such a low dose of 3 - 4.5 mg daily that there is absolutely no harm in using it. Many people have found their progression to stop or at least slow down immensely while taking LDN. Unfortunately though LDN is still rarely prescribed, therefore the sooner we get trials underway the better. Many people from around the world are trying to get their doctors to prescribe LDN but very few are lucky enough to find a good doctor who will help. Dr. Bihari in New York and Dr. Lawrence in Wales are under alot of pressure trying to help as many patients they can. At present they have to put many on a waiting list because there are little other doctors helping them by prescribing this drug. Your help is needed right now! Please sign this petition today and send it to as many people with as possible, together we can make a difference. Our team of campaigners for LDN hope to reach our goal of 100,000 signatures with your help. No matter where you live, you are important to us as we are campaigning for EVERYBODY WITH MULTIPLE SCLEROSIS. We will then send the results to politicians in all corresponding countries.
We signed the "Sign & Support the campaign for Research & Trials in 'Low Dose Naltrexone for Multiple Scler" petition!
# 11,408:
7:19 am PST, Feb 9,
Nicole Foerstner, Michigan
# 11,407:
7:02 am PST, Feb 9,
Name not displayed, Wisconsin
# 11,406:
3:06 pm PST, Feb 8,
Susan Hamilton, Washington
I have attempted to talk to my doctor regarding LDN, as I have had fibromyalgia and ibs for 15 years. My attempts have proven futile, I recently stumbled on the book "The Promise of Low Dose Naltresone Therapy", when I was at the Central Library in downtown Seattle....I hope to have more success in my next doctor visit, as I am going to take the book with me. More often than not, education has to come from the patient!
I have attempted to talk to my doctor regarding LDN, as I have had fibromyalgia and ibs for 15 years. My attempts have proven futile, I recently stumbled on the book "The Promise of Low Dose Naltresone Therapy", when I was at the Central Library in downtown Seattle....I hope to have more success in my next doctor visit, as I am going to take the book with me. More often than not, education has to come from the patient!
# 11,405:
9:01 am PST, Feb 6,
Sharon L., Wisconsin
I have a friend with advanced MS, and it has stricken members of my husband's family, as well: an aunt and cousin. Sharon L.
I have a friend with advanced MS, and it has stricken members of my husband's family, as well: an aunt and cousin. Sharon L.
# 11,404:
11:08 am PST, Feb 5,
Annette margaret Collinson, United Kingdom
i was diagnosed with primary progressive ms, im 53 and as far as i know ive had it ms 5 year. i heard about ldn through the internet asked my gp if he would prescribe it was told to have a word with my specialist/consultant. dont see my consultat till april and feel nothin is bein done for me.
i was diagnosed with primary progressive ms, im 53 and as far as i know ive had it ms 5 year. i heard about ldn through the internet asked my gp if he would prescribe it was told to have a word with my specialist/consultant. dont see my consultat till april and feel nothin is bein done for me.
# 11,403:
9:53 am PST, Feb 4,
Kathy Long, Wisconsin
# 11,402:
5:05 pm PST, Feb 3,
J Turner, Georgia
# 11,401:
5:39 am PST, Feb 2,
Vanessa Strange, Wisconsin
This is a very important study. LDN seems to have helped many, but validation is the key to it's acceptance. So, please reconsider any plans to stop this study,
This is a very important study. LDN seems to have helped many, but validation is the key to it's acceptance. So, please reconsider any plans to stop this study,
# 11,400:
3:34 am PST, Feb 2,
Laura A, United Kingdom
# 11,399:
12:30 pm PST, Feb 1,
Greta Turner, United Kingdom
LDN worked overnight for me. Legs stronger, no fatigue now, balance problems gone, eyesight improved. Getting on with everything wonderfully.
LDN worked overnight for me. Legs stronger, no fatigue now, balance problems gone, eyesight improved. Getting on with everything wonderfully.
# 11,398:
10:28 pm PST, Jan 31,
Zxcrlzev Zxcrlzev, Venezuela
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# 11,397:
1:34 pm PST, Jan 26,
Susan Smith, United Kingdom
# 11,396:
1:50 pm PST, Jan 25,
Name not displayed, Australia
Kind Regards,
Kind Regards,
# 11,395:
10:03 am PST, Jan 25,
Bridget Brister, New Mexico
LDN has helped me hugely with my Ankylosing Spondylitis and Fibromyalgia, it is my miracle med that's allowed me to walk again.
LDN has helped me hugely with my Ankylosing Spondylitis and Fibromyalgia, it is my miracle med that's allowed me to walk again.
# 11,394:
10:37 pm PST, Jan 21,
Leslie Jordan, California
# 11,393:
6:54 pm PST, Jan 17,
Deborah Stuart, United Kingdom
# 11,392:
3:28 pm PST, Jan 15,
Eleanor McQuade, United Kingdom
The sooner this is done the better for many many people who suffer from this dreadful disease
The sooner this is done the better for many many people who suffer from this dreadful disease
# 11,391:
1:02 pm PST, Jan 14,
Adam Brown, Pennsylvania
Too many good stories out there to pass this one up, seems like a lot of potential value here for people who are suffering.
Too many good stories out there to pass this one up, seems like a lot of potential value here for people who are suffering.
# 11,390:
10:01 am PST, Jan 14,
Anna Petrova Rodrigues, Portugal
# 11,389:
7:43 am PST, Jan 14,
Kenny Overcash, North Carolina
I have been fighting MS for almost 30 years. I took Beta Seron for most of that time. In the last 2 years, it has stopped working, and I was switced to Tysabri. It has shown some amazing improvements, but if LDN could accomplish even more improvements, I would be VERY interested in learning MORE!
I have been fighting MS for almost 30 years. I took Beta Seron for most of that time. In the last 2 years, it has stopped working, and I was switced to Tysabri. It has shown some amazing improvements, but if LDN could accomplish even more improvements, I would be VERY interested in learning MORE!
# 11,388:
2:35 pm PST, Jan 12,
Joy Livingston, California
I have suffered with RA for almost 6 years. This disease robs you of the life you want to live. It is extremely painful and the only drugs available are so toxic and dangerous one wonders why more hasn't been done to solve the mystery of autoimmune diseases. I have a great niece with MS and I will certainly tell her about my discovering this site.
I have suffered with RA for almost 6 years. This disease robs you of the life you want to live. It is extremely painful and the only drugs available are so toxic and dangerous one wonders why more hasn't been done to solve the mystery of autoimmune diseases. I have a great niece with MS and I will certainly tell her about my discovering this site.
# 11,386:
5:27 am PST, Jan 11,
Name not displayed, Nebraska
I have two cousins with MS, so anything that can be done to help them would be appreciated.
I have two cousins with MS, so anything that can be done to help them would be appreciated.
# 11,385:
8:03 pm PST, Jan 9,
Michele Bernier, Mexico
MY LUPUS LESIONS ARE GONE!
MY LUPUS LESIONS ARE GONE!
# 11,384:
11:44 am PST, Jan 9,
Fay Webb, West Virginia
One of my dearest friends has MS. It breaks my heart (and inspires me) to see him struggle physically to do things that make him feel productive. That is the worst part of it--the physical inability to do the things still desired by the heart. Please conduct more research and clinical trials. Thank you.
One of my dearest friends has MS. It breaks my heart (and inspires me) to see him struggle physically to do things that make him feel productive. That is the worst part of it--the physical inability to do the things still desired by the heart. Please conduct more research and clinical trials. Thank you.
# 11,383:
5:53 am PST, Jan 9,
Staci Heersink, Texas
As a pharmacist and Crohn's patient that almost died while receiving Remicade, I am eagerly waiting for options. I would be willing to participate in the studies.
As a pharmacist and Crohn's patient that almost died while receiving Remicade, I am eagerly waiting for options. I would be willing to participate in the studies.
# 11,382:
11:35 pm PST, Jan 7,
Marie Saunders, Australia
We urgently need to get the clinical trials underway in order help people with multiple sclerosis and for others that have auto-immune illnesses that can also benefit from Ldn. Isn't it time to start thinking about what's best for the people with MS and not what's best for the pharmaceutical companies.
We urgently need to get the clinical trials underway in order help people with multiple sclerosis and for others that have auto-immune illnesses that can also benefit from Ldn. Isn't it time to start thinking about what's best for the people with MS and not what's best for the pharmaceutical companies.
# 11,381:
6:15 pm PST, Jan 7,
Chris Fong, Australia
Research and trials are needed urgently - 2 general practitioners, 2 dermatologists and an immunologist I have seen in Australia have never heard of LDN and will not consider it as a treatment until there are readily available research papers on clinical trials.
Research and trials are needed urgently - 2 general practitioners, 2 dermatologists and an immunologist I have seen in Australia have never heard of LDN and will not consider it as a treatment until there are readily available research papers on clinical trials.
# 11,380:
11:52 am PST, Jan 6,
Nicole Dileo, Connecticut
We need it trialed urgently! People are in need!
We need it trialed urgently! People are in need!
# 11,379:
9:19 pm PST, Jan 5,
Jonathan Jeffreys, Virginia
As a victim of multiple sclerosis and having no success with either Copaxone or Avonex, I am anxious for clinical trials investigating the use of LDN and its potential benefits for M.S. patients like myself.
As a victim of multiple sclerosis and having no success with either Copaxone or Avonex, I am anxious for clinical trials investigating the use of LDN and its potential benefits for M.S. patients like myself.
# 11,378:
4:38 pm PST, Jan 4,
Name not displayed, Arkansas
# 11,377:
4:18 pm PST, Jan 4,
Name not displayed, Missouri
# 11,376:
10:48 am PST, Jan 4,
Name not displayed, Missouri
# 11,375:
10:57 pm PST, Jan 3,
Collette Reno, Arizona
# 11,374:
6:10 pm PST, Jan 3,
Henry Pontious, New Jersey
If more doctors would learn about this treatment, many more MS patients could receive this low cost and effective treatment and our health care industry could save many millions of dollars.
If more doctors would learn about this treatment, many more MS patients could receive this low cost and effective treatment and our health care industry could save many millions of dollars.
# 11,373:
1:52 pm PST, Jan 3,
Mark Rollings, United Kingdom
Let governments fund what's good for patients over what's good for drugs companies...
Let governments fund what's good for patients over what's good for drugs companies...
# 11,372:
6:36 pm PST, Jan 2,
Michelle Van Zandt Orlando, FL, Florida
# 11,371:
6:47 pm PST, Jan 1,
Gwen Di Benga, United Kingdom
I have Multiple Sclerosis and Crohn's. Dying to try LDN, with GP support and guidance.
I have Multiple Sclerosis and Crohn's. Dying to try LDN, with GP support and guidance.
# 11,370:
1:14 pm PST, Jan 1,
Name not displayed, Indiana
# 11,369:
11:44 am PST, Dec 31,
Lorena Hampton, Texas
With so many positives and very few negatives associated with LDN, clinical trials for FDA approval as an alternative to painful, side-affect laden current treatments should be made available immediately.
With so many positives and very few negatives associated with LDN, clinical trials for FDA approval as an alternative to painful, side-affect laden current treatments should be made available immediately.
# 11,368:
1:08 am PST, Dec 31,
Sandra Blyth, United Kingdom
MY SON IS JUST 6 YEARS OLD AND HE HAS MS....LDN NEEDS TO BE AVAILABLE EASILY NOW FROM ALLL OUR GP'S...WHAT IS THERE TO QUESTION..ITS CHEAP,SAFE AND HELPFUL TO MANY MANY CHRONIC ILLNESSES.
MY SON IS JUST 6 YEARS OLD AND HE HAS MS....LDN NEEDS TO BE AVAILABLE EASILY NOW FROM ALLL OUR GP'S...WHAT IS THERE TO QUESTION..ITS CHEAP,SAFE AND HELPFUL TO MANY MANY CHRONIC ILLNESSES.
# 11,367:
7:58 am PST, Dec 29,
Tony Tirado, Connecticut
Understanding its tough for doctors in keeping up with the latest information but do it yourself and persist no matter what with so many side affects with other meds its not clear why this is not advertised more than it is now only the money trail. Its about quality of life. I believe folks turn toward drugs (illegal or not) just to feel better.
Understanding its tough for doctors in keeping up with the latest information but do it yourself and persist no matter what with so many side affects with other meds its not clear why this is not advertised more than it is now only the money trail. Its about quality of life. I believe folks turn toward drugs (illegal or not) just to feel better.
# 11,366:
5:24 am PST, Dec 29,
Luciana Philippides, United Kingdom
# 11,365:
6:10 am PST, Dec 28,
Name not displayed, Georgia
# 11,364:
1:52 pm PST, Dec 27,
Sandra Senske, Michigan
For my daughter who was diagnosed with IBD at the age of 3 and now is told that she is out of medication options and should consider a total removal of her colon. She is 21 years old and suffers every day with pain and loss of control of her bowels. She is unable to work and is trying to get disability. Could save the government money if she could take an inexpensive medicine that would help her to become the productive citizen she once was.
For my daughter who was diagnosed with IBD at the age of 3 and now is told that she is out of medication options and should consider a total removal of her colon. She is 21 years old and suffers every day with pain and loss of control of her bowels. She is unable to work and is trying to get disability. Could save the government money if she could take an inexpensive medicine that would help her to become the productive citizen she once was.
# 11,363:
11:55 am PST, Dec 27,
Robin Tubbs, Kansas
# 11,362:
6:41 am PST, Dec 27,
Ray Baumann, Nebraska
# 11,361:
6:09 am PST, Dec 27,
Name not displayed, Germany
# 11,360:
6:00 pm PST, Dec 26,
Charlotte Milligan, Kansas
I beg you to please support clinical trials on this new product, Low dose naltrexone. We feel it could be of such benefit. Thank you
I beg you to please support clinical trials on this new product, Low dose naltrexone. We feel it could be of such benefit. Thank you
# 11,359:
2:23 pm PST, Dec 26,
Ginger Meyer, Missouri
# 11,358:
9:39 pm PST, Dec 24,
Name not displayed, New York
# 11,357:
12:10 pm PST, Dec 24,
James Graham Duncan, United Kingdom
we need more research
we need more research
# 11,356:
5:14 pm PST, Dec 23,
Dorothy Barna, Missouri
people are suffering without it
people are suffering without it
# 11,355:
1:21 pm PST, Dec 21,
Robert Cowherd, Arkansas
# 11,354:
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8:35 pm PST, Dec 20,
Robert N Cox, Arkansas
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# 11,353:
6:29 pm PST, Dec 20,
Lolita Sharp, Arkansas
# 11,352:
2:09 pm PST, Dec 20,
Clare Smith, United Kingdom
My Mother has MS and started on LDN 2 weeks ago. So far encouraging signs with regards to pain control, but why does she have to spend over £100 for 1 mg dose for one month. Not only does she have an awful degenerative disease, she also has to fund her own treatment!
My Mother has MS and started on LDN 2 weeks ago. So far encouraging signs with regards to pain control, but why does she have to spend over £100 for 1 mg dose for one month. Not only does she have an awful degenerative disease, she also has to fund her own treatment!
