My mum has MS and would like to at least give LDN a try, surely thats not to much to ask!
E
EDWARD DAVIS
11 years ago
My mum has MS and would like to at least give LDN a try, surely thats not to much to ask!
M
Martine McKue
11 years ago
People with autoimmune diseases deserve the chance of leading a life where they are actually able to function and achieve things! Many days are being wasted where the pain and depression are unbearable and the solution to this could be something as simple as LDN! We deserve the chance to live life!
G
Gill Corley
11 years ago
My husband has secondary progressive MS and we have just become aware of LDN. Finding out about a drug that could make living easier and even stop the progression has given him so much more hope for the future. This is why I am signing this petition.
B
Becky
11 years ago
I believe this LDN will change our lives forever! We need to help the sick and tell the world what we have in our back pockets!
M
Mona Larsen
11 years ago
A life saving drug that we know is safe. Ridiculous situation that EU must rectify if they are to keep or regain the trust of it's European citizens!
J
John Taylor
11 years ago
A vitally important drug. It is time we took note and stood shoulder to shoulder to stop Pharmacutical companies dictating our health to us in return for financial gain.
F
Freja Taylor
11 years ago
If this is not a comment on profit over humanity I don't know what is! Please EU do the right thing for us all, and not the right thing for your personal bank balances. Corruption on an epic scale seems the only feasible reason why this wouldn't be trialled and approved!
D
Darren Stokes
11 years ago
This drug is safe as houses let it pass
S
Susie Meehan
11 years ago
I have been trying unsuccessfully to get my doctors to look at this drug. Conventional medication is not working for me. I just don't get their reluctance. The drug companies are in control not the doctors.
A
Anna Rowley
11 years ago
This is not concentrating on one horrid disease but a plethora, come on everyone maybe it doesn't make the drug companies money, but think what it could save our countries and if not that think of the lives of each person directly concerned...not just the individuals, but their family, friends and the next generations to come. Please let's make it happen, now.
C
Clare Mould
11 years ago
I am a 39yr old women, i was dx with rrms on 6th May 2003, i have since progressed to spms, there is no treatment for spms, i have been looking into my one lifeline of slowing down the progression of this NASTY/DEBILITATING illness i have been given, therefore, I have been looking i have been looking into LDN. Apparently a prescription of this drug the for LDN, is not available on the NHS, even though if it was it is inexpensive and could save them millions.
Therefore, I am strongly petitioning against this and need this cheap drug made available.
A
Anonymous
11 years ago
I have crohns disease and would welcome the chance for this drug
J
Jenny Fernandez
11 years ago
This drug has proved effective for so many medical conditions. I have a number of autoimmune diseases and I will benefit from this LDN = Low Dose Naltrexone instead of the medication that is currently considered which will only exacerbate my current medical conditions dramatically. We need support with this drug trial urgently.
A
Adrian Makulow
11 years ago
We need LDN now
D
dawn jury
11 years ago
I have ms, and feel there is not anything on NHS out there for us.
A
angela guy
11 years ago
I suffer many auto immune disorders that leave me unable to work. LDN has been shown to improve these illnesses where no other drugs have except immunosuppresants. I am signing this petition in the hope that I can live a normal life in the future.
E
Elsie Silvey
11 years ago
I am so excited about starting on LDN. I finally found some hope for my condition. It is sad that doctors act like they would rather fight for "big medicine" than to help their patients.
Save the peopel
Save the peopel
My mum has MS and would like to at least give LDN a try, surely thats not to much to ask!
My mum has MS and would like to at least give LDN a try, surely thats not to much to ask!
People with autoimmune diseases deserve the chance of leading a life where they are actually able to function and achieve things! Many days are being wasted where the pain and depression are unbearable and the solution to this could be something as simple as LDN! We deserve the chance to live life!
My husband has secondary progressive MS and we have just become aware of LDN. Finding out about a drug that could make living easier and even stop the progression has given him so much more hope for the future. This is why I am signing this petition.
I believe this LDN will change our lives forever! We need to help the sick and tell the world what we have in our back pockets!
A life saving drug that we know is safe. Ridiculous situation that EU must rectify if they are to keep or regain the trust of it's European citizens!
A vitally important drug. It is time we took note and stood shoulder to shoulder to stop Pharmacutical companies dictating our health to us in return for financial gain.
If this is not a comment on profit over humanity I don't know what is! Please EU do the right thing for us all, and not the right thing for your personal bank balances. Corruption on an epic scale seems the only feasible reason why this wouldn't be trialled and approved!
This drug is safe as houses let it pass
I have been trying unsuccessfully to get my doctors to look at this drug. Conventional medication is not working for me. I just don't get their reluctance. The drug companies are in control not the doctors.
This is not concentrating on one horrid disease but a plethora, come on everyone maybe it doesn't make the drug companies money, but think what it could save our countries and if not that think of the lives of each person directly concerned...not just the individuals, but their family, friends and the next generations to come. Please let's make it happen, now.
I am a 39yr old women, i was dx with rrms on 6th May 2003, i have since progressed to spms, there is no treatment for spms, i have been looking into my one lifeline of slowing down the progression of this NASTY/DEBILITATING illness i have been given, therefore, I have been looking i have been looking into LDN. Apparently a prescription of this drug the for LDN, is not available on the NHS, even though if it was it is inexpensive and could save them millions. Therefore, I am strongly petitioning against this and need this cheap drug made available.
I have crohns disease and would welcome the chance for this drug
This drug has proved effective for so many medical conditions. I have a number of autoimmune diseases and I will benefit from this LDN = Low Dose Naltrexone instead of the medication that is currently considered which will only exacerbate my current medical conditions dramatically. We need support with this drug trial urgently.
We need LDN now
I have ms, and feel there is not anything on NHS out there for us.
I suffer many auto immune disorders that leave me unable to work. LDN has been shown to improve these illnesses where no other drugs have except immunosuppresants. I am signing this petition in the hope that I can live a normal life in the future.
I am so excited about starting on LDN. I finally found some hope for my condition. It is sad that doctors act like they would rather fight for "big medicine" than to help their patients.