So many of us need to, at very least, try LDN. It is cheap and could help those of us with 'Cell Proliferation' diseases.
Many conventional drugs just do not work for us.
Our Human Rights are being ignored by UK government who prevent our medics from prescribing LDN to those patients who COULD benefit from LDN.
S
Susan Palmer
12 years ago
Fed up with doctors lack of knowledge and disregard for patients well being
T
tracey ellis
12 years ago
i have ms for past 17 years and i wish to sign petition for the use of this drug
M
miranda andrea
12 years ago
I strongly believe based on my research and hearing others talk from taking this that it can have amazing results for some people!! The drugs companys are corrupt in my opinion and clearly there is no profit for them regarding LDN!
L
LYN MAXWELL
12 years ago
This should be available!
C
Chawakorn Hemitti
12 years ago
everyone should have a chance for a better life
A
Aad van Vliet
12 years ago
everyone should have a chance for a better life
D
derrick tate
12 years ago
Why would the government hold back on something that can help so many !
A
Anonymous
12 years ago
I support this petition
C
christine lewis
12 years ago
more GPs need to be knowledgable about ldn so many patients would benefit and ldn is much safer than so many other medications
D
Debbie Holden
12 years ago
I have PPMS & there are no drugs available. This drug appears to help some people with this type of MS & I would like my GP to be able to prescribe it without worry.
A
Annabelle Franklin
12 years ago
Please get this drug trialled now for the sake of all of us unable to work due to chronic conditions that have not responded to any of the drugs currently available.
C
chris Brown
12 years ago
hopefully this is still ongoing
D
Deirdre Craig
12 years ago
Thank you for your altruistic hard work. Keep going, you can see how appreciated you are by so many people with pain.
K
Kerry Duck
12 years ago
Please get this drug availiable, for all of us who suffer so much.
C
Cheryl Payne
12 years ago
Taking LDN since November 2013. Definitely helps my MS symptons
J
Jean O'Donovan
12 years ago
I can't believe that I've only just read about LDN for the first time today. I've had Hashimoto's Thyroiditis for 7 years and it has destroyed my life. I really want to give LDN a try.
B
Becca Eaton
12 years ago
I don't want to be in pain anymore nothing works for me. LDN is helping people like me with fibromyalgia.
B
Bridge Dillon
12 years ago
give me my life back. here is a drug with no side effects that has far superior results in treating fibromyalgia that the drugs I am already on which are higly addictive and have horrendous side effects but most importantly of all they do not work for pain relief. At best they partially work. They are also costing the country almost 200e a month last I checked and Ldn would cost around 30 euro a month I'm told.
S
simone smith
12 years ago
This is so important to be allowed to be made available on the nhs. This could help so many people to be able to take this safe drug.
So many of us need to, at very least, try LDN. It is cheap and could help those of us with 'Cell Proliferation' diseases. Many conventional drugs just do not work for us. Our Human Rights are being ignored by UK government who prevent our medics from prescribing LDN to those patients who COULD benefit from LDN.
Fed up with doctors lack of knowledge and disregard for patients well being
i have ms for past 17 years and i wish to sign petition for the use of this drug
I strongly believe based on my research and hearing others talk from taking this that it can have amazing results for some people!! The drugs companys are corrupt in my opinion and clearly there is no profit for them regarding LDN!
This should be available!
everyone should have a chance for a better life
everyone should have a chance for a better life
Why would the government hold back on something that can help so many !
I support this petition
more GPs need to be knowledgable about ldn so many patients would benefit and ldn is much safer than so many other medications
I have PPMS & there are no drugs available. This drug appears to help some people with this type of MS & I would like my GP to be able to prescribe it without worry.
Please get this drug trialled now for the sake of all of us unable to work due to chronic conditions that have not responded to any of the drugs currently available.
hopefully this is still ongoing
Thank you for your altruistic hard work. Keep going, you can see how appreciated you are by so many people with pain.
Please get this drug availiable, for all of us who suffer so much.
Taking LDN since November 2013. Definitely helps my MS symptons
I can't believe that I've only just read about LDN for the first time today. I've had Hashimoto's Thyroiditis for 7 years and it has destroyed my life. I really want to give LDN a try.
I don't want to be in pain anymore nothing works for me. LDN is helping people like me with fibromyalgia.
give me my life back. here is a drug with no side effects that has far superior results in treating fibromyalgia that the drugs I am already on which are higly addictive and have horrendous side effects but most importantly of all they do not work for pain relief. At best they partially work. They are also costing the country almost 200e a month last I checked and Ldn would cost around 30 euro a month I'm told.
This is so important to be allowed to be made available on the nhs. This could help so many people to be able to take this safe drug.