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LDN Petition to the European Parliament

889 Comments

D
Danecki
12 years ago

I am about to start taking it cause of stomack carcinom

D
D.O. Davies.
12 years ago

I have suffered from M.S.for 22 years and with no cure/treatment available would welcome this long-awaited trial.

J
John Denheen
12 years ago

On humanitarian grounds and as a tax payer for over 40 years I thoroughly endorse this petition.

J
Julie Phizacklea
12 years ago

There are so many people who need LDN. I have fibromyalgia and ME and I am about to start taking it, the cost for me per year is very expensive, but I think I really do need it. Feel really sorry for people who cannot have access to it.

C
Celia Ferguson
12 years ago

I have just started taking LDN for Parkinsons Disease with the blessing of my Consultant Neurologist who has been prescribing it for his MS patients with great success.

M
marianne verhoeven
12 years ago

LDN needs a registration, as for now it is not available for ms-patients because no doctor will priscribe it without a registration.

M
mr a mitchell
12 years ago

please make this drug front line treatment now.

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Nicola Jenkins
12 years ago

Have used this for 5 months and am really noticing my energy levels up and my walking has improved, I still need to rest butwhen Im active I feel so much better, Im sure I will keep seeing improvement in the nrxt mths too. I have ms my neurologist was willing for me to start LDN and use as well as, although he had already got me on a DMD.

C
Claire de Grasse
12 years ago

Please take a leadership role to show the rest of the world the way.

L
Loretta Gardner
12 years ago

I support this petition

A
Anne Elibol
12 years ago

I fully support this petition

A
anke meers
12 years ago

people should be able to get this drug in a safe way

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George menzies
12 years ago

I have had sle since 2004 the promised benefits from the usual drugs never happened so come on give US some help

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George menzies
12 years ago

I have had sle since 2004 the promised benefits from the usual drugs never happened so come on give US some help

A
alison loizou
12 years ago

I live in Cyprus and doctors here barely recognise fibromyalgia let alone heard of LDN. We need to spread the word and give hope to many who cold benefit from this wonder drug.

A
Anonymous
12 years ago

This is not a lot to ask, seeing as it's known to be working.

A
Anonymous
12 years ago

I am an RRMS sufferer and have heard of the good results this Drug has given so many people.I hope that the EU Parliament will listen to our requests and help to fund these crucial tests asap

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Helen McCrea
12 years ago

More and more people are developing autoimmune diseases, this drug could help them get some quality of life back, please help them

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soo
12 years ago

I am on LDN and my what a difference its made on my life . There is a lot of people out there who deserve to have this drug to help them.