LDN Petition to the European Parliament

Please provide funding for this drug to be made available in the UK

Please provide funding for this drug to be made available in the UK

Please make LDN avaliable on the NHS,i take ir for ME and it has made a big diference to my life but find it hard to pay for it privately.

Please make LDN avaliable on the NHS,i take ir for ME and it has made a big diference to my life but find it hard to pay for it privately.

I was diagnosed with PPMS in Sept 2009 and have been on LDN for 3 years.

I was diagnosed with PPMS in Sept 2009 and have been on LDN for 3 years.

20 years suffering from RA. The danish government has paid my Biological Medicine which has cost at least 1 million danish KR Now I`m on LDN and pay my own medicine as it is an inexpensive drug. I am very gratefull. Before I suffered on bio medicine, now i feel alive and free from sideeffects

20 years suffering from RA. The danish government has paid my Biological Medicine which has cost at least 1 million danish KR Now I`m on LDN and pay my own medicine as it is an inexpensive drug. I am very gratefull. Before I suffered on bio medicine, now i feel alive and free from sideeffects

Please push for this treatment to be licensed and researched further. Many Many people have gained freedom from chronic illness by using LDN.

Please push for this treatment to be licensed and researched further. Many Many people have gained freedom from chronic illness by using LDN.

Clinical research is the only way forward to finding out if the medication does work for people with autoimmune conditions. Don't make it all about the money or profits - it's about OUR quality of life and we do not want to be a burden to our society by being too ill to work and claiming benefits.

Clinical research is the only way forward to finding out if the medication does work for people with autoimmune conditions. Don't make it all about the money or profits - it's about OUR quality of life and we do not want to be a burden to our society by being too ill to work and claiming benefits.

Autoimmune diseases affect so many people and we deserve to be able to use a medication that can improve our quality of life and live life to the full again.

Autoimmune diseases affect so many people and we deserve to be able to use a medication that can improve our quality of life and live life to the full again.

My son who has severe ME/cfs and has been housebound for 4 years wants to have the benefit of LDN. I believe because of the current evidence this drug should be available now for a wide range of conditions without waiting for the relevant trials. People with ME/cfs are denied any effective treatment and upto 250,000 people in the UK are all but forgotten and abandoned by the NHS. This is a disgrace.

My son who has severe ME/cfs and has been housebound for 4 years wants to have the benefit of LDN. I believe because of the current evidence this drug should be available now for a wide range of conditions without waiting for the relevant trials. People with ME/cfs are denied any effective treatment and upto 250,000 people in the UK are all but forgotten and abandoned by the NHS. This is a disgrace.

I've experienced LDN as a truly spectacular treatment. It would be a huge waste not to explore fully the potential of this drug.

I've experienced LDN as a truly spectacular treatment. It would be a huge waste not to explore fully the potential of this drug.

Let us get this therapy available and heard of on the NHS for those who could lead a better quality of life. It is also able to halt devastating diseases, please work with us to get this available worldwide.

Let us get this therapy available and heard of on the NHS for those who could lead a better quality of life. It is also able to halt devastating diseases, please work with us to get this available worldwide.