Committed to trials of LDN as a treatment for autoimmune diseases

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About the LDN Research Trust

The LDN Research Trust was set up by a small core of people who have Multiple Sclerosis. The primary aim of the Trust is to initiate Clinical Trials of Low Dose Naltrexone.

Whilst working to raise funds for trials, we have helped over 15,000 people  to obtain LDN from a General Practitioner or Neurologist, either through the National Health Service or by private prescription.  We have also been able to help people, not just in the UK but in countries throughout Europe, as well as USA, Canada, West Indies, Australia, New Zealand, and others. By using this website and from our downloadable newsletters, you will be able to read the stories of some of these people.

We have helped many people with MS, Crohn's, IBS, ME and Cancer to name a few. The use of LDN is spreading.

Our ultimate goal is for everyone to be prescribed LDN on the NHS for all conditions where LDN could be of benefit.

The LDN Research Trust is a non-profit-making Registered Charity, and everyone is a volunteer.  

However, we are little different from other charities, in that there are unfunded elements which do ultimately cost us money to maintain and operate. To help us continue our work to bring relief to all people with Multiple Sclerosis, and other conditions we would appreciate help with fund raising, either in cash or in kind.  You can be sure that all contributions are greatly appreciated, however small. 

The Charity is a non-profit-making organisation whose aim is to enhance awareness of Low Dose Naltrexone (LDN), and the promotion and funding of research and clinical trials of LDN as a treatment for Multiple Sclerosis and other autoimmune diseases. The results of such research will be published for the benefit of the public.

We need to raise funds to get clinical trials underway, starting with those for Multiple Sclerosis, and then for other diseases suggested by Dr Bernard Bihari which might benefit from trials of LDN.

Our ultimate goal is for everyone to be prescribed LDN on the NHS for all conditions where LDN could be of benefit.

The Charity was set up by a group of people who themselves have MS and who have proved that LDN works for them. It is non-profit-making, and no salaries or wages whatsoever will be taken from the funds. Only expenses for the running of the Charity will be taken, and these will be at cost.

 

You can listen to over 400 interviews on our YouTube Channel, from LDN prescribing doctors, scientists, pharmacists and users for many conditions .

To download the LDN Information Pack which can be printed, to show your doctor.

The conditions where LDN could be of benefit. Countries around the World where are members are from.