We are a group of individuals dedicated to getting Low Dose Naltrexone (LDN) accepted in modern medicine, and trialled for the myriad of uses it shows benefit for.  These uses include autoimmune diseases such as Multiple Sclerosis, many cancers, Chrons disease, Rheumatoid Arthritis, HIV/Aids, Autism and many more conditions.   Each of us benefits from using LDN and we simply want to see it available to others. We have access to it because we know about it, but until everyone has heard of it and is given a fair chance to use it if they need to, we will continue our campaign.

In our unanimous opinion, it is scandalous that if another use is found for a generic drug after its patent expires, it cannot be made available without trials: these trials are too expensive when the sponsor wants to recover their investment. This is a blatant case of profit standing in the way of people’s lives. People are dying needlessly because they cannot get LDN, or because they are not being told about it. This is not an exaggeration, but neither is it intentional: it is just a consequence of leaving health care to the world of business. We need to short circuit this apathy right Now!

Jayne Crocker, Andrew Barnett, Malcolm Smith, Silvia Lane, Bob Thomson, Margaret Anne Gachagan, Janet Perry, Sandra and Sam Blyth and Bev Kean

Hopefully, this site will act as a simple signpost to all the fantastic work being done to bring LDN into the world where it needs to be.