LDNNow SP Feb2011

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!

Category:

News & Politics

Tags:

• Low Dose Naltrexone
• LDN
• Crohns
• Ulcerative Colitis
• Multiple Sclerosis
• Fibromyalgia
• Autism
• HIV/Aids
• Health
• Rheumatoid Arthritis
• LDNNow
• Hepatitis C
• Autoimmune Disease
• Cancer

[djkb1234]

I live in Northern Ireland and suffer from MS I have asked my consultant to prescribe it for me but was told that it was only given to suffers when everything else had failed!

It is scandalous that drug companies and some doctors are making millions out of our NHS, and it is evident that some "experts" have no interest in having a medical trial. I wonder why £££££££££££. I wish you all the best with your efforts.

Could you have an investigative TV programme have a look at this?