Guest guest Report post Posted January 17, 2005 Great idea, . Here is my email to Mr. : Dear Mr. : Did you know that the Multiple Sclerosis Society is heavily funded by pharmaceutical companies who manufacture the very expensive (but not very reliable) medications used to treat MS? And that if you call the MS Society and ask them to recommend a doctor, they won't recommend a doctor unless that doctor has promised in writing to prescribe one of these medications? I am an MS patient. I have found the best symptomatic relief from a medication called Low Dose Naltrexone (LDN). It is not marketed by any pharmaceutical company because it can't make them any money; the patent expired years ago. Many, many MS patients swear by LDN, and because of the internet, many more are learning about it every day. LDN is the top-rated MS therapy at Remedyfind.com, the non-commercial site that allows patients to rate their own medications. Many MS patients call LDN a life-saver: http://www.remedyfind.com/hc-Multiple-Sclerosis.asp And guess what? The MS Society has come out against LDN. Strange... I have quite a bit more information if you would like to pursue this. Quote Share this post Link to post Share on other sites