[Guest guest]

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.