It's too bad

[Guest guest]

because this group appears to have real ADVOCATES for the pharmaceutical

companies . . . I'm guessing through the medical community.

All I know for sure is for the last six years I've tried everything that came

down the road.

Something would start out promising and end up nowhere. I spent a TON of money

for it  - money I didn't have and the big drug companies make a fortune. I was

in pain and tired of hoping for the next new drug that might be on the horizon.

When I switched to a medication not even for immune disorders, I received the

first relief Ive had in years.

It's possible it wouldn't work for everyone just as I kept trying new

pharmaceutical's with little or no effect. But the cost for LDN is so low, the

side effects are next to none and the benefits are profound (for me and others).

I would say it's certainly worth a " look-see " .

Rheumatolgists and MOST GP's resist - why wouldn't they? The drug companies

aren't " courting " them for this medication. Their fellowships could be

jeopardized . . . there is NO INCENTIVE ($) or otherwise for docs to get on

board. The only possible advantage to them would be their patient's good

outcome. Sorry to say - in this big money medicene world - not enough.

I've been a part of the pushing of drugs on the seriously ill for the benefit of

drug companies . . . I don't see anything different with this group . . . so not

interested

K