Funding By MS Society For LDN Study

October 25, 2004

I just got an email from the nmss. They said that they have never

had any contact from Dr. Bihari about getting funds for an LDN

study. They gave me a link:

for any doctor who is interested in funding for research of a

potential MS drug. Does anyone have an email address for Dr. Bihari?

They certainly didn't say that they would fund such a study but they

didn't say they wouldn't. What I know is that if you don't ask they

will not.

Spcifically they said:

At the National MS Society, we support over 300 research projects

that have been deemed by our peer reviewers to be of excellent

quality and have great potential for providing new answers in our

quest to cure multiple sclerosis. These projects are by

investigators who applied to us for support. The individuals who

are claiming to be helping not only MS but many other disorders with

low-dose naltrexone have not applied to us for support, and have

shown no interest in actually doing the controlled clinical studies

that would prove their claims.

The very nature of MS (i.e., a problem one minute, feeling 'cured'

the next is a dream disease for any one making claims that are not

supported by scientific evedence).

I don't know how to contact Dr. Bihari. I would encourage him to

contact the NMSS through this link:

I know I feel better with LDN but if Dr. Bihari passes up this

chance to show the world what many of us know about LDN, I think

things look very suspicious.

I want to emphasize that I don't believe the NMSS is always good or

right but the are the only organization of which I am aware that has

the financial resources to sponsor such a study and one that doesn't

have any real conflict of interest.

Let's get a formal study done so LDN doesn't stay in the shadows.

Larry

PS, if you're interested in the full letter. Email me at

Larry@...

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