Re: Letter to MS Society - research funding

[Guest guest]

Hi Ben,

I was looking to see if there has been an update on your letter to

NMSS? If not, perhaps you might send same to the new MS team at Yale:

http://www.yale.edu/opa/v32.n25/story19.html

Of course, they got funded by NMSS so maybe that wouldnt work either.

But if you like I wil help you search out other locations to send to.

I struck out at NIH alternative medicine, they said since LDN is FDA

approve, it isnt alternative.

On another note, has anyone ever heard of patients funding their own

drug trial? What if we set up a non-profit donation collection org,

and once we had collected your estimate of $500,000, we could hire

one of those contract study administration companys, or take bids.

This is probably pie-in-sky thinking, but if I didn't think like that

I would not have typed " multiple sclerosis cure " into google and

found LDN !! OK, OK, I no it's not supposed to be a cure, but it is

the dame closest thing I've found yet. And no needles!

> -----Original Message-----

> From: [mailto:evansbenjamin@h...]

> Sent: Thursday, April 01, 2004 7:15 AM

> Hi everyone, I'm new to this board and still learning about low-

dose

> naltrexone which I stumbled across a few weeks ago.