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I was just looking at the NMSS (National Multiple Sclerosis Society)

web site and saw the following:

" The National Multiple Sclerosis Society provides funds for limited

short-term support of research in areas where preliminary data are

scant or nonexistent. This program is designed to support unique or

novel ideas with the potential to open significant new areas of

research on multiple sclerosis. Projects that are simply extensions of

on-going research or that already have ample supporting data will not

be considered. "

I agree that no drug company is going to undertake an FDA approved

study of LDN but the MS Society is supposedly not driven by a profit

motive but driven to find a cure.

There must be at least one idealistic researcher in the world who would

like to study a drug with the anecdotal promise of LDN and I'm sure

most of us would love to see the Society made to live up to its lip

service.

So, why has nobody applied for MS Society funding for an LDN study (or

if they have and been turned down, publisize that)?

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