MS: Getting the word out & Fundraising Tips Needed?

Question

I have an THEORY that MS and RA are in part caused by vitamin deficiency most probably due to MALabsorption. I want to get media coverage on asking people to get tested at cell level(step beyond blood).

I would like to set up a fund for raising money to give univ so they can complete a pilot study on this topic. I have NO clue as to where to start. Is there any organizations that could help me ?? I contacted National MS Society and left a message but their phone recording goes over there major funding coming from Pfiser & another pharmiceutical company so I am not holding my breath that they give money to look into malabsorption issue.

Any names, #s, email addresses of people who could help me(journalists,research $$).

I had my family member with MS tested and he does have boarderline vit D deficiency (scored 33.7 on scale of 32-100) AFTER taking 1400 IU of vitamin D daily? Sounds like absorption issue so doing further tests.

PLEASE HELP me help others get info about testing!

Answer 1

yeh it's true your saying...

Answer 2

Sorry, I can't help you but wish you luck.  I have a very dear friend with MS (actually my ex-husband) and he now spends most of his time in a wheelchair.  I support the Society with monetary contributions as best I can.  Again, good luck.