This Is MS Multiple Sclerosis Community: Knowledge & Support

Hey Everyone! My name is David Williams and I have worked in the MS and Neuroscience world for about seven years now. Although I'm not a patient, I have worked to help people with MS through community development initiatives. In 2001, I worked with Montel Williams doing numerous online chat sessions, an appearance at the Los Angeles Health Expo, helped launch the Montel Williams Foundation website, and even appeared on his show.

Big f@#kig deal!!!Montel Williams Foundation what a joke was their lots of talking and more talking.. He's got the balls to find some money the MRF needs a few mill, get it done!!!!

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Had ms for over 19 years now.

Yeah, the MWF didn't really get off the ground the way it should have. Like I said, I just helped launch the website. Montel has helped raise funds for MS, though. Awareness was raised a lot, too.

Who else do people think should step up around MS?

Who do u think ds?

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Had ms for over 19 years now.

I think we all have to step up. The issue isn't research $$ or even pharma money going into MS. That's happening. The problem is no one really knows which medication to take, and what other treatments can help.

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This link will take you to an interesting and informative March 24th interview Scott and Dr. Miller did with host Marc Pelletier of Futures in Biotech. It's about 1 hour. I think the interview was conducted in a way that would make it interesting to both scientists and MS novices.

http://www.twit.tv/FIB



Nicole A. McGarvey
Volunteer Area Director-Denver,CO
Myelin Repair Foundation - http://www.myelinrepair.org/
Discovery through collaboration

(303)-882-2672

Correspondence with representatives of the Myelin Repair Foundation should not replace consultation with one or more licensed neurologists or others who are trained to treat the symptoms of MS and other demyelinating diseases.

Nicole,

Thanks for the message. I'm interested in working with the Myelin Repair Foundation. With our real-world data used for research, we can partner to gain more answers.

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dswii, you are welcome at This is MS.

However, your advertisements for your for-profit company are against our forum rules. Kindly refrain from posting them any further. Thank you for understanding.

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Disclaimer: Any information you find on this site should not be considered medical advice. All decisions should be made with the consent of your doctor, otherwise you are at your own risk.

Arron,

I appreciate the rules of the forum, as ours are the same. The key here is that our data are collected for research purposes to help figure out what treatments will help patients TODAY. Patients can learn from other patients what works by seeing clinical outcomes, not just anecdotal evidence. I apologize if I broke the rules, but people should know about this. The breakthroughs we've already achieved in ALS are astonishing.

I apologize to the This Is MS community if I offended anyone.

Best,
David