Martin M.S. Alliance Foundation

Addressing Multiple Sclerosis in Communities of Color

welcome

“A health to you, a wealth to you,
and the best that life can give to you.”
- Anonymous

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Saturday, April 17, 2010
 Team “Face M.S.” will be participating in 22nd Annual National M.S. Society Walk through downtown Washington, D.C. (This is a beautiful 3 mile loop  beginning and ending at the Embassy of Canada - 501 Pennsylvania Ave NW WDC .  Metro Stop - Archives Navy Memorial/Pen Quarter. Estimated time for the walk is about 70 minutes)
Joining is easy just click below and register. 


https://www.regonline.com/FaceMS


A minimum donation of $25.00 is due at time of registration.  You may register up until 10am that morning.  My friends that are walking in spirit your donation is invaluable.  We will be combing donations and presenting one check to the M.S. Society on behalf of the Foundation.

To learn more about the walk
MS Walk - National MS Society, National Capital Chapter





I want to thank you for your continued support of the Martin M.S. Alliance Foundation and encourage you to experience firsthand the work of our outstanding board members and volunteers. I hope in the coming year we will become one of the leading resources supporting people touched by Multiple Sclerosis. The Martin MS Alliance Foundation’s job is to shed light on the issues of Multiple Sclerosis in communities of color through quality programs, easy to understand information and communicating on many different fronts within the community, the medical field and the corporate world.

Things to Think About:

Take the steps at least once a week, because you can and there is someone out there that wishes they could.

You know someone living with M.S. – you just don’t know it.






Disclaimer: The Martin M.S. Alliance Foundation offers information from various authoritative sources, including professionals, and sources of published record.  The Martin M.S. Alliance Foundation does not endorse any specific treatment regime.  All information and/or referrals are offered solely for the purpose of helping those affected by M.S. make informed decisions about their health care options and do not represent therapeutic recommendation or prescription. Any decisions regarding specific medications or treatment should involve consultation with your professional health care provider. Please be aware that we are an independent 501 (c) 3 charitable organization, Federal ID # 37-1478450.  We are not affiliated with any other organization.  All monies donated to the foundation are used to support the organizations programs

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