ABOUT this BLOG and How to use it

WELCOME to Stu's Views & MS News. A product of MS Views and News, a Not-for-Profit [501c3] organization. Founded in 2008, we provide educational Multiple Sclerosis information via live seminars and via the internet.

Key-Notes: Our live seminars average approx 60 people per educational program. Our blog is visited over 2900 times per week and our website is visited by thousands each month.

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On this blog see our Directory, Archives, recent Blog Posts & so much more. Use the Blog Search box (enter a keyword). See our Facebook information AND Links to other MS Organizations & bloggers. Scroll through entire page, to find information that could EMPOWER You. At the Bottom of this page, see informational videos and some for fun.

Disclaimer: "Stu's Views & MS News" / 'MS Views and News' does not endorse any products or services found on this blog. It is up to you to seek advice from your healthcare provider. The intent of this blog is to provide information on various medical conditions, medications, treatments, and procedures for your personal knowledge and to keep you informed of current health-related issues. It is not intended to be complete or exhaustive, nor is it a substitute for the advice of your physician. Should you or your family members have any specific medical problem, seek medical care promptly

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Friday, October 30, 2009

A new forum offered by the MSF: "African Americans with MS"

Some great news, the Multiple Sclerosis Foundation (MSF) has a new forum: African Americans with MS Forum.

Dr. Mitzi Williams & Lara Stepleman, PhD both experts on African Americans with MS will answer your questions. They see over 1, 000 African Americans with MS in the Augusta MS Center , GA


On this forum you will also be able to post questions to the people on the forum. A chance for you to meet other African Americans with MS across the UNITED STATES.


go to:http://www.msfocusforum.com/ - If you have a problem with the forum, email Derrick Lee at the MSF. ( derrick@msfocus.org)




Information provided by Helen Mangan - Support Group Coordinator for the MS Foundation.


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