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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Monday, June 13, 2011

About Stuart Schlossman - The provider of this Blog for those affected by Multiple Sclerosis


~~ Diagnosed with Multiple Sclerosis (MS). 

When I was diagnosed in 1998 with MS, there was little information available, without sourcing it all on the internet. Most people who I know, were skeptical about using the internet to find information. MANY whom I still know, do not know how to find things on the internet. 

This is why I do, what I do, in finding disseminating and providing information for those affected by MS, VIA this blog, via my website or via my weekly e-Newsletter. 

REGISTER if not receiving my weekly e-newsletter by clicking here: www.register.msviewsandnews.org

~~ Personally: I try to do, what I can, when I can.. Know what I mean? Learn more of me by visiting my website (www.msviewsandnews.org) and clicking on the "about Stuart" link.


Other places to find me or the information provide:
www.facebook.com/msviewsandnews  (MSV&N on Facebook)



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Disclaimer:  'MS Views and News' (MSVN), 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.

3 comments:

Peg Meerkatz said...

I was diagnosed in 1987 a era many MSers refer to as the period of diagnosis & adios. The doctors diagnosed you then you figured out the rest because no one (not even the doctors) knew much about MS. I now have secondary progressive MS and if I hear one more time home my outcome would have been better had I started disease modifying drugs when I was first diagnosed the long term prognosis would be better. Duh! There were no DMD's when I was diagnosed. I was pumped full of so much steriords I developed cataracts before age 30. I am happy to see all the research now being done but more has to be done for those with progressive MS.

Cherie said...

And I, for one, am grateful you took that restless need to know and converted it into a newsletter that has grown and evolved and is so userfriendly and unbiased. You are a gift and this person thanks you.

Stuart said...

Thank you Cherie... When will we have another story from the MS Nurse?