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What is Multiple System Atrophy (MSA) and How Does It Impact Me and My Family? 

Mission MSA
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The MSA Coalition kicked-off MSA Awareness Month 2023 with this webinar featuring Paul Beach, DO, PhD from Beth Israel Deaconess Medical Center and Amy E. Wynn, FNP from Vanderbilt University Medical Center where they addressed “What is MSA?” for both the patient, care partner and family members and provided the opportunity for attendees to ask questions and understand the clinical and psycho-social aspects of multiple system atrophy.
THIS EDUCATIONAL SESSION IS NOT INTENDED FOR THE PURPOSE OF PROVIDING MEDICAL ADVICE. All information, content, and material is for informational purposes only and are not intended to serve as a substitute for the consultation, diagnosis, and/or medical treatment of a qualified physician or healthcare provider. The information supplied through webinars or on our webpage, or by any representative or agent of the MSA Coalition, whether by telephone, email, letter, or other form of communication, is for informational purposes only and does not constitute medical, legal or other professional advice.

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28 фев 2023

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Комментарии : 11   
@brendadickenson3547
@brendadickenson3547 Год назад
Thank you all.
@moonstad6750
@moonstad6750 11 месяцев назад
Thank you... I think. Often hard to tell the good news from the bad news these days. Well presented and I'm about to binge the MSAcolalation videos. Mo
@tomtait2463
@tomtait2463 Год назад
Very well done! Tom
@brendadickenson3547
@brendadickenson3547 9 месяцев назад
My husband had dystonia and his neurologist at Shands asked if he would donate his brain to the brain bank at Shands and when he had his heart attack and fell.and only lasted a week. But our funeral home also knew ahead of time so it was not stressful. He had it lined up ahead of time, this was in 2004.
@c.c.3341
@c.c.3341 8 месяцев назад
Brenda I am very sorry about your dear husband. What a deeply compassionate gift he made to research ! I have Dystonia also and Dysautonomia and I feel very strongly that I that also have MSA, but living in a city where there are no experts on it is really tough.
@lindabarnes7358
@lindabarnes7358 7 месяцев назад
​@@c.c.3341my ok
@anthonychristian8030
@anthonychristian8030 Месяц назад
No sound
@c.c.3341
@c.c.3341 8 месяцев назад
What is the email for the MSA Coalition for information please?
@mikewolfe1833
@mikewolfe1833 5 месяцев назад
I do believe after yrs. Of looking and digging through my medical history in the last few years I’ve found to believe I have MSA. In 2021 I was diagnosed with Parkinsonism Parkinson’s disease REM sleep disorder central Bladder weakness Chronic Fatigue Sweating Also had mri of the spine. Showed up atrophy. I was told we won’t figure I was told the only way to know if I had it would be at i’ll Topsey
@mikewolfe1833
@mikewolfe1833 5 месяцев назад
I would like to find a center
@sunahamanagai9039
@sunahamanagai9039 11 месяцев назад
43:25 44:33
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