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Multiplesystematrophy. Living with MSA is a journey that requires courage, resilience, and a strong support network. Mission MSA is leading the charge to...
Read Multiplesystematrophy.org news digest here: view the latest Multiplesystematrophy articles and content updates right away or get to their most visited pages. Multiplesystematrophy.org belongs to a large group of moderately popular websites, with around 45K visitors from all over the world monthly. It seems that Multiplesystematrophy content is notably popular in Italy, as 32.7% of all users (15K visits per month) come from this country. We haven’t detected security issues or inappropriate content on Multiplesystematrophy.org and thus you can safely use it. Multiplesystematrophy.org is hosted with CloudFlare, Inc. (United States) and its basic language is English.
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Best pages on Multiplesystematrophy.org
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The MSA Coalition: Support, Educate, Advocacy & Encouraging Research
The Multiple System Atrophy Coalition is a charitable organization committed to support, educate patients, caregivers & encourage research to identify cause & cure for MSA
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The Multiple System Atrophy Coalition Surpasses $1 Million Milestone in Research Funding - MSA
Global efforts to achieve a greater understanding of multiple system atrophy, a rare and devastating neurodegenerative disease, have been enhanced by ten research projects receiving awards in 2016. Th...
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Guest Blogger: Anna Suarez, Communications Specialist | MAAC Rare Disease Day has arrived! On the last day in February the rare disease community can come together to raise awareness and share some co...
Multiplesystematrophy.org news digest
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6 months
By Jimmy Burt and Kathleen Romania
Can you feel joy and sadness at the same time? It seems like, nowadays, every Christmas season I experience this duality of emotions. I think my wife and her family do too. And I’d imagine George, my father-in-law, does especially.... -
6 months
You Can Go Home Again — with Preparation
By Alan J. Smally
MSA Coalition Board of Directors Patient Representative
Thomas Wolfe wrote “You Can’t Go Home Again,” but I thought maybe I could for Christmas. Although I was born up north, I had my first birthday in Sarasota, Florida, and lived there all through school. I have always considered Sarasota to be my home.... -
7 months
Navigating Emergency Room Visits and Hospital Stays
By Cathy Chapman
During the course of my journey with MSA, (I was diagnosed in 2012), going to the Emergency Room and having to stay overnight in the hospital was something I have had to experience multiple times. I want to share some tips that have been very helpful... -
7 months
By Tom Tait
Is this the last Christmas?
How do you get through Christmas with your loved one who was just diagnosed with possible MSA. The question always on your mind is, “Will this be the last one?” That question will come and go along the MSA journey during many events. I understand it...
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| Web host: | CloudFlare, Inc. |
| Registrar: | Public Interest Registry |
| Registrant: | Registration Private (Domains By Proxy, LLC) |
| Updated: | March 19, 2013 |
| Expires: | October 24, 2023 |
| Created: | October 24, 2012 |
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