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ONLINE GROUPS & VIDEO CHAT SUPPORT SESSIONS GUIDELINES

ONLINE GROUPS & VIDEO CHAT SUPPORT SESSIONS GUIDELINES

by defeatmsa | Nov 21, 2020 | Uncategorized

DEFEAT MSA UNITED FACEBOOK GROUPS  & VIDEO CHAT SUPPORT MEETINGS GUIDELINES (These policies are subject to change without public notice. Your continued membership in a Defeat MSA Alliance associated group implies consent to these policies.) 1) CONTENT: Content on...
“Finding Balance with MSA” – Joshua Calvert (Patient, Australia)

“Finding Balance with MSA” – Joshua Calvert (Patient, Australia)

by defeatmsa | Mar 23, 2020 | Patient Support Blog

My name is Josh I am 46 years of age. My passions include surfing gardening, travelling, and cooking. I worked as registered nurse for 24 years both in Australia and the United Kingdom. I have been married for 20 years and have a 14-year-old son. I live in Illawarra...
“Are we there yet?..No”- Anne Kastelic (Caregiver, Ohio)

“Are we there yet?..No”- Anne Kastelic (Caregiver, Ohio)

by defeatmsa | Feb 27, 2020 | Caregivers Blog

Caregiver Blog Post #2 The road to diagnosis… Are we there yet?…No Now?…No When are we going to get there? Said anyone who has taken a road trip.  Our trip took 3 1/2 years to get a doctor to agree to a diagnosis of “possible/probable...
Defeat MSA Announces Sponsorship of Global MSA Research Congress

Defeat MSA Announces Sponsorship of Global MSA Research Congress

by defeatmsa | Feb 19, 2020 | Advocate's Blog

ST. CLAIR SHORES, MI, February 19, 2020 – DEFEAT MSA ALLIANCE is pleased to announce its support as a primary funder of the 7th International Congress of Multiple System Atrophy: Toward a Cure for Multiple System Atrophy. Defeat MSA Alliance is a newly formed...

“But I’d of had to miss the dance…” – Anne Kastelic (Caregiver, Cleveland, Ohio)

by defeatmsa | Nov 22, 2019 | Caregivers Blog

“But I’d of had to miss the dance…” – Anne Kastelic (Caregiver, Cleveland, Ohio) Today I opened Facebook to see a call for a caregiver writing opportunity for Defeat MSA’s “Caregiver’s Blog.”  The idea is to share our story in an effort to help others on the MSA...
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