by defeatmsa | Mar 11, 2021 | Medical Research
NEW DRUG TRIAL FOR PEOPLE DIAGNOSED WITH MSA AND NEUROGENIC HYPOTENSION (BLOOD PRESSURE PROBLEMS): FROM THERAVANCE BIOPHARMA: For some people with MSA, parts of the nervous system may not work as well at regulating blood pressure, potentially resulting in a sudden...
by defeatmsa | Feb 14, 2021 | Advocacy Blog, Advocate's Blog
ST. CLAIR SHORES, MI, February 10, 2021 – 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. In 2020, Defeat MSA Alliance. along with...
by defeatmsa | Feb 1, 2021 | Advocacy Blog, Advocate's Blog
Help Defeat MSA – Include A Photo in Our New MSA Awareness Book! OBJECTIVE: To publish a small art photo book (printed on paper, approximately 50 pages, 20×20 cm, 7.9 x 7.9 in.) to represent those impacted by Multiple System Atrophy. As a bonus for each person...
by defeatmsa | Dec 2, 2020 | Advocacy Blog, Advocate's Blog
GIVE HELP, GIVE HOPE – ANNOUNCING THE 2020 RAYS OF HOPE HOLIDAY FUNDRAISER! Help Us Support MSA Research! Help Us Support MSA Patients! Help Us Support MSA Awareness! Help Us Educate Medical Professionals! 4 Ways to Support Our Efforts: Create #JustGiving Holiday...
by defeatmsa | Nov 27, 2020 | Advocacy Blog, Advocate's Blog
Announcing Defeat MSA Alliance #GivingTuesday 2020 Facebook Matching Fundraiser! Facebook has announced up to $100,000 Matching Funds Available on December 1, 2020 for #GivingTuesday. If you are giving this year – please consider helping Defeat MSA with a...
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