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Patient Support Blog

MSA BLOGS 

Caregiver’s Blog

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

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

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 MSA" and we were seeing...

Advocate’s Blog

GIVE HELP, GIVE HOPE – RAYS OF HOPE HOLIDAY FUNDRAISER!

GIVE HELP, GIVE HOPE – RAYS OF HOPE HOLIDAY FUNDRAISER!

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...

#GIVINGTUESDAY – ON DECEMBER 1 – FACEBOOK MATCH FUNDRAISER!

#GIVINGTUESDAY – ON DECEMBER 1 – FACEBOOK MATCH FUNDRAISER!

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 Facebook...

Researcher’s Blog

“ANNOUNCING NEW MSA GENETIC STUDY IN CANADA”

“ANNOUNCING NEW MSA GENETIC STUDY IN CANADA”

November 23, 2020 WINDSOR, ON - Defeat MSA Canada/Vaincre L’AMS Canada, Defeat MSA Alliance: Defeat Multiple System Atrophy and MSA United International enthusiastically announce a new genetic study in partnership with the Canadian Open Parkinson's Network (C-OPN)....

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