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 in Australia and New Zealand! Help Us Support MSA Patients and Carers in Australia and New Zealand! Help Us Support MSA Awareness in Australia and New Zealand!...

#GIVINGTUESDAY – ON DECEMBER 1 – FUNDRAISERS!

#GIVINGTUESDAY – ON DECEMBER 1 – FUNDRAISERS!

Announcing Defeat MSA Down Under #GivingTuesday 2020 Facebook or My Cause Fundraiser!  December 1, 2020 is #GivingTuesday. Please consider helping Defeat MSA Down Under with a Facebook Fundraiser, My Cause Holiday Fundraiser or a Direct Donation!  We Need Your Support...

Researcher’s Blog

“ANNOUNCING NEW MSA GENETIC STUDY IN CANADA”

“ANNOUNCING NEW MSA GENETIC STUDY IN CANADA”

November 23, 2020 WINDSOR, ON – Defeat MSA Down Under sister charities, Defeat MSA Canada/Vaincre L’AMS Canada, Defeat MSA Alliance: Defeat Multiple System Atrophy and MSA United International consortium enthusiastically announce a new genetic study in partnership...

SEMINAR: “A-Syn Conformational Strains and Patient Perspective”

SEMINAR: “A-Syn Conformational Strains and Patient Perspective”

MSA Researcher Raphaella So, PhD candidate (Toronto), and Defeat MSA Patient Advocate Beverly K. Wilson offer some informed insights on Multiple System Atrophy in a recent talk sponsored by our friends at Cure Parkinson’s UK. Beverly’s presentation describes the...

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