Our story…
What is MSA?
Multiple System Atrophy is a rare, rapidly progressing neurodegenerative disorder that affects the brain. Think: ALS and Parkinson's combined! In addition to movement disorders, swallowing and speech impairments, MSA impairs the systems that regulate blood pressure, heart rate and the bladder – many of the basic bodily functions that people take for granted every day!
People with MSA suffer from dangerously low blood pressure, speech and swallowing difficulties, sleep disturbances, breathing problems, rigidity and tremors. The life expectancy for those with MSA is typically 5 to 10 years. There is no remission of the disease. Almost 80% of patients are disabled within five years of the onset of the motor symptoms, and less than 20% of the cases survive beyond 10 years.
At present, there is no cure for MSA, no genetic tests to detect it, no therapy to slow it and very few treatments to manage its debilitating effects.
PLEASE CONSIDER DONATING TO OUR TEAM, OUR CHARITY AND HELP US DEFEAT MSA. WITH AWARENESS COMES FUNDING, WITH FUNDING COMES RESEARCH AND WITH RESEARCH COMES A CURE!
#MOVE4MSA #MOVEFORTHOSEWHOCANT 💜
Team members
Click on one of our team members below to make a donation.
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Move4MSA... Move4MyMom
Raised: $521.97
Team captain
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Kerri Bannon
Raised: $111.70
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Shannon Jeffery
Raised: $82.43
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Christine Lafleur
Raised: $54.63
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Jay Saucier
Raised: $0.00
Recent donors
| Donation date | Donor name | Donation amount |
|---|---|---|
| Oct 05 | Danielle Magvas | $54.63 |
| Oct 04 | Dave Delorme | $161.98 |
| Oct 04 | Bannon | $100.00 |
| Oct 04 | Shannon | $27.80 |
| Oct 03 | Curran Family | $33.16 |
| Sep 15 | Liz Campbell | $54.63 |
| Sep 15 | Pat Kalbfleisch | $108.31 |
| Sep 05 | Sylvie Tétreault | $54.63 |
| Sep 04 | Christine Lafleur | $54.63 |
| Sep 01 | Andrew McFadyen | $269.32 |
