Hello Friends! This fundraiser was created to raise awareness for the Multiple System Atrophy Coalition. My Mom, Kimberly Ann Kabasinski, passed away 4 years ago from complications of MSA. This disease is truly a nightmare. My Mom began to lose her balance, then her coordination, then her speech - the list goes on. She fought very bravely with this illness for 7 years. My Mom was truly one in a million. Her smile was contagious and she was the sweetest woman on the planet. She encouraged me to follow every dream, and was always right by my side cheering me on.
So please join me in raising awareness for MSA. Every $5 counts! It is my hope that someday a cure will be found for MSA.
Since 1989, The Multiple System Atrophy Coalition has focused on collaboratively building hope for those living with multiple system atrophy.
In support of families facing this disease, each year we host the world's largest live streamed MSA Patient & Family Conference. Our toll free MSA support line is staffed by past care partners who have extensive experience in managing all aspects of daily care.
Through activities like sponsoring and promoting prestigious MSA research conferences, supporting young investigators, and directing over $1.6 million towards 36 MSA research projects so far, the world's MSA research experts turn to us for partnership and collaboration.
This past year we hosted the 1st ever Global Meeting of MSA Charities in New York City. We sponsored the International MSA Congress bringing together over 200 MSA researchers to share their latest findings. During March MSA Awareness Month, we rang the NY Stock Exchange Closing Bell.
If you're looking to make a real difference on a global scale, The MSA Coalition is the charity to support this holiday season.
DONATE to this Holiday Hope campaign starting on Giving Tuesday November 27th.
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