The Multiple System Atrophy Coalition wrote:
Multiple system atrophy (MSA) took my father, Mark Versel, in 2012. My family knew nothing about this terminal disease at the time, and wish we had known about the Multiple System Atrophy Coalition sooner.
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 first-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 MSA Awareness Month in March, we rang the New York 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 27.
*** Please remember to ASK YOUR EMPLOYER if they offer matching gifts or check on this link:
Why not partner with us? CLICK "JOIN THE TEAM" today! Create your own fundraising and awareness page to benefit the MSA Coalition and tell your story.
Together We Are Building Hope for MSA.