March is Multiple System Atrophy Awareness Month!
Please DONATE NOW to support the fight against this devastating neurodegenerative disease.
At least 13,000 Americans and thousands more around the world need our help to fund critical research for earlier diagnosis, disease modifying treatments, and ultimately to discover a cure. Additionally, money is needed to educate the medical and MSA community, as well as for advocacy and awareness initiatives.
The Multiple System Atrophy Coalition is the leading nonprofit funder of global research, with a world-class scientific advisory board charged with vetting research proposals received from all parts of the world ensuring only the most promising MSA research projects receive our support.
Please donate today and your dollars will help support:
- Our Global Research Grant Program
- Our annual conference for patients and families (webcast live around the world)
- Training of volunteers to ensure our dedicated toll free support line continues
- Development of improved MSA educational materials for patients and carepartners
- Sponsorship of MSA educational events for health care professionals
- Sponsorship of travel grants for young MSA researchers to attend scientific conferences and present their work
- Sponsorship of the International Multiple System Atrophy Congress
- Staff to increase fundraising capacity which will directly lead to more dollars available for research, education, support and advocacy initiatives
- Development of a support and volunteer network to reach all affected by MSA
Your financial support to the MSA Coalition will keep alive the hope of finding a cure for Multiple System Atrophy through our Global Research Grant Program and sustain our efforts to support all affected by the disease.
Thanks so much for your generous support!
About Multiple System Atrophy
Multiple System Atrophy is a serious, life limiting neurological disease. It is so rare that most doctors have not even heard of it. Currently, MSA has no cure, no known cause nor any specific risk factors. People diagnosed with Multiple System Atrophy are swiftly robbed of their ability to walk, talk, chew, swallow and eventually breathe. They also become physically reliant on family members, friends or relatives to carry out most aspects related to daily living. For those diagnosed, it is a death sentence. There are no drugs that stop it's relentless progression. Research, education, support and advocacy are desperately needed.
About Multiple System Atrophy Awareness Month
In 2010, March was first officially declared as MSA Awareness Month. Since then, this annual event has grown to become a rallying point for the global Multiple System Atrophy community. Thousands of patients, care partners and advocates join their voices to share their personal stories and raise funds for the cause. As the nation's oldest and largest organization dedicated to this disease, and the leading nonprofit funder of global MSA research, the Multiple System Atrophy Coalition is encouraging everyone to support MSA Awareness Month.