Multiple System Atrophy (MSA) is a rare, neurodegenerative disorder impacting multiple bodily systems. Key symptoms can manifest in various combinations, including ataxia (impaired balance and coordination), significant postural hypotension (low blood pressure causing dizziness or fainting upon standing), bladder dysfunction (retention or incontinence), constipation, impotence, difficulties with speech and swallowing, sleep disorders, respiratory issues, and rigidity and tremor resembling Parkinson's disease. MSA can be regarded as a combination of three distinct presentations: Sporadic Cerebellar Ataxia Atypical Parkinsonism (Parkinson's Plus) Autonomic Dysfunction (Dysautonomia) Historically, these presentations were classified as three separate conditions: Olivopontocerebellar Atrophy (OPCA) Striatonigral Degeneration (SND) Shy-Drager Syndrome (SDS) The information contained on this website is intended for general knowledge and informational purposes only and does not constitute medical advice. This information is not intended to be a substitute for professional medical advice, diagnosis, or treatment. Always seek the advice of your physician or other qualified health provider with any questions you may have regarding a medical condition. Never disregard professional medical advice or delay in seeking it because of something you have read on this website. While we strive to provide accurate and up-to-date information, medical knowledge is constantly evolving. Therefore, we make no warranties, express or implied, about the completeness, accuracy, reliability, suitability, or availability with respect to the website or the information, products, services, or related graphics contained on the website for any purpose. Any reliance you place on such information is therefore strictly at your own risk. This website may contain links to other websites. These links are provided for your convenience only and do not constitute an endorsement of the linked website or its content. We are not responsible for the content of any linked website.
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About MSA
Ways to Help
Learn more about the symptoms, causes, and impact of MSA. Your support can change the future for MSA patients.
Our Impact
Ways we are trying to fund research is by holding regular fundraisers, such as Trivia Nights, Gala events, other ways are by donating but clicking the link below
Our Team
Meet the dedicated individuals driving our research forward and providing support to MSA patients and their families.