ALWAYS IN OUR HEARTS…
Throughout adversity, Mom maintained strength, dignity, grace, a sense of humor, and above all, love…
Multiple System Atrophy is a rare and terminal neurological disease. Diagnosis is often difficult, and treatment addresses symptoms, but there is no cure.
Confronted with a disease that is rare, debilitating, and terminal, patients and their loved ones face a difficult journey – largely alone. Much is needed to provide for better diagnosis, treatment, and support. Research is needed to find a cure, or at least a way to slow the progression of this disease. Above all, patients need hope…
MSA NJ is a non-profit organization formed to provide support for patients, families, caregivers, medical personnel, and any other affected persons or interested parties in the tri-state area impacted by Multiple System Atrophy.
Additionally, our goals include providing education about this disease and related matters, raising public awareness, and supporting research for treatment and a cure. Fundraising efforts are to support realization of these goals.