My Nonprofit Reviews

The MSA Coalition continues to be a resource, support, and outlet for me and my family even though my mother lost her battle with MSA in December 2016. Throughout her diagnosis, The MSA Coalition provided invaluable connection, answers, support, and HOPE. I have been fundraising for them in honor of, and then in memory of my mother since 2014 and continue to volunteer to this day.

The MSA Coalition was truly a life-saver. My mother lost her battle to Multiple System Atrophy in Dec 2016 , 4.5 years after her diagnosis. During that time the Coalition provided immeasurable support, advice, and resources. We are far from a cure to this nasty disease but my dad, brother, and I made it through with the support of these people.

With nowhere near the resources of the ALS or Parkinson's Foundations, the MSA Coalition made up of volunteers who really care. They want to keep on the fight for their loved ones that are no longer able to fight. The annual conference, live-streamed, is incredibly valuable to current patients, caregivers, and even for medical professionals who are still trying to understand the disease themselves. I look forward to seeing what the next couple of years bring.