Hoping to spread the news about MSA. I will send emails out today in hope of raising money go help find the cure for MSA
November 26, 2016
Help find a cure for MSA. A rare brain disease that affects the autonomic system of the body. Autonomic Systems are the body functions that works involuntary. In my case, it has impacted my eyes with double version, my lung capacity is at 50% which as made me home bound. I cannot go out in the heat, or the cold without taking a risk of infection or overheating. It has impacted my bladder, and bowels. Disrupted my sleep pattern, caused swallowing and speech problems. It has effected my balance, and given me ataxia. Limited some of my range of motion. Has made me dependent on a walker and a power chair. It has cause me to give up my dreams and hopes for the future. The latest is that it has impaired my hypothalamus, which regulates body temperature. Hence, I ask that you contribute what you can and none of the proceeds go to me but the MULTIPLE SYSTEM ATROPHY COALITION that supports research to develop a cure. My goal is to raise all I can to give hope to those like myself that is searching for a cure.