In describing our MDA community, I’ve often referred to us as being much like a human body. Our sponsors and volunteers are our backbone, and the families we serve are our heart. Without our sponsors and volunteers, we would collapse; without our heart, we would cease to exist.
MDA is continuously measuring the pulse of our MDA community and at all times is centered on the heart of our effort —...
MDA's Public WebEx , held on February 24, 2010, featured panelists Chris Rosa (Becker muscular dystrophy); L. Vance Taylor (limb-girdle muscular dystrophy) and Angela Wrigglesworth (spinal muscular atrophy) speaking about going to college with a neuromuscular disease.
Visit MDA's School Advocacy Resources page to see: