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ALS (amyotrophic lateral sclerosis, or Lou Gehrig’s disease) is a multisystem neurodegenerative disorder that primarily affects motor neurons, the nerve cells that control voluntary muscle movement. The loss of motor neurons causes the muscles they control to become weak and then paralyzed. Death, often within five years of diagnosis, usually is due to respiratory complications caused by paralysis of the muscles used in breathing.
MDA is the world’s leading nongovernmental funder of ALS research. Its worldwide program supports research efforts ranging from basic (early-stage) science, to preclinical testing and therapy development, to human clinical trials. Since its inception, MDA has dedicated more than $307 million to ALS research, services, education and advocacy programs.
Current MDA-supported ALS research is focusing on several areas, including:
Other critical MDA-funded ALS research contributions include:
MDA continues to be inspired by the words of the late Michael E. DeBakey, world-renowned heart surgeon and an MDA national vice president, who said, “There are no incurable diseases. There are only diseases for which no treatment has yet been developed.”
Muscular Dystrophy Association — USA
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