ALS (Amyotrophic Lateral Sclerosis or Lou Gehrig's Disease) is a deadly medical condition that affects thousands of people around the world. There is no cure, and the ALS Association is working diligently to find one. As one of the largest private funders of ALS research, they are building a future where a world without ALS might be a possibility. They give a voice to those who cannot speak and work closely with doctors to make sure ALS patients are receiving the care they need to extend their lifespan. See how one family leans on the ALS Association for support:

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