Established in 1987, The ALS Association Florida Chapter is fighting Lou Gehrig’s Disease on all fronts, or as we like to say, “Covering all the bases for people living with ALS in Florida.” We provide patient programs, advocate on behalf of patients with our government leaders, create awareness of the disease, and fund research. In addition, the Chapter provides financial support to our statewide multidisciplinary ALS clinics and research facilities, enabling them to increase patient care. The ALS Association leads the way in research, care services, public education, and public policy — giving help and hope to those facing the disease.
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