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The ALS Association is the singular national non-profit health organization dedicated solely to fighting ALS. Covering research, patient services, community support, public education, and advocacy, the ALS Association provides vital aid and hope for those affected by the disease.
The focus is two-fold: local efforts directly assist 395+ patients and families in the Northeast, while the National Office concentrates on impactful research and advocacy. All these achievements are made possible through the generous contributions of supporters.
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