The ALS Association is a non-profit organization dedicated to fighting Amyotrophic Lateral Sclerosis (ALS), a progressive neurodegenerative disease that affects nerve cells in the brain and spinal cord. Founded in 1985, the association focuses on research, patient care, and advocacy to improve the lives of those affected by ALS. The organization funds innovative research projects aimed at finding effective treatments and a cure for ALS. It also provides resources and support for patients and their families, helping them navigate the challenges of living with this condition. Through awareness campaigns, the ALS Association strives to educate the public about ALS and its impact.