The ALS Association is a non-profit organization based in Tampa, Florida, dedicated to supporting individuals affected by amyotrophic lateral sclerosis (ALS) and advancing research toward finding effective treatments. Located in the heart of Tampa at 501 E Kennedy Blvd Suite 1400, the organization serves as a critical resource for those seeking assistance, education, and community connection related to this progressive neurodegenerative disease. Through its focused efforts, the ALS Association strives to improve quality of life for patients and their families while fostering greater public awareness.

As a non-profit organization, the ALS Association offers a range of services that extend beyond direct support to patients. These include educational programs, advocacy initiatives, and fundraising efforts designed to accelerate scientific research. The organization works collaboratively with medical professionals, researchers, and caregivers to ensure that individuals living with ALS have access to the latest information and care options. This comprehensive approach helps to address the complex needs that arise throughout the course of the disease.

In addition to its support and outreach efforts, the ALS Association is a key player in the broader network of social service organizations within Tampa. It coordinates with other local agencies to provide holistic assistance that encompasses physical, emotional, and financial aspects of living with ALS. The organization’s commitment to transparency and clear communication makes it a trusted resource for families navigating the challenges of the disease.

Residents of Tampa and surrounding areas who require information or support related to ALS can contact the ALS Association at 888-257-1717. The organization’s presence in the community contributes to a stronger support system for those affected by ALS, emphasizing collaboration and compassion in every aspect of its work.