ALS Association

Non-profit organization supporting ALS research and patients

ALS Association is a non-profit organization dedicated to fighting amyotrophic lateral sclerosis (ALS), also known as Lou Gehrig's disease. The association is committed to advancing research, providing care and support to patients, and fostering public awareness about the disease.

History

The ALS Association was founded in 1985 with the mission to lead the fight to treat and cure ALS through global research and nationwide advocacy. It also aims to empower people with ALS and their families to live fuller lives by providing them with compassionate care and support.

Mission and Goals

The ALS Association's mission is to discover treatments and a cure for ALS, and to serve, advocate for, and empower people affected by ALS to live their lives to the fullest. The organization focuses on:

• Funding research to find a cure for ALS.
• Providing patient care and support services.
• Advocating for public policies that benefit ALS patients and their families.
• Raising awareness about ALS and its impact on individuals and communities.

Research Initiatives

The ALS Association is a leading funder of ALS research worldwide. It supports a wide range of research projects aimed at understanding the causes of ALS, developing new treatments, and ultimately finding a cure. The association collaborates with scientists, clinicians, and other organizations to accelerate the pace of research.

Patient Services

The ALS Association offers a variety of services to support individuals with ALS and their families. These services include:

• Access to ALS clinics and multidisciplinary care teams.
• Equipment loan programs to provide necessary medical equipment.
• Support groups and counseling services.
• Educational resources and information about living with ALS.

Advocacy and Public Policy

The ALS Association actively engages in advocacy efforts to influence public policy and increase funding for ALS research and patient care. The organization works with lawmakers, government agencies, and other stakeholders to promote policies that improve the lives of people with ALS.

Awareness Campaigns

The ALS Association conducts various awareness campaigns to educate the public about ALS and its impact. One of the most notable campaigns was the Ice Bucket Challenge, which went viral in 2014 and significantly increased public awareness and funding for ALS research.

Related pages

• Amyotrophic lateral sclerosis
• Ice Bucket Challenge
• Lou Gehrig
• Neurodegenerative disease

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