About ALS (Lou Gehrig's Disease)
Amyotrophic Lateral Sclerosis (ALS), also known as Lou Gehrig’s Disease, is a progressive neurodegenerative disease that slowly robs a person of the ability to walk, speak, swallow and, eventually breathe. With no known cause or cure, a person can expect to live typically 2 to 5 years from the time of diagnosis.
ALS has no racial, ethnic or socioeconomic boundaries and in only 10% of cases there is a family history of ALS. Today, there are approximately 30,000 people in the US living with ALS and 5,600 people are diagnosed each and every year in the US.
Create a world without ALS.
To discover treatments and cures for ALS, and to serve, advocate for, and empower people affected by ALS to live their lives to the fullest.
COMPASSION - INTEGRITY - URGENCY
Guiding Priciples are:
- People with ALS and their families come first
- One team, one vision, one mission
- Accountability and transparency
- Diversity and inclusion
- Open communication and dialogue
- Recognized interdependence between care and research.
- People with ALS and their families have:
- Access to consitent care, treatment and services
- Resource and support services that enhance quality of life
- Quality care and support leveraged by collaboration with partners
- Discover new life-extending treatment:
- Drive worldwide research agenda with urgency and boldness to improve outcomes for people with ALS
- Collaborate with partners in a comprehensive and diverse research model
- Facilitate the rapid development of new treatment options to extend and enhance quality of life while seeking a cure
About The ALS Association
The ALS Association is the only organization leading the fight to discover a cure for ALS from all angles - through robust research, care, and public policy programs. Our solution is an integrated approach that will lead us to viable treatments and cure for this terrible disease.
The ALS Association is at the forefront of the global research effort funding over $138 million in research and clinical management projects. To maximize results, The Association channels our funding, made possible through the generous support of donors, into global research projects focused on six tightly-related areas:
- Identifying ALS genes
- Understanding disease mechanisms
- Using stem cells for disease modeling and therapy testing
- Finding disease biomarkers
- Developing therapies
- Improving clinical trials
The ALS Association helps patients and families cope with the day to day challenges of living with ALS by providing information, resources, and referrals to many sources, including a wide variety of community services through our nationwide chapter network.
Our nationwide network of ALS Association Certified Centers of Excellence provide state-of-the-art, multi-disciplinary ALS care and services in a supportive atmosphere with an emphasis on hope and quality of life. To become certified as one of these centers of excellence, an ALS clinic must achieve national prominence, meet rigorous clinical care standards, and pass a comprehensive site inspection.
Our nationwide network plays a integral role in advocating for increased public and private support of ALS research and patient care. The ALS Association’s public policy efforts in Washington D.C. have raised the profile of ALS by working with the White House, Congress, National Institutes of Health, Centers for Medicare and Medicaid Services, Food and Drug Administration, Department of Defense, Department of Veterans Affairs, Social Security Administration, and Centers for Disease Control and Prevention.