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The ALS Association is the only national non-profit organization fighting Lou Gehrig's Disease on every front. By leading the way in global research, providing assistance for people with ALS through a nationwide network of chapters, coordinating multidisciplinary care through certified clinical care centers, and fostering government partnerships, The ALS Association builds hope and enhances quality of life while aggressively searching for new treatments and a cure.
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Citation Level
1985
English, etc
Website Key Features
Research Funding
The ALS Association funds cutting-edge research to find treatments and a cure for ALS.
Support Groups
Offers support groups for individuals and families affected by ALS to share experiences and coping strategies.
Advocacy
Advocates for policies that benefit people with ALS and their families, including increased funding for research and improved access to care.
Certified Clinical Care Centers
A network of certified clinical care centers that provide multidisciplinary care to people with ALS.
Education and Awareness
Provides educational resources and raises awareness about ALS to the public and healthcare professionals.
Patient Services
Offers a range of services to assist people with ALS, including equipment loan programs, respite care, and transportation assistance.
Global Research
Leads global research efforts to understand the causes of ALS and develop effective treatments.
Community Events
Organizes community events to raise funds and awareness for ALS research and support services.
Volunteer Opportunities
Provides opportunities for individuals to get involved and make a difference in the fight against ALS.
Online Resources
Offers a comprehensive online library of resources for people with ALS, caregivers, and healthcare professionals.
Similar Sites and Competitors
Additional information
Mission
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.
Vision
A world without ALS.
Headquarters
Washington, D.C., United States
Key People
Calaneet Balas (President and CEO)
Website
https://www.als.org
Contact
info@alsa-national.org
Social Media
Facebook, Twitter, Instagram, YouTube
Donations
Accepts donations to fund research, support services, and advocacy efforts.
Volunteer
Offers various volunteer opportunities to support the mission of the ALS Association.
Newsletter
Provides a newsletter to keep supporters informed about the latest research, events, and ways to get involved.
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