Advocacy partner: The ALS Association
About the ALS Association
Established in 1985, The ALS Association (Amyotrophic Lateral Sclerosis Assn) is the only national nonprofit organization fighting ALS on every front. By leading the way in global research, providing assistance for people with ALS, coordinating multidisciplinary care through certified clinical care centers, and fostering government partnerships, The Association builds hope and enhances quality of life while aggressively searching for new treatments and a cure.
Contact: Candyl Eyster – Associate Director, External Communications
Phone: 813-418-0769
Email: [email protected]
Upcoming events
Notice
There are no upcoming events.
About Advocacy Partners
The information above is provided by our partner. Learn more about our advocacy partners here.
Recent Posts
- My husband doesn’t get out much, but he enjoys following Comet’s secret life
- Keeping weight steady after tube feeding may help ALS survival
- Trial, error, and toe covers: Learning to adapt in life with ALS
- 5-year survival seen for over 40% of ALS patients on masitinib in trial
- Long-term air pollution exposure shows no clear link to ALS in UK study
