The Walk to Defeat ALS® is the #1 way to empower yourself to lend support to those fighting the disease and caring for someone living with ALS. Every year, thousands of people across the country come together to raise funds to support care service programs, enable cutting-edge research, and advance nationwide advocacy efforts for people with ALS and their families.
The Walk to Defeat ALS® is the #1 way to empower yourself to lend support to those fighting the disease and caring for someone living with ALS. Every year, thousands of people across the country come together to raise funds to support care service programs, enable cutting-edge research, and advance nationwide advocacy efforts for people with ALS and their families.
Take me out to the ballgame! Join The ALS Association Florida Chapter for our ALS Awareness Night with the Tampa Bay Rays as they take on the Miami Marlins on Sunday, September 26th!
Show your support for the ALS community and help us #StrikeOutALS. This annual event is fun for all - bring your family, friends, and co-workers and let's spread awareness of Lou Gehrig's Disease.
Join us for a virtual day of informative demonstrations and sessions for people living with ALS, caregivers, healthcare professionals, and supporters of the ALS community.
The Walk to Defeat ALS® is the #1 way to empower yourself to lend support to those fighting the disease and caring for someone living with ALS. Every year, thousands of people across the country come together to raise funds to support care service programs, enable cutting-edge research, and advance nationwide advocacy efforts for people with ALS and their families.
The Walk to Defeat ALS® is the #1 way to empower yourself to lend support to those fighting the disease and caring for someone living with ALS. Every year, thousands of people across the country come together to raise funds to support care service programs, enable cutting-edge research, and advance nationwide advocacy efforts for people with ALS and their families.
To register, please contact Kyle Kennedy at kkennedy@tmacmail.com. Your $150 includes 18 holes plus cart, event golf shirt, on-course games, food, open bar, and prizes! Deadline for registering is August 30th.
Lon Haldeman and Susan Notorangelo are working with area ALS Chapters to form a fund in the memory of their daughter Ericka Notorangelo Haldeman who passed away from infantile Lou Gehrig's Disease when she was less than 11 months old.
ALS is a horrific and always-fatal disease impacting patients and patient families throughout Wisconsin. It has no known cause. No known cure. And no effective treatment. Which is why it’s going to take all of us to take down ALS.
Learn more about this fun and fantastic community event and register by clicking here.
Join the fight by registering for The ManitoWALK vs ALS.