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.
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.
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.