OUR VISION:
To create a world without ALS.
OUR MISSION:
Leading the fight to treat and cure ALS through global research and nationwide advocacy while also empowering people with Lou Gehrig’s Disease and their families to live fuller lives by providing them with compassionate care and support.
SERVICES:
Providing quality services to patients and families living with ALS throughout the greater New York area, including New York City, Long Island, Westchester County, the Hudson Valley, and northern and central New Jersey.
RESEARCH:
Funding aggressive, cutting-edge research to find a cure that utilizes the newest techniques and fosters collaborative initiatives among government agencies, the private sector and scientists.
ADVOCACY:
Supporting The ALS Association's national advocacy program to expand government support of research and elicit programs to make treatments and care accessible and affordable for all ALS patients.
EDUCATION:
Heightening awareness of ALS in order to stimulate volunteerism, scientific and healthcare community activism, and public support that is essential to the fight against ALS.
