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In the quest to create a world without ALS, our vision is to care for
and support all people living with Lou Gehrig’s disease as we leave no
stone unturned in our relentless search for a cure.

To lead the fight to cure and treat ALS through global, cutting-edge research, and to empower people with Lou Gehrig’s disease and their families to live fuller lives by providing them with compassionate care and support.

Description:
To provide patients and families living with ALS (Lou Gehrig's disease) support and assistance to live fuller lives and remain as independent for as long as possible.

History:
The Chapter was founded in 2003 by Donna Mott-Lange after her father was diagnosed and passed from ALS. Donna promised her Father that people would have a place to turn for answers and referrals and to make others aware of the disease.

Contact people:

Donna Lange, Executive Director, (phone), (email) Jeanine Huber, Development Coordinator, (phone), (email) Dee Dee Rohr, Administrative Assistant, (phone), (email)

Address:

323 Rt. 5 W Elbridge, NY 13060 (See a map)