Our mission is to serve as a dedicated resource to ALS patients, their families, friends and caregivers. We aim to enhance the quality of life of all those affected by ALS whom we serve, to heighten community awareness of this devastating disease, and to strengthen public and legislative support in the fight against ALS.

Description:
ALS (often referred to as Lou Gehrig's disease) is an insidious disease, striking the nerves we need to manipulate the muscles we use daily. Roughly 30,000 people nationwide have ALS, more than 5,000 are diagnosed each year -- almost 2 times more men than women, and 1.5 times more military service members than the general population. It not only affects individuals, but also their entire circle of friends and families.
We provide services to ALS patients, families, and their caregivers in Nebraska and western Iowa. Our services include in-home consultations, support groups, community resources and referrals, an equipment program, a volunteer and respite program, and fundraising events for local patients services and national research efforts into the causes and cures for ALS.

History:
Inspired by longtime volunteers and a committed board of directors, ALS in the Heartland was formed and incorporated as a non-profit agency on June 4, 2006.

Contact people:

Steve Langan, Executive Director, (phone), (email) S. Romero, Patient Services Director, (phone), (email)

Address:

6277 S. 118th St. Omaha, NE 68137 (See a map)