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Hope Happens
Our Mission: To find a cure for ALS by funding progressive research and in the process create a new methodology for funding, researching and developing treatments for ALS and other neurological disorders.

Amyotrophic Lateral Sclerosis

More than 5,600 people in the U.S. are diagnosed with ALS each year. That’s 15 new cases per day. Upon diagnosis, each person is given between 2-5 years to live.

In the advanced stages of the disease, the cost for patient care averages $200,000 per year. The disease was discovered approximately 150 years ago, and ALS research in the last 10 years has been invigorated by the discovery of specific gene mutations which are responsible for the disease in a small proportion of people living with ALS. However, there remains no treatment proven to cure the disease or reverse its symptoms.

Source: The ALS Association


Opportunities

Hope Center investigators have characterized free radical pathways leading to nerve cell injury, identified a new class of free radical scavenger drugs with potential value for ALS and have examined connections between nerves and muscles. Current projects are testing newly discovered molecular pathways in ALS mice.

101 South Hanley Road
Suite 1320
St. Louis, MO 63105

p: 314-725-3888
f: 314-725-3892


Founder
Christopher Wells Hobler
1965 - 2005


Chris lost his battle against ALS on Wednesday, February 16, 2005, surrounded by his loving wife, family, friends and caregivers.
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The Hope Center
for Neurological Disorders

www.hcnd.org

HOPE HAPPENS was formerly

ALS HOPE: The Chris Hobler/James Maritz Foundation