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Few diseases are as cruelly debilitating as amyotrophic lateral sclerosis (ALS). But a Food and Drug Administration advisory committee this week gave patients a glimmer of hope by backing a new treatment that can slow their decline and provide precious more time to live.
ALS, or Lou Gehrig’s disease, is a neuro-degenerative affliction that gradually robs people of their ability to function. It afflicts about 30,000 patients in the U.S. with 5,000 new cases each year. Patients typically live only two years after a diagnosis as they lose their ability to control essential muscle movements and eventually to chew and breathe.
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