ALS Registry
- From: icyou
- Type: News Reports
- Joined: June 2007
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Added: October 24, 2007 | Time 04:31 | Views: 1,027
The ALS registry will collect and examine data from thousands of people with Lou Gehrig's Disease. Its data will be used to help determine risk factors for ALS, as well as interventions that are beneficial and which educational approaches are best.
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chicagogal says:36 weeks ago | Reply
I'm surprised a registry didn't already exist for people with ALS
Healthnut26 says:36 weeks ago | Reply
Glad to hear something is being done to find a cure for ALS! The ALS registry is a step in the right direction.
Posted By: multivu
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