The Project Blog
Articles, tips and advice related to ALS and those suffering from the disease, as well as their families, friends and caregivers from the Chris Ragan (one of the founders of the Peggy and Bernie Project and the son of Peggy).
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Peggy’s Blog
Follow Peggy Ragan’s journey with Amyotrophic Lateral Sclerosis (ALS), also known as Lou Gehrig’s Disease.
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News
Stay up to date on wht’s happening with the Project.
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Events
Upcoming Project and ALS events.
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