<p>In this episode, Alyssa speaks with Stacey Reason and Andrew Wakelin with the IamGSD organization.  Stacey and Andrew are both diagnosed with one of the muscle GSDs that we cover in this episode, McArdle disease.  You'll hear about their advocacy efforts through IamGSD and learn about the diesease from their perspectives as patients.  Enjoy!</p>

In this episode, Alyssa speaks with Stacey Reason and Andrew Wakelin with the IamGSD organization. Stacey and Andrew are both diagnosed with one of the muscle GSDs that we cover in this episode, McArdle disease. You'll hear about their advocacy efforts through IamGSD and learn about the diesease from their perspectives as patients. Enjoy!

<p>In this episode, Alyssa speaks with Stacey Reason and Andrew Wakelin with the IamGSD organization. &nbsp;Stacey and Andrew are both diagnosed with one of the muscle GSDs that we cover in this episode, McArdle disease. &nbsp;You'll hear about their advocacy efforts through IamGSD and learn about the diesease from their perspectives as patients. &nbsp;Enjoy!</p>

Episode 20 - IamGSD

This is CoRDS Cast, a rare disease podcast created by the team at Sanford Research. Our rare disease registry, CoRDS, connects patients and researchers everywhere. Here, you'll hear interviews with patients, patient advocates, physicians, and researchers to raise awareness about the 7,000 rare conditions affecting 1 in 10 people worldwide.

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Episode 20 - IamGSD

Episode 20 - IamGSD