The Plasma Podcast
Episode 6 – Interview with Megan Anne Ryan; Patient and Patient Advocate We have a special guest in honor of Rare Disease Day in today's episode. Megan Anne Ryan shares her authentic patient perspective and serves as a voice for patients worldwide. She is a proud native Texan who was diagnosed with a Primary Immune Deficiency, specifically Common Variable Immune Deficiency, in her twenties. Megan goes on to discuss the diagnostic odyssey which is all too often lengthy and challenging for patients. Her unique perspective serves to shed light on the importance of plasma donors and the staff involved in plasma collection. Advocacy Work Megan served as the Board Treasurer for the Jose Antonio Grifols Lucas I Foundation [https://www.grifols.com/en/our-foundations] and has further expanded her reach to the organization Undies for Everyone [https://undiesforeveryone.org/].
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