In making final preparations for this year’s Medicine X Conference at Stanford, I’m joined by Erin Moore. Erin is the mother of four children, one of whom lives with cystic fibrosis. We discuss her son’s diagnosis story, why she started blogging, and the diversity of her patient advocacy efforts. Later on in the podcast I learn about Collaborative Chronic Care Networks (C3N), Erin’s involvement in building a C3N for cystic fibrosis, and why Cincinnati is the best place for her family to live. Enjoy.
You can follow Erin on Twitter at @ekeeleymoore and at her blog, 66roses.com.
Run Time – 53:45
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