Patient Advocate Spotlight: Kristen Wheeden Steps into Lead Role for RDCRN Patient Groups sheila.wolfer@… Mon, 08/02/2021 - 21:09
Kristen Wheeden and her son, Brady
Kristen Wheeden and her son, Brady

Kristen Wheeden is executive director of the American Porphyria Foundation. In this interview, she describes how her son’s diagnosis drew her to patient advocacy. Wheeden is also the incoming chair of the Rare Diseases Clinical Research Network (RDCRN)’s Coalition of Patient Advocacy Groups (CPAG), after serving last year as co-chair.