Katie Sale, Executive Director of the American Brain Coalition, sits down with Mary Anne Meskis, CEO of the Dravet Syndrome Foundation, and Shannon Cloud, the Foundation's Patient Advocacy Director, for a conversation on the origins and impact of DSF. They discuss why the organization was founded, the critical advocacy work it leads, and the resources it provides to support patients and families affected by Dravet syndrome.

In this episode, ABC Executive Director Katie Sale sits down with Jane Powell, CEO & Executive Director, and Alejandro Bruner-Solas, Program Manager from PWN4PWN, for an inspiring conversation about advocacy, community, and living with narcolepsy. Together, they explore empowering individuals through peer support, workforce development, and inclusive programming, while sharing personal insights on navigating life with sleep disorders.

In this episode, Katie Sale, Executive Director of the American Brain Coalition, is joined by Kris Corbett, RN, author of Bravely Bleeding and person with lived experience (PWLE) of Cerebral Cavernous Angioma; and Cornelia (Connie) Lee, PsyD, CEO of the Alliance to Cure Cavernous Malformation. Together, they explore the power of advocacy, the importance of patient voices, and the urgent need for awareness and innovation in addressing cavernous malformations.