Season 3, Episode 8: Familial Cerebral Cavernous Malformations

This episode features Megan Loden, a mother to two rare disease patients. Megan's story starts in 2020 with a life-altering phone call that changed everything for her Identical twin girls. We delve into their journey from diagnosis to treatment and how her determination led her to become an advocate, chairing the Arizona Angioma Community Alliance.
Megan has a unique spirit filled with resilience, determination, and bravery. She shares her story, and we discover the power of support, advocacy, and the quest for a better tomorrow in this compelling episode.
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