Interview Series: Lisa Salberg, Founder and CEO of the Hypertrophic Cardiomyopathy Association (HCMA)

Interview Series: Lisa Salberg, Founder and CEO of the Hypertrophic Cardiomyopathy Association (HCMA)Issue #25 of "What's Her Problem?": Just one patient advocate can make a huge difference.Part 1 of my 5-part series of Heart Month posts, bringing awareness to a variety of topics in cardiology.This week’s questions:Are you a patient advocate? If so, how did you get started? If not, what do you think makes someone a great patient advocate?Show Notes:The Hypertrophic Cardiomyopathy Association (HCMA) Website: https://www.4hcm.org/Learn more about Centers of Excellence (COEs): https://www.4hcm.org/center-of-excellencehttps://www.4hcm.org/storehttps://whatsherproblem.substack.com/archivehttps://whatsherproblem.substack.com/notesRelated Posts:I was a guest on “Tales from the Heart” in 2024. You can watch that here:https://youtu.be/kiFXpo-dV1UReflections from the HCMA Annual Patient Meetinghttps://open.substack.com/pub/whatsherproblem/p/reflections-on-the-2025-hcma-annual?r=heamx&utm_campaign=post&utm_medium=webLet’s Discusshttps://open.substack.com/pub/whatsherproblem/p/lets-discuss?r=heamx&utm_campaign=post&utm_medium=webInterview Series: Sarah Homhttps://whatsherproblem.substack.com/p/interview-series-sarah-hom-accessibility?r=heamx&utm_campaign=post&utm_medium=web&triedRedirect=true This is a public episode. If you'd like to discuss this with other subscribers or get access to bonus episodes, visit whatsherproblem.substack.com/subscribe