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In this heartfelt episode, we sit down with Lisa Salberg, a pioneering advocate for hypertrophic cardiomyopathy (HCM) patients and the founder of the Hypertrophic Cardiomyopathy Association (HCMA). Lisa shares her deeply personal journey, beginning with her family's tragic history with HCM, a genetic heart condition that has affected multiple generations. Diagnosed herself at the age of 12, Lisa’s story is one of resilience, advocacy, and transformation.
Listen as Lisa recounts the challenges her family faced, including her sister’s untimely death due to HCM, which fueled her determination to create a support network for those affected by this rare condition. Through the HCMA, Lisa has built a community that offers essential resources, education, and emotional support to thousands of families worldwide.
The episode delves into the advancements in HCM treatment and the importance of genetic awareness and early diagnosis. Lisa’s own experience of undergoing a heart transplant in 2017, and the profound emotional impact of receiving a donor heart, highlights the life-changing potential of medical innovation and the power of human resilience.
Join us for an inspiring conversation about the importance of patient advocacy, the evolution of HCM care, and the enduring spirit of a woman who turned her family's struggles into a global mission of hope and support.
Episode Highlights:
LINKS:
https://4hcm.org/
https://www.drjeremykoenig.com/
https://www.instagram.com/drjeremykoenig/
https://www.youtube.com/@drjeremykoenig
LINKS:
https://www.drjeremykoenig.com/
https://www.instagram.com/drjeremykoenig/
https://www.youtube.com/@drjeremykoenig
Here's the link for this week's episode: https://drjeremykoenig.substack.com/p/the-polygenic-tapestry
In this heartfelt episode, we sit down with Lisa Salberg, a pioneering advocate for hypertrophic cardiomyopathy (HCM) patients and the founder of the Hypertrophic Cardiomyopathy Association (HCMA). Lisa shares her deeply personal journey, beginning with her family's tragic history with HCM, a genetic heart condition that has affected multiple generations. Diagnosed herself at the age of 12, Lisa’s story is one of resilience, advocacy, and transformation.
Listen as Lisa recounts the challenges her family faced, including her sister’s untimely death due to HCM, which fueled her determination to create a support network for those affected by this rare condition. Through the HCMA, Lisa has built a community that offers essential resources, education, and emotional support to thousands of families worldwide.
The episode delves into the advancements in HCM treatment and the importance of genetic awareness and early diagnosis. Lisa’s own experience of undergoing a heart transplant in 2017, and the profound emotional impact of receiving a donor heart, highlights the life-changing potential of medical innovation and the power of human resilience.
Join us for an inspiring conversation about the importance of patient advocacy, the evolution of HCM care, and the enduring spirit of a woman who turned her family's struggles into a global mission of hope and support.
Episode Highlights:
LINKS:
https://4hcm.org/
https://www.drjeremykoenig.com/
https://www.instagram.com/drjeremykoenig/
https://www.youtube.com/@drjeremykoenig
LINKS:
https://www.drjeremykoenig.com/
https://www.instagram.com/drjeremykoenig/
https://www.youtube.com/@drjeremykoenig
Here's the link for this week's episode: https://drjeremykoenig.substack.com/p/the-polygenic-tapestry