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Episode 33

Can patients with mitochondrial conditions afford to wait for the FDA?

Episode Description

Navigating child heart failure and mitochondrial disease. Dr. Heather Gatcombe shares her personal journey as a physician and mother navigating the complexities of mitochondrial disease and heart failure in her son. She discusses the challenges of diagnosis, the emotional toll of medical crises, and the journey through heart transplant. Dr. Gatcombe emphasizes the importance of understanding mitochondrial disease, the role of advocacy, and the potential future of mitochondrial medicine, including the impact of new treatments and the need for continued support and awareness.

Key Takeaways:

  • Mitochondrial disease can be difficult to diagnose due to its varied presentation.
  • Heart failure in children can arise from mitochondrial dysfunction.
  • Transplantation is a complex process that requires a multidisciplinary approach.
  • Post-transplant care involves managing potential complications and medication side effects.
  • Advocacy is crucial for rare diseases to ensure access to necessary treatments.
  • New medications can significantly improve the quality of life for patients with mitochondrial disease. And one of these medications is at risk of being discontinued meaning more people going back on the heart transplant list.

Dr. Heather Gatcombe is the mother of a child with mitochondrial disease and is on the Board of Trustees of the United Mitochondrial Disease Foundation and the Board of Directors of Enduring Hearts. She is an assistant professor at Emory University School of Medicine. The views expressed here are her own and do not represent those of Emory University.

https://www.linkedin.com/in/heather-gatcombe-md-3891875/

https://www.instagram.com/heathergatcombe/

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