Tiny Little Hearts Podcast: CHD and Heart Mom Life
Tiny Little Hearts Podcast is your honest, unfiltered space for the CHD (congenital heart disease / congenital heart defect) community. Whether you're a heart parent, a CHD warrior, or someone newly navigating a complex congenital heart diagnosis — this podcast was made for you.
Hosted by Katelyn McMahan, a mom of three girls whose world changed the moment she learned her youngest daughter had complex cardiac abnormalities. She searched for real stories — kids with complex CHD, single ventricle hearts, hypoplastic left heart syndrome, and other congenital heart defects— not the polished highlight reels, but the honest, raw truth of what this life actually looks like. She wanted to prepare her heart for the good, the bad, and the ugly.
Each episode features conversations with heart parents, CHD adults, providers, and others navigating the deeply real world of congenital heart disease, open heart surgery, and medical complexity. You'll hear practical advice, emotional honesty, and stories that remind you that you are not alone in this journey. Because this life is hard — and you deserve a place to feel seen.
Topics covered include: CHD diagnosis, heart surgery recovery, parenting a medically complex child, grief and resilience, NICU and PCICU experiences, fontan circulation, cardiac catheterization, and life after a congenital heart defect diagnosis.
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Tiny Little Hearts Podcast: CHD and Heart Mom Life
20. Caregiver Burnout: The Raw Reality
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In this episode, Katelyn McMahan discusses the often-overlooked topic of caregiver burnout, sharing her personal experiences and insights. She emphasizes the commonality of burnout among caregivers, the emotional toll it takes, and the importance of recognizing its triggers and signs. Katelyn offers practical strategies for self-care and highlights the significance of building a supportive community to navigate the challenges of caregiving. Ultimately, she encourages listeners to prioritize their own needs while balancing their roles as caregivers.
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