Ounces in Miracles: Life After Miracles with Traci & Bruce
Ounces in Miracles began as a podcast created by NICU moms, for NICU families — and it’s grown into a space where stories of survival, healing, and hope continue long after the hospital doors close. 💜 Join Traci and Bruce as they share the real, raw experiences of life after the NICU — from milestones and therapies to marriage, parenting, advocacy, and laughter in the chaos. Through heartfelt interviews and honest conversations, Ounces in Miracles: Life After Miracles brings both inspiration and connection to families of micropreemies, preemies, and medically fragile children. 🎙 Episodes feature: NICU mom & dad perspectives Life after the NICU — milestones, therapies & advocacy Rare diagnosis journeys Tips from medical professionals & specialists Mental health, relationships, and family resilience Because no one should walk the NICU journey alone — and the miracles don’t stop when you come home. 💫
Ounces in Miracles: Life After Miracles with Traci & Bruce
Ounces in Miracles began as a podcast created by NICU moms, for NICU families — and it’s grown into a space where stories of survival, healing, and hope continue long after the hospital doors close. 💜 Join Traci and Bruce as they share the real, raw experiences of life after the NICU — from milestones and therapies to marriage, parenting, advocacy, and laughter in the chaos. Through heartfelt interviews and honest conversations, Ounces in Miracles: Life After Miracles brings both inspiration and connection to families of micropreemies, preemies, and medically fragile children. 🎙 Episodes feature: NICU mom & dad perspectives Life after the NICU — milestones, therapies & advocacy Rare diagnosis journeys Tips from medical professionals & specialists Mental health, relationships, and family resilience Because no one should walk the NICU journey alone — and the miracles don’t stop when you come home. 💫

In this episode of Ounces in Miracles, we sit down with Jennifer, a NICU mom whose son Jaxson was born with a rare genetic condition called 22Q13 duplication. Jennifer opens up about her pregnancy, Jaxson’s NICU journey, the challenges of navigating a rare diagnosis, and the many specialists and therapies that have supported him along the way. She also shares the lessons she’s learned as an advocate and what she wishes more people understood about raising a child with unique medical needs. This episode covers: Jennifer’s pregnancy and Jaxson’s birth story Navigating the NICU and finding moments of hope Understanding 22Q13 duplication in parent-friendly terms Life after the NICU: therapies, specialists, and milestones Advocacy, resilience, and support for families with rare diagnoses 💜 Jennifer’s story is a powerful reminder that while the NICU journey is never easy, families don’t have to walk it alone.
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