
S2E11: Mia Cahill - From NICU Baby & Gastroschisis Survivor to Researcher
Sometimes, the most powerful research doesn’t start in a lab — it begins through lived experience.
Today, we meet Mia Cahill, whose journey into the research space started in a deeply personal way. Born in Ireland with gastroschisis, she grew up understanding what it means to fight for a start in life. That experience shaped not only who she became, but how she now connects with other families walking a similar path.
Through her work, Mia has dedicated her research to supporting parents of sick or premature babies — helping them find hope, comfort, and strength in the toughest of moments. She reminds us that what we can offer someone in a moment of crisis can make all the difference — that sometimes, it’s the smallest gestures that carry families through.
As she puts it, parents will remember more than their NICU babies ever will. The weight of that journey can stay with us far longer than the NICU stay itself. So, don’t put too much pressure on yourself. You’re in this for the long haul — to keep showing up, even years down the track.
Because a life is so much longer than a single NICU journey. A life-defining start doesn’t have to be the life‑defining moment.
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