The Premie Pod

How has it been 6 months already?! We have done so much in such a small amount of time! We have had incredible guests, ranging from mums to dads to healthcare professionals! We have coordinated a massive fundraiser where we raised $18,500 in 3 weeks for Red Nose Australia!! We have so much more to come, stay tuned.... Love,Kirsty, Dimitty & Meg @thepremiepod on all platforms [email protected]

Trigger Warning: This episode discusses infant loss and sudden infant death syndrome (SIDS), which may be distressing to some listeners. Please prioritise your wellbeing and take a break if needed.If you or someone you know is impacted by the loss of a baby or child, please know you are not alone. Support is available.📞 Red Nose Grief & Loss Support Line: 1300 308 307 (24/7)In this heartfelt episode of The Premie Pod, we’re honoured to be joined by Tenille James — a devoted mother to Kenny, Andie, and Harley.Tenille bravely shares her journey through premature birth, NICU life, and the unimaginable grief of losing her daughter Andie to SIDS at just 9 months old. Born at 35 weeks, Andie developed a critical condition called Persistent Pulmonary Hypertension of the Newborn (PPHN) shortly after birth, requiring intensive care and life support.Despite the odds, Andie came home — a true fighter. But the road ahead brought unexpected tragedy and heartbreak no parent should ever have to face.This episode is a moving tribute to Andie’s life and a powerful call to raise awareness around SIDS, grief, and the strength of families walking this path.❤️ Tenille’s story is raw, brave, and deeply human.🎧 Listen now — and please share to help us honour Andie and raise awareness.📌 Medical Disclaimer: The content in this episode is for informational and storytelling purposes only and is not intended as medical advice. Always consult a qualified healthcare provider regarding any medical concerns.

This is part two of last week's episode "IUGR, Ductus Arteriosus, Pericardial Effusion; Micah's Story" Mic, Micah's dad, plays a major role in financial, emotional and physical support for both Casey and Micah. Sometimes dads can get a little forgotten in NICU, so we're pleased to place a spotlight on a pretty incredible dad this week.

Their journey was filled with many challenges from Casey suffering pre-eclampsia to Micah suffering IUGR, having a large PDA, pericardial effusion, retinopathy of prematurity, an extubation, sepsis, ventilator-induced pneumonia, and a surgery for bilateral hernias.But this story isn't just about the medical hurdles they faced, it's about the emotional toll of the journey too. Casey and Mic open up about the raw, often unseen side of the NICU life: the fear, mental health struggles and how their strength and resilience together helped them both navigate this challenging journey.We invite you to share your experiences or words of support in the comments below.⚠️ DISCLAIMER:This video is intended for informational and storytelling purposes only. It is not medical advice. Please consult with a qualified healthcare provider for medical concerns or decisions.

This week, Katlyn shares her and her son, Cooper's, story! Cooper was diagnosed with congenital heart disease comprising of: - Double inlet left ventricle- Hypoplastic right ventricle- Transposition of the greater arteries- Atrial septal defect (ASD)- Ventricular septal defect (VSD)- Pulmonary StenosisWith such quite a significant diagnosis, the prognosis was not favourable. Even with so many people, including healthcare professionals, encouraging her to terminate the pregnancy, Katlyn chose her own path. She decided to give Cooper a chance. You will not want to miss this episodeDISCLAIMER: This episode is personal experience, not medical advice. Please seek counsel from your own medical practitioner for all medical enquiries.