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The Wolff Family’s Journey Through Loss, A Prolonged NICU Stay and What They Have Learned Along the Way

The Wolff Family’s Journey Through Loss, A Prolonged NICU Stay and What They Have Learned Along the Way

Released Thursday, 15th September 2022
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The Wolff Family’s Journey Through Loss, A Prolonged NICU Stay and What They Have Learned Along the Way

The Wolff Family’s Journey Through Loss, A Prolonged NICU Stay and What They Have Learned Along the Way

The Wolff Family’s Journey Through Loss, A Prolonged NICU Stay and What They Have Learned Along the Way

The Wolff Family’s Journey Through Loss, A Prolonged NICU Stay and What They Have Learned Along the Way

Thursday, 15th September 2022
Good episode? Give it some love!
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For our most recent podcast episode, I sat down with Jessica Wolff, a mother who has endured loss and 2 very different NICU journeys. For part one of this podcast, she shares personal details on her very complicated twin pregnancy and the difficult choices they had to make along the way. She reflects back on regrets both she and her husband, Pat have experienced as well as what helped them cope through their daughter, Lily’s 256-day NICU stay.

Jessica explains what helped them make the decision whether or not Lily should have a tracheostomy placed and she speaks candidly about what their expectations were after Lily’s tracheostomy placement, versus their reality. She offers frank advice for NICU families, especially those with similar situations who have children with feeding issues, ostomies, bronchopulmonary dysplasia or BPD, pain medication withdrawal, tracheostomies, and what going home looked like for their family with a ventilator-dependent child. 

You will be amazed by what this family has been through, but even more so by their strength and resiliency. Sweet Lily has touched so many lives in her short 4 years, and this is just the beginning of her story, I know she’ll pull on your heart strings as well. So sit back and listen to part one of this family’s story with Jessica Wolff. 


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Empowering NICU Parents Podcast

Is your baby currently in the NICU? Was your baby born prematurely? Or is your term baby in the NICU for high jaundice levels, low blood sugars, or because they have some Respiratory Distress and need oxygen or additional support? Are you wondering what in the heck is a small baby unit or kangaroo care? Why do NICUs use donor breast milk and what on earth does RDS, BPD, IVH, NEC, ETT, CPAP, HFNC, UVC, UAC, po, ng, NEC, ABG, CBG, CBC, and CMP stand for? Are you asking yourself how will we ever get through this, what questions should I even ask, and when will my baby come home? If you are a NICU parent who is scared, nervous, unsure, and full of questions, then hit the subscribe button so you do not miss another show!Welcome to the "Empowering NICU Parents Podcast" where we will answer ALL of these questions and SO MUCH more! Your host, Nicole Nyberg is a Neonatal Nurse Practitioner with years of NICU experience - but she also brings her unique perspective to this podcast as a mother of a 23-weeker. Along with sharing answers to the NICU medical questions you have, Nicole addresses and supports you through the incredibly difficult emotional struggles that only a NICU parent can understand. She provides you with knowledge plus tangible tips to guide, educate, empower, and support you through your baby's NICU journey and once they are home. Tune in to hear from someone who knows exactly what you're going through, another NICU Mama. Check out all of our show notes and additional information at empoweringnicuparents.com

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