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The Wolff Family’s Post NICU Journey Through Home Trach Care, Decannulation, and Unexpected Surprises Too

The Wolff Family’s Post NICU Journey Through Home Trach Care, Decannulation, and Unexpected Surprises Too

Released Friday, 30th September 2022
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The Wolff Family’s Post NICU Journey Through Home Trach Care, Decannulation, and Unexpected Surprises Too

The Wolff Family’s Post NICU Journey Through Home Trach Care, Decannulation, and Unexpected Surprises Too

The Wolff Family’s Post NICU Journey Through Home Trach Care, Decannulation, and Unexpected Surprises Too

The Wolff Family’s Post NICU Journey Through Home Trach Care, Decannulation, and Unexpected Surprises Too

Friday, 30th September 2022
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For this podcast, I continued my conversation with Jessica Wolff. We discussed what their life was like once they brought Lily home. She explains how they adjusted to caring for Lily with her tracheostomy along with the necessary life-saving equipment and how all of that completely changed once COVID hit. 

We discussed how the plan for Lily’s decannulation went completely sideways, how they coped with it, and how they learned that Lily actually needed a full laryngotracheal reconstructive surgery. Jessica proudly shares how Lily is doing today, medically, developmentally and emotionally and how they are navigating everything as a family, especially in preparation for sweet Lily to head to Preschool!

We conclude the episode speaking about Nolan, Jessica and Pat's son who they welcomed earlier this year who also spent some time in the NICU. 

Jessica shares some great information and advice pertinent to other families who are either currently in the NICU and weighing the heavy decision of a tracheostomy for their child, or for the families who have a child at home with a tracheostomy, as well as families who have suffered or may suffer a loss. Listeners will be surprised to hear some of the unexpected emotions that Lily and the Wolff family has had to work through once Lily had her trach removed. And again, you will be amazed by how strong and resilient Lily and the entire Wolff family is! I hope you enjoy the episode! 


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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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