Jen - Part 1 | Eating the Elephant(s)

Trauma. Grief. Heartache.  I know so many of us face these things on a daily basis.  Today’s story is no different.  Years into her journey, Jen is able to share details of her family, specifically of her two boys Carter and Silas. Hemophagocytic lymphohistiocytosis tragically changed life as Jen knew it, forever.  Topics we talked about that you do not want to miss: Carter and an “ear infection”  Silas born prematurely  Deja vu: fighting for Silas’ life Going from a typical healthy child to a disabled child in four months Losing 99% of your son Links and resources: Follow us on Facebook: www.facebook.com/WhenAutumnComesPodcast Join the WAC Society to talk about all things pod related: www.facebook.com/WhenAutumnComesSociety Follow us on Instagram: @WhenAutumnComesPodcast Catch up with Suz: @suzgeoghegan on insta See what Diane is up to: @diane.kay.erdman on insta Make sure you hit SUBSCRIBE so you don’t miss out on our upcoming stories of medical and special needs parenting from families like yours. And, if you enjoyed this episode, please leave us a 5 star rating and a review!  Thank You!  

Om Podcasten

We call ourselves the 4am Mom Club because more nights than not, our kids are awake at 4am. We both have very medical, complicated, rare, beautiful children. This is a podcast for medical and disability mamas (and the people who love them) who are facing a life they never expected. We share hope-filled stories of families, all shapes, colors, sizes and abilities, all in different phases of their medically complex or disabled caregiving journey. When Autumn Comes Podcast is a program of the Apricity Hope Project nonprofit. Our mission is to care for caregiver. Learn more at apricityhope.org