CDH Stories
Legacy’s CDH Story
I share these details to say that even under the direst circumstances, there is HOPE! Yes, there is pain, grief, and fear of loss, but there is always HOPE!
Oliver’s CDH Story
Ollie is almost two years old and the happiest, most loving, playful little boy. If you are a parent just finding out or in the thick of it, know that these Tiny Heroes are stronger than you think and will be ready to fight!
Charlotte’s Story - Congenital Diaphragmatic Hernia
Charlotte came home on December 29th with an NG tube and no medications except Pepcid and vitamin D. Within a week of being home, the pediatrician allowed us to take out the NG tube since Charlotte was taking a bottle and breastfeeding just fine. Our sweet girl is absolutely a Tiny Hero, and I hope that she continues to beat everything thrown at her!
Rhiley’s Story - Congenital Diaphragmatic Hernia
For all of the CDH parents out there currently in the thick of it like us, know that these babies are stronger than you can imagine. They fight like hell and are so resilient. Also, remember to give yourself grace and know that a whole community is available to help get you through what is most likely one of the hardest things you will ever experience.
Brielle’s Story - Congenital Diaphragmatic Hernia
Our sweet miracle has overcome so much in such a short amount of time, and my husband and I are so proud of her. Being a CDH mom on top of being a first-time mom has been a rollercoaster, but this sweet face makes it all worth it.
Avery’s Story - Congenital Diaphragmatic Hernia
Avery ended up being in the hospital for two and a half months and coming home with a G-tube and no oxygen needed. Now at almost a year old, she's G-tube free and hitting all her milestones. Her heart has developed well, and her echos have been good. It's amazing how strong these babies really are. Even though it's hard, it really is true when people say not to lose hope.
Autumn and Summer’s CDH Story
The surgeon was shocked, as were we. First, to see identical twins both with CDH and then the same exact defect. What do you say to the man who saved your children's lives? I just thanked him over and over. A huge weight had been lifted off my shoulders. What a rollercoaster ride!
Kai’s Story - Congenital Diaphragmatic Hernia
Kai is officially nine months and she is crawling, rolling over, and standing. She loves to dance and cuddle and play with her big sister. She always has a smile on her face as she continues to show the world how remarkably strong she is. She’s our Tiny Hero!