We still can't believe Hayden is doing as well as he is today. He has oxygen support at ¼ liter and does have a G-tube, but it seems pretty minor compared to what they were expecting for our little guy. He is both a miracle and a blessing, and we thank God every day that he proved everyone wrong.

Being a parent to a CDH baby is a whole load of anxiety, but they are the strongest babies in the world! Believe in yourself and believe in your baby. They are miracles!

Seeing what she's been through with CDH and how far she's come never gets old! She will be one in just a few days, and we are so thankful for her amazing surgeon and everyone involved in her care.

Kyson is thriving at home. We are so blessed and thankful for our little miracle. CDH is a scary diagnosis but these little warriors are such strong fighters! Have faith in your Tiny Hero - they can accomplish anything!

Our family is so blessed to have only spent 33 days in the NICU with Lilith. Everyone was amazed with how well she was doing, and at 12 days old, I finally was able to hold her.

Callie is doing really well, and her personality is emerging now that she is home. She still sees a lot of specialists very regularly, and we still have a lot of obstacles ahead of us, but we will continue to fight!

Sophia has been thriving at home ever since. She’s developing normally and growing like a weed. No one who meets her would ever know how rocky her start was!

This journey hasn't been easy, but you never know about things like this until it happens to you—all of the sleepless nights at the hospital, surgeries, all the waiting, the nerves. The list could go on and on. Every CDH journey is different but we are so alike in many ways.

Isabella is our little rockstar. She brings so much joy to those around her. We are praying for your Tiny Hero, too, and believing in your miracle; they really do happen!

We are amazed by our little superstar and could not believe how fast she became well enough to go home. She's now 8 weeks old, feeding and growing well.

Being able to hug her, see her smile, hear her babble is the best gift God could have given us. She's such a strong and intelligent baby. I can't wait to see what she does in life. I'm so happy Elizabeth chose us to be her parents.

Trey has been through a lot but always bounces back better than before. Yesterday, he started his senior year of high school. He is a strong, funny, and kind CDH survivor. Now, he is 17 years old and the light of our lives!

This was a long hard battle. I would do it a hundred times over for the life of my baby. Elisha is a fighter, and I'm proud to say that. I think this helped him through it all. Today, he will be 15 in September.

That day you first learn the words “Congenital Diaphragmatic Hernia” is one you will never forget. May 10, 2019, will forever be a hard day for me. Only two days before my first Mother’s Day, our world was shattered.

Jack is almost 6. He has had a bumpy ride. While he is still facing challenges, he doesn't let them get in his way. He is my Tiny Hero.

Leah is the most content, alert and happy wee girl! We appreciate every single minute with her. She is perfect, and people are shocked when they learn her story as she doesn't look like she was ever sick!

Cole continues to grow, laugh, and exceed our expectations every day. According to his pediatrician, he is in the 40-50 percentile for his weight, height, and head measurements.

Cash currently holds the record for the quickest CDH recovery at that children’s hospital. He is now 5 1/2 months old and thriving!

If you take anything from this long story of ours, it's that your kid isn't the only one that survives CDH; you do, too. None of this is your fault, and you're doing the best you can, so allow yourself some grace.

I'm forever grateful to her surgical team and the NICU staff, as well as our community, who rallied around us with donations, support, and prayers. Today, Brynlee is off all of her medication, developmentally on track, and the joy of my heart.