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Baby Girl Peters We will use this page to share updates about our baby girl.

12/08/2026

CDH affects more than the diaphragm—it also impacts lung development, making every breath a victory worth celebrating. 💙

Our Tiny Heroes show us every day what resilience looks like.

12/08/2026

If you’ve recently received a CDH diagnosis, we’re so glad you found your way here. 💙

While this journey may feel overwhelming right now, you are not alone. There is a community of families who have walked this road and are here to support you every step of the way.

Tiny Hero family, let’s fill the comments with words of hope and encouragement for those who need them today. 💙

26/06/2026

World Cup fun fact! Did you know one of Switzerland’s stars is also a CDH survivor?

Ricardo Rodriguez was born with congenital diaphragmatic hernia (CDH) and underwent emergency surgery shortly after birth. Doctors gave him just a 50% chance of survival.

Fast forward to today, and he’s representing Switzerland on one of the biggest stages in sports as a four-time World Cup player. 💙

Every CDH journey is different, but stories like Ricardo’s remind us that hope can lead to incredible possibilities.

We’ll be cheering him on! 🇨🇭⚽

Learn more about his story: https://www.the-sun.com/sport/16492452/ricardo-rodriguez-switzerland-world-cup-hernia/

And just like that our little miracle girl is THREE! She had the most magical birthday yesterday celebrating at one of h...
14/03/2026

And just like that our little miracle girl is THREE!
She had the most magical birthday yesterday celebrating at one of her favorite places!
We aren’t sure where the years have gone, but we do know that Miss Aurora is such a strong and beautiful little girl.
Her story didn’t start out ideal for any of us, but she continues to prove that she is a fighter and nothing will hold her back.
She’s developing such a strong personality that is both sweet and sassy and most of all silly.
We love you endlessly princess! 🩷

28/02/2026

February 28th is Rare Disease Day! The zebra is the global symbol of Rare Disease.

1 in every 2500 babies is diagnosed with Congenital Diaphragmatic Hernia, which classifies CDH as a Rare Disease under NIH guidelines. It is a structural defect (birth defect / congenital anomaly), and possibly a genetic defect as well. CDH is one of the lowest funded rare disease and birth defects per patient.

CDH Research International is a formal member of over a dozen rare disease alliances because when we all work together, our voices are louder! 🦓

Learn more at http://www.cdhi.org

26/01/2026

The Ronald McDonald House will always have a special place in my heart.

Because when my baby was in the hospital, and my world felt like it was crumbling,
they gave me a place to just be mom.

No hotel check ins.
No long drives back and forth.
No worrying about food, or showers, or where I’d sleep that night.

Just warmth.
Just comfort.
Just support, right when I needed it most.

They don’t just house families.
They hold them together during the hardest moments of their lives.

And I’ll never forget that.
Not ever.

©️Momming On Empty

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