The Babin Family Fundraiser

Our Goal: $500

DONATE NOW →


OUR STORY

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We were diagnosed at 20 weeks pregnant with CDH. The first high risk doctor told us it was only stomach up. We found out at week 32 it was everything, including the liver. Our son lived 35 days on ECMO. We wish we had the opportunity to meet Dr Kays. Tiny Hero is such an awesome resource.


WHY TINY HERO?

Everyone should have a chance to receive the best care. I wish we had known about Tiny Hero when our son was born.

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HOPE STARTS HERE HOODIE

You can also support our family by purchasing this exclusive Hope for the Holidays item. All proceeds from the sales go towards Tiny Hero. Tiny Hero is a 501(c)(3) organization built to help support families with CDH children.

What is CDH?

Congenital diaphragmatic hernia (CDH) occurs in an unborn baby when there is a hole in, or incomplete formation of, the diaphragm (the muscle under the lungs that is responsible for breathing).

CDH affects about one in every 2,500 babies (1600 cases in the U.S. each year), and occurs as often as cystic fibrosis and spina bifida, yet most have never heard of it. On average, only 50% of these babies survive. Learn more about what is CDH→

Where does my donation go?

  1. Family Grants - We help families get to very best possible care and provide financial aid when needed.

  2. Community Support - We create videos, update our blog and website, and produce printed materials to help expand our message of hope to a larger audience. 

  3. Inspiring Better Care - We partnered with the Fore Hadley Foundation to help fund productive research efforts across the country.

Jacob Dunford