Support for Little Liam's Medical Journey

When Liam was born in April 2024 he was diagnosed with a rare congenital birth defect, a long gap Esophageal Atresia/Tracheoesophageal Fistula. This occurs in less than .0002% of children. What this means is that Liam’s esophagus was in two pieces when he was born, and he didn’t have much esophagus to work with when repairing it. Since his initial repair at 1 day old, Liam has had to undergo 13 additional procedures and is in need of a specialist.

This is where you come in...

There are only two specialists in the country for his condition, one being in Florida, and insurance denied covering his treatment there. We were quoted $25,000 for his in-person evaluation/scope and need to raise $15,000 before they'll be able to move forward. We are actively seeking donations to help fund his treatment. We know that God will provide for us during this time, and we are so thankful to be surrounded by a caring and supportive community.

If you would like to donate directly to Colton and Ashton, you may do so via:

Cashapp: $ashnicole0411

Venmo: Ashton-Lindsey-5

Thank you so much for your continuous prayers and support for our family!