My name is Evelyn, and I’m reaching out on behalf of my niece, Kaylee Rivas. Kaylee was born with a rare and serious condition called Esophageal Atresia, a birth defect where the esophagus doesn’t connect properly to the stomach. This has meant that since birth, Kaylee has been unable to eat or drink through her mouth. In her short two years of life, Kaylee has had 5 surgeries in an effort to connect her esophagus to her stomach. None have been successful. Her most recent surgery was in July, and since then, she has remained hospitalized. She has spent more time in the hospital than at home. Through it all, Kaylee continues to fight with courage and a smile that lights up the room.

Her parents have done everything they can emotionally, physically, and financially to give her the care she needs. But the cost of ongoing hospital stays, surgeries, travel, and daily expenses is overwhelming. That’s why we are humbly asking for help.

We want to give Kaylee the chance to do what every child deserves:

To play with her friends, eat birthday cake, laugh without tubes and wires, and simply live life without constant medical complications.

Even if you can't donate, please share Kaylee's story. Every share is a step closer to finding the support she needs.

From the bottom of our hearts, thank you for your love, support, and prayers.

With gratitude,

Evelyn and the Rivas Family