Advancing MED13L Research: Support Kellan's Journey

We are reaching out with a heart full of hope and a plea for support for OUR beautiful one-year-old son, Kellan. Recently, he has been diagnosed with an extremely rare genetic condition called MED13L syndrome-a diagnosis that has changed our world in ways we could have never imagined.

What is MED13L Syndrome?

MED13L syndrome is an extremely rare neurodevelopmental disorder caused by mutations in the MED13L gene. This condition leads to a wide range of challenges including delayed milestones, intellectual disability, speech and motor impairments, seizures, and developmental delays. Because it is so rare, there are few treatment options and not much is known about the best ways to support children like Kellan.

For our sweet boy, every day is a new challenge, but also a new opportunity to fight for his future. He has a smile that lights up the room and a strength that inspires everyone around him. We know that with the right support, therapies, and treatments, he can live a fulfilling, happy life. But we can't do this alone.

Why We Need Your Help:

While we are doing everything we can to support Kellan’s development, we know that the journey to better care for him—and for other children with MED13L—requires more than just individual efforts. That's why we are partnering with the MED13L Foundation, an organization dedicated to advancing research, improving treatments, and raising awareness about this rare condition.

Funds raised through this campaign will go directly to the MED13L Foundation to support:

By donating, you are helping not only Kellan, but countless other children who are also facing this rare and difficult condition. You are funding vital research that could lead to breakthroughs in treatment and care for the future.

How Your Support Will Make a Difference

Every dollar you contribute will go toward funding the MED13L Foundation’s mission to drive research, advocate for better care, and provide families like ours with the resources they need to navigate this journey. While there is still much work to be done, your support gives us hope that together, we can make a real difference in the lives of children with MED13L syndrome.

From the bottom of our hearts, thank you.

Whether you can donate or simply share our story, your kindness means the world to us. We are beyond grateful for your support, and we promise to keep you updated on Kellan’s progress as well as the incredible work being done by the MED13L Foundation. If you'd like to follow his journey in more detail, please join our Facebook group: https://www.facebook.com/share/g/19SBdKFRUj/

With love and gratitude,

The Somerfelt Family

(Tyler, Monica, Nolan, Gavin and Kellan)