Story
The MED13L Foundation is a beacon of hope, ignited by the unwavering passion of families touched by MED13L Syndrome. Our mission is to create a brighter future for all those living with MED13L through the power of research, the strength of community, and the spirit of collaboration. Together, we are forging a path towards greater understanding and support, bringing light to the lives of families facing this rare genetic disorder.
Since our daughter, Caitlynn, was born we have been searching for answers to her condition.(the list of side effects are as long as my arm). We received great news in the fall of 2023, a diagnosis of Med13L. This brings us to a new chapter in our story. A potential for more treatment options in the future.
Please donate today to help fund the summer of 2025 conference. This will help families from All over North America connect, generate collaborative scenarios and most importantly generate opportunities for treatment in the future!
Thanks