Welcome Home to CSA

Group 2017

Thank you to the families, researchers and scientists that helped make The 2nd International Basic Science and Clinical Conference on Christianson Syndrome so SPECIAL!!

Our Mission Statement:
To advance the awareness and treatment of Christianson Syndrome through education and information, research, advocacy and support for individuals with Christianson Syndrome, their families, and other concerned parties.

Why was CSA created? The Christianson Syndrome Association is a non-profit organization founded by Debbie Nash and her family in August 2011 in honor of her son, Andrew. Andrew was diagnosed with Christianson Syndrome in August of 2010. Soon after receiving the diagnosis, the Nash family realized how very little was known about this newly found genetic disorder. From that point forward, it has been the goal of Debbie and her family to support the research into the cause and treatment for this disorder as well as raise awareness both nationally and internationally. Once diagnosed families need to be able to talk and network with other families to know that they are not alone. CSA was born out of Debbie’s desire to reach other families whose children are affected by CS and to unite them together as one family with the goal of raising awareness and to ultimately find a treatment to help our boys.

Christianson Syndrome Association
15201 Mason Road Ste 1000 #173
Cypress, TX 77433



2024 Loop for Luke

The sun was shining in Columbia MD for the 2024 Loop for Luke. So much love and laughter was shared by families and friends in support of Christianson Syndrome. This year's event raised almost $10,000.00 with participants raising awareness around the world. Thank you again to the Wright family and everyone else who helped make this a wonderful event!!