Welcome Home to CSA

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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.

The Christianson Syndrome Association (CSA) was founded in 2011 by Debbie Nash and her family in honor of her son, Andrew, who was diagnosed with Christianson Syndrome in 2010. What began as one mother’s tribute has grown into a welcoming home for families affected by Christianson Syndrome worldwide.

CSA brings together families, caregivers, advocates, and scientists—uniting them through shared understanding, strength, and hope. Together, we work to raise awareness, deepen understanding, and improve quality of life, with the shared dream of one day finding a treatment. At CSA, no family walks this journey alone—we are stronger together. WELCOME HOME TO CSA!