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The Children's Spine Foundation helps children diagnosed with complex spinal deformity access medical care. With the varied treatment options available, it can be a confusing and difficult time for families.

We help families obtain expert medical care by providing financial assistance for travel during this time through our Family Grant. Please click here for detailed information on the support available.


The Children's Spine Foundation is committed to improving clinical outcomes in patients with complex early onset scoliosis (EOS). Our infrastructure allows us to do this in the form of a clinical registry.

The registry securely and reliably tracks patients with EOS; that data is used as a basis of clinical research in many areas of complex spinal deformity. Click here for a complete list of our research.


The Children's Spine Foundation educates colleagues around the world to improve patient care and clinical outcomes. We support the participation of leading clinicians from outside of the US to contribute and share their data with us.

Our members participate in numerous expert panels and roundtable discussions both in the US and abroad. Click here for more info about our board members.