For parents and clinicians interested
in learning more about early
onset scoliosis



Access patient stories, contact leaders
in the field, request assistance
for care



Discover the latest research
in early onset


A collection of resources to bridge the gap between the science
and the treatment of early onset scoliosis.

Who We Are

Our Mission

To help children with spine problems live longer, better lives.

The Children's Spine Foundation is a community dedicated to improving the quality of care and the outcome of treatment for patients and families dealing with chest wall and spine deformities.

Our Results


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.

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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.

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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 providers.

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