For Doctors

Many doctors have never encountered an individual with sacral agenesis/caudal regression syndrome (SA/CRS).  There are no known specialists for this

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For Parents

                   Dear Parents of Children with SA/CRS, Hello new parents! I know

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A Letter from the President

With more than 1,000 individuals and families connected worldwide, iSACRA is proud to be the only international organization for people with

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Volunteer

iSACRA is always seeking volunteers for various activities.  If you have a talent or an interest in serving, please contact

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Donate

Donate Why do we raise funds? When you have a rare condition, you know all too well that: Lack of

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About iSACRA

This organization is a 501(c)(3) nonprofit based in the USA and is the world’s only international organization serving those who

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Contact

Please note we will not share your contact or personal information with outside parties without your written permission.  Please allow

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Board of Directors

iSACRA Board Members, June 2017 Jessica Rogers, President Jessica Rogers is a young adult with SA/CRS who was born in

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