| Welcome! The Jack Ryan Gillham Foundation is an organization committed to providing support to the families of critically ill children so that they may devote complete attention and care to the needs of their child. The Jack Ryan Gillham Foundation was established in September of 2007 in memory of our son, Jack, who passed away due to complications from a rare birth defect called Congenital Diaphragmatic Hernia (CDH). We appreciate your interest in the foundation and hope that you are touched by Jack’s life. Please check the Current Events page for regular updates and to find out about events we are planning to raise money and awareness for CDH and families who are affected by CDH. Please check out our Current Events page to see the work that we are all doing together to help continue Jack's legacy of hope and love and to help educate people about CDH. |
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