Support children with rare genetic disease, like Ian!

The Lapp family graciously wrote about their journey with their son, Ian’s, diagnosis of Glutaric Aciduria type 1 (GA1) and the Clinic for Special Children for our Annual Giving Appeal.

You can read their handwritten story below, with an opportunity to give children, like Ian, a bright future.

Continue reading Ian’s story HERE

How Can You Give?

Make a donation online with credit card: Give Here

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