Support children with rare genetic disease, like Ian!
Posted on December 16, 2019
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
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