I want to be able to encourage and strengthen other families through our sons journey. At age 3, my son was diagnosed with a rare disorder called, Dyskeratosis Congenita. The quest to find answers wasn’t easy. I wish I knew what I know now to help make this journey a bit easier. I decided to make this podcast even if it means I can help 1 or 3 people. I want to be the person you need, that I needed for years. My sons journey has made up better.
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