Mary Catherine Lynch arrived on December 8, 2011. After the initial shock that she was a SHE, we quickly learned something was not right. Then the real shock came; Mary Cate was diagnosed with Apert Syndrome, and since then our lives have been forever changed.
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We are looking forward to wonderful 2014! Mary Cate sends a virtual hug your way. We'll be posting updates about MC on our blog, so please check back often. We appreciate your kind words and support.
WE APPRECIATE YOUR GENEROSITY
Thank you for considering a donation! Children with Apert Syndrome can require 20 or more surgeries over the course of their life. Mary Cate has already endured 4 surgeries, and will continue to require more as she grows up.
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