2023 Gift Requests Maxley He loves Sesame Street and more specifically Elmo and super Grover. He has a heart…adminNovember 19, 2023
2023 Gift Requests Lucy Lucy is one in a million. She can light up a room with her smile.…adminNovember 19, 2023
2023 Gift Requests Magnus Magnus has PKS, but he doesn't let it stop him from being happy and full…adminNovember 19, 2023
2023 Gift Requests Sophie Sophie was misdiagnosed dandy Walker at 20 wks gestation. We delivered emergency c section due…adminNovember 19, 2023
2023 Gift Requests Dallas I don’t know about rare but he is a very pleasant lovable little guy. Always…adminNovember 19, 2023
2023 Gift Requests Beth Harlow's seizures are uncontrolled as with many children with Dravet Syndrome. The syndrome has many…adminNovember 19, 2023
2023 Gift Requests Aine Aine (Anya) is medically complex with a main diagnosis of 22q11.2 deletion syndrome. While there…adminNovember 19, 2023
2023 Gift Requests Isaac Isaac is a strong little guy who has faced many challenges head on. He was…adminNovember 19, 2023
2023 Gift Requests Wyatt Wyatt was born with a random genetic mutation that causes CFC Syndrome. There are currently…adminNovember 19, 2023
2023 Gift Requests Wyatt Wyatt has Lennox Gastaut Syndrome with no known genetic cause. He is part of the…adminNovember 19, 2023
2023 Gift Requests Alex Alex is just amazing. Loves pianos and his bottles. He healed from his hip surgery…adminNovember 19, 2023
2023 Gift Requests Gavin While there are less than 30 cases of Gavin's deletion and duplication in isolation, he…adminNovember 19, 2023
2023 Gift Requests Mark Mark has a rare genetic difference this has resulted in a long list of other…adminNovember 19, 2023
2023 Gift Requests Natalie It is difficult to summarize Natalie's story briefly, she has lived more, fought harder, struggled…adminNovember 19, 2023
2023 Gift Requests Jonah Jonah is a lovely boy with Pallister Killian Syndrome. Although he has global developmental delays,…adminNovember 19, 2023
2023 Gift Requests Lindsay My child is exceptional not rare. She is the most amazing little girl ever.adminNovember 19, 2023
2023 Gift Requests Anderson We moved from Michigan to Minnesota to be close to the few experts in the…adminNovember 19, 2023
2023 Gift Requests Liam We had Liam 3 weeks early and he was diagnosed at 3 weeks old with…adminNovember 19, 2023
2023 Gift Requests Jaden Jaden was born with Pallister Killian Syndrome and is now 21 years old. He just…adminNovember 19, 2023
