by Blake Powell | Aug 8, 2019 | Uncategorized
Our family cannot thank Oxford Kids Foundation enough for providing our son the grant for his treatment. There are no words I can say that would express the depth of our gratitude. All I can say is thank you, thank you, thank you for allowing my son to be able to do...
by Blake Powell | Aug 8, 2019 | Uncategorized
At 12 months old Tucker was diagnosed with Angelman Syndrome. Our geneticist told us he would never walk and our physical therapist at the time used the phrase “floor bound.” Tucker never gave up so neither did we. Nearing his fourth birthday Tucker had taken six...
