Story
On March 26th, our daughter Alannah was born five weeks premature. Hours later, she was diagnosed with OA-TOF and VACTERL associations - meaning she was born unable to swallow, with her food pipe disconnected from her stomach and also attached to her windpipe.
She was immediately transferred from Bath to Cardiff and underwent major surgery on day two. Because of a "long gap" between the ends of her food pipe, her recovery was intense. She fought bravely in the Cardiff NICU until we finally brought her home on May 3rd.
Emma and I are eternally grateful to the incredible NHS staff who saved her life and to our friends and family who carried us through. Living through that fear gave us a deep understanding of what other families face and our hearts go out to anyone going through the same struggle.
Today, Alannah is home and doing brilliantly. As her dad, I want to do everything I can to give back and support others navigating this diagnosis.
This September, I am cycling 450 miles solo from Keynsham to Milford, Donegal to raise money for TOFS—the charity providing crucial lifelong support to families of children born unable to swallow.
Please note: I am covering all my own travel, accommodation and ferry costs personally. Every single penny donated here goes directly to the charity to help families who need it most.
Thank you for your support,
George
