Story

On the 23rd April I will be running the London Marathon 2023 for TOFs Charity. 

Our youngest boy Samuel was born with a rare birth defect called Tracheoesophageal Fistula (TOFs) with Oseophageal astresia (OA). Samuel had corrective surgery at a day old and has had to have multiply further operations to stretch the scar tissue. Samuel also has some abnormalities with his heart that fortunately at the moment only require monitoring. I can't find the words to describe the emotions you feel as a parent when all isn't as it should be when your child enters the world and I will forever be grateful for the medical team that saved Samuel. The TOFs charity/family have been there from the start of our TOF journey, the support, information and guidance that the charity provide is invaluable. As this charity will be part of Samuels journey for the rest of his life it means so much to be able to try and give something back and therefore in October I will be running the London Marathon. Please sponsor me if you can, any amount will be greatly received.  

   

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Supporting

TOFS from TOFS (Tracheo-Oesophageal Fistula Support)

TOFS offers support to people born with Tracheo-Oesophageal Fistula (TOF) and/or Oesophageal Atresia (OA). These are rare congenital malformaltions of the gullet and windpipe. Immediate neonatal surgery is a treatment, not a complete cure. We are UK-based and receive no public-sector support at all.

27%

£407.50 raised of £1,500.00 target by 13 supporters

£340.00 donated and £67.50 in GiftAid

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When

From 22nd July 2022. Until 30th April 2023.

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