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.  


To save your purchase against your account or to accrue points Sign in or Sign up to create a new account.


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.


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

£340.00 donated and £67.50 in GiftAid

QR code

Scan the QR code to share the page


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


Start fundraising
Sign up

See the terms and conditions.   See the privacy policy.

If you require assistance, please get in touch.

Sign in

If you do not have an account, then please register with us.   You can request a password reset if you have forgotten your user password.

If you require assistance, please get in touch.