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TOFS Great North Run 2024

Story

On 8th September I will be taking part in the Great North Run, raising money for TOFS charity. 
TOFS charity has been a great source of support to me through tough and uncertain times after Beatrice was born unable to swallow. 
The TOFS website, Facebook page and CHEW magazine are useful and informative and allow parents to share experiences and receive support about TOF/OA which is a rare congenital condition. 
Your donation will help TOFS charity to carry on the wonderful work they do.  
Your donation means so much, thank you! 
This one’s for you Bea, so proud to be your mummy and watch you grow into a happy, healthy 7 year old. 

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Updates

Victoria Porter TOFS fundraiser 

Updated on Tue, July 2 2024, 7:48 PM

Supporting

TOFS - 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.

220%

£1,097.85 raised of £500.00 target by 22 supporters

£934.35 donated plus £163.50 in GiftAid

When

From the 25th May 2024 until the 1st October 2024

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