Emmas GNR for TOFS (COPY)

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Story

My long time friend’s son was born with OA/TOF alongside CHD. So I’m raising money to support the TOFS charity who are working hard to support the lifelong care for those born with this rare disease. 

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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.

1%

£10.00 raised of £750.00 target by 1 supporters

£10.00 donated

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When

From 15th May 2023. Until 22nd September 2023.

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