Fundraiser - Ted's TOF Teddy Toddle 2024

Story

Edward and I are taking part in the 2024 Teddy Toddle to raise funds for TOFS.

TOFS is the UK's charity dedicated to offering lifelong support to those born with Oesophageal Atresia (OA) and Tracheo-Oesophageal Fistula (TOF). These rare conditions affect 1 in 3,500 people and can have lifelong implications.

TOFS receives no support from the Government and relies completely on donations from supporters. Every pound can make a difference.

The reason why supporting TOFS is important to us (as many of you know) is Edward was born with OA/TOF without warning, Eve though we'd been under fetal medicine for the pregnancy due to indicators of a problem. The support of the charity gave me a way to take control over an unexpected and unknown medical journey that Edward faced.

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.

28%

£56.25 raised of £200.00 target by 2 supporters

£45.00 donated plus £11.25 in GiftAid

When

From the 8th June 2024 until the 15th June 2024

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