Brody’s TOFs Teddy Toddle 🧸

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Story

Brody was born with TOF/ OA which means he was born unable to swallow and needed emergency surgery. Although he is much better now he is in no way cured and will have to deal with this forever. But he is doing amazing and making us prouder every single day. 

Many parents are unaware that their baby is going to be born with OA / TOF. This stands for Oesophageal Atresia (OA) and Tracheo-Oesophageal Fistula (TOF) which are rare congenital conditions of the oesophagus (food pipe) and/or trachea (airway) that affects 1 in every 3,500 people. 

Brody will be participating in the TOFs Teddy Toddle on June 10th - June 17th 2023, where he will be completing 5K in 5 days (most definitely either chilling in his pram while we do all the walking or on one of our shoulders 🤣) but he will gain a lovely TOFs medal at the end 💜 

This charity is so close to our hearts and without the advice, support and help of this charity we wouldn’t be where we are today so we will be trying our best to raise as much as we can for this amazing organisation 💜


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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.

888%

£887.50 raised of £100.00 target by 20 supporters

£740.00 donated plus £147.50 in GiftAid

When

From the 10th June 2023 until the 17th June 2023

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