Fundraiser - Rachelâ€™s Ride London for TOFS

Story

I am cycling 100 miles, the furthest I ve ever ridden, on the 29th May to raise money and awareness for TOFS.org.uk

My daughter, Ruby, was born with a rare condition called Tracheo-oesophageal Fistula syndrome with oesophageal artresia (TOF OA). This means she could not swallow and had to undergo life-saving surgery at just one day old.

Fast forward to 6 years, multiple operations and spells in intensive care later and you would never know she had ever had any problems!

TOFs.org.uk were a tremendous support during the difficult early years for which we are forever grateful, and the reason why I want to help raise money today.

Ruby, your determination, strength and energy will be on my mind throughout the ride and I look to you for my inspiration x

Updates

Ruby

Updated on Sun, March 20 2022, 10:15 PM

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.

315%

£1,576.25 raised of £500.00 target by 47 supporters

£1,300.00 donated plus £276.25 in GiftAid

When

From 20th March 2022. Until 30th June 2022.

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