Story

We have been lucky(?) enough to be chosen by the lovely TOFS charity to run (or walk or possibly even crawl at the end) the virtual London marathon on the 3rd October. 

This charity is very close to our hearts after helping our family through a very difficult time when Clara-Leisa was born.

TOFS (Tracheo-Oesophageal Fistula Support) is a charity dedicated to improving the lives of all who were born with the TOF condition.

The TOFS charity also takes an active role in supporting research into the causes and implications of these conditions. They are closely connected with international collaborative work to improve outcomes for those born with OA/TOF.  

As a registered charity they receive no government funding and rely entirely on members' donations, voluntary donations and other sources of charitable income to fund their activities. 

We thank you for any kind donations. 

Chris and Vanessa.

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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.

225%

£2,248.12 raised of £1,000.00 target by 46 supporters

£1,822.50 donated plus £425.62 in GiftAid

When

From 3rd October 2021. Until 17th October 2021.

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