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Tracheo-Oesophageal Fistula Support

TOFS is a UK-based charity dedicated to providing emotional support to families of children born with Tracheo-Oesophageal Fistula, Oesophageal Atresia and associated conditions. Tracheo-Oesophageal Fistula (TOF) and Oesophageal Atresia (OA) are rare congenital conditions that affect one in every 3,500 babies. Learning that their child has TOF/OA can be an extremely difficult time for parents.

Who to contact

0115 961 3092
Tracheo-Oesophageal Fistula Support
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From that first moment to sharing the everyday challenges of bringing up a child with TOF/OA, TOFS offers friendship, support and information through:

  • one-to-one support from parents and relatives with experience of caring for a child with TOF/OA
  • social events and activities
  • our online community information leaflets and resources on many aspects of TOF/OA

Our membership of 1,100 includes new parents, families and health professionals. Contact us to find out how we can help you.

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Whilst every effort has been made to ensure the accuracy of the information provided in this directory, we do not accept any responsibility or liability for any errors that have occurred. It is recommended that you always check with providers that their service or organisation meets your requirements. We offer an impartial service and we cannot recommend or endorse any providers listed.

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