supporting the families of children born unable to swallow

During my working life as a paediatric surgeon I learned as much, if not more about TOF from parents and from TOFS meetings as I did from learned journals.

Leela Kapila, past Vice-President of the Royal College of Surgeons

Information on Procedures

Tracheo-Oesophageal Fistula (TOF) and Oesophageal Atresia (OA) are rare congenital conditions of the oesophagus (food pipe) and/or trachea (airway) that affect one in every 3,500 babies. Babies born with Tracheo-Oesophageal Fistula (TOF) and Oesophageal Atresia need to have surgical correction soon after they’re born. Some children may also need to have additional surgical interventions further on in their lives.

Every baby born with TOF/OA is different and will have different needs. With the benefits of modern medical intervention and the active support of groups like TOFS, the outlook for children with TOF/OA is very positive.

You can find out here about specific medical procedures. If you’ve got any questions, please contact the TOFS office.