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Information for people born with OA/TOF

OA/TOF were once considered paediatric conditions, and it is only in recent years – with the growing cohort of adults born with these conditions – that the long-reaching implications of being born with OA/TOF are becoming more acknowledged.We have split this section into two areas but some of the information is relevant to both.

Teens born with OA/TOF

Information and resources aimed at teenagers born with OA/TOF.

Find out more.

Adults born with OA/TOF

Information and resources aimed at adults born with OA/TOF.

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Get Support

At TOFS, we are committed to supporting those born with OA/TOF throughout their lifetime.

As well as the support we offer on this site, member’s magazine and via our TLC network, we also endorse a self-help Facebook group for adults.

UK Adults born with Tracheo-Oesophageal Fistula / Oesophageal Atresia.

Join TOFS

TOFS - Lifelong support for those born unable to swallow

Join TOFS and be a part of the largest community of parents, careers and those born with OA/TOFs in the world. Find out more…