Please contact TOFS (firstname.lastname@example.org) if you want to jump for TOFS!
TOFS helps make life easier for children and adults who were born unable to swallow due to the rare malformations oesophageal atresia and/or trachea-oesophageal fistula.
Surgery is essential and done in the first days of life. But it is a treatment, not a cure. Patients can suffer from obscure complaints, in some cases for life.
TOFS offers information about TOF/OA, and living with it, as well as personal contact. We also engage with healthcare professionals and sponsor some research.