St George's Centre
91 Victoria Road
Tel: 0115 961 3092
Tracheo-Oesophageal Fistula Support (TOFS) is a registered, UK-based charity dedicated to providing emotional support to families of children born with tracheo-oesophageal fistula (TOF), oesophageal atresia (OA) and associated conditions.
TOF and 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 TOF/OA need to have intensive neonatal care prior to corrective surgery, normally within days of birth. Some children have to undergo additional surgical interventions later on in their lives. Whilst many children born with TOF/OA will experience only a few problems, others may have difficulties with swallowing and digesting food, gastro-oesophageal reflux (where the acidic stomach contents pass back into the lower oesophagus) and respiratory problems. The effects of surgery and associated health problems can add a great deal to the usual challenges of parenthood.
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.
- Their online community.
- Information leaflets and resources on many aspects of TOF/OA.
TOFS is a recognised source of information for professionals with an interest in TOF/OA. TOFS also takes an interest in research into the causes and implications of these conditions.
Last updated on 25/10/2013
Disclaimer: This article is for information only and should not be used for the diagnosis or treatment of medical conditions. Patient Platform Limited has used all reasonable care in compiling the information but make no warranty as to its accuracy. Consult a doctor or other health care professional for diagnosis and treatment of medical conditions. For details see our conditions.