TOFS has developed from a small self-help group to an internationally recognised charity. Many of our volunteers and trustees are parents or relatives of children born with TOF/OA.
Our Council of Management is responsible for our development and strategic direction. Some of our trustees are parents or grandparents of children born with TOF/OA or VACTERL and some are adults who were born with the condition. This gives them all a unique understanding of the pressures our members face. You can contact any of our trustees through
the TOFS office.