Over thirty years on and now a registered charity, we continue to help families through the challenges of bringing up a child with TOF/OA, VACTERL and associated conditions.
Increasingly we also provide support to adults who were born with these conditions.
We do this by providing one-to-one support and a range of information and resources to families. TOFS is a recognised source of information for professionals with an interest in TOF/OA. We also take an interest in research into the causes and implications of these conditions.
We rely on support through membership fees, voluntary donations and other sources of charitable income to fund our activities.