The EA/TEF Family Support Connection is about families caring for one another, putting a smile on a child's face, and making a positive impact on someone's life. We do not give medical advice. Instead, we provide an ear for listening, a sounding board for ideas, a forum for questions, a shoulder to cry on and, most importantly, hope. We offer education and guidance on the practical aspect of caring for and raising a medically fragile child.
In our discussion forums, you can ask questions and hear stories from other parents.
We have produced several informative brochures to help you with many questions that arise when raising a child born with EA/TEF. Please access them using the menu to the left.