TOFS is the charity dedicated to offering lifelong support to those born with Oesophageal Atresia (OA) and Tracheo-Oesophageal Fistula (TOF).
We are the world’s largest English-speaking support group for OA/TOF with members in over 60 countries. We do this by supporting families, adults, and medical professionals.
tofs.org.uk
TOFS aims are:
Provide trusted information and support to OA/TOF patients regardless of age
Spread awareness of OA/TOF conditions and their implications post-repair
Facilitate peer-to-peer support and empower patients and their families to seek best outcomes.
We can only achieve our aims with your support. Please help us make a real difference in the lives of those born unable to swallow.
