supporting the families of children born unable to swallow

To all at TOFS, just a really big THANK YOU for being there. All I wanted was just for someone to listen and understand and you were there for me.

Jo Wright, parent of a child born with TOF/OA

Join the 200 club

As a ‘200’ Club member with a minimum donation of £1 per month for one year to TOFS (total £12), you will enter a monthly draw with a single prize of £50 each month.

You will be allocated a personal number and this will be entered into the draw each month.  This draw will happen on the second Tuesday of each month.

You will have a different number for each £12 donated to TOFS.

Winners will receive a cheque in the post and will be listed in the next available issue of CHEW and on the TOFS website.       
Your membership is renewable after one year.

Download and print the application form

Latest news…

Revised Memorandum and Articles of Association

Important notice for all members  

Research Study has made its first breakthrough

The American Journal of Human Genetics publish a paper submitted by TOFS patron, Dr Charles Shaw-Smith. 

A BIG thank you to all our fundraisers

Whether you’ve been running the Flora London Marathon or trekkin’ the Sahara - we’re very grateful…

TOFS 2009 conference

What would you like to see covered at our next conference?  Let us know NOW.

Interested in taking part in a study of the genetics of Oesophageal Atresia?

Find out more here

Other sources of information and support

Other websites you might like to take a look at.