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

Other sources of information and support

We’ve put together a list of links to other websites which provide information about TOF/OA and related conditions, and links to other organisations which provide support. Click here to visit the links page.

Latest news…

Are you an Adult TOF?

Interested in attending a ‘TOFS 16+...Adulthood’ conference?

2010 AGM and party-time!

Saturday 9 May - Rosliston Forestry Centre, Swadlincote, Derbys DE12 8JX

Are you a medical professional with an interest in Oesophageal Atresia?

You may benefit from attending the first-ever International Workshop on OA to be held on 27 and 28 May 2010 in Lille, France

TOFS - on Facebook

If you’re a TOF adult, or you have a child born with TOF, why not join our Facebook group?

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.