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

Publications

We provide a range of publications about the practical and emotional aspects of caring for a child with TOF/OA or VACTERL. Most of our resources have been written by medical and healthcare specialists or in partnership with them.

We understand how important it is to have the right information at the right time. Our experience has taught us that it’s usually best to learn about TOF/OA in stages. If you’re a new parent of a child with TOF/OA or VACTERL, we suggest you visit our section for new parents first. For a quick explanation of what TOF/OA is, take a look at what is TOF/OA?

You can download most TOFS leaflets for free or order copies from our office.

Our quarterly members’ newsletter, 

, is packed full of family updates, news and useful articles.

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Our book, The TOF Child, covers many aspects of caring for a child with TOF/OA. Written by medical professionals with a special interest in TOF/OA, The TOF Child covers key topics in detail, including feeding, family issues and sources of support.

The TOF Child costs £9.99 to members and £14.99 to non-members (in the UK)

You can view the book online. Click here

The_TOF_Child_website_copy.doc

To order The TOF Child, contact the office.

 

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Here is a publicity poster,  click on it to download the full sized version.