Welcome to a support network created by a parent in Ireland for people who are affected by Talipes / Clubfoot!

 

This site is created to bring people together world wide to form a Talipes support network. It will not offer you medical expertise. It will however offer practical help and information from others going through the same as you.

 

How to get started

 

1 - Update your profile page with some information and a profile photo.

2 -Introduce yourself by going to the Forum page. Tell us a bit about yourself and what brings you here!

3 - Catch up with Louis' story. A little boy with bilateral congenital talipes being treated in Ireland.

4 - Share helpful hints. You probably have something very useful to share with others to make coping with talipes easier.

5 – Add a discussion if you have a question for other TT members or just some food for thought!

6 - Start a blog! This is where you can share your own experiences and add to it as time passes, like a diary.

7 - Add photos and videos.

8 - Click on the banner below to help raise funds for Talipes Together when you shop from UK based online stores! A quick and easy way of helping us keep this website open!
 
 

This project received grant aid from Cill Dara Ar Aghaidh which is financed by the Irish Government under the Rural Development Programme Ireland 2007-2013 and by the European Agricultural Fund for Rural Development: Europe investing in Rural Areas.
Funding Document.pdf

EU Commission and Department of Community, Equality and Gaeltacht Affairs.