Talipes Together | Club Foot Support Network
Welcome to a support network created for people affected by Talipes / Clubfoot. We are here to share information, help and support!
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.
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!

Started by prem edward in Introductions. Last reply by Mia Barry 7 hours ago. 1 Reply 1 Like
Started by Pamela Leahy in Discussions. Last reply by Pamela Leahy 22 hours ago. 5 Replies 0 Likes
Started by Claudia Boggiano in Introductions. Last reply by Claudia Boggiano yesterday. 2 Replies 0 Likes
Posted by Mia Barry on January 17, 2012 at 3:30pm 0 Comments 0 Likes
Posted by Aisling Murray on January 12, 2012 at 11:13pm 0 Comments 0 Likes
Posted by Aisling Murray on January 10, 2012 at 7:51pm 7 Comments 0 Likes
23rd January 2012
Australian High Commissioner visit Bangladesh Clubfoot Programme. Read on...
17th January 2012
Grant will promote clubfoot research the world over. Read on...
16th January 2012
India - State opens up drive to cure clubfoot. Read article...
General
How parents feel about having a child with clubfoot - read on....
STEPS UK now has a bedtime book for sale about wearing boots and bars. It was hand made by a mother with a little girl with Talipes and it has now been printed. All proceeds go to STEPS UK charity. Link....
Steps South Aftica is calling for donation help for a little boy with club feet.
Arto Lekhgato is a cute little boy who lives with his mom and two older siblings in Otse, Botswana.
Arto was born with bilateral clubfeet and although he had some early casts applied at his local clinic, his feet remain uncorrected.
Time is not in his favor as he is almost 18 months old.
He should be walking by now and he isn't, which is hard on his mother and of course on him, although he doesn't realize what he is missing yet.
The Ponseti method is not available in Botswana yet, but we have found help in Cape Town to correct Arto's feet so he can live a life free from disability. We need to cover some of costs for his long journey:
- Travel from Gaborone to Cape Town for Arto and his mom
- Local transport in Cape Town
- Special foot abduction brace (shoes and bar) to maintain correction and prevent relapse
- Sustenance for Arto and his mom for the long journey and stay in Cape Town
Having access to the Ponseti treatment for clubfoot will be life changing for Arto and his family.
Your donation will give Arto the gift of straight and supple feet, so that he can walk and run like any other kid.
Link to STEPS page on Greater Good SA to make a donation.
http://www.myggsa.co.za/
© 2012 Created by Mia Barry.
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