Group for information and support for parents of children born with Talipes (Club Foot) living in Australia and New Zealand.

Offers information and support, as part of the International Rare Disease Support Network.

A support group for parentsof children with clubfoot, adults with clubfoot or anyone needing support with this condition.

A support group for parents of children with bilateral and unilateral clubfoot.

A discussion/support group for parents of children using the French Physiotherapy Method of treatment.

To discuss non-surgical methods of treatment, but specifically the Ponseti Method.

To offer support, encouragement, and information to people in the UK who have children with talipes, or who have been affected themselves.

A group to share stories, prayer requests, news and encouragement. Not limited to those with clubfoot.

Community for parents of children with this condition.