Please keep in mind that I have no medical training. I’m just a parent of a child born with bilateral clubfeet.
Our eldest child was born with bilateral clubfeet and Amniotic Band Syndrome affecting his left hand. In 1993 the internet was just a baby too. We didn’t know where to turn for information about these conditions. We made our decisions based on what our Doctors told us. We knew nothing about non-surgical methods of treating clubfeet and as a result, our baby had clubfoot surgery. I created this site so others could learn about the Ponseti Method. I hope this site will help others to find information and support. » Read Our story.
Please read this! IS YOUR DOCTOR USING THE PONSETI METHOD!?
I invite you to:
- submit your story to add to the site and read and comment on the stories that others have contributed ~ it’s these personal stories that make this site special
- donate your used orthopedic devices for reuse
- sponsor a forgotten child’s clubfoot treatment through CBM
- contribute to this site…. Through this site I have been able to help a number of people. Donations received will cover expenses such as hosting and domain renewal
This site is not run by an organization or charity. Please keep in mind that I have no medical training.