Congenital Talipes Equinovarus

Clubfoot | Congenital Talipes Equinovarus

Please keep in mind that I have no medical training. I’m just a parent of a boy born with bilateral clubfeet.
Bilateral Clubfeet

My eldest son, Evan, 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 his 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 Evan 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 Evan’s story.

Please read this!  IS YOUR DOCTOR USING THE PONSETI METHOD!?

I invite you to:

This site is not run by an organization or charity. I’m just a parent of a boy born with bilateral clubfeet. Please keep in mind that I have no medical training.

Clubfoot Stories

  • Nick’s Club Feet Story

    Hey everybody, obviously by the title you can tell my name is Nick. When I was born I also had two

  • Sydney’s Clubfoot Story
    Sydney’s Clubfoot Story

    My name is Sydney, and I’m 35 now. I was born with a severe unilateral clubfoot, my left. My mother told

  • Apollonas’s Clubfoot Story
    Apollonas’s Clubfoot Story

    My name is Alexandra and I am Greek. I have a son, Apollonas who was born with his right foot clubbed

  • Victoria’s Clubfoot Story

    Hi, I’m Victoria and I’m almost sixteen years old. I’ve recently started looking for stories written by people like me. I

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THANK YOU!

~ Ruth, Evan's Mom





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