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

  • Growing up with clubfoot *Kids point of view*

    Hey there! My name is Rayna and I was born with congenital clubfoot on both of my feet. I was born

  • double club feet

    I was born in 1955, in Berkeley hospital, Gloucestershire, UK. My mother was distraught at the thought of me having this

  • Nevaeh’s Clubfoot Story
    Nevaeh’s Clubfoot Story

    My daughter, Nevaeh, was born with bilateral clubfoot. When she was born, I didn’t even know what clubfoot was. She was

  • Born 1955 with club foot

    I was born with both feet pointing downward. My Mom told me that the doctor told her that I would be

SHARE-Story

 

facebook

Support this Website

If you would like to make a donation toward the costs of running this website, please click on the button below.

You will be taken to PayPal where you can make a secure donation. These funds will go directly to offset costs related to running this web site.

THANK YOU!

~ Ruth, Evan's Mom





css.php