Please keep in mind that I have no medical training. The information on this site has been gleaned from various sources.
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.
If you would like to make a $1 or $5 (or any other amount) 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. THIS BUTTON IS FOR DONATING TO THE UPKEEP OF THIS SITE NOT TOWARD SPONSORING A CHILD'S TREATMENT. $48.00 was donated last year (2008). $45.00 has been donated in 2009. Thank You!
