Guest guest Posted July 7, 2006 Report Posted July 7, 2006 IT's nothing big time but I have been working on adding my own page to my husband's website, (click Shaw's Page) emphasizing the Ponseti Method with information and photos of my " clubfooted " kids living a normal active life despite their so-called birth defects. It might be another source to send reluctant parents to - so they can visualize that it actually will be OK in the end if they use Ponseti treatments. I realize the surgical site members will probably poo-poo this, but I hope open minds will abound in the spirit of SUPPORT (notice I remembered to use all caps!) The whole site is still under construction so it's still a little rough but you're welcome to look around http://wildliferevivaltaxidermy.com Have a good day ee Mother of 3 Clubfooted Sons: - Bilateral Club Feet April 1998 Everett - Bilateral Club Feet September 2003 Garrison - Bilateral Club Feet March 2006 Visit us on the Web! www.WildlifeRevivalTaxidermy.com Quote
Recommended Posts
Join the conversation
You are posting as a guest. If you have an account, sign in now to post with your account.
Note: Your post will require moderator approval before it will be visible.