Guest guest Posted January 28, 2005 Report Share Posted January 28, 2005 Hi New Members! I try to read the messages as much as possible and reply whenever it seems that no one has replied already... Lately, the replies have been so numerous and quicker than mine because I'm on digest version, so I just wanted to post the link to my daughter's website in order to share our story to those just starting out... My daughter is now 3 3/4 years old. She had a mild right clubfoot. We are now on our third doctor, Herzenberg in Baltimore. For more details, check out: www.geocities.com/joannewalton2003/clubfootstory.html We are having our first local support group tomorrow in Fairfax VA at Borders at 1 pm. I know Shook posted a reminder about this, but figured I would mention that as a result of posting a few signs, there are now several local babies whose parents did not find this list and have switched to Dr. Herzenberg after receiving substandard treatment by a local doctor just starting out with the Ponseti method... The irony is that he is giving out my name and number to his patients and doesn't remember who I am! I hope he doesn't catch on or decides to figure out what he's doing wrong (besides using AFOs). We have a lot to talk about tomorrow! I highly recommend starting a local group. My daughter is very excited to go show off her fixed foot tomorrow for the babies! I will be bringing some handouts as well... Best, Joanne W. mom to Zoe, 3-25-01, right clubfoot Quote Link to comment Share on other sites More sharing options...
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