Guest guest Posted May 6, 2002 Report Share Posted May 6, 2002 Bonnie - You are so lucky to have a ped who is on top of this! So many are unaware of what is going on! You shouldn't need any help after they get their bands. My son doesn't even know that it is on. It has saved him from many bumps and bruises! Good luck with the casting! Dane's mom (DOC Band 2/14) --- In Plagiocephaly@y..., " frimadesignsinc " <frimadesignsinc@a...> wrote: > I joined your wonderful group yesterday. What a wealth of > information from start to finish. I'd like to introduce myself to > the group. My name is Bonnie and I live in Monroe, Georgia, about 45 > minutes east of Atlanta. We will be going to the Atlanta CT, once > the insurance issues are resolved or before hand. I'm married and > have three children. My little girl, Lilly is 2.5 years old. My > twin boys are 7 months, and Winn. The boys have been > diagnosed with Plagiocephaly. I honestly never even heard of it > until they were diagnosed. Thanks to your support group, I know I am > not alone in this. The boys had their x-rays about 1 month ago and > we have seen the neurologist who recommended the DOC Band from CT. > Thanks for the casting description information, I now can explain it > to the grandparents. I've planned fun time for Lilly while we go to > CT. They said to plan on 2.5 hours on the first and second visit and > then we will go once a week for 4 months. I'm just wondering, do you > think I'll need help after we get the helmets? My mom, who lives in > NJ, said she would come down. I'm obviously a little bit nervous. > Again, nice to meet you all. > Bonnie Quote Link to comment Share on other sites More sharing options...
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