Guest guest Posted October 3, 2004 Report Share Posted October 3, 2004 Thank you so much for your email. It actually made me tear up a little because it feels so nice to have so much support out there. I can't believe I found this website and I also can't believe there are enough of us out there to have a website. I do believe that Hannah will be mad and so upset when they do the casting. She doesn't even like someone holding her still to examine her. I know I will have a hard time but I have to support her and make her feel everything will be okay. I will post a message to everyone telling them how the casting went on Tuesday. Again, thank you for your kind words. I feel so fortunate to have made friends that are going through or who went through the same thing. Shari > > > Hi. My daughter is 5.5 months old and she was just diagnosed > with > > > plagiocephaly. She has torticolis too. We just had a catscan > > done > > > this morning which wasn't so great...she was fine but I was > > upset. > > > Next week she is getting fit for a helmet. I am having concerns > > > with the helmet and it does bother me but I know it will help > > her. > > > I would love some support, suggestions, feedback, success > stories, > > > etc...from anyone regarding treatments, PT and wearing the > > helmet. > > > I appreciate this. I have learned that support is important so > I > > > would love to hear from you. > > > > > > Thanks... Shari > > > > For more plagio info Quote Link to comment Share on other sites More sharing options...
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