Guest guest Posted January 9, 2010 Report Share Posted January 9, 2010 my sons plagio started out at 12mm at 4 mos, I didn't even know what was going on with him until I asked his Ped , thats when I realized it was "worse" than I thought. so I can see how others would not notice...but I did and it bothered me alot , and it worried me what he would think if he knew I could have fixed it and didnot, so after only 6 weeks in the band he is in the normal range and we are just going to wear a little longer to try and get more inprovement. I am so gald that we did do it . Its very frustrating when one Dr tells you its nothing and another one reccomeneds treatment, thats often the way in the medical world, just a matter of opinions. From: john_and_lincoln <johnrd007@...>Subject: Re: Upset and undecidedPlagiocephaly Date: Thursday, January 7, 2010, 4:56 PM Thanks for all of the replies. >> My wife had been repeatedly asking our doctor about our son's flat spot on his head, including making a special appointment at 3 months, and we were told not to worry that it would get better as he began to sit more. Well, my wife went in at 8 months and saw a younger new doc who sent us to Physical Theraphy. PT then sent us to Cranial Tech. We were told that he has plagiocephaly with a 12mm difference. They suggested that we get the band. We talked to our regular pediatrician who told us that he wouldn't get the band if it was his kid. Nobody seems to notice the difference, except my wife and I, and even then it doesn't seem that bad. I'm totally confused and upset> Quote Link to comment Share on other sites More sharing options...
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