Guest guest Posted April 18, 2008 Report Share Posted April 18, 2008 My daughter Sophia now 9 mos. also had this diag and was given the exercises by CT which she fought like crazy!!!! (They involve laying the kid down 5X a day - needless to say she won't even lay down to change her diaper without a fuss). After she was banded, we discontinued the habit of these after a hospital visit for RSV. When she graduated from her band, CT told me to keep the exercises up 5X a day until she was 18 mos. After reading some posts on the board, I got a second opinion from a pediatric physical therapist (which our ins covered) and am glad a did. She gave me exercises involving her sitting up and fun things using toys and bubbles to make sure she continues to keep the tort resolved (she favors her right and needs to turn to the left). I think CT is a good place to start but the second opinion is definitely worth it (the exercises are much more doable at this age). She also decreased the number of times a day we had to do these activities. I am going to bring her back when she hits each milestone - crawling and walking - she explained tort can reoccur at these times. Hope this helps! > > My son also had/has tort. I only have done exercises at home that were taught to me by the therapist at Cranial Tech. It has worked for the most part. While he prefers to look to one side and sleep on that side, he is definitely able and willing to move his head and sleep on the other side. Pictures have shown great changes in his neck strength also as he got older and we have done tummy time, sitting up, etc. I would recommend seeing someone at CT, the eval us free. The exercises are easy to do, although my little man did not always enjoy them. He is banded now and we still do them, along with talking to him so he has to look at us from different directions. It is correctable. > > > > torticollis > > hello there, > my son has just been diagnosed with congenital torticollis and > plagiocephaly he is 3 months old bless him! After trying to do some > research about it i cant seem to find a website that states that it > will correct itself back to normal after physiotherapy. > As im new on here are there any other members that are going through > the same thing that could offer me more info on torticollis and > possibly show me pictures of before treatment and after treatment. > I am (when i get time as i have 4 children) going to upload some pics > of kaen. > Thanks and hope to hear from any of you soon > > Lynn > > > > > > ______________________________________________________________________ ______________ > Be a better friend, newshound, and > know-it-all with Mobile. Try it now. http://mobile./;_ylt=Ahu06i62sR8HDtDypao8Wcj9tAcJ > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 19, 2008 Report Share Posted April 19, 2008 We only went to CT and I don't regret that. They are very knowledgeable and caring. I would go for an eval. and listen to what they have to say. Good luck. > > > > My son also had/has tort. I only have done exercises at home that > were taught to me by the therapist at Cranial Tech. It has worked for > the most part. While he prefers to look to one side and sleep on that > side, he is definitely able and willing to move his head and sleep on > the other side. Pictures have shown great changes in his neck > strength also as he got older and we have done tummy time, sitting > up, etc. I would recommend seeing someone at CT, the eval us free. > The exercises are easy to do, although my little man did not always > enjoy them. He is banded now and we still do them, along with talking > to him so he has to look at us from different directions. It is > correctable. > > > > > > > > torticollis > > > > hello there, > > my son has just been diagnosed with congenital torticollis and > > plagiocephaly he is 3 months old bless him! After trying to do some > > research about it i cant seem to find a website that states that it > > will correct itself back to normal after physiotherapy. > > As im new on here are there any other members that are going > through > > the same thing that could offer me more info on torticollis and > > possibly show me pictures of before treatment and after treatment. > > I am (when i get time as i have 4 children) going to upload some > pics > > of kaen. > > Thanks and hope to hear from any of you soon > > > > Lynn > > > > > > > > > > > > > _____________________________________________________________________ _ > ______________ > > Be a better friend, newshound, and > > know-it-all with Mobile. Try it now. > http://mobile./;_ylt=Ahu06i62sR8HDtDypao8Wcj9tAcJ > > > Quote Link to comment Share on other sites More sharing options...
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