Guest guest Posted September 27, 2009 Report Share Posted September 27, 2009 My name is Dawn. I have posted on here only a couple of times. This website has helped us a ton. I have learned so much about my daughters condition in this group. In addition, have received some great information in reguards to our options. To any new parents outwho have a recently diagnosed child of plagiocephaly. This is a great group to have in your corner. My daughter was diagnosed in March with plagiocephally. She wore her orthotic helmet for 4 months. She didnt mind it at all. Her result was awesome. I will never regret our decision to have her wear the helmet. I will not regret the work it took to get our insurance compay to pay for it. Dont give up on that one....its a pain, but it usually pays off. There is a lot of good information on appeal letters on here. I also used CAPPSKIDS.ORG to get a lot of good stuff. Thank you for having such a wonderful website to help us cope with our situation. I will continue to check in. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 27, 2009 Report Share Posted September 27, 2009 Congratulations!!!! Thanks for sharing your good news. Angie daughter graduated My name is Dawn. I have posted on here only a couple of times. This website has helped us a ton. I have learned so much about my daughters condition in this group. In addition, have received some great information in reguards to our options. To any new parents outwho have a recently diagnosed child of plagiocephaly. This is a great group to have in your corner. My daughter was diagnosed in March with plagiocephally. She wore her orthotic helmet for 4 months. She didnt mind it at all. Her result was awesome. I will never regret our decision to have her wear the helmet. I will not regret the work it took to get our insurance compay to pay for it. Dont give up on that one....its a pain, but it usually pays off. There is a lot of good information on appeal letters on here. I also used CAPPSKIDS.ORG to get a lot of good stuff. Thank you for having such a wonderful website to help us cope with our situation. I will continue to check in. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 28, 2009 Report Share Posted September 28, 2009 Congratulations Dawn. I'm glad you had good results. Enjoy your daughter's head. -christine sydney, 3.5 yrs, starband grad > > My name is Dawn. I have posted on here only a couple of times. This website has helped us a ton. I have learned so much about my daughters condition in this group. In addition, have received some great information in reguards to our options. To any new parents outwho have a recently diagnosed child of plagiocephaly. This is a great group to have in your corner. My daughter was diagnosed in March with plagiocephally. She wore her orthotic helmet for 4 months. She didnt mind it at all. Her result was awesome. I will never regret our decision to have her wear the helmet. I will not regret the work it took to get our insurance compay to pay for it. Dont give up on that one....its a pain, but it usually pays off. There is a lot of good information on appeal letters on here. I also used CAPPSKIDS.ORG to get a lot of good stuff. Thank you for having such a wonderful website to help us cope with our situation. I will continue to check in. > Quote Link to comment Share on other sites More sharing options...
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