While waiting for band #3 and his glasses I thought I would tell you about the Yahoo Plagio Support group. This is a great group of parents all dealing with the ups and downs of plagiocephaly and it's treatment. I joined the group in January 2005 and have since been made a moderator. This is the place to not feel so alone with this issue. There are almost 5000 members ( of course not all active) to help with your questions, listen to your frustrations, help with insurance, and share your progress stories, no matter what type of treatment you are using or thinking about using. We have parents using all brands of bands/helmets, parents doing repo, and parents of graduates who have been through it all and are now there to give advice and comfort. We have a photo section of our beautiful babies to look at, and lots of research articles and help links. You can make contact with other parents in your area or parents using the same facilities. I don't know what I would have done without the wonderful moderators and the members who so warmly opened thier arms to me when I thought I was just going to fall apart. You will find that through your experience ( however great or little it is so far ) you will be able to help others too. I must say Thank You to everyone who have been by my side through this long journey of ours.
Does anyone have any luck with insurance reimburstment for plagiocephaly, we are in the beginning stages with our daughter. I would like to get enough information before filing a claim with BC/BS.
Thank You
Posted by: Read Klos | March 20, 2007 at 04:39 PM