Our journey with plagiocephaly has begun, Little Miss Lynnsey is now wearing a helmet. Here is our story (so far):
At her two month check-up I first mentioned it to our pediatrician. I was advised to put the “fun” toys on her right side to help encourage her to look more to the right, as she was favoring her left, and to give more tummy time. It was the hope that these techniques would help with the flatness. We had done both of these things, but still the flattened spot persisted. At her four month check-up I discussed with our pediatrician that the flat spot on the left side of the back of her head had gotten worse since her two month check-up. At this point we were referred to a cranio-facial specialist to decide what actions, if any, to take.
Prior to Lynnsey’s four month check-up, Joe and I were fairly certain Lynnsey would be getting a helmet. We had researched plagiocephaly and it appeared that Lynnsey had a very classic case. First, I found an extremely helpful blog post from a mom whose daughter had to wear a helmet. She gave so much helpful information and encouragement. And then we found several youtube videos posted by parents whose children also had to wear a helmet. We were not surprised that on November 4, 2010, that the cranio-facial specialist suggested that Lynnsey be fitted for a helmet to correct her plagiocephaly. I think it was good that we had done some research ahead of time because we were not at all surprised by the specialists diagnosis.
The reasons we chose to get Lynnsey a helmet are (1) there is no guarantee the plagiocephaly would be corrected on its own. Many cases fix themselves as the child grows, but Lynnsey’s seemed pretty severe and she favors her left side which lead us to believe it would be more difficult to be corrected without an orthotic (i.e. her helmet), (2) we did not want Lynnsey to grow up and one day ask us why we didn’t do something when we could have-this is assuming that it would not correct its self, (3) it is only a three month process. We figured, three months now is really no big deal compared to all the years she might have a noticeably flat spot if we did nothing, and (4) thankfully we have good insurance and almost all, if not all, of it is covered, so there was not a financial burden affecting our decision.
Here are some photos of the process we have gone through:
First, Lynnsey had to get her head scanned for the helmet to be made. She slept through the first scan, which was pretty funny and surprising, but then we had to get another scan because the helmet needs made within two weeks of the scan being done and our insurance was a little slow on giving authorization. The scanning process was simple- thankfully they no longer have to do a plaster mold!

Scan-take 2. She did SO WELL both times

Helmet day 11-30-10!

Before-left side is flatter than right side Pretty pink helmet!


She was a little dramatic for literally a minute, and then perfectly fine!
I will continue to post about our journey with plagiocephaly and show how way super cute Miss Lynnsey is in her helmet. She is AWESOME! Go girl!
I do hope this post and future posts about plagiocephaly help other families who are just beginning down the path of handling plagio.