J.,
My son wore one of the craniocaps. He's 10 months now. He had a pretty sever flat spot on the right side of his head - called- "plagiocephaly"- and it's pretty much gone now. There is a little more to do, he outgrew his helmet and his therepist said we could go up a size, but she was happy with the result we got from the first helmet and that his head would continue to move until he was about 3, so what was left most likely will fix it's self.
I would suggest going to the specialist, just to see their evaluation and get all the information you can to make your decision.
It's just an evaluation and it might make you feel better that you just looked at options.Even if you decide not to have the cap. The specialist will tell you if it's a severe flat spot or a mild one. He'll give his suggestion, but if he/she's a good doctor, he'll leave the decision up to you. Most insurances will cover the helmet if the doctor sees a need for one. You can call your insurance ahead of time to get information on their coverage.
Here's a link to our family webpage...you can click on the pictures at the bottom and it will bring up the picture larger...the one with the cap is my son and this was midway through his cap....he really didn't mind it.
If it doesn't come through clickable, just copy paste in your broser.
http://stenzeltree.com/filmstrip.asp?picts=2006/cousins/0...
In our case, our son's spot was severly flat and we decided to get the helmet. It was the right decision for us, but you'll have to decide for yourself. My son started at 6 months. Their heads are really plyable at their young age. We noticed a change with in the first couple of weeks. He had a sever flattening of the side and he only had to wear it for 2 months. I was worried people would stare at him, but mostly no one said anything. Many people actually thought it was cute. Other kids really thought the helmet was cool when they saw it. Occasionally someone asked what happened and I just told them.."We're just rounding him out". We decided to use the cap, because of the level of severity the doctor thought it was. From the front you almost couldn't tell the flat spot, but from the side and back it was very obvious. Also, because of the severity, one side of his head was pushing forward. We ultimately decided to go with it, because from what we were hearing, it might have fixed itself, but not all the way and our son has such a good disposition. We were afraid if it didn't fix itself all the way, he'd be treated differently and it might affect him in some way.
There's a short period where you get your child used to wearing the helmet. Then you try a nap in it. Then you try sleeping all night....I can't remember, but I think it's about a week or week and a half starter time. Then you have them wear it for about 23 hours a day, with a half hour off every 4 - 5 hours.
It's kind of neat. When we finished, we got to keep the helmet and they offered to let us have the original mold they used to make the helmet, which we took. We have it now in a box to show Vincent when he's older. It's really neat to see how it was and how it is all at once.
The doctor we saw was Dr. Wood at Gilletts Children's Hospital. He was pretty straight forward with us. He said a lot of the flat spots he sees aren't too bad, but our son's was very sever. He said we could opt out of the helmet, but he wasn't sure if it woud pop out on it's own. He left my husband and I to talk and let us tell him when we were ready for him to come back and give him our decision.