Alrighty. So. Yes. Amos has a funky head. If he were a lady, I'd call him Miss Shapen. As it stands, he must be Mister Shapen.
We visited the second orthotist, a division of Hanger Orthotics, on Friday. She gave us a great deal of information about plagiocephaly and brachycephaly. She examined Amos' head, measured him, and declared him to be mildly to moderately plagiocephalic and brachycephalic. Meaning, he has a flat spot toward the right side of his head (plagiocephaly) but also a flattening of the back of the head (brachycephaly). We already knew that, but she had an even better diagnostic tool than just a measuring stick.
Hanger Orthotics uses a computerized scanner that digitalizes the head in 3D. Yup. We had the chance to see Amos' head on the computer and in person. She placed a stocking cap over his noggin, which made him look like the most adorable burglar ever. A receiver was placed inside the cap, and then she waved a wand all over his head in order to get the 3D image. It was pretty darn cool to watch.
Here is Amos' head.
As you can see, the red line indicates the middle of his forehead dissected through to the middle of the back of his head. For the most part, the left side of his head is forming well (that would be on the right side of the pic for you). The right side of his head, however, is troubling. That is where the original flatspot formed. It has shaped out better over the past few months of repositioning, but it isn't completely normal yet. The back of the head is flattenened and slopes to the right (the left side of the pic for you), but it is starting to round out. That is a very good sign.
Actually, the more I look at it, I think the red line should be moved over a few notches to indicate the true middle of his forehead, but it doesn't really matter. You can clearly see that Amos' head is misshapen.
So, measurements of Amos' head show that his width is almost the same as the length. Normal heads are longer than they are wide. It is possible that Amos' head will improve even more with continued repositional therapy. That means we keep him off of the back of his head. We encourage him to sit up as often as possible. When he sleeps at night or takes naps, we position him on his left or right side. For now, I will be concentrating mostly on positioning him on his right side in order to flatten out that bulge. I had been positioning him on his left quite a bit more, and it's clear from the scan that we've been successful in helping to round out that part of his skull.
It was agreed that we will continue to reposition Amos for another 5 weeks. We'll go back for another scan. They can superimpose the new scan over the old one to see how things have improved. If we're happy with the improvement, then all we may need to do is keep repositioning. If it's not clear that anything is changing, then we may consider a helmet.
I'm feeling good about this decision. It's sort of a happy medium between the two options. We've clearly seen that since Amos has learned to sit up, it is helping to reshape his head. I almost think it's helping faster than any of the repositioning I've done. Maybe. But, within a week of him sitting up, we saw the back of his head start to round out. That brings me much joy, people. Much joy.
He may still need a helmet. We'll see in 5 weeks. If he does, he'll probably wear it for 4 - 6 months. He'll need to keep it on for 23 hours a day. One hour off to bath him and to clean the helmet.
The downside for me, because the inner selfish lady is whining about it, is that this decision means at least 5 more weeks of losing sleep. Amos sleeps next to my side of the bed, and despite my efforts to wrap him up tight and to position him just so, he still manages to wriggle his way onto his back on occasion. I've gotten used to it, but gosh darn, I really miss sleeping.
Here is Amos' head just before he turned 6 months, and just before he started to sit up on a regular basis. You can kinda see that it is not as improved as the scan shows, which was taken a few weeks after he turned 6 months (and was a pro sitter).
Phil was trying to indicate where the middle of Amos' forehead was, but Amos keep flailing around.
So, that's the story. We'll keep on a keepin' on with our current methods. Then we'll see what we see.
Oh, and one of the more fun therapies we're using is to rub Amos' head with our hands. I will shape him into something great, like a bowling pin or an ashtray. Heheh.
Kim, if you are reading this, the second orthotist also said that neurosurgeons are notorious for being anti-helmet. I'd suggest that you do what we did: get a prescription for the helmet from your pediatrician or family doc that normally sees your little girl. Then, get a referral to an orthotist. We really like Hanger Helmets because of the scanning to get the head shape. The scan is used to create the helmet. Other helmets are created by taking a plaster cast of the baby's head, which can be a bit traumatic to the baby and the parents. The other helmets work just as well, but Hanger just has a friendlier approach to creating it.
For anyone dealing with plagiocephaly, there is a Yahoo group you can join.
I'll update as things progress. Send Amos' head some good vibes and thoughts!












18 beautiful people muttered something back:
Good news! I'm cautiously optimistic for you (as I tend to be) that the next visit shows even more improvement.
That's good news. I hope there continues to be a lot of improvement and that there won't be a need for a helmet in the end. My eldest son also had a misshapen head, but luckily it sorted itself out with me placing him properly when he slept, and by 1yo it was more or less perfect.
He's still so young, there's so much time. :-) I'm glad to hear that y'all have found a place that y'all feel confident with and good about. I really hope and pray that there will be good improvement and I love the image that you are literally shaping your son with your hands. So cute.
You are wonderfully positive and informative.
Good luck!
Someday, when little Amos gets to be a strapping 6 footer that all the girls just fall all over, I hope you'll be able to show him these posts. Because if he ever needs to be reminded just how much his parents love him, it's all right here.
Wow! That scan is incredible. I think that's the best thing as parents that you could have been shown. And when you return after 5 weeks, you will have a concrete comparison to mark his improvement.
Some parents might think "ah well, it will sort itself out" and be done with it. But not you two! You are taking an active role in helping to correct his condition.
Don't ever blame yourself for "caring too much." It's evident that your devotion to him is limitless. There can be no fault in that, no matter how easy it is to think so.
I have confidence that he will get better! And I'm very glad that you reached a decision that you're comfortable with. :-)
I'm glad you explained what I'm doing in the bath picture; otherwise, it kind of looks like I'm pushing my hand into his skull, which would be ridiculous since we want to be jamming our hands in from the sides for proper reshaping.
Glad he is improving. I do know some people who had helmets for their kids and said they were happy with the results, so even if it comes to that, well, it's not the end of the world. I hope the news continues to be good. :-)
Just in time lady! Thank ya, thank ya. We have an appt with the doctor today at 330 so then I will know what direction to go in. I appreciate your advice and will look up the hanger helmets.
Thank you for sharing this great technology with us. So glad Amos is becoming well-rounded. =) I hope the second scan shows significant improvement. Isn't hope a wonderful thing?
I glad that this doctor was better than the last one. Thanks for keeping us up to date.
Sending a wallop of good vibes baby's way.
I just know it's going to be fine.
Give him a hug and kiss from Frances in New York
Glad to see you finally got some better information and help.
I know how stressful it can be when something "isn't right" and you are faced with making decisions on a daily basis to try to figure it out/correct the problem. It can very nearly drive you crazy with anxiety over making the wrong choices.
Hand in there - Amos head still looks cuter than almost anything I've seen (have to put his second to another head I like.) ;-)
Love & Good Head Vibes!
That is good news!
I am just thinking, the repositioning can't be easy for you. Do you have to get up in the middle of the night to make sure he isn't laying (lying?) on the back of his head?
It seems somewhat funny, but we were all over the head rubbing technique! That stimulation gets the blood flowing! Our little one is adopted from Guatemala and when he came home, he wasn't on the U.S. growth charts at all. The doctor starting talking about microencephaly, but he rubbed his little head and he slowly making progress! At 13 months, he ranges in 15-50% in head circumference, weight and length.
Amos - wishing your head some good vibes!
ahhh cursed doctors! I was in the computer for the 15th but my appt. card said the 8th. So went to the doctors for NOTHING! I'm requesting a new referral from my ped. to go see an orthapedic doctor instead.
Suzanne - Thank ya! I'm still thinking he'll need a helmet, but I'm holding out hope that his head will cooperate.
Jenty - That's really good to know! Thanks for telling me about that. If you stop by again, can you tell me... was your son's head similar to Amos' scan picture?
Rachel - Thank ya! Yeah. It's like we're modeling clay every day, except it's his head. Haha.
LceeL - Aw, man! You are too kind. We'll see if Amos is strapping and/or 6 feet. His parents are not of ample stature, but there are lanky relatives.
Amanda - You are the best, lady.
You're right about the scan. It will help us with insurance issues. Also, I'm a visual learner, so it really helped me to see exactly what is good and what needs improvement. Technology. Ain't it grand?
Phil "shape of... an elephant!" - Yeah. The explanation was necessary so that people don't think you always taunt Amos with your large digits.
Good news! I hope he continues to improve without a helmet. I've heard a few of these cases lately where the child's head improved on it's own.
Either way, he still a cutie pie.
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