Guest guest Posted October 24, 2010 Report Share Posted October 24, 2010 DOC Band is referring to a brand of cranial molding orthosis sold by Cranial Technologies. You can learn more at www.cranialtech.com. The two top competitors are Hanger Orthotics and Orthomerica (Star Scanner, StarBand, Clarren Helmet). They deal with other orthotics, whereas Cranial Tech only does banding for plagiocephaly/ brachycephaly. Cranial Tech also uses PT's instead of orthotists, and their helmets are about 2 ounces lighter but children outgrow them more quickly because of the smaller amount of padding. Orthomerica locations are basically orthotists who chose to invest in a StarScanner. Hanger is a chain of orthotists, some of who offer bands in addition to other orthotics. If you google them and read their websites, it will make a lot more sense. There are also other local orthotists that sell cranial remolding orthoses from what I hear. My son had moderate plagiocephaly and mild/moderate torticollis (short/damaged SCM muscle on one side of neck, sometimes trapezius too). He worked with a PT for his torticollis. Torticollis is present in about 80% of babies with plagiocephaly, FYI. Even very mild torticollis needs to be fully treated, or it can cause worsening facial asymmetry in babies/ children with plagiocephaly and reduce the possible amount of correction with the helmet/ band or repositioning in young babies. Torticollis can also cause uneven or delayed motor development because the baby is uncomfortable or can't look toward one side of body. Even with somewhat mild torticollis and being in PT, my son had uneven use of his R vs. L hand (development of skills with R delayed a month or sometimes much more compared to L) and noticeable and worsening facial asymmetry caused by tort even after his plagiocephaly was corrected. I would think OT could have helped with this, though we never tried it. I got him to use his right hand by placing a box of toys on his right side every time he played. Of course, this didn't help once he could reposition himself. PT stretches had limited success for his torticollis, though many parents find it works very well. We finally got him a TOT Collar (google it), and that seems to be what is finally correcting his tort after 8 months of treatment. It has also helped his facial asymmetry a little since correcting tort usually reverses some facial asymmetry. Challenges or issues that occur with plagiocephaly vary. As I explained above, there are the issues that come with torticollis, which usually occurs in conjunction with plagio. For more about torticollis, visit the torticollis group. For plagio specifically, the most common issue is deformation of the head and face. If you don't think this is an issue, just imagine going to high school with half of your face squished! Nobody wants that for their child. The other issues come along with shifting of the facial features. Vision can be affected if the eye is either partially covered from the eyelid being pushed down, or if pressure changes in the eye damage vision. Torticollis can also cause temporary vision problems because it trains the brain to think the child is seeing with his/her head positioned neutrally when it is actually tilted to the side. The ears are usually shifted as well, and I've heard that some children seem to have more frequent ear infections because of this. The jaw can also be affected. This is more common with severe plagiocephaly. The uneven position of the jaw can cause TMJ. Finally, I've heard from some parents that the flat head made it difficult for their baby to learn to roll over. My son had difficulty going in one direction but could roll the other way. I think that it was more of a problem with his uneven motor development from the torticollis in his case, but that's just my theory. I've also heard that some children get more headaches from plagio, and I've heard from parents of older children with resolved tort that they still get a stiff neck/ aching after the tort is treated. So, in my opinion, the main issues that an OT might be concerned with are related more to torticollis than plagio. I'd recommend reading up on the tort board. > > Hello everyone, > I am an occupational therapy (OT) student and have not investigated plagiocephaly in detail. I have been reading some posts and I was wondering, what does DOC mean?! Also, can anyone explain some major challenges/issues that may have occured with plageocephaly?! Have any of you ever worked with an OT before and if so did it help? > If anyone could give me some input I would greatly appreciate it! > Thank you, > Mel > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 24, 2010 Report Share Posted October 24, 2010 , Thanks for ALL the information you posted to Mel. I found it to be so helpful. My son has the Hanger helmet and I too didn't know about the other bands. My son's left eye seems to be slightly smaller (because it doesn't open as much) as his left eye. The tech @ Hanger said it is "Lazy Lid", and said we can take him to a pediatric eye doctor. Have you experienced this? As for the torticollis, the tech @ Hanger did mention that our son has (mild) limited range on his left side of his neck. She didn't recommend therapy though. Should it be done? My son is 6 1/2 months old and has been wearing the helmet for 6 weeks now. Last week we were told that his progress is well, and he will need the helmet for maybe another month. Thanks ! --- Tommy's Mommy Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 25, 2010 Report Share Posted October 25, 2010 Thank you . I will look into physical therapy for our son. I appreciate the information. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 26, 2010 Report Share Posted October 26, 2010 My daughter does meet with an occupational therapist once a week and then has a physical therapist check on her once a month, both of whom we receive services for through ECI (Early Childhood Intervention - If you are interested in torticollis or other infant/toddler occupational therapies, your local ECI may have some internships or volunteer programs). I met with both in the beginning and they explained that at this age (6 months when we started with them), physical and occupational therapy is fairly interchangeable. I especially like that these therapists both go to my daughters daycare and do the therapy there, saving me time off of work and they also help to instruct the daycare providers on how to help my daughter. We have noticed an improvement with the therapy. My daughter now fights the original stretches for torticollis with a screaming vengeance so we have had to craft more exciting ways of getting her to stretch and exercise the weaker muscles. Also those stretches just didn't seem to be making a difference anymore. I also do yoga and massage with my daughter, as well as help her to stretch out and balance on a small exercise ball (it's actually one of those big colorful balls that you can buy at Walmart for $2). My daughter's torticollis is fairly well controlled for now and we generally only see the associated head tilt and a regression of muscle use when she is going through a growth spurt. (I'm told this is not uncommon to see) We did see developmental delays between left and right sides as was mentioned above and they could be as far apart as a month or more. However, since starting the therapy that time delay has decreased to an average 2 weeks. Hope this helps... > > Hello everyone, > I am an occupational therapy (OT) student and have not investigated plagiocephaly in detail. I have been reading some posts and I was wondering, what does DOC mean?! Also, can anyone explain some major challenges/issues that may have occured with plageocephaly?! Have any of you ever worked with an OT before and if so did it help? > If anyone could give me some input I would greatly appreciate it! > Thank you, > Mel > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 4, 2010 Report Share Posted November 4, 2010 , Thank you so much for providing information! I very much appreciate you taking time out of your day to help me better understand how I can help as an OT. I do agree that an OT could have helped your little one use the right hand more - that may be something you might consider in the future as well if you feel that is an area of growth. Again, thank you so much! Mel > > > > Hello everyone, > > I am an occupational therapy (OT) student and have not investigated plagiocephaly in detail. I have been reading some posts and I was wondering, what does DOC mean?! Also, can anyone explain some major challenges/issues that may have occured with plageocephaly?! Have any of you ever worked with an OT before and if so did it help? > > If anyone could give me some input I would greatly appreciate it! > > Thank you, > > Mel > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 4, 2010 Report Share Posted November 4, 2010 Thank you very much for replying! I am glad to hear that OT (and PT) have helped your little one - it is also great that the services are provided at the daycare so that extra time does not need to be spent at another location!! The information you provided is very beneficial and I feel as though I have a better understanding of plagiocephaly. Take care, Mel > > > > Hello everyone, > > I am an occupational therapy (OT) student and have not investigated plagiocephaly in detail. I have been reading some posts and I was wondering, what does DOC mean?! Also, can anyone explain some major challenges/issues that may have occured with plageocephaly?! Have any of you ever worked with an OT before and if so did it help? > > If anyone could give me some input I would greatly appreciate it! > > Thank you, > > Mel > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 5, 2010 Report Share Posted November 5, 2010 Mel - Your are welcome. I am keeping an eye on the R/L discrepancy and, though he's improved, I don't think it's 100% resolved. I'm going to wait and see a little longer. I want to see what happens when his hand preference is developed. I think he's going to be right-handed, so I'm hoping that it will resolve itself as he feels the urge to use his right hand more. If he still seems to have trouble, I'll look into OT. Thanks! > > > > > > Hello everyone, > > > I am an occupational therapy (OT) student and have not investigated plagiocephaly in detail. I have been reading some posts and I was wondering, what does DOC mean?! Also, can anyone explain some major challenges/issues that may have occured with plageocephaly?! Have any of you ever worked with an OT before and if so did it help? > > > If anyone could give me some input I would greatly appreciate it! > > > Thank you, > > > Mel > > > > > > Quote Link to comment Share on other sites More sharing options...
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