Jump to content
RemedySpot.com

Re: What can we expect...

Rate this topic


Guest guest

Recommended Posts

Are you in the USA? My answer is assuming you are...

It's hard to say how much correction you can expect. It depends on how well the

torticollis is treated, how compliant you are with band use, how much your

baby's head grows during the treatment period, etc. My son was banded at 9

months, and the neurosurgeon predicted 80% improvement for him if we could get

his torticollis resolved. He ended up going from 12 mm to 4 mm asymmetry, but we

were not able to fully resolve his torticollis, so that limited his results.

FYI, 4mm is the top of the normal range.

Your goal at the neurosurgeon's office is 1. to make sure the neurosurgeon

doesn't suspect anything besides plagiocephaly is causing the misshapen head, 2.

to get a prescription for an orthotic helmet, and 3. to find out where in your

area you can get the helmet. Some neurosurgeons don't like helmets, so if you

get a neurosurgeon who doesn't want to give you a prescription, you can instead

go directly to a helmet maker to have measurements taken, then try to get a

prescription from your pediatrician when the measurements come out in the

treatable range. The three largest helmet makers in the USA are Cranial

Technologies, Orthomerica (StarScanner/StarBand), and Hanger. Google them to

find locations near you and call for details and to find out if they will do a

consult without a prescription. FYI, Cranial Tech locations all do a free

consult without a prescription. Good luck at your appointment!

>

> Hello! I'm new to this group, just found it today.

>

> My son was born with torticollis which was diagnosed at his 2 month check up

along with his plagiocephaly. We've been working since he was 3 months with

various physical therapists to improve his torticollis enough so he could

eventually be fitted with a corrective helmet.

>

> His therapist finally gave the go ahead to see a neurosurgeon for the

corrective helmet and we go next week for our first appointment.

>

> I don't know anyone with experience with either torticollis or plagiocephaly,

and the physical therapist currently assigned to us though good at her job is

lacking bedside manner, hasn't been the best person to ask about what to expect.

>

> Can anyone share what we might expect and questions to ask? My son is now 8

1/2 months and all the therapist has been able to advise is that he'll for

certain get a corrective device and because of his age she's not too sure about

how much improvement to expect.

>

> Thanks!-

>

Link to comment
Share on other sites

As the other poster noted, it would be good to know where you're located. As for

correction, banding before 1 year is usually a good. Earlier is better, but you

are not really late. Make sure the person you're working with has good

experience with banding and has a positive perspective about the results you can

expect. The most popular band types are probably starband (orthomerica.com) and

docband (cranialtech.com). Cranial tech locations are generally good, since they

do only banding. Starband locations vary quite a bit depending how much

experience the ortho has with banding. We had a very good starband provider in

the SF Bay Area a few years ago.

The amount of correction is hard to say, but starting at this point you should

definitely see good progress. I always recommend taking your own photos every

week or two with approximately the same angle that shows the plagio well. This

will help you monitor the progress on your own. It is hard to see the changes

when you see your baby daily, so the photos help confirm you're moving in the

right direction.

-christine

sydney, almost 5 yrs, starband grad

>

> Hello! I'm new to this group, just found it today.

>

> My son was born with torticollis which was diagnosed at his 2 month check up

along with his plagiocephaly. We've been working since he was 3 months with

various physical therapists to improve his torticollis enough so he could

eventually be fitted with a corrective helmet.

>

> His therapist finally gave the go ahead to see a neurosurgeon for the

corrective helmet and we go next week for our first appointment.

>

> I don't know anyone with experience with either torticollis or plagiocephaly,

and the physical therapist currently assigned to us though good at her job is

lacking bedside manner, hasn't been the best person to ask about what to expect.

>

> Can anyone share what we might expect and questions to ask? My son is now 8

1/2 months and all the therapist has been able to advise is that he'll for

certain get a corrective device and because of his age she's not too sure about

how much improvement to expect.

>

> Thanks!-

>

Link to comment
Share on other sites

Join the conversation

You are posting as a guest. If you have an account, sign in now to post with your account.
Note: Your post will require moderator approval before it will be visible.

Guest
Reply to this topic...

×   Pasted as rich text.   Paste as plain text instead

  Only 75 emoji are allowed.

×   Your link has been automatically embedded.   Display as a link instead

×   Your previous content has been restored.   Clear editor

×   You cannot paste images directly. Upload or insert images from URL.

Loading...
×
×
  • Create New...