Re: New to group.... Need your input.

[Guest guest]

Hi ,

Yes, I am 100% satisfied w/Hannah's results. She still has a bit of

remaining asymmetry that was not correctible by any band (b/c of

inutero constraint), but the change is like night and day from where

we started! I'd make the same decision if I could go back and do it

again. Also, did you know there is a " no email " option for the

board? This won't clog your inbox with emails, but you'll have to

come to the group homepage to read and respond to messages. Most of

us do it this way b/c the volume of posts on this board is so much!

If you want to see Hannah's progress pics or read about our

insurance battle her website is below.

http://hannahsnoggin.typepad.com

> > I was told my son Brady had plagiocephaly that is causing

> > asymmetrical

> > placement of his ears. Our pedi sent us to Cranial Technologies

in

> > Dallas, Texas and wrote a letter of medical necessity and

> > prescription

> > to get the ball in motion with our insurance. I have since

learned

> > that my insurance is out of network for the DOC banding that

> Cranial

> > Technologies provides but I'm in network for the STARband. I

don't

> > know much about either process and was hoping to get some input

> from

> > mom's who have been where I am now. Any information you could

> > give me

> > would be helpful in this emotional time for me.

> >

> > I want to make the best choice for my son and I refuse to let

> > insurance dictate where we can and can't go. If I have to go out

> > of

> > networkI'm willing to do so!

> >

> > (I posted under another user name last night but that mail box

is

> > always so full it put me over my limit... sorry about that! I

set

> up

> > this new account just for this group.)

> >

> > Thanks,

> >

> > , Texas

>

>

>

>

> For more plagio info