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Re: Started the process

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That is great news! We've gotten a fair amount of improvement since 15

months. It has been very slow, but it adds up. We've kept in the

helmet over 6 months. Many people will tell you the Starband is not

effective after 6 months. In our case, we found this not to be true.

Also, you may hear people tell you that there won't be much improvement

past certain ages. We found that even past 22 months, if you are

patient, there is still change. You many also want to research

alternative treatments such as osteopathy, CST and chiro.

Good luck,

Kathy, mom to , 22.5 months

Karin wrote:

So despite being denied by insurance we have gone ahead a started

the process of getting a StarBand. It feels good to have a decision

made and moving forward with that decision. Levi was measured and my

little squirmy worm stayed still and we got the scan in only two takes!

I am uploading a picture of out little Levi in his little stocking he

had to wear for the scan in the "L" folder.

Our new Pediatrician is writing an appeal letter to our insurance, we

didn't even have to ask her to do it, yay, I love our new ped. I will

be writing an appeal as well. EI (early intervention) may cover it,

although I am not getting my hopes yet. It feels great that there are

so many people going to bat for us now, I just wish we could have had

all this action 9 months ago.

He'll be fitted on May 4.

Karin

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Thanks for the encouragement. What is CST?

Karin

> >

> >

> > So despite being denied by insurance we have gone ahead a started the

> > process of getting a StarBand. It feels good to have a decision made

> > and moving forward with that decision. Levi was measured and my little

> > squirmy worm stayed still and we got the scan in only two takes!

> > I am uploading a picture of out little Levi in his little stocking he

> > had to wear for the scan in the " L " folder.

> >

> > Our new Pediatrician is writing an appeal letter to our insurance, we

> > didn't even have to ask her to do it, yay, I love our new ped. I will

> > be writing an appeal as well. EI (early intervention) may cover it,

> > although I am not getting my hopes yet. It feels great that there are

> > so many people going to bat for us now, I just wish we could have had

> > all this action 9 months ago.

> >

> > He'll be fitted on May 4.

> >

> > Karin

> >

> >

>

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CST is cranial sacral therapy. (I think!!) Sent from my BlackBerry® smartphone with SprintSpeedFrom: "Karin" <k.marlett.c@...>Date: Fri, 23 Apr 2010 22:56:56 -0000<Plagiocephaly >Subject: Re: Started the process Thanks for the encouragement. What is CST?Karin> > > >> > So despite being denied by insurance we have gone ahead a started the > > process of getting a StarBand. It feels good to have a decision made > > and moving forward with that decision. Levi was measured and my little > > squirmy worm stayed still and we got the scan in only two takes!> > I am uploading a picture of out little Levi in his little stocking he > > had to wear for the scan in the " L " folder.> >> > Our new Pediatrician is writing an appeal letter to our insurance, we > > didn't even have to ask her to do it, yay, I love our new ped. I will > > be writing an appeal as well. EI (early intervention) may cover it, > > although I am not getting my hopes yet. It feels great that there are > > so many people going to bat for us now, I just wish we could have had > > all this action 9 months ago.> >> > He'll be fitted on May 4.> >> > Karin> >> >>

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Yes, CST is cranial sacral therapy.  A cranial osteopath with

experience in pediatrics may be a good place to start.  In addition,

has been seeing a chiropractor who does cranial adjustments and a

little CST almost weekly for months.  The alternative treatments have

helped 's head shape.  Recently, started PT since it turns out

he has some mild posture/muscle imbalances that probably contributed to

the plagio.

My 5.5 year son , who also has a little plagio, just started

regular CST therapy.  's chiro was too long of a drive for him and

the osteopath is difficult to schedule appointments with.  So, I found

a  recommended very local cranial sacral therapist.  So far

enjoys the CST treatments,.  It is too early to tell whether it helps

his head shape, but he has been more calm.

-Kathy, mom to 22.5 months and 5.5 years, both now with

very mild plagio

carrie_fl4@... wrote:

 

CST is cranial sacral therapy. (I think!!)

Sent from my BlackBerry® smartphone with SprintSpeed

From: "Karin" <k.marlett.cgmail>

Date: Fri, 23 Apr 2010 22:56:56 -0000

<Plagiocephaly >

Subject: Re: Started the process

 

Thanks for the encouragement. What is CST?

Karin

> >

> >

> > So despite being denied by insurance we have gone ahead a

started the

> > process of getting a StarBand. It feels good to have a

decision made

> > and moving forward with that decision. Levi was measured and

my little

> > squirmy worm stayed still and we got the scan in only two

takes!

> > I am uploading a picture of out little Levi in his little

stocking he

> > had to wear for the scan in the "L" folder.

> >

> > Our new Pediatrician is writing an appeal letter to our

insurance, we

> > didn't even have to ask her to do it, yay, I love our new

ped. I will

> > be writing an appeal as well. EI (early intervention) may

cover it,

> > although I am not getting my hopes yet. It feels great that

there are

> > so many people going to bat for us now, I just wish we could

have had

> > all this action 9 months ago.

> >

> > He'll be fitted on May 4.

> >

> > Karin

> >

> >

>

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