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My son is 11 1/2 months old, and he has positional plagiocephaly. It

has gotten progressively better since we first realized he had it at

about 6 weeks old. However, it is not completely better. His head is

almost perfectly round, but when you look directly down, his ears are

still a tad off. I look at some of the pics on plagio Web sites, and

his is not near what these children's heads are. However, we're still

concerned, and I'm wondering if anyone has had luck getting insurance

to pay for this. If it were obvious, of course, I wouldn't even

question whether to do it or not. But it's not obvious, and it has

improved so much that I wonder whether it really will even out on its

own.

Oh, and the mom asking if she was too late: My neurologist said that

while it is definitely easier to fix early on, he has seen children

as old as 5 years old have success with corrective therapy. He didn't

even bat an eye at waiting until my son was a year old to determine

whether or not to even consider intervention. And I have even seen

improvement within the past three months, or from 9 months of age

until almost a year old.

Anyway, I'm wondering if I'm going to have more trouble getting

insurance to help out since his IS NOT noticeable, thus may be

considered more of a cosmetic thing. Opinions, please!

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We have an insurance database where you can see if your insurance is

listed and what was paid. Usually they do go by measurements to

determine coverage but every policy is different. As to what your

Dr said, I don't know what treatment is available to a child over 2

for plagio besides very invasive skull surgery. As a rule, the

younger the child obtaining band/helmet treatment, the better the

outcome.

Natasha

Atlanta, GA

> My son is 11 1/2 months old, and he has positional plagiocephaly.

It

> has gotten progressively better since we first realized he had it

at

> about 6 weeks old. However, it is not completely better. His head

is

> almost perfectly round, but when you look directly down, his ears

are

> still a tad off. I look at some of the pics on plagio Web sites,

and

> his is not near what these children's heads are. However, we're

still

> concerned, and I'm wondering if anyone has had luck getting

insurance

> to pay for this. If it were obvious, of course, I wouldn't even

> question whether to do it or not. But it's not obvious, and it has

> improved so much that I wonder whether it really will even out on

its

> own.

> Oh, and the mom asking if she was too late: My neurologist said

that

> while it is definitely easier to fix early on, he has seen

children

> as old as 5 years old have success with corrective therapy. He

didn't

> even bat an eye at waiting until my son was a year old to

determine

> whether or not to even consider intervention. And I have even seen

> improvement within the past three months, or from 9 months of age

> until almost a year old.

> Anyway, I'm wondering if I'm going to have more trouble getting

> insurance to help out since his IS NOT noticeable, thus may be

> considered more of a cosmetic thing. Opinions, please!

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Hi,

Have you had your son evaluated by an orthotist facility to see if

they feel he would see significant correction from a helmet or

band? We do have some severity assessment forms here at the group

that could help in evaluating your son; they are in the

links/severity assessment of plagio folder. Insurance coverage

varies from member to member; even if some get a denial, many

proceed with the band and pay for it on their own while pursuing the

appeals process. If you'd like a snapshot of insurance

reimbursement, you can check out the Database section of the group

for " Who's Insurance Paid What. " You may even find that someone in

the group had your exact insurance. It's true some insurance cos

have minimum asymmetry measurements required for coverage. Do you

know what your son's measurements are? A consult with an ortho

might help you get these measurements. There are some links to

different insurance policies in the links/insurance/insurance

policies folder if you'd like to take a look at them. In addition,

some have maximum ages for coverage based on the insurance

companies' opinion of how old is too old to get correction. Cranial

Orthoses are coded " S1040 " usually Durable Medical Equipment, if you

want to call your insurance and check on coverage.

My thoughts on some of your post includes concern at your neuro's

comment that he/she has seen success with corrective therapy up

until 5 years of age... what is he/she referring to? Almost all

helmets and bands are only FDA approved for treatment up to 18

months, and sometimes the DOCband can be used up until 24 months.

After 2 years of age, only cranial vault surgery can be used. Other

than that, you're really just hoping for natural rounding (there is

no guarantee of this) or perhaps trying an alternative therapy such

as craniosacral. Waiting until your son was a year is very late on

the neuro's part to assess the banding option, but there is still

time to band if you choose to explore this option. The American

Academy of Pediatrics July 2003 release on Plagiocephaly clearly

states that helmets/bands have the best response when used between 4

and 12 months of age.

Have you been aggressively repositioning your son all this time? I

was able to treat my daughter Remy's plagio/brachy with just repo

only - we didn't band or helmet. We did set a deadline for trying

repo, though, at 8 months of age. We wanted to make a decision on

the banding option in a timely enough manner to be able to get good

correction from a band while she was still young enough. We saw a

dramatic improvement from 5 - 7 months, some rounding from 7 - 9

months, and a teeny bit of improvement from 9 - 11 months. Remy's

progress pics are in the photos/before and after/repositioned/Remy

folder if you are interested. It sounds as if you also have been

seeing good improvement over time as well, but still have some

doubts about his ears, etc. If I were you, owing to your son's

advanced age, I would base my treatment decision on how his head

looks right now, not how I think it might look in a few more

months.

Ultimately it's going to be your decision, but maybe it would help

to get info about insurance coverage, severity assessment, and a

consult with an orthotist to help with your decision. Where are you

located?

Christie (Mom to Repo'd Remy)

-- In Plagiocephaly , " erin1mama2003 "

<erin1mama2003@y...> wrote:

> My son is 11 1/2 months old, and he has positional plagiocephaly.

It

> has gotten progressively better since we first realized he had it

at

> about 6 weeks old. However, it is not completely better. His head

is

> almost perfectly round, but when you look directly down, his ears

are

> still a tad off. I look at some of the pics on plagio Web sites,

and

> his is not near what these children's heads are. However, we're

still

> concerned, and I'm wondering if anyone has had luck getting

insurance

> to pay for this. If it were obvious, of course, I wouldn't even

> question whether to do it or not. But it's not obvious, and it has

> improved so much that I wonder whether it really will even out on

its

> own.

> Oh, and the mom asking if she was too late: My neurologist said

that

> while it is definitely easier to fix early on, he has seen

children

> as old as 5 years old have success with corrective therapy. He

didn't

> even bat an eye at waiting until my son was a year old to

determine

> whether or not to even consider intervention. And I have even seen

> improvement within the past three months, or from 9 months of age

> until almost a year old.

> Anyway, I'm wondering if I'm going to have more trouble getting

> insurance to help out since his IS NOT noticeable, thus may be

> considered more of a cosmetic thing. Opinions, please!

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You've received some great advice. I too would call my insurance

company ASAP and find out what their measurement criteria is. Also,

the age limit, if any. My old insurance was only good for children

ages 4-12 months. My new insurance for ages 4-8 months (which seems

ridiculous). However, keep in mind that even if you've passed their

age limit you may be able to appeal it.

If you are concerned that repo won't give you the results you want,

then I would proceed with an evaluation before he gets any older.

Good Luck,

Dianna

Mom to

DOC Band 9/13

plagio/brachy

> > My son is 11 1/2 months old, and he has positional

plagiocephaly.

> It

> > has gotten progressively better since we first realized he had

it

> at

> > about 6 weeks old. However, it is not completely better. His

head

> is

> > almost perfectly round, but when you look directly down, his

ears

> are

> > still a tad off. I look at some of the pics on plagio Web sites,

> and

> > his is not near what these children's heads are. However, we're

> still

> > concerned, and I'm wondering if anyone has had luck getting

> insurance

> > to pay for this. If it were obvious, of course, I wouldn't even

> > question whether to do it or not. But it's not obvious, and it

has

> > improved so much that I wonder whether it really will even out

on

> its

> > own.

> > Oh, and the mom asking if she was too late: My neurologist said

> that

> > while it is definitely easier to fix early on, he has seen

> children

> > as old as 5 years old have success with corrective therapy. He

> didn't

> > even bat an eye at waiting until my son was a year old to

> determine

> > whether or not to even consider intervention. And I have even

seen

> > improvement within the past three months, or from 9 months of

age

> > until almost a year old.

> > Anyway, I'm wondering if I'm going to have more trouble getting

> > insurance to help out since his IS NOT noticeable, thus may be

> > considered more of a cosmetic thing. Opinions, please!

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> > > My son is 11 1/2 months old, and he has positional

> plagiocephaly.

> > It

> > > has gotten progressively better since we first realized he had

> it

> > at

> > > about 6 weeks old. However, it is not completely better. His

> head

> > is

> > > almost perfectly round, but when you look directly down, his

> ears

> > are

> > > still a tad off. I look at some of the pics on plagio Web

sites,

> > and

> > > his is not near what these children's heads are. However, we're

> > still

> > > concerned, and I'm wondering if anyone has had luck getting

> > insurance

> > > to pay for this. If it were obvious, of course, I wouldn't even

> > > question whether to do it or not. But it's not obvious, and it

> has

> > > improved so much that I wonder whether it really will even out

> on

> > its

> > > own.

> > > Oh, and the mom asking if she was too late: My neurologist said

> > that

> > > while it is definitely easier to fix early on, he has seen

> > children

> > > as old as 5 years old have success with corrective therapy. He

> > didn't

> > > even bat an eye at waiting until my son was a year old to

> > determine

> > > whether or not to even consider intervention. And I have even

> seen

> > > improvement within the past three months, or from 9 months of

> age

> > > until almost a year old.

> > > Anyway, I'm wondering if I'm going to have more trouble getting

> > > insurance to help out since his IS NOT noticeable, thus may be

> > > considered more of a cosmetic thing. Opinions, please!

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