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To Band or Not to Band

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This is a post from myself to any parent considering Orthotic

Management Treatment:

We as parents do the " best " we can for our children. There is

nothing else we can do.

I hope the following analogy will help in your decision process.

We can decide not to put braces on our children's teeth. However, as

an adult the child can always decide to wear braces to correct

alignment of their teeth. That being said, A child is unable to get

treatment for plagiocephaly once they reach adulthood.

My family was not willing or able to gamble on the most likely

outcome of not treating our son. We have been in a helmet for 5

months and have received 80 percent correction. I seriously doubt

that we would have been able to say the same without the helmet.

We are just into our new parenting career. I can say without a doubt

that getting the helmet was the best decision, both for us and our

son.

See Ben S. in the photos.......

Is Orthotic Management Treatment for Plagiocephaly a cakewalk?

Absolutely not. However, I can say it gets easier everyday.....

In closing, Children are cruel. I doubt very much as a teen that a

child will be " made-fun of " because they wore a helmet for 4-5

months as a baby. The same, I am afraid, will not be true for

untreated plagiocephaly. This was one of my major concerns. This

concern is getting less and less because of my son's helmet.

These are my opinions only. I welcome yours.

Jeff, Sandy and Ben Sponagle

New Brunswick , Canada

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Jeff-

I agree banding Dane was the best decision we have made as parents.

My son's asymmetries didn't respond to respositioning as we hoped.

I would like to add that many parents do also get great progress

from aggressive repositioning. They just often don't hang around as

much as us banders!

Beck, one of our mods, successfully repo'd her daughter .

After banding her oldest, , she was aware of the need to

reposition from day one!

Hooray to all of us however we correct the problem!

BTW- Ben is a cutie :)

Dane's mom DOC Grad

> This is a post from myself to any parent considering Orthotic

> Management Treatment:

>

> We as parents do the " best " we can for our children. There is

> nothing else we can do.

>

> I hope the following analogy will help in your decision process.

>

> We can decide not to put braces on our children's teeth. However,

as

> an adult the child can always decide to wear braces to correct

> alignment of their teeth. That being said, A child is unable to

get

> treatment for plagiocephaly once they reach adulthood.

>

> My family was not willing or able to gamble on the most likely

> outcome of not treating our son. We have been in a helmet for 5

> months and have received 80 percent correction. I seriously doubt

> that we would have been able to say the same without the helmet.

>

> We are just into our new parenting career. I can say without a

doubt

> that getting the helmet was the best decision, both for us and our

> son.

>

> See Ben S. in the photos.......

>

> Is Orthotic Management Treatment for Plagiocephaly a cakewalk?

> Absolutely not. However, I can say it gets easier everyday.....

>

> In closing, Children are cruel. I doubt very much as a teen that a

> child will be " made-fun of " because they wore a helmet for 4-5

> months as a baby. The same, I am afraid, will not be true for

> untreated plagiocephaly. This was one of my major concerns. This

> concern is getting less and less because of my son's helmet.

>

> These are my opinions only. I welcome yours.

>

> Jeff, Sandy and Ben Sponagle

> New Brunswick , Canada

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Team,

I can say for sure that if we have another kid we'll know better next

time to repo from the start. Of course <g> this is true for most

things, such as how to deal with morning sickness, breastfeeding,

what to do about that darn eczema, etc., etc., etc.

Ok, maybe not so funny, depends on my mood.

We're still discussing banding daily, even though we're having our

daughter fitted on Thursday. I know we'll go through with it, but

it's a tough decision.

BTW: I love the analogy to having braces. Is crooked teeth something

to be embarrassed about? I hope not--I had braces for 5.5 years as a

teen, and it didn't dawn on me to be embarrassed. Maybe _this_ is the

ultimate point: a baby/toddler doesn't know enough to be embarrassed--

it's we as adults who bring our prejudices with us. I am ashamed in a

way that I am battling my own embarrassment, even knowing that I

shouldn't be. I'm proud, proud, proud to be a mom to a beautiful,

smart, outgoing little girl, and I'm not going to e.g., not take

photos (mother-in-law's dumb idea) or not explain to people what the

deal is just because I'M uncomfortable.

Any thoughts? Thanks for letting me sound off.

concord

> > This is a post from myself to any parent considering Orthotic

> > Management Treatment:

> >

> > We as parents do the " best " we can for our children. There is

> > nothing else we can do.

> >

> > I hope the following analogy will help in your decision process.

> >

> > We can decide not to put braces on our children's teeth. However,

> as

> > an adult the child can always decide to wear braces to correct

> > alignment of their teeth. That being said, A child is unable to

> get

> > treatment for plagiocephaly once they reach adulthood.

> >

> > My family was not willing or able to gamble on the most likely

> > outcome of not treating our son. We have been in a helmet for 5

> > months and have received 80 percent correction. I seriously doubt

> > that we would have been able to say the same without the helmet.

> >

> > We are just into our new parenting career. I can say without a

> doubt

> > that getting the helmet was the best decision, both for us and

our

> > son.

> >

> > See Ben S. in the photos.......

> >

> > Is Orthotic Management Treatment for Plagiocephaly a cakewalk?

> > Absolutely not. However, I can say it gets easier everyday.....

> >

> > In closing, Children are cruel. I doubt very much as a teen that

a

> > child will be " made-fun of " because they wore a helmet for 4-5

> > months as a baby. The same, I am afraid, will not be true for

> > untreated plagiocephaly. This was one of my major concerns. This

> > concern is getting less and less because of my son's helmet.

> >

> > These are my opinions only. I welcome yours.

> >

> > Jeff, Sandy and Ben Sponagle

> > New Brunswick , Canada

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I think banding is perfectly acceptable. Decorate the band so it stands for something important for your child and make it special. Look at the band as a means for you to help you child grow into the best they can be. You wouldn't feel bad about getting a tutor to help a struggling child in school, so don't feel bad about the band. Also, the band provides protection from the bumps and falls our little ones experience. Use it as a means to spread the word about plagio to new moms and the importance of repostioning. Turn it into your personal crusade if you want to. Banding is not purely cosmetic, you are preventing eye, ear, and jaw problems that could develop. The bands can be really cute and a work of art if you look at them that way. Maybe send in a picture to Cranial Tech for their calendar or send her pic to your webmates. We are all going through or have gone through similar experiences. My daughter is going to be casted on Thursday. My husband is still pretty reluctant though.

Jen

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I, too, have been struggling with the embarrassment. I also realized

it's my embarrassment and I still try to take pictures of them when

their helmets are off, but I'm sure I will still take them with them

on, too. You're right, it's us who feel embarrassed, the girls

continue to smile and play away, saying who cares to us! Being a mom

of twins, you are approached A LOT more in public and I have noticed

that people have backed off a little now that they have helmets.

That is both a good and bad thing. It seems I may just need to get

over it and know that my daughters will thank me in the end!

Kirsten & Jocelyn

6 months today!

> > > This is a post from myself to any parent considering Orthotic

> > > Management Treatment:

> > >

> > > We as parents do the " best " we can for our children. There is

> > > nothing else we can do.

> > >

> > > I hope the following analogy will help in your decision process.

> > >

> > > We can decide not to put braces on our children's teeth.

However,

> > as

> > > an adult the child can always decide to wear braces to correct

> > > alignment of their teeth. That being said, A child is unable to

> > get

> > > treatment for plagiocephaly once they reach adulthood.

> > >

> > > My family was not willing or able to gamble on the most likely

> > > outcome of not treating our son. We have been in a helmet for 5

> > > months and have received 80 percent correction. I seriously

doubt

> > > that we would have been able to say the same without the helmet.

> > >

> > > We are just into our new parenting career. I can say without a

> > doubt

> > > that getting the helmet was the best decision, both for us and

> our

> > > son.

> > >

> > > See Ben S. in the photos.......

> > >

> > > Is Orthotic Management Treatment for Plagiocephaly a cakewalk?

> > > Absolutely not. However, I can say it gets easier everyday.....

> > >

> > > In closing, Children are cruel. I doubt very much as a teen

that

> a

> > > child will be " made-fun of " because they wore a helmet for 4-5

> > > months as a baby. The same, I am afraid, will not be true for

> > > untreated plagiocephaly. This was one of my major concerns.

This

> > > concern is getting less and less because of my son's helmet.

> > >

> > > These are my opinions only. I welcome yours.

> > >

> > > Jeff, Sandy and Ben Sponagle

> > > New Brunswick , Canada

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It seems I may just need to get

> over it and know that my daughters will thank me in the end!

-

Yes! They will thank you for taking care of this!

And as my dad always says " Some day this will seem like a long time

ago. " The time in the bands goes so quickly!

Most people looked at Dane simply out of curiousity. He loved the

attention!

Dane's mom DOC Grad

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Guest guest

just keep in mind that people fear the unknown and do not want to offend. they have no idea why your children are wearing bands. for all they know, you could be having a bad day and your child has some terrible disease or something. everyone loves babies, and no one wants to get depresed or depress the mother by asking questions that might bring out some devastating story that your child might be dying or something. i know this didnt come out eloquently, but they dont know how insignificant it is (not to belittle it either, because to us, this whole process is a huge ordeal). people just dont talk openly because they are afraid of upseting you. i once, as a 9 year old, or so, asked a woman about her baby. i cant remember what was different about it, to me that baby was cute. but, she bit my head off. she got really defensive and started yelling at me. she was really sensitive about it, and i hav enever asked about that kind of stuff again.

jen

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  • 1 year later...
Guest guest

Hi ,

Can you post some pics of 's head? What were the measurements? Are his ears aligned? Can you see any assymetry in his face? Sometimes both twins are banded and sometimes only one baby needs the band. I know there was a set of triplets at the Charlotte office and only baby A needed the band. If his head looks the same when he is 13 will anyone really notice? My instinct would say if I wasn't happy with his head shape now I wouldn't be happy with it at 13.

My dd had moderate plagio (11 mm cranial vault and 9 mm ear). Everyone thought she was absolutly beautiful (including me) and saw nothing worng. However, everytime I looked at the top of her head I saw that it just wasn't right. It took my parents awhile to see what I was talking about, now they say I made the right decision. She is now within the normal population range (cranial vault 3 mm, ears 4 mm). Sometimes you have to go with your mommy instinct.

HTH

mom to na

DOC Gradroguem22 <MICHELLE@...> wrote:

Hi all,I haven't been online in awhile, but some of you may remember and I. He received a Starband on 05/11/04 and is doing great. My question is actually concerning his twin brother . Whereas had left tort and some assemetry with severe (more than +2) brachy, has nothing wrong except mild to mod left plagio on the top part of his head (the bottom popped out with repo). All three of my children have very wide heads (they get it from my husbands side of the family). The PT told me it was the wideness of 's head that made his measurements go into the moderate category, not the difference from the actual flatness. The PT said she would right a med necessity letter if i if i wanted to pursue it so the insurance co would pay , but she said she would not

have him banded if it was her child. She said with no assemetry there would be no adverse effects of not fixing it. Also because it isn't very noticeable that hair would cover it.They will be 9 mo on the fifth so i know i need to make a decision. Everyone is against getting one, and i know that his plagio is in no way as bad as 's brachy, but i still worry that he will grow up and think i did something for his brother and not him. He also suffers with exczema on his head and face so i worry if he would even be a canidate for a band. Has anyone banded one child and not the other. i know 's isn't that bad, but I am really wrestling with this.Thanks,, 05/11/04 Starband, 8 3/4 mo, brachy, left tortColumbus, GAFor more plagio info

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Hello

Can you post some pictures?

I hope that I do not step on your toes with my coment, but to me it

seems as if you are " already " feeling guilty about just thinking of

not banding. If you feel deep down that you should do this, then you

need to not listen to the ones saying that everything is ok, and that

it can be hidden behind hair. That comment used to set me off.

Maybe if you take to get measurements it might be easier.

Willow my daughter was mod plagio (12mm), and I never had a second

thought about doing this for her. I have never had regreat for

putting her into her band. She is not perfect, but now atleast she

can have a short haircut and not have to worry about being stared

down. I'm sorry I can't give you a different kind of answer, but you

need to do what you feel is right.

Good luck, and let us know how you decide.

Sandy Willow's Mom

Torticollis resolved

Cranio Germany Grad

--- In Plagiocephaly , " roguem22 " <MICHELLE@C...>

wrote:

> Hi all,

>

> I haven't been online in awhile, but some of you may remember

> and I. He received a Starband on 05/11/04 and is doing

> great. My question is actually concerning his twin brother

> . Whereas had left tort and some assemetry with

> severe (more than +2) brachy, has nothing wrong except

mild

> to mod left plagio on the top part of his head (the bottom popped

> out with repo). All three of my children have very wide heads

(they

> get it from my husbands side of the family). The PT told me it was

> the wideness of 's head that made his measurements go into

> the moderate category, not the difference from the actual flatness.

> The PT said she would right a med necessity letter if i if i wanted

> to pursue it so the insurance co would pay , but she said she would

> not have him banded if it was her child. She said with no

assemetry

> there would be no adverse effects of not fixing it. Also because it

> isn't very noticeable that hair would cover it.

>

> They will be 9 mo on the fifth so i know i need to make a

decision.

> Everyone is against getting one, and i know that his

plagio

> is in no way as bad as 's brachy, but i still worry that he

> will grow up and think i did something for his brother and not

him.

> He also suffers with exczema on his head and face so i worry if he

> would even be a canidate for a band. Has anyone banded one child

> and not the other. i know 's isn't that bad, but I am

> really wrestling with this.

>

> Thanks,

>

>

> , 05/11/04 Starband, 8 3/4 mo, brachy, left tort

> Columbus, GA

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