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Re: Treating Toddlers

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Hi tte - my daughter wasn't a toddler, but I wanted to answer

some of your other questions:

1. What age did you treat your child and how successful was it?

she was 6 months - 14.5 months old, 90ish% succussful

2. Was it uncomfortable for your child?

she was ignorant of it on, but I suspect that each

child's disposition determines if it bothers them.

Most parents report that the kid never knew it was on.

3. How long was the treatment?

1st helmet=3.5 months, 2nd helmet=5 months

4.Have you noticed any delays with your child in developement?

her delay in crawling/rolling was due to her torticollis

(tight neck muscle). Once we were done with PT for

that, she hasn't had any other delays.

We saw an opthomologist yesterday to see if her residual

head tilt is due to an eye problem. (NO!!) But he did

see facial asymetry on the outside of her face still.

My boss sees a bigger cheek on one side too, we don't

really see any of it as we are used to her looks.

The good news is that the eye structure/orbit don't have

any asymetry inside her head and her vision wasn't

affected by the bulging forehead. That was a worry

to us as a side effect from her plagio.

5.Was it uncomfortable dealing with the " looks " from other

people?

I was in tears as we started the helmet - " No one will

come over and interact with her now " , " she'll be a

social outcast and her social skills will suffer " , etc.

WRONG! That helmet was like a magnet for fun, happy

people to say hi, tell her how cute she was, love on

her sticker selection that week, or share their

helmet story with us. BUT, a plain white helmet is

scary to strangers - go to a Hobby Lobby, s and

get stickers! The didn't stick to it, use a little extra

rubbing if they do.

I was afraid again as she exited the cast, " no one will

talk to her without her helmet on " . Of course, everyone

does...but now she doesn't have a pointy head!!

Good luck, CT is great!

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Hi tte & welcome to our group!

I am so sorry to hear of the poor treatment (or lack there of) from

your pediatrician. Unfortunatley though, that is a common story we

hear in our group. It really is such a shame.

Do you have the consultation scheduled with Cranial Tech yet?

Cranial Tech. does band children up til age 2 as long as the child's

sutures in their head remain open. We have had some other members

band over age 18 mos., but those are few. We have a current member

who is going thru DOC treatment older, I hope the mom will add her

experience & let us know how her child's head is progressing.

Luke most likely won't get 100% correction, but he still could

benefit somewhat from a DOCband. I would get into cranial tech for

an eval ASAP to see what they recommend.

I'll answer your other questions below:

> I would like to know the following:

>

> 1. What age did you treat your child and how successful was it?

A)My daughter Abby began her DOCband at 11.5 mos of age. Abby's

plagio was severe. She wore one band for 4.5 mos, graduated at age

15.5 mos with 50-60% correction which I'm thrilled with.

>

> 2. Was it uncomfortable for your child?

A) No, not at all. Abby never knew the band was on her head.

>

> 3. How long was the treatment?

A) DOCband 4.5 mos.

>

> 4.Have you noticed any delays with your child in developement?

A) Abby graduated from her band one year ago, she's now 27 mos with

no developmental delays.

>

> 5.Was it uncomfortable dealing with the " looks " from other

> people?

>

A) At first a bit, but you get used to it. I always say that it's

human nature for others to stare at something that is " different " .

I'd probably stare at a helmeted baby too if I didn't know what it

was for.

Please keep us posted on your decision & your appt with Cranial

Tech.. Best of luck. Welcome again.

Debbie Abby's mom 3/1/00 DOCgrad 2/16/01-6/22/01

MI

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Hi Nicollette,

My son, , is almost 1 (6 more days!), and he's been in his DOC band for

almost 3 months now, so I figured I'd chime in and let you know how we've

been doing. I am blessed that our health nurse knew that there was

treatment for 's brachiocephaly (flat on the back), and told us we

should get a referral from our family physician to go to the cranio dept. at

the hospital. I am grateful for her knowledge because I know not a lot of

people know there are things you can do about this. I know there are a lot

of moms on this forum who are trying to increase public awareness so parents

can force their doctors to help. Anyway...here go the answers...

1. What age did you treat your child and how successful was it?

started at about 9 months. We have seen some correction so far. It's

still flat on the back, and still have a ways to go, but there is definitely

improvement. We were told he'd probably wear the helmet for 5 months, so

I'm hoping for more improvement. I'm not expecting 100%, but any

improvement is good.

2. Was it uncomfortable for your child?

only cried when I put on the helmet for the first two days. He's

actually gotten to the point where when I take it off, he taps it against

his head as if to say put it back on. In all actuality it's saved his

little bean a few times! He's walking around furniture, and going up and

down stairs, so it's actually been a good thing to have from that point of

view too. :)

3. How long was the treatment?

As I said above we were told about 5 months. I don't care if he has to wear

it for 8 or 9 months, if it's going to help.

4.Have you noticed any delays with your child in development?

is catching on to things very quickly. He's smart just like his mommy

(lol), and musically gifted like his dad (drums/pots you know). I'm a first

time mommy, so I'm one of those who thinks my son is the cutest and the

smartest. :)

5.Was it uncomfortable dealing with the " looks " from other

people?

The first week I was self-conscious. doesn't care, and doesn't notice

the stares. I'm quite comfortable with it now. Sometimes people ask what

it's for, and then I get the surprises like the 9 year old girl who knew

what it was for because her teacher's son had one. I'm quite happy to talk

about it now because I know how little people know about it, and they just

may know someone whose child needs one. I'm sure there are many of us too

who wish we knew earlier that there are things we can do about this. It's

such a short amount of time in the helmet when you think about how old we

all live to...under a year in probably 70 to 80 years...not much time at

all.

Good luck with everything. You'll find lots of great support here. There

are SO many knowledgeable and caring people hanging out here.

Velma, Mom to

Calgary, Alberta, Canada

http://www.momsforlife.com/?vg39616

Date: Tue, 04 Jun 2002 11:00:59 -0000

From: " knicnac " <nikknac@...>

Subject: Treating Toddlers

Hi,

I have a 19 month old toddler boy named Luke. ...

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>

> I would like to know the following:

>

> 1. What age did you treat your child and how successful was it?

Started at 9.5 months for first band; and 14 months for second

band. Got about 60 percent approx. correction with first band and

probably a total of 90 percent for both bands. Got quite a bit of

correction with second band started later. He was categorized a

moderate/severe to start with a lot of facial asymmetry from birth

due to being breech baby with dislocated hip from intrauterine

confinement.

>

> 2. Was it uncomfortable for your child?

Fussed for about a minute then fine with it.

>

> 3. How long was the treatment?

5 months first band, 3.5 months second, 8.5 months total.

>

> 4.Have you noticed any delays with your child in developement?

He had delays initially due to torticollis. Now he is active

and running and getting into everything. Still has a little tilt we

are working on for torticollis.

>

> 5.Was it uncomfortable dealing with the " looks " from other

> people?

> All I can say is you do get used to it. After a while I even

forgot he was wearing when out until someone asked me about.

Candy, mom to

land

> I greatly appreciate any response form anyone who has dealt

> with this. It is a big decison for us and we so want to do the

right

> thing.

>

> Thank you so much,

> tte

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