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Re: Update from Australia

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Hi Joanne,

With all the parents I speak with, I always say that the most

important thing you can do is to find a physician who truly

understands plagiocephaly & its treatment. Finding a good physician

who takes your concerns seriously, is half the battle. If you're

constantly put off with statements like 'it'll round out on its own',

or 'don't worry hair will cover it when he/she is older' its time to

get a second opinion.

If a helmet is recommended, you should spend the time to find out

what experience the group has had with treating plagiocephaly and

specifically what success they've had with their helmet. How many

children have they treated? Is this a new program? How many years

has the individual been providing this service? What kind of

training have they had? How frequently do they follow up with the

child? Ask them specific questions about plagiocephaly and try to

guage their response. Are they comforatable discussing it, or do you

find the answers elusive? If you are uncomforatable, take the time

to do some more research. I am not familiar with what is available

in Austrailia, but if it is anything like the U.S., there are a lot

small helmet programs, and it will be up to you as parents to try to

assess the quality of treatment they can provide.

As an additional resource, at the international cranioafial meeting

this June I had the chance to speak with Dr. . Dr. is a

craniofacial surgeon from Australia who is considered one of the top

specialists in his field. We discussed how many parents on this site

were from Australia, and he informed me that he runs a plagiocephaly

clinic in his office and would be more than happy to answer any

questions the parents may have. His address is:

J. , MD

226 Melbourne Street

North Adelaide

South Australia 5006

Phone: 61 8 8267 1466

email: ddavid@...

Along with the fact that the " Aussie Mommies and Daddies " are at this

site learning everything they can about plagiocephaly, I think that's

a great start.

Sincerely,

Tim

littlefield@...

> > Hi all,

> > We finally saw the specialist about Jade's plagio. Unfortunately

he

> > says Jade is too old for her to get much benefit from a helmet.

She

> > is 10 months old next week.

> > I know that many babies in the USA get helmets as old as 12

months

> > but at the end of the day there are only 2 specialists in

Australia

> > who believe in helmets and without their referral its just not

> going

> > to happen for us.

> > It's disappointing to travel all that way to only find out that

its

> > too late. I had a good talk to this doctor and I clearly sensed

the

> > pressure that he is under from most doctors in Australia as they

> > simply don't believe in the use of helmets. So with this in mind

my

> > guess is that he will only treat babies which are at the perfect

> age

> > (3 to 6 months).

> > Jade still has some limitations in her neck movement and a small

> > tilt. The specialist says that we need to continue with physio

and

> > neck muscle stretching as this may help the plagio a little.

Thats

> > all we can do for her now.

> >

> > With the other specialist living over 2500km away from us, we

have

> to

> > accept that there is no hope of treatment in Australia.

> >

> > Thanks for all your support. Its time for us to sign off from our

> > quest for help.

> >

> > Simon

> > Australia

>

>

> For more plagio info

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