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Re: Digest Number 1466

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In a message dated 4/20/2002 2:30:07 AM Eastern Daylight Time,

writes:

> To the list, I contacted the reporter of the Philadelphia Inquirer article

> ....here it is.

>

- Thanks so much for sending the article! It's great - I'm sending it

to my mother! I think someone mentioned recently that it would be great to

have something clear and short to send to relatives who have trouble

understanding... Cyndi in VA

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In a message dated 4/20/2002 2:30:07 AM Eastern Daylight Time,

writes:

> To the list, I contacted the reporter of the Philadelphia Inquirer article

> ....here it is.

>

- Thanks so much for sending the article! It's great - I'm sending it

to my mother! I think someone mentioned recently that it would be great to

have something clear and short to send to relatives who have trouble

understanding... Cyndi in VA

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  • 7 months later...

In a message dated 11/30/2002 8:55:19 PM Eastern Standard Time,

writes:

>

> Does anyone have any recomendations for a DAN doctor in central PA

> or possibly the Blatimore, MD area?

>

>

>

Email me off list.

Michele

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  • 2 years later...

Diane, my heart goes out to you. That is SOOOOO horrible and upsetting.

I am wondering, from everyone out there with CT, what are the chances

of getting it in the opposite ear? My son has had 2 surgeries on his

left ear (he is 7 years old), and I feel we will probably need a

third (he is starting the stinky drainage again). Does he have a high

chance of getting this in his left ear as well?

Another question, is the no water rule only for canal wall down? Our

surgeon gave him permission to swim without ear plugs this summer,

and he has been in the pool everyday with a canal wall up surgery.

Thanks for advice!

Warm Regards,

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I had my CWD in 1979 and have never used ear plugs

while swimming (yes my Doc approves). I have had no

more c-toma's since 1979. Do what your Doc's tell you

as to using ear plugs or not, they are the experts.

tom hansen

--- jennifer <jennifer@...> wrote:

> Diane, my heart goes out to you. That is SOOOOO

> horrible and upsetting.

>

> I am wondering, from everyone out there with CT,

> what are the chances

> of getting it in the opposite ear? My son has had 2

> surgeries on his

> left ear (he is 7 years old), and I feel we will

> probably need a

> third (he is starting the stinky drainage again).

> Does he have a high

> chance of getting this in his left ear as well?

>

> Another question, is the no water rule only for

> canal wall down? Our

> surgeon gave him permission to swim without ear

> plugs this summer,

> and he has been in the pool everyday with a canal

> wall up surgery.

>

> Thanks for advice!

>

> Warm Regards,

>

>

>

>

>

>

__________________________________________________

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, I had CWU in 02/2005. I am going for my 2nd look

09/20/05. I have been without ear protection for at least a month.

So far, so good. I agree with Tom, Follow the Dr orders.

Bettie

>

> > Diane, my heart goes out to you. That is SOOOOO

> > horrible and upsetting.

> >

> > I am wondering, from everyone out there with CT,

> > what are the chances

> > of getting it in the opposite ear? My son has had 2

> > surgeries on his

> > left ear (he is 7 years old), and I feel we will

> > probably need a

> > third (he is starting the stinky drainage again).

> > Does he have a high

> > chance of getting this in his left ear as well?

> >

> > Another question, is the no water rule only for

> > canal wall down? Our

> > surgeon gave him permission to swim without ear

> > plugs this summer,

> > and he has been in the pool everyday with a canal

> > wall up surgery.

> >

> > Thanks for advice!

> >

> > Warm Regards,

> >

> >

> >

> >

> >

> >

>

>

> __________________________________________________

>

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  • 8 months later...
Guest guest

Funny you should ask this question. My son saw a specialist two days ago and we

spoke about it. His chest deformity, though, is a severe indent instead of a

bulge. It is so severe that when he was little, it caused a heart murmer and

lowered the blood flow, and many times he has had food caught in his esophagus

that couldn't get through. Twice we've had to call paramedics.

The specialist we saw is the one that has developed the new 3-D surgery for

scoliosis. He said that to do the surgery now (my son is 16) would be a major

surgery, and would take the same amount of recovery as his spinal fusion did.

He said that they put a plate in, under the ribs and pectus, to straighten them

out. It didn't sound like fun.

When he was little, and we had the heart problems, the doctors suggested he have

the surgery before kindergarten. However, when he reached the age of 4, they

determined that there was not significant enough problems with the heart to

warrant such a surgery. They told me that if we wanted the surgery for strictly

cosmetic reasons, they would do it, but after research on it, I just didn't have

the heart to put my little guy through that (he had been through enough at that

time).

Now I do regret him not having the surgery - but you never know and can't

predict the future.

I wish you well in finding out answers.

> From: " suzanna_melik " suzanna_melik@...

> Date: Thu May 18, 2006 2:04pm(PDT)

>Subject: My spine curvature and chest deformity

>

>Hi,I am new to the group. I have scoliosis and chest deformity because

>of it. I am 42 years old. My parents never paid attention to this. The

>bulge in my chest really bothers me. I am wondering if anyone else had

>this type of problem and what are the treatment options.

>

>Thanks,

>Suzanna

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Guest guest

> The specialist we saw is the one that has developed the new 3-D

surgery for scoliosis.

Hi,

What is this new " 3-D " surgery you mentioned, or is there a good link

I could go to that describes it?

Thanks,

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