Please Help My 13 Yo Daughter Posted: 05-15-07 19:00pm
My 13 yo daughter was recently diagnosed
with pectus carinatum. I was rapid and
progressive. My son was diagnosed in
november 2006 with the same thing. No
doctor believed it was not there even one
month prior to finding it. He did not have
a growth spurt and was seen on 8/22/06 by
a cardiologist and had an echocardiogram.
His report said normal chest wall. My
daughter was checked by a specialist on
12/4/06 when my son was checked and
treated with a brace.....She was fine. She
was checked again on 3/4/07, and she was
fine. On 4/1/07, I saw that her shoulders
were uneven and I checked her. Her sternum
was protruding. I begged for a vitamin d
level, and it came back very low. She
drinks lots of milk, and was taking cod
liver oil at least every other day prior
to the blood draw.
Okay, so we get her a brace, and she is
doing okay. But even before this she was
tired all the time. Around the same time
she had a fever for a few days, aches, and
tired. I remember that her eyes would also
swell and itch so much so that I was
afraid she was allergic to the cod liver
oil. I stopped it, but it continued. It
last for about two weeks, and is now gone.
She takes the same cod liver oil now
without any symptoms of allergy. She also
had horrible chapped lips, but no rash
that we know of.
She remains fatigued, and after a lab draw
for ebv she started to complain that her
right arm was tingling in the hand. She
thought the it was changing colors, but I
didn't see it. The next day she showed me
her hands, and her right hand was dark red
with purple tones. I could feel her radial
pulse, and it cleared quickly back to
normal color if she held her hand up. We
wen to the er, and they did venous and
arterial ultrasounds and flow studies. All
normal> in fact, they even tried to do
it with her hands dependant....They turned
but the flow was normal.
We went home and saw our family doc then
an appt with a vascular doc yesterday. He
sent her for esr and creactive protein.
They drew the blood in the left arm, and
before we were out of the hospital, her
left hand was purple blue and cold. It had
not done that before the blood draw. We
went back to the vascular doc in the same
office, and showed him. We were concerned
about thoracic outlet syndrome due to the
brace (which she has not worn in almost
two weeks that this has been going on),
and also kawasaki's disease. They did a
stat mri/mra of her thoracic area. Vasc
doc called me tonight to say it looked
normal, and no signs of thoracic outlet.
Esr and creactive all normal.
Okay, I am at a loss. She is so
tired......And I mean dramatically tired.
She was exhausted when we got home
yesterday. She has slept all day. Her ebv
labs were negative.
Her hands do not turn colors under cold
water......Only when dependant.
Her lymphocytes were elevated.
I am thinking about taking her to a
children's hospital er. I fear that
something is really wrong.
My family doc didn't even bother to return
my call when I called tonight.
Am I over-reacting?????? Should I take
her? I have waited for appt for vascular
doc for over a week....Now two weeks have
gone by and she seems worse.
Vasc doc was nice and caring.....He
suggested a rheumatologist, but he had no
idea what was wrong.
Should I wait it out for an appt with a
rheumatologist, or take her to the er?
I hate it when people make you feel like
an over-reactive mother, but this is so
not normal.
Thank you for helping me.
|
dynamicdebz
New User, Becoming EHEALTHy
Joined: 21 Apr 2007 Posts: 41 Location: Sheffield, UK
Posted: 05-17-07 16:01pm
Welcome mom2aboyngirl to the forum!
I unfortunately know nothing about the
pectus carinatum & have never heard of
the condition until now.
I felt as a supporter of this forum I
should make it my business to know a
little about the condition at least &
have done some research online.
The site that I found gave me the most
information was http://www.pectus.org/whatis.ht
m not sure if it will help you in
anyway but take a look, I felt it
explained everything in laymen terms.
I'm not even sure if you are in the right
forum, from the bit of research I have
done it comes across as being a genetic
disorder rather than immune (immune system
attacking it's own body). Maybe you know
better. They perhaps may be more armed to
answer you're query.
However whether it be this forum or the
genetics forum we will offer you all the
support we possibly can & I hope you
get the answers you are searching for.
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