I've been meaning to post this for awhile but...
I'm sorry all these posts aren't really in order.
At a visit to my obgyn I was getting my blood
drawn for my thyroid test and she asked if I
wanted a routine blood test. I said sure why
not. When the
results came in the doctor called. I remember
thinking it was odd that she called me herself.
She told me that I had an elevated risk for
Down
syndrome and that if I wanted to I could go to
a hospital that had more advanced equipment
and get an amniocentesis and a better
ultrasound. I asked if it was necessary and
she said
no we can watch it here and if we see anything
strange you can go to the other hospital. At
the ultrasound they found soft markers for DS.
They couldn't find a nasal bone and there
were spots on his brain. I had an ultrasound
monthy from then out. The ultrasound tech
said
that the heart looked fine. The next one
showed a tiny nasal bone. The doctor said
that they couldn't say for sure if he had it or
not...
nothing was absolutely certain. A friend said
that a friend of hers had a baby with soft
markers that came out "normal."
Somehow I knew that he would have DS.
Later on I had extra amniotic fluid but not
enough to be too worrisome. It eventually
resolved itself. The last few months we got
the news
that baby's femurs were shorter which they
said was another marker. Also the baby's
growth was in the 25th percentile then the
next month the
20th. The Dr said that if the growth was less
than 15th percentile then there was probably
something wrong with the placenta and we
would have to induce.
At 37 weeks his growth rate was less than 15th
percentile so we were off to the hospital. The
Dr. wanted to take it slowly to make sure
baby's lungs
would be developed. When I got checked in
they started pitocin to do a stress test. The
heart rate was great and all the numbers were
"beautiful"
despite the placenta being "ugly." (I love my
doctor's descriptive words :-) )After being
assured that baby would make it through birth
okay they turned off the pitocin for the night.
A friend
came over and they let me eat :) I didn't sleep
much that night!
The pitocin started early the next morning and
after too many awful contractions my beautiful
baby was born at 13:33. As it turned out the
cord was
short and not enough was getting to him.
Indeed he did have
Downs syndrome as you can tell by his eyes
and ears. However he does seem to have fairly
good muscle tone.
They didn't think he was breathing well
enough so they put him on oxygen. They also
did tests to find that he had a heart murmer
and would have to take an ambulance ride to
the nearest nicu. He stayed in intensive care
for about 10 days where he got heart tests,
antibiotics
and plenty of blood tests. The doctors
determined that he had an atrioventricular
canal defect which will need to be operated on
at about 4 or 5 months.
While there we saw more doctors than we had
in years including a geneticist who confirmed
the diagnosis and told us it was not the
genetic type of
DS.
He is now doing very well. He has regular
pediatric and cardiology visits and the doctors
are pleased with his progress.