I am 27 years old, and have been with my husband for four years, but
we recently got married in September. We became pregnant while on the
pill, but ofcourse were still very excited about the thought of becoming
parents. I think I was definitely ready to become a mother. I had even
told him that I was hoping we could try soon after the wedding. He said
that would be fine, since he too was very excited about being a daddy.
So, we broke the news to friends and family at about twelve weeks into
the pregnancy. I was feeling great, and wanted so much to share the news.
Of course the wedding plans changed a bit, but we still went forward and
decided to still get married. We had a perfect wedding, and our little
angel was with us on that day, four months into his life. We found out
at about six months that we were having a boy, and we were so excited.
We both cried at the ultrasound, you hate to admit you have a preference
because of course a healthy baby was the most important thing to us, but
I think we were so happy we were having a boy. Everyhting with the pregnancy
was going ok. The only that came up was that on my AFP test my HCG levels
were slightly elevated. They told me that all this meant was that at 37
weeks they would monitor me closely to make sure my placenta would be
ok to make it full term. I also was overweight at the beginning of my
pregnancy, not saying ofcourse that caused the PE or anything but I think
my weight concerned me at times.
Well, my guess is that at about 71/2 months is when I started to swell.
I brought it up with my doctor, but she said she felt it was normal. I
also started showing raised blood pressures, but they would lay me on
my side for fifteen minutes, and they would drop down a bit, and they
would send me off. Meanwhile I am a teacher who is on my feet all day
long, and it made no sense to me that she didn't consider bedrest. Well,
just before the holidays I had my 30 week appointment. For the first time
I had a plus one in my urine, and still had elevated blood pressure. My
doctor decided to have me do a 24 hour urine test, and bloodwork. She
told me to just go home, relax (not bedrest) and we'll see where things
will be in 2 weeks.
Well, at my 32, week appointment (Jan.2) things really started. I had
a plus three in my urine, high BP, and very swollen so she decided to
send me to L&D. Luckily my husband was with me. We were so scared,
but we tried to hang in there. We got to there and they immediately put
me on Magnesium sulfate, catheter, fetal monitor, and of course bedrest.
For about the next 36 hours I stayed in bed, and they did a 24 hour urine
and gave me steroids for the baby. They also did an ultrasound, which
showed the baby weighing 2 pounds 9 ounces, quite small I thought. I asked
about it, and they said placenta, amniotic fluid, and his measurements
looked good, so since I was a small baby maybe he was just going to be
small for his age. ( still major concern)
My dip sticks all were under plus one, and the first doctor even let
me have lunch on the second day, so I thought things were going ok, I
thought I may just have to stay there a while. Sure enough a new doctor
comes in and tells me the urine level was 3,000 and they thought I should
deliver, preferably by c-section for my health, and the babies. Of course
I thought he knew best so we went with that. I had my son on January 3,2002
at 7:45pm. He was perfect from the start, but tiny. He was 2 pounds 11.7
ounces, and he recieved 9.9 on his apgar. He didn't need a ventilator,
and was only on oxygen a short time. He went to the NICU and had a perfect
twelve days.
He made every step they hoped for. Off the bellyrubin lights, started
eating breast milk, went from 3ccs to 24ccs, and was gaining weight. He
was up to 2 pounds 14 ounces. On the early morning of January 15th, he
started to show signs of infection in his intestine. He had a residual
on his 3 am feeding. Let me not spend a long time on this difficult part
of my story. Our little prince, Dylan Thomas Simanek passed away at 3:56
pm on the 15th. He died from something that is called NEC. It is fairly
common, but from what we were told doesn't usually get so severe so quickly.
It can often be treated by antibiotics or surgery. Our son's intestine
perforated, and he died very quickly. It is has been a very devestating
experience that I think we have yet to even come close to understanding.
He was doing soo well, and we just still can't belive he is gone. We
are thankful though, for the twelve glorious days he spent touching our
lives, and our family, friends, and his nurses. He had some amazing nurses
who took very good care of him, and had a close bond with him. They all
use to tell us how they would fight over who would get to take care of
him.. His smiled lit up the room, and his strength amazed everyone. WE
WILL LOVE HIM FOREVER!
Now, my husband and I are trying to emotionally heal, and are fearful
that we will never have the opportunity to become parents again. My health
seems to be ok but am soo fearful I will get PE again, and have to go
through something like this. I don't think I could handle losing another
baby. But then again, I don't think my husband and I want to spend our
lives without children. So, hopefully we will one day find the strentgh
to try again. For now, I plan to investigate my care, Dylan's care, and
learn asmuch about PE as possible.