I had my first child at age 18, poor nutrition and my first baby. You would
have thought I would get preeclampsia then. But I didn't. I ended up with
preeclampsia with my second child.
At 35 weeks my doctor noted my blood
pressure was going up. He asked about lifestyle and if I had any changes.
Then he ordered a 24 hour urine, and to see him the following week.
At 36
weeks again they told me, lay down on your left side, again I didn't know
why. They took the pressures and then had me lay down for half an hour, they
came back in, and took it again, it was normal so they let me go home. By
this time I had been having the upper right pains, I too thought it was just
the way the baby was positioned so I never said anything at all. I also had
headaches in which the doctor told me to try drinking a coke, alternate hot
and cold. I let this go one for a week. That was around the 20th week or so.
By 37 weeks my visit again went the same, lay on left side to take the
pressure. It didn't go down after an hour. The doctor then explained to his
med student that my blood pressure was in the preeclampsia range 140/92
(normally I was 110/65. He ordered me to the hospital for a few hours worth
of blood pressure readings, and let me drive there, explaining that if it was
high after a few hours he would come to induce me. He never explained to me
what this was, and I was so afraid I didn't ask.
I called my husband at work
and told him I was swinging by to pick him up and that we would go to the
hospital, that my blood pressure was up. The nurse at the hospital that took
my readings was great. She explained more and told me that I was very swollen,
and asked if I was on bed rest. I told her no I wasn't. She told me I
probably should have been, and to rest as much as possible. The blood
pressure went down, and I was having some contractions. At first the nurse
thought she would be able to keep me because of them! When she called the
doctor to give him the readings he sent me home, to see him again in a week.
At 38 weeks I again went in to his office. He then reviewed my urine and
noted that I had an excessive amount of protein and since my pressure was
still up he was going to induce me the next day, before he had a sick mom
and baby. I delivered my daughter with a very swift labor, she came in under
2 hours. I was not on mag sulfate or any other preventative drugs, not even
aspirin. I however was lucky and did fine. My daughter had to go to the
NICU for a few days due to her blood sugar being low, but has had no problems
since.
Now that I am in my third pregnancy I am seeing a high risk doctor.
They told me that I had mild preeclampsia. They didn't mention HELLP but I
know I had to have that because they stated that I had a low platelet
count...under 20,000, and I had the pains but I just didn't know what they
were. I am hopeful that this pregnancy and postpartum will be uneventful.
It
just amazes me how many conflicting things there are out there about this
disease. All the doctors looked at me like I was stupid because I didn't have
preeclampsia in my first pregnancy, one even thought they just missed it!
I am concerned about the lack of knowledge out there, every doctor has
different opinions and treatments. Most seem to give aspirin, calcium, bed
rest, something to try to suppress it, others do mag sulfate as a standard
practice, mine did nothing extra. I just realize now how lucky I was given
no other medications or warnings.
Please help to support this foundation, so that hopefully our children will not have to deal with this! We need to get the information out there, especially to the medical community, they are stumped. Maybe if they just listen to us, they can get some answers. We break every "rule" of this disease on a daily basis! And I read that every hour 9 women die from this, and probably hundreds of babies. Yet they still call this "rare".
I am so glad that my daughter made it, now my only concern is...Will she get this?
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