After losing my first daughter to e.coli at 2-/2, I was desperate to
become a mother again. I tried IVF, putting in three embryo's because I
was told that my chances were not good (less than 10%) To everyone's
surprise, I became pregnant with triplets.
I am over 40, in good
health, except that I had been depressed and unable to function well
since the death of my daughter, and worried that improper nutrition and
stress over the wrongful death lawsuit might affect the babies.
At 21
weeks, I was diagnosed with preeclamsia and told by my perinatologist
that I would not deliver live babies. I stayed in bed, and was
monitored for my high blood pressure, low blood platelets, and
proteinuria although I felt fine. I had not gained much weight, and one
of the babies was not growing well. I underwent an amnio to see if the
third baby had trisomme, but she did not, and appeared to be fine except
for the small size.
At 27 weeks, she died.
At 28 weeks, I delivered
two baby girls b emergency c-section, both under lbs. Although my
perinatologist told me that I was in denial, and as soon as the babies
were born, I would feel so much better, this never happened. For me,
preeclampsia was a silent disease, only showing up through blood and
urine tests and high blood pressure.
With so little information
available about eclampsia, I was happy to find this website and that I
was not alone. I mourn for my two daughters, Brooke who would be four
and a big sister now, and for Hayley, my little one whom I never saw.
My "twins" are six months old now, and doing well, although they are
IUGR and still at the bottom of the chart for weight and height.
I long
to have one more baby, feeling as though something is still missing in
my life, but I worry about the chance of developing preeclampsia again
(not for myself, but for my unborn child) and feel such guilt over the
difficult fight my two little girls had to go through in their 3 month
hospital stay.
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