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Emiline' Story
Rick and I are here to share
with you our daughter Emiline’s story. Emiline
was born and went to be with the Lord on March 28th.
She stayed in our arms for one hour and ten minutes
but truly her story does not begin there. As with all
of us it began 9 months earlier. She was the eighth
child to bless our home and as an OB nurse I was very
familiar with the pregnant condition. As such I generally
opt for the lowest amount of interventions possible.
I forego all genetic testing and generally don’t
get an early ultrasound if it isn’t medically
needed. But this pregnancy seemed to be progressing
differently. By the time I was thirty weeks along patients
at work that we were delivering were asking me “Well
when are you going in?” this was the end of December.
When I responded not until April without fail they would
look at me with wide eyed bewilderment and ask me if
I had twins in there. At only 5ft tall I am accustomed
to resembling a pumpkin by the time the baby is due,
but this was certainly too early for that. I became
concerned and called my Midwife requesting an ultrasound.
I brought my husband with for that appointment, not
wanting to face the news of “twins” alone.
Little did we know at that time how lucky we would have
been to get that diagnosis. Instead we received a bulgy
eyed look from the OB GYN and all his cohorts and a
quik trip down to MN perinatology. Apparently our little
girl had lungs the size of butterfly wings atop her
heart and an abdomen that was so filled with fluid it
resembled mine. The official diagnosis was fetal-hydrops,
basically a fancy term for a tremendous amount of water
in her thoracic cavity and abdomen as well as polyhydramnious,
an abnormal condition of excess amniotic fluid. At this
point we did all the testing to try and find out why
with no answers to follow. All the known tests for WHY
came up negative. We then did all the investigating
into this strange syndrome of which we had previously
never heard. The bottom line was we could do nothing
medically to help her lungs grow. We had the horrible
fact to face that we were carrying a child with a condition
that the medical community would deem incompatible with
life.
So this is what we did. We prayed
a lot and implored everyone around us to do the same
asking God for a miracle, knowing full well He could
say yes or He could say no. I do believe that thousands
more rosaries were prayed in her behalf and prayers
were offered up in this cause than ever would have been
with a “Normal” child’s pregnancy.
And we used the time we did have to the best of our
ability. Medicine could offer us no cures but it could
offer time. Because of the massive amount of fluid on
her belly the stretching of the uterus would have thrown
me into labor prematurely. A combination of bedrest
and over a dozen therapeutic amniocentesis, a procedure
in which they stick a large needle into my stomach and
then into hers we were able to each week take off around
2 liters of fluid off Emmy and myself and thereby kept
her with us for 8weeks longer. I tried to do everything
within my power to keep her from regaining the fluid,
including restricting my fluid intake. I actually asked
the OB GYN if he thought that would help. He said he
didn’t think it would hurt, certainly underestimating
the power of a mother trying desperately to save her
child. It is never a good idea for a pregnant mom to
fluid restrict. The effort failed miserably to keep
her from gaining fluid although I could go long periods
of time without needing to empty my bladder. Sadly enough
whatever fluid I took in went first to her little body,
and to places it did not belong.
This is what we did with that
time. My children sang songs to their little sister
Emmy. I fed her chocolate and fruit salad every day.
We played hide and seek with her in my tummy. I hugged
her and cuddled her imploring God to not take her away
just yet. We had time to get to know her as her own
little person appreciating each day for what it was,
perhaps the last we would get to be with her.
What we did was unconventional
and was certainly frowned upon by many of the medical
community. In fact I have been told that a great number
of people said “well why is she continuing with
this? Aren’t they going to induce labor? Their
answer would have been to literally abort my child for
that is what an early induction with an otherwise healthy
mother truly is. We would have missed so much had that
been the road we followed. I would love to share some
pictures that a very talented professional photographer
put together for us. They hopefully will show you the
beauty and preciousness that God brought to us with
this little girl. Although we certainly would have preferred
that God say yes to that miracle we asked for He gave
us so much within that no, that we wouldn’t trade
little Emiline’s life for the world. This is her
message to us Life is Precious no matter how short,
no matter how disabled, no matter how useful or cost
effective NO MATTER WHAT!! Life is precious. I would
just like to close with a favorite refrain from a Song
that caught my attention one day.
We Live We Love
We Forgive and never give up
For the days we are given are gifts from above
So Today we remember to live and to love
Love your children, not because
they are ‘perfect’, not because they possessions,
not because they are accomplishments but because they
are gifts from God in whatever packaging He chooses
to send them to us, for how ever long he chooses to
lend them to us.
All children are a blessing
from God. Each of them a precious gift given to us to
hold for a few moments in time. We hold them with open
hands for only the Father knows when our moments are
up. When we speak of a child we wish to hold tight,
we always want more but with open hands we give back
to the Lord what wasn’t really ours anyway and
thank Him for the precious time He did give us.
I wish for the wisdom of God
on this difficult journey you are embarking upon.
Love
Rick and Gerri Nelson
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-The support, information and encouragement provided by the PPFL parents is not meant to take the place of medical advice by a medical professional. Any specific questions about care should be directed to a health care professional familiar with the situation.
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