Blogging Friends.... some very complicated emotions and feelings are
running amok within me right now. {No, I am not experiencing another mood
swing!! That was last night!! I survived, thank-you very much!!} I need to
write about these emotions and feelings. Get them "out of my system",
as that phrase goes.
Oops, I did it again. And
again. And again. And again. And again. And again. Times twenty children
who were born with congenital
diaphragmatic hernias. MY birth defect. Plus now two
additional children with different "special needs"/deliberating
health issues. I did it again. I have "met" so many children Online whose
very oxygen can be sucked away from them. See, several
years ago, when I was in my early 20's, I discovered this special little
boy--named Conner Phillip--who was born with a rare genetic illness called
Tay-Sachs disease. Long story short. Infants
with this condition develop "normally" until about six months. Then,
they slowly regress. Such children only live until the age of five years old.
There is no cure. I followed Conner's story closely, which was faithfully
written by his Mommy on a Web site. I prayed for him. This was emotionally trying at times knowing that he was going to die
anyway. But I do believe in miracles. Conner was only 22 months old when he
passed away on November 26th, 2006. This news, of course, broke my heart. I
even composed a poem in Conner's honor. Which, regrettably, I have mislocated.
Plus, Conner has an Angel figurine in my bedroom. After Conner died, I made a
promise to myself. Never discover any
more "terminally ill" {My choice of words at the time!!} children!!
I grow too attached. Thus, it is painful when these children pass. Well!!
This premature short-term memory loss sufferer/one step forward, two steps back
personality-type did just fine keeping her promise!! Fast forward. To January 2013. Over six years after
making this promise. When I felt God leading me to find families whose children
were born with congenital
diaphragmatic hernias. This birth defect can be fatal for various reasons. And I had no idea what I was getting myself
into!! I now have twenty--in
counting!!--children who were born with C.D.H., their hearts wrapped tightly
around my finger!! Including Sunni. Based
on Facebook, she does not have congestive heart failure!! Thanks be to God!! Sunni is back on feeds. Plus, she's looking and
feeling better!! Thanks for your
prayers!! Keep sending them Sunni's direction!! Well last week, I did it
again. I allowed yet another special little girl to wrap her heart and soul
tightly around my finger. She was not born with C.D.H., or craniosynostosis, for that matter. No.
Her name is Teresa. She's six,
was adopted into a loving American family from China, and is quite the little
fighter!! Teresa also needs prayers. Desperately. My comment today is self-explanatory.
Ann....
"Unfortunately, following the heart catheterization, the
doctors determined that the donor heart has been rejected.". Oh no!! I am
so sorry. Praying now for a new heart. That it bond and flow successfully with
Teresa's little body. But I have leapt ahead here. Praying--hard!!--for
Teresa's Berlin heart surgery. That there be absolutely zero complications. She
is a fighter, your girl. May God continuously watch over her. Six to eight
months of waiting for a new heart?! I cannot even imagine. Praying for it to be
sooner. Ironically, I can feel my own heart pounding....
--Raelyn