This blog was designed by Robin and I so we can share the story of KelliAnne's young life with the people that care about her most. KelliAnne entered our world in a hurry on May 16th, 2012, nearly 3 months prior to her August 3rd due date. She joined our family as a very sick 2 lb 4 oz little girl who has a long journey ahead of her... but that is just the tip of this little beauty's story.
8.04.2012
New Pics...
A few pics from the last couple weeks. KelliAnne has grown into some of the newborn clothes that adorn her wardrobe so her mom really enjoys dressing her up for any trip out of the house or even to go downstairs to the living room ;)
8.03.2012
C.E.L.E.B.R.A.T.E.
KelliAnne
has been home with us for just shy of one month. The last several weeks have
been an outstanding welcome into parenthood outside the NICU. Yes, there have been plenty of sleepless
nights, diaper blow outs, spit ups, and “what the heck does that mean” moments;
but we would not have it any other way.
There is
also quite a bit to celebrate. See below Tobin’s Top 10 Reasons to Celebrate:
1. It is Robin’s Birthday. She is one
amazing woman who has had quite a year. Happy Birthday Mama!
2. Today is actually supposed to be
KelliAnne’s birthday as well. Robin and I are still amazed that for the last
twelve weeks, we have watched her grow and get healthy out here in the real
world, and she was not even supposed to have even been here…. Apparently she did not want to share her
birthday glory with her mom and wanted her own BIG day.
3. Packing on the pounds-KelliAnne is
now up to 5lbs 10 oz. She came home weighing little over 4lb. We are still battling a bit of reflux but are
learning how to balance nursing, bottle feedings, and extra calorie fortified
feedings to get her big and fat.
4. Robin can almost, ALMOST read the
entire blog without crying.
5. KelliAnne has officially graduated
from the NICU. We had an appointment with the Children’s Spot, Saint Luke’s follow-up
clinic, to examine her developmentally. The same doctor who saw her the day she
was born, saw her yesterday and was ecstatic with her progress. She is now a healthy ‘term baby’ with no major
issues.
6. MRI – KelliAnne had an important MRI
done this week to follow up on the slight hemorrhaging she had in her brain. The hemorrhage has completely evolved, or
disappeared, and all other brain development that is to be expected by a term baby is now present. This was great news to a couple of parents
that have been awaiting ‘MRI Day’ for several weeks now.
7. NO MORE HEART/APNEA MONITOR. Yes,
that is right - the respiratory therapists reviewed the download of KelliAnne’s
apnea monitor and decided she no longer needs it.
8. Eye Exam – KelliAnne’s slight disease in her
left eye has not worsened, and is looking like it will clear up in the several
weeks. If it doesn’t the doctors are
watching very closely and are ready to do laser surgery at the first sign that
the disease is progressing. The good
news is that the laser surgery does not just stop the eye from getting worse
but actually can repair it to healthy condition. This is not what we originally thought.
9. Her body hair is actually clearing up
pretty good as well. As most of you
know, and if you didn’t notice from the pictures of me holding her, she has the
genes to be abnormally hairy. Just as
the doctors told us, the back, shoulder, and facial hair that covered her body
has pretty much all disappeared and.
10. - F.F.F. Faith, Family and Friends. The
last few months have been unexpected and trivial, yet completely awesome at the
same time. Dating back to mid-April when
Robin was first hospitalized and then put on bed rest, our faith, family, and
friends have been more then constantly showing up when we need them. We cannot
express how thankful we are for EVERYTHING that EVERYONE has done for us. We always
had good food, a clean house, a walked dog, plenty of thoughts, and enough
prayers to help us pull through this time. Words cannot express how grateful we
are for all of that. Throughout this time we have been told how strong Robin
and I are, and that our strength is the reason why KelliAnne, who was once
referred to as the “sickest kid in the NICU” came home at 35 weeks when we were
told no babies go home before 36 weeks. Our strength came from F.F.F.
And scratch #
4. She is crying again.
We love you
all and thank you again for helping us get through this journey. As you can
tell we are not updating the blog as frequently as there is not as much action,
but we will post a fun story and some pictures every once in a while so those
of you that don’t see KelliAnne too often can keep up with her story.
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