Ok....Here is the deal! FB is an awesome asset to keep in
touch and spread the word on what is happening with Miss K quickly. The
down side is that I never get things documented on my blog and am therefore
missing out on a lot of journaling. Therefore, I am going to TRY using my
blog as the MAIN place that updates will be. Likely I will post that
there is a blog update on FB with a link over to this blog. So, when we
get a heart.....this blog will be the place to come.
Like I said so
much has happened and nothing documented. For example, In May Miss K graduated
preschool. To think we almost didn’t send her because she was waiting for
a heart. Glad we didn't hold off because that heart ticker in the corner
of her blog is still counting up!
We have had a few
heart caths since my last post on here. We have treated some spotty
rejection episodes since then. Gone to the cabin, admitted Kaidence into
the hospital for an illness that sent her little body into shock (but she
recovered quickly) and other things here and there.
Kaidence's was
scheduled for a heart cath for July 3rd. It was quickly decided by her
cardio that it was much too long to wait. She felt that K's heart
pressures needed to be checked out. They had been fine all along but
regardless we cathed her heart last Tuesday. What a blessing that we did.
Turns out that Kaidence's hearts pumping pressures are high. We
have since learned that her heart biopsy came back clean and rejection free.
That was news we haven't heard for a very long time. The only
bummer was that with such a clean biopsy it only left one reason for the high
pressures....Heart Failure. K's heart is starting to fail. We
started her in a diuretic to help remove the extra fluid from her body in hopes
it will help with the pressures and keep the heart from working too hard. We
are also talking about tube feeds again because she is losing weight and no
longer being that great eater. We briefly talked about the next steps of care
if her heart continues in this direction.
That same week,
just days after the heart cath we received the amazing news that her PRAs
(antibodies we have to avoid in a new heart) had gone from 46% to ZERO.....This
was never expected because it rarely ever happens to this extent. These are
antibodies that have been in K's body since 8/2010 when she went into Severe
AMR (antibody rejection) and we spent all that time in the CICU. For her
these antibodies are 'bad guys’ and her body has held onto them ever since.
That is until now. This is nothing short of a miracle!
What does this
mean for Kaidence? At first it meant that now ANY heart that matched her
blood type could be given to her, opening up the donor pool. However,
after cardio discussed this with others it was decided that we still keep these
antibodies on her 'avoid' list for transplant even though she technically no
longer has them. WHY??? Your body has memory cells. Cardio worries
that it could be possible for those memory cells to be triggered by these
antibodies if her new donor heart tested positive for them. Then we could
be back to where we were in 2010 and NOBODY wants that. So for now it stinks
because it does make it harder to find that perfect match. However, in
the long run it will be a blessing and give Kaidence a better chance and
hopefully more time on this next heart with less rejection. I think in
the end we will be glad that things played out the way they have.
We are amazed that
these antibodies are no longer in her body. I was hesitant to post our great
news on FB because we have some heart buddies that are also waiting for hearts
with antibody issues. I felt bad having such wonderful news come our way.
Then I decided that if I could give anyone HOPE then it was what I should do.
Sometimes things happen that cannot be explained. In the end the
thing we have to remember is that the doctors aren't in charge and we aren’t in
charge. One person is in charge and that is our Heavenly Father.
It's so hard to let go of the control (even though we have never had it).
So just like I end
all these post....We will keep waiting! Some days the wait is easier than
others and some days the need for a heart seems more urgent then others.
In that same thought, we have been blessed and we are grateful.
Things could be much worse and for many, it is.
2 comments:
Thanks for the update, we think of Kaidence often and keep her in our prayers. It really is a miracle that her antibodies just dropped. Those miracles that can't be explained do give hope. I'm glad Kaidence is enjoying her little life. You are a good mom to give her those simple joys.
Thank-you for the update Shauntelle! I am the same way with FB.
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