http://bittersweetjaileen.blogspot.com/
Wednesday, May 13, 2015
Tuesday, April 7, 2015
Wednesday, January 7, 2015
2015 is not ready for Bri!
Brielle got her rifton walker a couple days before Christmas! We
had a goal that she would take a few steps before the New Year! She did it! Woot
woot! Just yesterday sick and all, she actually walked many steps in her walker!
So proud of my girl, she truly amazes me every day!
Here’s the video of her and her sisters cheering her on.
Here’s the video of her and her sisters cheering her on.
Bella tends to motivate her like a puppy :)
Friday, December 5, 2014
To the left, to the left! Brielle’s surgery was a huge success!
The
procedure took about an hour. (only reason it was so long is because of the Auditory Brain stem Response test.) When I walked into Post Op, I couldn’t believe she
looked so good! She usually doesn’t do well after anesthesia. One of the reasons
we were asked to prepare to stay the night, because we just don’t know what the
sedation will do to her. Before the procedure I spoke to the anesthesiologist,
and requested for him to do the most minimum sedation possible. This anesthesiologist
did an amazing job; they didn’t even put an IV in her! If you have an I-cell
child… this is music to your ears! These kiddos have very thick skin... I mean
that literally! Their skin keeps thickening through time because of the storage
in the cells. Last IV she had put in they popped 4 veins before they can get
one going.
She said “mama”
as soon as I walked in and was trying to tell me something. She looked drowsy
and was floppy but content. (She’s usually screaming, nauseous, very
uncomfortable, and needs to be medicated and hooked on machines until she feels
better.) As soon as I held her in my arms, I noticed she was very observant;
she was taking everything in. She kept talking (in her little language of
course); she was listening to herself. It was an amazing feeling to see her
discover new sounds and noises.
In the waiting room before going in to see her, the surgeon came
to give me the results. Bad news, she is completely deaf from her right ear. He
thinks the disease has damaged her inner ear with the storage in the cells. (Ugh..these
stupid storing cells!) THE GREAT NEWS is she should have full activity in her LEFT
EAR! Woot! Woot! I just can’t wait for all the things she is going to start saying. We thought she was spunky before, wait until she
can say her words clearly and add more to her vocabulary!!
When we got
home she was a little more coherent, I wanted her to rest so I put her down for
a nap. Ya... That didn’t last long; I was having a kick from all the
yapping she had going on in her crib. She is known to have intense
conversations with her stuffed animals, but today was REAL talk! Like “listen
here, I run this crib” kinda talk!
I am so
excited for her, one day in and her speech has already improved so much! I can’t even
imagine what I’ll be hearing from her tomorrow.
Thank You Jesus
and thank you all for always keeping Bri in your
prayers!
Thursday, December 4, 2014
break time
I sometimes
tell myself I need a break from my I-cell support group…
This week
we lost two little ones. Eryka Barre & Wynnie Johnson. Eryka made it to 4 years
of age and Wynnie to 6 years of age. I will not go into details on how they
left this world. Only thing I can say I-Cell disease is responsible.
I must admit, I am an emotional wreck every time I hear the news of one of our kids leaving
us. Crazy thing, I have never met any of these kiddos in person. The only
connection I have to their world is their parents/grandparents that share stories
and pictures on our support group online etc. Before meeting these families on
the support group, I went on a Google stalking spree; I wanted to learn every
little bit about Brielle’s disease.
A text book
can only give me statistics and scientific research. I was already aware of
that information when I spoke to the doctors. I wanted to know THE LIFE of a
child with I-CELL disease. Through my Google searches I found a blog about an
I-Cell baby girl Gabrielle Ross (who had already left this world when I found
her blog). After Gabby’s blog I found Dorian & Wynnie’s blog (twin brothers
with I-CELL) … found many more after those.
I’ve never
had an online relationship with anyone, but I can tell you that I definitely have
one with my I-CELL family.
Why is my
hurt so deep when we lose a child?... My mom has told me, “maybe you shouldn’t spend
so much time connecting with your group, it can’t be healthy for you”. I know
what she means, she knows I hurt every time I tell her a story of one of our
kids being in the hospital or leaving us.
Why?
… because I
know the feeling of losing a child. So I grieve with every parent. I grieve
their loss and grieve Jaileen’s loss and as terrible as it sounds; I
start grieving for Brielle.
… because
of that moment when you have to say Goodbye or See ya later, and you are left
with empty arms.
… because I
know I will relive this terrible nightmare all over again one day.
… because I
am living this journey with them and slowly my daughter is declining just like
them.
… because I
see how this disease has no mercy, it takes them all one by one.
… because
there is not one thing any of us can do about it.
So yes, maybe sometimes I ask myself, why I keep putting myself through this emotional
roller coaster?
Truth is
because even though those bad moments are BAD… Let me tell you that the good
moments are GOOD!!
… when we
share our children’s accomplishments
… when we
get a glimpse of their unique personalities
… when we
see how they all resemble each other in their own special way
… when we
learn from the parents that have been there
… when they
are happy and joyful; which is almost always
… when they
are beating the odds
… when they
pull through & believe me.. these kids pull through!
For as
tiny, limited and fragile these kids are.. boy, are they strong, courageous, and
determined to fight! I’ve had my share of kids, and been around many. I can
honestly say these kids are the happiest babies.
Sometimes, I
think people feel bad for us… Don’t! We have a happy life… I cannot tell you
how much joy a child this special brings to this world. For anyone that has
ever met Brielle, I don’t need to say it. She brings beauty out of every person
she encounters. Strangers are drawn to her. I share her life for everyone to
see the beauty that she is. Not for sympathy. This little one makes everyday
brighter.
Life is
good, but heaven sounds so much sweeter!
Fly high Eryka and Wynnie.
http://dorianandwynn.blogspot.com/
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