This. makes. me. very. sad.
Because.
I.
Summer !!!!!!
But, much to my dismay, summer has to
end, and we have to get ourselves back into a routine. Only this time,
our routine is getting another kid into the mix!! Sweet Tulah is
continuing to just do incredibly well. She has melded into our family
perfectly and has absolutely no problem loving us like crazy, or letting
us know when she isn't getting exactly what she wants!! I believe she
is very comfortable in her new family!!!
At
the beginning of August, Tulah got her first set of casts in order to
finish correcting her bilateral club feet. She gets a new set each
Monday. She does SO well with this! I have been told that while in China
she HATED this, and would cry (or most likely knowing her... scream) to
the top of her little lungs during much of the casting process. Well,
much to my surprise, this time around, she lays completely still, holds
my hand, and lets the Dr. do whatever she needs to do, without saying
(or screaming) a word!! In fact, the staff at the office has told us
more than once that she is the best club foot patient EVER!! WOW!! She
has come so far in just over 3 months!! What a difference a family
makes:))
She gets to pick her color each week
too! So far, her favorites are pink and purple! I'm happy with this too
since most of her outfits match those colors:)
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Tulah's first set of casts!!! |
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Tulah's 2nd set of casts!! |
At this time, she is currently in her
5th set of casts (Purple)! This should be her last set before her
surgery. On September 12th, she will have a tenotomy
to release some of the tendons in her foot that are very short and very
tight, making it impossible for her to move her foot up or down. She
also had this procedure in China, but due to the thickness and stiffness
of her tendons, she is requiring another one. At this same time, they
will also remove her precious little "extra" thumb. She will wear casts
again after her surgery, probably for about 6 weeks. Following that, we
will be going through some pretty intense physical therapy and she will
be in a brace. The goal is to her her up and walking as soon as we can.
After she is up and walking, we will proceed to correct her hips
sometime this winter.
Please remember to pray for our girl on September 12th!! I will update after the surgery as well!!!
Hi Tulah
ReplyDeleteMy name is Jenna. You are a brave courageous fighter. you are a special miracle from god, a gift from above, earthly angel,and you are a smilen hero. You are full of happiness, life, smiles, joy, fun,love, and spunk.
I was born with a rare life threatening disease, and have 14 other medical conditions, and developmental delays.
I wrote this poem
Each of us are Special
Each of us different,
No one is the same
Each of are us are unique in our own way,
Those of us who have challenges, we smile through our day.
Those who of us who have challenges, we smile through our day.
It doesn't matter what others say
we are special anyway.
What is forty feet and sings? the school chior
http://www.miraclechamp.webs.com
I will pray for your sweet girl! September 12th is easy for me to remember b/c our punkin goes in for her follow-up, sedated MRI to see how things healed (hopefully) after her detether surgery in May. I will have some quiet time while I wait, so know that someone in Ohio is praying for you! :o)
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