Kruz Davenport of Muscle Shoals,
Alabama
Born July 16, 2013
Diagnosed June 30, 2016 just before his
3rd birthday! Yes, the United States most recently diagnosed Little Giant!
I have had the pleasure of talking with Kruz's mom Jessica on and off for the past month or so. Shortly before Kruz was
officially diagnosed she reached out to me and wanted to know what to
expect. Although Joe and I feel her and her husband Kyle's pain and
know all too well the road they are starting to travel themselves, I
am thankful to have the opportunity to provide guidance
professionally and personally, but most importantly be there for them
as their new friends!
Jessica's team of friends and family
will be joining us in working on raising funding for our children's
research by way of the Little Giants Foundation. For this we are
beyond thankful.
Please visit their FB site for Kruz and
show them some love!
Taken from Kruz's mother Jessica and their
facebook site: Pray for Kruz: @KruznforaKure:
Today
we got the results and answers we have been searching 2 years for. He
does have what his nephrologist thought, Schimke Immuno-osseous
dysplasia, a very very rare form of
dwarfism.https://ghr.nlm.nih.gov/condition/schimke-immuno-osseous-dysplasia (I
know everyone will google just like we did, this link is from NIH and
explains the best)
This
will be one of the hardest things to try to put into words. So I will
start by sharing a little about Kruz. When Kyle and I found out we
were having a boy, we instantly started planning his life. From what
his name would sound like at a sporting event, to what sports he
would play. In high school, Kyle was "Mr. CCHS" and I got
"most athletic" so of course we just knew he would be big,
strong, and destined to play sports. We were planning his life for
him. Little did we know God would show us very soon who was in
control of his life, and a plan for Kruz far more than we could ever
plan or imagine.
Today
we got the results and answers we have been searching 2 years for. He
does have what his nephrologist thought, Schimke Immuno-osseous
dysplasia, a very very rare form of
dwarfism.https://ghr.nlm.nih.gov/condition/schimke-immuno-osseous-dysplasia (I
know everyone will google just like we did, this link is from NIH and
explains the best)
We have so badly wanted someone to tell us, "your son is fine, hes healthy", We may have no got that answer but he is happy, smiling, and loved. That is what I focus on each day. His doctor did say we may have caught it early enough he can live to be an adult. Statistics and life expectancy is just a number to us. We do know he will have kidney failure in 5 to 10 years though and we have to be very aggressive treating his symptoms of any sickness as they come. We have HOPE and we BELIEVE Kruz will help find the cure for him and other SIOD patients now and in the future. "I praise you for I am fearfully and wonderfully made" Psalm 139:4
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