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Our youngest son,
Gabriel, who had never any health
problems, began to get fevers, become
lethargic, lose weight and his appetite
among other things. After consulting
with our first physician, she diagnoses
him with a bad teething episode seeing
his gums were white and swollen. (Later
I found out white gums are a sign of low
hemoglobin.) I still felt something was
not right with him. I called my son’s
regular doctor (after the insurance
changed he could not see him anymore),
he advised me to follow my instincts and
get a second opinion. I scheduled
another appointment with a different
doctor and I began to pray this doctor
would investigate my son’s symptoms
more. |

Gabriel Caldwell-age
2, diagnosed with Leukemia

The Caldwell Kids,
Gabriel pictured left |
After giving her my long list
of concerns, “…he won’t walk anymore, he crawls,
he has even stopped drinking from his sippy cup
and only wants a bottle, he won’t say mama and
dada anymore, his stomach is sticking out, but
he is losing weight, he lies on the middle of
the floor on his stomach most the day...” this
doctor took my concerns and began to put things
into action. We got blood work drawn and an
appointment with the neurologist for his
developmental step back. Later that day I got a
call from a nurse telling me to rush Gabriel to
the hospital he had hemoglobin of 3.9. I didn’t
know what hemoglobin was at the time, but I know
it wasn’t good. I tried not to panic. I just
prayed, “Lord I know my son belongs to you, my
will is not there is something seriously wrong
with him, but if it is God as long as you get
the Glory out of the situation you will give us
the strength to endure anything.” A nurse there
advised me to transfer my son to Children’s
hospital of Michigan because Gabriel looked very
sick and she knew Children’s had more
experience. After the transfer and the
overwhelming, countless blood draws, a bone
marrow came, the moment I will never forget.
A nurse enters our hospital
room, on December 8, 2005, “Do you mind if I
take your older son to the playroom while the
doctors talk to you?” I consented to letting
him go, having my two year old in the hospital
all day, wondering what was going on with
Gabriel and being 4 months pregnant was tiring.
I thought of it as a break while two doctors and
a social worker pulled chairs into Gabriel’s
room. At 14 months, he lay in the crib sleeping
as the doctors began speaking to me. “As you
know we did a bone marrow on Gabriel yesterday
and we are now able to give you a diagnosis. We
discussed a few diseases we were trying to piece
together for Gabriel. The results of his bone
marrow where out of every 100 blood cells in his
body 90 are cancer, we have diagnosed him with
Acute Lymphoblastic Leukemia. Also known as ALL
B precursor…” At the moment I was unable to
focus on the way it made me feel. My almost
immediate response was “What do we do next?” I
knew we had to keep moving forward and not give
up hope.
I contacted the Red Cross to
inform my husband in boot camp his son has
cancer. The next day my baby was scheduled for
surgery, blood transfusions, platelet
transfusion, to start chemotherapy… it was a
whirlwind.
Since that day in December
God has given our family strength to survive.
We’ve had challenges and continue to. Children's
Chance has been a blessing to our family. Our
family moved to South Carolina the end of
January. We hadn't planned on the expense of
having an exceptional child. We have no family
here and had no friends. Traveling to the
hospital with three children, co pays,
food...were beginning to break us. I finally
asked my social worker at MUSC for insight on
organizations that could help our family with
our needs. She told me she was going to contact
Children's Chance. I was contacted by DeeAnn
and she turned my worries into hope. Children's
Chance not only help pay our bills, they also
sent us gas cards and food certificates. All I
could do is thank God for this organization.
After being blessed financially, DeeAnn
encouraged me. She knew exactly how I felt
because she had been here. She inspired me,
learning she helps make miracles happen for
families like her own. Children's Chance not
only fills a need but helps families as a
whole. That is what sets them apart and keeps
them in my heart and my prayers.
Still undergoing the top
third intensive chemotherapy and remaining
strong through everything. He is a hero and in
my heart he is already a survivor. Gabriel
recently had to get a G Tube placement, and we
are making a difficult decision to separate our
family, moving to Michigan where we have more
support through this intensive regimen of
chemotherapy. This may not be every man’s
battle, but for those who battle these cancers,
this is our life. Just like the meaning of
Gabriel’s name, God is my strength. May you be
blessed this Christmas season and I hope my
son’s testimony is a Witness of the Glory of
God.
With a grateful heart,
Angela Caldwell
-Story submitted by Angela
Caldwell, mother of Gabriel
Gabriel
Caldwell has most likely been through more in
his life already than most of us will ever
experience. And for that, Gabriel is truly a
Children’s Chance Champion!
              
Read
Matthew's story.
Read Amber's
story.
Read
Ruthie's story.
Read
Joel's story.
Read
Annastin's story.
Read Brittany's story.
Read the Ferguson family's
story.
Read Madelyn's story.
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To submit your family's
story about your own experience with pediatric
cancer to be featured in the Meet the Families
section, please email to:
samanthahiggins@bellsouth.net (include
pictures if you like)
or call the office at (803) 254-5996! |
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