Thanks to You All:

As I sit here and watch the sleet and snow we are getting today and
reading all the replys.......I am reminded of how blessed my life
is!

The last few days,  I've been sort of "re-living" that nightmare of
the week I learned of a disease called CML.  I never knew that there
were different kinds of Leukemia........boy,  did I learn as much as I
could after my doctor called me
on Thursday afternoon to tell me what was wrong and to tell me that he
had made me an appointment with an Onc./Hem. the next day.  He was
very kind to me and told me not to worry & fret.....that this was a
type of Leukemia that could be managed and that he had patients who
have lived many years with it.  All I knew about Leukemia was from
what my husband's office manager had gone through in '95 when she
almost died,  but was pulled through and has been living in remission
since.  I didn't know the difference between acute and chronic...but,
I was soon to find out.  And, boy, did I!   Now, I'm one of the
biggest "babies" when it comes to blood, needles, & pain. In my
younger years, I passed out at the drop of a hat when it came to
taking blood or IV's, you name it!
My first week after dx'es was a holy nightmare.  I had so many blood
tests taken and then came the wonderful BMB & BMA in the doctor's
office with nothing but some Lorazapan & Percocets........I remember
crying......I remember his saying he could not aspirate any marrow as
it was set up like concrete but he was extremely happy about the
sliver of bone which just didn't make sense to me at the time.  Then,
if that wasn't torture enough,  he sent me back down stairs to the lab
for more blood drawn.  By this time,  the drugs had hit and I was
pretty much out of it.  I barely remember any of that other than the
nurse had to go from one arm to the other as she couldn't find a vein
in the first.  I asked my husband later about all of this. (smile)
The visit a few days later, I learned the lab had lost some of the
tests, so I had to go through them again.  The genetics test took
nearly three weeks to come back......by this time, my husband had had
enough of their incompetence and had the doctor refer us to the same
doctor in St. Louis that had treated Betty, his office manager.  Right
away,  I learned the difference in how small labs & hospitals vs. one
of the top five hospitals in the World does things.  They treated me
with so much compassion and made me feel at ease around every corner.
When I almost passed out after one extensive blood draws ( 9
vials).....they were all right there helping.  I told my husband at
one of the days when I had to go to Labs, then Dr., then over to have
a BMB/BMA,  that I was sure that God was sitting up in heaven and
watching me and laughing.  Every time I sat for blood to be drawn, I
mentally had a talk with God and said, "Father, I know you are
thinking this is funny!"  "Of all the diseases,  why this?"   But,
after five years,  I can tell you that now,  it's a piece of cake.   I
don't have to have anyone go back with me to keep me focused by
talking to me........the girls who do the tests are so good,  I hardly
ever feel the stick of the needle and they are usually pretty fast and
done before the arm begins to throb.  The doctor I have now doesn't do
BMB's unless she sees something in the drawn blood that warrants it.
I can call her or her nurse practitioner any time and they are
available. I am pretty sure when I go back next month, they will then
stretch my visits out to every six months.  So,  through all the
awfulness of the beginning till now,  I learned......and now I am able
to maybe help someone else by telling them my story.   That's it,
fellow survivors.....we all have a story to tell.   That is what we
should remember............and share it with others.  Let them know
that they are not alone even though they may feel like it at the
time.

So,  God bless you all.......& try to remain focused on the good
things.........they are like mercy drops from heaven!

Love to all,
Suzieq
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[CMLHope]
A support group of http://cmlhope.com
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