December 20, 2006
To all of
you, who love and indulge
me, please stop sending
candy! If I eat one or two
Baby Ruth or Big Hunk bars a
day, I should be ready for
shipments of dark Dove
chocolate eggs for Easter!
I apologize to have left you
in limbo for so long. So
much has happened since my
Halloween update. On Nov.
2, surgeons removed my
spleen, gall bladder, and
60% of my pancreas. The
biopsy confirmed that the
pancreatic tumors were a
morphed version of multiple
myeloma so out they came.
Recovery went well for a
week but then I was
readmitted to the hospital
where a drain was inserted
in my back to empty a cyst
of fluid. “Not unusual” I
learn. Well, “unusual” was
the clear blue and plastic
siphon, accordion pump and
bag secured at my waist that
dangled like a waffle iron
down to my knee; not small
or dainty,
but huge, heavy, and
conspicuous. Thank goodness
for cold weather and long
sweater coats!
My weight is
again an issue. I haven’t
weight 85 pounds since grade
school but I do now, so Jim
is back on a one-man-crusade
to insure I eat often and
“take one more bite.” Then,
recovery from major surgery
has taken longer than I
expected. Even though I
heard the surgeon say “allow
eight to ten weeks to heal,”
I expected to bound out of
bed after the second week.
I was wrong. I didn’t. The
weeks between then and now
have been exhausting and
frustrating and painful.
But I’ve kept my goal in
sight: be strong enough to
board a plane to
Boston
on Dec. 20th!
Traveling is
part and parcel of my
revered oncologist
prescription. At our last
visit, he again urged me to
live in quality, not
quantity. He reminded me
that the cancer seems to pop
up every six months; the
“things” in between are side
effects. Here’s his proof:
I came home from
Seattle,
after the bone marrow
transplant, in late July
2005. The next cancer
trauma was in February 2006
when the tumor on my
shoulder was removed and the
tumor in my left hip was
radiated. “In between”
radiation burns caused
damage to the colon and its
subsequent removal. Six
months later, in August, the
pancreatic tumors showed
up. Since those (and a few
other little organs) have
been removed, I should have
another good six-month run.
As long as the doctors have
the equivalent of bailing
wire and duct tape and I
have organs to spare, cut
away. Here’s hoping and
praying for a long remission
run.
However, a
slight case of graft vs.
host disease is causing some
sores on my legs and
blisters in my mouth. The
prescribed prednisone
(steroid), while beneficial,
causes as much pain as the
disease it fights: swollen
feet, sleeplessness, and
night sweats to rival lather
rolling off a brick layer’s
back in Arizona’s summer
heat. But, I am alive and
at least well enough to
gripe about my state.
“Joy” is the
Christmas word that lifts my
spirit and it is mine this
morning as I write. In a
few hours, Jim and I fly to
Boston
for a glorious week with the
boys. The only Christmas
shopping I’ve done is via
Internet. . . both items.
My presence is their gift
this year. . . until they
drag me and Jim to Costco to
buy new sheets and towels
and food to fill their
pantries.
We will be
home in time to celebrate
the third anniversary of my
diagnosis: December 29,
2003. I will never forget
the doctor’s words, “I’m
afraid I have bad news for
you. You have multiple
myeloma.” How life has
changed during the past 36
months. I’ve endured more
than I thought possible,
laughed until I cried and
cried until no tears were
left. Some things are
drastically different: my
body, my perspective, my
sense of what’s important.
Some things have not
changed: my love for Jim and
Elliott and Taylor; my faith
that God is present, my
belief that we are all
sufferers on a journey
toward perfection of
character and soul. I’m
paying close attention to
the journey.
Annie Dillard
once wrote something like
this, “The way we live this
day, how we lived this hour,
is how we live our lives.”
“To the fullest” is my
daily, hourly goal and that
is my wish for you. . . that
“to the fullest” you will
enjoy the merriest of
Christmases and the Happiest
of New Years.
Janice
P.S. Still no
air date for the A&E
documentary. It is finished
but not yet scheduled. I’ll
let you know when I know!