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Warriors Page
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This
is my
father,
Joe Sabatine,
doing
what he
loves
best –
preparing
to fish!
First
diagnosed
20 years
ago. WLE
on back,
no further
treatments
suggested.
January
2001 diagnosed
Stage
IV with
met to
adrenal
gland,
which
was removed.
June 2001
mets to
both lungs
and bone.
January
2002 diagnosed
with multiple
micromets
to brain.
Passed
into eternal
life on
Thursday,
February
7th, 2002.He
was 58
years
old.
Joe
was a
loving
husband
to his
wife Sharon
for 38
years.
He was
loved
by many,
but especially
by his
children
and grandchildren.He
returned
this love
threefold.
His laughter
was distinct
and would
bring
a smile
to everyone’s
face.
He was
the type
of man
who would
do anything
for anyone,
and often
did. Even
in his
darkest
days he
did not
hesitate
to talk
with others
about
their
cancer,
and give
encouragement.
He had
such a
passion
for living
life to
the fullest,
and was
quite
the outdoorsman.
He loved
to fish,
duck hunt,
deer hunt,
sail,
camp,
snowmobile,
and even
raced
motorcross
when he
was younger.
My
father
will be
missed
so very
much by
so many
people,
but we
all know
he is
in a much
better
place
and no
longer
suffering.
His body
may be
gone,
but his
spirit
will live
on in
all who
knew and
loved
him.
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Jon
Michael
Warrington
was born
on July
10, 1973
in Minden,
Nebraska
to James
and Candice
Warrington.
The second
of four
sons,
Jon grew
up in
Gibbon,
Nebraska,
graduating
from Gibbon
High School
in May
of 1992.
As
a young
boy, Jon
enjoyed
camping
with his
family,
swimming,
playing
baseball,
and wrestling
with his
brothers.
In high
school,
Jon excelled
in football,
cross-country
and wrestling,
competing
at the
state
level.
He played
the drums
in the
school
band.
He also
acquired
a love
for horses
where
he trained
and competed
with his
mare,
"Missed
Flight".
He
grew up
in the
Baptist
faith,
and at
the age
of seven
accepted
Jesus
Christ
as his
personal
savior
and was
baptized.
He continued
his walk
with the
Lord the
remainder
of his
life.
As
a very
young
boy, Jon
was influenced
by his
grandfather,
MSgt Charles
Warrington.
As a result
of his
grandfather's
example
and love
of the
Marine
Corps,
Jon enlisted
in the
Marines
in May
1991 in
the delayed
enlistment
program,
at the
age of
17.
On
May 26,
1992 he
left for
MCRD in
San Diego.
After
basic
training,
re reported
for duty
at Camp
LeJeune
in North
Carolina.
There
he met
and fell
in love
with Sheri
Loper.
They were
married
on May
14, 1994.
In August
1995 he
was stationed
in Yuma,
Arizona
at LAV
test directorate
where
he spent
four years.
On
September
16, 1995
triplet
sons,
Calder,
Cullen,
and Cody
were born
to Jon
and Sheri
in Phoenix,
Arizona.
After
just a
short
time on
earth,
these
three
precious
babies
went to
heaven.
They have
since
been in
the hearts
and memories
of the
Warrington
family.
On December
31, 1996,
Jon and
Sheri
gave birth
to their
fourth
son, Colter
Wyatt.
He was
the light
of his
father's
life.
In
1999 Jon
was transferred
to SOI
at San
Onifrey,
California
where
he was
an instructor
until
his retirement.
In
June of
1998,
Jon was
diagnosed
with malignant
melanoma.
This started
his four
year battle
with this
dreadful
disease.
Through
his continual
struggle
with surgeries,
treatment,
and hospitalizations,
Jon continued
serving
his country
as a Marine,
attaining
the rank
of Staff
Sergeant.
Because
of the
limitations
of his
disease,
Jon was
medically
retired
in March
of 2001.
Jon,
Sheri
and Colter
moved
back to
Gibbon
to be
close
to family
and friends.
Jon continued
to valiantly
fight
his battle
with cancer.
He took
pleasure
in the
times
spent
with family
and friends.
Jon
passed
into heaven
on Saturday,
May 18,
2002 at
his parent's
home in
Gibbon,
surrounded
by his
family.
He
leaves
to mourn
his passing:
his wife
and son,
his parents,
brothers,
Kris and
wife Pam
of Gibbon,
Brion
of Omaha,
Dan of
Kearney,
two nieces
and one
nephew,
Grandparents,
Charles
Warrington
of Gibbon
and Virgil
and Ruth
Lusk of
Minden,
several
aunts,
uncles,
and cousins,
a host
of friends,
and Marine
Corps
comrades.
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This
is my dad,
Sam Westmoreland,
who was
diagnosed
with metastatic
melanoma
in January
2001. They
found 7
brain tumors
and 1 lung
tumor. This
is the result
of melanoma
on his face
about 4
years ago.
He was told
there is
no cure
and that
it was only
a matter
of time
before he
dies. Shortly
after he
was diagnosed
he decided
to try and
fight this
terrible
disease.
He went
through
a lot of
chemo and
radiation.
After none
of this
worked,
he was told
at the end
of August
or beginning
of September
that it
could be
a few weeks
or a few
months.
He was very
courageous
throughout
his battle
with cancer.
He passed
away on
September
24, 2001.
Even though
we all miss
him, I know
he is in
a better
place where
he will
suffer no
more. I
pray a cure
will be
found soon.
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This
is a picture
of my wife
Brenda,
38 years
old, who
was diagnosed
with Stage
3 Melanoma
in 1996,
small mole
lower back.
Had it removed
and was
told they
believed
it was all
removed.
Well four
years later
it returned
and she
was getting
headaches.
We both
knew what
it was and
she had
a MRI and
it showed
eighteen
brain tumors.
Brenda was
a trooper
all through
this nightmare.
She told
all her
friends
that she
was worried
about me
-- how I
would handle
all of this
after she
was gone.
She was
not worried
about herself.
She asked
the oncologist
what was
going to
happen,
how she
would die.
He told
her and
she turned
to me and
said let's
get out
of here
and she
never said
another
word about
it. We were
married
for 12 years
they were
the best
years of
my life
and I miss
her so much.
I hope and
pray for
a cure to
this insidious
disease
and all
the misery
it causes
so many
people.
I know Brenda
is with
God and
she suffers
no more.
Till I see
you again
my darling.
All my love,
Bob
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My
son LeRoy
Smith
was diagnosed
with mm
in Nov.
of 1996.
Mole on
lower
left back
removed
and sent
away to
PA and
was told
all was
clear.
Was diagnosed
as only
.7. In
July of
1998 noticed
lumps
under
left arm.
I'll always
remember
the surgeon's
sad look
when he
came out
of surgery
and said
it was
melanoma.
Still
he fought
hard.
Owned
his own
trucking
business,
all from
hard work,
went on
a full
year of
interferon,
always
positive,
always
a smile.
I never
knew till
he was
gone,
he was
told then
that he
had between
3 to 5
yrs. He
was going
to beat
it and
be a survivor.
He regained
his strength
and weight
and we
thought
he was
doing
great.
Summer
of 2000
we entered
our Kenosha
Cty Relay
for Live
Event.
I raised
the highest
single
donation
of over
$2000.00.
Then September
of 2000,
just after
getting
home from
work went
into seizure
and rushed
to hospital.
Found
golf ball
sized
brain
tumor,
had surgery,
radiation,
made 2
trips
to TX
to Burzinski
Clinic,
once again
went back
to work
until
Jan. 2001
looked
in mirror
and like
overnight
a massive
lump right
above
his heart.
Biopsy
and was
melanoma.
Through
it all
he remained
so strong
continuing
to go
up north
snowmobling
with his
family
between
chemo
treatments.
Then more
small
brain
tumors,
did the
gamma
knife,
went on
massive
chemos,
all to
no avail,
sold his
business,
tumors
progressed
and lost
some speech
and major
crisis
when he
could
no longer
drive.
Driving
had been
his life.
He loved
his flag
pole,
it was
a gift
from one
of his
drivers,
and he
died at
4:30 p.m.
beautiful
sunny
day on
Flag Day,
June 14,
2001.
His wife
went out
and lowered
the flag.
His twin
sons were
13 on
January
12, 2002.
Oh, how
we all
miss him.
His loving
Mom and
Family

Tribute
from the
company
LeRoy
hauled
for:
His forever
smile
said it
all
No one
loved
his family
more,
No one
loved
his friends
more,
No one
loved
his work
more,
And no
one but
no one
loved
his truck
more.
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Here
is my precious
sister Anissa
Chambers
Spann, 30
years young,
who died
of melanoma
on July
29th, 2001.
She was
a beloved
sister,
daughter,
mother of
three wonderful
children,
wife, and
friend to
anyone she
came in
contact
with. Her
smile and
warm personality
could brighten
up any room.
She never
had much
monetarily,
but she
was always
content
as long
as her husband
and her
children:
Tommy, Clint,
Taylor,
and Carly
were taken
care of.
Her battle
with melanoma
was a short
one, lasting
only three
months from
diagnosis,
but she
fought courageously,
maintaining
her smile
and sense
of humor
until the
end. She
is gone,
but SHE
WILL NEVER
BE FORGOTTEN,
and I'm
sure that
Heaven is
a better
place now
that she
is there.
Your family
and friends
Love you
Anissa,
and we long
for the
day to see
your warm
smile throughout
eternity!!!
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This
is my
Mom, Donna
Reith.
She was
finally
diagnosed
with Stage
III MM
in July
'91 after
she went
through
5 biopsies
over the
period
of a year.
Her Primary
appeared
on her
nose.
All 5
were read
incorrectly.
By the
time it
was diagnosed,
she was
Stage
III with
one lymph
node positive
for MM.
She went
through
a total
of 17
surgeries
as a Stage
III, many
were reconstructive
as they
removed
1/2 of
her nose
due to
the primary
Melanoma.
She attempted
interferon
in '91,
but the
side effects
were incredibly
severe
and treatment
was terminated.
She remained
NED until
March
4, 2000
when a
large
lump was
buldging
out of
her back
and growing
at a rapid
pace.
The Core
Needle
Biopsy
indicated
it indeed
was Metastatic
Melanoma.
As months
would
pass,
she would
develop
metastases
in both
lungs
and in
her brain.
She
tried
EVERYTHING
and then
some to
combat
this beast.
She participated
in two
different
clinical
trials
after
FDA Approved
treatments
failed
her. She
was involved
in Phase
I trials
for Perillyl
Alcohol
as well
as Endostatin.
She was
dropped
from both
studies
due to
progression.
When the
brain
mets caused
seizures
and left
her unable
to communicate,
she decided
to try
Gamma
Knife,
without
success
unfortunately.
Two months
before
she died,
she developed
several
very large
blood
clots
in both
lungs
and in
one of
her legs.
Meanwhile,
the brain
mets was
progressing.
Mom needed
to make
a choice
between
Hospice
and continuing
the battle.
There
was no
choice
in her
mind.......she
continued
to fight.
She began
Temador
just 12
hours
before
she died.
She was
an inspiration
and a
Godsend
to all
who had
the pleasure
of knowing
her. She
loved
life so
much and
fought
very hard,
always........always
with a
positive
attitude
and a
smile
to share
even during
the worst
of her
battle.
She passed
away peacefully
on April
14, 2001.
To
those
who love
her, she
will forever
be the
strongest,
most amazing
woman
we'll
ever know.
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My
sister Irene
died of
malignant
melanoma
on July
8, 1988.
She was
29 years
old. She
had resigned
her commission
as a Captain
in the U.S.
Marine Corps
to purse
full-time
training
for the
Hawaii Ironman
competition.
She was
diagnosed
with melanoma
shortly
after she
began her
training,
and died
without
completing
the event.
I completed
the Vineman
Ironman
in July
1999 as
a tribute
to everything
she has
taught me
about life
and the
role of
happiness
in staying
emotionally
and physically
healthy.
I miss her!
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This
photo
of Jerry
Keeling
was taken
only months
before
he was
diagnosed
with nodular
melanoma
in April
1998.
He was
dressed
in costume
for a
role in
one of
the many
plays
he performed
at our
community
theater.
I'm certain
that he
is still
singing,
blending
his rich
baritone
with the
other
voices
of the
Angel
Choir.
Jerry
confronted
melanoma
with the
same quiet
determination
as he
did most
things.
He resolved
to stay
positive
and not
give up,
and in
the end
he faced
death
with dignity,
grace,
and even
humor.
He
left a
legacy
whereas
by example
he taught
those
who knew
him to
not dwell
on what
might
have been,
but rather
to embrace
the possibilities,
and to
not fear
death
as an
ending,
but to
anticipate
it as
a new
journey.
Gerald
M. Keeling
December
11, 1951
- October
20, 2000
Son, Brother,
Husband,
Father,
Grandfather
and child
of God
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Here's
Joe Tuso,
dancing
with his
sweet
wife,
Jean.
Melanoma
took his
life,
but not
his spirit,
on Feb.
4, 2001.
He fought
a long
and hard
battle,
but never
gave up
hope--we
know he
wants
you all
to keep
up your
fight
in the
hopes
of a cure
for this
terrible
disease.
He valued
all of
the friendships
and words
of encouragement
he received
on this
MPIP board.
He was
first
diagnosed
in August,
1998,
became
Stage
III in
July of
2000,
Stage
IV in
December
of 2000,
and passed
away Feb.
4, 2001.
He was
willing
to try
ANYTHING
to be
around
longer,
even if
a treatment
only had
a 1% chance
of helping
his MM,
he would
have pursued
it. His
wife,
five daughters,
son-in-laws,
12 grandchildren
and mother
will miss
him greatly,
but are
very thankful
for the
wonderful
impact
he's had
on their
lives.
In one
of the
books
he translated,
Beowulf
was described
as "...the
mildest
of men
and the
gentlest,
kindest
to his
people."
This,
too, is
true of
Joe.
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Kyle
Edvard
Ericksen
was born
on 1/14/1971
and died
9/25/2000.
He was
29. Kyle
only lived
15 months
after
he was
diagnosed
with the
beast.
His treatment
was experimental
and it
failed.
He loved
music,
the ocean,
skateboarding,
his dog
Tucker,
his family,
and life.
He was
the light
of our
life;
a very
big and
painful
hole will
always
remain
in our
hearts.
We miss
him so
very much.
He has
one sister
Kindra.
The following
is a poem
that I
once saw
posted
on MPIP,
I borrowed
it, and
had it
put on
a tile
for Kyle's
headstone.
Music
was so
important
to him.
Kyle,
your music
will always
continue
life is
much like
music.
A well-lived
life plays
on forever
in the
minds,
and the
hearts,
and in
the very
souls
of all
who hear
it. Each
life's
song is
but a
blend
of the
notes
given
to us
by God
at the
moment
of our
birth.
We put
the story
to the
melodies
that we
choose
by the
way we
live each
day. Throughout
our lives,
we add
to this
mix the
notes
from the
lives
of all
who touch
us deeply.
And they,
in turn,
live on
in us…
and the
music
continues.
Let Kyle's
"Song"
be remembered...
and live
on… in
all who
knew him.
We
love you
Kyle,
Mom, Dad
and Kindra
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This
is my husband
Randy. He
was first
diagnosed
with melanoma
in June
of '95 when
he had a
mole removed.
In January
of '96,
during a
routine
check-up,
his doctor
felt an
lump in
his neck.
The following
biopsy revealed
what we
had feared:
the melanoma
had spread
to his lymph
nodes. Randy
underwent
extensive
surgery
(modified
radical
neck dissection)
and started
a one year
Interferon
therapy
right afterwards.
He tolerated
the IFN
very well;
he felt
great and
started
to run again
(some of
you might
remember
his runner's
story).
In May 1998,
the melanoma
returned!
It had spread
to his liver,
spine, adrenal
gland and
pancreas.
He underwent
Bio/Chemo-Therapy
and had
a partial
response;
meaning,
that he
only had
a few spots
in his liver
and his
spine left.
Then, in
March of
2000, he
- once again
- had new
tumor growth
in his abdomen.
Unfortunately,
all the
therapies
and surgeries
he again
underwent
couldn't
help save
his life.
He passed
away on
February
16, 2001
-- only
12 days
after his
35th birthday.
Randy
was the
most wonderful,
honest,
inspiring
and courageous
person
I've ever
met. He
changed
my life
forever
and I
hope,
with all
my heart,
that he's
still
watching
over me.
"Some
people
come
into
our
lives
and
quickly
go.
Some
people
move
our
souls
to dance.
They
awaken
us to
new
understanding
with
the
passing
whisper
of their
wisdom,
and
make
the
sky
more
beautiful
to gaze
upon.
Some
people
stay
in our
lives
awhile,
leave
footprints
on our
hearts,
and
we are
never,
ever
the
same
again."
~
Author
unknown
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Kenneth
L. Luke
Age 44
Mar 2,
1956 -
April
18, 2000
Caregiver
was Mom
(Jan)
Diagnosed
in June,
1994,
primary
mid-upper
back:
malignant
melanoma
- superficial
spreading
type,
0.62,
Clarks
Level
III. He
had a
WLE at
a major
hospital
specializing
in MM.
The SNB
had not
yet been
developed.
Other
than periodic
checkups,
no further
treatment
was ordered.
In
April,
1999 the
melanoma
returned
with a
vengeance,
resulting
in a complete
left axilla
lymphadenectomy
(26 positive
nodes).
Over the
next 9
months,
Ken was
treated
at three
well-known
hospitals,
all melanoma
specialists.
He had
numerous
surgeries,
received
two different
vaccines,
IL-2,
DTIC and
radiation
but the
melanoma
continued
to spread.
He encountered
many problems
along
the way
and his
condition
deteriorated
rapidly.
By the
end of
January
his liver
had suddenly
exploded
with tumors,
he experienced
severe
problems
with IL-2,
treatment
was stopped
and he
was released
from the
NIH trial.
In early
February,
a JWCI
doctor
said they
had nothing
for him
and I
was advised
to "just
keep him
comfortable".
Shortly
thereafter,
he went
on hospice
and passed
away during
Holy week,
on April
18, 2000.
Ken
always
looked
younger
than his
years,
still
played
sports,
loved
to do
stats
and was
known
for his
infectious
smile
and winning
personality.
His devotion
to his
family,
loyalty
to his
friends,
pride
in his
work,
passion
for sports
and great
sense
of humor
made up
his wonderful
persona.
As a corporate
accountant,
preparing
financial
statements
for an
international
corporation,
Ken met
and worked
with people
around
the world.
When he
passed
away,
condolences
poured
in from
all corners
of the
globe,
each remembering
a man
with a
great
smile,
a magnetic
personality
and one
who always
carried
himself
with class
and dignity.
Throughout
his battle,
when bad
news seemed
to be
the only
news,
Ken always
remained
positive,
vowing
that the
"beast"
would
never
steal
his spirit.
Ken never
knew how
many lives
he touched
and how
his courage
became
an inspiration
to all.
He was
truly
a very
special
person,
a brave
warrior
and our
hero.
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Shayna who
was born
on March
1st 1974
at 3:53
pm on a
Friday,
Shayna kept
me in labor
for 36 hrs
(pain) and
when she
was born
I knew she
would be
my life.
What a beauty,
she would
make people
stop in
their tracks
and say
how beautiful
she was,
I even entered
her in beauty
pageants
and she
won 1st
place every
time. Aside
from her
beauty she
was mine
and I loved
and doted
on her.
She was
an only
child for
almost 10
yrs and
wanted a
baby sister
or brother
so much
that the
day I told
her she
was going
to get her
wish, she
cried with
joy. Shayna
was born
in Southern
California
but when
she was
14 we moved
to Nebraska
to give
the kids
a better
"safer"
upbringing.
Shayna struggled
through
her teen
years and
at the age
of 20 gave
birth to
her daughter,
the child
she wanted
more than
anything
else in
the world.
Shayna finally
got her
act together
and was
such a good
mom. She
went back
to school
so she could
become a
nurse and
was working
full time
and taking
care of
her daughter.
Her life
was coming
together
when she
got sick
and before
she knew
what was
going on
she had
a hysterectomy
and all
kinds of
invasive
things done
to her body.
It took
my breath
away that
if she wouldn't
have had
her daughter
she would
never have
the chance
to have
a child
of her own.
Shayna was
dx. on December
21st 1996,
but the
worst was
yet to come.
She had
just been
given a
death sentence
because
her cancer
was so aggressive
and so fast
spreading
that they
knew it
would be
very hard
to stop
it. Melanoma
a simple
SKIN cancer,
that is
what most
people think,
that you
cut it off
and its
gone, well
its not
a simple
SKIN cancer
at all.
PLEASE read
about it
and learn
because
what you
don't know
can and
will kill
you. Shayna
lost her
fight to
melanoma
on September
1st.1998
at 1:04
am at her
home with
her daughter
sleeping
soundly
not really
"knowing"
Mommy was
gone for
always.
Shayna fought
hard but
it (melanoma)
was to deadly
to beat,
she left
her little
sister(14)
and twin
brothers(6)
along with
her little
girl(4)
and a devastated
Mom. Our
lives here
will never
be the same
without
Shayna,
but not
a day or
night goes
by without
us talking
and thinking
about her.
A mom is
NEVER ready
to lose
a child,
it changes
you forever,
it is so
unnatural
to outlive
your "baby"
but because
I have the
blessings
of my other
children
I will survive.
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I
am submitting
this photo
of my wife,
Kathy Salling.
The photo
was taken
in 1960,
the year
we married
and the
year she
became a
Registered
Nurse (RN).
Kathy was
born Sept.
3, 1939
and lost
her battle
with Melanoma
on Mar.
28, 2000.
In between
we had 4
kids and
7 grandkids.
Kathy's
primary
tumor appeared
in 1976
and after
surgery
and an experimental
immuno therapy
program
she was
pronounced
"cured."
In 1998
she suffered
a recurrence
in the form
of skin
mets and
sub-Qs on
her upper
body plus
liver mets.
After 5
cycles of
Bio/Chemo
(Legha Protocol)
cleared
the liver
mets, we
started
Varidose
Vaccine
at JWCI
( Dr. Glenn
Tisman.)
She subsequently
developed
mets to
the bone
( a titanium
rod replaced
the humerus
in her left
arm), brain
mets requiring
radiation,
stomach
lining and
small intestine
mets plus
numerous
sub-Qs returned.
She also
had mets
in her abdominal
cavity outside
her colon.
During her
2 year fight
after the
recurrence,
she had
about 40
tumors surgically
removed
but in the
end we just
couldn't
remove them
all. It
seems she
had mets
everywhere
in her body
except the
lungs.
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Sally
& Dickey
Stilwell
This is
a photo
of me and
my husband,
Dickey,
who lost
his battle
with Melanoma
at the age
of 29. We
were together
in total
just over
3 years
but had
only been
married
5 months.
There aren't
words to
describe
how Dickey
changed
my life.
I now know
the meaning
of true
love. So
now he is
my guardian
angel and
I only hope
that he
can take
care of
me from
the heaven's
above. |
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This
is Beth
Brawn (on
right) and
her sister,
Brenda L.
Cervi, March
21, 1963
- March
30, 2000.
Original
mm removed
from back
in 1996,
lymph nodes
were clear.
New spot
(unrelated
to first
according
to Dr.)
appeared
in October
1999. Removal
and biopsy
done in
Nov 99.
CT scan
done in
December
as soon
as biopsy
came back
and MM had
already
spread to
lungs, liver
and brain.
She refused
all treatments
as they
gave her
2 months
to live.
She opted
for better
quality
of life
rather then
effects
of some
of the treatments
she was
given the
choice of.
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Name:
Paul Schmidt
Born:
2/10/1961
Family:
Husband
and father
of four.
Diagnosed
stage 1:
June 1999
Diagnosed
stage 4:
Jan 2000
Died:
June 25,
2000 |
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This
is Cindy
Blanc.
The MPIP
is dedicated
to the continued
struggle
against
the disease
which took
Cindy's
life but
could not
conquer
her spirit.
We have
a memorial
page
on the MPIP
in Cindy's
honor.
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