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Warriors Page
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This
is my
husband
Steve
diagnosed
in January
of 2002.
He was
such a
beautiful
loving
man that
was genuinely
sweet.
Steve
never
had a
negative
comment
when you
asked
him how
he was
doing,
even right
after
his surgeries
he always
said he
was "doing
good".
Steve
was a
kid at
heart;
he loved
to work
on the
bikes
with our
3 boys
and go
fishing
and would
even be
caught
racing
the kids
to the
supper
table
most nights.
Steve
had his
first
WLE in
March
of 2002
with primary
on his
right
forearm.
Steve
decided
to go
with the
Interferon
and so
started
in June
of 2002
and we
stopped
in October
of 2002
when Steve
started
having
seizures,
it was
then I
knew that
he had
a tumor
on his
brain.
At the
end of
October
Steve
underwent
brain
surgery
to remove
as much
of the
tumor
as they
possibly
could.
On New
Years
Eve was
when we
found
out that
all of
his organs
were affected
as well,
all he
wanted
was to
see his
boys graduate.
Steve
and I
were always
a team
and even
when things
got harder
for him
he always
did his
best to
help me.
5 days
before
he past
away he
was able
to attend
our youngest
sons 6th
birthday
and for
as uncomfortable
as he
was he
told everyone,
"I'm doing
good".
That
night
Steve
asked
me to
call his
best friend
to take
him to
church
and so
I did,
when they
came back
from church
his friend
was just
in tears
and told
me that
when he
asked
Steve
how he
was doing
that morning
while
they were
in church
Steve
told him
"I'm not
doing
so well"
and from
that day
on Steve
was unable
to get
out of
bed. Monday
I had
our 2
youngest
boys taken
out of
the house
to stay
with friends,
I just
couldn't
let them
see their
Daddy
like this
and let
them say
their
goodbyes.
Tuesday
came and
Steve
was so
very restless
and every
hour on
the hour
Steve
would
shout
out "
honey
I love
you" no
matter
who was
in the
room with
us. That
Wednesday
I drove
to Minneapolis
to pick
up his
oldest
son from
the airport
and try
as I might
nothing
could
prepare
him to
see his
father
in that
condition
but when
we arrived
home Steve
knew that
he was
there
and held
out his
arms and
told him
" come
here and
give me
a hug
I love
you".
It was
then that
I told
Steve
" now
all the
boys are
home"
and he
looked
at me
with his
beautiful
blue eyes
and said,
" I love
you" and
took his
last breath
and past
away on
January
18th 2003.
I miss
him so
bad it
hurts,
but I
know that
he is
watching
over for
us and
grinning
for ear-to-ear
watching
his 3
beautiful
sons grow.
I love
you always
Steven,
Alicia
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This
is my
beautiful
sister
Jennifer.
Diagnosed
stage
III in
1998.
She had
just turned
32 when
Melanoma
took her
away from
us. I
miss her
every
day and
wish I
could
see her
beautiful
face and
talk to
her again.
I would
always
read these
memorials
and feel
so bad
for the
people
who lost
their
loved
ones and
think
not my
sister.
Never
did I
ever imagine
having
to put
her memorial
on this
page.
I always
thought
her amazing
strength
and faith
in God
would
get her
through
the battle.
That's
just what
it was
a battle.
I guess
She was
too strong
for this
earth
and God
wanted
her for
better
reasons
unknown.
That's
the only
way I
can comfort
myself
when I
have to
face the
fact that
she is
no longer
with us.
We
were close
in age
and did
many things
together.
We shared
a love
for BonJovi.
We went
to concerts
together
all the
time.
Jennifer
had a
great
passion
for life
and only
wanted
to better
herself.
She was
going
to college
and wanted
to become
a physical
therapist.
She put
everything
on hold
when this
disease
progressed
to stage
IV in
Oct 2001.
She wanted
to wait
till she
was better
to continue
doing
anything.
She needed
to focus
on beating
this disease.
She underwent
several
different
treatments
but nothing
could
tame the
beast
inside
her. Jennifer
had great
faith
in her
religion
and always
prayed
to God
and St
Pio to
save her
from this
dreadful
disease.
But on
June 10th
2003 God
took her
home.
Melanoma
stripped
my sister
of her
life and
the things
she wanted
to accomplish.
The one
thing
I know
is that
she is
most definitely
an angel
of high
rank up
in heaven.
She earned
her wings
while
on this
earth.
Jennifer
was so
courageous
and strong.
She never
complained
or asked
why me?
She lived
each day
with a
smile
on her
face and
only wanted
to live
and spend
time with
her family,
her friends
and her
golden
retriever
Maury.
I wish
I could
have my
sister
my best
friend
back to
go through
this journey
of life
with me.
I miss
her, need
her, and
love her
so much.
Jenn,
We love
you and
miss you
every
day! You
are always
in our
hearts.
Till we
meet again
my beloved
sister.
We Love
you!
Jennifer
Margaret
Toscano
4/19/71-6/10/03
Our Angel
In Heaven
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My
mom Janice
Nolin
Burke,
lost her
fight
with Melanoma
on 7-22-03.
She was
extremely
beautiful
to everyone
who knew
her.
She was
my best
friend
and I
am going
to miss
her so
bad. She
was diagnosed
in June
of 1997.
She has
had so
many operations,
chemo,
radiation,
experimental
procedures
that I
guess
her body
could
take no
more.
I am comforted
by all
of the
support
from all
my friends
and family
and also
I am thankful
to all
of you
here on
the MPIP
website.
Each and
everyone
of you
has helped
me to
understand
this cancer
better
and that
the feelings
that I
am going
through
are normal.
I will
miss her
so much.
I know
a minute
will not
go by
that I
don't
think
about
her.
Leigh
Burke
Shaughnessy
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Meet
my brother,
David Long.
His battle
with melanoma
began in
January
1999 and
ended with
a peaceful
passing
in June
2003. He
fought a
courageous
battle and
we were
by his side
every step
of the way.
David lived
his 41 year
life to
the fullest
- exploring
the rivers
and oceans,
the stars
and the
planets,
expressing
himself
by painting,
woodworking,
sculpting,
writing
poetry and
songs, playing
the guitar,
and building
and riding
Harley Davidson
motorcycles.
Instead
of focusing
on building
bank accounts
and developing
a professional
career,
David focused
his energy
on being
a good friend
to everyone
who knew
him and
exploring
nature's
intricacies
with a childlike
wonder.
I will miss
you bro,
and I look
forward
to being
reunited
with you
when my
time comes.
Until then,
I will live
my life
to the fullest
because
I know that
is what
you would
want me
to do. |
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This
is my brother
Ronnie.
He was diagnosed
in February
1992 with
stage IV
mailignant
melanoma.
He had a
mole on
his upper
back that
had grown
and had
started
bleeding.
He had a
biopsy and
we, his
family were
told he
had less
than 1 year
to live,
he lived
for 9 months,
without
ever knowing
how bad
his diagnosis
was, his
Doctor suggested
to us that
we not tell
him he was
going to
die for
fear he
would just
give up.
He was so
brave throughout
that 9 months,
he went
through
many rounds
of chemo
and radiation
to the point
his upper
body looked
charred.
My husband
Bryan and
he were
like brothers,
Bryan him
to most
of his treatments…Hospice
was called
in so I
knew it
wouldn’t
be long
before we
had to say
goodbye.
On Thursday
night, Oct.
15th, 1992,
5 days from
his 36th
birthday,
he went
home to
be with
The Lord.
Those 9
months were
so precious
to me, to
say the
least. To
watch him
go downhill
like he
did, It
was the
hardest
thing I’ve
ever done.
We told
each other
“I love
you” often
during that
time, something
we had never
actually
said before-it
always went
without
saying.
We lost
our Dad
in 1966,
he was 9
and I was
5….I now
take comfort
in knowing
that they’re
together
again, knowing
I will join
them some
day. Until
then, rest
in peace
guy’s until
we meet
again…PJW |
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This
is the Andrews
family;
Mike, Beulah,
Amy, Jenny
and Aaron
(this picture
was taken
a decade
ago!) Dad
was diagnosed
with MM
where the
"sun doesn't
shine!"
in July
2002 (patnet
Mike). My
Dad is most
remembered
for his
funny sayings,
teasing,
and for
the love
he had for
his family.
Mom and
Dad were
high school
sweethearts
and were
married
over 35
years. They
were still
very much
in love.
Dad got
to meet
Jesus on
May 6, 2003
at 12:29
a.m., he
was 53 years
old. We
will all
miss him
terribly....his
wife, children,
parents,
sister,
his seven
grandchildren
(they call
him Popie)
and many,
many more.
One of the
sayings
Dad is famous
for is "No
matter where
you're at,
there ya
are!" and
we know
exactly
where he
is now.
See you
in heaven
Daddy!
AmyIN
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This
is a picture
of my sister
Lynda...patnet
under Lynda.
She was
a wonderful
lady. Lynda
was first
diagnosed
with stage
III Melanoma
in 1994.
Following
surgery,
she was
NED until
the fall
of 2000....she
lost her
battle in
2001. She
was loved
by many...she
was a wonderful
mother and
wife...and
my big sister...and
I loved
her very
much. She
was 8 years
older and
was also
kinda a
second mom
figure to
me. I miss
her greatly. |
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Russell
E. Chirico
March 12,
1969 - November
11, 2002
"My
Lil'Ogar,
Forever
Love"
are the
words
inscribed
on the
inside
of my
husband's
wedding
band;
let me
explain.
SHREK
was one
of our
favorite
fairytale
movies;
we must
have watched
it 1000
times,
if not
more.
SHREK
himself
was truly
nothing
more than
a gentle
giant
as was
my husband.
As you
can see
by Russ's
picture,
there
was nothing
"lil"
about
him. Standing
6'3, 4%
bodyfat,
and 235
lbs, he
was my
Prince
Charming
(my lil'Ogar).
Our story
is one
of a fairytale
drenched
with romance
that met
up with
a deadly
dragon
nnamed
Melanoma
and ended
too soon.
We were
married
April
13th of
2002 and
diagnosed
one week
after
the honeymoon.
My husband
danced
into Heaven
at the
tender
age of
33 only
6 months
after
we were
married.
Russ was
a husband,
brother,
son, friend,
a protector,
he was
TRUE.
He loved
life and
lived
it to
the fullest;
always
sharing
laughter
with family,
friends,
and Bosco,
our Jack
Russell
that went
everywhere
with "his
daddy".
My husband
had such
a confidence
about
himself.
He could
walk into
a room
and just
his presence
would
demand
your utmost
attention.
Not only
did he
have an
abundance
of physical
strength,
but inner
strength
as well.
Melanoma
may have
attacked
his body,
but it
couldn't
attack
his soul.
His faith
was steadfast
and strong;
me moved
mountains
with it
and is
continuing
to do
so today.
He never
met a
stranger
and created
instant
friendships
that would
last a
lifetime.
His beautiful
smile
could
tame a
tiger,
and 1
wink of
his crystal
blue eyes
would
melt your
soul.
They always
melted
mine!
He was
bold and
sensitive,
always
speaking
his mind
and yet
not afraid
to share
his true
feelings.
my husband
was REAL.
Here is
a little
info about
us. We
left each
other
love notes
in the
driveway
written
in sidewalk
chalk
and hid
little
cards
all over
the house
with "sweet-heart"
notes
on them.
Every
Friday
night
I would
proclaim
"I'll
cook you
breakfast
in the
morning!",
and every
Saturday
morning
I would
awake
to the
smell
of fresh
brewed
coffee.
Strangers
would
walk up
to us
enjoyed
working
out together
in the
gym, but
most of
the time
just ended
up giggling
rather
than exercising.
Russ drank
red wine
to impress
me, and
only told
me he
hated
it after
we were
married.
He proposed
to me
at the
end of
a candlelit
trail
strewn
with rosebuds.
One month
after
he died,
I found
the paper
where
he had
practiced
memorizing
what he
wanted
to say
in the
proposal,
it was
perfect!
I will
forever
love my
husband.
On the
evening
of November
11th,
I softly
held his
head as
he quietly
danced
into the
Heavens
to join
his older
brother
and sister,
Tim and
Janine.
Heaven
is a place
that has
become
so very
real to
me. my
husband
is there.
I patiently
await
the day
God calls
on me,
and my
husband
will embrace
me at
the gates
as we
dance
through
eternity
together
in our
Fathers
Kingdom.
ETERNITY!
I love
him and
miss him
fiercly.
Camie
Chirico
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Dann,
age 54,
the love
of my
life and
my husband
for 30
years,
went home
to Heaven
on November
11, 2002.
We were
married
when he
was 23
and I
was 18.
He
fought
MM valiantly,
and through
the whole
battle
we believed
that God
makes
no mistakes
and that
He is
good all
the time,
not just
when things
are going
our way.
That still
holds
true for
me.
God
gave me
a very
special
moment
in the
hospital
two days
before
Dann left.
These
were five
friends
and myself
standing
around
his bedside,
and he
took off
his oxygen
mask,
looked
straight
at me
and said,
"I will
love you
forever
and ever
and ever."
I was
so thankful
for his
words
and that
he chose
to say
it when
there
were people
in the
room with
us. There
were plenty
of times
we were
alone
that he
could
have said
it. But
I think
he wanted
everyone
to know
how much
he loved
me. I
know that
not only
I, but
also those
other
five people,
shall
never
forget
this expression
of love.
I love
you, Dann,
and because
of our
faith
in Christ,
I know
I also
shall
be with
you again
when I
am called
home.
Your
loving
wife,
Dircy
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This
is a picture
of the
love of
my life,
my husband
and soulmate,
Dave Weeks.
He had
also a
great
love affair
with the
game of
golf besides
being
president
of his
own corporation.
He was
first
diagnosed
with melanoma
in January
of 1997
with a
rare case
of malignant
melanoma
under
his right
thumbnail.
By the
end of
January,
1997 he
had had
surgery
to amputate
the majority
of his
right
thumb.
By the
beginning
of February
he had
been to
see the
oncologist
and started
regular
appointments
every
3 months.
They advised
just as
a precaution
to try
interferon
but it
was such
an abnormally
high dose
that he
had to
quit.
There
is much
to be
said for
the quality
of life.
It was
his decision
as it
was his
life.
He had
so many
surgeries
I lost
track.
This was
minor
compared
to the
last month
of his
life.
In July
of 2002,
he started
having
great
stomach
problems
and finally
his family
practitioner
admitted
he could
go no
further.
We went
to the
stomach
specialist
who immediately
set up
a ct scan
within
3 days.
The day
of the
scan,
we were
told to
go directly
across
the street
and be
admitted
to the
hospital.
I was
told he
had some
sort of
obstruction
in the
small
bowel.
When they
operated,
they told
me afterwards
that they
did a
resection
to solve
that problem
but the
larger
part of
this is
that there
were nodules
everywhere
and that
it was
very advanced.
It would
be very
quick.
He was
in the
hospital
for 10
days knowing
his outcome.
I don't
know how
he did
it. He
came home
on 8-2-02
and died
on 8-20-02
at home.
He was
60 years
old. I
didn't
want to
make this
sound
like a
medical
journal
because
there
was so
much more
to him
than the
melanoma.
He had
a great
sense
of humor
and very
positive
attitude
about
all the
tests
he had
to have.
He never
complained
once.
I believe
to the
bottom
of my
soul that
he knew
all of
this deep
inside.
We had
just moved
into a
brand
new house
and I
think
under
normal
circumstances
I would
have gotten
more resistance
from him
but I
think
this was
his way
of making
sure I
was closer
to my
family.
I'll
love you
forever,
Honey.
Love,
Kathy
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A
picture
of John
and myself.
John passed
away on
February
22, 2003.
He was a
great brother
and friend.
The MPIP
Board and
the people
who use
it were
very special
to John.
Love you
John.
Jim
See
Jim's
memorial
freedive
to 116'!
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This
is my wonderful
sister Carol
"Carrie"
Cedillo.
She is pictured
here with
her husband
Keith and
their two
girls Lindsay
and Courtney.
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This picture
is of Carol
(top left),
the oldest
of six kids,
at our sisters
wedding
only 15
months before
she died.
She died
of malignant
melanoma
at the age
of 41, on
July 5,
2002 at
7:00 pm.
Carol "Carrie"
was born
and raised
in Elmhurst,
Illinois
with her
three brothers
and two
sisters.
She was
first diagnosed
with malignant
melanoma
with a mole
on her back
in 1993.
Almost 5
years to
the date
of that
diagnosis
she found
a lump on
her arm
on the same
side as
the mole
on her back.
The battle
of a lifetime
was just
beginning.
She underwent
surgery
and one
year of
interferon.
Carol fought
vigilantly
through
every severe
side effects
that this
drug could
possibly
offer. She
continued
to work
on the few
good days
she had
and stay
as involved
as possible
in her girls
lives. After
being NED
for almost
two years
she started
having hip
pain in
May of 2001.
On September
11 the bone
scan showed
"hot
spots"
of melanoma
in her left
hip and
femur bone.
She had
hip replacement
on November
1, 2001
and did
remarkably
well. Only
6 weeks
later to
be told
that it
is now in
your lungs
and liver.
She did
two rounds
of bio chemotherapy,
to no avail,
and then
some experimental
treatment.
The beast
eventually
made it
to her brain.
Carol would
try ANY
treatment;
she so desperately
wanted to
be here
for her
husband
and her
girls. Even
two weeks
before she
died, when
she was
so weak,
she was
going through
tests to
try another
brutal treatment.
She fought
so hard
even at
the end.
My
sister
had the
unending
support
of her
wonderful
husband
Keith
and her
two beautiful
girls
Lindsay
and Courtney.
They were
there
for her
day in
and day
out and
we all
admired
their
family
strength.
Carol
had so
much support
from her
family
and friends
and was
always
so appreciative
of everyone's
help.
She was
admired
and loved
by so
many with
a sense
of humor
that was
all her
own. She
left behind
words
and phrases
that family
and friends
can really
appreciate
now and
laugh
at. Our
lives
will never
be the
same without
her but
SHE WILL
NOT BE
FORGOTTEN.
Many of
her wonderful
qualities
will live
on in
her girls.
We miss
her dearly
and not
one day
goes by
that I
don't
think
of her
and wish
things
could
be different.
There
are still
so many
things
I need
to tell
her. Until
we meet
again
in eternal
life we
love you
and miss
you.
Carol
"Carrie"
Cedillo
February
13, 1961
- July
5, 2002
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In
Remembrance
of Nate's
Smile
Life
is a mixture
of sunshine
and rain,
Laughter
and pleasure,
teardrops
and pain,
All days
can't
be bright,
but it's
certainly
true,
There
was never
a cloud
the sun
didn't
shine
through
-
So just
keep on
smiling
whatever
betide
you,
And you'll
find when
you smile
your day
will be
brighter
And all
of your
burdens
will seem
so much
lighter
And nothing
on earth
can make
life more
worthwhile
Than the
sunshine
and warmth
of a beautiful
smile.
Let
not your
heart
be troubled:
Ye believe
in God,
believe
also in
me.
John 14:1
Gone
fishing
in a Beautiful
Place
See you
all soon!
Love,
Nate
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This
is a picture
of our
21-year-old
son, Allan
Dennis
Bryce,
with his
girlfriend,
Missy.
Allan
was a
CAD-CAM
engineer
who loved
Missy,
paintballing,
playing
D&D, cars,
computers,
and hanging
with his
friends.
He diagnosed
with MM
at age
17 in
August
1998 -
two months
after
graduating
from high
school.
The MM
site and
all the
lymph
nodes
under
his left
arm were
removed,
which
was pretty
tough
on this
left-hander.
He was
an the
INF/Melacine
protocol
for two
years,
during
which
time he
had no
further
mets on
any scans
and pretty
much lived
his life
like he
had always
done.
He finished
his treatment
in October
2000,
and he
and his
Mom celebrated
by getting
something
he wanted
more than
anything:
a tattoo!
He got
a tribal
symbol
and Mom
(at the
age of
45!) got
a hummingbird.
They were
both thrilled.
Our happiness
turned
out to
be short-lived,
however.
His first
set of
scans
three
months
after
completing
INF treatment
showed
lung mets,
and then
six months
later,
brain
mets.
He underwent
gamma
knife
surgery
and seemed
to do
well for
several
weeks.
However,
he suffered
a brain
bleed
and was
totally
paralyzed
on his
left side.
After
only two
and a
half weeks
in Rehab,
however,
his persistence,
courage
and hard
work resulted
in his
ability
to walk
again
with assistance.
We were
able to
bring
him home,
but our
happiness
was short
lived.
Four days
after
bringing
him home,
he suffered
another
brain
bleed
and was
brought
back to
the hospital.
From
the day
he was
diagnosed
up until
this second
bleed,
Allan
never
felt sorry
for himself,
or moaned,
or said
"why me?".
He took
every
bit of
bad news
with a
grain
of salt
and a
"So what?
Let's
just take
care of
it" attitude.
When the
second
bleed
happened,
though,
he was
devastated.
It was
almost
like he
knew that
this would
be the
beginning
of the
end. After
a few
days back
in the
hospital,
Allan
started
to suffer
seizures.
We were
basically
told to
take him
home because
there
was nothing
anyone
could
do for
him any
more.
We brought
him home
on November
26th and
celebrated
his 21st
birthday
on November
29th with
all his
friends
and family
beside
him. He
slipped
into a
coma on
December
7th, and
died on
December
8th with
his loving
father
at his
side and
holding
his hand.
Allan's
courageous
spirit
and bravery
has inspired
everyone
who knew
him or
came in
contact
with him.
We are
glad he
is no
longer
in pain,
but we
all miss
him terribly.
In
addition
to his
parents,
Sharon
and Dennis,
he is
survived
by his
two brothers,
Davidson
(19) and
Stephen
(17);
grandmother
Marion
Reuther;
many aunts,
uncles,
cousins,
friends,
and the
love of
his life,
Melissa
Burdick.
Allan
Dennis
Bryce
11/29/80
- 12/8/01
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This
is my
dad Mike
Highley.
He was
a great
musician
and loved
guitars.
My dad
was first
diagnosed
with melanoma
very suddenly
in July
2001.
He bravely
battled
along
with our
entire
family
for 10
months.
He was
diagnosed
with stage
4 melanoma
with brain
mets.
We attempted
all conventional
and alternative
medicines.
Through
this whole
thing
my dad
always
had his
sense
of humor
and everyone
loved
him. He
was a
devoted
father
to me
and my
sister
Christy
and was
a very
loving
husband
to my
wonderful
mother
Pam. They
were married
for 32
years.
My dad
had many
friends
and touched
many people's
lives.
He is
missed
so much
every
day. Mike
lost his
battle
on May
13, 2002,
at Hospice
of Dayton
in Ohio.
We love
you Dad
(&
Grandpa),
Mom, Cindy
&
Christy
Brittany
&
Danielle
(his 2
granddaughters)
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This
is Daina
Kapochus,
she was
32 when
she lost
her battle
with melanoma.
In 1990,
when she
was 20 years
old, a mole
she had
since birth
started
to grow
and itch.
Many doctors,
including
her dermatologist,
had told
our family
since she
was little,
that this
mole was
fine, nothing
to worry
about. Then
came 1990
and the
WLE--malignant
melanoma.
All margins
clear, 4.5
mm depth.
She was
free of
the beast
until April
24th, 2001
when we
found it
in her liver.
85% of her
liver was
occupied
by tumors
at this
time. We
went to
NCI for
a trial
and they
turned her
down, 31
years old
and I guess
she wasn't
considered
a good success
rate. We
proceeded
to receive
treatment
at Fox Chase
Cancer Center
in Philadelphia
PA. Wonderful
oncologist--Daina
fought bravely
and with
great courage
for 18 months
after diagnosis.
She was
beautiful,
intelligent-she
was a registered
Pharmacist
in New Jersey,
and we feel
undescribable
sorrow at
having lost
her. The
cancer may
have taken
her body--but
will never
take her
spirit,
which lives
in all of
us that
remain,
and it can
never take
away our
many precious
memories
as they
are forever
locked within
our hearts.
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This
is my
wife Gayle
F. Newsom.
She died
on December
12, 2001,
she was
50 years
old. Over
eleven
years
from having
a malignant
mole removed
she was
diagnosed
with Stage
IV melanoma
Memorial
Day 2001,
in the
lung and
liver.
We celebrated
our 27th
wedding
anniversary
on December
7th with
a trip
to the
Grove
Park Inn
in Asheville,
NC. It
was the
first
time in
6 months
we had
any type
of vacation
and we
just relaxed
and enjoyed
each other.
She was
weak from
the fight
but never
lost faith
in God
and always
had hope
she would
beat this
disease.
She held
on to
the Bible
verse,
"I can
do all
things
through
Christ
who strengthens
me".
We had
the best
marriage.
She was
more than
a wife,
she was
my best
friend.
She leaves
two of
the finest
sons a
father
could
have Matthew
23 and
Wesley
21. What
a good
mother
she was.
I miss
her so
much.
I know
that she
is with
God and
at peace
in Heaven.
To all
those
who have
lost a
loved
one I
truly
hope they
believe
in Christ
and a
life beyond
the grave.
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This
is my beautiful
husband
Chris and
I on our
wedding
day in Cozumel,
Mexico in
May of 2001.
He had just
stopped
taking Interferon
after nine
months right
before the
trip because
they found
another
lump in
his neck.
He still
managed
to look
handsome
no matter
what torture
the treatments
put him
through.
He fought
this terrible
monster
for three
years and
never complained
or gave
up hope.
He wanted
to live
so badly.
He wanted
to stay
here with
the people
he loved.
I won’t
go on about
his battle
with the
beast here;
I’ll leave
that for
the PatNet
page. This
is devoted
to the wonderful
way that
Chris lived
his life.
He was the
smartest,
strongest,
kindest,
funniest,
most loving
person anyone
could ever
meet in
their life.
There isn’t
a single
person in
the world
that could
have a negative
word to
say about
Chris. Everyone
who ever
met him
fell in
love with
him. He
was such
a happy
person.
He made
other people
happy. When
we were
together
all we ever
did was
laugh. He
had the
best laugh.
He always
took care
of everyone,
his parents,
his brother
and sister,
his friends
and most
of all me.
We are all
lost with
out him.
But yet,
we know
how lucky
we were
to have
had him
in our lives
for the
time that
we did.
I never
thought
that I would
be a widow
at 27, but
the love
I have for
Chris gets
stronger
every day,
and I know
that some
people never
have a love
like that
ever. So
I am grateful
for that.
He is my
Angel and
I know that
he is watching
over me
from a better
place. And
we will
be together
again someday,
we have
to, I promised
him.
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In Loving
Memory
of
Christopher
James
Berg
April
25, 1973-
September
3, 2002
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Linda
Brandolino,
Dec. 2nd,
1951 - Dec.
1st, 2002,
was diagnosed
with melanoma
in August
of 2001.
In early
2002 scans
revealed
brain metastases.
More than
anything
Linda wanted
as much
quality
time with
family as
she could
get and
she accomplished
that, enjoying
family,
friends
and home
up to the
very end.
She lived
to see her
daughter
and son-in-law
graduate
from college,
the birth
of her first
grandchild
and she
and her
husband
celebrated
their 25th
anniversary.
Linda was
50 years
old. Her
family consists
of husband
Daniel,
children
Ellen, Justin,
Lindsay
and Adam
and grandson
Byron. She
was a preschool
teacher
and published
author.
But her
best role
was Wife
and Mom.
Her sweet
smile, compassionate
heart, uncomplaining
yet fighting
spirit have
left us
a great
legacy.
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