World Aids Day focuses on
what you can do to combat the disease
Alex Paul/Democrat-Herald Kalee Garland, who has was
born with HIV/AIDS, and
Bob Bowers, who has lived
with the disease for 23
years, spoke Thursday at
Linn-Benton Community College
during World Aids Day.
At first glance,
dressed in black, with tattoos running up
and down both arms, and a skull-like silver
belt buckle,
Bob Bowers is an imposing figure.
That is until he starts to to talk about
living with HIV/AIDS for 23 years. Tears
start flowing and the tough guy persona
melts away.
The tears, he says, aren’t
about his life. They are for the millions
of people around the world who have died
from the disease or its complications. Many
of them were his friends.
Thursday,
Bowers and
Kalee Garland, 21,
who was born with HIV which turned into
“full blown AIDS” when she was just 7 years
old, spoke at Linn-Benton Community College
during World AIDS day. Their visit was sponsored
by the college’s Student Life and Leadership
office.
“We have lost 25 million brothers and sisters
so far,” Bowers said. “Yet, this is a preventable
disease.”
An Oregon native,
Bowers said
AIDS is an
extension of social issues including extreme
poverty, racism, and physical and mental
abuse. Bowers lost his mother when he was
10 and never knew a real father figure.
He went looking for love and often in the
wrong places. At 19, he was living a fast
life of drugs and unprotected sex in
Los
Angeles.
At 21, he was diagnosed with what was then
called Gay Related Immune Deficiency. He
said
AIDS no longer garners front page headlines
because people believe there are “drug cocktails”
that have defeated the disease.
“Those cocktails are actually chemotherapeutic
medications,” Bowers said. “They are powerful,
they make you sick. It isn’t pleasant and
they cost thousands of dollars per month.”
They also don’t work for everyone with
AIDS.
Bowers said
HIV/AIDS does not discriminate
by social class. It is not a homosexual
disease.
“It’s not who you are, it’s what you do,”
Bowers said. “If you want to shoot dope,
don’t share needles. If you want to have
sex, use a condom.”
Garland is a San Diego, Calif. native who
learned about her disease after a teacher
thought she had been abused at home. Bruises
were outward signs of her disease.
“I love my life. I was supposed to die at
age 7,”
Garland said. “I am not a survivor;
I am a fighter.”
Garland has endured the inability to fight
off infections caused by the disease, including
battling meningitis four times and having
68 spinal taps during her many stays in
hospitals. She has also suffered from the
ignorance of others, including teachers,
when it comes to
HIV/AIDS.
Garland is engaged to be married and says
her fiance does not have
HIV/AIDS.
Bowers
was married for 11 years and his wife did
not have HIV/AIDS, nor does she now. He
has been in a 3-year relationship with a
woman who does not have HIV/AIDS.
Protection,
Bowers and Garland agree, is
mandatory, not just because of
AIDS, but
also to protect yourself from more than
two dozen sexually transmitted diseases.
The two encouraged the audience to be involved
by becoming educated, getting tested, volunteering
with programs such as the Valley Aids Information
Network and supporting legislation to find
a cure for the disease.
To learn more about AIDS/HIV, visit Bowers’
website,
www.hivictorious.org
Bob
featured on
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in conjunction with
the ACT V AIDS Ride
in Madison, Wisconsin.
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and Jay at
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Student, born
with HIV, gives
talk
By THERESA HOGUE
Gazette-Times reporter
When Kalee Garland
was 7 years old,
her teacher called
Child Protective
Services because
she saw Garland
covered in bruises
and feared the worst.
But the worst was
not exactly what
her teacher had
expected.
Garland
was not being hurt
by her mother. She
was battling AIDS.
The diagnosis was
unexpected to everyone,
especially
Garland’s
mother, who until
that moment hadn’t
realized that she
had been infected
with HIV by a boyfriend
long before
Garland
was born.
Garland was born
with the virus,
and by age 7 she
had full-blown AIDS
— and a very bleak
prognosis. Doctors
didn’t expect her
to live longer than
six months.
But now, at age
21, Garland is a
university student
in San Diego with
a fiancé and exciting
plans for her future.
For the past week,
she’s been traveling
around Oregon with
her friend,
Bob
Bowers of HIVictorious,
talking about
her
life with AIDS to
school kids, community
groups and whoever
else will listen.
Bowers is the nephew
of Corvallis resident
David Williams.
The Corvallis Elks,
of which Williams
is a member, has
hosted Bowers and
Garland’s appearances.
They will speak
at area high schools,
Community Outreach
Inc. and other locations,
including a keynote
address at Linn
Benton Community
College. It is scheduled
for Thursday as
part of International
World AIDS Day.
“I saw
Bob and totally
connected with him
... He had
tattoos,
and he reminded
me of Henry Rollins,”
she said, referring
to the famed — and
heavily inked —
author and former
lead singer of the
punk group Black
Flag.
When Bowers started
talking about his
own experiences
as an
HIV-positive
adult, he also shared
his mission through
HIVictorious, which
is to educate and
demystify the world
of
AIDS/HIV. He
asked Garland if
she might be interested
in traveling to
Oregon in the fall
to help him share
that message.
“I jumped at the
chance,” Garland
said. She’s already
done multiple
presentations
on AIDS through
the University of
California at San
Diego, and feels
it’s important to
help people understand
the truth about
HIV.
“People with HIV
and AIDS are just
human,” she said.
“We’re not running
around infecting
people. You have
to engage in a behavior
that’s high risk
to contract it.”
Garland survived
her early years
with AIDS by taking
a combination of
highly toxic
AIDS
medications, but
by the age of 10,
she began refusing
treatment because
the side effects
were too great.
For a time, she
participated in
an
experimental
treatment where
she was infused
with a donor’s white
blood cells, but
the experiment was
discontinued, so
throughout her teen
years, Garland went
untreated.
That turned out
to be a mistake.
Garland contracted
meningitis four
times between the
ages of 16 and 18,
and the final time,
it was so severe
that doctors had
to implant a shunt
through her head
that drained into
her stomach. She
decided it was time
to get back on her
medications.
Today, her viral
load is now undetectable,
and her T-cell count
is at 80, where
it used to be in
the teens. T-cells
are a kind of white
blood cell that
help fight off illness.
A healthy human
usually has a count
of 600 to 1,200.
She doesn’t know
what the future
holds, but says
any prognosis she
receives will be
taken with a dash
of skepticism. After
all, doctors didn’t
expect her to survive
past age 8 anyway.
And while she wants
to make sure other
young people know
that people with
AIDS and HIV shouldn’t
be feared, she wants
to impress upon
them that the disease
itself is nothing
to take casually.
“You’re not invincible,”
she said.
Speaker uses
his story to fight
AIDS: Bob Bowers
got it from a needle
23 years ago
By THERESA HOGUE
Gazette-Times reporter
When heavily tattooed Bob Bowers shows up at a high school and announces that
his nickname is Pirate, he definitely gets attention from the teens he’s talking
to. He knows that his tough-guy appearance wins him respect that a middle-aged
guy in a suit with a Powerpoint presentation won’t earn.
But the 44-year-old Bowers needs every ounce of attention he can get, because
he’s got a tough message to get out. Bowers has been HIV-positive for 23 years,
and has been trying to educate Americans about HIV/AIDS ever since his own
diagnosis in the early 1980s.
On Saturday, he’ll come back to his home state to speak in Corvallis at an
HIV/AIDS awareness fund-raiser dinner.
Bowers, who graduated from North Bend High School, was 21 years old and living a
hard-partying life in Los Angeles when he started feeling sick. His lymph nodes
were swollen and he was fighting off fatigue.
“I was doing drugs at the time, so it was hard to tell the difference between
being high or being sick,” he said.
Bowers, who had used intravenous drugs, had heard of AIDS but never considered
that he was at risk. A doctor’s diagnosis told him differently.
“I was clueless,” Bowers said. His doctor told him to prepare for the worst. At
the time, the diagnosis was a death sentence. But fate, and medication, kept him
alive while more than 40 of his friends died.
In 1999, when a close friend died from AIDS-related illness, it was “the last
straw,” Bowers said. He began dedicating himself to public speaking.
“My biggest gift is not eloquence and big words,” he said. “I’m extremely
passionate. I live it, I breathe it.”
Bowers has formed a non-profit organization called HIVictorious, and spends most
of his time traveling. His presentation at the Corvallis HIV/AIDS Awareness
dinner is the first time he’s had a chance to speak in his home state.
Bowers has been invited to speak by the Corvallis Elks Lodge, where his uncle,
David Williams, is a member. Williams said he’s been inspired by the work his
nephew has done. He’s also found himself learning through Bowers’ experiences.
“I’ve had my eyes closed (to HIV/AIDS) for years,” Williams said. But now he’s
eager to help his nephew with his message.
As for Bowers, he feels that he has helped change lives.
“When you speak the truth you get people to a safe place.”
Taken from "The
real world of AIDS:
A snapshot of
HIV
in Madison today"
By Kelly Schlicht,
May 8, 2007
HIVictorious’
leader Bowers looks the part of a champion; his well-toned, muscular frame does
not bear the characteristically gaunt, emaciated look of someone undergoing AIDS
treatment. His outlook on life mirrors his outward appearance. Through highs and
lows, Bowers has battled HIV/AIDS since 1983. He educates others on the
still-present danger of the disease, stressing that “the H in HIV stands for
human.”
He describes the shock of many audiences when they realize the scheduled AIDS
speaker is a reasonably healthy-looking straight man as evidence that stigmas
still exist in society. This stigma, he explains, makes many other people living
with HIV/AIDS in smaller cities reluctant to speak out, in fear of being called
gay or treated like a leper. However, Bowers quickly points out that the gay
community was the first group to fully accept him, “like a family,” despite his
HIV status.
Bowers fears that youth apathy toward AIDS not only proliferates the shameful
stigmas surrounding the disease but also increases the spread of infection.
“They’re hearing it more from textbooks not from the media, not from the horse’s
mouth,” Bowers says in regards to current HIV/AIDS education. “They have no clue
the true reality of the course of the disease and what it’s capable of.”
AIDS speaker:
Students 'have a
place'
Bowers will touch
on living with and
battling HIV
By Lindsay Fiori
of the Marquette
Tribune
Twenty-three
years is longer
than most of us
have been alive,
but that is how
long Bob Bowers
has been living
with HIV. In that
time, he has gained
much knowledge and
experience on the
disease and will
be sharing then
with the Marquette
community tonight
at 7:30 p.m. in
the Weasler Auditorium
as the
keynote speaker
for AIDS Awareness
Week.
"We
hope he can educate
more people and
get them involved
in the
fight against
AIDS because it
affects us all,"
said Aarti Bhatt,
chair of Watumishi
and a junior in
the College of Health
Sciences. "It's
a big deal. It's
not just a medical
issue, but a social
issue too."
Watumishi,
the student organization
dedicated to promoting
AIDS education and
advocacy, heard
about Bowers from
the AIDS Resource
Center of Wisconsin,
according to Bhatt.
Watumishi
contacted Bowers,
43, of
Madison,
who said he was
more than willing
to be a part of AIDS Awareness Week.
"It's
really important,
especially on the
college level, for
people to understand
where they have
a place in this
fight whether it's
in their jobs or
in student groups,"
Bowers said. "There
is work you can
do right now to
have a direct impact."
In
his talk, Bowers
will address issues
such as politics,
funding and involvement
to show how the
face of AIDS has
changed over time.
"I
want to address
the political climate
in the fight against
AIDS, which has
to do with everything
from funding to
issues addressing
law makers and how
important that is
in the overall fight,"
he said.
Bowers
will also speak
about his personal
experiences in
battling
HIV. At age 21,
Bowers said he was
living on the streets
of Los Angeles addicted
to speed. He shared
a needle only once,
but that was enough.
A doctor diagnosed
him with AIDS-related
complex in 1985.
AIDS-related complex
is today called
HIV symptomatic,
which means the
patient has HIV
and certain
symptoms,
Bowers said.
"The
first case of AIDS
reported in the
United States was
in 1981, so there
was little knowledge
at the time I got
infected," he said.
"It was very frightening.
I had seen people
I knew drop dead
from it because
they had no medications
whatsoever."
Bowers
said he began speaking
in 1986 at a
high
school near Hollywood.
He spoke off and
on until 1999 when
he dove into speaking
fulltime after the
AIDS-related death
of one of his closest
friends.
"He
was one of my best
friends in the world,"
Bowers said. "He
supported me all
along. His death
was the last straw."
Julie
Pintar, a senior
in the College of
Nursing, met Bowers
while working at
Camp Heartland
last
summer.
"I
feel lucky that
I got to work with
him and become friends
with him," she said.
"He is an amazing
person who has dedicated
his life to the
cause."
Pintar
said she believes
Marquette will benefit
from having Bowers
speak because many
people don't think
it could ever happen
to them. Hopefully,
he will inspire
more people to take
steps to remain
negative and to
get tested, she
said.
"My
main goal is to
empower people with
truth and some of
the realities of
sexuality and STDs
in general," Bowers
said. "I try to
present that in
a very real manner
so people can understand,
empower themselves
and decide what
they want to do."
Instead
of letting HIV bring
him down, Bowers
has used it to positively
change his life,
according to Pintar.
"I
am not defined by
HIV any longer,"
he said. "I have
as much a chance
for life as you
do."
Bob
Bowers stands at
the front of a room
full of college
students. Every
eye is fixed on
his enormous arms,
trying to read them.
His body is covered
in dozens of tattoos.
Flaming skulls and
spider webs twist
around his wrists,
up to his shoulders
and across his chest.
There are too many
to count. His friends
call him "Pirate."
The
ink on his body
was injected with
a small
needle that
moves up and down
at a rate of several
hundred vibrations
per minute. It penetrates
the skin only by
one millimeter but
can leave grown
men in tears.
It
only takes one look
to know Bob has
felt some pain in
his life. His
tattoos
tell a story. Somewhere
in the living mural
is a beginning and
an end. Bob goes
back to the parlor
year after year
adding to his body
new cryptic images.
"I
shared a needle
with my girlfriend
one time," Bob said.
In 1983 Bob and
his girlfriend wanted
to get high and
so they shot up
some crystal
meth.
It changed Bob's
life forever. Two
years later he was
diagnosed with the
AIDS virus.
One
more tattoo means
one more year of
survival. He celebrated
20 years with a
tattoo of a blue
bird. AIDS is trying
to kill him but
Bob is fighting
back. I don't want
sympathy and I don't
want people to perceive
me as a victim,
he said.
Bob
will do anything
to survive the disease.
He lives one day,
one dose at a time.
Drugs have turned
his automatic death
sentence into a
painful but manageable
disease. He estimates
that his prescriptions
cost about $3,000
per month.
"I'm
a walking testament
to
modern medicine,"
Bob said. He opened
a medicine bottle
and poured a heap
of pills into his
hand-the "morning
dose." He tried
to pop the handful
into his mouth all
at once but couldn't
do it, there were
too many.
He
passed around a
hypodermic needle
for everyone in
the
classroom to
see. The needle
is more than an
inch long. His body
stopped producing
testosterone a long
time ago so he will
inject some of the
hormone into his
thigh. "That's a
lot of meat to go
through!" he jokes.
He
has a big smile
on his face. To
him, this all feels
like a miracle.
The drugs keep him
alive.
Years
ago he was being
injected with mice
cells just to experiment
for
potential treatments.
Some of the drugs
he was once prescribed
made him so sick
he couldn't eat
a house salad without
vomiting.
In
1989 he started
what was known as
"monotherapy," or
AZT. It was the
first drug approved
for the
treatment
of HIV. The drug
stops the virus
from spreading to
new cells but does
nothing for cells
already infected.
To Bob the medication
is like a Band-Aid
over a gaping wound.
"There is a multitude
of ways they attack
it but they're just
slowing it down,"
he said.
Bob
used monotherapy
for seven years
until the FDA approved
new drugs called
protease inhibitors
in 1995. Bob started
taking the combination
therapy, also known
as the "cocktail."
According to the
Center for AIDS
Information and
Advocacy, combination
therapy "radically
altered the course
of HIV disease."
But
the
cocktail made
Bob feel sicker
than ever. He began
to wonder what chemotherapy
must feel like.
"They wear on your
body and your mind.
Then try going to
work, shitting yourself,
vomiting yourself."
The side effects
of the medications
got worse. He stood
in his shower for
hours vomiting everyday.
"We
kept hope for a
new drug." One pill
made him numb from
his mouth to his
belly, like a shot
of Novocain from
the dentist's office.
One pill put him
in a wheelchair.
He didn't care about
the
side effects;
Bob was surviving
to see tomorrow.
He
kept score as the
"cocktail" had a
great impact on
the
AIDS community.
Deaths attributed
to the disease dropped
drastically wherever
combination treatment
was available. In
1997, for the first
time since 1990,
AIDS dropped from
8th to 14th place
as a leading cause
for death in the
United States, according
to the national
Centers for Disease
Control and Prevention.
In 1999 the National
Institute of Allergy
and Infectious Diseases
announced they had
finally traced the
origin of AIDS to
a group of subspecies
of chimpanzees in
Africa. Bob had
been living with
the disease for
16 years already.
Bob
can look back and
remember everything
that has happened.
He can remember
his friends dying.
He can remember
all his girlfriends
and his 11-year
marriage. While
living with AIDS,
Bob owned a gym
in Los Angeles and
he can remember
that, too. He looks
back and thinks
about his mother
dying of breast
cancer when she
was 35 years old.
"I
never thought I
would see 35, no
way," he said. Bob
is now 43. "It's
a miracle." Most
of all, his dreams
have kept Bob going.
"Every dream I ever
had even before
I had AIDS has come
true," he said.
When
Bob was 21 years
old he went to the
doctor. He thought
he had simply been
partying too much.
Swollen glands,
fever and fatigue
called for a blood
test and the results
came soon after.
That
was how it all started:
the treatments,
medications,
blood
tests and
injections.
The insults, anger
and confusion, they
all started, too.
In 1985, the only
thing spreading
faster than AIDS
were the
misconceptions
about the virus.
HIV
and AIDS were called
"gay diseases" and
people believed
they could be spread
from sharing water
fountains or kissing.
Bob was afraid to
share a soda with
anyone. Some of
the doctors refused
to enter the room
because they were
afraid. Other doctors
wore protective
gloves and masks
just to talk to
Bob.
"People
have no clue as
to the passion,
the anger I have
that today we know
exactly
how AIDS
is spread," he said.
Bob is on an endless
pursuit to spread
awareness about
the disease.
He
started fighting
AIDS in his body.
Now he is fighting
it from spreading
to other people.
He is fighting at
home, at elementary
schools, rehab centers,
prisons and even
in the nation's
capitol. He flew
to Washington D.C.
to lobby for cheaper
drug prices because
people with AIDS
are dying on waiting
lists in the United
States. Bob is fighting
to live and he is
fighting for everyone.
"People
really get it when
you tell it real,"
he said. "I try
to put into context
what it is like
to
live with HIV
and AIDS." To Bob,
spreading the
truth
about HIV and AIDS
is as important
as finding a cure.
"If you think about
the
homophobia,
the
job discrimination,
the ignorance involved.
Throw in
compassion
and everything changes,"
he said.
Bob
is living proof
that the human spirit
can
survive against
all odds. "I don't
have to tell you
that we all have
our own shit to
deal with, mine
just happens to
be AIDS," he said.
People
ask Bob how he got
here and he tells
them it is a combination
of everything. Its
more than just the
drugs, they are
far from a cure;
more than his friends,
many of them have
died; more than
just his tough childhood,
he is a grown man
now. "None of those
things slowed me
down and I'm not
about to let
HIV/AIDS
slow me down," he
said.
You can read more
about Bob A.ka.
Da Pirate and view
more news and stories
here:
"IN DA NEWS"
When
I first met
Bob a little more
than a year ago I was amazed
at how mentally strong he was.
Bob was the first person I had
ever met, that I knew of, that
was HIV positive. His
attitude on life really made
me think twice about little
things that I use to dwell on
daily.
His passion and commitment to
educating others comes across
in his website.
Bob knows
first hand the facts about the
disease. He has dedicated
a lot of time and effort to
hopefully changing someone else's
life for the better through
his website.
Through my job I use to only
refer to
Bob as that guy I did
a story on about his life and
his
fight against HIV.
Now a year later, I can call
him my friend.