Botswana’s strategy
to fight AIDS shows most promise
Alexandra Zavis
GABORONE, Botswana — Catherine had already buried two sisters
because of AIDS when she was diagnosed with the dreaded disease.
After doctors broke the news, she stopped eating. “I thought
that was the end of my life,” she said.
Three years later, the bubbly young woman in a floppy sun hat is
sharing her marriage plans with fellow patients as they wait for
medicines that are bringing new life to one of the countries worst-hit
by AIDS.
In 2002, Botswana became the first African country to offer free
treatment to all who needed it. With more than a third of adults
infected, many doubted it could fulfill the promise.
But the largely desert nation now has half the estimated 110,000
people in immediate need on life-prolonging anti-retroviral medicines,
showing that treatment is possible on the world’s poorest
continent.
“If HIV was left to take its course, this country would be
literally destroyed both economically and socially,” said
Segolame Ramotlhwa, operations manager for the national treatment
program dubbed Masa, or New Dawn. “Not treating is not an
option.”
AIDS has ripped through sub-Saharan Africa, killing 2.4 million
people this year alone, according to U.N. figures. In Botswana,
life expectancy has plunged to 39 years, AIDS patients overwhelm
hospital wards and funeral homes offer 24-hour service.
Medicines that have turned the disease into a manageable chronic
condition in wealthier nations remain out of reach for most in Africa,
home to more than 60 percent of the estimated 40 million people
globally infected with HIV, the virus that causes AIDS. The cost
is prohibitive and few countries have the infrastructure to dispense
them on a large scale.
Botswana, which is slightly smaller than Texas, has the advantage
of a small population of 1.7 million. Diamonds have made the country
comparatively wealthy, and most people live within five miles of
a clinic.
But Health Minister Sheila Tlou says the most important difference
is Botswana’s commitment to fight the pandemic. Its pledge
to provide treatment drew critical support from donors such as the
Bill & Melinda Gates Foundation and major pharmaceutical companies,
but the government is paying more than 90 percent of the cost itself.
“African countries say they have no money, but if a war is
brewing, in the blink of an eye, that money would be there,”
Tlou said. “So you need that commitment. Instead of spending
money on Cadillacs, put money where the people are.”
The massive treatment effort is straining limited resources, though.
Development funds have been diverted to health, which accounts for
a quarter of the national budget.
Some 52,000 patients are being treated free at 32 sites nationwide,
while 7,300 others obtain their medicines privately.
The results are visible. Patients who once arrived in wheelchairs
and on stretchers now walk to clinics. Others believed to be on
their deathbeds are back at work.
The treatment is complicated, and missed doses can cause resistance
to build. But churches and other groups help ensure patients have
a “buddy” to support them, and doctors say the rate
of adherence tops 85 percent.
The availability of treatment also is encouraging more people to
get tested on a continent where stigma remains high.
Catherine was rail-thin and covered in sores, but she waited two
years to find out if she had the virus that killed her siblings.
“That time there was no treatment, so I didn’t want
to check,” said the mother of two, still too ashamed to give
her last name. “There were many funerals because of this disease.”
Authorities estimate that up to 35 percent of those infected here
now know their status, far higher than in other countries.
Understanding of the disease also is spreading. Patients once locked
in silence now chat openly with each other in waiting rooms, swapping
details of their CD4 counts and viral loads.
But fear, ignorance and denial still keep many away until it is
too late. Catherine’s fiance reminds her to take her pills
but refuses to be tested himself.
When Cynthia Leshoma was first given anti-retrovirals, she was so
depressed she swallowed all the medicine at once and washed it down
with cleaning fluid.
When she emerged from a coma three days later, she decided to turn
her life around. She quit drinking, joined a support group and learned
to take her medicine. Earlier this year, she was crowned Miss HIV
Stigma Free in a beauty pageant that aims to change attitudes about
the disease.
“In Botswana, we are lucky because the government is offering
us medicine,” said Leshoma, counting out pills on a restaurant
table after her cell phone tells her it is time. “People die
because of stigma, not because of AIDS.”
Hoping to get more people on treatment, Botswana started routinely
offering HIV tests throughout the health system in 2003. Now, so
many patients agree to get tested that doctors worry whether they
will be able to keep up with demand.
(Associated Press)
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