WHAT MONEY CAN BUY
Millions of
Africans die needlessly of disease each year. Can Bill Gates change that? BY MICHAEL 5PECTEK
Each May,
representatives from the hundred and ninety-two member nations of the World
Health Organization travel to Geneva to set policies for the coming year. The
assembly lasts a week, and the delegates often find themselves devoting as much
of that time to politics as they do to matters of life or death. This year, on
the opening day, Elena Salgado, the assembly's president, spoke bluntly about
the growing chasm between the "rich world," where people live in
health and comfort, and everywhere else. The mortality rate for infants in the
developing world is sixteen times greater than it is for infants in the West,
she told the delegates. And at least one woman dies every minute from
avoidable complications of pregnancy. Half of these deaths occur in Africa,
where hundreds of millions of children, and almost as many adults, suffer
needlessly from illnesses that most people in the West have never heard of. The
W.H.O.'s director general, Lee Jong-wook, warned that even the modest health
goals that the United Nations has established for the new millennium are
unlikely to be met. In fact, he said, in many places death rates are rising.
The most
anticipated speech—and the least diplomatic—also came on the first day: Bill
Gates addressed the assembly in his role as the founder of the world's most
powerful charity, the Bill & Melinda Gates Foundation, which he and his
wife started five years ago. The foundation's endowment is nearly twenty-nine
billion dollars— more than the gross domestic product of Tanzania—and its
principal goal is simple: to rid the world of disease, particularly the many
illnesses that are essentially ignored because they affect the world's poorest
people. "Global health is our lifelong commitment," Gates told me
that day. "Until we reduce the burden on the poor so that there is no real
gap between us and them, that will always be our priority. I am not so foolish
as to say that will happen. But that's our goal."
Gates had arrived
from Seattle just after dawn, going directly to a breakfast with health
ministers from ten African nations. It was a dismal day, rain pounded the gilt
windows of the Palais des Nations, and the sky seemed heavy enough to touch the
ground. The meeting was held in a room panelled in dark-green wood and filled
with enormous mirrors. A buffet of coffee, tea, fruit, and doughnuts had been
set out for the ministers. In front of Gates's seat, there was a Diet Coke and
a plastic cup. When Gates entered, the ministers started to clap. Gates bowed
his head, winced, and sat down. "I know your jobs are super, super
important," he told them. "And I am excited about the progress that
can be made for the health of your people." He looked tired, and seemed
slight in a mauve shirt and gray business suit. One by one, the ministers told
him their troubles.
“In Nigeria, the
health system simply doesn't work," Eyitayo Lambo, the country's health
minister, said. His counterpart from Botswana, Sheila Tlou, echoed those
thoughts. "H.I.V. and malaria have dismantled our country," she said.
"We need help just to get back to where we were." The other ministers
told similar stories. Tuberculosis, H.I.V., and malaria were rampant, as were
lymphatic filariasis, schistosomiasis, river blindness, and other, even less
well-known diseases. Each person began and ended by thanking Gates; in January,
the foundation had contributed seven hundred and fifty million dollars to the U.N.'s Global
Alliance for Vaccine and Immunization, to fight easily preventable diseases,
like diphtheria, whooping cough, and measles. (Gates had also provided funds to
vaccinate forty-two million children against hepatitis B.) The ministers
thanked Gates for helping to promote a safe, cheap drug for visceral
leishmaniasis (a malaria-like disease that affects nearly half a million people
a year), for investing in the first seemingly effective new dnig for sleeping
sickness in fifty years, and for supporting research into a vaccine for
pneumonia that could reduce African deaths by fifteen per cent.
Two days earlier, the Tribune of Geneva had run an article
headlined "THE HEALTH OF THE WORLD DEPENDS MORE ON BILL GATES THAN ON THE
WORLD HEALTH ORGANIZATION." Few of those at the assembly could disagree.
The annual budget of the W.H.O. is SI.65 billion. Since 2000, the Gates
foundation has spent six billion dollars to address health issues in the Third
World—more than nearly every contributing nation, and far more than any other
charity. This time, Gates arrived in Geneva with a check for two hundred and
fifty million dollars, to help pay for the foundation's most ambitious venture
yet: the Grand Challenges, a series of fourteen fundamental obstacles to
scientific progress which, if solved, would lead to dramatic improvements in
the health of the world. The challenges, which include goals like developing
vaccines that require no needles or refrigeration, were first issued in 2003
(along with a two-hundred-million-dollar grant), and a thousand scientists from
seventy-five countries responded with proposals.
It would be hard to overstate the impact that the Gates foundation
has had: the research programs of entire countries have been restored, and
fields that had languished for years, like tropical medicine, have once again
burst to life. In a world where a fast reaction to the threat of disease is
imperative, bureaucracies like the W.H.O.—which make decisions by consensus—are
often too cumbersome to compete at the speed of a mutating virus. Gates and his
wife need consensus only between themselves. At times, the foundation appears
as brazen as Gates has always been at Microsoft, which he started thirty years
ago, and where his combative style has made him one of the most polarizing
figures in the history of American business. "Bill and Melinda don't
believe in half measures," Richard Klausncr, the former head of the
National Cancer Institute, who is the foundation's director of global health,
told me. "Every time we get a grant proposal, we ask what fraction of the
problem will be solved by this work. Always. And if there is no answer there
is no grant." The rock star and anti-poverty evangelist Bono put it
another way: "This isn't about compassion. It's about results. It's not
some sort of well-meaning-hippie stuff. Bill Gates is not into nice sentimental
efforts or whimsical support of hopeless causes. When Bill walks into the room,
we are not expecting to have a nice warm fuzzy feeling."
Gates was scheduled to address the assembly at 3 P.M. First,
however, there were some politics to endure. While he and I sat in a conference
room on the second floor of the Palais, the delegates below were bogged down,
for the eighth straight year, in hours of bickering over whether Taiwan could
take part in the meeting. The country was not even seeking the right to
vote—just to observe. Taiwan has always been a center of influenza—including
the current epidemic of bird flu—and played a role in the rapid spread of SARS
in 2003. It is not recognized by the United Nations, however, and there was
never any chance that the request would be approved. Lofty goals are often set
in Geneva—on H.I.V., polio (an effort now heavily underwritten by the Gates
foundation), maternal health, and malaria, for example—but they are rarely
met.
Malaria, the world's most prevalent parasitic disease, kills as
many as three million people every year—almost all of whom are under five,
desperately poor, and African. In most years, more than five hundred million
cases of illness can be attributed to the disease, although exact numbers arc
difficult to assess because many people don't (or can't) seek care. It is not
unusual for a family earning less than two hundred dollars a year to spend a
quarter of its income on malaria treatment, and what they often get no longer
works. In countries like Tanzania, Mozambique, and the Gambia, no family,
village, hospital, or workplace can remain unaffected for long. Malaria
governs their lives. "It just blows my mind how little money has been
spent on malaria research," Gates told me as we were waiting for the
Taiwan debate to end. "What has prevented the rich world from attempting
this? I just keep asking myself, Do we really not care because it doesn't
affect us? Is that what it is?" Gates looked grim but went on. "Human
suffering as a result of malaria is incomparable. By many measures, it's easily
the worst thing on the planet." When Gates gets animated, his voice starts
to slide in unexpected directions, and so does he. By the end of our
conversation, he was talking in bursts and rocking back and forth in his chair.
"I refuse to accept it," he told me. "I refuse to sit there and
say, O.K., next problem, this one doesn't bother me. It does bother me.
Very much. And the only way for that to change is to stop malaria. So that is
what we are going to have to do."
There has never been a time when malaria has not been a major
global health problem; its symptoms have been reported for thousands of years.
Only the plague—and, perhaps soon, H.I.V.—has influenced the demographic and
geographical history of humans more. Malaria had become widely recognized in
Greece by the fourth century B.C., and was responsible for the decline of many
of the city-state populations that were then at the center of the world.
Treatment and cures have been sought for millennia. The Chinese qing hao
plant—which today is the source of the most promising anti-malarial drug,
artemisinin—was first described, more than two thousand years ago, in a medical
treatise called "Fifty-two Remedies," discovered in the Mawangdui
tombs, in Hunan province. The Centers for Disease Control was founded in
Atlanta, not Washington, at the end of the Second World War largely because its
initial mission was to control malaria, which remained a significant problem in
the southern United States and in Europe throughout the nineteen-forties;
malaria was particularly severe in the Mediterranean. It was malarial
infections, more than war wounds or any other cause, that prevented Allied
soldiers from fighting in the Italian campaign during 1943.
Malaria starts suddenly, with violent chills, which are soon
followed by an intense fever and, often, disabling headaches, convulsions,
and delirium. As the parasites multiply, they take over the entire body. Anemia
is common, because malaria parasites live by eating the red blood cells they
infect; they can also attach themselves to blood vessels in the brain. If it
doesn't kill you, malaria can recur for years. The disease is transmitted to
humans by female anopheles mosquitoes infected with one of four species of a
parasite called plasmodium; by far the most dangerous of the four is Plasmodiumfakiparum.
It is also the most prevalent. Together, the mosquito and falciparum are
the most deadly couple in the history of the earth—and one of the most
successful. A virus like measles, polio, or even H.I.V. consists of just a few genes. Malaria has five thousand
genes, and its ability to mutate rapidly to defend itself and evade new drugs
has made it nearly impossible to control. It wasn't until the eighteen-nine ties
that Ronald Ross, a British physician working in the Indian Medical Service in
Hyderabad, discovered that malaria was transmitted by mosquitoes.
After the Second World War, malaria-control campaigns were initiated
in many countries, and with the notable help of the insecticide DDT successes
were striking. Malaria was eradicated from the United States in 1951; like
measles, polio, and other illnesses that no longer threaten us, it is
completely unknown to children and largely forgotten by adults, We tend to
think of malaria, if at all, as something distant and exotic, like the British
Raj, which suffered so badly from it—a malady that required a stiff upper lip
and the quinine that comes in a gin-and-tonic. The World Health Organization
sought to eliminate malaria even before it attempted to eradicate smallpox.
The nineteen-fifties was an era of particular confidence in the power of
medicine; a new polio vaccine had been discovered, and so had antibiotics.
In countries like South Africa, Sri Lanka, and Mozambique, after
extensive spraying, malaria had almost vanished. India brought the number of
cases down from seventy-five million in 1951 to around fifty thousand in 1961.
Large swaths of the disease in Southeast Asia were also on the brink of
eradication. Yet by the late nineteen-sixties the success had come to a halt.
DDT was seen as devastating to wildlife, and mosquitoes had begun to grow resistant
to it. (Many subsequent studies have shown, however, that the insecticide is
not as dangerous to the environment when used sparingly.) The United States
banned DDT in 1972, and other developed countries followed. In most of Africa
and Asia, where malaria efforts have always been funded by the West, the
pesticide became politically unacceptable. Six years after Sri Lanka stopped
using it, the number of cases rose from seventeen to more than half a million.
By that time, though, malaria had essentially been banished from the developed
world, and with it any incentive for continued research.
Less than ten per cent of all investment in health research is
devoted to the diseases that affect ninety per cent of the world. To address
this imbalance, in 2002 the U.N. created the Global Fund to Fight AIDS,
Tuberculosis, and Malaria. Richard Feachem, the fund's director, is a professor
of public health at Berkeley, he founded the Institute for Global Health, and
he once served as dean of the London School of Hygiene 6c Tropical Medicine,
which has always been the world's most important center for malaria research.
Feachem dresses in tweeds, and has graying hair and a thin, oval face; glasses
dangle from a cord around his neck. Despite his current role, he retains the
dispassionate manner of a scholar; he understands politics, but worries that
too many people have begun to ignore history. "In the first year I had
this job, malaria was never mentioned," he told me in Geneva. "In the
origins of the fond, the momentum was entirely about H.I.V. Malaria was an
afterthought." At an annual cost of twelve billion dollars, however,
malaria is responsible for almost forty per cent of public-health spending in
Africa.
Poverty cannot be
addressed unless malaria is, too. And the attempt to end poverty has gained
great currency in the past two years. Last December, Gordon Brown, the British
Chancellor of the Exchequer, promised that his country would purchase hundreds
of millions of doses of any successful vaccine— thus providing incentive for
investment which pharmaceutical companies had always lacked. In June, the
Gates foundation, which had already donated more than a hundred and fifty
million dollars for malaria research, announced a new round of global health
grants, worth more than four hundred million dollars. A few days after the
Gates announcement, President Bush pledged more than S1.2 billion to fight
malaria in Africa over the next five years, by expanding access to remedies
that already exist and that are known to work: mosquito nets treated with
long-lasting insecticide, indoor spraying, and the distribution of effective
medicines, such as the therapies that include artemisinin. (Bush has announced
such initiatives before—and then failed to fulfill them. Much of the money has
simply been shifted from other commitments.)
There have been great moments of optimism in the past, too,"
Feachem told me, "but there has always been this sense of malaria
fatalism. There has been the idea that this is just pan of Africa and being
African." For much of the past twenty years, Feachem said, political
leaders throughout the world have been waiting for a vaccine to appear as if by
magic. "It is a moral outrage. This is an utterly preventable holocaust,
and the numbers are far higher than the W.H.O. says. They have put the dead at
one million for years, and now it is really three million in terms of deaths
to which malaria might have contributed. So I don't think it's yet the time to
break out the champagne. You have to remember we almost eradicated malaria
before. And what has happened? Not only have we failed but by any reasonable
measure more people have suffered from malaria in the past fifty years than in
the history of mankind. It has been a remarkable march backward."
In most parts of the world, malaria parasites have become
resistant to chloroquine, which had been the first-choice treatment in Africa
for decades. Chloroquine, a synthetic chemical similar to quinine, costs only
fifteen cents a dose, and is easy to make. Sulfidoxine-pyrimethamine, or SP—the
second-choice treatment—has also failed widely. The only consistently
successful alternatives are the artemisinin-based combination therapies—a
mixture of drugs helps prevent resistance—but they have been in short supply
and are ten times as expensive as treatment with chloroquine. If those drugs
should fail, nobody knows what would come next. "The problem is getting
worse in many ways," Feachem said. Studies consistently show that
mosquitoes are transmitting the virus more frequently. There are also more
breeding sites, denser populations in affected areas, and higher death rates
owing to drug resistance. "We are seeing more urban outbreaks in countries
like India," Feachem continued. "We are seeing other, more ominous
signs, too. Malaria has become endemic at altitudes where it never used to
occur. Some of that may be because die mosquitoes are adapting, but most of it
is simply a result of human population density—people living where they never
used to live." (Some of the disease's spread, too, can be attributed to
global warming, as mosquitoes migrate to newly temperate areas.)
Fifty per cent of the world's population is regularly exposed to
malaria—an increase of almost ten per cent in the past decade. When the
parasite returns to a place where success had been dramatic, as was the case
with Sri Lanka in the sixties, the consequences can be particularly
devastating. In such populations, because they have never been exposed, most
people simply lack the protective antibodies required to bolster their immune
systems. It took the republics of the former Soviet Union fifty years to
eradicate malaria, but only five years for the parasite to return in force. It
will take many years to eradicate it again. Resistance to drugs and pesticides
has become far more widespread in the past decade, and many public-health
systems in the Third World have broken down completely. African governments,
faced with the staggering burden of H.I. V. {which not only increases
susceptibility to malaria but places impossible demands on services and
medical personnel) and often civil conflict as well, continue to grow poorer,
and their people become sicker.
In 2000, all fifty-three African chiefs of state met in Abuja,
Nigeria, and issued a document known as the Abuja Declaration, in which they
pledged to halve malaria mortality and disability by 2010. Today, more people
are sick and dying than before. "The mistake was not in putting out the
targets," Allan Schapira, a policy coordinator at Roll Back Malaria,
which was created by the U.N. in 1998, told me. "The mistake was in not
putting the hammer down to make it happen." But that would have required
about three billion dollars a year. "The economic conditions of the
industrial world are better than at any other time in history," Schapira
said. "Affluence is much greater. People should have strong pangs of
conscience." New money has been committed—for drugs and research.
Scientific prospects appear genuinely promising; but excessive confidence has
derailed efforts to overcome malaria before. And some people feel that if there
is no victory this time, the defeat will be even more difficult to overcome.
There is one sad fact about the malaria community," Kent
Campbell, a former chief of the malaria branch at the Centers for Disease
Control, told me. "We have always been so wedded to failure that we don't
even have the leadership necessary to risk the additional failure to get where
we need to be. This would cost two or three dollars a person." He was
referring to treatment and prevention services for Africans. "It has gone
on for too long. I would love to believe that in the United States this effort
is being driven by a decent desire to help, but I don't think most Americans
give a rat's ass about the death of millions of African kids each year. I
don't think they ever have."
Tuele Hospital sits on a low hill in the Muheza District of
Tanzania, halfway between Mt. Kilimanjaro and Dar es Salaam. Much of the
coastal plain is given over to plantations of sisal and coconut. The roads are
rutted and made of dirt, and along the sides women in brightly colored caftans
gather to sell cashews, charcoal, bananas, cellular-phone cards, old tires,
and bowls full of a small green fruit that looks like a lime and tastes like a
mango. The rains were late this year, delaying the worst of the malaria season,
but the dry weather hurt the crops. Everyone in this part of Tanzania raises
some vegetable or fruit. Nobody could survive without them.
The day I arrived, this spring, the rain came down in torrents.
Forests around Muheza have been cleared in many places in the past decade,
which makes it an ideal breeding ground for the anopheles mosquito. Malaria is
already Tanzania's leading communicable disease. The likelihood of getting
sick is influenced by the number of infectious bites any person receives in a
year, which is known as the entomological inoculation rate, or E.I.R.—the
basic yardstick for transmission. Tanzania has a uniquely wide spread; E.I.R.s
ranging from less than one to more than a thousand infectious bites per person
have been documented. In the region near Tanga—Muheza lies just forty
kilometres to the west—people are bitten by an infected mosquito an average of
seven hundred times a year (about twice each night). That is among the highest
rates of malarial exposure in the world.
At the Tuele hospital, which has two hundred and sixty-five beds
and serves a district of three hundred thousand people, malaria accounts for
more than half of all admissions. In the dry season, there are often two people
in a single bed; when the rains get heavy, there are two to a bed and two or
three lying on the floor between the beds. Tanzania spends four dollars per
person on health care each year, and with that sum doctors confront an almost
epic range of maladies: river blindness, rotavirus (the most common cause of
diarrhea in children, responsible for more than six hundred thousand deaths a
year), elephantiasis, and sleeping sickness are all relatively common. So are
measles and pneumonia. But none of those diseases are as destructive as H.I.V.
or malaria. The infant-mortality rate in Muheza is a hundred and thirty-three
per thousand births, far higher than the national average of slightly more
than a hundred per thousand. (In Europe, the average figure is about five per
thousand.) The malaria burden is harsh in terms of death, but it goes far
beyond that. Sick people can't work or take care of their families. When one
child is dying of malaria, a mother is often forced to ignore the others.
T. K. Mutabingwa, a gruff man in his fifties who holds a tenured
position at the London School of Hygiene &. Tropical Medicine, has watched
children die nearly every day of his adult life. He is one of Africa's most
prominent malaria researchers and has been working at Tuele for more than
twenty-five years. "My Ph.D. was a study that showed chloroquine was doing
nothing for pregnant women," he told me. That was many years before the
government tried to switch to other drugs. Perhaps they didn't read it."
Since the early nineteen-eighties, Mutabingwa has been trying to find die most
effective and least intrusive therapies for mothers and children. One of the
genuine mysteries about malaria—and one of the greatest opportunities for
researchers—is how people develop immunity. When a bite from a mosquito
infected with falciparum doesn't make you sick, it acts like an inoculation;
that's why children who survive to the age of five are much less likely to die.
Adults in Africa may get very sick, but the disease rarely kills them. Pregnant
women, however, are an exception. The first time a woman becomes pregnant, she
is highly susceptible to malaria; in subsequent pregnancies, the risk is
lower. For years, epidemiologists had assumed that pregnancy simply weakened
the immune system.
"That didn't make complete sense, of course," Mutabingwa
told me. "Why would these same women do better in the second pregnancy?
And even better in the third? Those weaken your immune system, too." Ten
years ago, Patrick Duffy, of the Walter Reed Army Institute of Research, and
Mi-chal Fried, from the Seattle Biomedi-cal Research Institute, both colleagues
of Mutabingwa, discovered that a distinct form of the falciparum parasite
binds to a specific receptor on the placenta. The first time a woman becomes
pregnant, if the parasite latches onto those receptors, she has no defenses.
After that, however, her immune system learns to recognize the parasite and
makes antibodies that provide at least some protection. The discovery has
immense implications both for drug treatment and for the development of a
vaccine: if those antibodies can be reproduced successfully, they may be able to
protect women even before they become pregnant.
Mutabingwa offered to show me around the hospital. Women dressed
in robes, their heads obscured by flowing scarves, lined a long, low breezeway
connecting the main wards. Each woman had at least one child, bundled in
swaddling, sitting by her feet, or nursing. None of them cried; the children
seemed like statues while their mothers waited wordlessly to see a nurse,
Nearly half of the adults in the hospital have H.I.V., Mutahingwa said, and
almost all the children have ma-kria. A considerable number have both. We
entered the women's ward, where electric-blue mosquito nets hung in cones over
every bed. The hospital is often the only place in which a woman will have the
use of a net. One mother had just arrived from a village nearby, after a
ten-kilo metre bus ride over a series of craters that serve as a road. She was
covered in dust and wrapped like a mummy. In her arms she cradled a seemingly
lifeless child; malaria had made the baby severely anemic. Two feet away, a
three-year-old boy with an I.V. tube in his hand lay on a gurney, screaming
over and over, "Mksno wangu! Mkonoiaangu!" ("My hand!
Myhandf) "At times, you get to a clinic and they don't have cups for
water," Mutabingwa said. The boy was one of the lucky children who had
made it to the hospital before lapsing into a coma.
"You know, if you do this for a while the danger is not to
care," Mutabingwa said. We walked over to the combined H.I.V. and
chronic-tuberculosis ward (there is neither space nor money to separate them).
A single fluorescent bulb cast an eerie glow across the room. Every bed was
occupied, some by more than one person. H.I.V., tuberculosis, and malaria
(which together kill five million people a year) fuel each other. Anybody with
one is far more likely to fall prey to either of the others. "These women
arc here because of acute malaria," Mutabingwa said. "After five or
seven days, they are usually released. There is not that much we can do for
them after that." We headed back toward the women's ward. A young woman,
about sixteen, was sharing a bed with another woman, a few years older. A baby
with malaria lay between them. The two women were sistets, and the older one
was visiting. She had tuberculosis. Mutabingwa could not conceal his
irritation. "This is not infection control!" he cried out to nobody
in particular. "It is really very dangerous for her to be here." The
older woman shrugged, got out of bed, and left.
While I was in Tanzania, I stopped at villages near Tanga, on the
eastern coast, and, with the help of my driver, spoke to people there. When the
subject turned to malaria, the sense of futility was pervasive. "We don't
have the kind of money you need for nets," one mother told me. Nets, which
are remarkably effective, cost about four dollars and must be treated
regularly with insecticide. "My husband doesn't think it's worth the
expense," the woman said. Mosquitoes almost always feed at night, yet only
two per cent of the children and women in Tanzania sleep under nets or live in
homes that have been sprayed with insecticide. AtTuele, I asked several women
if they had bed nets—and all said no.
Later that day, I went to visit Stephen Magesa, an entomologist
with Tanzania's National Institute for Medical Research. Magesa has spent most
of his career assessing the effectiveness of bed nets that have been
impregnated with insecticide. "In 1991, we showed that even in very
intense areas of transmission we could reduce the burden," he said.
Magesa is a quiet, donnish man. He spoke deliberately but without emotion.
"The study was not big enough to show an impact on mortality. But we did
show very dearly that the mosquitoes did not survive." More important,
the researchers found benefits even for those people who did become infected:
they had fewer parasites in their blood and less severe fevers. "We know
the nets work. We have known it for almost twenty years," Magesa said.
Actually, people have been using nets to protect themselves from
mosquitoes for more than two thousand years. Herodotus described Egyptians
living in marshy areas who would wrap themselves in fishing nets. In the nineteenth
century, British colonists in India routinely slept under nets to stave off
bites. (At that time, nobody knew what caused malaria.) It turns out that you
don't even have to sleep under a net for it to protect you. In one study, in
Ghana, child mortality increased by seven per cent for every hundred metres
that children were away from nets; other research, in Kenya, has demonstrated
that death rates, the incidence of anemia, and even the level of parasites in
the bloodstream were lowered in children who lived within three hundred metres
of houses that had nets.
Bed nets do require attention. They must be properly installed,
used regularly, and treated with insecticide every six to twelve months. And
although the four dollars they cost would be money well spent for even the
poorest family, African governments have never made much of an effort to help.
In 2003, fewer that five per cent of children living in sub-Saharan Africa
slept under nets. New technology should change that. Several companies have
begun to manufacture nets that have insecticide embedded within their fibres.
They don't need to be sprayed and they last for nearly five years—the years
that are crucial for infants and young children.
Magesa's arguments have long been ignored. "I am sitting here
watching my hair go gray and waiting for those nets," he told me as we
sipped iced tea in his cramped office. "Every year, a million more kids
die. A decade ago, they were saying, 'Let people die; there is nothing we can
do.' Then Gates came along and he said this is not acceptable. That was more
important than his money. He put malaria back on the world's stage. But will he
be able to keep it there?
"We are watching children die— our children—and they die
every day," Magesa said. "You could save between thirty and fifty per
cent of them with nets alone. If you added improved hospital services and
proper medicine, you could save eighty per cent. But we already know how much
eight hundred thousand African children are worth to the rich world. We have
known it for a long time."
One afternoon, early in August, I met Bill and Melinda Gates for
dinner at the home of the foundation's president and co-chair, Patty Stonesifer,
who lives with her husband, the journalist Michael Kinsley, on the prosperous
shores of Lake Washington. Their house sits directly across from the
technological Xanadu occupied by Gates, Melinda, and their three children. As
I stood on the dock staring at the sailboats dotting the water, I noticed a
small motorboat heading our way.
Bill Gates was behind the wheel, with Melinda acting as navigator. When it
seemed as though they were going to glide into the dock, they cut the engine,
drifted in, and tied up. Gates was dressed in a T-shirt, a Polartec sweater,
and khakis. He looked as if his most recent haircut had been performed with
blunt scissors and a soup bowl. Melinda was dressed casually in a sweater set
and black pants. She is athletic, and one could not help contrasting her tan
with the definitive pastiness of her husband.
The Gates
foundation—while run by Stonesifer, chaired by Gates's father, and founded by
both Bill and Melinda Gates—has been portrayed largely as the expression of one
man's obsession. That turns out to be untrue. Stonesifer is close to both
founders, and she has been with the philanthropy since the planning stages.
Gates and his wife sign off on all grants larger than ten million dollars, but
Stonesifer is responsible for hiring staff and managing the foundation. After
working at Microsoft for nine years, becoming its highest-ranking female
executive, she retired in 1996. She had become very wealthy, and takes no
salary from the foundation. Stonesifer is not particularly fond of publicity;
she is utterly frank, but prefers to work behind the scenes. At times, her lack
of pretense leads her to be underestimated. But not by Gates. "If this
foundation works, it's because of Patty," he told me. "She is one of
the best managers I have ever known."
In addition to
its work on public health, the foundation has chosen to support libraries,
education, and the underprivileged. By most measures, the grants and the
commitment in those areas are enormous: so far, the foundation has made nearly
$2.5 billion worth of educational awards; eight hundred million dollars more
has been allocated to programs in the Pacific Northwest, where Gates has spent
his life. They are each dwarfed, however, by the investment in public health.
The Gates foundation has more than vast wealth: it has the power of a
government without actually being bound by a nation's political or economic
constraints. "We are in this unusual position where we can spend one
hundred million dollars on something we think might work and it can tail and
nobody gets fired" was the way Gates described it to me. "Political
institutions just can't handle risks like that." The foundation has drawn
liberally from America's leading medical institutions: in addition to
Klausner, who will leave next month to pursue a private venture, Regina
Rabinovitch, who was hired from the Malaria Vaccine Initiative, directs the
infectious-disease program; Helene Gayle, who is in charge of the foundation's
H.I.V., TB, and reproductive-health programs, is one of the most visible black
women in American science. There are at least a dozen other similarly
experienced and sought-after scientists on the staff.
Bill Gates has
always had an interest in science. Yet it was Melinda who first suggested that
they concentrate on global health. Gates didn't get it: he was interested in
population control and thought that improving the world's health might even
run counter to that goal. ("It was only when I dug into it a bit that I
came to understand that better health leads to lower populations with more
resources," he said.) Melinda French grew up in Dallas. She studied
economics and computer science at Duke and stayed to earn an M.B.A. She joined
Microsoft in 1987, helping to develop such products as Encarta, Expedia, and
Cinemania, and she ran a division that produced several hundred million
dollars in annual sales. The two were married in 1994, and Melinda left the
company two years later, when their first child was born. Gates owns more than
a billion shares of Microsoft, which at times have been worth as much as a
hundred billion dollars. Today, after his contributions to the foundation, his
net worth stands at roughly half that amount. "We knew that we wanted to give
virtually all of it away instead of having it go to our kids," he said.
"But we certainly thought that it would happen when I wasn't working full
time at Microsoft."
On the eve of
their wedding, Gates's mother wrote a letter to Melinda in which she stressed
the great opportunities the two would have as a couple to improve the
world—and the unique responsibilities that came with immense wealth. "It
was really quite beautiful," Melinda said. "And that was what got us
going." Their interest in population control led them to look more deeply
into public health, and the realization that diarrhea, respiratory diseases,
and other syndromes were killing millions of people every year. "The whole
thing was stunning to us," Gates said. "We couldn't even believe it.
You think in philanthropy that your dollars will just be marginal, because the
really juicy obvious things will all have been taken. So you look at this stuff
and we are, like, wow! When somebody is saying to you we can save many
lives for hundreds of dollars each, the answer has to be no, no, no. That
would already have been done." Gates's voice rose as he talked. In the
background, a seaplane swooped down onto the lake. "We go to events where
people are raising money for various illnesses where lives are being treated as
if they were worth many millions of dollars. And here we were learning that you
can save even more lives for a few hundred each. We really did think it was too
shocking to be true."
Gates began to approach scientists for advice. One of them, William
Foege, is a former director of the C.D.C. and one of the country's most
experienced public-health officials. I ran into Foege not long ago and asked
him about his first encounters with Gates. He laughed and said, "The guy
came to me and said he wanted to learn about public health and he wanted to
help. Do you know how many times before I have heard those sorts of things?
Rich people say that all the time. I gave him a list of eighty-two books. I saw
him a couple of months after that and I asked, 'How are you doing on those
books?' And he said, Well, I have been so damn busy I have read only nineteen
of them.' I still didn't know whether to believe him, so I asked, Which was
your favorite?' He didn't hesitate for a second. That 1993 World Bank report
was just super,' he told me. 1 read it twice.'" By then, Foege had signed
on as an adviser to the foundation. He now splits his time between Seattle and
Atlanta.
The 1993 World Bank Development Report helped change the way
public-health officials calculate the relationship between disability and the
value of life. In the report, for the first time, bank economists focussed on
the concept of the "disability-adjusted life year" (DALY), which has
come to serve as the standard measure of how to assess the burden of a disease.
In the past, the impact of any illness—cancer, the common cold, and everything
in between— was usually evaluated on the basis of how likely it was to kill
you. But life without good health also carries enormous costs for individuals,
families, and societies. The disability-adjusted life year combines years of
potential life lost owing to premature death with years of productive life lost
to disability. Blindness is an example of a health problem that, while not
causing death, can dramatically reduce one's quality of life or ability to
function within society. Alz-heimer's disease is another.
Even so, the World Bank report, at three hundred and twenty-nine
pages, makes for some dry reading. When I asked Gates if he had indeed read it
twice, he replied, "I've read it more than twice. It's really a nice piece
of work." The DALY concept led Gates and his wife to their first large
grant, a hundred and twenty-five million dollars, for the Children's Vaccine
Program. They refer to that grant as "the 125." 'That led to the
750," Melinda added, an initial seven-hundred-and-fifty-million-dollar
donation to the Global Alliance for Vaccines and Immunization, which they
matched this year. "After the 125, we had a dinner for about a dozen scientists
at the house," Melinda went on. "We were both extraordinarily impressed
with their knowledge, their expertise, their desire to solve problems. And
toward the end of the dinner Bill posed the question: 'If you had more money,
what would you do?' and the room came alive. Just to hear what their ideas were
was so exciting for us. It was a revelation. And we both walked away from that
dinner thrilled, because we had been surrounded by people that were so
brilliant at Microsoft. And we saw immediately that these were the same type of
people."
The National Institutes of Health helps pay for most of the basic
biomedical research carried out in the United States, but it does not produce
drugs or vaccines. That has always been a job for pharmaceutical companies,
which, like any business, concentrate on creating products that people will
buy. There is almost no financial incentive to make a vaccine for malaria; the
West doesn't need it. African children don't lobby Congress; they have no
money, and neither do the countries they live in. Philanthropy has not filled
the gap. "I always say to people with a lot of money, 'Do you want a
disease?'" Gates said, " We can give you this whole disease, or a
whole region or a country. Whatever you want.'" He went on, "We heard
again and again this recitation of places where all this great work had
occurred and then it would just get stalled. There was just nobody to push it
to the next level. It's all the greater crime that something like malaria
never got more attention. We gave a small grant at first, like thirty million
dollars, and everybody said, Wow! That is the greatest increase in non-government
spending in the history of malaria research!' And I thought, Oh, you are kidding."
The Gates foundation offices, in Seattle, are aggressively nondescript.
There is no name on any building or door, and no architectural grandeur. The
foundation receives thousands of grant proposals every year. (Program officers
appraise them first, and then rely on outside committees of experts for
guidance before deciding whom to fund and how much to award.) The criteria are
straightforward. "We look at three things," Richard Klausner told me
one day in his office. 'The burden, the inequity of that burden, and the
inequity of attention." Diabetes, for example, is a big problem in the developing
world, but it gets a lot of attention and also affects the rich part of the
world, so neither pharmaceutical companies nor Western scientists need Gates
money.
Gates sends a constant stream of e-mail to Stonesifer, Klausner,
and the other top scientists at the foundation. Although he remains the
chairman of Microsoft and seems no less consumed by its affairs, he still finds
time to pore over every major grant that the foundation makes, and he asks
dozens of highly technical questions about each of them. "Bill is a guy
who enjoys spending his free time reading and rereading immunology textbooks
and learning a bit \ more about molecular biology," Klausner said.
Bob Dylan's "Chronicles: Volume 1" sat prominently on Klausner's
desk, next to a fat book filled with N.I.H. budget projections. "Guess
which one I would rather read?" he said. "Well, Bill would choose the
other." Once, when I asked Gates if he watched television, he said,
"Not really." Then he conceded that he liked to watch while he was on
his treadmill, particularly the show "24." "Although a little
less after Kim left," he said, referring to the role played by the actress
Elisha Cuthbert. When I started to mention something about a recent episode,
Gates jumped in before I could finish the first sentence. "No!" he
shouted. "Don't say one word until December the sixth. That's when the
last season comes out on DVD. Ill be able to discuss it the next day—well, it
might take me two days."
Nothing animates Gates more than the attempt to find vaccines for
AIDS and malaria. He has been the International AIDS Vaccine Initiative's most
prominent and consistent supporter. He told me that he hoped to live to see
vaccines for both diseases used widely. When he is criticized in the
public-health world, it is usually because he has focussed so prominently on
cutting-edge, next-generation
vaccine research, rather than on the use of more conventional
technology that could have immediate effects. "Ge-nomic data, of course,
is the future," he told me. "We are really down to a rational-design
approach to drugs. We can even sort immune cells and see what proteins come out
where." Gates is right: at some point in the next generation, our
understanding of genetics will undoubtedly help produce fundamental advances
in medicine. For now, though, many wonder if an emphasis on simpler solutions
would save more lives. "The Gates approach is highly scientific,"
Allan Schapira, of Roll Back Malaria, told me when I was in Geneva. Schapira
spends most of his time figuring out how to best deploy bed nets and to stave
off drug resistance in Africa. "I don't want to say it's wrong," he
said of Gates's approach.
"There can be valuable questions." But he personally
found it hard to concentrate on the future when so many people are dying now.
Even Klausner, on more than one occasion, has discussed with me the pitfalls in
counting on high-tech solutions when other answers already exist.Appeals for
low-tech solutions by public-health leaders and by African scientists like
Stephen Magesa were traditionally ignored, because they cost too much. In
places where the government spends less than ten dollars a year on each
citizen's health, bed nets, drugs, and the use of various pesticides (which
has kept the United States malaria-free) are out of the question. In Zambia,
malaria kills one child out of five. This May, the Gates foundation decided to
award thirty-five million dollars to MACEPA, the Malaria Control and Evaluation
Partnership in Africa, to help Zambia. The program will be administered by
Kent Campbell, who spent many years at the C.D.C. The immediate target is to
cut deaths by seventy-five per cent within three years. But the greater goal is
to create a model of what is possible in a poor African nation. The government
of Zambia will purchase hundreds of thousands of insecticide-treated mosquito
nets, thousands of doses of ar-temisinin combination therapy, and enough
insecticide to spray every house in the country. "We need to prove that
children don't have to die," Brian Chi-ruwo, the Zambian health minister,
told me. "And with this money I think we
can.
There is almost universal acknowledgment that the research pipeline
for new malaria drugs has never seemed belter. There are also techniques that
lessen the likelihood that the parasite will become resistant. One of the most
promising of these techniques is the use of intermittent preventive treatment
for infants. In recent studies, scientists gave babies three doses of medicine
during the first year of their lives, whether or not they had malaria, when
they received routine immunizations to other diseases. Such preventive
therapy has already been shown to help protect pregnant women; and in early
studies the children's risk of contracting malaria was cut by more than half.
So was the incidence of severe anemia. Still, drugs require money (lots of
it), vigilance, and a functioning health-care system, and the emergence of
resistant strains will always pose a threat.
A malaria vaccine, on the other hand, would save many more lives,
and at a far lower cost. "There is a huge distinction you have to make
between a chronic treatment and something you take once in your life,"
Gates said. "Mumps is complicated. Rubella is complicated. So is polio.
But a onetime treatment and boom"—he clapped his hands together.
"There you go."
Nobody has ever made a vaccine that works against a parasite, but
scientists have spent decades trying. The organism itself is stupefyingly complex;
but the relationship of a mosquito, the falciparum parasite, and a human is
far more so. Anopheles mosquitoes require a meal of blood in order to lay
their eggs—and they almost always feed at night. Malaria begins when a female
mosquito bites somebody who has already been infected. The mosquito becomes infected,
too, then passes that infection to its next victim in a form of the parasite called
sporozoite. Once sporozoites enter the body, they glide into the bloodstream
and travel to the liver, where they divide repeatedly. Two days later, about
the time that the parasites leave the liver, ten original spo-rozoites have
created millions of progeny. They then invade red blood cells and begin to
feed on them, and within two weeks they will number more than thirty billion.
Last year, for the first time, a vaccine offered partial
protection against infection. In a study on more than two thousand children in
Mozambique, the risk of developing severe malaria was reduced by fifty-eight
per cent. The vaccine attempts to stimulate immunity by using one of the
proteins on the surface of the malaria parasite when it invades the liver. It
was produced by GlaxoSmithKline and, along with more than a dozen other
experimental vaccines, was supported by the Malaria Vaccine Initiative. Most of
the funding came from the Gates foundation.
Although this vaccine is not a miracle cure, even partial
protection against a disease that kills millions would help. Nonetheless, the
foundation is intent on finding a vaccine that works better. Regina Rabinovitch
said, "We would like to take a vaccine and have it be ninety-nine per cent
effective—a mosquito bites you, it takes a blood meal, shoots some parasites
into you, and within five minutes those parasites are dead." The problem
is that such a response would require a high level of the right kind of antibodies.
It would have to work early, in the blood or just as the sporozoites enter the
liver—before they destroy billions of red blood cells. "That is the holy
grail for you and me and the United States military," Rabinovitch said.
Malaria has always had a profound effect on the military. During the war in
Vietnam, for example, there were places in which the number of malaria cases
reported by G.I.s each year equalled— and even exceeded—the number of U.S.
troops.
"But this is where it gets a bit messy," Rabinovitch
continued. "Let's say we got that immunity and it waned after five years.
You would then be immuno-logically naive." For an American soldier, she
said, it wouldn't matter, because "you're only there for two years or
less." But, she went on, "if you are a child who is living in Africa,
who is dying at the highest rates, what would happen if that immunity wore off?
All of a sudden, you would be like an infant again—the people who are at
greatest risk. So if we had a vaccine and its effects didn't last, children
would be at risk once again beginning when they are about five years old. So we
really want something that provides protection from severe disease, and death,
so that if you still get infected you will generate an immune response, and the
likelihood that you will die or become severely sick is lower.
"The goal is to turn a six-month-old into a ten-year-old, so
that he has protective immunity. This is called the 'leaky-bed-net model.' We
know that it doesn't decrease all exposure. It acts as a baited trap with a
human inside and the mosquito touches the net and neurologically becomes a
little nutso and dies."
The parasite's greatest weapon is its ability to avoid the immune
system by continually changing both its surface proteins and its location:
every time it moves from a mosquito's gut to its salivary gland and from there
to our liver and red blood cells, it changes form. The tools of molecular
genetics are finally letting scientists attack each different stage of the
infection—and there are now many vaccines in development. Some work at the
blood stage and some at the liver stage. I asked Rabinovitch how she chooses
which to fund. She smiled. "We are supporting all of them," she said.
"This foundation is agnostic when it comes to malaria religion. We just
want something that works."
The Seattle Biomedical Research Institute is more than
twenty-five years old, and the scientists there work solely on eliminating
infectious disease. Last year, the institute moved into a new building a couple
of miles from the Gates foundation, with laboratories equipped with
gene-sequencing machines, microchip arrays, and powerful new computers. It's
a Bill Gates kind of place. Institute scientists are working on several
malaria vaccines. One of them is based on research by Michal Fried and Patrick
Duffy, who is on loan from the Army. Their discovery of a distinct form of falciparum
which adheres only to the placenta suggests that they might be able to create
a vaccine for pregnant women. Their goal is to prevent sickness, not necessarily
to prevent infection.
Stefan Kappe, a young German parasitologist at the institute,
takes an entirely different approach. He has been studying the mosquito
itself. Since the parasite moves from a human into a mosquito, as well as in
the other direction, Kappe is trying to find a way to prevent infection by
disabling falciparum before it can make it to the liver. Exposure to radiation
weakens the sporozoites that mosquitoes carry in their salivary glands. When
those sporozoites are injected into a person, they stimulate immune activity
and protect him from malaria. That is how most basic vaccines work. A measles
vaccine, for example, is a live strain of the virus that has been weakened to
the point where it can do no harm; yet it tricks the immune system into
creating antibodies to defend itself against genuine measles viruses.
Until sequencing technology made it possible to manipulate genes
in the parasite, this approach never seemed worth pursuing. The parasite has to
be alive to spark the immune system, and it would have been unethical to
inoculate people with live parasites— even weak ones. Nor would it ever be
possible to X-ray enough mosquitoes to protect the world from them. So Kappe is
using genomics to destroy only those genes, which are essential for the
parasite to grow in the liver. He, too, is supported by a grant from the Gates
foundation. "I would never have received funding for this particular
project—any classical review mechanism at N.I.H. would have come back and said
no, too far-out," he said. "The Gates people know it's far-out. But
sometimes far-out works."
Kappe wondered what would happen if he could weaken die falciparum
parasite enough to stimulate the human immune system without endangering it.
It's a tricky prospect, because the parasite needs to do at least part of its
job. Weaken the parasite too much and it would not be capable of inducing a
useful immune response; but, if it isn't weakened enough, the inoculation would
simply give people malaria. Reiving on the full spectrum of modern genetic
tools (as well as on educated guesses), Kappe was able to identify several
genes diat help falciparum to grow and to survive. He dien started deleting
individual genes, to see what effect that caused. "We were lucky to find
two genes that when we delete them the parasite really gets stuck in its
development," Kappe told me. "What matters die most here is that
these deletions don't affect other parts of the life cycle." Without
these genes, the falciparum parasite cannot cause infections in red blood
cells, because it never makes it out of the liver.
The only place you can keep enough mosquitoes to do this kind of
research is an insectary—which is a cross between a zoo for insects and a
laboratory, There are just a few in the world; they require constant
oversight, lots of space, and a perfect climate. The insectary at the
institute is a very humid room, and, as we entered, several of Kappe's
colleagues, working with dissecting microscopes, were removing parasites from
the glands of mosquitoes. Behind the researchers lay long pans with hundreds
of tiny eggs about to hatch. A female anopheles will lay a raft of about a
hundred eggs at a time. The males live for sex, last about a week, and then
die. Kappe's vaccine has worked in mice, stranding the parasite in the liver
and preventing further infection. But he has a long way to go before he can
test it on humans. "
This association between the parasite and the mosquito is millions
of years old," he said. "It's absolutely a brilliant example of
evolution. But if we want to succeed we will have to reproduce this intricate
relationship exactly. We have to create that environment and then manipulate
it. I come from genetics and from the world of parasite biology. I believe that
with modern technology we can make live vaccines that are protective. I don't
think that is in the future. I think it's now."
David Schellenberg, a clinical epidemiologist from the London
School of Hygiene &, Tropical Medicine, has spent much of die past decade
in Africa, and he sees the struggle in a less exalted way. On the day of my
visit, he was standing in the middle of his office at the Ifakara Health
Research and Development Centre, on the northern edge of Dar es Salaam, along
with a young Tanzanian man who works for him. Schellenberg was excited. A rough
wooden box sat on a table in front of them. Jumper cables snaked out of one end
of the box, and a car's cigarette lighter was at the other end. Schellenberg
thanked the man profusely. "This could be as important and valuable as
anything we have ever done for malaria," he told me as I entered the room.
He was not entirely joking. Schellenberg is running some of the most important
malaria drug trials in Africa—testing whether a few doses of preventive
medicine will help protect infants from the disease. The contraption on the
table had been rigged to charge the batteries of computers in the many study
villages where electricity is often absent. "We need computers to work out
there if we are to collect data and store them properly. But, with the
electricity so bad, the computers are completely unreliable."
Schellenberg is a soft-spoken, studious-looking man with
close-cropped hair, blue eyes, and gold wire-rimmed glasses. Like any doctor
who has worked both in the lab and in the village, he is well aware of the
difference between efficacy and effectiveness. When researchers announce diat
diey know how to do something because they have the scientific data to back it
up, diose data are based on efficacy—not effectiveness. "The difference
between what you see in the clinical world and what you find in the real world
can be enormous," Schellenberg said. "And in the real world sometimes
you don't feel you can afford the fine print." Some of the earliest trials
involving preventive treatment of pregnant women and of children were conducted
at Ifakara. "Often a clinical trial proves something can work—the use of
bed nets, for example, or a new regimen of drugs," Schellenberg said.
"But does that mean that everyone in every village or city in Africa will
accept the results?"
Schellenberg and his wife, Joanna, who is also a malaria
researcher, have two sons, eleven and seven. They moved back to Africa from
England last year. Their first posting lasted six years, but their older son
contracted drug-resistant malaria and almost died. "He was airlifted to
Nairobi, and he had chest surgery," Schellenberg told me. "Then he
had pneumonia and that led to abscesses. We very nearly lost him. He is fine
now, but it was scary. You can imagine after that there was a lot of
soul-searching about whether or not to return. But we are here because this is
where we really belong." He said this with no remorse. "Look, we are
lucky. We were able to call a plane and get him out of there. So he lived. That
is not the way it is for the other children who get this disease. There are no
planes. No drugs. No doctors. And no real hope of surviving. So when we asked
ourselves, "What are we doing by coming back,' we had to think about
that."
The Gates foundation supports much of Schellenberg's work—and
other studies of intermittent therapy as well. He is grateful. But Schellenberg,
like many of his colleagues, is concerned about what he sees as a growing
preoccupation with futuristic technology. "Ten years ago, we were saying
that a vaccine would not be available for at least ten years. Now we seem to be
saying the same thing. I think we need not put our hopes in magic bullets when
we have the arsenal to make such an impact now. What we need are magic guns,
not magic bullets," he said. "We need to be able to deliver what we
already have." Schel-lenberg admits that while he is attracted to the
"shiny, scientifically exciting stuff, a lot of what we are doing in
southern Tanzania now is not scientifically challenging. It's like that wooden
box with the cigarette lighter. We are making simple things. And the questions
we are asking are not very exciting in scientific ways. But they are urgent.
This is what we need to do now. We need to make things work. Not just work
under ideal conditions."
Bill Gates approaches life as if it were a problem that needed to
be solved. At times, he appears as if he had stepped out of a Henry James novel:
a confounding mixture of innocence, arrogance, and belief in what is right—the
American Man. Gates's eager, energetic view of the world is stamped on
everything he does: from his house, where guests can program their rooms to
reflect their taste, to the software company he founded. Microsoft, whatever
else it is or has become, began as a collection of smart people who realized
that technology, when driven by the right kind of intelligence, rules the
world. Gates feels the same way about improving public health. His faith in
progress is absolute. "The complexity of biology and how it works is so
interesting," he told me one day. "And, in terms of human welfare,
the idea of getting rid of these diseases—which could be in our lifetime—is
just very exciting."
That final sentiment makes many public-health officials nervous.
"The eradication of disease and the alleviation of suffering depends more
on developing the skills of talented people than on technology," a
generally favorable editorial about the foundation recently declared in the
British scientific journal The Lancet. Gates has put aside more than a
billion dollars to help disad-vantaged American students earn college degrees.
The Lancet editorial suggests that a similar educational investment in
developing countries might do more good than many programs that emphasize
science alone. Both historical and contemporary studies have shown that the public
health of a nation only improves through a combination of social and political
measures. Medicine matters, of course, but it is far from the only thing that
does. (The United States is the richest country in the world and the most
technologically advanced, yet it ranks twenty-ninth among world nations in life
expectancy and thirty-eighth in infant mortality.) "In calling on the
world's researchers to develop innovative solutions targeted to 'the most
critical scientific challenges in global health,' the Gates Foundation has
turned to a narrowly conceived understanding of health as a product of
technical interventions divorced from economic, social, and political contexts,"
the Canadian health economist Anne-Emanuelle Birn wrote recently.
Gates has heard these criticisms, and the foundations's recent
commitment to a full-scale attack on malaria in Zambia illustrates that. It is
impossible to doubt the sincerity of Bill or Melinda Gates, or to question the
impact they have had, and will have, on the world. Yet it would be hard to expect
the iconic American technologist, a man who has made one of the world's great
fortunes by harnessing the flow of information, to abdicate the future. "I
do believe in progress," he told me in Seattle. "Capitalism is an
unusual system, in that somebody can have so much wealth. But then again it's
an unusual system because money can actually flow from the luckiest to the unluckiest
and hopefully in clever ways so that it's not just writing checks.
"We do not measure ourselves at all by the amount
given," he continued. "We have taken on the top twenty killers, and
for everything we do we look at the cost per life saved and real outcomes in terms
of how things get improved. It's fun, and it is also an enormous
responsibility. But having my job at Microsoft is also fun and a huge
responsibility. That is true for being a parent. Many of the most important
things in life are like that. Why else would you want to get up in the
morning?" *