Ahead of him, leading the trail with an air of assurance, walks a local witchdoctor.
Aided by a couple of
artificial lights, the two figures venture deeper into the darkness,
running their hands along the cavern's limestone walls for guidance.
Bats meandering above their heads, the men enter a vast cave chamber
dotted with a handful of rocks.
"What I want to know is,"
Torner breaks the silence," have you ever seen anyone pray for
something evil down here?" he asks the witchdoctor. "So they can get
hold of someone? Like an albino?"
An albino himself, Torner
has been traveling around Tanzania to debunk the widespread
misconceptions about the congenital disorder. Dozens of albinos have
been mutilated and slaughtered in the country in recent years, because
of rumors being spread that their body parts can bring wealth and good
luck.
Josephat Torner: Living with albinism
Albino activist fights for equality
Albino rights activist climbs mountain
To stop the atrocities, Torner thought he needed to confront the group he believed was the source of these rumors: witchdoctors.
And that's what brought him to the depths of this cave, face to face with his "enemy."
"We call you a spirit because a white person like you is the devil," readily admits the witchdoctor.
"You're saying I'm a white demon?" Torner hits back, "we are demons?"
The reply: "Yes, because you're white."
'In the Shadow of the Sun'
This dramatic confrontation is one of the most intense moments captured in a new documentary, called "In the Shadow of the Sun."
The independent film,
shot by director Harry Freeland, chronicles the life story of Torner and
his fight for acceptance of albinos in a country where little is known
about the genetic disorder.
"My heart always is
still looking the recognition of people with albinism in this world,"
says Torner, who's been an advocate for albino rights since 2004. "Just
to recognize that we are here."
Torner and Freeland
spent six years creating the film. The director's inspiration to make a
documentary on albinism came nearly a decade ago, when he had one of his
first encounters with someone with the disorder in Senegal.
It's my dream in my life that people with albinism are respected and given all rights which other human beings are being given.
Josephat Torner, albino activist
Josephat Torner, albino activist
"A woman approached me
in the street, held out her child and said 'here, take it back, where it
comes from," remembers Freeland. "She had a child with albinism and
because I'm white, she thought the child belonged to me in some way --
her husband had left her for having a white child and accused her of
sleeping with a white man."
Leading man
People with albinism are
born with genes that do not make the normal amounts of the pigment
called melanin. Those born with the disorder, which affects people from
all races, inherited the genes from their parents who may or may not
have any of the associated traits.
But many people don't
understand the effects of the condition and as Freeland discovered, in
parts of Africa albinos often suffer social stigma, prejudice and even
attacks.
Keen to make a film
documenting the plight of this group of people, Freeland headed to
Tanzania, the country reported to have one of the biggest albino
populations in the world. There, he came across many amazing stories,
but he didn't find his leading man until he met Torner.
"I just heard him speak
and instantly, I just knew he was the one to lead the film," says
Freeland. "I think so many stories that come out of Africa are negative,
and everything about Josephat is positive."
Despite growing up with a
disorder that left his skin and hair pale, as well as his strength and
eye sight weak, Torner has succeeded in making the best of his
situation.
Over the years, he's
overcome struggles and discrimination to receive an education and get
married. A father of two, Torner' has even climbed Africa's tallest
mountain, Kilimanjaro, to prove that albinos can achieve greatness.
"It was really very
difficult to climb," he admits. "But I was climbing because at that time
I had an agenda behind for what is happening to this world," he adds.
"We are killed, we are hunted, we are chopped. So I climbed with a
special message ... to the African countries: that we are able. But
[also] protect us, give us a chance, don't stigmatize, don't isolate,
don't hide us to the darkness room -- just open the way."
'Why are they killing us?'
In Tanzania, there's been 72 reported people with albinism killed over the last five years.
Harry Freeland, director
Harry Freeland, director
In 2009, the Tanzanian
government embarked on a campaign against the killers of albinos,
particularly in the Lake Victoria region. Freeland says at the heart of
the problem are witch doctors making claims that albino body parts can
bring wealth.
"In Tanzania, there's
been 72 reported people with albinism killed over the last five years,"
says Freeland, noting that the actual number could be higher. "And
there's been 34 people left mutilated that have survived attacks."
Some of the victims were people Torner used to know.
"I was angry," says Torner, recalling the moments following his confrontation with the witchdoctor.
"He answered it to me
directly, without even trying to hide anything. So I was angry, of
course, because I remember my brothers and sisters whom I lost, because I
will not see them forever and while he's there he's continually
surviving," he adds. "So, you ask yourself, 'what's the problem? Why are
they killing us? Why are they hunting us?'"
Torner realizes he may
never get a suitable answer to those questions. Yet, this doesn't stop
him from doing all he can to bring attention to his message of creating a
more inclusive society.
He hopes that his
community work and the documentary focusing on his efforts, coupled with
the outreach from other organizations and the government, will
eventually make Tanzania a place where albinos aren't forced to stay in
the shadows.
"It's my dream in my
life that people with albinism are respected and given all rights which
other human beings are being given," he says.
"This is what is in my
heart -- when I would see justice to people with albinism; when I would
see the lifespan of people with albinism is increasing, this is still a
dream to my life."
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