Sharon Ndanu, a student at Kenyatta University speaks to the Nation
during Albinism day on June13, 2015, at KICC. Albinism affects
approximately one in 17,000 people in North America but is much more
prevalent in East Africa, where it affects as many as one in 1,400
people. PHOTO| ANTHONY OMUYA | NATION MEDIA GROUP
In May 2015, Tanzania’s deputy minister of Home Affairs, Ms
Pereira Silima, issued an unambiguous warning to the members of her
country’s National Assembly.
“I want to assure my
fellow politicians that there won’t be any parliamentary seat that will
be won as a result of using albino body parts,” she declared.
Ms Silima’s warnings appear to have gone unheeded during the run-up to Tanzania’s recently concluded elections.
The
Tanzania Albino Society says that at least four persons with albinism
have been killed since campaigning officially began on August 23.
There
is reason to believe that some of those running in the election were
turning to a form of witchcraft that uses albino body parts allegedly to
bring good luck.
Albinism affects approximately one in
17,000 people in North America but is much more prevalent in East
Africa, where it affects as many as one in 1,400 people.
Around the world, people with albinism are subject to widespread discrimination.
A
February 2015 report of the United Nations Human Rights Council notes
that, “as of October 2014, over 340 attacks against persons with
albinism, including 134 killings, have been recorded in 25 countries.”
The
situation is particularly severe in parts of East Africa, where
superstition fuels a lucrative trade in albino body parts, which are
used in potions and amulets believed to bring good fortune.
PROTECTING ALBINOS
In Tanzania alone, official figures show that at least 75 persons with albinism have been murdered since 2000.
In Tanzania alone, official figures show that at least 75 persons with albinism have been murdered since 2000.
Campaigners
believe the real number to be much higher. Countless others have
survived attacks, many of them losing fingers and limbs in the process.
The body of a person with albinism is believed to carry a market price of up to $75,000.
Yet
with the harvest of albino body parts being particularly acute in the
impoverished regions surrounding Lake Victoria, it is widely believed
that East Africa’s wealthiest and most powerful, most notably
parliamentarians themselves, make up the primary markets for this costly
form of witchcraft.
The Tanzanian Government has
joined other administrations in the region, including Malawi and
Namibia, in trying to protect persons with albinism.
Measures
including a ban on witchcraft and the arrest of scores of witchdoctors
have sought to stem the harvest of albino body parts.
However, more is needed to effect a change in popular attitudes.
That is why, on June 3, 2015, the Senate of Canada adopted a motion concerning the rights of persons with albinism.
The
motion sees parliamentarians as critical in educating citizens about
human rights and the challenges confronting people with albinism, and in
advocating tolerance and adherence to the rule of law.
COMBATING PREJUDICE
It calls on parliamentarians to exercise their influence within their communities to combat prejudice and disinformation, to reach out to fellow citizens about the multiple layers of human rights challenges confronted by persons with albinism, and to become advocates for tolerance and the rule of law, especially in the lead-up to elections.
It calls on parliamentarians to exercise their influence within their communities to combat prejudice and disinformation, to reach out to fellow citizens about the multiple layers of human rights challenges confronted by persons with albinism, and to become advocates for tolerance and the rule of law, especially in the lead-up to elections.
Vicky
Ntetema, an award-winning former BBC journalist from Tanzania, in 2008
published a report exposing the use of albino body parts in witchcraft
by politicians in Tanzania.
She serves as the
executive director of the Canadian-based NGO, Under the Same Sun, a
leading advocate for the rights of persons with albinism worldwide.
“I call upon you African leaders to wipe the tears of mothers of
persons with albinism who suffer from stigma and discrimination because
they have children with the genetic condition,” she appealed in a recent
Facebook post.
“I call upon you African leaders to
console grieving mothers whose children have been mutilated and murdered
so that their body parts can be used by witchdoctors to make their
clients successful.”
Vicky’s message is clear: the rights of people with albinism are human rights.
Politicians
in Tanzania and across East Africa have not only the power and
responsibility to ensure that those rights are protected, but also the
influence to combat the ignorance that puts so many innocent lives in
peril.
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