The plight of albinos
Lazarus
Sauti
Some
countries in the African continent are the worst places to be for an albino.
Because African albinos are especially noticeable, it is difficult for them to
enjoy the sacrosanct right, the right to life in some parts of Africa.
People
with albinism – a congenital disorder that robs skin, eyes and hair of their
pigment, are attacked and hunted like animals.
They
are also deprived of basic health services vital for their survival, according
to the World Health organisation – a specialised agency of the United Nations
that is concerned with international public health.
Further,
on the continent well known as the cradle of humanity, people with albinism are
believed to possess special powers, but not in a good way – myths that Rutendo
Mawere, a highly innovative, motivational and interactive Zimbabwean media and
human rights activist, describes as wild and terrifying.
“Albinism
is believed to be contagious so people are afraid to touch people with the
disorder.
“More
so, some people believe albinism is the result of a curse from the spirits on
the family with a member with such condition, so it is thought to be unwise to
associate with such a family,” she noted.
In
most, if not all, African societies, pregnant women are discouraged from
looking at people with albinism as the belief is they will give birth to a
child with the condition.
In
the Democratic Republic of Congo (DRC) and Burundi, the flesh of people living
with albinism is thought to contain ingredients that can bring luck, fertility,
wealth and ward off evil spirits.
Due
to these petrifying myths, adds Mawere, lives of people with albinism are in
danger.
True
to Mawere’s word, in Malawi, for instance, an 11 year-old girl was kidnapped in
January by her uncle, who was told he could get US$6 500 for her body.
Sadly,
two other albino children were also abducted, and a 68-year-old woman was found
dead and dismembered that same month, according to the United Nations High
Commissioner for Human Rights, Zeid Ra’ad Al Hussein.
Amir
Manento, a retired judge and human rights activist, also said around 30 000
people with albinism are thought to be living in Tanzania, where they have to survive
with the risk of being killed and their body parts fetching high prices for
witchcraft.
According
to a report by the International Federation of Red Cross and Red Crescent
Societies, he added, a complete set of Albino body parts – including all four
limbs, genitals, ears, tongue and nose – can fetch up to US$75 000.
Manento
also asserted that in October, Tanzanians will go to the polls to vote in
presidential and parliamentary elections, and this is possibly the worst time
to be a person living with albinism in the country.
“Every
election period brings with it a new cycle of killings. In between we have
other smaller elections translating to more abductions, more killings.
“We
see an increase of witchcraft and the use of human body parts, particularly
albino body parts, in the run-up to the general elections.
“Albino
body parts are associated with good luck, and as the country gears up for the
elections, the demand for good luck charms goes up. Sacrifices during this time
are thought by some to be a sure way of guaranteeing victory in the polls,” he
asserted.
Isaac Maigua Mwaura, Kenya’s first
albino Member of Parliament, says it is time measures are put in place to end
these killings and abductions.
Mwaura added that strict laws need
to be established and adhered to by all affected countries.
“Enforcement of laws is one of the
weakest links in this war. We have become the hunted. Neither we nor our
children are safe. Fathers are betraying their children’s trust and selling
them off like unwanted baggage. Mothers are conspiring to traffic their own
flesh and blood to senseless deaths.
“Therefore, governments must
establish strong laws and policies to promote and protect the lives of people
with albinism,” he said.
Tapiwa Gwenlisa Marange of Alive
Albinism Initiative – a platform to educate society and empower people with
albinism in Zimbabwe, believes political, business and religious leaders as
well as individual members of society must educate societies to understand that
a person with albinism is a human being and having such a child is not a
gateway to quick riches.
“Society needs to understand what
albinism is; it needs to be more empowered and supported to co-operate. Therefore,
political, business and religious leaders as well as nongovernmental organisations
should not only empower people with albinism with life skills, but should encourage
the society to respect their rights,” she explained.
The
WHO agrees, “Governments
should also increase public awareness of the condition and listen and respond
to the concerns of organisations representing people living with albinism.”
The
international public health agency also encouraged individual African states to
carry out surveys that determine the prevalence of albinism, and build up
proper policies for assisting people with albinism.
“Individual
states should develop appropriate strategies that integrate albinism awareness
in the school curricula, especially to correct misconceptions about the condition,
educate counsellors in schools about albinism as well as train health care
providers at clinics and hospitals about albinism,” noted the WHO, adding that
the strategies should also encourage community self-help support groups.
“Albinism
has to be recognised as being a medical condition and not a curse.
“As
a result, African countries need to train their health care staff to deliver
albino children the same way they do black-pigmented children and offer
counselling services to couples who deliver such children.
“African countries need to respond
to the needs of their people living with albinism by providing free skin
lotions and subsidized or free glasses.”
The Tanzanian government, after being encouraged by the United
Nations, officially banned witchcraft in an effort to stem the killings of
people with albinism.
In view of that, fellow African governments must also ban
witchcraft; and security agencies in respective African countries must be
placed on high alert to provide maximum protection to people with albinism.
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