Zambia: body of albino found in Chipata with missing tongue, arms and eyes

A gruesome murder in Chipata, Eastern Province, Zambia.

It is not the first time that the Eastern Province is in the news with an attack on a person with albinism. Also last year, in 2019, the province made headlines with the murder of an albino. Often, Zambians point an accusing finger to neighboring Malawi when a mutilated body of an albino is found. However, just recently, in January of the current year, a prominent Zambian, MDD president Dr Nevers Mumba, alleged that ritual killings are common in Zambia and have always happened towards elections. 

Incumbent president Edgar Lungu is facing a presidential election in 2021. The ruling Patriotic Front (PF) party is split into two camps over his candidature whereas of course also the opposition has its own presidential candidate. (webmaster FVDK). 

Body of albino found in Chipata with missing tongue, arms and eyes

Published: March 26, 2020
By: Zambia reports – Chris Phiri 

POLICE in Chipata have picked up a dead body of an albino without a tongue, arms and eyes.

Eastern Province Police Commissioner Lackson Sakala said police recoverd the body at Yamene farms along the Chipata/Lundazi road yesterday.

Mr. Sakala said the incident occurred between 15 hours and 17 hours adding that the deceased was found in a maize field at a distance of about 60 metres from the Chipata/Lundazi Road.

He said when police officers visited the scene of the suspected murder they discovered that some body parts were missing.

“After inspecting the body they discovered that the following body parts were missing; there was no tongue in the mouth, the tongue was cut, both eyes were removed and both arms were also removed by way of amputation. The victim at the time he met his untimely death was wearing a jean trousers, red t-shirt and black shoes,” Mr Sakala said.

He said the body had since been deposited in Chipata Central Hospital Mortuary awaiting postmortem.

“May I appeal to those that may miss their relative, an albino to come through so that they identify this unknown albino who was murdered yesterday. As police we have actually instituted investigations into this gruesome murder,” Mr Sakala said.

Copyright © 2020 ZR.

Source: Body Of Albino Found In Chipata With Missing Tongue, Arms And Eyes

Chipata (eastern Zambia)

Malawi persons with albinism launch anti-killings campaign

Following a court order, presidential elections are going to be held on July 2. The Malawi Electoral Commission (MEC) has stipulated that the official campaign period will run from May 2 to June 30. 

The Association of People with Albinism in Malawi (APAM) fears that this will increase the already fragile position of people living with albinism in Malawi. History teaches us that attacks on people with albinism increase during election campaigns. The Malawian government fails to react properly. Since 2014, 171 attacks against people with albinism were carried out of which 25 persons were killed and 13 were reported missing. Hence, the Association of People with Albinism in Malawi has launched an anti-killings campaign. 
(webmaster FVDK).

Malawi persons with albinism launch anti-killings campaign

Published: March 24, 2020
By: xinhuanet.com         

The Association of People with Albinism in Malawi (APAM) has launched a campaign to condemn killings of people with albinism for rituals ahead of the fresh presidential polls in the country.

APAM President Ian Simbota, told local media Sunday after the launch that members of the Association fear for their lives as some study showed that persons with albinism are targeted for rituals during elections. Simbota told Xinhua Monday that as of March 23rd, 2020, APAM had recorded 171 cases of attacks against people with albinism of which 25 persons were killed and 13 were reported missing since 2014. (italics added by the webmaster FVDK)

“We received the February 3 judgement with mixed reactions because on one hand we were happy that we will be given back our ballot power but on the other hand looked at the threatening times that we always go through because of the same election exercise,” said Simbota.He said during the campaign the APAM members want to sensitize mostly political leaders to desist from beliefs that killing a person with albinism and getting their body parts for rituals can make them win an election. 

“Those things don’t exist, it’s just some evil way of thinking. We are the voters and politicians should use us as such and not as rituals; it does not work,” said Simbota.”We are a population of 134,636 people and those are the votes that we are worth,” he added. In 2015 UN Human Rights Expert on Albinism Ikponwosa Ero, linked the killings of persons with albinism in Africa to elections, saying many political hopefuls believe that body parts of persons with albinism can be used as charms for one to win an election. (bold added by the webmaster FVDK)

Source: Malawi persons with albinism launch anti-killings campaign

Democratic Republic of Congo: albino woman reveals kidnapper wanted to kill her and use her bones in witchcraft

With 2.4 million square kilometers, at least 250 ethnic and language groups and a total population of nearly 100 million people, the Democratic Republic of Congo (DRC) is one of Africa’s giants. The following map illustrates the real size of the DRC.

The number of people living with albinism in the DRC is unknown, but they are a vulnerable group, sometimes hunted down as animals, like in neighboring Central and Southern African countries. In the article below an albino woman, Lisa, narrates her story, how she escaped from being murdered. She was also sexually abused. Lisa lives in a remote area of South Kivu, an administrative region bordering Rwanda and Burundi. Much of the article focuses on sexual violence and unfortunately Lisa’s experiences are shared by many other women in the DRC.

People living with albinism are discriminated and enjoy even less protection from the State than other Congolese citizens. Superstition, witchcraft, lack of protection, human rights violations, ritual murder, sexual abuse. Read Lisa’s story and shiver.  (webmaster FVDK).

Sex abuse survivor reveals kidnapper wanted to kill her and use her bones in witchcraft

Lisa – an albino who lacks pigmentation in her hair, eyes and skin – tells the Record how a man lured her away from home in the Congo so he could murder her and perform magic rituals with her remains.

Survivor Lisa was abducted by a man who wanted to use her bones in witchcraft rituals (Image: simon murphy)

Published: February 24, 2020
By: Daily Record UK – Stephen Stewart

He wanted to butcher her and use her bones in magic ceremonies.

Sexual abuse survivor Lisa – an albino who lacks pigmentation in her hair, eyes and skin – is quietly telling how a man wooed her, expressing his undying love before luring her away from home to murder her and perform rituals with her remains.

Her delicate features remain impassive as she recounts her horrific ordeal. Her condition – which affects the production of melanin, the pigment that colours skin, hair and eyes – can be a gruesome death sentence in the Democratic Republic of Congo. 

The Daily Record and Sunday Mail have run a series of hard-hitting stories this week after we travelled there to uncover the reality for women in the country once dubbed the “rape capital of the world”.

According to the Home Office, 40 per cent of women in the area we visited – South Kivu –   have suffered sexual violence.

Before she was kidnapped, Lisa had already suffered. The 22-year-old has one child born of rape. She was attacked when she was 18 as she worked in the fields around her village.

Often, women like Lisa have to be treated in poorly-equipped hospitals where doctors have to perform gynaecological surgery using the light of their mobile phones thanks to the frequent power cuts.

She said: “I was in the field working when I was raped. A man came and forced himself on me and I got pregnant. I gave birth to a boy. At first, when he was born, he was unwell but now he is fine and I love him very much.”

In DRC, there are many mothers who became pregnant after being attacked.

In the eyes of the law, their children do not exist but, thanks to SCIAF, Scotland’s Catholic international aid agency, they can now get a birth certificate, which gives them access to healthcare and education.

Lisa, who lives in a remote area of South Kivu, added: “Albino people like me are often discriminated against here. There are people who say that albinos can work magic. People point at me in the village and say bad things.

“One day, a man came to my village and he was very nice to me. He said he had fallen in love with me and he talked me into going on the bus with him to the city of Bukavu. He took me to a house and left me there.

“Another man came and asked me if I knew the other man. I had to admit that I didn’t really know him that well. It was then that he told me the other man was bad and trafficked albino people.

“He wanted to kill me and use my bones in witchcraft. I left as soon as I could and went back to my own village. Things are better now. I did not go to school and I can’t read or write but I would like my boy to study and do great things.”

Lisa has been supported by the generosity of Scottish people through SCIAF, which supports local projects promoting women’s rights, gender equality and provides services to the survivors of sexual and gender-based violence.

Gran Sylvia, 41, is another woman who has survived sexual abuse and is now receiving support through SCIAF.

She was abducted by rebel gangs and had to leave behind her two-month-old baby.

She was forced to become the “wife” of a rebel commander and was abducted for four years. During this time, her baby and mother had died and her husband had remarried.

She was left traumatised and now receives counselling, seeds, tools and training in how to grow food to feed the family and sell any surplus.

Sylvia said: “They made me walk and they hit me on the back with the butt of their guns. I left everything. If you said you were tired, they would say, ‘OK, you want to rest?’ and they would shoot you.

“I saw two people shot like this. We were all afraid. Those who refused to have sex were killed and their bodies fed to the pigs. I saw so many people die.

“This life was the worst.”

Thanks to the support of Scots through SCIAF, things have turned around. She added: “The counselling helped very much. After this, I still felt hurt but not as badly as before.

“I say, show me the one who brought this programme here and I could kiss them. Whenever I hear SCIAF is visiting, I feel happy.”

SCIAF funds medical care and surgery for women who have suffered sexual violence.

The rape epidemic means that doctors at Katana hospital are now world experts in fistula surgery despite the basic conditions.

Dr Michael Chanikire, 38, said: “When I work with these women, I think they could be my mother, wife or sister. It hurts to see people hurt in these ways. They are often traumatised by their suffering.

“I have worked in Europe and one of the main medical issues there is cancer but here we see a lot of fistula problems caused by the trauma of rape and sexual violence. There are times when we have no electricity and we have to use the lights on our mobile phones to perform surgery.

“Women fear coming here as there are many rebels in the area and they will know she has come for treatment and they know she will be asked about what has happened to her.

“Sometimes, it feels like we doctors have come through hell dealing with the things we have to do. It is rewarding too, though. My mother sees me wearing my white coat and she feels so proud of me.

“She knows I am doing my best to help women and that makes her very happy.”

Source: Sex abuse survivor reveals kidnapper wanted to kill her and use her bones in witchcraft

Africa’s shameful acts of racism: the plight of persons with albinism (PLWA) in Africa

Under construction – comments (webmaster FVDK)

Some of the protestors with various placards that called on the Liberian Government among other things, increase their budgetary support (Courtesy of Daily Observer, Liberia).

Africa’s Shameful Acts of Racism: The Plight of Persons with Albinism (PLWA) in Africa

Published: December 2, 2019
By: Edmund Zar-Zar Bargblor, The Daily Observer (Liberia),  Webmaster Admin 

Racism is the belief that a particular race is superior to another, and that a person’s social and moral traits are predetermined by his or her inborn biological characteristics.   On the African Continent, we have seen the impact of colonialism and its attributes of racism and discrimination.

The former Apartheid system in South Africa and its institutionalized racial segregation was an extreme expression of European treatments of Africans. The miserable treatment of people living with Albinism by fellow Africans is not only unfortunate, it is shameful.

The condition known as ‘Oculocutaneous albinism’ (OCA) is a genetically inherited autosomal recessive condition and OCA2, tyrosine-positive albinism, is the most prevalent type found throughout Africa. Due to the lack of melanin, people with albinism are more susceptible to the harmful effects of ultraviolet radiation exposure.

The National Institutes of Health reported that about 200,000 Americans are affected; and around the world, it is between one in 17,000 and one in 20,000 people are people living with albinism. However, it is prevalence in parts of Africa, but it is far higher than the global average. People living with Albinism makeup about one in 4,000 people in South Africa and perhaps one in 5,000 in Nigeria. According to a 2006 review published in the journal BMC Public Health, the prevalence in Tanzania is one in 1,400, but this estimate is based on incomplete data. Since Tanzania’s total population is more than 40 million that would suggest an albinism community of about 30,000. A census is underway, however, and the Albinism Association of Tanzania believes the total figure could be more than 150,000.

People living with Albinism suffered in the hands of fellow Africans

The human rights organization Amnesty International quoted the Malawian police’s description of the gruesome murder of Mr. Machinjiri: “About four men trafficked him to Mozambique and killed him. The men chopped off both his arms and legs and removed his bones. Then they buried the rest of his body in a shallow grave.”

There are superstitions in some parts of Africa that albino body parts bring wealth, power or sexual conquest, and that having sex with a person living with the condition of albinism cures HIV and AIDS. Attackers sell albino body parts to witch doctors for thousands of dollars, according to Amnesty International. In Tanzania, some 75 people living with albinism were reported killed between 2000 and 2016.

Also, there have been reports of people living with albinism killings in South Africa; although such crimes are less common there than in Malawi, Tanzania and Burundi. Last February, a South African court sentenced a traditional healer to life in prison for murdering a 20-year-old woman living with albinism.

The Office of the UN High Commissioner for Human Rights (OHCHR), the UN agency that deals with human rights issues reported in 2016 that hunters of people living with albinism sell an entire human corpse for up to $75,000, while an arm or a leg could fetch about $2,000”.

In many African countries, it is sad and shameful the atrocious manner in which people living with albinism are treated; their lives are compounded by “exclusion, stigmatization, and denial of basic rights such as the right to education and health,” according to Amnesty International.  People living with Albinism continue to experience social isolation and stigma which includes name-calling, mockery, and exclusion from certain community activities.

It is reported in Zambia that at least ten people living with albinism are murdered in ritual killings every year.  Some believe their body parts bring wealth or luck. Those born with the genetic condition are calling for an end to this madness. There are more than 25,000 people living with the condition in Zambia.

Madame Janet Kakusa Wonani of Zambia, Founder/President of Light of The World Foundation. She works closely with children with Albinism in Zambia, irrespective of limited financial support.

According to the Albinism Foundation of Zambia (AFZ), Executive Director John Chiti, more than 25,000 persons with albinism in Zambia are currently in need of sunscreen lotion.

In an interview with Africa Renewal, Ms. Ero, said that the albinism situation in Africa, “is a tragedy.” She referred to the 7,000 to 10,000 people living with albinism in Malawi and thousands of others in Tanzania, Mozambique and other countries as “an endangered people”, facing a “risk of extinction if nothing is done.” Tanzanians call people living with albinism zeru, zeru, meaning “ghosts.”

Prevailing Superstitious Mindsets

Superstitious mindsets in some African countries continue to seek murdered for body parts, including infants and babies. Most of the attacks have taken place in Tanzania. Murders and attempted attacks, though in smaller numbers, have also been documented in Burundi, Kenya, Swaziland, Guinea, Nigeria, South Africa, Congo, Zambia, Namibia, Ivory Coast, and Burkina Faso.

The Converson.com conducted research and looked at media reports published between 2008 and 2011 on albinism and murders in Tanzania. It published a data set of 563 media reports in both English and Swahili from Tanzanian national newspapers.

The data showed that the Tanzanian press portrayed and explained violent attacks against persons with albinism in four ways. They were:

  • criminal activity,
  • cultural practices,
  • a socio-economic phenomenon,
  • a human rights issue.

Ms. Kway-Geer, the first Member of Parliament in Tanzania with albinism described her individual testimonials, first-hand accounts of difficulties as:

“When I was at primary school, people used to laugh at me, tease me – some didn’t even like to touch me, saying that if they touched me they would get this color. People used to abuse me on the road when I took the buses to school. They would run after me – crowds of kids following me – shouting ‘zeru, zeru’. (zeru, zeru, is a derogatory term).

Recommendations

The Conversation.com has identified the following recommendations.

  1. There is an urgent need to address the violence faced by this vulnerable group. Public health awareness is an important first step.
  2. Adequate health services for skin and vision disabilities should be prioritized.
  3. Putting out messages that counter the stigma against people living with Albinism is also important, as is access to education.
  4. Interventions must consider Albinism’ human rights. For example, putting children with albinism in camps may protect their right to life and security,but it restricts their rights to freedom of movement, and family life.

In addition, African Governments should seriously advocate against harmful practices against people living with albinism.  State parties should take all appropriate measures and offer support and assistance to victims of harmful practices, including legal sanctions, education, and advocacy campaign to eliminate harmful practices perpetrated on persons with albinism, such as witchcrafts, abandonment concealment, ritual killings, etc.

Conclusion

One thing for sure, the people living with Albinism did not create themselves; they were created in the same way you and I were created by the God who doesn’t make a MISTAKE. Their birth process is the same as you and me! Their mothers’ carried them for nine (9) months in their wombs before giving birth to them.

Who are we – be it an individual or government to decide that they should not live because they are different? Did God ask he needs our HELP to make His decision? The Almighty God does not need the assistance of mortal humans to run his affairs. The actions of those individuals perpetuating violence against persons suffering from albinism are no different than King Leopold II of Belgium, Adolph Hitler of Germany, Napoleon Bonaparte of France, and White racists today.

In Genesis 1:31(NIV): “God saw all that he had made, and it was very good…” God himself said it was Good, NOT bad. God doesn’t create anything UGLY! So, why individuals, including governments, are killing these innocent people? In addition, 1 Thessalonians 5:22 instructs us to “Abstain from all appearance of evil.” Accordingly, the GENOCIDE against these poor innocent people must be STOPPED!

Now, take a closer look at the beautiful tapestry of the people living with Albinism provided here. The question that readily comes to mind is any of you better looking than the people living with Albinism provided in these photos? I DOUBT IT! Therefore, let the persecution and killing of people living with Albinism STOP before the wrath of God descends upon us.

As Africans, it is embarrassing to read or hear that other Africans are discriminated against due to their race. Racism is contrary to God’s plan for humanity. The divisions we face today in contemporary Western nations are due to Race, the color of one’s skin or ethnic background.  And obviously, this perception is not part of God’s plan.

The Albinism Society of Kenya held a Mr. and Miss Albinism beauty pageant in Nairobi to support those with the hereditary condition. (https://www.bbc.com/news/in-pictures-46439699).

In the words of Maya Angelou: “We, the black people, the most displaced, the poorest, the most maligned and scourged, we had the glorious task of reclaiming the soul and saving the honor of the country. We, the most hated, must take hate into our hands and by the miracle of love, turn loathing into love. We, the most feared and apprehensive must take the fear and by love, change it into hope. We, who die daily in large and small ways, must take the demon death and turn it into life.”

Indeed, Children living with albinism in Africa are our brothers, sisters, daughters, and sons, let us protect them always, they are all God’s children as well.

Source: Africa’s Shameful Acts of Racism: The Plight of Persons with Albinism (PLWA) in Africa

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