It is not known with certainty how many people in Africa are affected by OCA, which stands for ‘Oculocutaneous albinism’ (see below). It maybe a quarter of a million, it may be more. What we do know is the plight of persons with albinism. The lack of melanin which brings this condition with it, results in unhealthy effects of ultraviolet radiation exposure. Moreover, widespread superstition causes many wicked people to believe that albino body parts bring wealth and/or power. As a result, persons with albinism are chased, kidnapped, murdered.
The article below contains many examples of these gruesome practices which occur in many African countries. The author, Edmund Zar-Zar Bargblor of the Liberian newspaper, The Daily Observer , is to be commend for drawing attention to these outdated and cruel practices which constitute a serious violation of the human rights of people with albinism and have no place in a modern society.
Warning: the following article contains graphic details of cruel ritualistic activities (webmaster FVDK).
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.
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:
“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).
The Conversation.com has identified the following recommendations.
There is an urgent need to address the violence faced by this vulnerable group. Public health awareness is an important first step.
Adequate health services for skin and vision disabilities should be prioritized.
Putting out messages that counter the stigma against people living with Albinism is also important, as is access to education.
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.
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.
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.”
FRANCISTOWN: Acting High Court judge Modiri Letsididi sentenced two ritual killers to a total of 27 years imprisonment yesterday. The judge said Thuri Poicho and Njayi Kamuanga were under the influence of alcohol when they committed the murder. He said he had considered everything submitted on their behalf by their attorneys Charles Tlaagae and Muriro Furusa.
“Both accused were influenced by immaturity and had pleaded guilty to the charge. That show contrition and remorse on their part,” said Letsididi.
He added that Poicho was a first offender and has no previous conviction. He noted that the accused persons have been in custody since August 2001 and the charge has been hanging on their heads ever since. The judge commented that the two have lost their previous employment as herdsmen as a result of the offence. He noted that the accused persons did not benefit from the ritual killing ordered by a certain Ntshemang. However, he said the court is duty bound to protect society and the sanctity of life. “This court should demonstrate to the society that such crimes should not be tolerated. Both accused persons participated in unprovoked assault of the deceased, cutting his private parts and tongue in order to gain. In my view, there is no worst crime than this,” said the soft-spoken judge. He noted that Kamuanga has a previous conviction for a crime committed two months before the ritual murder. Therefore, he sentenced him to 14 years and gave Poicho 13 years for the ritual killing of Aaron Phobe.
On Monday, state counsel Keneilwe Lephalo said one Ntshemang approached the convicts and showed them a lot of money if they gave him the private parts of a human being. He promised them P8 000 for the job. They then conspired to kill Phobe and get the organs. “They assaulted him with a knobkerrie on the head until he fell unconscious on the ground. They removed his tongue and genitals and then delivered them to Ntshemang who had packed his vehicle in the bush who promised to pay them P8,000 the next day,” she submitted.
The investigations led to the arrest of Poicho on August 14, 2001 at Nnyambesi cattlepost and Kamuanga at Satau cattlepost. “They were taken before a judicial officer Phetsolo Nare, where Kamuanga was the only one who deposed a confession statement. In so hitting the deceased with a knobkerrie, they intended to cause his death. They acted unlawfully and had no lawful justification for their conduct,” submitted Lephalo.
Immediately after the judge was satisfied that the accused’s plea was unequivocal, he asked the two defence attorneys whether there are any extenuating circumstances in the case. They adopted the same submission that P8,000 offered by Ntshemang was a fortune for their clients who are herdsmen and the amount had a bearing on their reasoning. In mitigation, Poicho’s attorney Tlaagae submitted that his client was unknown in criminal circles and the court should impose a sentence that would give him a chance to rehabilitate.
“He pleaded guilty, and acknowledged to the society that what he did was morally and legally wrong. He benefited nothing from P8,000 they were supposed to be paid and they never saw Ntshemang again,” submitted Tlaagae. He urged the court to impose a sentence that would not break the accused. Mitigating on behalf of Kamuanga, Furusa submitted that the court should take into consideration the personal circumstance of his client. He said Kamuanga confessed at the time of his arrest and thus saved valuable time for investigating officers and court. “He was incited by allegedly rich person to commit this crime. Ntshemang was never prosecuted and the accused has to bear punishment on behalf of Ntshemang,” said Furusa.
The case reproduced below refers to the trial of Sepeni Popo who in 2006 was found guilty of killing a Molepolole woman, Binki Balotlegi, in what was believed to be a ritual murder. Sepeni Popo was sentenced to death.
I first reported this case – many, many years ago – on my website ‘Liberia: Past & Present of Africa’s oldest Republic‘, notably on the page ‘Ritual killings in other Sub-Saharan countries: Lesotho‘. The case of Sepeni Popo is one of the rare cases still available online. Unfortunately, most links referring to cases of ritual murders reported on these country pages have gone missing over the years, reason why I decided to adopt another approach on the present web site: reproducing literally the articles concerned, but with extensive reference to its origin, giving the original author and publishing house or web site all credits they are entitled to. (Webmaster FVDK).
Published: July 26, 2007 By: Lekopanye Mooketsi
Death row inmate fails to get Court of Appeal reprieve
The fate of death row inmate, Sepeni Popo lies with President Festus Mogae, after he failed to get a reprieve at the Court of Appeal this week. The condemned prisoner can only escape the hangman’s noose if the President exercises his prerogative of mercy to save him. But Mogae, a confessed retributionist, has never pardoned a death row convict.
Popo was sentenced to death last year, by the Lobatse High Court for killing a Molepolole woman, Binki Balotlegi in what was believed to be a ritual murder. He confessed that he was promised P1,000 for the murder. Three other men who were charged with him were later acquitted and discharged of murder.
In his appeal, Popo’s lawyer, Themba Joina argued that the trial judge, Ian Kirby was wrong in failing to recuse himself and that the confession statement by his client was wrongly admitted in court.
He submitted that the judge should have found extenuating circumstances and refrained from passing a death sentence. The defence wanted Kirby to recuse himself from the case because at the time it was registered, he was the Attorney General and as result he might have been an interested party. However, the Court of Appeal ruled that there was no need for Kirby to recuse himself since he did not directly deal with the case when he was Attorney General.
Joina argued that there was no evidence that Popo had been advised of his right to legal representation before the confession statement was taken. He added that the court erred in not ordering a trial within a trial before admitting the confession statement.
Joina submitted that the hand written statement was not produced in court and there was no evidence as to what happened to it. He said the original statement was the only document which could prove to the court what actually transpired when the confession was made.
The Court of Appeal ruled that that it was clear from the evidence that Popo freely and voluntarily made the statement to a judicial officer. The court was of the view that this was a particularly brutal murder and the injuries were horrible.
The court ruled that the murder was deliberately planned for a reward. In dismissing the appeal, the judges said there was no evidence to diminish Popo’s moral culpability.
In his confession statement, Popo said a man asked him and his colleagues to get a baboon without fur. He said when they asked him what he meant, the man said he wanted them to find a woman’s private parts for him. Popo said each of them was promised P1,000 after delivering the goods. He said he later arranged with his accomplices to find out what the man was looking for. He went into detail about how they found their prey.
After a drinking session, they later led a woman to an isolated spot where they brutally attacked her. Popo said after they killed the woman, one of his partners cut off a piece of her private parts.
He said they parted after the job was finished and he went to sleep. Panic struck him the following morning when he realised that his cap was missing. “When I recalled carefully I came to the conclusion that it was left at the crime scene,” he said.
The confession statement narrates what Popo did up to the time when police spoke to him, including washing his clothes to remove blood stains. He told the judicial officer about his unsuccessful attempts to get the promised payment after the mission was accomplished.
A must read. Though a very lengthy report that I reproduce here, it contains such a wealth of information on albinism, people living with albinism, their fears, their dangers, the measures taken by the Government of Tanzania, that I thought I must conserve it and present to you. I will not even try to summarize it or give some sketchy details, judge for yourself. (Webmaster FVDK)
Published: February 9, 2019 3:01AM EST By: Human Rights Watch
Many children with albinism in Tanzania share similar stories of hardship. The “temporary holding shelters” strategy introduced by the Tanzanian government in the late 2000s may have contributed to a decline in the number of physical attacks, but Human Rights Watch observed that it led to the emergence of additional challenges.
In July 2017, Human Rights Watch interviewed 13 children and young people with albinism, aged 7 to 18 years old, and 26 other people, including family members, education professionals and nongovernmental organizations in the Mwanza, Shinyanga and Simiyu regions of Tanzania. There, we found that Tanzanian government policies designed to protect children with albinism incidentally had a negative impact on their rights to family life, an adequate standard of living and inclusive education. In order to protect their privacy and shield them from potential repercussions, the names of most interviewees referred to hereafter have been changed.
While the Tanzanian government appears sensitive to these concerns, it should now intensify efforts to reinsert children with albinism into their communities and provide them with inclusive education, while continuing to investigate and prosecute those responsible for attacking children with albinism. By doing so, Tanzania has an opportunity to emerge as a strong African leader in ensuring the safety, inclusion and dignity of people with albinism, as outlined in the Regional Action Plan on Albinism in Africa, the first-ever continental strategy to address violations against people with albinism, adopted in 2017.
What Is The Best Interests of the Child Principle?
The Best Interest of the Child principle derives from the United Nations Convention on the Rights of the Child. It requires state parties to prioritize the interests of the child in any action that may impact them. This includes taking into consideration the child’s own views and desires, his identity, his need for care and development and his right to a safe family and community environment. These factors should be considered altogether and balanced against one another if in contradiction. State intervention should be based on individual assessments of the particular child whose situation requires it.
Recommendations To the Government of Tanzania
Increase public sensitization efforts aimed at dispelling deadly and discriminatory myths about albinism, notably through workshops and public service announcements on radio and television, particularly in rural and isolated communities.
Ensure that all teachers in the public education system are trained to adequately provide for the specific needs of children with albinism.
Ensure that resources are at the disposal of schools to meet the specifications needed of children with albinism, notably by providing for textbooks and exams with larger fonts and assistive devices to read the blackboard.
Pursue efforts to promote the safety of people with albinism by investigating threats and crimes against people with albinism and holding those responsible to account.
Work with parents and communities to ensure the safe and orderly reunification of children with albinism with their families, with the goal of progressively dismantling the temporary holding shelters.
Recommendations to International Donors
Support projects dedicated to sensitizing the Tanzanian public to albinism and training teachers to provide for the specific needs of children with albinism in public schools.
Support the Tanzanian government in reuniting children with albinism with their families and ensuring their return to a safe, inclusive community.
Albinism in Tanzania
Albinism is a genetic condition that causes a deficit in the biosynthesis of melanin, a pigment that colours the skin, hair and eyes. While albinism is a rare condition in Europe and North America, affecting one out of about every 17,000 to 20,000 people, it is slightly more widespread in Sub-Saharan Africa, with prevalence rates of 1 in every 5,000 to 15,000 births. Tanzania’s 2012 national census identified 16,477 people with albinism. Today, it is estimated that there are over 18,000 people with albinism in the country.
People with albinism usually have a paler, whiter appearance than their relatives. The deficit of melanin can also result in low vision and an increased vulnerability to sun’s ultra-violet radiation. Consequently, people with albinism living in Sub-Saharan African are about 1,000 times more likely to develop skin cancer than the general population.
As noted by the United Nations Independent Expert on the enjoyment of human rights by persons with albinism, “The complexity and uniqueness of the condition means that their experiences significantly and simultaneously touch on several human rights issues including, but not limited to, discrimination based on color, discrimination based on disability, special needs in terms of access to education and enjoyment of the highest standards of health, harmful traditional practices, violence including killings and ritual attacks, trade and trafficking of body parts for witchcraft purposes, infanticide and abandonment of children.”
In many parts of East Africa, people with albinism are targeted for their body parts, which some believe hold magical powers and bring good fortune. Traditional healers and “sorcerers” have over the years claimed that people with albinism are “ghosts” who never die but merely disappear. In 2009, the International Federation of the Red Cross reported that a senior police officer in Dar es Salaam, Tanzania’s economic capital said that the body of a person with albinism could fetch up to US$75,000.
Over the last decade, Under the Same Sun, a Canadian non-governmental organization working to empower people with albinism, estimates that over 200 people with albinism, many of them children, have been killed in Africa or had their body parts amputated. In Tanzania alone, the group reported that at least 76 people with albinism were killed since 2006.NGOs and local groups reported that criminals have stolen bones from the exhumed remains of people with albinism.
The last reported killing, in February 2015, took place in the region of Geita, in Northwest Tanzania, when men abducted a one-year-old baby with albinism from his mother and “hacked [him] to death.” The men were said to have hit the mother with a machete when she refused to hand over her child, an activist who was with her when she woke up at the hospital told Human Rights Watch.
Faced with increased international scrutiny at the end of the 2000s, Tanzania began to mobilize resources to fight off traffickers and protect people with albinism. Local organizations told us that since 2007, hundreds of children were removed from their families, sometimes with no consultation or consent, and placed in shelters where they were effectively isolated from society.
According to activists who spoke to Human Rights Watch, orders from the government to protect people with albinism were enforced by district commissioners, who oversee security in their respective districts.
“There is an order from the district that says that if anything happens to [a] child with albinism, local leaders would be responsible. It something happens, the whole community will be suspected,” the manager of a local organization working with people with albinism told Human Rights Watch. “Because no one wants trouble in their backyard, there was a big push from the communities to send the children to the shelters.”
The Tanzanian government also moved to combat impunity for ritual crimes, notably by investigating, arresting and prosecuting those who attack or sponsor attacks against people with albinism. In 2015, the Tanzanian government announced a ban on witchdoctors, which came out of a special joint task force between the police and the Tanzanian Albinism Society. As reported by the BBC at the time, then Home Affairs Minister Mathias Chikawe declared there would be a nationwide effort to “arrest them and take them to court” if witch doctors continued their practices. Over 200 suspects, including some allegedly involved in killings of people with albinism, were reportedly arrested by the authorities.
Ten years after the wave of killings and attacks began, these appear to have decreased because of Tanzania’s protective measures and stronger response to ritual crimes and attacks against people with albinism. The temporary holding shelters, however, remain. “The shelters were emergency, temporary solutions. But 10 years is not temporary anymore,” an activist for the rights of people with albinism told Human Rights Watch.
Under international human rights law, children with albinism have the right to live in a family environment. Local NGOs are now making efforts to reunite children and families. The Tanzanian government should do more to reunite families, to combat stigma within communities and ensure that family caregivers have the financial and social support they need to care for these children.
The government’s response should be guided by the best interests of the children involved, and balance the child’s protection and safety with the preservation of the family environment and the enjoyment of other rights. This is particularly important as the government has begun to send some children from the shelters back to their communities.
Separation from the family and movement restrictions
Most of the 13 children and young adults with albinism Human Rights Watch interviewed described how the killings and the ensuing protection measures implemented by the Tanzanian government separated them from their families.
While in many cases, separation was a decision of the parents, five children said they were ordered to go to a shelter or boarding school by government officials (police or district education officers), with no regard for their parents’ consent. Human Rights Watch was not able to confirm this assertion from their parents. Once in the shelters or special boarding schools, the children’s freedom of movement was severely curtailed on security grounds.
Marco, an 18-year-old man with albinism, described to Human Rights Watch how his father had been obliged to let him go to the shelter: “When the killings and attacks happened, the government moved me to the Buhangija temporary shelter (Shinyanga region). Police officers came home and spoke to my dad but he refused to take me to Buhangija immediately because he wanted to find out more about it first. The first time, the police left without problems. The second time, they left with me.”
Augustin, a 14-year-old teenager from Shinyanga who was attacked by criminals who cut his left forearms and fingers on his right hand when he was four-year-old, said the district education officer took him to the shelter when he was seven or eight. “He picked me up at a bus stand. At first, no one explained to me why I was being taken there. I was sad at the beginning because I missed my parents. It felt like a punishment. Now, I understand it was to protect me from bad people,” he told Human Rights Watch.
The mother of Victoria, a young woman with albinism from Shinyanga region who stayed for three years in Buhangija, confirmed that parents did not have any choice but to let their children go: “The government wrote a letter to the school Victoria was attending giving notification that children with albinism should be sent to Buhangija [shelter]. We were given a specific date and time by which she had to be there, which was two days later.”
Victoria’s father added: “When the government said we had to bring Victoria to Buhangija, I didn’t know why. There was security here…. But I had to accept the order. I don’t know what would have happened if I had refused.” 
NGOs that promote the rights of people with albinism also reported pressure by the government on local schools and the community to send children away to the shelters, by threatening to hold community leaders and members accountable if a child who remained at home was attacked. “For communities, having a child with albinism among them felt like a burden – because you have to provide protection – so the shelters were a good solution to get rid of that burden. You don’t have to respond to police enquiries if something happens,” a national advocate for the rights of people with albinism told Human Rights Watch.
In addition, parents of children with albinism and organizations working with people with albinism told Human Rights Watch that regardless of whether children had been voluntarily or involuntarily placed in shelters, once they were under the protection of the state, they were no longer allowed to go home – even for vacations – without a letter from the village chairperson, approved by the district commissioner, guaranteeing the area’s safety. An NGO worker explained the process to Human Rights Watch:
The parents [must] first get a letter from the chairperson of the village and then send it to the district commissioner. The chairperson’s letter should say that the area is safe, that we know the child with albinism is visiting the parents. Without the chairperson’s letter, the district commissioner cannot issue his own letter. Some parents complain and say that they have the right to take the children home. But they generally understand.
Severin, a 14-year-old boy with albinism, said he never went home on vacation while he lived in the shelter. “Once in Buhangija [shelter], we were told we needed a letter to be allowed to go home. My parents didn’t try to get the letter. I felt bad not to be with my family during the vacations because I missed them,” he said.
The parents of Victoria, a young woman with albinism who stayed for three years in Buhangija, who have university degrees, said it was easy to obtain such a letter from the authorities. “When the parents are bringing the letter, it assures the school that there is full security in the family and in the village [for children with albinism],” the mother said. “We wouldn’t have been allowed if we had tried to bring [our daughter] home for good. It was impossible to come out of Buhangija [shelter] without permission. There was full security.”
A representative of an international NGO sponsoring the education of children with albinism told Human Rights Watch that these restrictions also apply to children who have been moved out of shelters and into private schools under their sponsorship program.
As a result of the government’s restrictions, some children had not been home for several years, and some were no longer in contact with their family. In one case, Lucy, a 12-year-old girl with albinism, told Human Rights Watch at the time of the interview that she had not seen her mother in two years and did not know where her family was:
I was 6 years old when I got to Mitindo [shelter in Mwanza]. My mother brought me there because she saw the thieves [people attacking children with albinism] and so she took me to the [shelter]. I was left there alone by my mother and I felt sad because she said she’d come back but did not. She came back only once I went [to a private school, where I am being sponsored by an international NGO] in 2015. She came only for one day to ask who was paying my school fees and asked whether they could pay for my brothers too. I don’t know why she hasn’t come back. We don’t get to speak on the phone. I don’t have her number. So I don’t know about my mother and brothers right now.
According to representatives of local organizations working with people with albinism, another reason why some children placed in shelters no longer see their family is because their parents left no records of where they came from, and tracing the family after several years is difficult.“When some parents brought their children to the shelters, some didn’t leave any contacts and in other cases they did but the phone numbers don’t work,” a local NGO worker told Human Rights Watch. A staff member of another NGO said the temporary holding shelters had become akin to orphanages: “Parents took advantage to drop their kids there. Some children with albinism have been there for four or five years now without seeing their parents.”
The separation from family exerts a heavy emotional toll on young children with albinism. Peter, an 18-year-old man who stayed at the Buhangija for eight years, said his brother was the only one visiting him. “I didn’t want to come [to the shelter]. I was too young. I used to cry all the time. I was a child, I missed my mother, my grandmother and my sister,” he told researchers. “Only my brother would come to visit. I did speak with my mother however, maybe once a month by phone. I felt good talking to her but I missed her.”
Despite the difficulties children with albinism face in the shelters, some, including Severin, said they saw advantages in living among other people with albinism: “My parents did not come to visit at Buhangija. But it was good to be with other children with albinism because we felt we had a right to stay in the world.”
To protect children with albinism from physical attacks, a number of shelters and boarding schools have enforced drastic security measures that deprive children of their freedom of movement.
In July 2017, Human Rights Watch visited Buhangija, a former boarding school for students with disabilities transformed into a temporary holding shelter for children with albinism in 2009. At the time of the visit, 226 children were living in the shelter, out of whom 142 were children with albinism (the others were deaf or blind children attending the inclusive school located next to the shelter). At the shelter, Human Rights Watch researchers observed a barren compound made up of five dormitories surrounded by tall walls topped with barbwire. Children with albinism who attend class walk about 100 meters to the school. The rest of their free time is spent within the compound, which has no recreation space or trees to provide for shade, useful in helping people with albinism shield themselves from the sun.
“My first impression of Buhangija was that it was so difficult because we were staying in [the shelter] for the whole day and I’m a very mobile person. So I first felt very bad but as days went by, I got used to it,” Marco, an 18-year-old who left the shelter in 2017 told Human Rights Watch.
The principal of a secondary boarding school that caters to children with and without albinism in Mwanza region told Human Rights Watch that the movement of children with albinism is restricted even beyond the temporary holding shelter, and in the case of his school, because it lacks resources to adequately protect them outside the compound: “The main challenge with people with albinism is protection and safety,” he explained. “I’ve been asking since last year for one district policemen to be on site at night but there isn’t enough [district]money to do that. So, we talk to those students and discourage them from walking around alone, especially at night.”
A 15-year-old girl with albinism attending that secondary boarding school said they are not allowed to leave the dormitories: “The environment here is not good. We are not allowed to stay outside because the school doesn’t have enough security. Classes usually finish at 2:15 p.m. and we have to be in our dormitories by 2:40 p.m.”
NGOs have reported that children with albinism living in these shelters are progressively being sent back to their communities. While this is important progress, it is essential that the process of reinserting children in their communities complies with the best interests of the child principle. Authorities should ensure that the views of children and their families are taken into account, that children have access to education in their community, and that the community has protection systems in place.
Such consultations did not take place in the case of Mariam, a seven-year-old girl from Simiyu region, who was reunited with her 85-year-old grandmother. “After she was removed from Buhangija, the government forced me to take care of Mariam because her mother and father are not providing for her, “recalled the grandmother.” This happened without the government consulting me beforehand…. They just dumped the child on me.” Mariam does not attend the local school because, her grandmother said, she could not afford to buy textbooks.
Stigma and bias in the community
Eight children with albinism interviewed by Human Rights Watch recounted how they experienced stigma and bias in their communities, including name-calling.
Josefina, a seven-year-old living with her grandparents in the Shinyanga region, for example, said other children call her “Mbuliwmelu,” which means “white goat” in the local Sukuma language. “When that happens, it makes me feel sad and very angry, but I stay silent,” she said.
In the Simiyu region, the grandmother of Mariam, a seven-year-old young girl with albinism, said Mariam frequently faced similar experiences:
Most people have a negative perception of Mariam because of her color. They don’t even want to welcome Mariam in their home. If they see her, they’ll see her colour and will see that if she spends too much time in the sun she has sores. If she plays, they fear blood will come out of her. They call her “Mbulimwelu”. Mariam is always sad when they call her like that, and sometimes she locks herself in the house and starts crying. In those cases, I just leave her alone.
In some cases, parents have rejected or attacked their own children. Twelve-year-old Lucy, for instance, now lives at a private boarding school after receiving a scholarship from an international NGO. Choking on her tears, she said her mother told her that her father abandoned her prior to sending criminals to try and kill her: “My mother told me that my father refused me. I don’t want to go back [to my hometown] because it is my father who sent the thieves to get me.”
Despite efforts by the government of Tanzania and NGOs to sensitize the general public in recent years, progress remains fragile, especially in rural areas, where people with albinism continue to face stigma and the rejection of their community and, at times, their own families. This can lead to poor self-esteem among young people with albinism, and difficulties in finding work opportunities later in life. An 18-year-old man with albinism told Human Rights Watch in Shinyanga region that he thought people like him have a harder time at finding work: “My life would definitely be different if I was not a person with albinism. If you have a black skin, you have many more opportunities. You can do the physical work, whereas person with albinism have to be careful because of their skin.”
But, as the parents of four children with albinism pointed out, not all communities and families reject children with albinism. “When I had my first child with albinism, I was happy and thought this was normal. My family was happy too and if they weren’t, they didn’t let it show,” their mother said. “It is the choice of God. God is giving. We should agree with them, be close with them,” their father added.
Barriers to education
“People with albinism don’t get education,” a community organizer with albinism told Human Rights Watch. “Firstly because of their low vision. Teachers don’t know how to deal with that. Secondly because [of lack of] interaction [with others]. There is teasing in school. People with albinism face a lack of interaction with local community. People see us as bad people. They see us as people who can’t contribute because of our bad education or lack of education,” he added.
Ensuring a free, safe and dignified access to education is key to upholding the fundamental human rights of people with albinism and to combatting the stereotypes and stigma that continue to expose them to mistreatments and fatal risks.
Children with albinism face a range of barriers impeding their access to education.
Many families of children with albinism for instance are unable to enroll them in school because they lack sufficient income, or fear that having them walk to school may expose them to dangers. The grandmother of Mariam, the seven-year-old girl with albinism, said she is ready to go school but that she doesn’t have the resources to send her. “I wish for Mariam to become a doctor or a teacher. I don’t want her to be a wife. But it costs money to buy books and everything.”
Children with albinism may also face health risks at school due to their sensitivity to the sun. Laura, a 15-year-old student at a public secondary school, told Human Rights Watch that despite efforts to train teachers on the needs of children with albinism, the school still put the health of children with albinism at risk: “This school is not good. They force us to do activities in the sun. Teachers can also punish you if you say you can’t do activities in the sun. They caned me three times and it was very painful.”
In addition, children with albinism do not always get the inclusive education they should be entitled to. In that respect, the existence of the temporary holding shelters and other special boarding schools, while providing safety and an opportunity to attend classes, promotes segregation and denies children the opportunity to learn with their peers without albinism and to feel included in their communities. As 12-year-old Lucy explained to Human Rights Watch, “It was not nice to only be with children with albinism because we stayed without difference – we must mix.”
Children interviewed by Human Rights Watch also said that schools sometimes fail to provide children with albinism with appropriate accommodations for their low vision. This would include assistive devices, such as magnifiers, enlarged printed material, writing in large letters on the blackboard, and seating children with albinism in the front of the classroom.
Gloria, a 14-year-old student with albinism who wants to become an engineer and build airplanes said she had different experiences in public and private schools: “Before, I was going to a public school. I didn’t like it there because there was no good care. In class, the teachers would be writing with small letters on the blackboard. I’d ask them to make the letters bigger, but they’d say that they can’t,” she told Human Rights Watch. “[The private school] was better. They wrote with big letters on the board – it was easier for me to follow the classes and get good grades.” 
Some public schools are taking positive steps. The principal of a Mwanza region public secondary boarding school that caters to the general public as well as to several children with disabilities and children with albinism told Human Rights Watch: “There is no segregation. All students are taught together. We have many special education teachers and they are all trained by the government. I insist that children with albinism sit at the front row and that the teachers write with big letters on the blackboards and that exams and other exercises are printed with big font for them,” he said. Yet, the resources are scarce: “We get some equipment from the ministry, but not enough. We have no monoculars [to help children with albinism see the blackboard], for instance.” 
Lawrence is a shy nine-year-old boy who attends public school and his father is very proud of him. “When we took him to school for the first time, teachers were very aware of albinism, maybe they had been trained,” Charles said. “The only challenge Lawrence faces is his vision. Sometimes he has difficulties reading the blackboard [but] he gets support from the teachers and sometimes they explain or move him to the front. Lawrence does very well at school and sometimes is at the first position.”
It is important that all teachers be familiarized with the specific needs of students with albinism and that the schools be provided with adequate resources to ensure they can achieve their full educational potential. More efforts are also needed to sensitize family-members and communities about albinism, to ensure that children with albinism in Tanzania can thrive both inside and outside the classroom.
 Lekalakala, P., Khammissa, R., Kramer, B., Ayo-Yusuf, O., Lemmer, J. and Feller, L., “Oculocutaneous Albinism and Squamous Cell Carcinoma of the Skin of the Head and Neck in Sub-Saharan Africa,” Journal of Skin Cancer, August 12, 2015, https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4549604/ (accessed January 25, 2019).
 Human Rights Watch interview with Augustin (pseudonym), Tanzania, July 2017.
 Human Rights Watch interviews with A.Y. and Z.M. (pseudonym), the parents of Victoria (pseudonym), Tanzania, July 2017.
 Human Rights Watch interview with representatives of three NGOs working in this field, names withheld, Tanzania, July 2017.
 Human Rights Watch interview with community activist (pseudonym), Tanzania, July 2017.
 Human Rights Watch separate interviews with representatives of three NGOs working in this field, names withheld, Tanzania, July 2017; Severin (pseudonym), Tanzania, July 2017; and A.Y. and Z.M. (names withheld), Tanzania, July 2017.
 Human Rights Watch interview with NGO representative (pseudonym), Tanzania, July 2017.
 Human Rights Watch interview with Severin (pseudonym), Tanzania, July 2017.
 Human Rights Watch interviews with A.Y. and Z.M. (names withheld), parents of Victoria, Tanzania, July 2017.
 Human Rights Watch interview with NGO representative (pseudonym), Tanzania, July 2017.
 Human Rights Watch interview with Lucy (pseudonym), Tanzania, July 2017.
 Human Rights Watch interview with representatives of three NGOs working in this field, names withheld, Tanzania, July 2017.
 Human Rights Watch interview with a representative of one NGO working in this field (pseudonym), Tanzania, July 2017.
 Human Rights Watch interview with a representative of one NGO working in this field (pseudonym), Tanzania, July 2017.
 Human Rights Watch interview with Peter Mwanzi (pseudonym), Tanzania, July 2017.
 Human Rights Watch interview (pseudonym), Tanzania, July 2017.
 Human Rights Watch interview with Marco Ndimo (pseudonym), Tanzania, July 2017.
 Human Rights Watch interview with A.M. (pseudonym), Tanzania, July 2017.
 Human Rights Watch interview with J.P.M. (pseudonym), Tanzania, July 2017.
On numerous occasions Liberian leaders have publicly denounced the ritual murders that take place in the country. We can mention President William Tolbert (1971-1980), Gyude Bryant (Chair of the Transitional Government after the Second Civil War, 2003-2006) and President Ellen Johnson Sirleaf (2006-2018). The fact that the presidents Samuel Doe and Charles Taylor were not so outspoken on this subject, certainly not in public, has special reasons……..
The article below on Ellen Johnson Sirleaf’s warning and reaction does not constitute the first and only time that she denounced the phenomenon of ritualistic killings in her country. More on it at a later stage. (Webmaster FVDK)
Published: November 20, 2015 By: The Guardian
Liberia’s president, Ellen Johnson Sirleaf, vowed on Thursday to crack down on those responsible for a rise in ritual killings in the West African country as it seeks to emerge from the shadow of an Ebola epidemic.
In some areas of central Africa, body parts are prized for their supernatural powers and are used in black magic ceremonies. Local media have reported at least 10 related murders in Liberia in the past few months. (Italics added by the webmaster, FVDK).
Johnson Sirleaf said in a speech: “We are witnessing the rise in what appears to be ritualistic killings and armed robbery in the country, thus threatening our security.”
“I am instructing the security forces to rigorously enforce the law to the letter and bring this ugly situation under immediate control.”
It is not yet clear why ritual killings are rising and Johnson Sirleaf offered no explanation. Some residents have speculated that presidential hopefuls seeking to replace Johnson Sirleaf when her final term expires in 2017 are using black magic to boost their chances.
Liberia was declared Ebola-free for the second time in September after reporting more than 4,800 deaths but its economy is struggling to recover.
Johnson Sirleaf said in the same speech she would seek to boost power supply and access to electricity and build additional infrastructure in the last two years of her term.
Published: April 16, 2008
Writing by Daniel Flynn; Editing by Clar NiChonghaile
A sorcerer performs a dance in front of a sacred fire in Bitouga, some 600 km from the Gabon capital Libreville, in this September 2007 photo. REUTERS/Antoine Lawson
LIBREVILLE (Reuters) – When the body of 13-year-old Ralph Edang N’na was found drained of blood and with gaping wounds in his genitals, chest and neck last month, many in Gabon thought it was politicians who had ordered his killing.
The murder of children and young adults, whose organs are eaten or used to make magical amulets, has increased in recent years in the oil-rich central African nation. Campaigners say some Gabonese politicians use the black magic rituals to boost their chances of winning lucrative government posts.
With elections to local municipal councils due on April 27, many fear a spate of gruesome child murders.
Every week, mutilated bodies are discovered in the capital Libreville, despite police patrols, and streets quickly empty after nightfall. Anxious parents are keeping a close watch around schools to prevent children from being snatched.
“It’s before elections and ministerial reshuffles that the vilest crimes are committed and the capital empties of certain kinds of politicians who go to the interior to carry out witchcraft,” said pastor Francois Bibang, a member of the Association to Fight Ritual Crimes (ALCR).
In ritual killings, which still take place in several African countries, people, often children, are killed to obtain body parts and blood in the belief they will bring social success and political power.
The ALCR says that in February alone there were 12 such killings in Gabon.
“Unfortunately, this practice seems to be spreading again in Gabon,” said Jean-Elvis Ebang Ondo, who founded ALCR after his 12-year-old son was kidnapped, killed and mutilated in 2005.
The government set up a National Observatory for the Rights of Children in November 2006 to implement the U.N. charter on children’s rights, enshrining the right to health, education and protection from abuse.
Gabon, with just 1.6 million people, is one of sub-Saharan Africa’s largest oil producers but most of its population continue to live in poverty, while members of a rich elite drive shiny new cars along Libreville’s sea front boulevard.
Omar Bongo, the world’s longest-serving president, has ruled the country since 1967 and used the oil funds to weave a web of patronage which has created bitter competition for lucrative political jobs.
Ondo condemned “the silence of the state” and called on residents to “fight off these assassins who sow terror in the heart of Gabonese society”.
After a penal code approved in January omitted any mention of ritual crimes, Ondo called on the government to find out how many people had been killed in this way.
But no clear figures exist for how many children and teenagers are slain in ritual killings in Gabon.
The head of an association against ritual crimes, Frederic Ntera Etoua, said 290 killings had occurred since 1986 in the thick jungles of the Ogooue-Ivindo province in the northeast, where Ralph Edang N’na was killed.
“There is a pyramid organization with politicians at its head who pursue the famous ‘spare parts’ then the recruiters who are middle men and then the suppliers and sellers who find the innocent victims,” said Bibang.
Parliamentary speaker Guy Nzouba Ndama opened the latest session of the assembly on March 3 by denouncing ritual crimes by politicians.
So far no politicians have been convicted for involvement in such crimes. An attempt to prosecute a legislator from the oil-rich region of Gamba last year failed after he claimed parliamentary immunity.
Philippe Ndong, a psychology teacher at Libreville university, traces the rise in ritual crimes to 2001.
“As legislative elections approached, mutilated bodies were discovered around the country,” said Ndong. “An 8-year-old girl was snatched in Ndolou department and killed in Mouila. The man allegedly responsible was a candidate to parliament who entered the government after this crime.”
Ndong cites other ritual murders. In 2002, a man in his 20s, Lucien Bigoundou, was killed in the Digoudou forest of central Gabon while on a hunting trip with companions who cut off his genitals and other parts of his body.
In March 2005, the bodies of two 12-year-old boys were washed up on a Libreville beach — one was Ebang Ondo’s son. A month later, six-year-old Warlys Igor Mboumba was found dead in a Libreville gutter, his body drained of blood.
In January 2006, the bodies of three children under four were discovered in the trunk of a car in a private yard.
And last April, two men suspected of sodomizing a 3-year-old boy and draining his blood in a ritual killing were lynched.
“It is up to the government to put a swift end to this impunity or risk seeing a rise in mob justice,” said pastor Emile Ngoua, a member of the ALCR.
Muti murder in Clewer, near Witbank, South Africa – suspect dies in police custody
BY NALEDI SHANGE – Published on 22 March 2018 – 10:44
One of the men implicated in the killing of an elderly woman in Clewer near Witbank has died in police cells‚ said Mpumalanga police.
“The remains of a 65-year-old woman were found at Clewer near Witbank. Three men have been arrested in connection [with this]. However one of them collapsed and died while in police custody. An investigation is underway‚” said Brigadier Leonard Hlathi.
Further details on how the suspect died were not immediately available.
The victim‚ believed to be Aletha Maree‚ had been reported missing after her home was burgled on February 25‚ said the SA Crime Community Watch group.
“Many aspects however are leading us to believe that it will most likely be [the remains of Maree] that were found some nine kilometres from where SACCW earlier recovered some personal belongings of the missing person where a large search then took place‚” spokesperson Maureen Scheerpers said last week.
DNA tests were being conducted to verify the identity of the remains. Maree was believed to have to been killed as part of a muti ritual. Maree is one of three people from Witbank who have recently been killed in what is believed are muti-related killings.