This is not the proper place to dwell on the excesses of the Trump Administration. Moreover, I wouldn’t’t have enough time or space to do it. However, the following is obviously a violation of the right to asylum. People with albinism need protection of the state and the community, notably in Africa, where the risks of being attacked, kidnapped, mutilated or murdered for reasons of witchcraft are clearly present given the numerous reported cases. It’s a daily reality for a person living with albinism in Sub-Saharan Africa to fear for one’s life. Hence, it is absolutely understandable that a person with albinism who does not get the protection he or she needs, flees to a place where the superstitious and violent practices as they occur in SSA are absent.
This explains the reason of fleeing to the US by a Nigerian with albinism, named Aisha (real name withheld for private and safety reasons). The Trump Administration’s asylum crackdown shattered her dreams of a quit and peaceful life in the US.
How on earth could one decide to deport her to Uganda, a place known for being unsafe and dangerous for persons with albinism?
Uganda is not a ‘safe third country’ for people living with albinism, whatever the US Department of Homeland Security may say. It’s an outright scandal, and human rights violation – unfortunately neither the first nor the last of the Trump Administration.
Moreover, the policy of deporting unwanted persons to a so-called safe third country, often poor countries (lamentably, the US is not the only western country resorting to these practices) has definitely (neo-)colonial characteristics. Another reason to reject it. (webmaster FVDK)
‘I was devastated’: the Nigerian with albinism deported under Trump’s asylum crackdown
Published: July 1, 2026 By: Sarah Johnson (name has been changed at the subject’s request) – The Guardian
Growing up and living with albinism in rural Nigeria was tough for Aisha*. She and her two siblings with the condition were shrouded in stigma and lived in constant fear of being mutilated or killed. Her sister was attacked twice and her brother was kidnapped as a child by people who wanted to sell his body parts.
A bus arrives in Jinja, Uganda, before a march against discrimination, held by people with albinism and their supporters to mark International Albinism Awareness Day.
Three years ago, Aisha, 35, entered the US via the border with Mexico and registered as an asylum seeker. Her brother had already been granted asylum and her sister’s case was soon to be successful, too.
But in March she was informed that her claim would not be heard and that she would be deported to Uganda instead – a country in east Africa deemed safe by the US Department of Homeland Security.
“I was devastated and shocked when the judge denied my case,” says Aisha. “All the evidence was there – my siblings were attacked in Nigeria.
“In Uganda the same thing happens, they take people for [witchcraft] rituals and everything. I don’t know what else they needed for me to show them that I have a legitimate case.”
Albinism is an inherited genetic condition that reduces the amount of melanin pigment formed in the skin, hair and eyes. It occurs in all ethnic groups throughout the world. In subSaharan Africa, the prevalence of albinism is the highest worldwide, and it affects more than one in 4,000 people in some countries, according to the World Health Organization.
In countries throughout subSaharan Africa, including Nigeria and Uganda, people with albinism face severe threats, including ritual killings, rape and mutilation. These attacks are driven by harmful superstitions that their body parts bring wealth, political success and good luck.
Aisha’s lawyer, Ravindar Arora, who also represented her two siblings, calls the decision to deny her asylum “ridiculous”.
“Having worked as an immigration lawyer in the US for 15 years, I’ve got a good sense of what is a winnable asylum claim and what’s not,” he says. “This should have been a slam dunk.”
He adds that the Trump administration’s immigration crackdown has been playing havoc with people’s lives and his job. “It’s insane. Trump’s first term was not great … attorney generals were plucking out cases, writing their own decisions and overturning decades of precedent in the process. That was bad enough. This is easily 10 times worse.”
According to Ikponwosa Ero, director of advocacy at Under the Same Sun, a charity helping people with albinism, the rise of anti-immigrant rhetoric and farright movements in the US and Europe is leading to more asylum claims for people with albinism being denied.
“[These cases were successful] up until the last couple of years, with the changes in administrations worldwide where people are looking more inward,” she says. “Before that, we had an estimate of an over-90% success rate. But with the changes in administrations and political approaches [that’s no longer the case].”
Under the Trump administration, the US has entered into several new asylum cooperative agreements (ACAs) accords that allow governments to transfer asylum seekers to third countries rather than adjudicating their claims domestically.
Under these arrangements, people may be removed to a “safe third country”, even if they have no ties to that nation. One exception to the ACAs is if someone would be persecuted or tortured in the third country.
Arora says he submitted evidence in Aisha’s case showing that people with albinism are not safe in Uganda. “We even had an expert witness testify, who is from Uganda and who lives with albinism. The judge tried to turn that around on us and said she was living in Uganda, so it must be safe,” he says.
The Ugandan government’s action plan for persons with albinism 2020-25 says they are “a vulnerable group that faces multiple and intersecting forms of discrimination and human rights violations”.
It adds: “They have been subjected to discrimination, banishment, cutting of body parts and amputation of limbs, torture, and murder due to … unfounded beliefs [in witchcraft].”
Arora believes Aisha has a strong case and even if it is rejected at the next stage, the Board of Immigration Appeals, they will appeal again.
Aisha, who has married and had a child since she arrived in the US, says: “I don’t even know what to think. I was really hopeful and then my [asylum request] was denied. Still, I remain hopeful that I will be able to pursue my goals and live a normal life here.”
• This article was amended on 30 June 2026 to remove some personal information.
The life of Nelisiwe Shiba, a woman born with albinism, was never the same after dodging the night she was meant to ‘disappear’ for good, as per the age-old legend that people like her do not die — they simply vanish.
They can even leave the house in the middle of the night without informing anyone, as the legend goes, and take on a mysterious journey to a forest or mountain – never to be traced again.
However, just hours before the evening when such was scheduled to happen to Shiba (35), she was given a timely tip-off by a community resident supposedly sent by a member of the very group that had plotted to make her vanish forever. The member seemingly had a change of heart.
This took place in one of the small rural communities of Northern Hhohho, whose name she preferred not to disclose. She was 25 at the time and had a small child.
Since then, Shiba has been living with the kind of fear that grips people with albinism nowadays — that when the sun sets, they could fall victim to ritual killing disguised as mysterious disappearances. Albinism is a genetic condition in which a person is born with little or no melanin pigment, resulting in lighter skin, hair, and eyes and often causing vision problems.
Harmful myths falsely claim that people with albinism possess magical powers or bring wealth, a misconception that has contributed to discrimination, attacks, and ritual killings.
Elaborating on her account in the wake of International Albinism Awareness Day, commemorated on June 13 to promote the rights, dignity and inclusion of persons with albinism worldwide, Shiba mentioned that she had previously been oblivious to grave dangers faced by people like her.
“After I graduated from Limkokwing University, I relocated to Northern Hhohho because I got a piece-job as a shopkeeper in a grocery shop owned by a relative. The community there was very welcoming and I never felt unsafe, even at night,” she said.
The only challenge she knew and had experienced as a person with albinism was discrimination. Being vulnerable to murder for ritual purposes was a myth to her until the day she got a grave warning that saved her life.
Recounting the events of that day, she stated:
“The community member came to the shop where I worked.
He said he wanted my father’s contact number. I was sceptical about giving it to him, but he insisted with some urgency.”
She yielded after the man bluntly told her that she was not safe and must ensure she did not close the shop late that day.
“He called my father and I overheard the conversation. He informed him about a plot to take my life and that it was a done deal. I had been sold, that night would be the one I disappeared,” she stated.
Shiba also overheard that a certain witchdoctor or sorcerer was part of the group and had approved her as a suitable target. He would be there to oversee the ritual process of the killing. The fact that she had a small child, though without albinism, was viewed as a bonus. Shiba was going to ‘disappear’ with her child.
“When he finished the phone conversation, before departing, he gave me another stern warning not to tell anyone what I had heard.
Shortly afterwards, I received a call from my father, who told me to pack up and find someone to carry on with the shop the following day because he would be fetching me before evening,” she explained.
Shiba remembers being emotionally traumatised by the visit and feeling weak at the knees with fear due to sudden realisation she was never completely safe due to her albinism.
Early that evening, her parents arrived in a car and took her and her child away without giving any hint that it was, in fact, a desperate escape.
She recalled that the community member who warned her father hinted during the phone call that the homestead involved in the deadly plot was nearby.
These were people she interacted with almost daily and would never have suspected to harbour such intentions. Looking back, she says the incident became a turning point that fuelled her distrust of people — something that persists to this day. It takes time for her to let down her guard.
“I don’t hitchhike or accept lifts unless it is from someone very close and trusted. I rely on public transport and would rather go back home than accept a lift from strangers,” she added.
Since that day, she has also become sensitive to noises at night. The slightest sound in or outside the house wakes her up, and she listens carefully to determine its nature.
Over the years, Shiba channelled that fear into advocacy by joining the Swaziland Association of Persons with Albinism (SAPA), where she has since risen to the position of president.
“I’ve also become a motivator for persons with albinism and try to fight for our rights. Apart from threats to our lives, we suffer social discrimination a lot, as many people have wrong information about albinism,” she said.
“There’s still a long way to go in educating the nation and debunking all the myths.”
The Swaziland Association of Persons with Albinism (SAPA) has raised alarm over persistent discrimination, dangerous superstitions and violence against people with albinism.
The association warned that the situation amounts to an ‘undercover genocide’, not just in the kingdom, but the wider Southern African Development Community (SADC) region. The concern was expressed by SAPA Executive Director Philemon Gama during the commemoration of International Albinism Awareness Day held at the Deputy prime minister’s office on Friday.
The event was attended by Minister of Tourism and Environmental Affairs Jane Mkhonta-Simelane, who represented Deputy Prime Minister Thulisile Dladla. Representatives from disability organisations and SAPA members were also in attendence.
Gama said misinformation about albinism remains widespread, contributing to stigma, exclusion and in some cases, violent attacks. He noted that harmful beliefs—such as the idea that people with albinism do not die but disappear, or that their body parts bring luck—continue to place them at risk of ritual killings.
He cited recent incidents in the Southern African Development Community (SADC) region, including the killing of children with albinism in Madagascar and another case in Malawi involving a relative. He cited cases in the country, recalling the 2010 murders of two children in the Shiselweni region and a another in the Hhohho region in 2016, which he said demonstrate that the threat is not theoretical but real.
“These are not was olated incidents. They reflect a deeper problem driven by superstition and silence. In many cases, disappearances are not properly reported due to cultural misconceptions,” Gama said.
Beyond safety concerns, he highlighted systemic discrimination affecting access to opportunities, including financial assistance. He said persons with albinism were often met with skepticism when seeking support, limiting their ability to improve their livelihoods.
Gama welcomed government efforts to improve living conditions for persons with albinism, including a housing initiative announced by the deputy prime minister’s office. Under the programme, five houses were allocated, with two already completed and handed over at Mhlangatane and Mayiwane, while three remain under construction.
He further called for SPF 50+ sunscreen to be included on the national essential medicines list, arguing that it should be provided free due to the health risks associated with prolonged sun exposure.
SAPA also urged stronger regional and continental legal protections, calling on governments and the African Union to intensify efforts to prevent ritual killings and discrimination. Gama appealed to communities, traditional leaders and the media to actively challenge harmful beliefs and ensure responsible reporting.
He stressed that awareness must extend beyond annual commemorations.
“This issue requires consistent attention, education and action throughout the year if we are to achieve meaningful change,” he said. Gama concluded by calling for sustained advocacy and stronger institutional support to ensure the safety, dignity and full inclusion of persons with albinism in society.
Warning: the following post contains graphic details of abductions, mutilations and other criminal acts including murder which may upset readers.
Unfortunately, the abduction, mutilation and killing of persons with albinism for ritualistic purposes have never disappeared in the Southern African country of Malawi. I have devoted considerable attention to this in the past.
Without pretending to be exhaustive I refer to the following posts: 2015, 2016, 2018, 2019, 2020, 2021, 2022, 2024. Interested readers may use the dropdown menu (under ‘African countries’) for all posts on Malawi. For last year, 2025, I may refer to an article published by The Guardian, A friend killed, and inquiries shelved: life fighting the stigma of albinism in Malawi (not covered on the present ste). It draws attention to the increasing fear among people with albinism in light of the scheduled elections.
As has been reported before, there exists a link between an increase of reported ritualistic killings and elections (see my March 18 post) – and Malawi does not seem to be an exception – whereas the Association of Persons with Albinism in Malawi (APAM) has drawn attention to the connivance of certain politicians who obstruct fair investigations into reported attacks on people with albinism and ritual murder cases or sweep them under the rug, see my 2021 post on the subject.
The Malawi-based journalist and media professional Benson Kunchezera has a strong focus on development reporting, particularly in areas such as agriculture, digital innovation, public health, and environmental sustainability. Besides the just mentioned areas of interest and competence he is also interested in human rights issues in particular the position of persons with albinism and their plight in some countries notably Malawi. I commend him for drawing international attention to the precarious position of people with albinism in Malawi and highly recommended reading his recently published article on this topic.
Malawi’s renewed attacks on persons with albinism raise alarm
Attacks, abductions, and grave tampering targeting persons with albinism have resurfaced across Malawi in 2026, reigniting fears that the country’s progress on protecting this vulnerable community is unravelling. Civil society is fighting back — but without a renewed national action plan, advocates warn the worst may be yet to come.
The story of Flora Saidi remains one of the most painful reminders of the violence faced by people with albinism in Malawi. According to accounts documented by advocacy organisations supporting persons with albinism in the country.
Flora Saidi
It was a Monday morning in 2003 when Flora Saidi left her home in Kadewere village under Traditional Authority Chowe in Mangochi, hoping to find piecework to feed her family. She left behind her 19-year-old son, Saidi Daitoni, a young man with albinism.
When she returned home empty-handed later that afternoon, her son had managed to earn a small amount of money. They agreed to share it with his girlfriend, who was visiting. Saidi left with her to look for change so they could divide the money properly. He never returned.
The following morning, Flora began searching for him. By then, he had disappeared. Police were informed, and after a search, his body was discovered near a residence he had visited the previous evening. Some of his body parts had been removed. The perpetrator was later sentenced to 155 years in prison with hard labour.
PERSISTENT THREATS IN RURAL MALAWI
Malawi has 134,636 persons with albinism, with over 117,000 living in rural areas. It is in these rural communities where poverty, limited law-enforcement presence, and entrenched myths combine to create dangerous conditions.
Persons with Albinism, especially in the southern African regions face persecutions, because their body parts are believed to bring lack of wealth after being mixed with some concoctions by a witch doctor.
Others believe that when they have unprotected sexual intercourse with a person with albinism they can get cured of HIV/ AIDS.
The Association of Persons with Albinism in Malawi (APAM) has documented fresh cases in districts including Mulanje, Kasungu, and Dowa. Grave tampering and disappearances have reignited fear among families who had begun to feel cautiously safe.
In February 2018, Amnesty International published a joint report by the Ministry of Justice and Constitutional Affairs and the Malawi Police Force with 148 cases reported in Malawi’s four districts.
Recently, in 2026, more than 4 cases of persons with Albinism have been recorded by the Malawi Police Service ranging from attacks, abductions and tampering of graves in some parts of the country.
“We thought we were coming to an end of these attacks,” Maynard Zacharia, APAM’s National Coordinator, told FairPlanet. “Now we are seeing signs that the underlying issues were never fully resolved.”
Maynard Zacharia
COMMUNITY PROTECTION IN ACTION
In response, APAM has intensified its on-the-ground efforts. The organisation is not only condemning attacks publicly but also mobilising communities in hotspot districts such as Machinga.
One strategy involves relocating children with albinism from high-risk areas to safer homes. In some cases, this means placing them in boarding facilities or with vetted guardians where security is stronger. At the same time, APAM is lobbying authorities and partners to invest in secure-housing projects with reinforced doors, burglar bars, and community-based surveillance systems.
Beyond physical protection, APAM is conducting awareness campaigns aimed at dismantling the myths that drive violence. Working with chiefs, faith leaders, and local youth groups, activists hold community dialogues that confront harmful beliefs directly. In village meetings, survivors and families share testimonies, reframing albinism as a genetic condition rather than a mystical anomaly.
“These conversations are not easy,” Zacharia told FairPlanet. “But we have seen that when traditional leaders publicly reject the myths, attitudes begin to shift.”
The organisation is also pressing for the conclusion of more than 28 long-pending court cases involving murder and abduction. By monitoring proceedings and engaging legal-aid partners, APAM hopes to prevent cases from stalling indefinitely — a pattern that erodes public trust.
Kaiyatsa told FairPlanet that fear remains a major barrier to reporting threats. In rural areas, families often hesitate to approach police due to mistrust in the justice system and fear of retaliation.
According to him, the situation was further complicated by the controversial pardon of police officers previously convicted in connection with an albinism-related killing. For rights groups, the decision sent a damaging signal.
“To victims’ families, it suggested that justice can be undone,” Kaiyatsa told FairPlanet. “To would-be offenders, it reinforced the perception that accountability is not guaranteed.”
Michael Kaiyatsa
In response, CHRR and other organisations have stepped up advocacy for witness-protection mechanisms and independent monitoring of investigations. They are pushing Parliament and relevant ministries to allocate dedicated funding for protection programmes and to ensure that cases are prioritised within the judiciary.
REVIVING NATIONAL COMMITMENTS
Malawi once drew international praise for adopting a National Action Plan on the Protection of Persons with Albinism. However, the plan expired in 2022 and has yet to be renewed, leaving what activists describe as a dangerous coordination gap.
“Commitments on paper are not enough,” Zacharia says. “We need implementation that reaches the village level.”
REBUILDING TRUST FROM THE GROUND UP
On the ground, solutions are increasingly community-driven. In some districts, local committees made up of chiefs, police representatives, teachers, and activists meet regularly to assess risks and share information. Informal early-warning systems — such as community WhatsApp groups with coordinated night patrols-have been introduced in certain high-risk areas.
Civil society organisations are advocating for long-term assistance for affected families, including counselling, educational support for orphaned children, and income-generating projects for households that have lost breadwinners.
These initiatives aim not only to respond to attacks but to address their ripple-effects — school dropouts, psychological trauma, and deepening poverty.
A FRAGILE BUT DETERMINED PROGRESS
Organisations such as the Scotland Malawi Partnership insist that regression is not inevitable. They point to the increasing visibility of persons with albinism in advocacy spaces, media platforms, and leadership roles.
Flora Saidi, though still grieving, has participated in community meetings where she shares her story. Her testimony serves both as a warning and a call to action.
For Malawi, the struggle to protect persons with albinism is about more than ending ritual killings. It is about strengthening rural policing, restoring faith in the justice system, and dismantling centuries-old myths.
For people like Flora Saidi, safety is still uncertain, but hope lies in the quiet work happening in villages and communities across Malawi.
Their efforts may not end the attacks overnight. But for families living in fear, each community meeting, each court case and each safe home built is a step toward something simple with the chance to live an ordinary life without fear.
Warning: the article presented here contains graphic details which may upset readers.
On March 17, I posted Tanzania court upholds death sentence in rural murder. A Babati man who had been found guilty of murdering his stepson for ritualistic purposes heard the final verdict for his crime: the capital punishment.
A few days later, Joseph Muhuila, an Iringa man, was given the same sentence by the High Court of Tanzania: death by hanging, for killing his four-year-old son, Timothy Muhulila, allegedly for ritualistic practices. The cruel crime occurred on April 12, 2025.
Iringa Region is one of Tanzania‘s 31 administrative regions, located in the middle of this East African country, in size comparable to e.g. Guinea-Bissau in West Africa. In 2022 the region had a population of about 1.2 million people.
So, within a short space of time, the law in Tanzania dealt decisively with ritual murderers who have been found guilty. On the one hand, this shows beyond any doubt that ritual murder does indeed occur in this country of over 70 million inhabitants, spread across more than 120 different ethnic groups. (There was, incidentally, no doubt about this, as Tanzania is often in the news for the wrong reasons due to the abduction, mutilation and ritual murder of people with albinism. Also see my 2019 post on the precarious position, discrimination, kidnapping and murder of people with albinism in Tanzania.) On the other hand, it is also a hopeful sign that the country’s highest authorities are serious about prosecuting the perpetrators of these violent crimes, which are based on superstition, greed and contempt for the right to life of innocent people, sometimes small children or other vulnerable individuals. (webmaster FVDK)
Iringa man sentenced to death for killing four-year-old son in ritual killing case
Published: March 18, 2026 By: Friday Simbaya – The Citizen
When I first read the article presented below and published by the Guardian, entitled ‘The children are not safe here’, about a Nigerian couple – Olusola and Chinwe Stevens – fighting infanticide in their own home country, I remembered an earlier article describing this courageous couple and their admirable work. In 2018, to be precise on May 9, 2018, I published a post entitled ‘Nigerian couple working to eliminate infanticide in Nigeria‘, on two Christian missionaries, Steven Olusola Ajayi and his wife Chinwe who in 2004 had opened a shelter for so-called ‘evil children’, the Vine Heritage Home.
Without any doubt, this is the same couple and the same home presented in the 2026 Guardian article below. The 2018 article on the missionary couple was originally published on a website called ‘This Is Africa’. It was an opinion-article. Unfortunately, the exact title is missing. lIn 2018 I had juist started the present site on ritual killings, superstition, witchcraft, infanticide and human rights, and – with hindsight – at that time there was still lack of a systematic presentation.
Unfortunately, the original 2018 article no longer exists on he internet. This is precisely the reason why I have opted for the actual approach to copy-paste articles selected for my postings (together with my comments), as I had this experience before. See the section Why publish this site?
Infanticide is a crime, caused by ignorance and superstition. Nigeria is certainly not the only African country where systematic infanticide exists, i.e. the systematic killing of small children, babies. I regularly read about infanticide in other countries where sometimes desperate mothers kill their newborns. But the shelter created by Olusola and Chinwe Stevens, VIne Heritage, is for other babies whose life is threatened: new born babies who are considered ‘evil’ children, who are believed to be bad omens. Babies with disabilities, albino babies, twins, are suspected to bring curses and bad luck. Hence… they are killed, buried alive, or ‘simply’ disappear.
I express my deep respect to the Stevens couple and am convinced that their work is not in vain and that it will ultimately contribute to the eradication of a terrible crime that has existed for too long. (webmaster FVDK).
If you would like to support The Guardian financially, please click here.
‘The children are not safe here’: the Nigerian couple fighting infanticide
Triplets Paul, Pauline and Paulina at the Vine Heritage Home Foundation, Gwagwalada, aged six months in July 2025. Photograph: Adesegun Adeokun/The Guardian
In a few isolated communities in central Nigeria, some babies are believed to be bad omens. Olusola and Chinwe Stevens run a thriving home for babies at risk. But what happens when the families want them back?
Esther Stevens’ life nearly ended as soon as it began. She was born in 2007, in a village on the outskirts of Abuja, Nigeria’s capital city. Her mother died giving birth to her, and in the eyes of some villagers, that meant the baby was cursed. According to tradition, there was only one way to deal with such a child. The villagers tied the newborn to her mother’s lifeless body and prepared to bury them together.
When word reached a Nigerian missionary living in the community, she rushed to the burial site and pleaded for the baby’s life. After the villagers and relatives refused, she appealed to the traditional priest who had been called on to perform the rite. “Finally, the priest agreed and said, let them give her the evil child and see what the child will become,” Esther said. “The child, that’s me.”
The missionary took Esther to a children’s home in Abuja run by a Christian couple, Olusola and Chinwe Stevens, who brought her up as their own. Today, Esther is 18, tall, with a broad smile. She laughs easily and has a quick sense of humour.
In Nigeria, children are widely regarded as gifts from God or the spirit world, but according to some traditional belief systems, certain children were once thought to bring misfortune. Children born with albinism, visible deformities or disabilities were said to bring curses, or to be omens sent from ancestors or deities. In parts of southern Nigeria, particularly among the Igbo, twins and triplets were feared. Although these beliefs have largely faded, in isolated pockets of the country, they persist. In some of these communities, says the human rights activist Leo Igwe, the death of the mother in childbirth is believed to be the fault of the child.
The couple who run the children’s home where Esther grew up have been confronting these practices since 1996. Sent by the Christian Missionary Foundation to Abuja, the Stevenses discovered that some children were still being killed: poisoned, abandoned to starve or buried alive. In 2004, they created the Vine Heritage Home Foundation, a refuge for vulnerable children. Twenty years later, they provide a home for more than 200 children.
When Nigeria moved its capital from Lagos to Abuja in 1976, the new site was presented by the government as a neutral location, symbolically distant from centres of ethnic and regional tensions. But less than 40 miles away from this gleaming modern capital, with its wide boulevards and high-rise buildings, are communities that become nearly impassable in the rainy season. Many of these communities depend largely on subsistence farming, and the few healthcare facilities are poorly equipped and understaffed. According to Olusola, 75% of the children living in Vine Heritage are there because their mothers died in childbirth. (Nigeria is “the most dangerous country in the world to give birth”, according to UN data from 2023, which shows that one in every 100 women dies during childbirth or shortly after, many from postpartum haemorrhage.)
After their shocking discovery, the Stevenses began going around the communities, begging the families to hand over to them any of the “cursed” children rather than kill them. Then they began to speak with other local missionaries, asking them to spread the word that they were willing to take in any child deemed evil.
One of their contacts, missionary Andrew Tonak, told me that Chinwe is one of the most open-hearted people he has met, a mother and leader whose counsel, generosity and instinct to give have touched countless lives. Tonak is 61, and has lived in Kaida village, about 40 miles west of Abuja, since 2000. He recalled visiting women who had just given birth to twins. On his next visit, he would often be told, “The children are no more. They died.” Over the years, he says he has rescued 20 children from the village and neighbouring communities.
By the time some of the children now at Vine Heritage were rescued, they were already weakened by poisoning or severe malnutrition. Most required urgent medical attention. But increasingly, communities are becoming aware of the Stevenses’ work and now bring newborns to them directly, before harm can come to them.
Olusola said: “On their own, they come asking, ‘Please, where is that house where they keep the children?’ And then they bring them.”
Today, Vine Heritage is home to more than 200 children, from newborn to young adults. The oldest, Godiya, is 21 and has been at Vine Heritage since she was a baby. The newest arrival before my visit, a baby born on 27 May 2025, has been fighting for her life in a hospital crib since the day she was brought to the home.
About four years ago, Vine Heritage moved from a cramped facility that was originally designed to accommodate 55 children, to a much larger compound in Gwagwalada, built with funding from the EU in partnership with global charity ActionAid. The home has 18 dedicated staff working in shifts to provide round-the-clock care for the babies and toddlers. In a spacious hall, everyone gathers for morning prayers, group meetings and TV time. (Like any home full of children, there’s a constant battle for control of the remote.)
As I followed Olusola on a tour of the neatly laid-out grounds, he moved in a sprightly fashion, his greying beard framing a warm smile. At the youngest children’s dormitory, a chorus rang out: “Daddy! Daddy! Daddy!” They are not allowed out unaccompanied, and their small faces were pressed against the windows.
Esther Stevens, 18, who has been living at the home since birth. Photograph: Adesegun Adeokun/The Guardian
The multiple-birth siblings all have names that sound alike: Victor and Victoria, Mabel and Bethel, Zion and Zipporah. Among the youngest residents are triplets named Paul, Pauline and Paulina. Their parents arrived at the home one morning about six months ago, cradling the newborns in their arms. “I asked, ‘Why did you bring them?’ They said, ‘We don’t want them to die,’” Olusola recalled. The parents have visited once since then. They love their children, but fear that if the babies remained in their village, they would be killed.
Esther is clearly a favourite among the younger children. They love to follow her around and clamber on to her back, and as she and I chatted, they hovered close by. Esther knew nothing of her true origins or how she had come to live in the house until she was 14. She had been among the first children to arrive, joining the household in 2007 when there were only nine or 10 others. Olusola and Chinwe have one biological child, Praise, now 24 and studying at university. In those early years, Esther assumed she was also their biological daughter. As more children joined over time, she believed she was simply growing up in an orphanage run by her own parents. All the children bear the surname Stevens. “I knew it was an orphanage home, but I thought I was their real child. I look like mummy,” she said, and she does share some resemblance to Chinwe, with the same complexion.
Esther’s illusion was shattered when members of her biological family unexpectedly arrived at the home. At the time, the missionary who had rescued her as a newborn was preparing to leave the community. Before departing, she contacted Esther’s biological family to ask if they wanted to see where she had taken their child, knowing that once she left, they might never have the chance. “My grandmother came from the village and said she wanted to see me,” Esther recalled. “She wanted to see if I was still alive. When she told my father I was alive, he came to see with his own eyes.”
To prepare her for the meeting, Olusola sat her down and told her the truth about her past. “I was more than shocked,” she said quietly. “I felt sad. I felt bad.” Wanting to know more, Esther asked for her file. She read it cover to cover. What hurt most was discovering that her family had never come for her in all the 14 years she had been there. “Finding out about my parents’ true identity … It was just … I shed tears because they didn’t even care.”
Kaida, a village in Gwagwalada, is the closest community to Abuja’s city centre where there is evidence that infanticide may still sometimes take place. There are no tarred roads to the village, and the route is rough and bumpy, but it is better connected than most. There is a patchy phone signal here.
In Kaida, I met Abubakar Auta, a father of 13 and a husband to two wives. His twins Eric and Erica were sent to Vine Heritage about seven years ago. Like almost every adult in Kaida, Abubakar and his wife, Amina, farm for a living. To supplement their income, Amina digs sand from the river to sell to builders. She arrived to meet me straight from her work, dripping wet, sand clinging to her bare feet. Of her husband’s 13 children, seven are hers. Abubakar said he sent the twins away to “save their mother from suffering”. He believed they would not be safe in Kaida. Speaking to me in Hausa through a interpreter, he explained, “If I had left my children here, people would keep their eyes on them, and that would make them a target.” (Eric later died at the children’s home after falling ill.)
Kaida village has solar power, which provides a few hours of electricity each day for its two clinics: one government-run, the other operated by missionaries trained in community health. The government facility stands silent and empty. Locals say its staff are rarely present. The missionary clinic, by contrast, is alive with activity.
While I was there, a community health worker tended to a woman whose young grandson had a toe injury, the wound still raw and red. The woman had told me earlier on, in her home, that she had previously given birth to three sets of twins. All of them died within months. “They just fell sick,” she said. “In a short time, they were dead.”
Olusola Stevens with some of the children at Vine Heritage Home in Gwagwalada, July 2025.Photograph: Adesegun Adeokun/The Guardian
Her eldest child in his early 20s, sitting nearby, looked up and interrupted. “It was an evil hand that killed them,” he said, his tone defiant. At his words, his mother fell silent and turned her face aside, making it clear she wanted no part in that line of conversation.
The village head described the killing of children as belonging to “a time when people did not know these children were human beings”. He repeatedly used the phrase “in those days” to explain that their “eyes are now open” and such killings no longer happen. (He confirmed that the practice continued until at least a little more than 10 years ago, and that his “those days” referred to the years before then. Lakai has served as village head for the past 26 years.)
Community members are reluctant to speak openly, whether out of fear of stigma, distrust of outsiders, or the sensitivity of exposing cultural taboos. What I was able to piece together from these guarded, euphemistic conversations suggests that decisions involved a mix of family elders and traditional religious leaders. Leo Igwe, the human rights activist, acknowledged the role of patriarchy in situations where women surrender their babies to die. In 2019, ActionAid ran a survey in 57 villages around Abuja in which 16% of male respondents openly expressed support for the practice.
The shroud of secrecy has made it hard to tackle these beliefs. When I contacted various government officials, each one said they had never heard of such practices. Infanticide is against the law, but enforcement is hampered by secrecy and denial. Arinze Orakwue worked for nearly 20 years for the state body responsible for rescuing vulnerable children. From the early 2000s, he visited many communities where infanticide is practised, meeting with traditional chiefs and local leaders in an effort to change entrenched beliefs. “Many of them are living in denial. They tell you that it used to happen in their community a long time ago but it doesn’t happen any more.”
As more children were brought to their home, the Stevenses realised the scale of the problem. In 2013, when they decided to speak publicly about infanticide, the Federal Capital Territory government summoned them, accusing them of spreading falsehoods and damaging Nigeria’s image, just to attract attention and donations. Yet this scepticism faded after officials were shown clear evidence. The government eventually commissioned the couple to run awareness campaigns in the affected communities. They have built new partnerships, most notably with ActionAid. “The greatest problem is denial,” said Andrew Mamedu, ActionAid’s Nigeria head. “The community will insist, ‘Oh, there’s nothing like that.’ But when you go there, you see the evidence. You see the altars to the dead twins. Sometimes, the parents can’t account for their children. They are pregnant and before you know it, they’ve given birth and the baby is gone.”
ActionAid’s approach to the problem was patient, practical and deliberately indirect. Staff set up committees in each community – made up of men and women, young people, traditional rulers and religious leaders – and framed their aim as community development. “We don’t start with infanticide because they would just drive us away,” Mamedu said. The teams began by focusing on livelihoods, education, hygiene and access to healthcare, and only then moved on to tackling infanticide, under the broader banner of maternal and child health. Committee members acted as local advocates. One of their most effective tools was radio, still the most widespread and trusted source of news in northern Nigeria.
Chinwe Stevens at home.Photograph: Adesegun Adeokun/The Guardian
The strategy produced some measurable gains. In two communities ActionAid’s advocacy helped secure government investment in health centres. In four communities, the killings gradually stopped. Parents who had handed over children returned to the home to ask for them back. New local “champions” began to emerge, ordinary people willing to speak up. Still, the effort had its limits. Resistance from influential elders persisted, and when funds ran short in 2022, much of the work was left unfinished.
The Stevenses continue to work closely with missionaries stationed across the area. But not all rescues come through Christian networks. In Godiya’s case, it was a Muslim cleric who stepped in. “The Islamic preacher went to the community to preach and make converts, just like I do,” Olusola recalled. “He saw a child strapped to the dead body of her mother. They were preparing the grave. He asked, ‘Please, this child, what happened?’ They told him she was an evil child, and that their culture was to bury such children with their mothers. He said, ‘Can you permit me? Let me call my pastor friend so he can come and pick up the child.’ So he called me, and we went to the community and took her.”
When the Stevenses first established the Vine Heritage Home, their vision was simple: to raise the rescued children as their own and, once they were older, return them to their communities so they could become agents of change in the very places that had once rejected them. In recent years, 36 children have been returned to their families. In each case, the families themselves came asking for the children. But reintegration is rarely smooth. For one thing, many of these rural communities speak local languages understood by few outsiders.
When Esther visited her family in Dako village for the first time in December 2021, she met her siblings: two older brothers, two older sisters, and a younger sister. She was the only child from her mother, who had been the last of her father’s three wives. Two of her siblings were already married with children. They were glad to see her, but communication was difficult. “I couldn’t talk with them because they speak Basa,” she said. Only her elder brother could speak English, because he was in school.
The contrast in education was stark. When Esther told them she was in her third year of junior secondary school, they thought she was lying; most of the people her age in the village were still in primary school.
At Vine Heritage, every child goes to school. Of the current residents, 182 are enrolled, from primary and secondary pupils to university students like Godiya, who is studying sociology at Nasarawa State University, just across the border from Abuja. Godiya dreams of a career that comes with a uniform – any one will do. Esther has just finished secondary school and hopes to begin university later this year to study law. For many like her, returning to their villages would probably end those dreams.
Sometimes, a compromise is possible. Fifteen-year-old Mabel and Bethel spend their school holidays in Kaida village with their family, then come back to the home once classes resume. Their family first came to reclaim them when they were 10 years old. “I was happy, but I was not happy,” Bethel said. “I was happy that I had seen the place where they gave birth to me, but I was not happy to leave here,” she added. “Whenever I go there, nobody disturbs me, but I always want to come back.”
Beyond communication difficulties, the adjustment to rural life can be harsh. Children accustomed to running water, electricity and regular meals must fetch water from streams, adapt to harder living conditions, and endure the curiosity or suspicion of villagers.
The Stevenses usually wait until they consider the children old enough to understand before telling them how they came to the home. When Godiya turned 17, in 2021, her people came looking for her. “At first I said I was not going to see them because for how many years they did not come,” she recalled.
Gloria, 11, playing with other children at Vine Heritage Home.Photograph: Adesegun Adeokun/The Guardian
“It took us two hours to convince her,” Olusola said. “I pleaded with her, telling her that their coming was a sign of progress.”
Since then, Godiya has stayed in touch with her family, but she only made her first trip back in January 2025. Without proper roads, the only way to reach Bari village was by motorbike. Hours after leaving Gwagwalada, she finally arrived exhausted, and the entire village gathered to stare. “Everybody was just looking at me,” she said. “I didn’t understand the language and the journey was stressful. They were speaking, but I didn’t understand them.”
The youngest of nine children, Godiya was welcomed with joy by her older sisters, who embraced her through tears. They urged her to come back for Christmas, but she was dismayed by the lack of electricity or phone network, and currently has no plans to return.
Esther’s experience in Dako was similar. “When I went to the village, everybody came to see me,” she said. Some of the stares unsettled her. “The community was scary. The way some villagers look at you, as if there’s some evil thought in their mind. I was so scared because I didn’t want anything to happen to me.”
Sometimes, the danger is real. Four years ago, eight-year-old Monday was sent back to his village at his grandfather’s request. Monday’s mother had died giving birth to him. The family had recently converted to Christianity, and after Monday’s father remarried, the grandfather felt it was the right time to bring home the boy once deemed “evil”. But just two weeks later, Monday was returned to Vine Heritage. The elders in the village had been resentful, asking the grandfather how they should feel when others had killed their own children but he had brought his back alive. Fearing for the boy’s safety, the grandfather decided it was better for him to leave. “He called me and said, ‘I am returning your child to you,’” Olusola said.
When a family asks for their child back, the Stevenses try to find out if it is safe for them to return. But they cannot prevent every tragedy. About eight years ago, the Stevenses visited a mother who had recently given birth to an albino girl. She assured them that attitudes towards albinos in her community had changed in recent years, so they did not insist on bringing the new baby to the home. “I was asking questions: has anybody threatened you or the child? She said no,” Olusola recalled. Shortly afterwards, word reached him that the baby had died without explanation. He has never been able to discover what happened.
The years have taken their toll on Chinwe and Olusola. About two years ago, Chinwe’s health began to deteriorate, and Olusola urged her to move into a small flat nearby so she could focus on recovery. During school holidays, two of the oldest children, including Godiya, take turns staying with her, helping with everyday needs, while the others visit in small groups from time to time.
Chinwe has had a stroke, developed high blood pressure and undergoes regular dialysis. I visited her in the modest flat where she lives alone, after spending her entire married life surrounded by dozens of children. She spoke candidly about how she poured herself into caring for others while neglecting her own health. Apart from the small income the Stevens received as missionaries, they earned nothing, relying entirely on donations to care for the children. Now, Chinwe herself depends on donations to cover her medical expenses.
On the walls hang photographs of her in a graduation gown, taken when she earned her doctorate in agriculture from the prestigious University of Nigeria, Nsukka. Another, from two years ago on her 59th birthday, shows her nearly three times her current, frail size. Pointing to one, she said softly, “Look at me then, and look at me now.” She managed a wry laugh.
Olusola said the home had its future leaders among the older children, those willing to step up and already involved in administration and management. Some, he explained, had made it clear that even after graduating from university, they intended to remain committed to running the home. Whenever he was away for meetings, they kept things running. Unless visitors specifically asked to see him, the children received guests, handled day-to-day operations, managed money and accounts, and reported back to him. “The only thing they can’t do is sign cheques,” he said. “I have already told them that in the next 10 years, I will sit back and the home will be in their hands.”
Most donations to Vine Heritage come from individuals. On the day I visited, a donated cow stood in the compound. But with Nigeria’s soaring inflation, now at its highest in nearly three decades, many longtime supporters have cut back or stopped entirely. “Sometimes, when you phone people to remind them of their promise to pay school fees, they get irritated,” Olusola said. “Because of Nigeria’s economy, some of the people that used to support the home before are now finding it difficult.”
Mamedu, at ActionAid, believes the issue is more complex. The challenge, he says, lies in how the home is run. It is neither a formal organisation nor a business. There is no business plan, governance structure, or consistent paperwork like a typical NGO or charity would have. It is registered as a foster home. There are no clear systems for tracking how funds are spent or how accounts are managed.
“We supported the home to try to institutionalise the process,” Mamedu said. “We trained the staff on hygiene, childcare, some record keeping, even partner management. From the start, we told Olusola, let’s have a central way to account for every fund that comes in, so that when we say we don’t have money, it’s backed by proper records. But he tells us that this is not an orphanage; it’s a home.”
ActionAid still supports the home, providing monthly funds for food and covering urgent medical bills for the children. But the future is uncertain. The Stevens’ family-first approach has undoubtedly saved lives and nurtured emotional bonds among the children, Mamedu believes. But the original vision of reintegrating children into their communities appears to have faltered, which means the home keeps growing. Olusola admits that he once believed those communities would be more developed by the time the children grew up. He had expected more progress.
I asked Olusola if he would have done things differently. “When God asks you to do something you only obey,” he said. “It never occurred to me that we would ever have more than 20 children. After saving seven children, we had a pause of about one-and-a-half years, and we thought that would be all. We made our decision that whatever we gave to our biological child, we would give the rest.” But after the seven-year hiatus, Olusola recalled, “the floodgates opened, and more children started coming”.
King Mswati III (born in 1968, crowned king in 1986) is Africa’s last absolute monarch. He rules with his mother, Queen Nfombi. King Mswati III renamed his country then called Swaziland to Eswatini in 2018.
King Mswati III introduced a number of measures and changes which brought some relief to the country that had been ruled by his father, King Sobhuza II, with an iron fist since independence from the British in 1968. Officially, Sobhuza II was King of Swaziland for 82 years and 254 days, the longest verifiable reign of any monarch in recorded history.
King Mwsati’s s rule is not undisputed. In fact, his lifestyle and human rights violations have been criticized at several occasions. However, as the story below tells, he showed positive leadership – ‘leadership by example’ – in advocating the rights of people with albinism.
At various occasions I have drawn attention to the precarious position of people living with albinism in Africa. They are discriminated, bullied, attacked, and sometimes killed – murdered, as some people believe that their body parts can bring luck, wealth, prestige or power.
For this reason I wish to commend King Mswati III and the Queen mother for their precious example and I hope that the example given by Their Majesties will not only be followed by the people of Eswatini but also in neighboring g countries where the position of people with albinism is also threatened by prejudice an superstition. (webmaster FVDK)
King Mswati III
Cultural leadership confronts albinism discrimination head-on
People living with albinism together with those living with disabilities at the recently ended Incwala Ceremony. Eswatini customs and culture prohibited such communities of people from getting closer or inside royal residences. His Majesty King Mswati III has since changed this long-held custom to accommodate people living with albinism and disabilities (Pic: Sibusiso Shange)
Published: February 18, 2026 By: Khaya Simelane – Times of Eswatini
MBABANE – In Eswatini cultural visibility is becoming protection for people with albinism and a tool to dismantle stigmatisation.
A new breath of fresh air is changing and shaping the narrative around a community long confined to the periphery and deep fear.
For decades, thousands of Africans born with albinism have mastered the art of invisibility. Whether at communities, schools, sports and everywhere, they have, out of their will, been forced to remain invisible, even if against their will.
From a young age, they have been made to feel different. With many labels around them prevalent across African communities, none has driven them to remain invisible than the one recently introduced in which they are labelled ‘ma-Millions’.
This labelling, though sometimes uttered jokingly, relates to the widespread belief that the body parts of people living with albinism are ‘powerful’ to make one a millionaire.
According to Menzi Sukati, founder of the Albinism Society of Eswatini (ASESWA), the prevalent belief that people with their condition are sources of wealth is exactly what perpetuates their killing.
As a result, he said from a tender age, most commonly in the rural villages and crowded locations, they have grown up calculating risks before stepping outside, either to play or hang out with their peers.
Night travelling is strictly discouraged while during elections, many of them keep a low profile, he added.
This stems from an entrenched myth across the continent that has portrayed people with albinism as mystical beings whose body parts can generate wealth, political power or supernatural protection.
Those myths have fuelled ritual attacks, mutilations and killings that have left families traumatised and communities fractured.
King’s counter-image efforts
At last year’s Umhlanga Ceremony and again during the recently concluded Incwala, the country’s most sacred cultural ceremony, people living with albinism were visibly invited and welcomed.
According to Senior Archivist and Cultural Anthropologist Lethumusa Simelane, King Mswati III has once again stood in the moment of time and embodied inclusivity and Ubuntu.
Simelane stated that what the Monarch has done can not only be limited to only fighting stigmatisation against people with albinism.
Instead, the King has moved beyond the acceptable norm to harmoniously review and relax some of the country’s cultural traditional practices governing ceremonies and royal residences (tigodlo).
“When talking about what the King has done, we must never forget that growing up, we knew that certain people were not allowed closer or inside royal residences,” said the anthropologist.
He explained that culturally, such beliefs had nothing to do with the person’s natural being, however more with the foundational systems governing African monarchies.
“Therefore, the King, cognisant of the changing times reached the a difficult decision by appealing to the custodians of our culture and sought their permission to relax some of these practices. The King realised that he cannot be a King to some, while others are pushed away from him,” said Simelane.
The renowned Eswatini historian likened the King to the Biblical Christ, who, despite Jewish law and beliefs decided to defy and dine with people with leprosy.
The historian underscored that when respected leaders, like the King publicly contradict myths; they shift social norms more effectively than legislation alone.
In his remarks, he confidently stressed that the King had once again become the symbol of Ubuntu and a true father, sending a strong message that there was no place for uncultured beliefs in the kingdom.
Transformative
Simelane added that in a region where visibility can invite danger, the sight of them standing confidently at the centre of national tradition carried unusual weight.
He said for a community accustomed to the margins, standing at the heart of culture can be transformative. Against this continental backdrop, he said the kingdom’s recent cultural inclusion offers a sharply contrasting image.
Incwala is not just a festival in the casual sense. It is a deeply spiritual ceremony (prayer) centred on kingship, renewal and national unity.
Participation, therefore, signals belonging to the moral and cultural fabric of the nation.
In many African societies, stigma is often justified in the language of tradition. When harmful myths are rooted in culture, dismantling them requires trusted cultural authority.
In Eswatini, the monarchy remains one of the most influential institutions across rural chiefdoms and community structures.
The images of people with albinism participating in the recently ended Incwala Ceremony deserved to be applauded, and for the King to be formally appreciated, according to Simelane.
In a continent where some children with albinism have been relocated to boarding schools for protection, being publicly welcomed into a royal ceremony reframes belonging.
Myth
Albinism is a rare, genetically inherited condition characterised by little or no production of melanin in the skin, hair and eyes. It is non-contagious.
In sub-Saharan Africa, an estimated one in 4 000 people are born with the condition, although prevalence varies by country.
The condition brings medical vulnerability, particularly to skin cancer and visual impairment in equatorial climates.
To every observer, the King has outdone the Tanzanian Government and instead of the courts he used culture to dismantle stereotypes around albinism.
According to an article by researcher Charlotte Baker published in The Conversation, human rights violations against people with albinism in Tanzania have included discrimination, verbal abuse, exclusion from education and health services, as well as killings, abductions, mutilations and even grave exhumations to obtain body parts for sale.
The violence has prompted Tanzanian and international civil rights groups to file a case before the African Court on Human and Peoples’ Rights against the Government of Tanzania, arguing that it had failed to protect this minority.
The court found that, although some steps had been taken, the state violated the right to life by failing to protect them as required under Article 4 of the African Charter.
It also ruled that Tanzania breached the right to non-discrimination by not doing enough to combat myths and stereotypes.
The ruling ordered nationwide awareness campaigns for at least two years, amendments to the 1928 Witchcraft Act to criminalise attacks, implementation of a national action plan, improved access to health services including sunscreen and eye care, educational support, and the establishment of a compensation fund for victims.
Baker notes that since 2007 more than 700 attacks and killings across 28 countries have been reported to the Canadian organisation Under the Same Sun, although many cases go unrecorded.
In Tanzania alone, there have been 209 reported attacks since 2007.These numbers tell a story of fear that extends far beyond one country.
Government driving advocacy
Meanwhile, the Eswatini Government has intensified its efforts towards promoting the rights, welfare and inclusion of people with albinism.
On February 13, 2026, the Deputy Prime Minister (DPM) Senator Thuli Dladla received a donation of sunscreen lotions and protective lip balms donated by the kingdom’s TV station to people with albinism.
The DPM, when accepting the donations extended her appreciation to the Monarch for leading the way, noting that it was pleasing to see organisations and entities across the country take leaf and follow in the footsteps of the King and Queen Mother.
“The gesture by Their Majesties has affirmed to all and sundry that people with albinism are human too. Even the doubting Thomas’s that were pushing them away from Their Majesties and the country’s cultural practices have been silenced,” said the DPM.
Dladla mentioned that by extending the cultural space to people with albinism, the Monarch did more than host guests. It publicly affirmed that they are part of the kingdom’s identity.
According to Dladla, Simelane and Sukati, the King has done more than spearhead a law meant to protect, promotes and embrace people with albinism, as well as their rights.
Advocacy efforts have included sunscreen donations and awareness campaigns, recognising that ultraviolet exposure poses a serious health risk.
Without melanin, skin is highly susceptible to damage and untreated skin cancer can drastically reduce life expectancy.
The DPM further stressed that indeed inclusion of people with albinism at high-profile events must translate into action and policy.
A senior traditionalist when contacted stated that when the highest traditional authority in a country affirms the dignity of people with albinism, it sends a message to rural homesteads and urban neighbourhoods alike.
Commenting anonymously as no formal appreciation has been extended to Their Majesties as per culture; the traditionalist joyfully appreciated the inclusion of the albinism community in cultural activities in order to fight the stigma around them.
The well-known traditionalist mentioned that for a child born with albinism in the country today, the image of participation in Incwala or Umhlanga offered a counter-narrative to fear.
“Instead of being told to hide, that child can see proof of belonging,” he said.
Legal obligation
According to the Office of the United Nations High Commissioner for Human Rights (OHCHR), the United Nations (UN) body mandated to promote and protect human rights globally, people with albinism continue to face widespread discrimination rooted in ignorance, superstition and harmful myths.
The OHCHR states that persons with albinism are often denied equal access to healthcare, education and legal protection. In some regions, they are reportedly subjected to extreme violence fuelled by false beliefs about their condition.
It emphasises that governments have a legal obligation to protect them, prosecute perpetrators of attacks and implement comprehensive strategies to eliminate stigma and discrimination.
In recognition of these challenges, the UN General Assembly proclaimed June 13, as International Albinism Awareness Day in 2014, observed annually since 2015.
The day seeks to raise global awareness about albinism, combat myths and misconceptions while further promoting the rights, dignity and inclusion of persons with the condition.
Through this international observance, the UN calls on states and communities to shift from silence and superstition to protection, awareness and meaningful inclusion reinforcing the principle that people with albinism are human beings entitled to life, equality and full participation in society.
Meanwhile, the African Union (AU) has adopted a strong human-rights-based approach to combat discrimination and violence against persons with albinism across the continent.
Through its Regional Action Plan on Albinism in Africa (2021–2031), formally adopted by the AU Executive Council in 2019, the continental body seeks to end attacks and other human rights violations targeting persons with albinism.
The framework focuses on four key pillars, namely; preventing attacks, protecting victims, ensuring accountability for perpetrators and promoting equality and non-discrimination.
The AU recognises albinism as a disability and situates protection measures within its broader disability rights framework, including the Protocol to the African Charter on Human and Peoples’ Rights on the Rights of Persons with Disabilities in Africa.
It also highlights the heightened vulnerability of women and children, calling on member states to implement specific protective measures.
In coordination with the United Nations and civil society organisations, the AU urges African governments to adopt national action plans, strengthen legal systems and intensify public awareness campaigns, particularly around International Albinism Awareness Day on June 13, to confront the root causes of stigma and violence.
Together, these continental and global efforts underscore a growing commitment to replace myth and marginalisation with protection, dignity and full inclusion.
Complacency
Still, some scholars across the continent have warned against romanticising the moment. Across Africa, attacks have sometimes declined only to resurface during periods of economic hardship or political contestation.
Election cycles in certain countries have historically coincided with spikes in ritual violence fuelled by rumours that charms made from body parts can secure victory. (Italics and bold letter-type added by the webmaster FVDK).
Structural inequality, unemployment and desperation create fertile ground for exploitative myths.
“The real test is whether people with albinism feel secure in remote communities, whether police respond swiftly to threats and whether courts prosecute offenders consistently,” noted one scholar.
The African Court’s ruling against Tanzania has set a legal precedent across the continent, signalling that states have enforceable obligations to protect persons with albinism. It reinforces that attacks rooted in superstition are not cultural nuances but human rights violations.
At the same time, Eswatini’s cultural inclusion demonstrates that tradition can be mobilised in defence of dignity.
The current site presents little news about ritual practices, including ritual murders (“muti murders”) in Mozambique, mainly due to a bias in my research, which focuses primarily on Anglophone countries in sub-Saharan Africa.
Warning: I have included the last news article below (implicating Peter “Cool Dud” Muparutsa (66) of the RUNN Family fame, who has found himself at the centre of a storm after being accused by some relatives of the ritual murder of a Mozambican woman for fame during his hey days in music – for illustrative purposes: to indicate that ritualistic practices are not an unknown phenomenon in Mozambique – and would like to emphasize that inclusion in no way implies that I endorse the accusation. (webmaster FVDK)
‘Undocumented’ Mozambican sangoma in court over possession of human tissue
A Mozambican traditional healer, 26, Aizeque Zacaria Cumbuia, appeared in the Ga-Rankuwa Magistrates’ Court on Friday, for possession of human body parts.
Published: August 22, 2025 By: Mbalenhle Zuma – Sunday World (South Africa)
A 26-year-old Mozambican traditional healer, Aizeque Zacaria Cumbuia, appeared in the Ga-Rankuwa Magistrate’s Court on Friday, charged with possession of human tissue.
The discovery was made on August 7 during a police investigation into a gruesome murder in Brits. A female victim was killed, her body parts removed, and her remains burned.
“We were horrified to find human tissue in the suspect’s possession,” said a police spokesperson, underscoring the gravity of the case.
Found with murder victim’s body parts
Cumbuia was allegedly found with human tissue in a room where he practised as a sangoma (traditional healer).
“The evidence was uncovered during a thorough search linked to the Brits murder investigation,” the spokesperson added.
According to the National Prosecuting Authority (NPA), Cumbuia may also face charges of kidnapping, murder, defiling a corpse, and violating South Africa’s Immigration Act, as he is suspected of being in the country illegally.
The murder is linked to the 2023 killing of 20-year-old Gontse Makhubela. Her organs were allegedly found in Cumbuia’s possession.
During his arrest he was found in possession of human remains believed to be that of Makhubela, 20.
The young woman was allegedly lured by another man, Serame Moroke. The instruction allegedly came from Cumbuia, for Makhubela to be killed for ritual purposes.
Victim lured from shop by ‘client’
Makhubela was establishing her post-matric life when she was brutally murdered.
She was working as an intern at a furniture shop. Her assailants, posing as potential clients at the shop, lured her to her death.
Two other suspects, including another Mozambican traditional healer, have been arrested.
In court, the case was postponed to August 28, 2025, for a formal bail application. The state has, however, voiced out that they plan to oppose Cumbuia’s bail.
A prosecutor stated: “The severity of these crimes and the ongoing investigation demand that the accused remain in custody.”
Traditional healer in court for possession of human tissue linked to murder investigation
Aizeque Zacaria Cumbuia (26) a traditional healer from Mozambique appeared at the Ga-Rankuwa Magistrates’ Court. He is facing a charge of possession of human tissue
Published: August 22, 2025 By: IOL (South Africa)
Aizeque Zacaria Cumbuia, a 26-year-old traditional healer from Mozambique, made a brief appearance at the Ga-Rankuwa Magistrates’ Court, facing a serious charge of possession of human tissue.
The allegations against Cumbuia emerged from police operations that were initially focused on a separate murder case, according to National Prosecuting Authority spokesperson, Lumka Mahanjana.
She explained that police discovered evidence on August 7, when they found human tissue within the premises where Cumbuia practiced his traditional healing.
“This was discovered by police officers when they were conducting investigations in relation to a Brits murder case, where a deceased female was killed, body parts removed, and her body burned,” Mahanjana said.
Police have stepped up their efforts to trace the circumstances surrounding the crime, and Cumbuia’s alleged involvement has only intensified their inquiries.
During the court proceedings, the magistrate heard that the state intends to oppose any application for bail, arguing that Cumbuia’s release could pose significant risks to the ongoing investigation and the safety of the community.
The matter has been postponed until August 28 August when Cumbuia is expected to make a formal bail application.
Case of a Mozambican traditional healer accused of ritual murder postponed (YouTube)
Screenshot – to listen to the report, please click here
Published: August 22, 2025 By: SABC News – South Africa
The National Prosecuting Authority (NPA) is confident of a successful prosecution in the trial of a Mozambican national found in possession of human remains believed to be that of a murdered 20-year-old woman. 26-year-old Isaac Shikomboya’s arrest follows that of two other people who were apprehended after being found in possession of the slain victim’s cellphone. The two men led the police to Shikomboya. The case has been postponed to Thursday next week for a bail application.
Warning: I have included the news article below for illustrative purposes – to indicate that ritualistic practices are not an unknown phenomenon in Mozambique – and would like to emphasize that inclusion in no way implies that I endorse the accusation. (webmaster FVDK)
Weekender Reporter VETERAN producer and musician, Peter “Cool Dud” Muparutsa (66) of the RUNN Family fame, has found himself at the centre of a storm after being accused by some relatives of the ritual murder of a Mozambican woman for fame during his hey days in music.
The explosive allegations were thrown at the ageing producer by his grandnephew — Macdonald Nyamajiya — who claimed that Muparutsa later married him and his two brothers off to the slain woman’s blood-thirsty avenging spirit.
He alleged that the woman’s restless ghost has been haunting their family.
The matter was heard before Chief Mutasa’s community court recently after Muparutsa had reported Nyamajiya, accusing him of tormenting him through the “frivolous” allegations.
Muparutsa produced before the court a tirade of text messages, in which Nyamajiya accused him of being a heartless murderer and ritualist, who had destroyed his family.
“If you are free, come to Dangamvura today so that we see each other face-to-face. You know your stories or give me an address of where you stay so that I come there myself.
“Let us not meet in the spirit, but let us meet during daylight, enough is enough,” reads one of his text messages.
Another message, dripping with rage, reads: “I am not afraid of you, you are not God. Personally, it is now boring me because you are responsible for our suffering, so we have to meet. There shall come a time where we will be assaulting each other and striking each other with axes.
“I do not want a grandfather who makes me his scapegoat. What you have done is enough. If you do anything to me, know that you and your family will perish. Play your guitar at church later after you have finished appeasing this spirit,” he charged.
Startled by the venom, Muparutsa confirmed the accusations.
“I am being accused by my older brother’s daughter’s son of wizardry, possessing goblins, and causing all the mishaps in their family. I was shocked when I went through his text messages,” he said.
In response, Nyamajiya told the court that he had written the offensive messages out of deep pain.
“My late mother was a Muparutsa and my father hails from Bocha. However, I grew up within the Muparutsa family and use their surname.
Growing up, we were told that he (Peter) has goblins, and that he was being haunted by an avenging spirit because he killed someone in Mozambique.
“In April, the spirit started manifesting on my younger brother and we consulted healers, who told us that our grandfather, Peter, was responsible for it.
“My brother acted as if he was paralysed and would shout Peter’s name. It is still happening up to now,” he alleged. He further claimed that the spirit insisted that he and his two brothers were spiritually ‘wedded’ to a female goblin by the musician.
“It is said that he killed a woman of the Tembo Clan, and is the one whose spirit we were married to. She was from Mozambique.
“The woman claims she was killed for rituals to enhance his musical fame. Every healer we consulted pointed an accusing finger at him,” said Nyamajiya.
Another family member, Bridget Muparutsa, weighed in, saying the allegations have haunted them for generations.
“We heard about it as we grew up. We would get married and come back home widowed because our husbands would have died. We wanted to be here with the rest of the family, but in the process of taking the matter to Headman Muparutsa, Peter brought the case before this court,” she said.
The matter took an unexpected turn after Chief Mutasa ruled that Nyamajiya had no right to sue Peter.
“Macdonald, you are not a Muparutsa, it is your mother, who was a Muparutsa. If a Muparutsa killed someone, it is not possible for the avenging spirit to torment you because you are not a member of the Muparutsa family by blood.
You cannot come here accusing your uncle because you are not a Muparutsa. His family should report him, and not you,” warned Chief Mutasa.
He further warned Nyamajiya against being dragged in his uncles’ family feuds.
“Do not be too convinced of what you are hearing — what if it is someone else that is using his face? Do not be used to fight battles that are not yours. Let the Muparutsa family approach my court to sue him, not you. I am not favouring anyone in this matter, but we need to help you guys,” said Chief Mutasa.
Nyamajiya was fined a beast for disrespecting his uncle.
“You were disrespectful. For that, you must pay him a beast. You cannot challenge an elder in this manner,” he ruled.
Chief Mutasa also ordered the Muparutsa family to unite and consult traditional healers together to settle the matter.
Elsewhere on this site I provide ample information on the phenomenon of albinism and the plight of Africans living with albinism. It is not only a heath issue. It is also a human rights issue. People living with albinism are targeted on the African continent, they are discriminated, attacked, mutilated and sometimes murdered for ritualistic motives. This horrible practice must end.
Fortunately, organizations such as the Source of Nile Union of Persons with Albinism (SNUPA) are making efforts to make the lives of people with albinism more bearable and to fight against the stigmas attached to albinism. They are to be commended for their valuable work but we must realize that it is a matter that concerns us all. (FVDK)
The hidden struggles of living with albinism in Uganda
Published: July 22, 2025 By: Rhonet Atwiine – Nile Post, Uganda
There are not many in-depth studies of the phenomenon of ritual murders and even less of the killing of children for ritualistic purposes. The article below discusses the ritual murder of children in Ghana and Kenya, examines who the perpetrators are and why they came to their crime.
The study by Emmanuel Sarpong Owusu is a must read. The author is to be commended for a serious and interesting study.
Interestingly, a number of the author’s findings and conclusions – based on online news reports in eight media outlets in Ghana and Kenya and on interviews with 28 experts – are consistent with my experiences after years of studying ritual killings in Sub-Saharan Africa. In particular I wish to mention here the main factors driving the motivation of the majority of the ritual murderers: superstition, greed and illiteracy, whereas the for various reasons failing reaction of authorities and the resulting lack of rule of law facilitate the impunity and the continuity of the cruel and outdated phenomenon.
According to the study, in Ghana, the media reported at least 160 ritual murders between 2012 and 2021. Of this number, 94 (about 58.8%) were children. Of the 102 ritual murders in Kenya in the study period (2012-2021), 66 (64.7%) were children.
I refer to the study below for more details. Please note that, unfortunately, three links in the original article seem to be incorrect: (i) ‘juju in Ghana’ leads to general information on juju (link should be placed under ‘juju’); (ii) ‘juju in Kenya’ leads to nowhere; (iii) reference to members of occult sects leads to ‘juju in Kenya’. (webmaster FVDK).
Ritual murder of children: study in Ghana and Kenya explores who’s doing it and why
Published: April 15, 2025 By: Emmanuel Sarpong Owusu – The Conversation, UK
Superstition, an irrational belief in paranormal influences or a false attribution of events, is an age-old phenomenon found in probably all human societies or cultures. It encompasses a wide range of beliefs, practices and behaviours. Some of these have harmful or even deadly consequences.
In many African communities, there are widespread beliefs relating to the use of human body parts for traditional healing rituals. Human body parts and blood are said to enhance the potency of traditional medicines and rituals that supposedly guarantee wealth, business success, fertility, protection and longevity, among others.
Ritual killings, including those of children, are reported regularly around Africa. A case in point is the targeting of children with albinism for ritual purposes in Tanzania. One research report says one in five people in Mozambique and one in four people in South Africa believe that rituals and traditional medicines made with human body parts are more potent and effective than those using nonhuman objects.
Children are particularly targeted for killing because they can’t repel attacks, and because of beliefs about the potency of their body parts. The victims in more than half of all the ritual murders reported in Ghana and Kenya in 2022 were children.
I am a legal scholar with years of research on superstition-driven crimes against vulnerable groups in African settings and the criminal justice response to such crimes. In a recent study I explored the magnitude, characteristics and motivations, as well as the socio-cultural and economic contexts, of ritual child murder in Ghana and Kenya. My study was carried out through in-depth analysis of news reports of ritual murders for a period of 10 years, coupled with semi-structured interviews with academics and other experts.
I found that the major factors contributing to the persistence of ritual child murders were superstition, economic hardship, illiteracy and inefficient criminal justice systems. A new consumerist ethos also plays a role: wanting a life of luxury and the admiration that comes with it.
The study seeks to enhance awareness of the ritual child murder phenomenon and encourage support for the enforcement of child rights protection laws. When policymakers know more about the scale and circumstances of ritual child murders, they are better equipped to act on it.
Ritual murders in Ghana and Kenya
Belief in juju is widespread in Ghana and Kenya. This is the belief that people can mystically control events by using incantations (“magic words”) and, sometimes, objects.
My study analysed data drawn from online news reports in eight media outlets in Ghana and Kenya. I used media content because the countries don’t have national data sets on ritual homicide, and empirical research is limited. Secondly, I interviewed 28 experts in criminology and criminal justice, sociology, African religions, and child and family welfare and social protection. These participants were selected using the purposeful sampling technique.
In Ghana, the media reported at least 160 ritual murders between 2012 and 2021. Of this number, 94 (about 58.8%) were children. This suggests that an average of 9.4 children fall victim to ritual murder each year in the country. Of the 102 ritual murders in Kenya in the study period, 66 (64.7%) were children. This represents an annual average of 6.6 in the country.
In both countries, most victims (over 80%) tend to be drawn from families of low socio-economic backgrounds in rural and semi-rural communities. In Kenya, children with albinism are also targeted.
The overwhelming majority of offenders are males. There are three main categories of perpetrators of ritual child murders:
the juju practitioner or traditional healer who usually prescribes the required body parts and effects the medicine or ritual
the client who consults traditional healers and stands to benefit directly from the ritual or medicine
the (hired) ritual murderer, who abducts the victim and extracts the required body parts.
Data from media reports show that most of the perpetrators apprehended are those directly involved in the killing. They are usually aged between 20 and 39 years and of low socio-economic status in rural communities. However, some interviewees insisted that some rich and prominent persons are also involved.
In Ghana, uncles, fathers and stepfathers were the dominant perpetrators in cases where victims and perpetrators were known to be related. Unlike other types of homicide, ritual child murder generally involves strangers nearly as often as it involves family members and acquaintances.
Motivations and responses
The dominant motivation for ritual murder is financial gain. This conclusion is drawn from the media accounts and the interviews. Perpetrators are promised money in exchange for specific human body parts. Others kill to use the body parts for rituals that are supposed to ensure a long life, fertility, business growth, or protection against evil. In Kenya, some perpetrators kill in fulfillment of their obligations as members of occult sects.
Other factors that sustain the practice – based on media reports and interviews – are superstition, unemployment and economic hardship. Adding to these are illiteracy, which fosters unfounded beliefs, and an inefficient criminal justice system, which enables these crimes to thrive.
Poor parental supervision is an important risk factor for ritual child murder. In both countries, over 70% of the ritual murder victims were under 10 years old. They were abducted or murdered while going to or returning home from school. Others were abducted while running errands such as fetching water from a stream unaccompanied. Some may have been playing outside their homes unsupervised, or running errands by themselves for relatives.
In both countries, the criminal justice system’s response is evidently ineffective. In Kenya, over 90% of perpetrators are not apprehended. Of 68 suspects arrested in Ghana, only four convictions were reported. Crime scenes are poorly managed and preserved by police officers and detectives in both countries.
Crime scene videos show the victims’ remains being removed by authorities and conveyed to the morgue without diligent forensic examination of the body and the crime scene for evidence.
What governments can do
The belief in the power of juju and associated rituals and medicines cannot be wished away. It can only be combated in various ways:
bringing the activities of traditional healers and occult-related sects under closer scrutiny
promoting education and awareness, emphasising the need for supervision of children
Ritual murder of children: Study in Ghana and Kenya explores who’s doing it and why
Volunteers assist forensic experts and homicide detectives from the Directorate of Criminal Investigations (DCI), to exhume bodies of suspected followers of a Christian cult named as Good News International Church, whose members believed they would go to heaven if they starved themselves to death, in Shakahola forest of Kilifi county, Kenya April 25, 2023. (PHOTO/ REUTERS)
Published: April 18, 2025 By: The Eastleigh Voice, Kenya
The dark side of superstition and the reality of ritual child murder
Published: around April 20, 2025 By: IOL, Sunday Tribune – South Africa
EMMANUEL SARPONG OWUSU, A DOCTORAL RESEARCHER AND LECTURER AT ABERYSTWYTH UNIVERSITY IN WALES, WRITES ABOUT SUPERSTITION-DRIVEN CRIMES AGAINST VULNERABLE GROUPS IN AFRICAN SETTINGS.