Zimbabwe’s All Women Anti-Poaching Unit

Conservation becomes a community enriching project.

Photo of Zimbabwe’s Hwange National Park by Christine Donaldson on Unsplash.

The unit is called Akashinga, Shona for The Brave Ones, and it could not be more aptly named.

Founded by Damien Mander, an Austrailian former special forces soldier, Akashinga is a part of the International Anti-Poaching Foundation, a non-profit dedicated to preserving the Phundundu Wildlife Area. 

Phundundu is a 115-square-mile area in the Zambezi Valley ecosystem which is home to 11,000 elephants and other endangered wildlife. In the past 20 years, frequent poaching has taken its toll on the reserve, resulting in the loss of thousands of elephants. While killing wildlife without a permit is illegal, animal trophies such as bones, tusks, and teeth can be sold on the black market for an amount equivalent to a month’s salary.

According to Akashinga’s website, anti-poaching initiatives often close off “traditional grazing areas, places of burial, worship, water points, food sources and traditional medicine,” making communities feel that endangered plants and animals are more important than their humanity. This resentment can fuel poaching attempts for which offenders can be arrested and sometimes killed. These experiences then reinforce the idea that endangered flora and fauna are of greater importance than the community, creating a cycle of resentment and violence.

To address this phenomenon, Akashinga takes a community-first approach to conservation. By recruiting women from the communities surrounding the Phundundu to serve on the unit, the organization is able to use conservation initiatives to enrich communities. Akashinga’s website describes the effort as having a “community-driven interpersonal focus, working with rather than against the local population for the long-term benefits of their own communities and nature.” To this end, 62% of operational costs are returned to local communities.

In this light, it is significant that the unit is made up entirely of women. According to National Geographic, research shows that in developing countries, women invest 90% of their income in their families, while men only invest 35%. Women are at the grassroots of community life, and when their wages are invested in their families, the entire community proffits.

But this is not the only reason that women are so right for the job. Mander had formerly trained male rangers for years before changing to an all-female model. He said that women are far better rangers; they are less likely to take bribes from poachers, and are skilled at de-escalating high tension situations. In National Geographic he commented that a gun in the hands of a man is a toy, but with a woman it is a tool.

Women also prove to be more resilient. Only three women quit the army-style training necessary to become part of the unit. When Mander was training men, all but three recruits quit after the first day. In National Geographic Mander said that, “we thought we were putting [the women] through hell, but it turns out, they’ve already been through it.”

This resilience is not without cause. Many of the women of Akashinga are victims of abuse, and have experienced their own trauma and exploitation. The BBC writes that Kelly Lyee Chgumbura, a unit member, was raped at seventeen and forced to drop out of school, abandoning her dream of becoming a nurse. She then had to give her baby to her rapist's mother, in accordance with Shona norms where if a mother is unable to provide for her child, the father’s parents become its guardians.

“My goals had been shattered,” she told the BBC, “It was like I couldn’t do anything more with my life.” A few years later, Chgumbura was recruited by her village head to try out for a ranger position. She was selected for the unit, and with a steady career now has a chance to win back custody of her daughter.

Being a ranger provides a sense of purpose as well as an income. “When I manage to stop poachers, I feel accomplished,” Chgumbura told the BBC, “I want to spend my whole life here on this job, arresting poachers and protecting animals.”

Like Chgumbura, most of the unit have faced traumatic experiences and lacked the agency and resources to protect themselves. “Who better to task with protecting exploited animals,” Mander told National Geographic, “than women who had suffered from exploitation?”

Phundundu is the first reserve worldwide to be managed entirely by women, but it will not be the only one for long. According to its website, Akashinga plans to welcome 1,000 new recruits who will protect 20 reserves. They aim to accomplish this by 2025. 






EMMA BRUCE is an undergraduate student studying English and marketing at Emerson College in Boston. While not writing she explores the nearest museums, reads poetry, and takes classes at her local dance studio. She is passionate about sustainable travel and can't wait to see where life will take her. 



Blue Out on Insta

Blue Out on Instagram: Support for Sudan through Social Media Awareness

Sudan Flag Sticker on a Car. pjbury. CC BY-NC-ND 2.0

Recently, a specific shade of blue has been popping up around Instagram in the form of profile pictures. This Blue Out was started by Instagram influencer Shahd (@hadyouatsalaam). She is a Sudanese-born, New York City-based activist—or how she likes to identify herself, “a political scientist by degree and a social media influencer by interest”, according to her recent Insta post, introducing herself to her new followers. 

Shahd created this movement for the sole purpose of raising awareness to what is currently going on in Sudan. Protests in Sudan began in December of last year, when there was a price-spike in basic commodities (i.e. bread). It was not until April 11th, after a mass, multi-day sit-in, that the Sudanese people did see the change they wished for. The current President, a man named Omar al-Bashir, and his party were being jailed or put on house arrest. The protestors believed this to be a victory. They were wrong. General Awad Ibn Auf, the Vice President, soon gave a televised statement explaining the new governmental system that was going to be put in place—one run by three separate military factions called the Transitional Military Council (TMC). He stated that they intended to remain in power for two years until the country could elect a new President, also claiming a three-month state of emergency and curfew. The people did not accept these conditions and in under 24 hours, Ibn Auf resigned and General Abdelfattah al-Burhaan become the new chairman.

Since General Abdelfattah al-Burhaan’s new appointment, negotiations between the people and the TMC have been chaotic. Once again being fed up, the Sudaneese people, with the people of the Sudanese Professionals Association (SPA), organized a mass strike from the 28th of May to the 29th. These strikes immediately became violent and the TMC used these mass demonstrations to portray the SPA in a vicious light. On June 3rd, government forces began shooting at the protestors which, reportedly, left 118 dead and many more injured. Since then, an Internet black out has been in place and thus sparked social media outcry.

But why should this matter to us? The answer is simple: because we have the power and the privilege of accessing the Internet with the capable means of shouting loud enough that somebody will listen. Over the past two weeks, because of the uproar on social media, there have been an influx of articles written about what is going on, how long it has been going on, what is the important information that we need to know about the revolution in Sudan. One Instagram user, Rachek Cargle (@rachel,cargle), with the help of “an incredible group of activists” has even composed a masterlist of articles ranging from immediate updates to fundraising efforts, according to her post that calls for any more information to add. 

Unfortunately, with the uproar, there have also been people who cruelly want to capitalize on the movement for clout reasons. Just last week, a post went viral that claimed for every re-post to a page or story, the originators of the account would donate meals to the Sudanese people. Very soon, the page was labeled as a hoax given curious peoples’ inquiries into how they would provide the food, where is the funding coming from, and other questions which the page either did not answer or gave vague responses to. From these instances, it is important to remember that when trying to get information out, there needs to be a more thorough and conscious effort on the part of other social media users to not just mindlessly click-and-post, but rather, do a quick search about what the post is, and then determine whether or not it is legitimate. 

Using the privilege we have—whether it be from simply having the means to repost an article or getting in contact with local government officials so they can talk about what is going on—is a butterfly-effect that will change how the Sudanese revolution will go. Being complacent or a bystander is just as harmful as supporting the violence because inaction is not action, inaction does not bring about change but lets things remain as they are, because they are not directly affecting us. I encourage those of you reading this article to look at the Instagram influencers I have mentioned as well as the hashtag #Iamsudanrevolution. There you will find countless posts, articles, links, and organizations that can inform you, help you, and guide you on how you can help. For immediate action, check out Cargle’s post which is a picture of protestors with SUDAN in bold, blue letters and the subtitle of Information & Support Round Up. There you will find the link to the master document which will provide the beginning of any information you want to know. 

I must repeat—acting as a bystander perpetuates the actions that are harming individuals because it is neglecting them the action they need. Use your privilege for something productive. 




OLIVIA HAMMOND is an undergraduate at Emerson College in Boston, Massachusetts. She studies Creative Writing, with minors in Sociology/Anthropology and Marketing. She has travelled to seven different countries, most recently studying abroad this past summer in the Netherlands. She has a passion for words, traveling, and learning in any form. 



Living With Albinism in Sub-Saharan Africa

In Malawi, Mozambique, Tanzania, and beyond, children and adults with this rare condition face widespread violence based on superstition—and fight for the right to live their lives free of persecution.

On the left, a baby with albinism. Kaysha. CC BY-NC-ND 2.0

On January 1 of this year, unknown assailants climbed through the window of Kwenda Phiri’s home in Nhkata Bay, Malawi, and hacked him to death, chopping off his hands and fleeing with them. Their motive? Phiri had albinism, meaning that—due to a rare genetic condition—he was born without pigment in his skin, hair, or eyes. Unfortunately, Phiri’s killing was far from an isolated incident. Across sub-Saharan Africa, people with albinism face physical violence and persecution based on superstition, often leaving them unemployed, isolated, and fearful of even leaving their homes.

Kidnapping and dismemberment, such as in the case of Phiri, is common, as body parts from people with albinism can bring in up to $75,000 on the black market. Witchdoctors perpetuate myths about the magical qualities of people with albinism, and make outlandish claims that their body parts can be used in charms and potions to summon wealth, power, and good luck. Babies born with albinism may be considered a curse and slaughtered at birth, especially in certain regions: in Tanzania, where the condition affects up to 1 in 1400 citizens, people with albinism are called zeru zeru, meaning “ghosts,” and assumed to bleed a different color or be immortal. Such superstitions have fueled more than 520 recorded attacks in 28 countries since 2006; Tanzania had the highest number, at more than 170 incidents. Attackers and witchdoctors rarely face legal action, and not a single buyer in this gruesome segment of the black market has ever been prosecuted.

The Nkhata Bay, Malawi, area, near where Kwenda Phiri was killed. Matthew and Heather. CC BY-NC-ND 2.0

For people with albinism who manage to escape fatal attacks, prospects for education and gainful employment are often dim. In Tanzania, only half of children with albinism complete primary school, and even fewer attend secondary. The condition typically affects vision, leaving children without access to glasses to struggle and underperform academically. Adults with albinism are met with few job opportunities, and often fall into poverty. Women with albinism suffer specific and especially dangerous injustices. Unfounded myths run rampant that sex with a women who has the condition can cure HIV/AIDS, leading to many women with albinism contracting AIDS through this heinous variety of ritual rape. Even after death, persecution persists: Many families whose relative with albinism has passed away do not hold the funeral in public, for fear that the grave might be dug up and the corpse stolen. This practice of quiet, unnoticed burial may also perpetuate superstitions regarding immortality.

Attacks are especially prevalent in certain countries—namely Tanzania, Malawi, and Mozambique, according to Turkish news outlet TRT World. Indeed, Nyasa Times, the online breaking news source that reported Phiri’s murder, stated that “Malawi faces ‘systematic extinction’ of people living with albinism if they continue to be murdered for their body parts.”

The general culture of neglect and harmful behavior toward people with albinism also exacerbates concerns about skin cancer, to which people with albinism are particularly susceptible given their lack of pigmentation. Parents often do not know about the importance of covering up in the sun and copiously applying sunscreen; in fact, some actually take their children with albinism into the sun to intentionally darken their skin, leading to dark-colored pre-cancerous lesions that only encourage the parents to continue. Only 2 percent of people with albinism in sub-Saharan Africa live beyond age 40—largely due to the scourge of cancer—and most children with albinism as young as 10 already have some early form of the disease.

In response to the unchecked spread of skin cancer, a company called Kilimanjaro Suncare, or Kilisun, has designed a sunscreen especially for people with albinism. When the product was released in 2012, it was used to help 25 children; as of 2017, it was being given free of charge to 2,800 people at clinics taking place every four months. Over half of those receiving Kilisun were children.

While skin cancer can be mitigated with appropriately distributed medical care, resolving the culture of violence against people with albinism will be a longer and more arduous process. In its 2017–2018 report, Amnesty International acknowledged the situation of people with albinism in Mozambique for the first time ever, estimating that 30,000 people experienced discrimination for their condition and pointing to a spike in incidents of persecution. In Tanzania, a charity called Under One Sun runs an education program for students with albinism and a summer camp for students who have been abandoned by their families due to their condition, as well as performing public advocacy and outreach through seminars and film screenings. The Albino Foundation offers similar advocacy services in Nigeria, aiming to empower people with albinism and educate the Nigerian and global societies about the realities of the condition.

For some individuals with albinism, art has served as a powerful means to address the injustices hindering their lives on a daily basis. Singer-songwriter Salif Keita—who endured bullying and rejection as a child in Mali due to his albinism, and who founded a global foundation in 2006 to aid those who are afflicted—dedicated a benefit concert in November 2018 to a five-year-old girl with albinism who was kidnapped, tortured, and killed in Mali in May of that year. More than 100 politicians, diplomats, and people with albinism attended the event.

Arriving to Sengerema region in Tanzania, where a life-sized statue dedicated to people attacked due to their albinism can be found. TANZICT Project. CC BY-NC-SA 2.0

In Sengerema, Tanzania, a monument has been erected to honor those who have been assaulted and murdered due to their albinism. The statue portrays a dark-skinned father and mother; the father holds his light-skinned child with albinism on his shoulders, and the mother places a hat on the child’s head to keep them safe from the rays of the sun. Around the monument are etched the names of people with albinism who have been attacked, representing an homage to those lost to the anachronistic attitudes of the past. Standing tall above the ground, the life-sized statue—which was made by Tanzanian artists with disabilities—imagines a possible future in which people with albinism can live safely and normally regardless of their pigmentation.





TALYA PHELPS hails from the wilds of upstate New York, but dreams of exploring the globe. As former editor-in-chief at the student newspaper of her alma mater, Vassar College, and the daughter of a journalist, she hopes to follow her passion for writing and editing for many years to come. Contact her if you're looking for a spirited debate on the merits of the em dash vs. the hyphen.








Forgotten, but not Gone: Zika’s Return to the Media

Earlier this week the Duchess Sussex of Meghan Markle canceled a trip to Zambia, citing exhaustion and concerns over the presence of Zika virus in the country. The Zika virus had been rather dormant in the media over the last year, all but vanishing in the wake of Trump speeches, trade wars, and Brexit. It had, however, remained a constant concern for those living in certain countries or traveling to them. Markle’s encounter with the Zika virus and the subsequent headlines have helped to push it back into public view, and once again, questions are being raised about its origin, transmission, and what is being done to fight it.

The Duchess of Sussex. Office of the Governor - General - GG.govt.nz. CC BY 4.0.

The Zika virus was first discovered in the Zika Forest in Uganda in 1947. The first recorded carriers were monkeys, but the forest was also home to over 70 species of mosquitoes, and they became the primary source of viral transmission. The disease was eventually discovered in humans in 1952, but for the most part remained confined to animals until 2007, when the first human outbreak was documented on the Island of Yap in the Federated States of Micronesia. In 2015, the virus made international headlines when Latin America and the Caribbean saw an explosion of human-related cases. As was the case in Africa, mosquitoes were the main culprits of transmission. However, in 2016, the virus saw a sharp decline in new cases, and with it a decline in news coverage.

Adults infected with Zika often display no symptoms. Those who do usually report mild fevers, rashes and muscle pain. The impact on unborn babies is far more devastating. Zika infections during pregnancy have resulted in miscarriages and babies being born with microcephaly, a condition in which a child's head is much smaller than it should be (Markle and husband Prince Harry had recently announced that they were expecting a child, and concern for the child’s welfare was thought to be Markle's main concern when she opted out of her trip to Zambia).

The Zika Virus is spread mainly through mosquito bites. James Gathany - https://phil.cdc.gov/phil/details.asp?pid=9257. Public Domain.

While a full-on cure for the virus remains elusive, health and government officials have been able to curb infections by going after the mosquitoes that carry and transmit the disease. In preparation for the 2016 Olympics in Rio de Janeiro, the Brazilian government launched a large-scale effort to fumigate the city for the insects, while in England a biotech company called Oxitec developed genetically modified mosquitoes, which, when released into the wild, would mate with infected mosquitoes and pass a gene on that would prevent those mosquitoes from reproducing. In the United States, The Centers for Disease Control made a point of advising those traveling to countries with high rates of infection to use insect repellants.

Microcephaly- a birth defect linked to the Zika virus. Centers for Disease Control and Prevention. Public Domain.

Many world issues persist despite the ebbing and flowing of news coverage. Though not the hot story it once was, the Zika virus is still a viable threat and will remain so until a vaccine is found. Those traveling to countries that have been deemed areas of risk should take all necessary precautions to prevent infection, or, like the Duchess of Sussex, simply the put the trip off until another time.


JONATHAN ROBINSON is an intern at CATALYST. He is a travel enthusiast always adding new people, places, experiences to his story. He hopes to use writing as a means to connect with others like himself.