Ministers Call for Coalition to scale up land restoration massively worldwide

Climate Change, Conferences, Environment

NEW DELHI, Sep 11 2019 – 1. On the road to the Climate Action Summit, the Minister of Environment, Forest and Climate Change of India and President of COP14, His Excellency Mr. Prakash Javedkar, and the United Nations Deputy Secretary-General, Her Excellency Ms. Amina J. Mohammed, hosted a high-level luncheon on land and climate on 9 September 2019, on the margins of the UNCCD Fourteenth Session of the Conference of the Parties (COP14). The event was co-facilitated by the United Nations Convention to Combat Desertification (UNCCD) and the United Nations Environment Programme (UNEP).

2. During the meeting, participants underscored that land resources are the basis for human health, livelihoods, food security, and for our economic, cultural and spiritual well-being. Some 25 per cent of the world’s land is degraded (IPCC, 2019), affecting the lives of 3.2 billion people, particularly smallholder farmers, those in rural communities and the world’s poorest populations (IPBES, 2018). Women in particular are on the daily frontline struggle to salvage the large area of agricultural land already affected by land degradation. And the stewardship of indigenous peoples is essential to safeguard the world’s remaining biodiversity. All vulnerable groups who depend on sustainable land management and who can contribute to land restoration need our support.

3. Participants welcomed the IPCC’s special report on Climate Change and Land which constitutes the first comprehensive study of the entire land-climate system. As such, they agreed that it is a fundamental contribution to global negotiations on climate change, biodiversity and sustainable land management, and calls for synergies between the Rio Conventions. The report provides a sound basis for ambitious actions contributing to climate change adaptation and mitigation, biodiversity conservation as well as to combat land degradation and enhance food security.

4. Participants stressed that restoring degraded lands and achieving land degradation neutrality (SDG 15.3) provided an integrated solution to increase ecosystems and populations resilience as well as to enhance the capacity of our land for carbon sequestration. Land use must therefore be an integral part of the climate solution, rather than a cause of GHG emissions. This will strengthen biodiversity conservation, increase livelihoods and human security. It will also curb emissions from degrading lands and help close the projected emissions gap between Nationally Determined Contributions (NDCs) and the Paris Agreement objectives. Most importantly, land degradation neutrality will improve the living conditions of affected populations and the health and productivity of their ecosystems.

5. Participants agreed that land restoration will deliver co-benefits to many Sustainable Development Goals and that the three Rio Conventions can actively work together to support restoration activities as an important contribution to the 2030 Agenda for Sustainable Development.

6. Participants agreed that the critical role of land restoration for climate mitigation and adaptation must be visible. The Climate Action Summit will send a strong political signal for more public funding and private investments to enable land restoration for impact at the scale needed, through gender-responsive, transformative projects and programmes that seek to generate and sustain fundamental and sustainable positive change. Every 1 USD invested in land restoration is expected to generate up to 10 USD in returns for society through more efficient agricultural practices, integrated water management, and vital ecosystem functions (GPFLR, 2018).

7. Participants indicated that time had come to turn the vicious circle between land and climate into a virtuous one by reinforcing the positive elements of the relationship, helping to manage emissions on the one hand and adapting to climate impacts on the other. Participants therefore called for more concerted policy action, more investments, and more capacity to scale up land restoration to achieve land degradation neutrality. They expect the Nature-Based Solutions Coalition to propose concrete and ambitious actions at the Summit.

8. Participants supported the global effort to achieve land degradation neutrality through ambitious initiatives such as the Bonn Challenge target of having at least 350 million hectares of degraded land under active restoration by 2030 and the Great Green Wall for the Sahara and Sahel Initiative. Participants also welcomed the UN Decade on Ecosystem Restoration 2021-2030 (UN General Assembly resolution 73/284) as a unique opportunity to galvanize political will, increased investments, and action on the ground for land restoration at massive scale across the world.

9. Participants called for the UN Climate Action Summit to be the starting point for the establishment of a coalition of countries, to accelerate massive scaling up of land restoration activities worldwide, and to act as the building block of the UN Decade of Ecosystem Restoration (2021–2030). A coalition of active countries could federate and accelerate the achievement of existing ecosystem restoration goals of all into the UN Decade – a decade of action and impact on the ground for the planet, for the people and for prosperity.

10. Participants included Armenia, Austria, Bolivia, Brazil, Burkina Faso, Chile, China, Colombia, Costa Rica, Fiji, Finland, France, Gambia, Germany, Haiti, Iceland, Italy, Japan, Morocco, Nicaragua, Niger, Nigeria, Norway, Peru, Republic of Korea, Saint Lucia, Saint Vincent and the Grenadines, Samoa, South Africa, Tajikistan, The United Kingdom, the European Union as well as CBD, GCF, GEF, FAO, IPBES, IPCC, UNCCD, UNDP, UNEP, UNFCCC, UNRC India and the World Bank.

For further information, please contact:

    • Ms. Wagaki Wischnewski, wwischnewski@unccd.int, Cell: +91 74284 94332/+49-173-268-7593
    • Mr. Tim Christophersen, tim.christophersen@un.org, Cell : +254706044045

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‘Conference Emphasises Need for Partnerships to Create a World Without Leprosy’

Active Citizens, Aid, Asia-Pacific, Civil Society, Conferences, Development & Aid, Editors’ Choice, Featured, Global, Headlines, Health, Human Rights, Regional Categories, TerraViva United Nations

Human Rights

Yohei Sasakawa, chair of The Nippon Foundation and World Health Organisation (WHO) Goodwill Ambassador for Leprosy Elimination, delivered a keynote address at the 20th International Leprosy Congress (ILC). Credit: Stella Paul/IPS

MANILA, Sep 11 2019 (IPS) – Forty years ago, Yohei Sasakawa saw his father moved to tears after meeting and witnessing the suffering of people affected by leprosy – also known as Hansen’s disease. Not only did the patients have a physical illness, but they also suffered from social exclusion and discrimination. It made the young Sasakawa vow to work for the elimination of leprosy from the world – just as his father had been doing.


Decades later, after visiting 120 countries and having meetings with countless policy makers and state leaders, Sasakawa – now the World Health Organisation (WHO) Goodwill Ambassador  for Leprosy Elimination – is delivering on his promise.

At the first day of the 20th International Leprosy Congress (ILC), being held in Manila, Philippines, the chairperson ofThe Nippon Foundation (TNF) called for activists, scholars and those affected the globe over, to rally behind the goal of a world free of  stigma, discrimination and violation of human rights of those affected by leprosy. The ILC, which ends Sep 13, is supported by TNF sister organisation the Sasakawa Health Foundation (SHF).

Sharing his experiences, he recalled how he, TNF and SHF lobbied the United Nations to recognise the elimination of stigma against leprosy-affected people as a human rights issue.

Sasakawa reminded delegates that it was a tough journey against several odds as policy makers and diplomats  showed little interest in the human rights of leprosy-affected people. He told the congress how during a 2003 U.N. Human Rights Council meeting in Geneva, only five members attended the event to discuss stigma as a human rights violation in a room that could accommodate 50.

Not one to give up, Sasakawa kept pursuing the issue until finally in December 2010 the U.N. General Assembly unanimously adopted the resolution on elimination of discrimination against persons affected by leprosy and their family members and accompanying principle and guidelines was passed.

“I believe the elimination has been an important milestone in my journey,” Sasakawa said.

But despite the U.N. resolution and various local laws at country level worldwide abolishing policies like segregation and isolation of the leprosy-affected, society still stigmatises and discriminates against Hansen’s disease patients as well those who work within the field, like health care workers etc.

He said one example of this remains is the classification of leprosy as a neglected tropical disease.

“I would like to express my opposition to leprosy being considered as one of the neglected tropical diseases. Leprosy has never been neglected even for a moment by both persons affected and by people who have worked hard for their betterment. In my opinion, this medical terminology feels like it is looking down on the patients and also shows a lack of respect towards those are fighting against leprosy today. Leprosy is an ongoing issue.”

However, Sasakawa also acknowledged that in other areas — such as the partnerships and networking — there has been great progress. The Global Partnership for Zero Leprosy network was a significant step forward.

“The  collaboration will greatly enhance our work towards achieving ‘Zero Leprosy,’” he said, adding that the strengthening of these partnerships, especially with the governments, was crucial to reach the common goal of a leprosy-free world.

“Whenever I go abroad, I always meet with the national leaders of the countries. We cannot solve the issue of leprosy without their understanding and support. Without their support, we cannot secure the budget for activities to eliminate leprosy and the associated discrimination,” he reminded the congress.

Rachna Kumari, of International Federation of Anti-leprosy Associations or ILEP, who is based in Munger in Eastern India’s Bihar state, told IPS: “We cannot end stigma just by treating leprosy as a health issue.”

If only health workers are assigned to work on leprosy, they will work on medication. That is not enough to solve the problem we face. So, we need education. Government must include information on leprosy in school books. There must be billboards and large posters which can educate both patients and healthcare workers. Only with such a holistic approach we can win this,” Kumari said.

Earlier, delivering the keynote speech, the Philippine Secretary of Health Francisco Duque asserted that his government remains serious about respecting the rights of leprosy-affected people.

“The vision of our Universal healthcare for the Filipino people is deeply tied to the aspirations of the 2016-2020 global strategy for the leprosy and goal number 3 of the SDGs or the sustainable development goals. We remain committed to these goals and aspirations. We are committed to zero stigma, zero disability, zero transmission and  zero disease,” Duque told the congress.

Duque also stressed the importance of partnerships to achieve the goals yet unmet.

“We are only a  few months away form 2020 and our midterm strategy is only getting underway. We must work together. This year’s conference emphasises the need for partnerships to create a world without leprosy. And our success and your success may define the relations we have made and continue to make.

Acknowledging stigma as a “barrier for early detection and treatment“ of leprosy, Huong Thi Giang Tran, WHO’s Director for Disease Control in the Western Pacific also said that stigma limits the opportunity for life and leads to social and economic exclusion. She called for the addressing of stigma at the policy level.

 

Let’s Get Climate Action into Traction with Gender Equality

Civil Society, Climate Change, Featured, Global, Green Economy, Headlines, Peace, TerraViva United Nations, Women & Climate Change

Opinion

Ulrika Modéer is UNDP’s Assistant Administrator and Director of the Bureau of External Relations and Advocacy, and Anita Bhatia is UN Women’s Deputy Executive Director for Resource Management, Sustainability and Partnerships.

Credit: UN Women

UNITED NATIONS, Sep 11 2019 (IPS) – Climate change is already altering the face of our planet. Research shows that we need to put all our efforts over the coming decade to limit warming to 1.5°C and mitigate the catastrophic risks posed by increased droughts, floods, and extreme weather events.


But our actions will not be effective if they do not include measures to ensure social justice, equality and a gender perspective. So, how do we integrate gender equality in climate change actions?

The impact of climate change affects women and girls disproportionately due to existing gender inequalities. It also threatens to undermine socio-economic gains made over previous decades.

With limited or no access to land and other resources including finance, technology and information, women and girls suffer more in the aftermath of natural disasters and bear increased burdens in domestic and care work.

Women and girls have also seen their water collection time increased and firewood and fodder collection efforts thwarted in the face of droughts, floods and deforestation, occupying a significant portion of their time that could have been used for their education or leisure.

This is not only theory. For example, women and children accounted for more than 96 per cent of those impacted by the flash floods in Solomon Islands in 2014 and in Myanmar, women accounted for 61 percent of fatalities caused by Cyclone Nargis in 2008.

Women and girls also remain marginalized in decision-making spheres — from the community level to parliaments to international climate negotiations. Global climate finance for mitigation and adaptation programmes remain out of reach for women and girls because of their lack of knowledge and capacity to tap into these resources.

Despite these challenges, women and girls play a critical role in key climate related sectors and have developed adaptation and resilience-building strategies and mitigation techniques, such as driving the demand for renewable energy at the household and community levels for lighting, cooking and productive use solutions that the international community must now support.

Women are holders of traditional farming methods, first responders in crises situations, founders of cooperatives, entrepreneurs of green energy, scientists and inventors, and decision-makers with respect to the use of natural resources.

Women comprise an average of 43 percent of the agricultural work force in developing countries1 and manage 90% of all household water and fuel-wood needs in Africa. Some studies have shown that if women were afforded equal access to productive resources as men, their agricultural outputs would exceed men’s by 7 to 23 percent. It is therefore imperative to embrace and scale-up the initiatives of the 51 per cent of the world’s population.

In recent times, women and girls have used their knowledge and experience to lead in mitigation efforts. From developing apps to track and reduce the carbon emitted as a result of individual consumption, to reducing food by connecting neighbors, cafes, and local shops to share leftover and unsold food 2.

Young women scientists, like South-African teenager Kiara Nirghin, are making a difference in the fight against climate change. They are building on the legacies of women and girls such as Nobel Prize winner Wangari Maathai, who empowered communities to manage their natural resources in a sustainable way.

At the same time, UNDP and UN Women have been collaborating to advance gender equality and women’s leadership on climate change. For example, in Ecuador, the two UN agencies have teamed up with the government to support the inclusion of gender in the country’s climate action plans.

UNDP and UN Women have also collaborated globally to ensure that gender remains a key factor when world leaders make critical decisions on climate change.

If policies and projects take into account women’s particular roles, needs and contributions to climate action and support women’s empowerment, there will be a greater possibility to limit warming to 1.5°C in line with the 2030 Agenda for Sustainable Development. We must continue to engage women and women’s organizations, learning from their experiences on the ground to build the evidence for good practices and help replicate more inclusive climate actions.

The UN Secretary-General’s Climate Action Summit in New York on September 23, 2019 is a unique opportunity to elevate at the highest level the need for substantive participation of women and girls in efforts against climate change.

At the Summit, there will be several initiatives put forth to address climate change, including one focusing on gender equality. The initiative recognizes the differential impact of climate change on women and girls, and seeks support for their leadership as a way to make climate actions more effective.

It calls for the rights, differentiated needs and contributions of women and girls to be integrated into all actions, including those related to climate finance, energy, industry and infrastructure. It promotes support for women and girls in developing innovative tools and participating in mitigation and adaptation efforts and calls for accountability by tracking and reporting progress towards achieving these goals.

For climate action to get more traction and be effective, we need a critical mass of Governments and other stakeholders to sign on to the Climate Action Summit’s gender-specific initiative. The world cannot afford to keep limiting the potential of women and girls in shaping climate actions, as all evidence points towards the benefits of their involvement.

There is already interest by United Nations Member States, as shown in the increased integration of gender considerations in their national climate plans, but a broader movement is needed. We need multi-stakeholder partnerships and engage a critical mass of supporters – governments, UN entities, financial mechanisms, and civil society organizations to support the gender-specific initiative of the SG’s Climate Action Summit.

The time for gender-responsive climate action is now.

1 Food and Agriculture Organization of the United Nations (FAO), The State of Food and Agriculture: Closing the Gender Gap for Development (Rome: FAO, 2011a).
2 Olio, a food-sharing app was founded by women from Sweden, the UK and USA. For more info: https://unfccc.int/climate-action/momentum-for-change/women-for-results/women-leading-a-food-sharing-revolution; One Million Women was founded by a woman in Australia to get one million women to change their lifestyles to mitigate climate change. The group has an app that provides the tools to cut carbon pollution in home energy savings and clean energy options, minimising food waste, reducing over-consumption, investing and divesting (your money) wisely, sustainable fashion, low-impact travel, etc. For more info: https://www.1millionwomen.com.au/

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Nothing For Us, Without Us – Hansen’s Disease-Affected Tell International Gathering

Asia-Pacific, Civil Society, Conferences, Development & Aid, Featured, Global, Headlines, Health, Human Rights, Regional Categories, TerraViva United Nations

Human Rights

Jennifer Quimno of the Coalition of Leprosy Advocates of the Philippines (CLAP) (centre) is joined by Sri Lanka’s Shagana Thiygalingam (L) and Amarasinghe Manjula (R) after Quimno delivered the recommendations presented by the Global Forum of People’s Organisations on Hansen’s Disease to the International Leprosy Congress in Manila on September 11. Credit: Ben Kritz/IPS

MANILA, Sep 11 2019 (IPS) – Stronger government action to fight stigma and discrimination, more government funding for health and non-health support programmes, and a larger role for people’s organisations in developing policy towards Hansen’s disease treatment and eradication are still needed for eliminating the disease.


This was some of the recommendations made by participants of the first ever Global Forum of People’s Organisations on Hansen’s Disease today, Sept. 11 during a presentation to global academics, scientists, researchers, health staff, partners and those affected by the disease at the 20th International Leprosy Congress (ILC).

Jennifer Quimno, secretary of the Coalition of Leprosy Advocates of the Philippines (CLAP), was chosen by the forum participants to represent the group.

“I really felt I was carrying everyone’s voices with me,” Quimno told IPS.

Ending stigma, improving cooperation

The ILC, which is currently being held in Manila, Philippines, is hosted every three years and was last held in China in 2016.

Prior to the start of the congress, Japan’s Sasakawa Health Foundation (SHF) and The Nippon Foundation (TNF), which support elimination of the disease as well as various organisations of persons affected by the disease, held a global gathering from Sept. 7 to 10. For the first time, organisations of those affected by Hansen’s disease from 23 countries across Africa, Asia, Latin America and the Caribbean met to share their know-how and experiences in eliminating Hansen’s disease.

Along with recommendations for eliminating discriminatory laws and practices, including social, psychological, and economic support in Hansen’s disease management programmes, and giving people affected by the disease a greater voice in policy formulation, the forum debated that a shift in terminology from “leprosy” to “Hansen’s disease” be promoted to help combat the historic stigma associated with the disease. No consensus was reached, however.

The recommendations called for comprehensive action and the involvement of non-health agencies and other stakeholders, because areas such as clean water and sanitation, proper housing, education, and dignified work are all, in the view of people’s organisations, critical to efforts to stamp out the disease.

The forum also called for a much greater role for people’s organisations in sustaining Hansen’s Disease treatment, rehabilitation, and services, and in promoting dignity, equality, and respect for human rights.

“Hansen’s disease is more than a disease caused by a bacterium. Poverty, institutional, social and political neglect, complacency and the structural invisibility of vulnerable populations contribute to the perpetuation of Hansen’s disease,” the final draft of the forum’s recommendations read.

Other key recommendations presented to the ILC by the forum include: More funding for research to fill scientific knowledge gaps that still exist (much remains unclear about the transmission of the disease); greater focus by national programmes on case detection, disability prevention, and rehabilitation during treatment; and more funding for “care after cure” programmes, including psychological, social, and economic rehabilitation.

To combat the stigma associated with the disease, the forum urged the widest possible dissemination and adoption by governments, NGOs, and other stakeholders of United Nations guidelines for the elimination of stigma and discrimination. 

The conclusions also made a firm demand for the elimination of all existing discriminatory laws and practises globally, saying that this would further require “affirmative and reparation policies,” in order to be truly effective in promoting equality.

The people’s organisations also made a call for a greater role in government policy-making toward leprosy. They did not neglect improvements in their own capabilities as well. While calling on governments to develop measurable action plans, the people’s organisations noted they must improve their effectiveness by through strengthening networks, and engaging more productively with governments.

Hope for the future, but a few uncertainties

Participants at the global forum who attended the first day of the ILC expressed hope the recommendations would lead to positive action, but noted uncertainties remain.

“Being able to do this at the ILC is a milestone for us, to have our perspective heard,” Frank Onde, president of CLAP, told IPS. While people affected by Hansen’s disease have regularly participated in the ILC, Onde felt this was the first time recommendations were presented in an organised way.

For Indonesia’s Ermawati, a member of PerMaTa, “Attending this congress is like a dream, to come from my village to be involved in a gathering like this,” she told IPS. “It’s inspiring, and I hope it would inspire others [affected by leprosy] to join us and help others.” 

Ermawati was hopeful the recommendations would lead to greater awareness and reduce stigma, particularly the discrimination against women in her country. “I hope it leads to greater acceptance, particularly of us women. In my country, the stigma is very great.” One problem faced by Indonesian women afflicted with leprosy is that they cannot marry; if laws in an area do not actually prohibit it, the culture in most places encourages men to shun these women.

Shagana Thiyagalingam, who is from Sri Lanka, felt that Quimno’s presentation was inspiring. Quimno spoke of how after both she and her father had contracted the disease, but how she still continued her studies currently works with the government health department. “Her story was so motivational,” Shagana told IPS. “It should encourage other women to come forward and feel less stigma.”

Thiyagalingam’s traveling companion Amarasinghe Manjula was likewise inspired by Quimno’s personal story.

While optimistic about what lies ahead, CLAP’s Onde, and his Indonesian counterpart Paulus Manek, the president of PerMaTa, expressed a few reservations. “The barriers [between people’s organisations and government agencies] really need to be minimised,” Onde said.

Manek saw the size of the ILC gathering itself as a sort of barrier to effective action. “It’s almost too big,” Manek said. “I see people here, they are interested in one or two issues only. Maybe there should be a closer focus on fewer issues at once.”

He also suggested that new guidelines from the United Nations Human Rights Council would be useful.  

“It would help us,” Manek said. “I think the media can also help to spread awareness and stopping discrimination.”

Quimno for her part was hoping to see some concrete actions taken as a result of her presentation on behalf of the global forum. “There are so many gaps to fill, so I would hope these people here would commit to studying and planning actions to take on the things we recommended. That would be progress.”

 

The Multiplicity of Zanele Muholi

Each photograph contains only one subject: Muholi. The self-portraits were taken over a three-year period. All photos courtesy of Zanele Muholi and Seattle Art Museum

The exhibition is dimly lit. And it’s supposed to be—it’s part of what makes it great. When I walked through the press preview, someone requested that the lights in the galleries be turned up. Our guide politely declined. The South African photographer and “visual activist” Zanele Muholi, whose “self-portraits captured with a camera” compose the show, had come through just that morning to tweak the lighting the way they liked it, sure of how they’d like to be seen.

Somnyama Ngonyama, Hail the Dark Lioness consists of around 75 black-and-white self-portraits that spill out of Seattle Art Museum’s Jacob Lawrence and Gwendolyn Knight Gallery and into the hallway and gallery that abut it. The walls are painted black, charcoal gray, and white, providing no bright contrast of any sort. Eight of Muholi’s portraits are blown up to the size of walls, almost physically involving the viewer in the composition; the others range in size, the smallest being the size of a large hand.

Each photograph contains only one subject: Muholi. The portraits were taken over a three-year period from 2014 to 2016 as Muholi traveled the world, giving guest lectures and participating in residencies in places like Oslo, Norway; Richmond, Virginia; and Mayotte, a French territory off the east coast of Africa.

“They are taken in various places wherever I wake up, so a sense of space is connected to my realities as I respond to many things I have encountered,” the artist told me. “This is my own way of undoing many things, including racism, but I use my own body as a subject of my own art.”

Muholi’s work is powerful because it recognizes the multiplicity of blackness and of self. It’s a reminder that to be black—as a condition, as a culture—is a complex state of being that’s often reduced to a single thing and, therefore, misread. Muholi’s personal ties to their queer and black community back in South Africa only deepen the ways in which their self-portraits can be read. Aesthetically, the work is both editorial and DIY, serious and playful.

The child of a Zulu mother and a Malawian father, Muholi was born in Umlazi, South Africa, in 1972. Muholi was a baby when their father died, and their mother worked as a maid to provide for the family. After completing an advanced photography course at Market Photo Workshop in Newtown, Johannesburg, Muholi had their first solo exhibition at Johannesburg Art Gallery in 2006.

In 2002, they cofounded and worked as a community-relations officer for the Forum for the Empowerment of Women, a black lesbian organization based in Gauteng, South Africa. They also reported and photographed for the blog Behind the Mask, which focused on gay and lesbian issues in the African continent.

This work set the stage for one of Muholi’s most discussed projects, their ongoing series Faces and Phases that began in 2006, for which Muholi photographs black lesbian, transgender, and intersex South Africans from their own community. The portraits came at a time when queer black South Africans were experiencing a wave of hate crimes and murders.

That series—which now includes more than 250 portraits—features queer couples and trans, lesbian, and genderqueer individuals presenting themselves to the camera, looking directly into the lens. It is, in part, a visual archive that does not play into any stereotypes or fears about this community, but rather respects and validates this community’s existence. These people whom Muholi photographs and works with are collaborators who accompany Muholi wherever they go.

Muholi’s work in Somnyama Ngonyama flows along a similar vein. “This [show] is on race, specifically responding to a number of events that are taking place in South Africa and beyond. There’s a lot of ongoing racism that is taking place and we hardly have the opportunity to respond as art practitioners or creatives to speak to such atrocities, violent racism, and displacement of our people,” the artist told me. “I’m not talking about myself only, but I’m talking about many other people whose voices are there but not heard.”

Most of the self-portraits in the exhibition at Seattle Art Museum feature Muholi looking directly at the camera, engaging the viewer. In the pictures, their skin appears uniformly darker than in real life, the whites of their eyes whiter, a result of them cranking up the contrast postproduction. They emphasized to me that there is no artificiality of any kind in their photographs, using only available light and spaces.

Eschewing high-quality materials, Muholi searched for discarded, mundane, cheap materials in each of the locations they traveled to, and then manipulated those findings to transform them into something greater than the sum of their parts. Often, these “un-African” materials were fashioned to resemble or recall something African, something that reminded Muholi of home. Rubber bicycle tires become a head wrap and dress; wooden clothespins become an elaborate headpiece; steel wool becomes a crown in tribute to their mother, Bester.

Whether using markers, wooden chopsticks, cheap dream catchers, power strips, vacuum tubes, blown up rubber gloves, scissors, chairs, hair buns from H&M, or actual money, Muholi embodies many different characters and selves. It’s more than just playing dress up, but rather an intended confusion for the viewer, each different character—lion, jester, king, queen, nurse, prisoner, lover—calling into question what we see when we see each other.

This embodiment challenges the presumed audience about their assumptions—here in Seattle, that audience is mostly white people—and about their own visual archive of black people. In the photograph Ntozakhe II, Parktown, 2016, Muholi is fashioned after the Statue of Liberty. Are black people in the United States truly free? If the Statue of Liberty were black, would our concepts of freedom and justice be different? In another wall-size photograph, Bhekisisa, Sakouli beach, Mayotte, 2016, Muholi’s body lies almost hidden among the rocks on a beach of Mayotte. To a viewer, what could that evoke? Refugees? As a critic, I’m keenly aware that I bring myself and my history to whatever I look at. Muholi is asking me to dissect and strip away that stuff.

When I mentioned Cindy Sherman—a white American artist known for her movie-like photographs in which she inhabits different characters—Muholi grinned. They get that comparison a lot. “Cindy cannot connect to our reality—not ever, not tomorrow,” the artist said, referring to the black community.

Each different character—lion, jester, queen, nurse, prisoner, lover—calls into question what we see when we see each other.

For comparison and context, they offered that black American visual artist Renee Cox is a better reference point. How we think about what an artist does requires an attentiveness, a willingness to look beyond our own ways of thinking, the connections we make, our own perception of the canon.

At the opening reception for the exhibition, I stood in the drink line behind an aloof-looking older white man who was making conversation with a younger black acquaintance about the show. He leaned in, familiarly, conspiratorially, referencing the photos: “They’re frightening, though, aren’t they?”

His acquaintance gave a humorless chuckle before grabbing a drink and slipping back into the crowd.

Frightening. My brain wrestled with the word as I watched the man sip his drink unbothered and wander back into the celebration. My thoughts drifted back to earlier in the day when a white woman asked Muholi if their portrait Julile I, Parktown, Johannesburg, 2016 was a reference to Édouard Manet’s Olympia. In the picture, Muholi is lying, naked, in front of tall stacks of newspapers while a length of plastic pads wraps around their leg.

Muholi was quick to correct the woman: No, no, this photo was taken days before an operation they were to have that would take tumors out of their uterus. This self-portrait was about the state of panic they were in surrounding whether or not they’d survive the surgery. Manet was not on their mind.

In no portrait does Muholi give a smile. The photos are not meant to appease in that sense. But that does not mean that there is a lack of emotion in the show. Rather, there’s an abundance of emotion.

“There are images that are super ugly,” the artist told me. “There are images that will make the next person feel like, ‘Wow!’ There are other images where you’re like, ‘Why do we have to look at this?’ It is through those images in which I want other people to find their own responses.”

That made me wonder about the responses I’d witnessed. Could it be that Muholi’s blackness was read as something to be feared, and their pain was read as beauty? The white woman referencing Manet misread the pain of Muholi’s photograph and saw beauty. The white man looked at Muholi’s willingness to present their body—their culture, their history, their sexuality, their many selves—and saw something frightening, perhaps his own fear. Maybe he saw that he didn’t know what he didn’t know.

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The Emergence of a Global Voice for Hansen’s Disease Affected Persons

Active Citizens, Asia-Pacific, Civil Society, Conferences, Development & Aid, Featured, Global, Headlines, Health, Human Rights, Regional Categories, Sustainability, TerraViva United Nations

Human Rights

Her experience and the chance “to help strengthen Colombia, the world, and my family” through participating in the Global Forum of People’s Organisations on Hansen’s Disease, sponsored by the Nippon Foundation and the Sasakawa Health Foundation, was like “rising from the ashes” for Lucrecia Vazques from Felehansen Colombia. Vazques’ family was hit hard by leprosy, with not only herself, but her son and one-month-old granddaughter being afflicted. Credit: Ben Kritz/IPS

MANILA, Sep 10 2019 (IPS) – The Global Forum of People’s Organisations on Hansen’s Disease, which was attended by members of people’s organisations from 23 different countries, wrapped up in Manila, Philippines, today Sept. 10 after four days of discussion and deliberation.

The main outcome was a set of recommendations, which included participants stating that those affected by the disease should have more inclusive roles in the global campaign against leprosy.

Asked to share his impressions of the forum with his fellow participants, Joshua Oraga, who is a member of ALM Kenya, a local Hansen’s disease non-profit, told the audience, “We should all familiarise ourselves with the WHO [World Health Organisation] guidelines on strengthening the participation of persons affected by leprosy in leprosy services. That should be our creed, because if you look at that document, you will see that we are the only stakeholders who have an end-to-end role.”

He said that those affected by leprosy or Hansen’s disease had a role in overcoming stigma and discrimination.

“We have a role in the promotion of equity, social justice, and human rights, we have a role in addressing gender issues, we have a role in the dissemination of information, education, communication…. We have a role in advocacy, we have a role in counselling and psychological support, we have a role in training and capacity-building, we have a role in referral services, we have a role in resource mobilisation…. So, we are everywhere!”

Oraga’s enthusiastic impressions in a way defined the outcome of the forum organised by Japan’s Sasakawa Health Foundation (SHF) and The Nippon Foundation (TNF), which support elimination of the disease globally and provide information and awareness about the disease through their dedicated website titled Leprosy Today.

The recommendations will be presented on the first day of the International Leprosy Congress (ILC), which is also being held in Manila from Sept. 11 to 13. The recommendations addressed increasing awareness of Hansen’s Disease among the public and governments, calling for greater government support for people’s organisations’ advocacies, taking a larger role in helping to form anti-leprosy policy, and working to build sustainability and more effective networks among organisations spread around the world.

A true people’s forum

To Dr. Takahiro Nanri, Executive Director of SHF, the real value of the recommendations lies not in their details, but in the manner in which they developed.

Nanri noted that the forum’s carefully-planned agenda was quickly thrown off-schedule by the spirited discussions among the participants. “The people really led the forum, and did the work they wanted to do, and I am very happy about that.”

“The recommendations were good ones, but what I think is really important is the process we saw,” he added.

Oraga was likewise pleased and motivated by his experience. Oraga, who had leprosy as a youth, said, “This is the first time I have had the opportunity to take part in a meeting at this level, so imagine my excitement and happiness to be able to come here.”

Oraga also expressed his gratitude for the work that Yohei Sasakawa, World Health Organization’s (WHO) Goodwill Ambassador for Leprosy Elimination and chairperson of TNF, has done over the last four decades. Sasakawa’s foundations have contributed over USD200 million in financial support for the WHO’s Global Leprosy programme. He also advocated for discrimination and stigmatisation against people affected by Hansen’s disease to be included in the United Nations human rights agenda. The resolution was passed in 2010.

“He has done so much for leprosy around the world, and personally I am grateful. Just think of it, because of Mr. Sasakawa, in three years, maybe leprosy will just be like any ordinary sickness,” Oraga said.

Lucrecia Vazques of Felehansen, Colombia also felt the forum was an extraordinary experience. “It’s been wonderful,” she told IPS through a Spanish translator. “It is like resuscitating after a hard moment.”

Vazques’s bubbly personality belies her own difficult experience with Hansen’s disease, which not only afflicted her, but her one-month-old granddaughter and her son, who was diagnosed first.

“It was hard,” Lucrecia said. “I had no knowledge whatsoever.We thought we would die.”

“But there was something to fight for, and to live for, and here I am. This forum means rising from the ashes. And if I had the choice, I would rise from the ashes again, and I would be right here, to help strengthen Colombia, and the world, and my family,” she said.

Looking ahead

But there is much work to still do.

“Because this was a people-led forum, it gives us direction. As you know, our resources are not limitless. We have an obligation, but it is of course better if we can maximise our efforts, and the recommendations help,” Nanri said.

Nanri reiterated the value of the “process” that he saw evolve during the forum, particularly in the context of the Joint Campaign on World Leprosy Day 2020, which will be observed on Jan. 26 next year.

“This was a step. You don’t go from the ground to the 10th floor in one jump. So now the first step has been taken. The next step is to get the groups around the world to do the activities at the same time,” which is the goal of the joint campaign. “When these recommendations are presented at the ILC, the next step can begin,” he said.