We saw this coming. As humanitarians, our risk assessments in different parts of the world have always factored in the potential for extreme weather events and the spread of vector-borne diseases, of drought, desertification, and mass displacement. Emergency first responders like us work up scenarios for interventions and gain experience each time we put our planning to the test in real crises.
It is 50 days into the lockdown in Kashmir since roads were blocked off, schools shut, and internet and communication services stopped.
In less than ten days world leaders will be gathering at the United Nations in New York for the Climate Action Summit. Their goal is simple; to increase ambition and accelerate action in the face of a mounting climate emergency.
For many this means ambition and action that enables countries to decarbonize their economies by the middle of the century. But that is only half the equation. Equally ambitious plans are also needed to build the resilience of vulnerable sectors and communities being battered by climate related disasters of increasing frequency, intensity and unpredictability.
As companies begin to focus on hiring people with disabilities, we need to shape how they think and act on this interest.
In an alarming imbalance struggling families in rural Bangladesh spend almost US$2 billion a year on preventing climate-related disasters or repairing damage caused by climate change ― far more than either the Bangladesh government or international bodies.
New analysis of historical satellite imagery indicates that Nepal’s forest area has nearly doubled, from 26% of land area in 1992 to 45% in 2016. The midhills have experienced the strongest resurgence, although forests have also expanded in the Tarai and in the mountains. This makes Nepal an exception to the global trend of deforestation in developing countries
In a life peppered with tragedy, Mary Shelley wrote in 1818, “Have I not suffered enough, that you seek to increase my misery?” That this accurately sums up the fate of many women in South Asia who suffer a major health shock such as a serious illness or a disability or both, is hard to dispute.
Human trafficking is perhaps one of the most well-organised crimes being committed in India. How else do we explain the phenomenon of adolescent girls and young women from remote villages across India being found in brothels in our cities?
International Leprosy Congress just wrapped up in Manila, Philippines last week. Alongside policy makers, diplomats, medical researchers, doctors, donors and academics, several Hansen's disease-affected people’s organisations also participated in the 3-day congress that was co-sponsored by The Nippon Foundation (TNF) and Sasakawa Health Foundation (SHF).
Rachna Kumari of Munger in Eastern India’s Bihar state is not yet 30. But she's already been married at 18, abandoned by her husband after she was diagnosed with leprosy and become an award-winning advocate of the disease. She has traversed a long road. And this week she undertook another step in her journey to fly to Manila, Philippines, as a delegate at the 20th International Leprosy Congress (ILC).
From the ashes of a tragedy that wiped out almost 90% of the city of Hiroshima on 6 August 1945, an institute called the Hiroshima Peacebuilders Center
(HPC) rose like a phoenix of hope that is pioneering the creation of a global pool of peacebuilders. It is driven by the 2030 Agenda for Sustainable Development declaration that "there can be no sustainable development without peace and no peace without sustainable development.”
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.
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.
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.
Octogenarian Yohei Sasakawa has travelled to more than 90 countries across the globe; from areas of conflict, to the jungles of Brazil, shaking hands, hugging and washing the feet of Hansen’s disease-affected people. His message is simple: Stop stigmatisation and eliminate the disease.
As a series of conflicts in the Hindu Kush Himalayan region come into sharp focus, sidelining local populations, the long-term environmental costs may leave the region degraded, poor and desperate.
Increasing awareness of the continuing existence of Hansen’s Disease (leprosy) is critical to sustaining effective public health efforts against the disease, eliminating the social stigma associated with it, and halting its transmission.
August is immensely important in the history of the Asian subcontinent, marking the month that India and Pakistan gained independence
from the British in 1947. Now, in 2019, it has once again proved momentous, when, ten days before
India’s Independence day celebrations, prime minister Narendra Modi’s
government revoked the autonomy of Indian-administered Kashmir – a status provided for under the Indian Constitution.
Organisations supporting people affected by Hansen’s disease (leprosy) have social rather than capitalist aims, but they need to take a business-minded approach to their work if they wish to be sustainable, experts at a global conference in Manila, Philippines said.
Being part of a platform where leprosy-affected people from all over the world can freely interact, exchange and share opinions, ideas, experiences and strategies was always something Tasfaye Tadesse dreamt of.
Professor Takahiro Nanri is the executive director of the Sasakawa Health Foundation, co-organiser of the Global Forum of People’s Organisations on Hansen’s Disease, which will take place from Sept. 7 to 10 in the Philippines.