Neema Namdamu, 42, grew up in the village of Bukavu in eastern Democratic Republic of Congo where children with disabilities were considered a curse.
As a child Namdamu contracted polio, leaving her paralysed from the waist down. Her neighbours advised her mother to do what they felt was the "right thing": to leave the child alone in a hut until she died of starvation.
Djibouti’s President Ismail Omar Guelleh knows that his country is in need of an education system that is, “innovative, based on universal principles and values and adaptive of the local realities”.
Fifteen years ago, Sattamma – a daily labourer in the Rangareddy district of southern India’s Telangana state – was abandoned by her husband after she was diagnosed with Hansen’s Disease.
On late Monday morning, a motley group of more than a thousand youth gathered in a hall in Sharm el-Sheikh, Egypt, to listen to Sophia — a humanoid robot capable of displaying humanlike expressions and interacting with people. Yahya Elghobashy, a computer science engineering student from Cairo, sat excitedly in the audience. A few meters away from him, also in the audience, was Abdel Fattah el-Sisi — the President of Egypt.
Dr Rahat Chawdhury is the Deputy Program Manager at the National Leprosy Program of Bangladesh. His is the umbrella organization of hundreds of doctors, technical experts, counsellors, strategists, health advocates, field workers and thousands of leprosy-affected people as the beneficiaries.
Dr Erwin Cooreman
is the Team Leader of WHO's Global Leprosy
Programme. This week, he is in Dhaka to attend the National Conference on Leprosy, which was inaugurated by the prime minister of Bangladesh Sheikh Hasina. In her speech, she reiterated her commitment to make the country Zero-Leprosy by 2030.
Sandhya Mandal has never felt so vindicated. For the past four years, the 36-year-old community health worker from Meherpur – a rural district bordering India – has been traveling 50 km every day along dusty roads on an old motorbike, searching for leprosy patients who needed urgent treatment. But in her community, instead of compliments, neighbours and relatives raised questions about her work and her character. “They ask why I come home so late and what is this ‘work’ that I really do. Some even imply that I might be doing something like prostitution,” Mandal tells IPS.
“The window of opportunity to avoid catastrophic climate change is fast shrinking,” executive director of the Green Climate Fund (GCF), Yannick Glemarec, tells IPS.
Good news: the graph depicting climate investments has been steadily increasing. Climbing from the 2012 figure of $360 billion in climate investments across the world to close to $600 billion currently.
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).
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.
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.
Professor Ai Kurosaka remembers the day she first interacted with a person affected by Hansen’s disease. It was 2003 and Kurosaka, then a graduate student of sociology at the Saitama University in Japan, had been assigned to interview ex-patients and their family members to document what kind of discrimination they faced. It was a very difficult task because nobody wanted to speak or identify themselves.
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.
Kumaribai Jamkatan, 51, has been fighting for women’s land rights since 1987.
Though the constitution of India grants equal rights to men and women, women first started to stake their claim for formal ownership of land only after 2005–the year the government accorded legal rights to daughters to be co-owners of family-owned land.
Jam Bai, an Indigenous farmer from Korchi village in western India, is a woman in hurry. After two months of waiting, the rains have finally come and the rice saplings for her paddy fields must be sown this week while the land is still soft.
During his 22-year career in the health sector, Marcus Samo has seen the Federated States of Micronesia (FSM) suffer from an increased burden of disease while at the same time the resources to address them have either remained the same or decreased.
It’s a good day for Dexter, a 25-year-old fisherman from Pohnpei in the Federated States of Micronesia. He’s just been told that he is cured of leprosy.