News

UN Special Rapporteur to join virtual launch of partnership with charity Lepra

  • Date

    Tue 5 Jul 22

Health education in Bangladesh 2012

UN Special Rapporteur on the elimination of discrimination against persons affected by leprosy Alice Cruz is helping launch a new partnership between international charity Lepra and the University of Essex.

The new partnership is looking to help people affected by leprosy and other vulnerable groups throughout the world including India.

Alice Cruz will give the keynote address at the virtual launch event on Wednesday 13 July titled ‘We will overcome leprosy together’. Her address will be followed by a panel discussion with people affected by leprosy, doctors, scholars, and WHO representatives.

Register for the Zoom Webinar online and see the full programme online.

Panel members will include representatives from the University of Essex’s Institute of Public Health and Wellbeing and Human Rights Centre plus the Blue Peter Public Health and Research Centre in India and the World Health Organization’s Regional Office for South-East Asia.

Partnership launch

Professor David O’Mahony, the University of Essex’s Dean of Partnerships (Research), said: “We’re really excited about our partnership with Lepra, and this event will help highlight how together we will be able to work and cooperate on the important work that Lepra delivers across the world in the combat against leprosy.

“There are wide range of opportunities for our respective organisations and for our researchers and students – from undergraduates to PhD students – to benefit from this partnership and we look forward to working together.”

Jimmy Innes, Lepra CEO, said, “I’m delighted that we are holding this launch event to celebrate this new partnership between Lepra and the University of Essex. We both share the same physical home in Colchester, and we both come with rich and diverse histories that offer us great complementarity. For Lepra, we relish the chance to work with the university’s students and staff, to help engage in our work addressing leprosy in India and Bangladesh, and in pursuit of a world that is free from prejudice and disability due to leprosy.”

Lepra and the University of Essex will be collaborating on projects and academic research where Lepra and the University share common interests, to advance the fields of public and global health.

Working together they will address the current and pressing issues such as human rights and advocacy, medical and para-medical science, social science as well as human science.

Event panel and testimonials

The event panel will include Mr Rajni Singh, Bihar State Coordinator, Lepra; Dr Aparna Srikantam, Director of Lepra Blue Peter Public Health and Research Centre in India; and Dr Venkata Ranganadha Rao Pemmaraju, Ag Team leader, Global Leprosy Programme, World Health Organization, Regional Office for South-East Asia; and Dr Asrat Mengiste, NTD Technical advisor, Centre for Innovative Drug Development and Therapeutic Trials for Africa, College of Health Sciences Addis Ababa University.

Those attending will also hear testimonials from Ms Manikyamma Kummarapalli, Lab Assistant for Lepra at the Blue Peter Public Health and Research Centre, India, and Businessman and Entrepreneur Mr Md Shah Ajom Shumon, who is a Community Leader and Secretary of Pabna District Federation of the People affected by Leprosy in Bangladesh.

Lepra's work

Leprosy is an infectious disease, affecting a person’s peripheral nerves, often leaving them with disabilities including the inability to walk, use their hands or see. Leprosy is curable with a course of multi-drug therapy, that is provided free of charge. Due to fear and lack of knowledge, there are over three million people across the world living with undiagnosed leprosy and every day the disease causes more damage to their health, livelihood, and future.

Last year, despite the global pandemic and lockdowns, Lepra directly reached more than 290,000 people through diagnosis, treatment and holistic care. More than 225,000 people were further engaged in their home communities through health education and events to raise awareness of leprosy and other neglected diseases, to reduce transmission and promote wellbeing.

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