For over four decades, the Nepal Leprosy Relief Association has walked alongside the most marginalised people in Nepal — bringing medicine, dignity, and hope to communities that history had forgotten.
The Nepal Leprosy Relief Association — NELRA — was founded in 1978 by a group of Nepali physicians, social workers, and community leaders who recognised that leprosy was not merely a medical problem but a profound crisis of exclusion. At the time, Nepal had one of the highest leprosy prevalence rates in South Asia, yet patients in hill districts and remote Terai communities had no access to treatment whatsoever.
NELRA's founders established the first dedicated leprosy outpatient clinic in Kathmandu in 1979, followed rapidly by mobile units that reached the Bagmati, Gandaki, and Koshi zones. Working in close partnership with the government of Nepal and the World Health Organization, NELRA became the primary implementing partner for Nepal's national MDT rollout in 1982 — making Nepal one of the first countries in South Asia to offer multidrug therapy at scale.
Through political upheaval, natural disasters including the 2015 earthquake, and the COVID-19 pandemic, NELRA has never suspended its field operations. Today, the association runs seven district offices, two rehabilitation centres, a dedicated children's scholarship programme, and a nationally recognised legal advocacy cell — touching over 62,000 lives across all seven provinces of Nepal.
NELRA co-led the rollout of Multidrug Therapy across Nepal in 1982 alongside the Ministry of Health. This work reduced Nepal's leprosy prevalence rate from 19.4 per 10,000 population in 1985 to below 1 per 10,000 by 2010 — achieving the WHO elimination threshold for the first time in the country's history.
When the Gorkha earthquake struck in April 2015, leprosy patients in Sindhupalchok, Nuwakot, and Dhading lost not only their homes but their entire treatment supply chains. NELRA deployed emergency teams within 72 hours, delivering 8,400 MDT kits and establishing two temporary rehabilitation shelters serving 340 displaced patients.
In the early 1990s, NELRA launched its Dignity Advocacy Programme — a systematic effort to challenge the caste-based exclusion of leprosy-affected individuals from public life. The programme produced Nepal's first legal brief on leprosy discrimination, which was submitted to the National Human Rights Commission in 2003 and influenced amendments to the Public Health Act.
NELRA's work is guided not by charity but by rights. We believe leprosy-affected people are full citizens whose dignity, participation, and leadership must be central to every programme we design and deliver.
NELRA treats access to leprosy treatment, rehabilitation, and social inclusion not as gifts to be given but as rights to be claimed. Every programme is designed to build the capacity of patients and affected communities to advocate for those rights independently of external support.
No programme is designed by NELRA without the participation of people who have lived experience of leprosy. Our Community Advisory Panels in each of Nepal's seven provinces hold veto power over programme design decisions that affect their communities — a structural commitment, not a consultation gesture.
Every field intervention is tracked against a defined theory of change with independent monitoring and evaluation. NELRA publishes its full programme data annually, including failures and shortcomings, in accordance with the International Aid Transparency Initiative standard that NELRA adopted in 2016.
NELRA's clinical mandate ends only when a patient is economically independent, socially reintegrated, and legally protected. Treating the disease is the beginning of our work, not the end. Our case-management model assigns each patient a single coordinator who remains their point of contact from diagnosis through full rehabilitation.
We walk alongside. We do not hand down. Patients are partners, not beneficiaries.
Solutions are designed for Nepal's geography, culture, and political reality — not imported wholesale from elsewhere.
We publish what works and what does not. Accountability to communities comes before accountability to donors.
NELRA was established under the distinguished patronage of Princess Shanti Singh, whose leadership shaped the organisation's character and ambitions for over two decades. She was succeeded by a line of dedicated chairpersons who each advanced the mission.
Princess Shanti Singh lent her royal stature and personal conviction to the cause of leprosy relief at a time when the disease carried the deepest social stigma in Nepali society. Her decision to publicly associate with NELRA at its founding in B.S. 2027 was itself a powerful act — signalling to the country that leprosy-affected people deserved care, not condemnation.
During her 23-year tenure as Chairperson, she oversaw NELRA's transformation from a small Kathmandu-based organisation into a nationally recognised institution. She personally campaigned for the removal of discriminatory practices in public life, engaged international partners to fund the MDT rollout, and mentored the generation of leaders who succeeded her.
Six leaders have carried forward the responsibility of the Chairpersonship since Princess Shanti Singh's tenure, each serving NELRA at a distinct chapter in Nepal's leprosy relief story.
Scroll to explore the full timeline
Founded in Kathmandu by Dr. Laxmi Prasad Shrestha and six colleagues. First office opened in New Baneshwor.
Nepal's first dedicated leprosy outpatient clinic opened in Kathmandu, seeing 312 patients in its first year.
Co-leads Nepal's national Multidrug Therapy rollout with the Ministry of Health and WHO — one of Asia's first.
First mobile medical units deployed to Terai districts — Saptari, Siraha, and Mahottari — reaching previously inaccessible populations.
Launches Nepal's first structured programme challenging caste-based exclusion of leprosy patients from public life.
Receives the Prime Minister's National Award for Public Health — Nepal's highest civilian recognition in health services.
Submits landmark discrimination brief to the National Human Rights Commission, directly influencing Public Health Act amendments.
Nepal reaches WHO leprosy elimination threshold — below 1 per 10,000 — for the first time. NELRA central to this achievement.
Deploys emergency teams within 72 hours of Gorkha earthquake. 8,400 MDT kits delivered. 340 patients sheltered. Zero treatment interruptions.
Launches children's scholarship programme supporting 340 students from leprosy-affected families in 5 provinces.
Pivots all operations to home delivery during lockdown. All 62,000 active patients maintained on treatment throughout the pandemic.
Launches Vision 2030 — a partnership with all 7 province governments and WHO Nepal targeting zero new Grade-2 leprosy disability in Nepal.
Images from NELRA's field operations across Nepal's provinces.
Forty-six years of work has brought Nepal to the threshold of eliminating leprosy disability. Help NELRA cross that threshold.