Our Vision is a World where Leprosy is Defeated and Lives are Transformed.
The Leprosy Mission is the world’s oldest and largest leprosy-focused organisation.
Leprosy defeated, lives transformed
Following Jesus Christ, we seek to bring about transformation; breaking the chains of leprosy, empowering people to attain healing, dignity, and life in all its fullness.
Our Christian identity and values are at the heart of who we are and everything we do. Because we follow Jesus Christ, we value Compassion, Justice, Integrity, Inclusion, and Humility.
We will do everything we can so that by 2035, children can be born into a world without being at risk of leprosy.
We are one of New Zealand's oldest charities being in New Zealand for over 100 years. We have a dedicated staff based in Auckland and raise funds and awareness for people affected by leprosy around the world.
The Leprosy Mission was founded in 1874 by Irish missionary Wellesley Bailey. On a mission in India he met a group of people sitting under a tree. They had been banished from their village because of their leprosy.
Deeply moved, he returned home determined to make a difference. He declared, “If there was ever a Christ-like work in the world, it is to go amongst these poor sufferers and bring them the consolation of the gospel.”
Nearly forty years later he visited New Zealand with his wife Alice in 1912 and inspired local people to begin their own support chapter. The Leprosy Mission New Zealand was formed to raise awareness about leprosy and provide financial support to bring hope and healing to people affected by the disease.
The Leprosy Mission is part of the Global Partnership for Zero Leprosy, joining with organisations like the World Health Organisation (WHO), working towards ending leprosy transmission by 2035.
Some communities still believe that and shun people with leprosy. It is just a bacterial disease, though uncured it causes immense damage and disability Leprosy – also called Hansen’s Disease – is caused by bacteria attacking nerves in our extremities, such as hands, feet, face, eyes. Leaving them numb.
It is only mildly infectious. You would have to spend years with an infected person before you were likely to catch it. This is why it tends to affect families and was once believed to be hereditary. It is not. You can’t catch leprosy by touching someone. It spreads through moisture droplets in the air, from someone who has not started their cure.
95% of people may be naturally immune, but immunity is lowered by poor nutrition, sanitation, and hygiene.
Fingers and toes to claw inwards. In the eyes, it can lead to infections, cataracts and even preventable irreversible blindness. Fingers and toes may claw inwards. In the eyes, leprosy can lead to infections, cataracts, and even preventable irreversible blindness. This often occurs because the disease damages the nerves that control blinking. Without the protective reflex of blinking, ulcers and infections in the hands and feet become common. When the skin loses feeling, people may ignore normal bruises, cuts, and burns, allowing these unprotected wounds to become severely infected, which can lead to disfigurement and amputations.
A common complication is footdrop, as the nerve that controls our walking is destroyed. Without being able to automatically raise our toes as we walk, our feet get bruised and scraped, leading to infections that in turn lead to amputations or even death. That is why one of the most effective aids is a pair of protective sandals.
Better still, is to stop leprosy before it can cause this harm.
The Leprosy Mission is committed to the safeguarding and protection of everyone we work with, including beneficiaries, volunteers, TLM staff and the staff of partner organisations.
For all of history, there was no cure for leprosy. That is what made leprosy healings in the Bible such remarkable miracles. Leprosy was an irreversible life sentence – often a death sentence. Today, though, we have a cure: six months to a year of a specific combination of medications.
If leprosy is found and cured early permanent disability can be completely avoided
That is why we also educate local health workers, doctors, nurses, paramedics, rural medical practitioners, and family planning staff about leprosy - so they can identify cases and refer people for treatment as quickly as possible.
This is very significant because there is no reason a child receiving MDT needs to be kept away from school, or an adult kept from earning their living. This still does happen though, because …
The ancient stigma and fear of leprosy remains its greatest burden
Some communities retain deep fear of leprosy and the disabilities it causes, based on ancient myths, superstitions and even discriminatory laws that persist to this day. People in such a community may not believe that MDT can set someone free from leprosy.
As a result, people affected by leprosy are often rejected by families, friends, employers, and communities. Many lose jobs and struggle to find a livelihood. Others lose their homes and children are excluded from school.
Because of this stigma, many people with leprosy are afraid to come forward for treatment. They hide in shame and isolation, until the disease has caused deep damage to their lives.
When people do begin treatment, the death of the bacteria in their bodies can cause an extreme inflammation called Leprosy Reaction, with pain, sickness, swelling and fever. These people require a lengthy hospital stay to complete their treatment. They cannot afford this level of care themselves, so selfless people like you generously support their care.
As a Leprosy Mission supporter, your gifts, donations, prayers, and all other forms of your support are working in some of the poorest and remote areas in the world.
Leprosy is still a major health threat in one of world’s poorest, most crowded countries.
Successful community health since 1999
Intensive case finding.
Tackling leprosy with local partners: ENAPAL.
Around 70 percent of people diagnosed with leprosy live in India
Reducing world’s third worst rate of new leprosy cases.
Preventative health, raising awareness on issues like leprosy, TB and malaria.
3,000+ people receiving leprosy treatment.
Working with TLM PNG to reduce leprosy’s burden: medical, social, economic.
Partners with TLM TL to reduce leprosy’s medical burden and social cost.
Andre Stuart
Board Chair
Gillian Whitley
Executive Director
Jasleen Kler
International Programmes Manager
Leanne Ryburn
Marketing & Fundraising Manager
Martin Malkaney
Finance Manager
Andrew Stott
Blair Matheson
Graham Mills - Treasurer
Jo Burnet
Nadine Rutter
Nicholas Fagerlund
Rev Kathleen Gavin
The Leprosy Mission New Zealand is a vital member of the Leprosy Mission Global Fellowship. Through a robust and enduring partnership with the New Zealand Government's Ministry of Foreign Affairs and Trade, we implement sustainable programs across the Asia-Pacific region. These initiatives encompass health, disability, livelihood development, gender and inclusion, WASH (Water, Sanitation, and Hygiene), education, community governance, and advocacy.