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Video – Sarita’s Story

When I visited Lalgadh Leprosy Hospital for Easter 2014 I was blessed to meet some beautiful people. I know I have made friends for life as a result of my time spend there. One of the ladies I met was Sarita, she was part of the outreach team who travelled with us to the remote villages. On these trips she preformed many tasks, one of which was introducing us to the villagers, helping to translate and share their stories.

I also spent time with her in the small jewellery making workshop which she manages. She provides training and support for people in a similar situation to her own. Sarita, seen here on the left,  is a very warm, confident and outgoing person but this was not always the case.

Click on this video link to hear her story:

workshop loRes


Increase in patient numbers

The Nepal Leprosy Trust hospital in Lalgadh, south eastern Nepal reached its highest recorded number of patients with 601 outpatients on Sunday 12th October – 58 leprosy and 543 general.  This is very good news as there still remains a reluctance to present with leprosy related symptoms due to the associated stigma.

Busy OPD over600patients_Sun12Oct2014_loRes

These continuously increasing numbers suggest a wonderful increasing visibility and drawing power of LLSC’s hospital services under the Good Lord’s hand and with its reputation for low cost (or free) high quality caring clinical diagnostics and patient treatment  – things that characterise compassionate Christian care.  Perhaps you could  spare a thought or a prayer for the stretched Out Patient Dept (and In Patient Dept) staff, especially the doctors, nurses and paramedics who battle through the pressures of these huge numbers each day, willingly and caringly despite the present uncomfortable heat.

Queuing for treatment in Out Patient Dept, Lalgadh Leprosy Services Centre, Nepal
Queuing for treatment in Out Patient Dept, Lalgadh Leprosy Services Centre, Nepal

Craft Fair in Farmleigh

Tuesday 23rd September 2014.

Thanks to everyone who attended the Nepalese Cultural day in Farmleigh last Sunday. We really appreciated the interest and support for both our craft sale and in hearing about our mission in Nepal.  Sales of Christmas stock was surprisingly high although not altogether unusual as the felt Santa Cones are really loveable. It was such a glorious warm sunny Sunday!

Photo: Alison Irwin
Photo: Alison Irwin
Felt Making

There was a lot of interest in how the felt santa cones are made.     They start out as pieces of dyed  wool fibres, which are kneaded and matted together, by hand, using warm water and soap. As the wool shrinks and tightens the pieces are formed into specific shapes to give an end result.  To form the santa, pieces of cone shaped wood are used as a structure to support the felt as it dries which in turn absorbs the shape of the cone.

The natural lanolin in the wool, the warm soapy water and the hand movements are extremely beneficial to hands that have suffered as a result of leprosy infection.  The finished products provide income generation opportunities for the artisans,  who are supported by NLT Kathmandu.

Felt Santa



Nepal Day Craft Fair in Farmleigh, Phoenix Park. Sunday 21st September 2014 from 12pm – 5pm.

Join us for a family fun day in the beautiful setting of Farmleigh estate. Nepalese crafts, cultural performances, food, photographic exhibition plus much, much more. Come and say hello to us at the NLT stall.  We will be selling Nepalese jewellery, batik cards, felt beaded hearts, and stars in a fantastic range of colours.

NLT Kathmandu
NLT Kathmandu

This photo was taken in April as Durga, Sunita and Sarmila hand sew on beads and put the finishing touches to the felt hearts, angels and star shapes for our order for Ireland. This is one section of the  NLT craft workroom in Kathmandu, it is outdoors under a light canvas roof.  I watched as the artisans sat cross legged sewing, they can remain working in this position for hours.

Santa_Cone _crop_011

These happy felt faces are looking for a home for Christ… it is a little early in the year, and with summer still here, to finish typing  the above  word!

Demolishing stigma

Stigma – A mark of disgrace associated with a particular circumstance, quality, or person.

Oxford dictionary

“It all began with a small patch on my skin that didn’t feel anything, but now I feel tingling in my toes and feet.”

Leprosy is caused by bacteria, mycobacterium leprae, affecting the nerves in the skin, face, hands and feet.

“As time went by my hands and feet would get injured. I feel no hurt.”

Leprosy can permanently damage the nerves so that they feel no pain, hot or cold, just like an anaesthetic.

“Cuts get infected, and ulcers develop. I feel no discomfort.”

The patient feels no pain, injuries are not rested and may get infected badly.

“My family don’t like the disease, they hide me, and make me live alone. I feel loss.”

Stigma can begin between husband and wife, parents and children.

“My children are discouraged from going to school. I feel shame.”

The wider community can affect the families of leprosy sufferers.

“We cannot go to the well with everyone else, our neighbours shout at us. I feel anger.”

Fear and misunderstanding in the community can lead to separation.

Lalbusty Tulashi – at the top of the hill – this is the only water point and  pump in the village.
Lalbusty Tulashi – at the top of the hill – this is the only water point and pump in the village.

“I’ve lost my job, as my boss does not want me around. I feel hunger.”

Economic loss can cause the family great hardship.

“I went to the hospital at Lal Gadh Leprosy Services Centre (LLSC), the doctor tells me I have leprosy. I feel despair.”

The actual diagnosis can be the most painful part, for patient, family and community.

Ashok Shrestha, OPD Lalgadh Leprosy Services Centre
Ashok Shrestha, OPD Lalgadh Leprosy Services Centre.

Mr Mohad Aniul_shame_107








“The nurses take care of my wounds and ulcers and give me medicine. I feel compassion.”

The secondary effect of having damaged nerves is infections, this is what most people see as leprosy, the leprosy bacteria is treated by antibiotics.

“I sleep in a hospital bed and have a full meal. I feel safe.”

Often patients may be malnourished and need to be admitted as in-patients.

“The hospital staff hold my dry hands in theirs and make me laugh. I don’t feel untouchable.”

Stigma begins in the heart, and we overcome it by the way we live, by the example we show.

“I am much better now, so I can go home, I meet other leprosy patients in my area. I feel a new community beginning.”

Leprosy patients form self-help groups (SHG), to look out for each other. Men and women, young and old, Muslims, Christians and Hindus of different castes all sit together and share their struggles, offer advice, laugh and cry, touch and comfort each other, building self-esteem and confidence.

“In the SHG we can start to learn again, to read and write, to understand health issues. I feel I am growing.”

Self-help groups receive support from LLSC with adult and health education.

“The SHG begins a monthly savings scheme. I feel hope.”

Self-help groups receive seed capital from LLSC and encourage leprosy patients to budget and save.

“I start a small business and earn money to support my family. I feel pride.”

The savings scheme can lend money to its members to start an enterprise to break the downward cycle of poverty.

Monthly savings scheme helps me to start a small fruit and veg market.
Monthly savings scheme helps me to start a small fruit and veg market.

“My children respect me again, and my spouse welcomes me in the home. I feel love.”

The family often adapts and heals remarkably easily.

“My children can return to school. I feel they have a future.”

Public health education, through street drama or discussion provided by LLSC can help bring down barriers in the community.

“The SHG invites LLSC to start a Village Alive Programme in our village. I feel I am becoming a leader.”

The Village Alive Programme is an intensive three year health, education and development programme, that the self-help group initiates with the support of LLSC and agreement of the local community.

“Our village is doing well, the community looks to me to help and guide them. I feel no disgrace.”

Mr Mohad Aniul.
Mr Mohad Aniul.

Demolishing stigma by Nepal Leprosy Trust.

All the above quotes are drawn from leprosy affected people in Nepal and this story highlights a common journey of recovery for them as enabled by NLT.



Village alive

Drinking clean water, washing your hands, seeking treatment for infections: such things may be second nature in Ireland. But for many villagers in rural Nepal, a lack of education hinders their knowledge and ability to live healthy and ward off preventable diseases.

Thanks to a 3-year grant from Irish Aid and effect:hope The Leprosy Mission Canada, Nepal Leprosy Trust Ireland is now supporting some of the very poorest in Nepal to live more productive lives in a project called Village Alive Programme  or VAP.

NLT has organised groups in two Dalit villages (a group of people traditionally regarded as untouchable) to effect and promote health improvements. After training and support from NLT staff, a volunteer in each village qualifies as a Rural Health Facilitator, who helps the groups to identify major health problems and tackle them through health education: the use of clean water, and improved sanitation.

village water pumpThe project also includes a micro-finance element, which encourages men and women to develop their own small businesses.

Measurements will be taken to gauge the success of the project, and it is hoped that the long term incidence of Leprosy will reduce as a result of improvements in the standard of living.

For more details see: sponsor a village