Look behind the lens of leprosy with photographer, Tom Bradley

We asked photographer, Tom Bradley, to share his experiences from Bangladesh and how your support really can transform the lives of these forgotten communities.

“As I watch Shopna examine patches on the faces of brothers Chaina and Joy, aged six and nine, she takes down their details, marking them both as suspect leprosy cases, Masuma spots another boy in the crowd with facial patches, noticing that he looks just like Joy. She soon discovers that the boy was his twin brother, Bijoy. He too has the telltale patches on his skin – three children from one family potentially affected by leprosy.

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6-year-old twins, Joy and Bijoy, may have leprosy. Photo: Tom Bradley

Shopna is a Field Organiser for The Leprosy Mission’s partner Mukti, and she’s assigned specifically to diagnosing new cases of leprosy, along with her co-worker Ripon. My name’s Tom Bradley; I’ve been photographing people affected by leprosy for almost a decade now, and I’ve been following both Shopna and Ripon for the day, as they have been called out to examine two suspect cases of leprosy in a village in western Bangladesh. Accompanying me are Leprosy Mission staff Masuma and Jiptha, both of whom are also trained to recognise leprosy cases.

But Bijoy isn’t the only extra case that day. As Shopna begins to examine him, another boy, 10-year-old Durantha, is pushed to the front of the onlooking crowd of children. He also has patches on his face. And he is not the last unexpected case that day either.

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10-year-old Durantha has patches on his face. Photo: Tom Bradley

We walk through the village on this very hot and humid morning, followed by a number of children and a few adults. Most of the men are out working in the fields, and a few of the women steal away from their work preparing food, looking after the house and children and tending to any livestock left at home.

As we leave the village, we walk along narrow paths, slightly raised up with earth to divide the square rice paddies.

It seems it’s difficult to even leave the village without spotting yet another child with patches of leprosy.

Meanwhile Shopna and Masuma, walking a little behind us, are called off to someone’s house, having just been informed of another child who has patches on their face. Two more suspect cases are discovered. Having caught up with us, Shopna takes over from Jiptha to take down the boys’ details.

As we move onto the next village, just across the road, Shopna comes across a young man with patches on his arm. The patches show signs of clear anaesthesia, and then Shopna realises his mother is affected by leprosy, although she was cured some time ago. The young man, Dukhiram, is confirmed as a new case and Shopna notes down his contact details so he can be supplied with the vital MDT tablets as soon as possible.

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Shopna checking the patch on Dukhiram’s arm. Photo: Tom Bradley

The next village is much the same as the first, and though we’re going primarily for my benefit, to interview an old patient I have met before, Shopna is busy wading through the crowd picking out people with patches on their face.

The work seems neverending – so many suspected new cases found.

Shopna hasn’t yet been doing this work for a month, but already enjoys it greatly.

“When I visited the field last month, I felt very encouraged. If I visit more areas I can identify more people affected.” Shopna tells me. “I feel it’s such a great opportunity to work with them and help them get treatment in time. I feel really proud doing this work.”

I can see Shopna enjoys her new job and is so good at interacting with the people she meets, smiling and reassuring them, but also listening with genuine concern if they talk about their problems.

“Now so many women come to meet with me and talk about different issues,” she says.

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Shopna works tirelessly to ensure people with leprosy are diagnosed and treated. Photo: Tom Bradley

Shopna’s job, which takes her out into the community most days in the week is absolutely vital in effort to combat leprosy in the area, where people living in remote villages may not get the treatment they need otherwise, their leprosy left undiagnosed.

On this day alone she registers ten new suspect cases and one new confirmed case. The suspect cases will all be followed-up regularly, so that if their patch does indeed turn out to be leprosy they can be put on treatment and cured, hopefully, without complication. The longer leprosy is left untreated, the more potential it has to cause severe disability and have an even greater impact on someone’s life.

People like Shopna work tirelessly to prevent this from happening, a real lifeline to the people they meet.”

You can see more of Tom’s work on his website or on Twitter/Instagram @tombradleyphoto

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Why I love working for The Leprosy Mission

As she comes to the end of her 2 years on the Graduate Development Scheme, one of our two Graduate Trainees, Laura Stopczynski, shares her thoughts about working for The Leprosy Mission England and Wales.

Leprosy is a cruel disease which still destroys thousands of lives every single day. Witnessing what leprosy can do and listening to heart-breaking yet powerful stories from around the world, I have been humbled and reminded of God’s extravagant grace and love he has for his world, and for his people.

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Laura met Mahendra during her visit to Anandaban Hospital, Nepal in 2017.

Being part of the team here, allows me to play my small part in making a difference and seeing lives truly being changed by the work of The Leprosy Mission. My role gives me the opportunity to use the skills that God has given me to bless others and day to day work towards something greater.

Through working at The Leprosy Mission, I get to hear stories and see with my own eyes miracles of light happening all around the world.  It’s a privilege to be part of a global family who despite living at opposite ends of the world, all have a common goal to see people affected by leprosy set free. It’s honestly such a great place to work.

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Laura with colleagues from across The Leprosy Mission Global Fellowship as part of the Asia Learning Workshop, 2017.

 

You can apply for The Leprosy Mission’s graduate scheme here.  (Deadline August 1st).

You’ve cured six year old Akira!

NTD and Research Coordinator Shabina Sadiq reflects on her recent visit to Sri Lanka.

I met Akira and her mum over a year ago when I went to visit The Leprosy Mission’s projects in Sri Lanka.

Like any child she was shy to begin with but very playful, mischievous and with a curious nature, wanting to know why so many people wanted to talk to her mum and not her. Her mum has leprosy and her dad left them when he learnt about his wife’s diagnosis. Akira was only a baby when he left and she has never seen him since.

Whilst we are talking to her mum, she mentions to the Project Officer and Doctor standing next to her my daughter has a skin patch on her upper arm”.

They immediately turn to Akira and ask to look at the patch.

It is small, the size of a finger print, but significant enough for the Project Officer to say “bring her in to the centre and we will take her for tests”.

Immediately, I find myself looking straight at Akira thinking ‘she looks fine’. Akira, oblivious to what is happening around her, looks at me smiling and pointing, as if to say let’s go and play outside.

I turn back to her mum and suddenly realise that I do not need to worry. Akira’s mum is a Leprosy Champion. I am standing beside an amazingly strong woman  who, like any mother, will fight for her child’s good health.

Over a year later I find myself back in Sri Lanka. Akira’s mum recognises me immediately and comes to shake my hand saying “it’s like meeting an old friend again”. She then points behind me.

I turn and see Akira in the distance, giggling with laughter and waving.

She has completed her MDT and looks like most happy children. She still has the mischievous look in her eye, one that at times I can relate to.

She looks healthy, loved and full of hope.

May 9 Blog
Six-year-old Akira’s future is full of hope after being cured of leprosy.

I have seen what can happen when people with leprosy receive the treatment they need quickly – this transformation is thanks to our amazing donors. It’s difficult to think about how different Akira’s life may have been if she hadn’t received the support and care she needed immediately.

Thanks to your support, our teams in Sri Lanka are able to change lives.

Thanks to you, teams in Sri Lanka are able to reach out and support people like Akira’s mum, giving them the confidence, skills and strength to overcome the stigma and discrimination associated with leprosy. Leprosy Champions, such as Akira’s mum, are able support others in their communities.

You have made it possible to train local project staff so they can recognise the signs of leprosy immediately – stopping leprosy in its tracks and preventing disability.

Thanks to you, leprosy doesn’t have the opportunity to steal hope and joy from little children like Akira.