The hope is that circulation of the above photo via social media will help reduce the stigma against albinism and also the irrational fear some people have of catching it.
The photo is very reminiscent of those with Princess Diana holding hands with AIDS and leprosy sufferers in the 1980s and which had a positive effect on public perceptions within the UK.
We are extremely grateful to our good friend Mr Venance Gomegwa for designing and supervising the construction of better housing for the family. It has taken a great deal of his time and energy but the outcome is excellent and the family are delighted.
For two years FUM helped with further training for Dr Mary Mkamwa, a skin specialist. She is now fully qualified and one of her responsibilities is for the 52 people in Nzega District who suffer from albinism. This includes the family in Mambali.
Sadly the mother died recently of skin cancer, a common problem due to the lack of protective melanin in their skin.
To help Dr Mary in her work FUM made a one-off donation to provide a year's supply of factor 60 suncream for each of the 52 sufferers. They will also receive regular check-ups with Dr Mary.
In autumn 2018 Sebastian, our excellent volunteer liaison officer in Nzega District, told us of a particularly distressing family situation that he had come across in his work as a Social Welfare Officer. He asked if there was any way that FUM might provide some help for the family.
FUM's constitution does not allow us to support individuals or families; only institutions such as clinics, colleges and schools can be supported. So FUM Secretary, Rod Smith, suggested a crowd-funding initiative and we were delighted that in just over two weeks it raised £1500. We are very grateful to all who contributed.
They live near the remote village of Mambali, almost 100 km south west from Nzega along rough dirt tracks. The family of seven all suffer from albinism, a genetic condition where their skin lacks the melanin pigment that gives protection from the sun. Eye damage and skin cancer are often side effects.
More enlightened people in Tanzania accept those with albinism but in areas where traditional beliefs are stronger sufferers can be isolated, or even in danger, despite the government's efforts to promote acceptance.
With no land to cultivate the family has been reliant on begging. The aim is to help them become self-sufficient for the future but this cannot happen in isolation. Following the expression of support from FUM members the District Commissioner (DC) visited the family and addressed the local community. As a result support for the family is now coming from several directions.
In recognition of the village's support for the family FUM will provide funds for much needed extra toilets at the Primary School.