Referring to the stigma he faces in Somalia because he has albinism, 25 year-old Elmi Bile Mohamed says: “People tell me I am a cannibal and that I will eat their children. They are terrified of me.”
Mr Mohamed has struggled to find a place to live in the capital, Mogadishu, since leaving his rural home in the central region of Hiraan. His brothers also suffer from the condition.
“We were continuously insulted and tortured by our community. We were beaten up and mocked for the pale colour of our skin, hair and eyes,” he says.
“I thought I would find a better life in Mogadishu but I was wrong.”
Mr Mohamed searched and searched for a room in a shared house but was rejected at every turn.
He ended up paying $30 (£23) a month to live in a storage shed in Hamar Weyne district, the oldest part of the city.
“People think I am cursed,” he says. “They often throw a mixture of salt water and raw eggs onto my doorstep because they believe this will protect them from me.”
Mr Mohamed eventually found a job as a cleaner in a restaurant earning between $1.40 and $4 (£3) a day.
It didn’t last long.
He was fired after customers stopped going to eat there, saying they feared he would infect them with albinism even though it is not a contagious disease, rather a genetic condition.
“I went from restaurant to restaurant looking for another job but nobody would employ me,” he says. “I ended up begging on the streets, holding up a placard with my phone number on it so people could make donations via mobile payments.”
The money he earns from begging is rarely enough to cover his meals and rent, let alone the sunblock and glasses he needs to protect his sensitive skin and eyes. People with albinism have little or no melanin, the pigment that colours eyes, hair and skin and offers protection from the sun.
“I cannot afford to buy sunglasses,” Mr Mohamed says. “There is so much dust and highly polluting traffic in the market where I beg. My eyes are constantly in agony and my sight is deteriorating rapidly.”
“Sometimes people give me their leftovers to eat. Other times I have nothing.”
Mr Mohamed’s dreams of running away to Mogadishu to earn money to send back to his family, especially his albino brothers, have been shattered.
It is not clear how many people with albinism live in Somalia as there is no data available. The country has been affected by conflict and instability for more than three decades so it is impossible to gather reliable information.
Earlier this year, about 80 families living with albinism in Mogadishu came together to form an association, Somali Albinos, which they hope will raise awareness about their plight and help reduce stigma.
So far, they have been sent 86 bottles of sun cream from Somali women living in the diaspora.
It is recommended that people with albinism wear high-factor sunscreen, protective clothing and sunglasses to reduce exposure to sunlight.
Their lack of melanin means they are at increased risk of getting sunburn and skin cancer. It also leads to eye problems as melanin is involved in the development of the retina, the thin layer of cells at the back of the eye.
“Other Somalis with disabilities have formed organisations which lobby for help from the government and international organisations,” says the group’s chairman, 40 year-old Mohamed Abukar Abdiqadir. “They now have rights. We don’t.”
“I was elected as the leader of our association because I am a hero and I never give up,” says Mr Abdiqadir, who has six children. Like him, they all live with albinism.
He scrapes together a living by selling dried and tinned food from a trolley in Hamar Weyne market. He always wears a hat to protect himself from the harsh sun.
“The reason people hate and fear us is ignorance,” he says.
“The evil and discrimination we face must not stop us from fighting for our rights and feeding our families. If Somalis learn about albinism, they will realise we are people just like them.”