We treated Negatu during our 2019 Complex Mission - read lead nurse, Raj Mashiana's reflections on his journey. Read more
During our 2019 Complex Surgical Mission, Project Harar operated on 37-year-old Ahmed who came to us with a left mandibular ameloblastoma. Read more
Maftu recieved surgery for her ameloblastoma in 2018 and returned in 2019 for further corrective surgery. Read her story. Read more
In 2018, Project Harar was able to provide Mohammed with life-changing surgery. Following a successful operation, four year-old Mohammed came out of his shell and was finally able to speak, attend school and play like a normal child. Read his story. Read more
When Banchigize was born, his mother had never come across such a condition. Horrified by what she saw, fear for her son’s future and talk of his looks in the community kept her awake at night. Read his story. Read more
10-year old Abinet arrived at Project Harar's complex surgical mission in 2016 with a nasal lipoma (a small lump on the end of his nose) which was causing him difficulties with breathing and sleeping. He also faced problems at school - the other kids held their noses and called him names. He was really badly bullied. Read more
In 2015, 11 year-old Fami arrived in Addis Ababa hoping for treatment for her ameloblastoma (a type of facial tumour). Sadly, the surgeons could not find a way to operate that year, and she was sent home. She received treatment in 2016 and then again in 2018 by our international team of specialists. Read more
Three years ago, a small growth appeared on Gemechu’s cheek that continued to enlarge. Eventually, it got so large that if left untreated, it would threaten his life. The growth was a giant ameloblastoma, which caused Gemechu great pain both physically and emotionally. Not only did his face constantly ache, but he also experienced discrimination from those around him. Read more
Hafis received surgery for a giant tumour that had grown in his mouth enabling him to eat, open his mouth and smile again. Read about his transformation. Read more
Seso was treated for Trismus, a condition that caused her mouth to remain tightly closed - she has had this since she was three years old. Read more
When little Merwa was born, her mother Rocla was shocked and frightened. She had never seen a child with a cleft lip before. ‘I was really scared when I gave birth to Merwa and saw her for the first time,’ she said. ‘Nothing can prepare you for that feeling.’ Read more
At the age of 15 many girls are conscious of their appearance, but for Mechot the way she looked affected every aspect of her life. Over three years a giant cell tumour had rapidly grown in the roof of her mouth, making eating, speaking or even smiling extremely difficult. Read more