Rathanak is a two-year-old toddler who lives in Cambodia with his parents and twin brother. His mother works long hours at a garment factory, and his father is a hairdresser who earns a small daily income. When his parents are at work, he and his twin are looked after by their grandmother. Rathanak enjoys eating fried egg and caramelized pork, and he loves playing with toys alongside his brother. Rathanak was born with polydactyly of his right hand, meaning that he has an extra thumb. This makes it difficult for him to grasp objects and interferes with his play. As he grows older, he has also started to feel shy and self-conscious because his hand looks different from those of other children. Fortunately, on February 25th, surgeons will perform a polydactyly repair procedure to remove the extra digit. Our medical partner, Children's Surgical Centre, is requesting $379 to fund this procedure. After surgery, Rathanak is expected to have improved hand function and better coordination. The procedure will help him use his right hand more comfortably and confidently, allowing him to play, learn, and perform daily activities more easily. Rathanak's mother shares, “I hope that after the surgery my son can use his hand normally, and feel confident like other children. I don’t want him to feel shy or different anymore. I just want him to grow up happy and proud of himself.”

Benjamin is a six-year-old boy from Tanzania. He is the third-born in a family of three children, and lives with his parents, whose livelihoods depend on small-scale business activities to sustain their household. Benjamin's family describes him as a bright and curious child, who enjoys learning and playing with other children in the community. Benjamin has been diagnosed with bilateral genu varus or "bow legs," a condition where the knees curve outward while the feet and ankles touch. Several factors could cause this condition, such as growth disorders, vitamin deficiencies, or excessive fluoride found in contaminated drinking water. As a result, the knees can be angled inwards or outwards, making it difficult to walk, and potentially causing long-term joint damage. The condition has affected Benjamin's posture and mobility, making prolonged standing and walking increasingly difficult. Without treatment, the condition could continue to worsen as he grows, potentially limiting his movement and participation in school and daily activities. Our medical partner, African Mission Healthcare, is requesting $810 to fund treatment for Benjamin. The procedure is scheduled to take place on March 24th at our medical partner's care center, Kafika House. Treatment will hopefully restore Benjamin's mobility, allowing him to participate in a variety of activities, and greatly decreasing his risk of future complications. Benjamin's father said: "I wish for his legs to be strong, so that he can walk independently with his friends to school, without us worrying about his well-being."

Fozan is a beautiful four-year-old boy with a bright smile from Ethiopia. He loves playing football, solving puzzles, and singing children’s songs. He also enjoys spending time playing with his older brother. Fozan is the second child in his family. His mother is a housewife, and his father works as a taxi driver. The family lives in a rented house and works hard to provide for their children. The condition came to the family’s attention when Fozan’s aunt took her own baby to a clinic for a procedure. During the visit, the doctor discovered that her baby had an undescended testicle and explained the condition to the family. After learning about this, Fozan’s aunt informed her brother. When Fozan’s father checked his son, he noticed that one side of Fozan’s scrotum appeared empty and immediately took him to a clinic. The doctor explained that surgery was needed at an early age, which made the family feel anxious and worried about the condition, and the doctor referred them to another hospital for further evaluation and treatment. At the referral Hospital, doctors confirmed the need for surgery. Fozan was placed on a waiting list, and the family waited anxiously for three months. Later, when Fozan’s father returned to check on the waiting list, the hospital staff informed him that they had tried to contact the family but could not reach them by phone. They also told him that Fozan had been referred to Bethany Kids for treatment. Soon after, Fozan and his father visited our facility, where Fozan was carefully examined. Fozan was diagnosed with cryptorchidism, a condition in which one or both of the testicles remain undescended. If left untreated, Fozan has an increased risk of developing hernias, testicular cancer, and fertility problems in the future. Fozan will be receiving assistance from our medical partner, African Mission Healthcare (AMH). Fortunately, he is scheduled to undergo corrective surgery on March 13th. AMH is requesting $754 to cover the total cost of his procedure and care. Fozan’s father conveyed his gratitude, stating, "I am truly delighted with the service and hope the surgery will be successful. I am excited, especially when the doctor told me that my child's surgery will be performed laparoscopically."