Shinka is a 6-year-old boy from Kenya. He is the last born in a family of seven children. His father, who was the sole breadwinner of the family passed away in 2017 after a short illness. To provide for the family, the eldest son, who finished his high school studies last year, sells milk to earn some money. Sometimes the earnings are not much, and they have to rely on family members for financial support. The family does not have medical coverage and is not able to raise the money needed to pay for Shinka's surgery. In May of last year, Shinka started experiencing some difficulty when passing urine. At some point, he had stopped going to school for a few weeks. His mother shared Shinka's condition with his uncle who took him to a local health center for review. Shinka was examined and referred to our facility. When he came with his uncle for examination, doctors were able to diagnose his condition and also found a condition called cryptorchidism that first requires a bilateral orchidopexy surgery. If left untreated, Shinka has an increased risk of developing hernias, testicular cancer, and fertility problems in the future. Shinka will be receiving assistance from our medical partner, African Mission Healthcare (AMH). Fortunately, he is scheduled to undergo corrective surgery on January 11th. AMHF is requesting $646 to cover the total cost of his procedure and care. Shinka’s uncle says, “We are very much worried as a family about Shinka’s condition. His studies are affected, and we want him to go back to school as soon as possible.”

Phikhirona is a shy 8-year-old student in grade one. Her family consists of her father, formerly employed near Children's Surgical Centre crafting prosthetic limbs, and her two elder sisters. One, aged 13, is currently in grade 5, while the other, aged 11, is navigating grade 4. Unfortunately, her mother succumbed to breast cancer several years ago, so her older sisters watch after her. In her first year of attending school, she has interest in Khmer subjects. Back at home, her cooking skills are being developed by her older sisters, who are teaching her how to prepare her favorite dish - fried pork with vegetables. Phikhirona was born with polydactyly of both hands and feet. This means that she has an extra digit on the side of both hands and polysyndactyly of her feet. On each foot, she has an extra toe that is connected, via fusing or webbing, to an adjacent toe. She faces difficulty wearing conventional shoes due to the presence of extra toes and fingers, and unfortunately, she endures teasing from other children as a result. Fortunately, on January 29th, surgeons will perform a polydactyly repair procedure to remove the extra digits of her hands. Our medical partner, Children's Surgical Centre, is requesting $299 to fund this procedure. After surgery, she will feel more comfortable about her appearance, and she won't be ashamed of how her feet look. Her father shared: "I hope that the surgery will not cause any infection and the extra fingers will not grow back."

Jonathan and his mother are refugees from Southern Sudan. He is the 1st born in a family of three children. He is a special needs child after being diagnosed with autism when he was young. His mother says he developed jaundice as a neonate, which was not well controlled, which she believes led to brain damage. Hence, she cannot work because Jonathan requires constant support. It takes the help of relatives and friends to help her make ends meet. Since 2021, Jonathan has been experiencing frequent adenoid infections, accompanied by difficulty sleeping, breathing, as well as pain, making him cry a lot. He has been treated many times with not much change. They were introduced to our partner's care centre, Nazareth Hospital, by one of the doctors from South Sudan. After consultation, the surgeon advised to have an adenoidectomy, but the family is not able to raise the fee required. If not treated, Jonathan will have more problems. Our medical partner African Mission Healthcare is requesting help raising the $565 to fund the surgery planned January 28th. Jonathon's mother shared: “It is not easy to bring up or care for a child with autism, but at least I try my best. It is worse when he has a painful or disturbing condition like this. I kindly seek help so that he may be treated and at least I can have one less problem to deal with. I would appreciate it.”