Pisey is a 12-year-old, seventh-grade student from Cambodia. Pisey's father works long hours as a truck driver and her mother stays home to care for Pisey and her two younger siblings. Pisey's favorite subject is math and she wants to be a teacher when she grows up. In her free time, she enjoys reading books. Pisey has been experiencing frequent and recurrent sore throats, accompanied by a fever and difficulty swallowing. The frequent sicknesses often lead to missed school days. Pisey was recently diagnosed with enlarged tonsils and adenoids, which, if not treated, will cause her symptoms to persist and possibly intensify over time. Our medical partner, Children's Surgical Centre, is requesting $265 to fund a tonsillectomy and adenoidectomy for Pisey, which is scheduled to take place on March 21st. Surgeons will remove her tonsils and adenoids, hopefully relieving Pisey of her symptoms and helping her live much more comfortably. Pisey's mother said, "After surgery, we hope Pisey can swallow better to eat her food and she can return to school."

Kelly is a 23-year-old Business Administration student from Kenya. Her family members assist in offering her with living support, especially since her father passed away in 2022, and her mother suffers from a condition that requires constant care. In January 2024, Kelly's left knee was struck by a door, leading to swelling and pain in the area. Subsequently, the swelling burst, resulting in pus formation. She sought medical attention at a nearby hospital, but unfortunately, her condition did not improve. Kelly was taken our medical partner's care center, AIC Kijabe Hospital, where she was diagnosed with a small, proximal tibia sequester. Surgery was recommended, without which there was a risk she could lose her leg. Fortunately, our medical partner, African Mission Healthcare, is helping Kelly receive treatment. On April 8th, surgeons at AIC Kijabe Hospital will perform a sequestrectomy debridement external fixation to prevent the infection from spreading, and save her leg. Now, Kelly's family needs help to fund this $1,500 procedure. Kelly says: “I stopped going to college because of the infection. I cannot walk or use my leg because of the infection. I am requesting for treatment support to help preserve my leg.”

The birth of twins Jane and her sister brought joy to their parents. She is the 4th born in a family of five. She is a bright grade 1 student who likes reading, drawing and colouring. Her family hails from a small village, and both her parents are farmers. Soon after birth, her parents discovered the challenge of Jane being born with multiple birth conditions: Bilateral clubfeet, hydrocephalus, and spina bifida. They shared that they were quite shocked as they had not heard or experienced any of them before. Treatment for hydrocephalus and spina bifida required a collaborative effort between orthopaedic specialists and neurosurgeons. At ten days, she underwent a spina bifida surgery at a local hospital to address the neural tube defect affecting her spine and then hydrocephalus. Jane is a resilient girl and has overcome so much, carrying a big smile on her face. She now needs treatment for her clubfoot condition as her feet are bent inward, hindering her mobility. She is scheduled to undergo surgery, which will be impactful to her because she will be able to walk confidently like other children and continue with her education. “My desire is to see my daughter walking well and any kind of help is greatly appreciated,” Jane’s mother told us.