John is a quiet 11-year-old boy from Kenya. John's story is a journey of compassion and the unwavering support of a dedicated well-wisher. His origin is drawn back in Tanzania, where he faced the disturbing reality of being disowned by his real parents due to his disability on his feet. John was left helpless in the unfamiliar surroundings of central Kenya. For the past seven years his guardian has stood by his side, offering not just a shelter but also a sense of belonging. John’s chapter started to change when a team of AIC Cure International doctors visited his neighborhood for a mobile clinic. He was reviewed and scheduled for surgery and underwent a successful surgery on his left foot and his left foot has healed well. John still has clubfoot of right foot. He is currently in the hospital to undergo right foot treatment, which involves serial casting to adjust the position of his foot to achieve the desired correction. Clubfoot is a condition in which the foot is twisted out of shape. This causes difficulty walking and even wearing shoes. Surgeons from our medical partner's care center, AIC Cure International Hospital are scheduled to now perform clubfoot repair surgery on February 19th. Our medical partner, African Mission Healthcare Foundation, is requesting $1,286 to fund John's clubfoot repair. After treatment, he will be able to walk easily. Once he heals, John aspires to go back to school and study and one day achieve his dream of becoming a doctor in future. John told us: “I am looking forward to seeing my foot corrected, walking properly, playing football with my friends and continuing with my studies like other children, and achieving my dream of becoming a doctor in future to also impact lives of children born like me."

Anne, a seven-month-old baby from Kati, is adored by her parents and three siblings. Anne was diagnosed with hydrocephalus, a condition in which excess cerebrospinal fluid accumulates in the brain and increases intracranial pressure. She previously underwent surgery to correct the condition, but the surgery was unsuccessful. She requires a shunt to drain excess fluid from the brain and reduce intercranial pressure. Without treatment, Anne will experience severe physical and developmental delays. Our medical partner, Project Medishare, is helping Anne receive treatment at Hospital Bernard Mevs, the only site in the country where this care is currently available. On April 10th, surgeons will perform a ventriculoperitoneal shunt (VPS) surgery, giving an opportunity for Anne to grow into a strong and healthy young girl. Now, Anne's family needs help to fund this $957 procedure. Anne's mother says: "I hope this surgery will allow my daughter to grow up healthy"

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.