Liza is a determined 18-year-old high school student from Cambodia. She lives in Kandal Province with her parents and two younger siblings. Her father works as a welder, and her mother stays at home to care for the family. She is the eldest child and is currently studying in Grade 11. Her younger sister is in Grade 9, and her younger brother is in Grade 6. She dreams of becoming a doctor one day and enjoys listening to music and reading books in her free time. Liza was born with severe spasticity affecting both her upper and lower limbs, causing abnormal muscle tightness and an abnormal gait. In November 2025, she received botulinum toxin (Botox) injections into her hamstrings and other spastic muscles in her lower limbs, which noticeably improved her walking for a period of time. However, about four months later, her condition gradually worsened again, and her right leg developed a contracture. This has made walking increasingly difficult and has limited her mobility and independence in daily activities. Although the previous treatment provided temporary improvement, the return of the contracture has once again made movement challenging and affected her confidence in walking. Fortunately, our medical partner, Children's Surgical Centre, is helping Liza receive treatment. On May 22nd, surgeons will perform a contracture release surgery to release the tight muscle and improve the position and movement of her ankle. This treatment will help her walk more easily, improve balance and comfort, and allow her to move with greater confidence. Liza's family can contribute $75, but needs help in raising $497 more to fund her procedure and care. Liza said, “When my walking improved before, it gave me hope for the future. I pray this surgery will help me walk better again so I can continue my studies and move closer to my dream of becoming a doctor.”

Michael is a 10-year-old student from Kenya. When his mother was pregnant with him, she went through a very hard time. She had married into a different tribe, and this brought her a lot of pain. “I was rejected because I was seen as a foreigner,” she said quietly. “This made my pregnancy very difficult. Then my only son was born with clubfoot, and life felt too heavy to bear.” Clubfoot is a condition where one or both feet turn inward, affecting the bones and muscles. Michael lived with this condition on both of his feet for almost ten years without treatment. As he grew older, walking became painful and tiring. “My feet are very sensitive,” Michael said. “I cannot walk without my slip-on shoes. I want to walk fast or even run, but I cannot.” Many times, he leaned on walls for support while watching other children walk and play freely. His mother's pain grew deeper when her in-laws rejected her and her husband, saying their child was cursed. Michael’s father supported them at that time. But after everything they went through, they stopped looking for treatment, and Michael grew up with the condition. Even so, they still hoped that one day things would change. In 2025, that hope came back when they moved to a new village. A neighbor told Michael's mom about CURE Children’s Hospital of Kenya. Fortunately, Michael traveled to visit our medical partner's care center, AIC Cure International Hospital. At the clinic, the doctors examined Michael and quickly scheduled him for surgery. There, surgeons will perform clubfoot repair surgery on March 25th. While Michael is scheduled for surgery, his family cannot afford it. Our medical partner, African Mission Healthcare, is requesting $1,286 to fund Michael's clubfoot repair. After treatment, he will be able to walk easily and attend school without disruptions. "I am looking forward to getting better so that I can continue with my studies and engage with my friends in playing football," Michael told us.

Mdoe is a 14-year-old boy from Kenya. Shortly after his birth, Mdoe showed signs that his intestines were not working properly. He was brought to several hospitals, but was not given a clear diagnosis. Mdoe's condition worsened. He was visibly in pain, restless, and crying constantly. Mdoe's mother was determined to find help. She took him to a larger facility, where doctors explained that his intestines were intertwined and that he would need surgery. He would require a colostomy bag to help him pass stool. After a few days of monitoring, they were discharged. But only days later, complications arose, and Kinago underwent surgery at the same hospital. Life after surgery was far from easy. His mother took him for clinic checkups several times, striving to remain consistent with his care. But back at home, reality pressed in. Both parents engage in small-scale farming, stretching each harvest to provide for their eight children. Eventually, the cost of continued clinic visits became impossible to sustain. Now fourteen, Mdoe has never been able to attend school. It breaks his heart to watch children his age walk to class while he remains at home. His condition requires him to change his colostomy bag regularly, yet he has been using the same one since early childhood. Some schools refused to admit him. Over time, discouraged and burdened by school fees, his mother stopped trying. Fortunately, our medical partner, African Mission Healthcare, can help. On February 12th, Mdoe will undergo abdominal surgery that will improve Mdoe's quality of life. His family needs help raising $1,081 to fund his procedure and care. Mdoe's mother shared, “It is painful when your child asks you why he cannot go to school like other children. I see the longing in his eyes, and I wish I could take this condition away from him. I may not have wealth, but I have never stopped fighting for him, even when the journey felt too heavy for my shoulders.”