Matiyas is a two-year-old boy from Ethiopia. His mother is a homemaker who looks after Matiyas and his younger sister, while his father is a taxi driver. Since birth, he has been fighting a severe, ongoing battle with chronic tonsillitis, a condition that deeply impacts his daily life and overall well-being. His struggle is at its worst during the night. Because his tonsils are constantly swollen, he faces significant airway blockage that makes it nearly impossible for him to breathe through his nose while he sleeps. Instead of resting peacefully, he spends his nights gasping for air and struggling to catch his breath, leaving both him and his parents exhausted and worried. Our medical partner, Saglan Wajee General Hospital, is requesting $700 to fund a tonsillectomy for Matiyas, which is scheduled to take place on May 23rd. Surgeons will remove his tonsils, hopefully relieving Matiyas of his symptoms and helping him live more comfortably. Matiyas's parents shared, "Our deepest hope is for our little boy to finally breathe easily, sleep peacefully through the night, and wake up refreshed instead of gasping for air."

Hok is a 67-year-old man from Cambodia. He is married and lives with his wife and youngest child, who works at a bank. He has four children, all of whom are married and visit him with their families. He enjoys caring for his grandchildren and spending time with them. In 2014, Hok was involved in a motor vehicle accident that caused a fracture of his left femur. Despite several surgeries over the years, the fracture has remained unhealed. The unhealed fracture and protruding, painful nail in his left femur make walking difficult. He currently relies on crutches to move around. Fortunately, surgeons at our medical partner, Children's Surgical Centre, can help. On September 3rd, Hok will undergo a fracture repair procedure, which will remove the old nail, repair the fracture with plates and screws, and use a bone graft from his iliac crest to support healing of the femur and reduce the pain and discomfort caused by the damaged hardware. His family can contribute $100, but needs help raising $500 more to fund his procedure and care. Hok said, “I hope this surgery will help my leg heal properly and reduce the pain caused by the protruding nail. I look forward to walking more comfortably and returning to my normal daily activities.”

Reaksa is 14 years old and a 10th grader from Cambodia. She is the only child in her family and lives with her parents. Her father works as a chef in a restaurant, while her mother works as a cleaner. She enjoys studying Khmer literature, which is her favorite subject at school, and hopes to become a teacher in the future. In her free time, she likes drawing and listening to music. Her favorite foods are sour fish soup and fried vegetables. Around the age of 10, Reaksa's mother first noticed that her daughter’s back was becoming curved. Over the years, the curvature gradually worsened. She now has severe scoliosis, with her spine bending significantly toward the right side and associated kyphosis. Her condition has begun to affect her daily life. She has difficulty walking and sitting for long periods, and the discomfort she experiences while sitting makes it difficult for her to concentrate in class. Despite these challenges, she continues to attend school and work toward her dream of becoming a teacher. Until now, her family has not been able to afford the treatment she needs. Her family learned about our medical partner, Children’s Surgical Centre (CSC), through social media and sought treatment. On August 18th, she will undergo posterior spinal fusion (PSF) from T3 to L3, a surgical procedure that uses instrumentation to correct and stabilize the curved portion of her spine. She needs help of $1,500 to help cover the costs of her surgery, the implant, and post-operative care, including physiotherapy. The surgery aims to improve the alignment of her spine and prevent the severe curvature from progressing further. Reaksa's mother said, “I hope this surgery will help manage my daughter’s severe spinal deformity, improve her comfort and posture, and allow her to stay active and continue her studies and daily activities. I want her to feel more confident and comfortable as she grows.”