Sobel is an unemployed 21-year-old who lives in Phnom Penh province with six other members of his family - his father and five siblings who all live together at home. His father is retired. Before his injury, Sobel had an engineering job and enjoyed playing volleyball with friends. In July 2023, on his way home from work, Sobel's motorcycle skidded on the rain-soaked surface, sending him crashing onto the pavement. He lost consciousness for several hours. His sister took him to a local hospital with a skull fracture, broken collarbone, and broken upper arm. He has been diagnosed with a brachial plexus injury on his left side. The brachial plexus is a nerve network that transmits signals from the spine to the shoulder, arm, and hand. Injuries to this nerve network can result in loss of function and sensation. Sobel is unable to lift his shoulder or hand, consequently stripping away his ability to work. The thought of navigating life with only one arm is hard for him to imagine. Sobel traveled to Kien Khleang National Rehabilitation Centre to receive treatment. This is the only center in the whole country where this treatment is available. On January 2nd, he will undergo a brachial plexus repair surgery. After recovery, he hopes to restore function in his arm and hand and find a job to help his family. Our medical partner, Children's Surgical Centre, is requesting $709 to fund this procedure. Sobel said: "I want to work like before and hope the surgeons can help me."

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.

Ly is a one-year-old girl from Cambodia. Ly's father is a farmer and her mother stays home to care for Ly and her two older siblings. Ly enjoys eating noodle soup, and likes to play with toys. Ly was born with polydactyly of both feet. This means that she has an extra toe on each foot. If the extra toes are not removed, it will become difficult for her to use her feet as she grows older and she could feel uncomfortable around others. Fortunately, on April 22nd, surgeons will perform a polydactyly repair procedure to remove the extra toe. Ly's family is able to contribute $100 but our medical partner, Children's Surgical Centre, needs an additional $199 to fund this procedure. After surgery, she will be able to walk easier and her parents will not worry about other children making fun of her feet. Ly’s mother shared, "I hope she will be able to have normal feet just like other kids when she grows up."