Vichheka is a 26-year-old from Cambodia. Along with caring for her daughter, Vichheka and her husband sell grocery products from their home. When Vichheka was a toddler, she fell off the front stoop of her home, possibly creating a left hip deformity. Her parents brought her to Children's Surgical Centre (CSC) for examination; it was decided that surgery was not needed at the time. Since then, she has suffered from frequent spasms down her left leg, made worse by prolonged periods of standing while working. A relative suggested she return to CSC to determine if there was a solution to her ongoing pain. Now doctors would like Vichheka to undergo contracture release surgery on her rectus femoris, a muscle in the upper leg to finally heal her condition. After recovery, Vichheka should be in less pain. Now, she needs $572 to fund her procedure. Vichheka shared "I hope I can walk easier with no more pain after this surgery, so I can help my husband and raise my child."

Su is a 12-year-old boy from Burma who lives in an Internally Displaced Persons (IDP) camp with his family. Su had to discontinue his studies while in fourth-grade, and his family was forced to leave their home because of the conflict in Burma. Su’s grandparents are his primary caregivers as his parents divorced, got remarried and moved away. His half-brother, uncle, aunt, and infant cousin also live with the family. Su’s grandmother and aunt take care of their home, while his grandfather, uncle and half-brother work as day laborers. Su initially noticed signs of his condition in January, when he felt pain on the left side of his mouth, and had a slight swelling on the left side of his face. One month later, he was taken to the clinic by his aunt, where it was discovered that he had three cavities on the left side of his mouth. The doctors removed the decayed tooth on the top jaw but left the lower two as the swelling was significant. Su stayed in hospital for one week to recover, while receiving antibiotics. He was released from the clinic once the pain and swelling had decreased, but shortly after, the symptoms resurfaced, more intense than before. Presently, the left side of Su’s face is significantly swollen, and he feels acute pain. He has difficulty eating and can only chew from the right side of his mouth. He cannot lay down on the left side due to the swelling and pain, which gets worse at night. Su also feels pain in his neck when he drinks or swallows food. Su needs to undergo a CT scan, a procedure in which X-ray images taken from several angles are combined to produce cross-sectional images of the body. This will help doctors diagnose his condition and formulate an appropriate treatment plan. Su's family is however unable to raise the required funds needed for the imaging procedure. Our medical partner, Burma Children Medical Fund, is requesting $414 to cover the cost of Su's CT scan and care, scheduled for March 25th. Su is keen to return to school when his condition is treated. He loves to paint and draw in his free time and would like to be an artist someday. Su's grandfather is worried about his condition, but hopeful about his future. He says, “Whatever he wants to do in his future, I will support him fully, as his parents are gone.”

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.