Hassan is an only child whose parents separated before he was born. Prior to his birth, Hassan's mother worked alongside his grandmother, doing farm work to earn income. After Hassan was born, his mother had to stop working so she could take care of him. Hassan was diagnosed with spina bifida at birth, a condition that occurs when a developing baby's spinal cord fails to develop or close properly while in the womb. Hassan had a swelling on his back that was open and leaking. He was admitted in hospital for a few days while his mother was taught how to dress the wound. An MRI and a CT scan were done and he was scheduled for surgery weeks later. While home, his mother continued with the wound dressings as instructed until the leaking stopped. During one of the post-natal clinics, Hassan and his mother were referred to our medical partner's care center, BethanyKids, for treatment. Upon arrival at BethanyKids, Hassan was examined and was additionally diagnosed with hydrocephalus, a build up of fluids in the brain. He was then scheduled for a spina bifida repair surgery, and the mother was told that once he recovered, he would be scheduled for a shunt insertion surgery. Due to financial challenges and a loss of income for Hassan's mother, the family is unable to meet the medical expenses. Without treatment, Hassan is at risk of lower-limb paralysis, infection of the exposed nervous tissue, development of tethered cord syndrome, and possible developmental delays. Fortunately, our medical partner, African Mission Healthcare, is helping Hassan receive treatment. On March 15th, surgeons at BethanyKids will conduct a spina bifida closure surgery to promote Hassan's healthy growth and development. Now, Hassan's family needs help to fund this $1,151 procedure. Hassan’s mother says, “A while back, I had already given up on Hassan's treatment. Because the community had never seen such a condition, I was told that I would always get children who have different medical conditions. After coming to this facility, I realized that this was not the case. My hopes were raised again and now I’m looking forward to the best outcome in Hassan’s treatment.”

Dane is a studious fourth-grader. She and her family live in Banteay Meanchey province, where her parents sell spices at the local market. She has a 7-year-old sister in second grade. At school, she likes Khmer history, mathematics and likes reading books. She hopes to continue her education and be a teacher some day. Three years ago, Dane and her younger sister's hands and legs were burned from a gas explosion. Despite receiving burn care at a local pediatric hospital, numerous burn scars persist on her hands and her legs, especially on Dane's right fingers. This condition significantly hampers her overall hand function. She is unable to grasp objects and has one affected finger that is nonfunctional. The visible effects of her hand condition contribute to her feelings of embarrassment. She has difficulty writing and is shy in school. When Dane's family learned about our medical partner, Children's Surgical Centre, she traveled for six and a half hours seeking treatment. On January 30th, surgeons at CSC will perform a burn contracture release surgery to help her use her fingers and hand more efficiently. Now, her family needs help to fund this $495 procedure. Dane said: "I hope I can use my fingers after this operation, and can hold things better in school."

Phikhirona is a shy 8-year-old student in grade one. Her family consists of her father, formerly employed near Children's Surgical Centre crafting prosthetic limbs, and her two elder sisters. One, aged 13, is currently in grade 5, while the other, aged 11, is navigating grade 4. Unfortunately, her mother succumbed to breast cancer several years ago, so her older sisters watch after her. In her first year of attending school, she has interest in Khmer subjects. Back at home, her cooking skills are being developed by her older sisters, who are teaching her how to prepare her favorite dish - fried pork with vegetables. Phikhirona was born with polydactyly of both hands and feet. This means that she has an extra digit on the side of both hands and polysyndactyly of her feet. On each foot, she has an extra toe that is connected, via fusing or webbing, to an adjacent toe. She faces difficulty wearing conventional shoes due to the presence of extra toes and fingers, and unfortunately, she endures teasing from other children as a result. Fortunately, on January 29th, surgeons will perform a polydactyly repair procedure to remove the extra digits of her hands. Our medical partner, Children's Surgical Centre, is requesting $299 to fund this procedure. After surgery, she will feel more comfortable about her appearance, and she won't be ashamed of how her feet look. Her father shared: "I hope that the surgery will not cause any infection and the extra fingers will not grow back."