Keisha is a 5-month-old baby girl from Haiti. She is the first child of her parents. Keisha has been diagnosed with hydrocephalus, a condition in which excess cerebrospinal fluid - the fluid which surrounds the brain - accumulates in the brain and increases intracranial pressure. The accumulation of fluid has caused Keisha’s head to expand beyond a normal range. Without treatment, Keisha will experience severe physical and developmental delays. Keisha is scheduled for surgery to put a flexible plastic tube called a shunt in her brain to redirect the cerebrospinal fluid into another part of her body. Draining the excess fluid from Keisha’s brain will reduce the pressure and greatly improve the quality of her life. With proper treatment, Keisha will hopefully develop into a strong, healthy young girl. Keisha is scheduled for surgery on December 8th at Hospital Bernard Mevs, the only site in the country where this care is currently available. Our medical partner, Project Medishare, is requesting $957 to cover the cost of surgery. Her family is grateful Keisha is able to have surgery to prevent long-term damage to her brain.

Mercy is a determined young lady, a sixth born in a family of nine children. Her father is a small scale farmer and her mother a homemaker. She goes to secondary school in Meru County, but is currently behind on her studies due to delays caused by a condition impacting both legs. Mercy was born with a condition known as bilateral genu varum (sometimes referred to as bowlegs), which causes her legs to curve outward at the knees. The condition has greatly affected her mobility. She finds it difficult to walk long distances, she gets tired quickly, and is unable to fully engage in activities with friends. Her self-esteem has been dramatically impacted by constant teasing from her peers, who find her way of walking different. Fortunately, Mercy is scheduled to undergo a surgery called bilateral Proximal Tibial Osteotomy (PTO) at our medical partner's care center AIC CURE International Hospital. The treatment will heal her legs, allow her to walk easily and support her to engage better both in school and with friends. Mercy hopes to become an orthopedic surgeon in order to help other children in the future. “I am looking forward to see my legs being corrected, to live more actively and continue with my education. God bless you for the support,” Mercy told us.

Residing in Kampong Thom province alongside her parents, two brothers, and two sisters, Sine's family earns their livelihood from the nearby rice paddies. Sine's favorite food is Khmer noodle soup, and she finds she loves Cambodian Studies. During her free time, she engages in reading and enjoys playing with her siblings. When she grows up, she wants to attend a prestigious university and ultimately pursue a career as a doctor. Sine was born with a hairy nevus - a type of birthmark characterized by a darkly pigmented, often raised patch of skin covered with hair. These birthmarks can vary significantly in size and appearance, ranging from small and barely noticeable to larger and more prominent. Hairy nevi are present at birth and are caused by an overgrowth of pigment cells in the skin. While most hairy nevi are harmless, larger ones may carry a slightly increased risk of developing into skin cancer, particularly melanoma. As Sine has gotten older, her insecurities around her birthmark have led to her missing a lot of school. In the pursuit of a solution, Sine and her mother traveled to Kien Khleang National Rehabilitation Centre, the care center of our medical partner, Children's Surgical Centre (CSC) for treatment. The doctors at CSC devised a treatment plan for Sine. On November 15th, 2023, Sine is scheduled for a partial removal of the nevus, with a follow-up in six months for additional planning and removal. Skilled surgeons at CSC will conduct the initial operation, employing skin grafting from her scalp to excise part of the nevus. This intervention aims to restore Sine's confidence, enabling her to resume regular school attendance, and to minimize her future health risks. CSC is requesting $726 to help fund the cost of this transformative procedure for Sine. Her mother shared, "I hope she can feel better and will want to play with her friends."