Bakari is 6-year-old boy from Tanga, Tanzania. He is known for his charm, sociability, and outspoken nature. He is the first child to his mother, with his father having passed away. His mother, due to remarriage and relocation to another region, Mwanza, had to leave him in the care of his grandmother and uncle. Currently a student, Bakari recently embarked on his primary education, finding joy in the time spent at school with his peers, though limited in activities due to the condition he was born with. Bakari faces a physical challenge as he was born with a condition affecting both of his feet, causing them to twist inward and downward, significantly impacting his mobility. Early in his life, he had an opportunity for treatment in Tanga, but unfortunately, his father’s demise led to a lack of follow-up post-operative care, resulting in a relapse. At the age of two, his grandmother took him to the hospital for treatment, but insufficient financial resources prevented them from completing the necessary procedures, leading to yet another relapse. Determined to secure proper treatment for Bakari, his grandmother patiently gathered savings and, in late 2023, brought him to Arusha, specifically to Nkuaranga Hospital. During their visit, the doctor informed them that, due to Bakari’s age, he required more complex surgery, which the grandmother couldn’t afford. The doctor then directed them to Kafika house. Upon arrival, he was assessed by the team there. Bakari has clubfoot of both feet. His treatment plan will start with manipulation and casting, followed by corrective surgery. Clubfoot is a condition in which the foot is twisted out of shape. This causes difficulty walking and even wearing shoes. The team at Kafika House will begin clubfoot treatment on January 19th. Our medical partner, African Mission Healthcare, is requesting $935 to fund Bakari's clubfoot repair. After treatment, his mobility will significantly improve. Bakari’s grandmother says: “I really hope my grandson's feet will be okay. I have struggled to see him get treatment hoping his future will be okay.”

Samuel is a 10-month-old baby boy from Haiti. He is the first born child of his parents. Samuel has been diagnosed with hydrocephalus, a condition in which excess cerebrospinal fluid accumulates in the brain and increases intracranial pressure. As a result of his condition, Samuel has been experiencing increasing head circumference. Without treatment, Samuel will experience severe physical and developmental delays. On February 1st, Samuel will undergo surgery at Hospital Bernard Mevs to treat his hydrocephalus. This is the only site in the country where this care is currently available. Surgeons will place a shunt to drain the excess fluid from Samuel's brain, reducing intracranial pressure and greatly improving his quality of life. With proper treatment, Samuel will hopefully develop into a strong, healthy young boy. Our medical partner, Project Medishare, is requesting $957 to cover the cost of this surgery. His parents are looking forward to their child being healthy after surgery, hopeful that he can live a good life ahead.

Luz is a three-year-old girl from a mining town in central Bolivia. Her mother is a farmer and her father sadly passed away from a heart attack soon after she was born. Luz has a cardiac condition called ventricular septal defect, in which a hole exists between the two lower chambers of her heart. Blood leaks through this hole without passing through her lungs to obtain oxygen, leaving her weak and dependent on an external oxygen tank. Fortunately, our medical partner, The International Cardiac Alliance can help. Luz is scheduled to undergo heart surgery on March 21st. Our medical partners are requesting $1,500 to fund her procedure. Luz's mother says, "I am looking forward to my daughter being able to play normally and start preschool after her surgery!"