Loise is the third born in a family of eight children. She's in the 5th grade and is passionate about reading. She aspires to become a doctor. Her mother is a homemaker and her father is a teacher. Loise’s clubfoot was diagnosed shortly after birth. Her left foot was turned inward and downward. Due to the lack of hospital services in their region, Loise has had to live with this condition which affects her mobility. Loise’s medical journey began with a visit to a mobile clinic where she was seen by an orthopaedic specialist. The doctor recommended that she start with serial casting, a gentle and effective treatment for clubfoot purposed to soften the tissues and realign her bones before surgery. She is presently in the hospital undergoing serial casting and needs to undergo a surgical procedure that will make it possible for her to wear shoes, walk upright, improve her self-esteem, and continue her education. Her surgery is scheduled for February 28th and her family is raising $1,224 to cover the cost of care. Loise said: “I am looking forward to walk upright without pain and continue with my education.”

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.”

Kenay is a sweet eleven-month-old baby boy from Ethiopia who loves to play with his mom. He is the fourth child of his parents. Kenay has started weaning and is eating Plumpy Nut, a nutrition supplement donated by the government and organizations to children with malnutrition, as Kenay was underweight. Kenay’s dad is a farmer and has land, but because of the drought, they couldn’t harvest enough, even for the family’s consumption. Initially, Kenay got his emergency colostomy from Sekota Hospital, which was supported by the community. However, he became so sick and underweight that his mother and some family members lost hope in his ability to survive. Fortunately, his mom heard about our medical partner’s care center, BethanyKids, from a social worker, and upon learning that they could get treatment for his condition, their hope increased. Bethany Kids covered the family’s transportation and accommodation to bring Kenay to the hospital, where the medical team first put him on a nutrition program for over four months to treat malnutrition. Now, Kenay’s weight is normal, and he is fit for surgery. Kenay was born with an anorectal malformation, a congenital abnormality that leads to a complete or partial intestinal blockage. He needs to undergo a series of procedures to eliminate bowel dysfunction. The long journey with multiple issues with his colostomy care has significantly impacted the psychological health of his parents, and they are requesting financial assistance with his surgery cost. Kenay is scheduled to undergo surgery to correct his condition on November 22nd. Our medical partner, African Mission Healthcare (AMH), is requesting $1,500 to cover Kenay’s procedure and care costs. After his recovery, Kenay will no longer experience bowel dysfunction or be at risk of developing health complications in the future. Kenay’s mom said, “I hope my child will get treatment, and I hope he will heal after the treatment. I hope I will see him growing up and start a decent life.”