Spencer is the last born in a family of four children. His father is a fisherman, and mother stays home to care for Spencer. Shortly after birth, Spencer's stomach became swollen. He was diagnosed with Anorectal Malformation - a birth condition in which the rectum is malformed. He was scheduled for a colostomy opening surgery, but Spencer's parents did not have any money for the surgery. They went back home with some medication to help pass stool as they were looking for money. After one month, they gathered some money and underwent the surgery. Spencer is now scheduled for an anorectoplasty surgery, where the surgeon will further correct the malformation. Our medical partner, African Mission Healthcare, will perform the surgery on February 27th and is requesting for $743 to fund the surgery. Spencer’s mother says, “As a parent, it's very painful to see your child suffering yet there’s nothing you can do to help. I hope that my child will be able to recover and live a normal life.”

Amina is a 11-year-old girl from Musoma region in Tanzania, the seventh child in a family of ten siblings. Her parents are small-scale farmers who rely solely on their harvest for sustenance and income generation. They often struggle to meet their needs, and climate change has resulted in poor harvests over the past year. About a year ago, Amina developed a swelling on her chin. Initially, it was considered insignificant as it did not bother her, but over time, the swelling grew larger and began to cause her significant discomfort when she was eating. This prompted concerns from her parents, who initially sought advice from a nearby pharmacy. However, the cream provided proved ineffective. Consequently, the family took her to a nearby hospital, where she was diagnosed with a mass requiring surgical removal. Due to financial constraints, her parents could not afford Amina's treatment so they went back home. Sometime later, the outreach team of our medical partner's care center visited their village, and the family was directed to Kafika House for further review and treatment. The team also assisted the family with transportation costs as they could not afford it. Fortunately, our medical partner, African Mission Healthcare, is helping Amina receive treatment. On April 2nd, surgeons will remove the mass and ease Amina's symptoms. Now, Amina's family needs help to fund this $724 procedure. Amina's mother says: “Please help with my daughter’s treatment. I hope she recovers from this condition so that it won’t be a problem as she grows older.”

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.