Cleophas is a 7-year-old boy from Kenya. He is the 5th born in a family of six children. Cleophas was born with clubfoot, a condition where his foot is twisted. He was also born with hydrocephalus, an issue where fluids accumulate in his brain. To help with his hydrocephalus, doctors put a shunt in his head to drain the extra water. But even with the shunt, Cleophas still has trouble walking because of his clubfoot. He tiptoes as he walks and often falls. Fortunately, Cleophas visited our medical partner's care center, AIC Cure International Hospital. There, surgeons will perform clubfoot repair surgery on April 23rd. Our medical partner, African Mission Healthcare Foundation, requests $1,286 to fund Cleophas's clubfoot repair. After treatment, he is expected to be able to walk comfortably without tiptoeing and continue with his education without interruption. Cleophas' mother shared, "I look forward to seeing my son walking comfortably like other children."

Priscah is a social butterfly from Kenya who loves playing with toys and teddy bears. She is three years old and the youngest in her family, with three older siblings. She was brought to the hospital by her mother. Priscah's mother separated from her husband after Priscah was born. She works multiple jobs to provide for her children. Despite the challenges of being the sole provider, Priscah's mother is strong and determined, pouring all her love into her children. Priscah has clubfoot of both feet. Clubfoot is a condition in which the foot is twisted out of shape, which causes difficulty walking and even wearing shoes. Priscah has undergone serial casting and a previous surgery, but they were unsuccessful. She needs to undergo clubfoot repair surgery. Our medical partner, African Mission Healthcare (AMH), is helping Priscah receive this treatment on February 6th. After surgery, Priscah will be able to walk and play easily with her friends at school. AMH is requesting $1,286 to fund Priscah's treatment. Priscah's mother said, "I am looking forward to seeing my daughter walking well and joining school with other children, and any support to ensure that this dream is achieved will be greatly appreciated."

Aung is a nine months old baby boy from Burma. He lives with his parents, grandparents, aunt, uncle, and two elder sisters. His father works as a day laborer, while his mother takes care of the household. They also run a small farm where they grow rice for both their family to eat and to earn an income. However, their monthly earning is insufficient to cover their basic living costs and Aung's medical expenses. As a result, they are indebted. Aung was born at home with the assistance of a midwife. Neither the midwife nor the mother noticed any abnormalities at that time. However, the day after his birth, Aung's grandmother observed swelling in his left foot and genitals, as well as a mass on his right flank. Last May, Aung and his mother sought treatment at the public hospital in Yangon, where he was admitted. There, he underwent tests, including hormone evaluations, along with multiple X-rays of his chest, abdomen, pelvis, and both legs. The doctor informed his mother that a rare congenital condition was suspected, and that amputation might be necessary if there were any changes in his leg color or when he reached six months of age to prevent complications. Oral medications and bi-weekly follow-up appointments were provided. Over time, Aung's leg and scrotum swelling worsened. However, due to ongoing conflict near their village and financial constraints, Aung's parents were unable to attend further follow-up appointments. Doctors now want Aung to undergo an MRI, an imaging procedure that uses magnetic fields and radio waves to produce images of bodily organs. This scan will hopefully help doctors diagnose his condition and formulate an appropriate treatment plan. Our medical partner, Burma Children Medical Fund, is requesting $968 to cover the cost of Aung's MRI and care, scheduled for January 26th. Aung's mother expressed, "I hope to witness my son's full recovery. His condition brings me immense sorrow, and I do not know why this has happened to him. I would like to extend my heartfelt gratitude to BCMF and the donors for helping my son. Once he receives complete treatment, my wish is for him to excel in his education and achieve success in life."