Two-month-old Dayana is the first child of her mother, who is a food vendor, and her father, who works in construction. She battles a condition called coarctation of the aorta. One of Dayana's major blood vessels connected to her heart is too narrow, this causes blood to back up into her heart, which can lead to heart failure. Fortunately there is a treatment than can cure her condition. During surgery, doctors will expand the aorta to allow blood to flow normally. She is scheduled for treatment on February 8th and our medical partner International Cardiac Alliance is helping her family to raise $1,500 to support the cost of care. Dayana's mother says, "We have been very afraid for our daughter's life ever since she was born, and so we are so glad to have this opportunity!"

Gian is a one-year-old baby boy from Kenya. Both of his parents are Intern Teachers and Gian is their only baby. About seven months ago, Gian’s father noticed there was something different about Gian's body. They took him to a nearby health center where, after examination, they were advised to take him to a major Hospital. They brought him to Nazareth Hospital and was diagnosed with cryptorchidism, a condition in which one or both of the testicles remains undescended. If left untreated, Gian has an increased risk of developing hernias, testicular cancer, infection, testicular torsion, and fertility problems in the future. Gian will be receiving assistance from our medical partner, African Mission Healthcare (AMH). Fortunately, he is scheduled to undergo corrective surgery on April 4th. AMH is requesting $483 to cover the total cost of his procedure and care. Gian's father said, “When we took him to the health center, we were told this can cause problems for him in the future. We now seek help so that he can undergo the treatment and at least grow up like any other boy."

Manfa is the only child in his family. His parents are rice and potato farmers in rural Mondolkiri Province in Cambodia. He loves to eat fried potatoes using the potatoes they grow on the farm and enjoys watching cartoons on his mom's phone. Manfa was diagnosed with osteogenesis imperfecta, a congenital condition in which bones are brittle and prone to breaking. He has experienced multiple fractures in his lower limbs since he was six years old. On March 4th, Manfa will undergo osteotomy, a procedure where his tibia bone will be reshaped to facilitate improved walking balance and prevent pain for him in the future. Our medical partner, Children's Surgical Centre, needs your support to fund the $469 procedure, post-op medications, and physiotherapy costs. Manfa's father shared: "In the future, I'm worried my son will not be able to attend school. I hope he can walk better than before and continue his dream to work as a teacher."