Aye is a 25-year-old woman from Thailand. She lives with her parents, grandfather, aunt, brother, sister and daughter. She and her sister are homemakers, while her father is a day labourer. Her brother works in a garment factory, and her mother and aunt are unemployed. Since Aye was 12 years old, she has experienced difficulty passing urine on and off. In October, this worsened and she now has blood in her urine and severe pain in her lower back. Doctors want Aye to undergo a CT scan, a procedure in which x-ray images taken from several angles are combined to produce cross-sectional images of the body. This scan will hopefully help doctors diagnose her condition and formulate an appropriate treatment plan. Our medical partner, Burma Children Medical Fund, is requesting $414 to cover the cost of Aye's CT scan and care, scheduled for December 20th. Aye said, "I have been experiencing these symptoms for so many years but because of financial problems, I have never receive proper treatment."

Rayan is a one-year-old boy from Tanzania. He is the first child of his parents, and he is an active and interactive child who loves playing with other children. His father takes on casual jobs to earn a living, while his mother is a homemaker. Rayan was born with a congenital condition affecting his left hand, in which two fingers are joined together, causing concern for his parents regarding its impact on his future. Fortunately, Rayan's mother learned about our medical partner's care center Kafika House from a previous patient and made the decision to take him there. At the center, Rayan was diagnosed with left-hand syndactyly, a condition that is corrected through surgical intervention. The plastic surgeons intend to carry out a release procedure to separate his left hand's third and fourth fingers. Fortunately, our medical partner, African Mission Healthcare, is helping Rayan receive treatment at their care center Kafika House. On March 7th, surgeons will perform a contracture release surgery to enhance the mobility of his fingers. Now, his family needs help to fund this $874 procedure. Rayan’s mother says: “I hope my son’s hand will be okay and that the condition will not affect his future.”

Shinka is a 6-year-old boy from Kenya. He is the last born in a family of seven children. His father, who was the sole breadwinner of the family passed away in 2017 after a short illness. To provide for the family, the eldest son, who finished his high school studies last year, sells milk to earn some money. Sometimes the earnings are not much, and they have to rely on family members for financial support. The family does not have medical coverage and is not able to raise the money needed to pay for Shinka's surgery. In May of last year, Shinka started experiencing some difficulty when passing urine. At some point, he had stopped going to school for a few weeks. His mother shared Shinka's condition with his uncle who took him to a local health center for review. Shinka was examined and referred to our facility. When he came with his uncle for examination, doctors were able to diagnose his condition and also found a condition called cryptorchidism that first requires a bilateral orchidopexy surgery. If left untreated, Shinka has an increased risk of developing hernias, testicular cancer, and fertility problems in the future. Shinka will be receiving assistance from our medical partner, African Mission Healthcare (AMH). Fortunately, he is scheduled to undergo corrective surgery on January 11th. AMHF is requesting $646 to cover the total cost of his procedure and care. Shinka’s uncle says, “We are very much worried as a family about Shinka’s condition. His studies are affected, and we want him to go back to school as soon as possible.”