Rivaldo is a four-year-old boy from Haiti. He lives with his mother and grandmother in a neighborhood of the capital, where he goes to pre-school. He loves to read and play games with his classmates and neighbors. Rivaldo has a cardiac condition called ventricular septal defect where a hole exists between the two lower chambers of his heart. Blood leaks through this hole without passing through the lungs to obtain oxygen, leaving him weak and short of breath. Rivaldo will fly to the Dominican Republic to receive treatment. On July 24th, he will undergo cardiac surgery, where surgeons will sew a patch over the hole in his heart so that blood can no longer leak through it. Another organization, Haiti Cardiac Alliance, is contributing $8,000 to help pay for the surgery. Rivaldo's family also needs help to fund the costs of surgery prep. The $1,500 will cover labs, medicines, check up and follow-up appointments. It also supports passport obtainment and enable social workers from our medical partner, International Cardiac Alliance, to accompany Rivaldo's family overseas. Rivaldo's mother says, "Our family is all very thankful to everyone who is helping to save our son's life."

Nataly is a student from Bolivia. She is an only child and lives in La Paz with her mother who works as a housekeeper in a hotel. Nataly is in the 9th grade and likes studying math and engineering. She dreams of pursuing a career in aeronautics. Nataly has patent ductus arteriosus, a heart condition where a hole exists between two major blood vessels next to the heart and causes blood to leak through the hole. This condition leaves her dizzy and weak. On June 5th, she will undergo cardiac surgery at our medical partner's care center, Hospital del Niño Dr. Ovidio Aliaga Uría. During surgery, surgeons will close the hole so that blood can no longer leak through it. After surgery, Nataly will have improved activity endurance. Nataly's family needs help to fund the costs of cardiac care and surgery. The $1,500 requested by our medical partner, International Cardiac Alliance, covers cardiac exams and diagnostics, surgical costs, follow-up care, and medications. Nataly shared, "I am excited to have this surgery so that I can feel normal and have energy and strength!"

Sam Ang lives with a group of friends in Kandaal province in Cambodia. He works as a truck driver. His family and siblings live nearby, where they run a small grocery stall on the roadside. In his free time, Sam Ang goes fishing in the Mekong River or checks the news on his phone. A previous injury that was left untreated is limiting his function on his right arm. He is also experiencing a loss of sensation and discomfort, making it difficult to drive long hours at his job. Surgeons at our medical partner, Children's Surgical Centre, plan to do a nerve procedure to improve function and sensation in Sam Ang's arm. Surgery and physiotherapy will allow him to carry out his job and everyday activities without difficulty. Now Sam Ang and his family need $572 to fund his surgery, post-op medications, and physiotherapy. Sam Ang shared, "I hope I can improve my arm so I can go back to work and help support my family."

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."

Rose is a 50-year-old woman from Kenya. Her husband works as a vegetable vendor in Nairobi and they have two adult children. Rose has a chronic wound on the left leg. Her doctors say she has severe cellulitis or a bacterial skin infection. The condition causes her pain and makes it difficult for her to walk. The wound in the leg needs to be treated by debridement or removing the damaged tissue so it can heal better. Rose also needs a skin graft to avoid infection. Fortunately, our medical partner, African Mission Healthcare, is helping Rose receive treatment. On March 14th, surgeons will perform a debridement and skin graft procedure to heal the wound and prevent the leg from being amputated. Now, Rose needs help to fund this $1,185 procedure. Rose says, “I risk losing my leg if not treated. This wound is worsening and needs urgent care.”

Aymy is a loving housewife and mother of two children. A year ago, Aymy began to experience severe pain and frequent acid reflux. During these bouts of pain, her husband misses work to stay home and care for their children. Aymy was found to have gallstones and was advised to undergo a cholecystectomy, the surgical removal of the gallbladder. If left untreated, her symptoms will continue to worsen and put her at risk for further health complications. Aymy is scheduled to undergo the procedure on March 5th with our medical partner, World Surgical Foundation Philippines (WSFP). The Philippine Health Insurance Corporation is supporting a portion of the cost of the procedure and WSFP is raising the remaining $1128 to cover the cost of Aymy's surgery and care. Aymy says, "I am grateful to everyone who will donate for my surgery. We cannot afford the treatment, especially when the necessities are costly. Thank you for making this possible for me and my family."

Residing in Kampong Thom province alongside her parents, two brothers, and two sisters, Sine's family earns their livelihood from the nearby rice paddies. Sine's favorite food is Khmer noodle soup, and she finds she loves Cambodian Studies. During her free time, she engages in reading and enjoys playing with her siblings. When she grows up, she wants to attend a prestigious university and ultimately pursue a career as a doctor. Sine was born with a hairy nevus - a type of birthmark characterized by a darkly pigmented, often raised patch of skin covered with hair. These birthmarks can vary significantly in size and appearance, ranging from small and barely noticeable to larger and more prominent. Hairy nevi are present at birth and are caused by an overgrowth of pigment cells in the skin. While most hairy nevi are harmless, larger ones may carry a slightly increased risk of developing into skin cancer, particularly melanoma. As Sine has gotten older, her insecurities around her birthmark have led to her missing a lot of school. In the pursuit of a solution, Sine and her mother traveled to Kien Khleang National Rehabilitation Centre, the care center of our medical partner, Children's Surgical Centre (CSC) for treatment. The doctors at CSC devised a treatment plan for Sine. On November 15th, 2023, Sine is scheduled for a partial removal of the nevus, with a follow-up in six months for additional planning and removal. Skilled surgeons at CSC will conduct the initial operation, employing skin grafting from her scalp to excise part of the nevus. This intervention aims to restore Sine's confidence, enabling her to resume regular school attendance, and to minimize her future health risks. CSC is requesting $726 to help fund the cost of this transformative procedure for Sine. Her mother shared, "I hope she can feel better and will want to play with her friends."

Three month old Keziah lives with her parents and two older siblings in Kenya. Her father, who works as an artist, is the sole breadwinner for the family. Keziah was born with open spina bifida and bilateral club feet. Spina bifida is a type of neural tube defect, in which the spine does not properly close around the spinal cord. While she has undergone some therapy for her condition, without additional treatment, Keziah is at risk of lower limb paralysis, infection of the exposed nervous tissue, and developmental delays. Our medical partner, African Mission Healthcare, is requesting $1,151 to cover the cost of Keziah's spina bifida closure surgery. The procedure is scheduled to take place on January 5th at BethanyKids Kijabe Hospital. This surgery will hopefully spare Keziah from the risks associated with her condition, allowing her to grow and develop along a healthy trajectory. Keziah's father says: “She is a jovial kid. We are sad that she is unwell. I hope that she is treated, and she can walk in the future.”

Witneyla is an 11 month old infant from Haiti. She is cared for by her single mother, who loves her very much. She has no brothers or sisters. Witneyla has been diagnosed with hydrocephalus, a condition in which excess cerebrospinal fluid accumulates in the brain and increases intracranial pressure. As a result of her condition, Witneyla has been experiencing increasing head circumference. Without treatment, Witneyla will experience severe physical and developmental delays. Our medical partner, Project Medishare, is requesting $957 to cover the surgery for Witneyla at Hospital Bernard Mevs, which will treat her hydrocephalus. This is the only site in the country where this care is currently available, and the procedure is scheduled for September 18th. This critical treatment will place a shunt to drain the excess fluid from Witneyla's brain to reduce intracranial pressure and greatly improve her quality of life. With proper treatment, Witneyla will hopefully develop into a strong, healthy young girl. Her mother is hopeful that this surgery will allow her child to grow up healthy.