Hayu is an energetic, curious, and playful young boy from Ethiopia. He enjoys exploring his surroundings and playing with anything he can find. He shares a particularly close and affectionate bond with his father. Hayu lives with his parents, two sisters, and older brother in a loving family environment. Hayu was born with hypospadias, a condition that causes urinary dysfunction. Without treatment, he will continue to experience uncomfortable symptoms and will be at risk of future complications. Fortunately, Hayu is scheduled to undergo corrective surgery on October 21st. Our medical partner, African Mission Healthcare, is requesting $1,293 to cover the cost of his procedure and care. Hayu’s father, saying: “My greatest wish is for my child to regain his health and undergo a successful surgery. I am deeply grateful for the support and services provided by this organization. Without this assistance, my child might still be waiting for the treatment he needs. May God bless this organization and everyone involved in helping children like my son receive the care they deserve.”

Anna is an eight-year-old student from Haiti. She lives in Port-au-Prince with her mother, father, and two younger brothers. Her father is a store clerk, and her mother is a teacher. She is in the third grade and likes all of her classes. Anna has a cardiac condition called Tetralogy of Fallot. This condition involves several related defects, including a hole between the two lower chambers of the heart and a muscular blockage of one of the valves. These defects prevent her body from obtaining the oxygen it needs, leaving her weak and short of breath. Anna needs to fly to the Dominican Republic to receive treatment. On October 19th, she will undergo heart surgery, during which time surgeons will sew a patch over the hole in her heart and remove the blockage from her valve. Another organization, Haitian Hearts Foundation, is contributing $8,000 to pay for surgery. Anna's family also needs help to fund the costs of surgery prep. Our medical partner, International Cardiac Alliance, is requesting $1,500 to cover labs, medicines, and check-up and follow-up appointments. It also supports securing travel documents for the family and travel costs for the social workers from our medical partner, who will accompany Anna's family overseas. Anna's mother says, "Our family is hopeful that after this surgery, our daughter will have normal health for the first time."

Legrand is a preschooler from Haiti. He lives with his mother, who works as a farmer and market vendor, and his grandmother in a small agricultural community in central Haiti. Legrand has a congenital heart condition called patent ductus arteriosus (PDA), in which an opening between two major blood vessels near his heart. This causes blood to flow abnormally, placing extra strain on his heart and contributing to weakness and difficulty gaining weight. Legrand needs to travel to the Dominican Republic to receive treatment. On October 21, he will undergo a procedure in which doctors will use a catheter to place a small device that closes the opening between the blood vessels, allowing blood to flow more normally. Another organization, the Haitian Hearts Foundation, is contributing $5,000 toward the cost of his treatment. Legrand's family also needs help to fund the costs of surgery prep. Our medical partner, International Cardiac Alliance, is requesting $1,500 to cover labs, medicines, and check-up and follow-up appointments. It also supports securing travel documents for the family and travel costs for the social workers from our medical partner, who will accompany Legrand's family overseas. From Legrand's mother, "I know that God has blessed us to reach this hospital to take care of my son!"

Jeremia is an 11-month-old baby boy. He is the only child in his family and lives with both parents, who work as pastoralists. They keep cattle and occasionally cultivate maize during the farming season to support their family. Jeremia has clubfoot on both feet, a congenital condition in which feet are twisted inward. Without appropriate treatment, this condition can make walking difficult and affect his ability to wear regular shoes comfortably as he grows. When Jeremia was born, his parents were unaware that medical treatment could help correct the position of his feet. Hope came when the Kafika House outreach team visited their village and identified Jeremia as a child who could benefit from treatment. For his parents, this discovery opened the door to an opportunity they had not previously known was available. Following an assessment, Jeremia has been scheduled to begin clubfoot treatment on October 20th. Our medical partner, African Mission Healthcare, is requesting $341 to fund Jeremia's clubfoot repair. After treatment, Jeremia will have improved mobility as he grows. “We are grateful for this opportunity to help our son walk comfortably,” says Jeremia's mother

Albertina is a two-week-old girl from Tanzania, and the youngest child in her family of nine children. Her mother maintains their home and cares for the children, while her father works as a fisherman to provide for the family. Albertina was born with clubfoot on her left foot, a congenital condition in which the foot is turned inward. Without appropriate treatment, this condition can affect her ability to wear shoes and walk comfortably as she grows. Soon after her birth, Albertina's family was referred to our medical partner's care center, Kafika House, for assessment and treatment. The referral gave the family hope that their newborn daughter could receive the specialized care she needed. Albertina is scheduled for treatment, and will be fitted with a foot abduction brace (FAB), which she will wear as part of her treatment plan until the age of five to help prevent her clubfoot from recurring. The treatment will begin on October 20th, and our medical partner, African Mission Healthcare, is requesting $341. After treatment, Albertina will have the opportunity for better mobility, and enjoying her childhood milestones. “We are grateful that our daughter has a chance to receive treatment, and grow up like other children,” said Albertina's mother.

Christie is a four-year-old girl from Haiti, who lives with her parents and two older siblings in a neighborhood of Port-au-Prince. She is in preschool, and is learning to read. She loves dressing up and playing with her friends. Christie has a cardiac condition called patent ductus arteriosus. A hole exists between two major blood vessels next to her heart; blood leaks through this hole, leaving her weak and short of breath. Christie will fly to the Dominican Republic to receive treatment. On May 13th, she will undergo cardiac surgery, during which doctors will use a device on the end of a catheter to plug the hole so that blood can no longer leak through it. Another organization, International Cardiac Alliance, is contributing $4,000 to pay for surgery. Christie's family also needs help to fund the costs of surgery prep. Our medical partner, International Cardiac Alliance, is requesting $1,500 to cover labs, medicines, and check-up and follow-up appointments. It also supports securing travel documents for the family and travel costs for the social workers from our medical partner, who will accompany Christie's family overseas. Christie's mother says: "Our family is so thankful that our daughter has this chance to travel and to get her heart healed!"

Jade is a 17-month-old baby girl from Bolivia. She lives with her mom, who used to work as a maid, her dad, who is a driver, and her older brother. Jade was born prematurely at 6 months 2 weeks, and spent four months in NICU; it was during this time that doctors informed her family that she would need heart surgery, but that they preferred to wait for her to grow. Jade has a cardiac condition called patent ductus arteriosus. A hole exists between two blood vessels next to her heart. This condition prevents Jade's blood from circulating properly, causing her weakness and leaving her at risk of heart failure if the condition goes untreated. On August 5th, she will undergo cardiac surgery at our medical partner's care center, Hospital del Niño Dr. Ovidio Aliaga Uría. During surgery, surgeons will sew the hole closed so that blood can no longer leak through it. Jade's family needs help to fund the costs of cardiac care and surgery. Our medical partner, International Cardiac Alliance, requests $1,500 to cover the cost of cardiac exams and diagnostics, surgical costs, follow-up care, and medications. Jade's mother shared, "I just pray my little daughter will have a successful surgery so she can have a happy life."

Hervens is a 17-year-old high-school student from Haiti. He lives in a neighborhood of Port-au-Prince with his parents, four brothers, and two sisters. His parents are both small-scale vendors. Hervens is in his second year of high school and likes art and literature. Hervens has a cardiac condition called atrial septal defect. A hole exists between the two upper chambers of his heart; blood leaks through this hole, leaving him weak and short of breath. Hervens needs fly to the Dominican Republic to receive treatment. On June 23rd, he will undergo heart surgery, during which doctors will sew a patch over the hole so that blood can no longer leak through it. Another organization is contributing to pay for surgery. Hervens's family also needs help to fund the costs of surgery prep. Our medical partner, International Cardiac Alliance, is requesting $1,500 to cover labs, medicines, and check-up and follow-up appointments. It also supports securing travel documents for the family and travel costs for the social workers from our medical partner, who will accompany Hervens's family overseas. Hervens says: "I am looking forward to having more energy, and to being stronger after my surgery!"

Kenawaka is a playful and cheerful 15-month-old boy from Ethiopia, who enjoys spending time with his older sister. He lives with his parents and sister in a rented home. His father works as an accountant to support the family, while his mother is a homemaker. Kenawaka's mother first noticed that something was different when she took Kenawaka to the hospital for circumcision. After examining him, the doctor told them that he would need specialized assessment and treatment, and referred them to a public referral hospital in the capital city. Following the referral, Kenawaka's parents waited another year due to a long surgical wait list. Though they were increasingly anxious, they could not afford care in a private facility so they continued hoping that they would be attended to soon. Recently, the referral hospital informed Kenawaka's parents to bring him to our medical partner's care center, BethanyKids Myungsung Christian Medical Centre (BKMCM). Kenawaka was diagnosed with hypospadias, a condition that causes urinary dysfunction. Without treatment, he will continue to experience uncomfortable symptoms and will be at risk of future complications. Fortunately, Kenawaka is scheduled to undergo corrective surgery on September 25th. Our medical partner, African Mission Healthcare, is requesting $1,293 to cover the cost of his procedure and care. Kenawaka's father said, “Thank you so much to everyone at BethanyKids. We are truly grateful to all the staff for their kindness and care. Everyone has treated us with so much respect and made us feel comfortable throughout this journey. We are very happy and thankful for the support Kenawaka has received. We love our son so much, and our greatest wish is to see him healthy and happy after his surgery.”

Eyosyas is a cheerful five-year-old boy from Ethiopia who loves playing with his older sister, watching cartoons, and spending time with his family. He lives with his parents and older sister. His father works as a daily laborer in construction, while his mother cares for the family. When Eyosiyas was still a baby, his mother noticed that something was different about his body. She was advised by a doctor to wait and observe. Four years later, his mother's concerns returned after a relative sent her a photo of her cousin's son, who was the same age as Eyosiyas. Comparing the two boys' development, she questioned whether Eyosiyas's condition was normal. She took him back to the health center for another examination. Eyosyas was diagnosed with cryptorchidism, a condition in which one or both of the testicles remain undescended. If left untreated, Eyosyas has an increased risk of developing hernias, testicular cancer, and fertility problems in the future. Eyosyas was referred to our medical partner's care center, BethanyKids Myungsung Christian Medical Centre, and will undergo surgery on July 24th. Our medical partner, African Mission Healthcare, is requesting $754 to cover the cost of his procedure and care. Eyosiyas's mother shared, "I am so happy to be here and to have this opportunity for my son. As a parent, I never imagined we would receive such high-quality care free of charge. We are deeply grateful to BethanyKids and everyone who made this possible. Thank you so much for your kindness and support. May God bless you all."

Nan Maw is a 24-year-old woman from Burma. She lives with her friends in Bangkok in an apartment rented by their employer. She works as a waitress, while her brother and mother still live in their village in Karen State, Burma. When Nan Maw was healthy and working full-time, she would send half of her salary home to support her mother. She dreams of building a concrete house back home for her family. Nan Maw was born with an atrial septal defect (ASD), a condition in which a hole exists between the two upper chambers of the heart. Sometimes ASDs may close on their own during development, but sometimes this condition requires surgery to repair the hole and prevent long-term damage to the heart and lungs. Due to her condition, she can only engage in part-time work as she gets tired too easily. Nan Maw is scheduled to undergo heart surgery on August 31st at our medical partner's care center, Kasemrad Prachachuen Hospital, to correct her atrial septal defect and improve her quality of life. Our medical partner, Burma Children Medical Fund, is requesting $1,500 to help cover the cost of Nan Maw's procedure and care. Nan Maw said, “I would like to thank your organization, BCMF, and your donors for your help. If you do not help me, I would have had to give up on my treatment because I know that I could not afford it by myself. I am very happy and thankful to all the donors. You have helped me feel that I can dream again. Before I developed these symptoms, I dreamed of working hard, saving money, building a house back home, and opening my own restaurant. Since I first noticed my symptoms, it felt like my dreams were lost. But now, I can dream again.”

Robinas is an intelligent 11-year-old boy who lives in Ethiopia with his parents and cousin. His father is a teacher who works hard to provide for the family, while his mother has been living with a chronic illness that has kept her at home for several years. Despite these challenges, his parents have remained committed to supporting both his education and his health. Robinas is on a full scholarship at a private school, where he consistently ranks among the top students in his class. His dedication and hard work have earned him several medals in recognition of his outstanding academic performance. Outside the classroom, he enjoys playing football, reading books, and spending time with his cousin. Robinas was born with hypospadias, a condition that causes urinary dysfunction. Although his parents noticed the condition at birth, they were advised to delay surgery until he was older, as the procedure would be safer once he had developed further. Over the years, the family visited several hospitals but were consistently told to wait. Eventually, doctors at a private hospital confirmed that Robinas was eligible for surgery; however, the cost was beyond the family’s financial means. They were then referred to a public hospital, where they faced a long waiting list. This prolonged waiting period has been emotionally difficult for the family, especially as Robinas has begun asking his father why he is different from other boys. After six months, the family finally received wonderful news. They were informed that Robinas had been referred for surgery at our partner’s medical care center, BethanyKids Myungsung Christian Medical Centre (BKMCM). Robinas is scheduled to undergo corrective surgery on June 29th. Our medical partner, African Mission Healthcare, is requesting $1,293 to cover the cost of his procedure and care. Robinas’s father shared, “Thank you so much for BethanyKids’s help with the children and for supporting my son. I feel terrible when I’m unable to afford that surgery, but the support means so much to us. Thank you again, God bless you all.”