Ulemu is a friendly 11-year-old boy, the firstborn of two children from Malawi. The family lives in a small, single-room mud-built house with a thatched roof. His mother earns a living by selling tomatoes from a small bench outside their home, and the family depends largely on this income to meet their daily needs. Ulemu's mother shared that he has been experiencing pain that often starts in his groin area, and travels up towards his abdomen, around the navel. She noticed that the pain is particularly severe during cold weather. She took him to the referral hospital several times in search of medical help, but unfortunately the surgery list was always long, and he has not been able to receive the surgery he needed. After hearing from several friends that Nkhoma Hospital was providing surgical services, she decided to bring him there. Getting to Nkhoma was not easy for the family. Because of their limited resources, even finding transport was a challenge. The journey took around five hours, and during the trip, his mother had to carry Ulemu on her lap at times. At Nkhoma Hospital, Ulemu was assessed and diagnosed with a left inguinal hernia, a condition that occurs when abdominal tissue protrudes through a weak spot in the lower abdominal muscles, causing a bulge in the groin area. Doctors explained that he would need surgery to correct the condition. For Ulemu's mother, finally receiving a diagnosis brought some relief, but learning about the cost of treatment brought another worry. The family could not afford the surgery fees. Ulemu's illness has also affected his education. For a boy who has recently completed his primary school examinations, his mother hopes that treatment will allow him to continue with his education without the interruptions caused by pain. Fortunately, Ulemu is scheduled to undergo hernia repair surgery at Nkhoma Hospital. Our medical partner, African Mission Healthcare, is requesting $421 to fund Ulemu's hernia repair surgery. The procedure will take place on August 13th and, once completed, will provide Ulemu relief from the pain that has affected his childhood and education. Ulemu's mother said, “I want my son to receive the help he needs, so that he can be well again and continue with his education.”

Constant is a two-year-old boy from Malawi. He is the last-born child in a family of four children, and his mother manages the home while his father runs a small electronics business to support the family. Constant has an right inguinal hernia, a condition that occurs when abdominal tissue protrudes through a weak spot in the lower abdominal muscles, causing a bulge in the groin area. The condition has brought periods of discomfort and worry to his young life. His mother has watched him grow while also keeping a close eye on the swelling, especially when it becomes more noticeable. At his age, Constant should be free to play, explore and enjoy being a child without his family having to worry about a condition that may require surgery. His parents have sought help because they want to see him treated and able to grow without the discomfort and uncertainty that have accompanied the hernia. After assessment at Nkhoma Hospital, Constant's mother was advised that he would need hernia repair surgery. When the family learnt about the cost of treatment, they were worried as they could not afford the full amount. His mother is hopeful that, with support, her little boy can receive the treatment he needs and be able to grow up healthy, active, and free from the burden of this condition. Fortunately, on August 11th, Constant will undergo hernia repair surgery at Nkhoma Hospital, our medical partner's care center. His family is contributing towards his care, but still needs to raise $421 more for his treatment. Constant’s mother said, “As his mother, all I want is to see Constant grow up healthy and free from this problem. He is still so young, and I want him to be able to play, run and enjoy his childhood without us worrying about the swelling. I am hopeful that with the help of the donor program, he will receive the surgery he needs and have a better future.”

Tasmiya is a bright, curious five-year-old girl from India. Tasmiya's father works in the carpet industry; her mother is a homemaker. Her favourite fruit is mango, and like any child her age, she wants to run, play, and go to school with her friends. She is the second of four daughters, and her father describes her as a girl who loves to study. Her face lit up whenever school was mentioned, but her injury made it difficult for her to continue her education. About a year ago, Tasmiya was playing with a friend when she accidentally fell into hot water, causing severe scald burns. The burns covered a large area of her chest, affecting both sides, including tissue near her breasts and chest wall, as well as her right thigh. As the burns healed, they left thick, raised scarring across her chest and thigh, and most disabling of all, a scar contracture at her right elbow that has pulled the joint out of its normal position. The contracture in the right elbow has left her unable to fully extend or use her arm normally. Simple daily tasks like writing, dressing, and carrying a school bag are difficult for her right now. Tasmiya has not been able to go to school or continue her education, something her father says weighs on her, since she loves learning. As she grows, the scarring on her chest also carries the risk of restricting normal development if left untreated. Tasmiya's family learned about our medical partner, G.S. Memorial Plastic Surgery Hospital and Trauma Center, and sought treatment. On September 2nd, specialty surgeons will perform a burn contracture release surgery. This will release the contracture and help restore use of her arm, allowing her to write and carry a school bag, dress herself, and do everyday things other five-year-olds do without a second thought. Now, she needs help to fund this $1,442 procedure. Tasmiya's father shared, "I am happy that she will have her surgery done, and I am confident because my neighbour, who had severe contractures, was treated here and is fully healed. I have full faith in Tasmiya's recovery."

Sineth is a 13-year-old 8th grade student from Kampong Cham Province in Cambodia. She lives with her parents and younger sister, who is in Grade 4. Her parents are rice farmers and work hard to support their family. Sineth enjoys studying Khmer literature, which is her favorite subject at school, and hopes to become a doctor in the future. In her free time, she likes listening to music and chatting with her friends. Her favorite food is fried pork with ginger. Sineth has scoliosis, a condition in which the spine curves abnormally to one side, often resembling a "C" or "S" shape. Her spinal curve has gradually worsened over the past three years and is now approximately 50 degrees in the thoracolumbar region. Although she does not currently experience pain, the increasing curvature affects her posture and makes it difficult for her to sit comfortably for long periods. This can make it harder for her to stay comfortable and concentrate during class, and the curvature may continue to worsen as she grows. Sineth's family was referred to our medical partner, Children’s Surgical Centre (CSC), by another hospital. They traveled approximately four hours from Kampong Cham to seek specialized care. On August 17th, surgeons at CSC plan to perform posterior spinal fusion to help straighten and stabilize her spine and prevent the curvature from worsening. She needs $1,500 in support to cover the cost of her surgery and related medical care. This treatment will help support her spinal health as she continues to grow and allow her to remain active and continue her education. Sineth's parents said, “We hope that this surgery will help straighten and stabilize our daughter’s spine and prevent her scoliosis from getting worse. We wish for her to grow well, stay active, and continue her studies and daily activities with confidence and comfort.”

Yesak is a joyful two-year-old boy from Ethiopia. He is known for his bright smile, active nature, and love for playing with his friends. He enjoys playing football and riding his bicycle. As the first child of his parents, he is curious, intelligent, and quick to remember new things. He loves exploring his surroundings, spending time with other children, and learning through play. Yisak lives with his parents in a rented house. His father works in the insurance sector, while his mother works as a messenger. Yesak was born with hypospadias, a condition that causes urinary dysfunction. Yesak's parents first discovered his condition when they took him for circumcision. During the visit, the doctor explained the condition to them. The news left the family worried and frustrated, but the doctor reassured them that the condition was treatable and advised them not to lose hope. The doctor referred Yisak to a higher-level hospital for specialized treatment when he became older. Without treatment, he will continue to experience uncomfortable symptoms and will be at risk of future complications. Fortunately, Yesak is scheduled to undergo corrective surgery on June 26th, and our medical partner, African Mission Healthcare, is requesting $1,293 to cover the cost of his procedure and care. Yisak's father said, "Thank you very much. We were warmly welcomed and treated with kindness by the staff. The services provided were professional and exceeded our expectations. We are grateful for the care and support given to Yisak and hopeful for a positive outcome for his condition."

Tennyson is a playful 11-year-old boy from Kenya. He is currently in grade 3 and loves drawing and playing with friends. His father is a construction worker, while his mother is a home maker. Tennyson has clubfoot of right foot, a condition in which the foot is twisted out of shape. Tennyson was also born with a hearing impairment. His mother first noticed that his right foot was bending when he was three years old. “He struggled to walk and would often complain of pain, and as he grew, it only got worse,” she recalls. They sought help at a nearby hospital but were informed that the condition could not be treated there. With no clear solution, they returned home. As time passed, the condition worsened. The pain increased, Tennyson's foot began to swell, and walking became more difficult. Eventually, Tennyson had to stop going to school because he could no longer walk. One of his teachers grew concerned and reached out to the family. After learning about Tennyson’s condition, the teacher informed his mother about a mobile clinic by AIC CURE Hospital, where Tennyson could undergo a review. At the clinic, Tennyson was assessed and scheduled for serial casting and a clubfoot surgery. He has been undergoing the casting and is now ready for the repair surgery, which has been scheduled for May 25th. Our medical partner, African Mission Healthcare, is requesting $1,286 to fund Tennyson's clubfoot repair. After treatment, his foot will gradually straighten and restore his ability to walk. Tennyson's mother says: “I am praying that his foot will be straightened, so that he can walk without pain, go back to school, and live like other children.”

Ny is 54 years old and a fruit seller from Banteay Meanchey Province from Cambodia. She is married and has one son, two daughters, and one grandson. She currently lives with her husband, who works as a construction laborer. In her free time, Ny enjoys listening to the news on the radio and listening to monks' sermons. Ny is diabetic, which has affected her vision. She was diagnosed with retinal detachment on her right eye. She has been experiencing constant tearing and blurred vision, which makes it difficult for her to see clearly and affects her ability to sell fruit properly. Because of her poor vision, she also finds it difficult to travel far places. She has difficulty seeing things clearly, recognizing faces, and going anywhere outside. When Ny learned about our medical partner, Children's Surgical Centre, she traveled for eight hours seeking treatment. On February 26th, eye surgeons will perform a retinal detachment repair procedure in her right eye. After recovery, she will be able to see clearly. Her family can contribute $50, but needs hep raising $656 more to fund her procedure and care. Ny said, "She hopes that after surgery, her vision will improve, the tearing will stop, and her vision will not deteriorate any further. She wishes to return to selling fruit and move around independently as before."

Laysing is a two-year-old boy from Preah Sihanouk Province in Cambodia. He lives with his parents and his four-year-old sister. His father works for a private company, while his mother stays at home to care for the children. He enjoys playing with toys alongside his sister, and his favorite meal is soup, especially lemongrass sour soup. Laysing was born with scoliosis, a condition in which the spine curves abnormally to one side. His parents first noticed the condition when he began walking. As he has grown, the scoliosis has caused him to tire easily when walking or playing. The condition makes everyday activities difficult and sometimes causes discomfort. Laysing's parents are concerned about his posture and possible complications in the future. Laysing's family heard about our medical partner, Children's Surgical Centre (CSC), and traveled four hours to attend a consultation. After extensive testing, doctors recommended that Laysing have spinal surgery. Without treatment, Laysing's symptoms will continue, and he will be at risk of future complications. On March 23rd, surgeons at CSC will implant a metal "growing rod" into Laysing's spine to help correct the curve and allow for further spine growth. CSC is requesting $1,500 to cover the costs of his surgery, the implant, and post-operative care, including physiotherapy. This treatment will help him stand taller, move more comfortably, and reduce fatigue. After recovery, he should be able to play, walk, and participate in daily activities more easily, improving both his quality of life and his confidence. Laysing's mother shares, “I pray that after the surgery, my child will feel stronger, stand taller, and live freely without discomfort, embracing a future full of hope and happiness.”

Brian is 10 years old and a student from Kenya. He is the youngest of four children. He was born with a condition known as Hemiplegic Cerebral Palsy (CP), which has greatly affected his mobility. Brian cannot walk and only crawls from one place to another. This has made daily activities difficult for him and his family. After his birth, his mother was referred to a nearby hospital for specialized care. Brian underwent several physiotherapy sessions, hoping to see improvement. Unfortunately, his condition did not get better. As a widow, Brian’s mother works tirelessly, taking on casual jobs like crushing stones into ballast and selling them, to provide for her family. Despite the hardship, she has never given up on finding help for her son. Brian attends a special school within their village that supports children with different disabilities. Brian was diagnosed with clubfoot on his right foot. Clubfoot is a condition in which the foot is twisted out of shape. This causes difficulty walking and even wearing shoes. Fortunately, Brian traveled to visit our medical partner's care center, AIC Cure International Hospital. There, surgeons will perform clubfoot repair surgery on February 20th. Our medical partner, African Mission Healthcare, is requesting $1,286 to fund Brian's clubfoot repair. After treatment, he will be able to walk on his feet, play with other children, become more independent, and continue with his education without limitations. “When I first learned about my son’s condition, I was in great shock. I did not know what the future would look like for him,” Brian’s mother recalls softly. She added, I hope to see my son receive treatment, walk on his own, play and interact freely with other children, and continue with his education without any challenges.”