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."

Pyae is a 16-year-old girl from Burma. She lives with her parents, her sister, and her brother in Mandalay. Her father works as a day labor and her mother sells fruits pickle at home. Pyae and her siblings are students. Pyae was diagnosed with a heart condition that requires valve replacement. Heart valves control the flow of blood between chambers, but certain conditions may narrow the heart valve or cause the blood to flow backwards. Normal valve function is necessary to prevent long-term damage to the heart and lungs. Currently, Pyae has chest pain, gets tired easily, and is unable to eat and sleep well. Our medical partner, Burma Children Medical Fund, is requesting $1,500 to fund a heart valve replacement for Pyae. The treatment is scheduled to take place on May 15th at our medical partner's care center, Kasemrad Prachachuen Hospital in Thailand, and once completed, will hopefully allow her to live more comfortably. Pyae said, "If it is not BCMF and its donors, I will not have the right to receive the surgery.” Pyae’s mother said, “I would like to say thank you so much for your support and your cares to us. This kind of opportunity and support, we can not find and receive it inside Burma. I would like to contribute back to BCMF someday in the future.”

Aitana is a young girl from Bolivia. She lives with her mom and her dad, who have a small convenience store. Aitana has a twin sister and an older brother; they live in the northern part of Bolivia. Where they live, there are no cardiologists. So, when her mom noticed that her heart was beating too fast, she took her to a different area where she found out she had a heart condition and needed surgery. Aitana has a cardiac condition called an atrial septal defect. A hole exists between the two upper chambers of her heart: blood leaks through this hole, leaving her weak and short of breath. On April 15th, Aitana will undergo cardiac surgery at our medical partner's care center, Hospital del Niño Dr. Ovidio Aliaga Uría. During surgery, surgeons will sew a patch over the hole so that blood can no longer leak through it. Aitana'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. Aitana's mother shared, "We were looking forward to this day, I trust everything will go well, I pray for that."

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.”

Rehema is a 16-year-old girl from Tanzania. She is the second-born in a family of six children and lives in a large household where her father has two wives. Rehema’s mother, the second wife, plays a central role in caring for her children, while the family relies mainly on animal keeping for survival. Rehema is currently in class five, determined to continue her education despite the challenges she faces. Rehema was diagnosed with genu valgus. This is a condition that has affected both her legs for five years and has gradually worsened. Several factors could cause this condition, such as growth disorders, vitamin deficiencies, or excessive fluoride found in contaminated drinking water. As a result, the knees can be angled inwards or outwards, making it difficult to walk and may cause long-term joint damage. Walking long distances, such as going to the market, fetching water, or going to school, has become painful and exhausting for her. Her parents worry deeply about her future, especially as the pain continues to limit her mobility. Doctors have planned for a right distal femoral osteotomy (DFO), a procedure that will help correct the deformity, reduce her pain, and allow her to continue her schooling with confidence. Our medical partner, African Mission Healthcare, is requesting $777 to fund treatment for Rehema. The procedure is scheduled to take place on January 9th at our medical partner's care center, Kafika House. Treatment will hopefully restore Rehema's mobility, allow her to participate in a variety of activities, and greatly decrease her risk of future complications. Rehema says, "I really hope that one day I will be able to help my mother with chores without her being concerned most of the time."

Clamson is a young student from Haiti. He lives with his parents and younger sister in a city in northern Haiti. He likes going to kindergarten and to church. Clamson has a cardiac condition called a ventricular septal defect. A hole exists between the two lower chambers of his heart; blood leaks through this hole without passing through his lungs to obtain oxygen, leaving him weak and short of breath. Clamson will fly to the Dominican Republic to receive treatment. On January 22nd, he will undergo cardiac surgery, during which surgeons will sew a patch over the hole in his heart so that blood can no longer leak through it. Our medical partner, International Cardiac Alliance, is contributing $5000.00 to pay for surgery. Clamson's family also needs help to fund the costs of surgery prep. They need help raising $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 Clamson's family overseas. Clamson's mother shared, "Our family has been praying for this surgery ever since we found out about our son's heart problem. We are glad the time has finally arrived!"

Nicole is a beautiful six-year-old girl from Kenya. She lives with her single mother and three siblings. Her mother does casual work on other people's farms to support her children. She is in the first grade and loves to sing. Nicole dreams of becoming a gospel musician when she grows up. Nicole has clubfoot on her left foot. Clubfoot is a condition in which the foot is twisted out of shape. This causes difficulty walking and even wearing shoes. “My heart is heavy. I feel like my daughter didn’t do anything wrong,” says Nicole’s mother. “I just hope she can walk like other kids,” she added. Nicole walks with difficulty, often tiptoeing and sometimes falling. She cannot play freely with her friends and feels sad when other kids laugh at her while she walks. Fortunately, Nicole traveled to visit our medical partner's care center, AIC Cure International Hospital. There, surgeons will perform clubfoot repair surgery on December 10th. Our medical partner, African Mission Healthcare, is requesting $1,286 to fund Nicole's clubfoot repair. After treatment, she will be able to wear shoes, walk easily, and enjoy playing with her friends. Nicole's mother shared, "I have high hopes that at CURE Hospital, she will get better, be able to continue her education like other children, and achieve her dream of becoming a gospel musician."

Erlinda is a young student from Bolivia. She lives in central Bolivia with her parents, who both work in agriculture, and her five brothers. Erlinda stopped attending school last year because she felt too weak. Erlinda has a cardiac condition called aortic stenosis. One of the valves of the heart is too narrow; this causes blood to back up, leading to weakness and heart failure. On November 19th, she will undergo cardiac surgery at our medical partner's care center, Hospital del Niño Dr. Ovidio Aliaga Uría. During surgery, surgeons will reconstruct the valve so that it opens to a more normal size. Erlinda'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. Erlinda's father shared, "I hope this surgery goes well so that my daughter can have a healthy heart and can go back to school!"