Danna is a three-month-old baby girl from Bolivia. She lives with her mom, dad, and an older brother. Her father works in tourism, while her mother takes care of the children at home. Danna's mother noticed that she was not growing properly or gaining weight, so she took her to the hospital where her heart problem was discovered. Danna has a cardiac condition called patents ductus arteriosus. A hole exists between two blood vessels next to her heart. This condition prevents Danna's blood from circulating properly, causing her weakness and leaving her at risk of heart failure if the condition goes untreated. Danna also has Down syndrome. On September 22nd, 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. Danna'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. Her mother says: "I have a lot of hope, I pray the surgery goes well, she needs this surgery urgently."

Deborah is a two-year-old baby girl from Haiti. Deborah is very cheerful and outgoing. She likes to play with her neighbors and sing. She lives in a city in northern Haiti with her parents and older brother. Deborah has a cardiac condition called ventricular septal defect. A hole exists between the two lower chambers of her heart; blood leaks through this hole without passing through the lungs to obtain oxygen, leaving her weak and short of breath. Deborah will fly to United States to receive treatment. On July 23rd, she will undergo cardiac surgery, during which surgeons will sew a patch over the hole so that blood can no longer leak through it. Another organization, HeartGift Foundation, is contributing $18,000 to pay for surgery. Deborah'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 Deborah's family overseas. Deborah's mother says: "It's a miracle that our family has this chance for our daughter to have surgery. We are very thankful to everyone!"

Susan is a six-year-old girl from Kenya. From an early age, Susan experienced delayed developmental milestones. She was only able to sit at eight months and did not begin walking until she was two years old. As she grew, her parents noticed that she had difficulty speaking and pronouncing words. They hoped that, with time, she would improve, but the challenges persisted. Her parents enrolled her in school, believing that interacting with other children would help her learn to communicate better. Unfortunately, Susan continued to struggle both academically and socially. While her peers progressed to the next grade, she had to repeat a class because she was unable to keep up with communication and learning activities. Seeking help, her family first took her to a nearby hospital, and later, through a friend’s recommendation, she was referred to our medical partner's care center, AIC Kijabe Hospital. After undergoing audiology assessments, Susan was diagnosed with severe hearing loss. The major reason she cannot speak clearly is that she is unable to hear properly. When her parents learned the cost of hearing aids, they were worried. Susan’s father depends on casual construction and farming jobs to provide for his wife and their three children, while her mother works as a waitress at a local food joint. Despite working tirelessly, the family cannot afford the support Susan urgently needs. Our medical partner, African Mission Healthcare, is helping Susan receive treatment. On 21st May, she will be fitted with hearing aids that will improve her hearing. With consistent speech therapy, her communication skills will also improve, so she catch up with her peers. Now, Susan's parents are seeking support to raise $1,171, to aid in treatment for their daughter's hearing, help her find her voice, and continue her education with confidence alongside other children her age. Susan’s mother says, “Susan is a very active and bright child, but because she cannot hear properly, she struggles to keep up with other children her age. Being able to hear would help her speak more clearly, interact confidently, and progress well in her education.”

Hikma is a charming 20-month-old girl who lives with her parents and older brother in Ethiopia. Her parents were small-scale farmers until they were displaced due to war in their area. Now, her mother is a dedicated home maker, and her father works as a daily laborer. As with many other displaced families, it has been difficult for them to afford their daily necessities. Hikma was born with an anorectal malformation, a congenital condition that can lead to a complete or partial intestinal blockage. However, the symptoms were not obvious until she was around one year old. Her mother was deeply distressed by what she observed and immediately informed Hikma’s grandmother, who then began seeking for medical assistance. To avoid social stigma, however, the family tried to keep Hikma’s condition private. Eventually, the grandmother came across a Catholic missionary organization, which connected the family with a field coordinator of our medical partner's care center, BethanyKids Myungsung Christian Medical Centre (BKMCM). With the support of relatives and the Catholic missionaries, Hikma's family raised funds to travel to Addis Ababa. Upon arrival at the hospital, doctors explained that Hikma would need a series of surgeries to eliminate bowel dysfunction. The family was relieved and encouraged to hear that Hikma could be helped. Presently, Hikma has already undergone the first surgery, a colostomy creation, and recovered well. Now, Hikma needs support for her second surgery, which will occur on April 20th. Our medical partner, African Mission Healthcare Foundation, is requesting $1,500 to cover the total cost of Hikma's procedure and care. After her recovery, Hikma will no longer experience bowel dysfunction or be at risk of developing health complications in the future. Hikma’s mother said, “I would like to thank you sincerely for your support and the services you provided. Thank you again. I truly hope my child will grow up to be a wonderful woman.”

La Min is a 12-year-old boy from Burma. He lives with his parents and three brothers in Myawaddy, Karen State, Burma. His father is a day laborer, and his mother takes in laundry. He and his two older brothers are students, but his younger brother is too young to go to school yet. The family’s monthly income is not enough to cover the family’s daily expenses, so they often borrow money from a neighbor to get by. Since 2023, La Min has been experiencing swollen tonsils which make it difficult for him to breathe. He coughs and snores at night and has difficulty sleeping, so he sometimes has to sleep sitting upright. Because of his difficulty breathing, he gets tired easily, so his parents sometimes do not allow him to play football or cane ball with his friends. La Min was recently diagnosed with enlarged tonsils, which, if not treated, will cause his symptoms to persist and possibly intensify over time. Our medical partner, Burma Children Medical Fund, is requesting $1,500 to fund a tonsillectomy for La Min, which is scheduled to take place on March 17th. Surgeons will remove his tonsils, hopefully relieving La Min of his symptoms and helping him live more comfortably. La Min said, “I look forward to eating anything I can again. Right now, my mother just cooks plain food, so I want to eat something delicious again.”

Kwardun is a three-year-old boy. He is the second oldest in his family and lives in a household where access to specialized healthcare is limited. Kwardun’s mother is responsible for caring for the children while managing household duties. His father financially provides for their family. Kwardun is an energetic and social child who enjoys playing with other kids in the community. However, his clubfoot has affected his ability to walk properly. As he grows older, the deformity has begun to limit his mobility, causing him to tire quickly and struggle to keep up with his peers during play. Without treatment, this condition could worsen and significantly affect his independence and future participation in school. Kwardun was diagnosed with bilateral clubfoot. Clubfoot is a condition in which the foot is twisted out of shape. The tissues connecting the muscle to the bones are shorter than usual, and this causes difficulty walking and even wearing shoes. Fortunately, Kwardun's family traveled to visit our medical partner's care center, Kafika House. Surgeons will begin clubfoot treatment on February 10th. Our medical partner, African Mission Healthcare, is requesting $1,171 to fund Kwardun's clubfoot repair. After treatment, he has a strong chance of improved mobility and a more active childhood. Kwardun's father says, “He wants to run and play like the other children, but his foot makes him walk slowly and fall often.”

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!"

Lia is a young student from Bolivia. She lives with her mom, who is a homemaker, her dad, who is a truck driver, and her two younger siblings. Lia's mom noticed that her daughter had a constant headache, body aches, and dizziness. She took Lia to the doctor, which led to her being diagnosed with a heart condition called patent ductus arteriosus. A hole exists between two blood vessels next to the heart. This condition prevents Lia's blood from circulating properly, causing her weakness and leaving her at risk of heart failure if the condition is not treated. On December 16th, 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. Lia'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. Lia's mother shared, "I just hope my daughter has good health after the surgery, and stops being sick so often."

Janaika is a 33-year-old woman from the Philippines. Her partner is a motorcycle delivery driver. When opportunities arise, he also takes on construction jobs to supplement his income. Five years ago, Janaika was diagnosed with mixed hemorrhoids. She continues to experience discomfort, pain, and bleeding. She finds it difficult to move in and out of bed. Janaika needs surgery to prevent her symptoms from getting worse. Fortunately, our medical partner, World Surgical Foundation Philippines (WSFP), is helping Janaika receive treatment. She is scheduled to undergo a hemorrhoidectomy on November 8th. The Philippine Health Insurance Corporation is covering a portion of the cost of her treatment, and WSFP is raising the remaining $1,257 to cover Janaika's procedure and care. Janaika says, "I am very grateful because you are giving others like me a chance to have surgery who cannot afford it due to the high cost. Thank you for being a bridge that allows us to create a better future —one that will allow me to work again and improve myself."