Salato is a 5-year-old boy from Tanzania. He is a part of the Maasai tribe and comes from a large Maasai family with seven children. His father is a livestock keeper. Due to their remote location, the family relies on livestock and selling cattle as their main source of income to cover their expenses. Salato was diagnosed with genu valgus. His legs bow inward so that his knees knock. This condition is typically caused by an excessive accumulation of fluoride in the bones, which often stems from contaminated drinking water. As a result, Salato faces difficulty walking long distances and experiences considerable discomfort due to the abnormal gait he has developed. This condition has also limited his ability to help his father with the livestock and hampers his ability to socialize with others. During an outreach visit from our medical partner, African Mission Healthcare (AMH), Salato and his parents had the opportunity to attend a clinic where he received education about his condition. The church kindly assisted in facilitating his transportation to the hospital. Upon arrival, the team warmly welcomed him and conducted a thorough assessment. As a result, a plan was formulated to correct the abnormality in his right leg surgically. However, Salato and his parents are unable to afford the costs associated with his treatment. Fortunately, our medical partner, African Mission Healthcare (AMH), can help. Salato will undergo a corrective procedure on August 2nd. Treatment will hopefully restore Salato's mobility, allow him to participate in a variety of activities, and greatly decrease his risk of future complications. AMH is requesting $880 to cover the cost of Salato's treatment. Salato’s guardian says, “He often feels left out when he can’t socialize with his peers. We hope the treatment will help him fit in his society.”

Saw resides in a refugee camp along the Thai-Burma Border with his wife, two daughters, and son-in-law. His wife is a homemaker, and Saw stopped working as a day laborer due to his worsening health. He is proud of his family: One of his daughters is a student, the other is a pharmacist, and his son-in-law is a medic at the camp's hospital. He likes to forage for vegetables in his free time. Saw has been diagnosed with a right irreducible inguinal hernia and is scheduled to undergo hernia repair surgery in October. This surgery is essential to relieve his pain and discomfort and improve his overall quality of life. Saw said, “I want this discomfort and pain to disappear. I cannot do anything because of the pain. I hope that after surgery, I will be able to have a normal life again and will no longer be in any discomfort.”

Gregon is struggling to hear. He has severe bilateral hearing loss that requires attention. He needs hearing aids for both ears. He attends school, but his mother plans to send him to a special school to learn sign language. With the hearing aids, he will be able to hear well and join the special school where he will learn to speak and study hard. Gregon is an only child raised by a single mother who lives in an urban area in the country's capital, Nairobi. Gregon's Mother says, "He enjoys schooling but cannot recognize voices. My child needs to hear to go to school."

Axel, who is a five year old kindergartener, lives with his parents in La Paz, Bolivia. His mother is studying engineering, while his father works in construction. Axel was born with a coronary fistula, a rare condition in which a hole exists between one of the arteries on the outside of the heart, and one of the chambers of the heart. Because of this condition, blood leaks through the hole, weakening Axel, because his heart does not receive sufficient blood flow. Fortunately, our medical partner, International Cardiac Alliance, is here to help Axel access the treatment that he needs. On September 12th, doctors at Hospital del Niño Dr. Ovidio Aliaga Uría will sew the hole closed, so that blood can no longer leak through it. After surgery, Axel should be able to go on to live a strong and healthy life. Now Axel and his family need your help to fund this procedure, which will cost $1,500. Axel's mother said: "Our family is very happy to know that our son was chosen for surgery, and we are praying that everything will go well!"

Nafie is a 22-month-old toddler from Ethiopia. He loves water play and often touches things to see what is before him. He is the only child of his parents. His dad and mom are day laborers who graduated from high school. Nafie's mom noticed he was experiencing discomfort when using the restroom. She sought medical treatment and doctors determined that he was born with hypospadias, a congenital abnormality that causes urinary dysfunction. Without treatment, he will continue to experience uncomfortable symptoms and will be at risk of cancer and infertility in the future. Due to Nafie's condition, his parents are stressed and concerned about his future. They are appealing for financial assistance to help their son undergo a hypospadias repair surgery that will correct the abnormality and enable Nafie to live a full and quality life filled with dignity. After the procedure, Nafie will be able to pass urine as his peers do. Fortunately, Nafie is scheduled to undergo corrective surgery on September 22nd. Our medical partner African Mission Healthcare (AMH) is requesting $1,293 to cover the total cost of his procedure and care. Nafie's dad said, “It was really hard to believe that there is this kind of condition or there are children that went through this kind of situation. We were so scared and worried when we learned about his condition. We couldn’t think that it was correctable by treatment. We were relieved and felt happy when the doctor told us that the condition was correctable by surgery.” Nafie's mom also shared, “After the surgery, we hope he will be normal and just as other children.”

Carlos, who is two months old, lives with his parents in the hills above La Paz, Bolivia. His father is an electrician, while his mother is a fruit seller. Carlos was born with a rare cardiac condition called coarctation of the aorta. As a result, Carlos' aorta - which is the the main blood vessel leading from the heart - is too narrow, causing blood to back up into the heart. In order to remedy this condition, Carlos will need to undergo surgery. Our medical partner, Haiti Cardiac Alliance, is helping Carlos' parents to access the care their child needs. On July 20th, surgeons at Hospital del Niño Dr. Ovidio Aliaga Uría will widen Carlos' aorta, restoring normal blood flow. Now Carlos and his parents need your help to fund this $1,500 procedure. Carlos' mother said: "Our son has been in hospitals ever since he was born. Our family is hopeful that after this surgery he can come home to live with us!"

Gerry is a 48-year-old man from the Philippines. He is a dedicated husband and father who works hard as an on-call driver to support his family. For more than 20 years, Gerry has experienced mild abdominal pain. He visited a hospital for medical attention and was supposed to receive surgical treatment. However, due to the hospital's limited capacity and high influx of emergency cases, Gerry's surgery was deferred. As time passed, Gerry's symptoms worsened and he experienced intense pain more frequently. It became increasingly difficult for him to carry out his daily activities, work, and provide for his family. Now, Gerry is once again seeking medical attention. Fortunately, our medical partner, World Surgical Foundation Philippines (WSFP), can help. Gerry visited WSFP's care center where he had another medical checkup. Doctors advised that Gerry undergo a cholecystectomy, the surgical removal of the gallbladder. Now, Gerry is scheduled to undergo a cholecystectomy on June 24th. Philippine Health Insurance Corporation is covering a portion of the cost of the procedure, and WSFP is raising the remaining $1128 to cover the cost of Gerry's surgery and care. Gerry shared, "This free surgery is truly beneficial to us because we are really struggling financially. We have no money to spend for my needed treatment, so I'm so grateful to WATSI and the World Surgical Foundation Philippines!"

Helen is a young student from Haiti. She lives with her parents in a neighborhood of Port-au-Prince; she is in first grade and likes her math and reading classes. Helen 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 her lungs to be oxygenated, leaving her weak and short of breath. The surgery that Helen needs is not available anywhere in Haiti, so she will fly to the United States to receive treatment. On May 22, she will undergo cardiac surgery, during which surgeons will sew a patch over the hole in her heart to close it. Another organization, HeartGift Foundation, is contributing $14,000 to pay for surgery. Helen's family also needs help to fund the costs of surgery prep and travel. The $1,500 bill covers labs, medicines, and checkup and followup appointments. It also supports passport obtainment and the social workers from our medical partner, Haiti Cardiac Alliance, who will accompany Helen's family overseas. Helen's father said: "Our family is all very excited and hopeful to know that our daughter's heart can be fixed soon!"

Ally is a 4-month-old baby from a remote area of northern Tanzania. He has three siblings, and his parents practice small-scale farming. They grow agriculture crops for the family's consumption and sell the surplus harvest to cover some of their expenses. However, climate change has severely affected their livelihood; in the past three years, their harvest has been inadequate to meet the family's food needs. Ally was born with clubfoot of his left foot. Clubfoot is a condition in which the foot is twisted out of shape, which causes difficulty walking and even wearing shoes. On February 24th, surgeons at our medical partner, African Mission Healthcare (AMH), will perform clubfoot repair surgery that will allow Ally to be able to walk as he grows. AMH, is requesting $935 to fund this procedure. Ally's mother says: “I hope that my son lives free from this condition. I hope this treatment will make it possible.”