Wine is a three-year-old boy who lives with his parents and siblings in Karen State - an area of Burma that is in a state of crisis and conflict. Wine’s father is a construction day laborer and his mother stays at home with Wine and his siblings. Wine's older brother lives in Bangkok and his sister lives in Shan State and is able to send Wine's household money every month. His other four siblings are students. Wine was born in 2019 with a condition called hydrocephalus. Hydrocephalus is caused by a brain malformation or birth defect that causes excessive cerebrospinal fluid to accumulate in brain cavities. Cerebrospinal fluid is a clear, colorless liquid that surrounds the brain and spinal cord, protecting them from injury. It carries nutrients to the brain and spinal cord and takes away waste. In a healthy person, the amount of this fluid produced by the brain is absorbed by the body. In hydrocephalus, the fluid fails to drain and accumulates, leading to pressure on the brain. Wine's symptoms include a lump on the bridge of his nose. His eyes frequently water, and he cries a lot when he is in severe pain. Additionally, his head is gradually increasing in size as the fluid continues to build. The condition is most often treated by inserting a shunt. The shunt diverts excess cerebrospinal fluid (CSF) from the brain to another part of the body where the fluid can be reabsorbed. Wine visited a doctor when he was born to address the issue. While he was in the process of receiving treatment across the border at a hospital in Thailand, the Thai-Burma border shut down due to the outbreak of COVID-19. With the closure of the Thai-Burma border, Wine and his family could not go back to his follow-up care. Fortunately, after the Thai-Burma border reopened, Wine was able to meet with our medical partner, Burma Children Medical Fund (BCMF). Wine received a CT scan at Mae Sot General Hospital and the doctor was able to diagnose the issue and scheduled Wine to undergo surgery immediately on June 2nd. BCMF is now requesting $1,500 to help fund this procedure. Wine's mother said, "I want him to be able to walk, sit, and be healthy like other children his age. My husband and two of my children work, so I can take good care of Wine. I cry a lot whenever I see Wine suffering from pain, but now I feel like I no longer have to shed a tear for him because of that. I don’t want to be rich, nor do I want him to be rich. I only want Wine to be healthy and happy."

Peterson is a 24-year-old man from Haiti. He lives with his parents and younger sister in a city on the southern coast of the island. When he feels well enough, he helps his family with their market stand. Peterson has a cardiac condition called atrial septal defect. A hole exists between the two upper chambers of his heart; blood leaks through this hole without passing through his lungs to obtain oxygen, leaving him weak and short of breath. Peterson urgently needs surgery, but this is not available within Haiti. So Peterson will fly to United States to receive treatment. On March 2nd, he 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, Baylor Scott and White Heart Hospital, is contributing $15000 to pay for surgery. Peterson'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 Peterson overseas. "I would like to say thank you to everyone who is helping to fix my heart," said Peterson.

Michael is a beautiful baby who likes playing with blocks and waving his arms in time to music. Michael has a cardiac condition called tricuspid atresia: he was born without one of the four valves that is normally present in the heart. As a result, blood cannot flow through his lungs and body normally, leaving him sick and short of breath. On March 1st, Michael will undergo cardiac surgery, during which doctors will perform a technique called a Glenn procedure to create a conduit to allow blood to bypass the missing valve and more easily circulate through Michael's body. Another organization, Gift of Life International, is contributing $5,000 to pay for surgery, but Michael's family is still in need of $1,500 and have turned to the Watsi community for support. Michael's mother says: "It has been very frightening to see my son have such difficulty breathing, and I am so glad we can finally find a way to help him."

Esther is a 22 year old woman, living in Kenya. She is currently in her final year of school, pursuing a course in hospitality. Esther is supported by her mother, a widow, who runs a small grocery. Two weeks ago, Esther slipped on a staircase and broke her left ankle. At the local facility where Esther was initially taken, she was administered pain medication. An X-ray was performed at a second facility, and it was recommended that Esther undergo surgery to repair the fracture. Esther chose to visit the doctors at our medical partner, African Mission Healthcare Foundation, and now she is scheduled for surgery on January 5th, at AIC Kijabe Hospital. While Esther is currently unable to walk without support and without pain, the scheduled fracture repair surgery should restore her mobility. Now she needs your help to cover the $979 cost of the procedure. Esther says: “I am unable to go to school due to the fracture. I cannot walk and need the surgery to be able to use my leg again.”

Meet Night, a jovial and playful five year old girl. Night lives with her parents and two younger siblings in a traditional home in Kenya. Her father works selling second hand clothing, while her mother stays home to take care of the children. Shortly after she was born, Night's parents realized that something seemed wrong. They brought Night to a health facility in Turkana County where they lived, and were referred on to BethanyKids Hospital. There she was diagnosed with hydrocephalus, which meant that fluid was collecting in her head. Surgery was performed, and a shunt was placed to continuously drain the fluid from Night's head. A year later, however, Night's head began to increase in size, and she developed weakness on the right side of her body. The doctors at the local health facility urged Night's parents to take her back to BethanyKids Hospital for additional treatment, but Night's parents didn't have enough money to do this. With the help of our medical partner, African Mission Healthcare Foundation, Night is now scheduled to undergo a craniotomy on January 5th at BethanyKids Kijabe Hospital, when surgeons will drain excess fluids from Night's brain. Night's father is providing as much of a co-pay as possible for this procedure, but the family needs your help to raise the remaining $1,500 required to cover all of the costs of Night's surgery and care. Night’s father said: “Night is not able to communicate well because of her condition. This surgery will help her to be able to speak.”

Revania is an 8-month-old baby. She is the firstborn and an only child, bringing much joy to her parents. Her parents are trying their best to provide for their baby, but their income is dependent on the unpredictability of agriculture in Tanzania, where they live. Revania has clubfoot of both of her feet. Clubfoot is a condition in which the foot is twisted out of shape. This causes difficulty walking and even wearing shoes. Fortunately, Revania's family traveled to visit our medical partner's care center, Arusha Lutheran Medical Centre. There, surgeons will perform clubfoot repair surgery on December 2nd. Our medical partner, African Mission Healthcare Foundation, is requesting $935 to fund Revania's surgery. After treatment, she will be able to grow up healthy and active. Revania’s mother says, “It was scary at first not knowing how to help my daughter, but I wish she will get better.”

When U Eain was 10 years old, he became a monk. Now, at the age of 33, he lives with five other monks in a monastery in Yangon, Burma. As a monk, U Eain doesn't have an income. Instead, every morning, two of the novice monks from his monastery collect food donated by followers in Yangon. In addition, worshipers who visit the monastery donate vegetables, fruits and curries to eat. When the monks preach in other villages, they may receive small cash donations, and when U Eain's parents visit him every year, they provide U Eain with a small amount of money. In this way, the monks are able to cover their basic needs. In February, U Eain went to a town in Mon State to preach. During his second day there, he felt very tired and struggled to breathe, and ultimately, he had to stop preaching. He went to a local clinic, where he received two injections that helped him to feel better. The next day, he returned to his monastery in Yangon. Once he was home, he developed a fever and felt very tired, so he went to a nearby clinic. There, he received an electrocardiogram (ECG). After his results came back, the doctor told him that there were problems with his heart, and U Eain was referred to Yangon Government Hospital for an echocardiogram. On April 19th, U Eain had the echocardiogram, and then brought the results back to the nearby clinic. Due to numerous issues uncovered by the test, U Eain will need cardiac surgery to replace two valves in his heart. Fortunately, our medical partner, Burma Children Medical Fund, is able to help U Eain access the care that he needs. On October 21st, doctors at Pun Hlaing Hospital will replace the two valves in U Eain's heart, relieving him of the chest pains, rapid heartbeat, fatigue and difficulty breathing that he suffers from now. With his limited income, U Eain needs your support to raise the $1,500 to cover the cost of the procedure. He is hopeful to feel himself again soon and looks forward to returning to preaching and teaching. U Eain said: “I am so happy to receive treatment. I would like to say thank you so much to all of the donors.”

Abigaelle is an 18-month-old infant from Haiti. She has two siblings: one brother and one sister. She is a happy and cheerful baby who loves to smile and play! Abigaelle has been diagnosed with hydrocephalus, a condition in which excess cerebrospinal fluid accumulates in the brain and increases intracranial pressure. As a result of her condition, Abigaelle has been experiencing an increase in head circumference. Without treatment, Abigaelle will experience severe physical and developmental delays. Our medical partner, Project Medishare, is requesting $957 to cover the cost of surgery for Abigaelle at Hospital Bernard Mevs to treat her hydrocephalus. This is the only site in the country where this care is currently available. The procedure is scheduled to take place on July 13th. This critical treatment will place a shunt to drain the excess fluid from Abigaelle's brain to reduce intracranial pressure and greatly improve her quality of life. With proper treatment, she will hopefully develop into a strong, healthy young girl. Abigaelle's family shares that they are looking forward to their child being healthy.