Nuru is a young girl with a big family. Her father is a cattle breeder. Cattle breeding has been hard for the past few years because of climate change, so the cattle have been dying because of starvation. Nuru has always wished to go to school, but it has been hard for her to start because the nearest school is located around 6 km away from home and her condition makes it impossible for her to walk that distance every day. Nuru was diagnosed with bilateral genu valgus. Her legs bow inward so that her knees touch. This condition is typically caused by an excessive accumulation of fluoride in the bones, which often stems from contaminated drinking water. As a result, Nuru has a difficult time walking. Our medical partner, African Mission Healthcare, is requesting $880 to fund corrective surgery for Nuru. The procedure is scheduled to take place on January 6th. Treatment will hopefully restore Nuru's mobility, allow her to participate in a variety of activities, and greatly decrease her risk of future complications. Nuru’s father says, “My daughter has been suffering for a while. I wish for her to be able to do what she wishes independently.”

Andy lives in a neighborhood of La Paz with his parents and younger sister; he is in the fifth grade and likes playing video games and spending time with his friends and family. Andy was born with a heart condition called ventricular septal defect: a hole exists between the two lower chambers of his heart, and blood leaks through this hole without passing through his lungs to obtain oxygen, leaving him weak and short of breath. During surgery, doctors will sew a patch over this hole to close it. His surgery costs $1,500, and Andy's family needs help to pay for it. Andy's mother said, "Our family is very hopeful that after this surgery Andy will have more energy and will grow bigger and stronger!"

Maria is a 59-year-old lady from Kenya. She is married and has six children; all grown up and working manual jobs to support themselves. Maria and her husband depend on their small farm. For over 5 years Maria has had abdominal pains, especially in the epigastric region. She has been treated many times in different hospitals. This year the pain became much worse and a scan showed a she has cholelithiasis. She came to Nazareth Hospital and our partner surgeon advised her to have a laparotomy. Unfortunately, due to hereconomic status, Maria and her family cannot manage to raise the $788 cost for this treatment. If not treated, Maria will continue to have the pain and may have more complications like pancreatitis or gall bladder obstruction. “I have stayed in pain for many years and even my children are tired of taking me to the hospital every time. I am kindly hoping to have this sponsorship so that I can be treated once and for all so that my life can be normal again. My family lives a life of struggle, we cannot make it to pay for this surgery, so I will appreciate and thank God if helped,” said Maria quietly.

Rin is a 43-year-old mother of one. She is a construction worker and divorced from her husband. She has one son who lives with her. In her free time, she likes to listen to Khmer songs and do things around the house. Earlier this month, she was working on a roof near a high-voltage wire and suffered multiple electrical burns on her hands, feet, and head. She was taken to a referral hospital, but only received minimal dressing for her burns. The tissue damage is extensive, and she is in pain and unable to use her hands. When Rin learned about our medical partner, Children's Surgical Centre, she traveled for three and a half hours seeking treatment. On September 15th, surgeons at CSC will perform a skin graft surgery to to help regenerate the damaged skin. Now, she needs help to fund this $805 procedure. Rin is hopeful that after surgery her hands will be better and she will be able to work again.

Exavier is an adorable 5-month-old baby from Haiti who has been diagnosed with hydrocephalus, a condition in which excess cerebrospinal fluid accumulates in the brain and increases intracranial pressure. As a result of his condition, Exavier's head circumference has increased. Without treatment, he will experience severe physical and developmental delays. Our medical partner, Project Medishare, is requesting $897 to cover the cost of surgery for Exavier at Hospital Bernard Mevs. This is the only site in the country where this care is currently available, and the procedure is scheduled to take place on August 26th. This critical treatment will drain the excess fluid from his brain to reduce intracranial pressure and greatly improve his quality of life. With proper treatment, Exavier will hopefully develop into a strong, healthy young boy. Exavier's family shares that they hope the surgery with allow him to grow, attend school, and play with the other children.

Rozaleny is a 70-year-old woman from the Philippines. She lives with her husband, who is a tricycle driver. For the past few months, Rozaleny has been experiencing pain and difficulty sitting. After three months of enduring this pain and discomfort, she decided to seek medical care. She was diagnosed with external hemorrhoids and was advised to undergo surgery to prevent her condition from worsening. However, Rozaleny and her husband could not fund her needed treatment due to financial constraints. Fortunately, our medical partner, World Surgical Foundation Philippines (WSFP), is helping Rozaleny receive treatment. She is scheduled to undergo a hemorrhoidectomy on July 30th at WSFP's care center. During this procedure, surgeons will remove her external hemorrhoids. A portion of the cost of her treatment is being supported by the Philippine Health Insurance Corporation, and WSFP is raising the remaining $1,137 to cover the cost of Rozaleny's procedure and care. After her recovery, she will no longer experience pain and will avoid future complications. Rozaleny's husband shares, "This free surgery will really be a big help to us. We can't afford to pay for her treatment. We're eternally grateful to Watsi and World Surgical Foundation Philippines for all their help."

Yoon is a bright and loving 12-year-old girl. She lives with her mother and uncle in Karen State of Burma near the border with Thailand. She was a student in grade three but stopped studying in August 2020 when she was no longer able to walk. Yoon enjoys painting pictures and reading books. In the future, she wants to go back to school and continue her studies. She helps out her mother with household chores. Her uncle is unemployed whereas her mother is an agricultural day labourer. One day at home, Yoon fell down when she tried to stand up to go to the bathroom. Her feet felt painful and were pointing downwards. After that, she did not try to stand up again and would move around her house on her knees. Her mother would have to carry her to the bathroom. Due to their financial situation, her mother was not able to seek treatment despite being very worried for her daughter. Over time, Yoon noticed that her feet were increasingly pointing downwards and were stiff. Her legs would feel painful and were also stiff. Sometimes, she could not stretch out her legs due to feelings of tightness and pain. Her mom shared that she would cry whenever her legs pained, and she would have to wait until the pain lessened by itself. Additionally, her hands began to weaken until she could not hold food with her hands. At the same time, her speech became slurred and her voice became hoarse. On June 17, Yoon arrived at our medical partner's care center, Mawlamyine Christian Leprosy Hospital (MCLH), and was admitted that same day. She received a physical examination and was diagnosed with cerebral palsy and tightness of Achilles tendon in both of her legs. The doctor recommended she receive surgery on both of her feet, which would help her walk again, and scheduled the procedure for June 21st. When Yoon’s mother told the doctor that they cannot afford to pay for surgery, the doctor referred Yoon to Burma Children Medical Fund (BCMF) for assistance accessing further treatment. Our medical partner, BCMF, is requesting $1,500 to cover the cost of an Achilles tendon lengthening procedure for Yoon. This procedure will elongate her Achilles tendon, allowing increased motion at the ankle joint. Without treatment, Yoon's condition will continue to cause her discomfort and will further limit her movement. Her mother said, “I cried almost every night when I saw my daughter in this condition. She always cried and complained about her feet. She always asked me to bring her to the hospital to get treatment. Whenever she asked me, I felt very sad and I would cry in secret. I want her to get treatment, but I cannot afford to pay for it. Due to COVID-19 and the current fighting in Burma, I cannot make enough money or save it. Often, I would only eat fishpaste and rice, but give her meat so that she can have something nutritious. When I heard that she has donors who will help her receive treatment, I felt very happy and thankful to BCMF for this kindness. I never thought she would receive such an opportunity. It makes me so happy that I do not know how to express it in words.”

Rose is a 7-month-old baby from Haiti. She lives with her father and grandmother, and they shared that she loves to smile and play with her family! Rose has been diagnosed with hydrocephalus, a condition in which excess cerebrospinal fluid accumulates in the brain and increases intracranial pressure. As a result, Rose has been experiencing an increasing head circumference. Without treatment, Rose will experience severe physical and developmental delays. Our medical partner, Project Medishare, is helping Rose receive treatment at Hospital Bernard Mevs, the only site in Haiti where the treatment she needs is available. On May 27th, Rose will undergo surgery to drain the excess fluid from her brain to reduce intracranial pressure and improve her quality of life. With this treatment, Rose will hopefully develop into a strong, healthy young girl. Project Medishare is requesting $897 to cover the cost of her surgery. Rose's father shared that he hopes for a healthy life for Rose in the future.

Vania is a hardworking 14-year-old student from Haiti. She lives in an urban area of the island nation's capital, Port-au-Prince, with her parents and three younger brothers. She enjoys studying, especially science and literature. Unfortunately, Vania has not been able to attend school for two years because of her heart condition. She suffered from rheumatic fever early in her childhood. The illness damaged one of the four valves in her heart, leaving her with a condition called rheumatic mitral regurgitation. Her heart cannot pump blood adequately through her body, which leaves her weak and short of breath. The good news is that surgery can help. Vania will fly to the Cayman Islands to receive treatment. On May 16th, surgeons will remove her damaged valve and implant an artificial valve in its place. Another organization, Have a Heart Cayman, is contributing $17,000 to pay for the procedure. But Vania's family also needs help to fund other medical and travel costs, which is where our Watsi donors come in. They are raising $1,500 to cover lab work and medicine for Vania, along with checkup and followup appointments. It also will help pay for her to get a passport and support social workers from our medical partner, Haiti Cardiac Alliance, who will accompany Vania and her family overseas. Vania says, "I am looking forward to this surgery so that I can feel more normal and go back to school."

Feven is a beautiful 7-month-old baby girl from Ethiopia. She has two older brothers and five sisters. She loves to play with her mom. Her dad is a farmer and he works hard, but his income is not enough to maintain the family so his brother often helps. All their children are in school and Feven's mom sometimes is able to sell items at the market. Feven was born with a birth defect called anorectal malformation. She developed bowel obstruction because of her condition and had an emergency colostomy surgery. Her parents shared that they are highly affected psychologically and are sad and worried about their baby. Feven now needs a follow up surgery to help her eliminate bowel dysfunction. She is scheduled to undergo surgery to correct her condition on March 22nd. Our medical partner, African Mission Healthcare, is requesting $1,500 to cover the total cost of her procedure and care. After her recovery, Feven will no longer experience bowel dysfunction or be at risk of developing related health complications in the future. Her mom shared, “We were so worried. But thank God he gave us this opportunity.”