Scot joined Watsi on October 16th, 2016. Two years ago, Scot joined our Universal Fund, supporting life-changing treatments for a new Watsi patient every month. Scot's most recent donation supported Joyline, a 14-year-old girl from Kenya, to fund fracture repair surgery.
Scot has funded healthcare for 35 patients in 9 countries.
Scot has funded healthcare for 35 patients in 9 countries.
Joyline is a 14-year-old student at a primary school in Kenya, where she lives with her parents and two younger siblings. Her parents are small-scale farmers who plant potatoes and beans, mainly for home consumption, with some sold for an income. They live in a home without electricity, using firewood as their source of heat, while getting their water from a nearby river. Joyline reported that she started feeling pain in her leg in November of last year. Her parents brought her to two different facilities, where the only treatment provided was pain medication. Walking has become difficult to the point she had to stop going to school and is unable to walk on her own. Fortunately, surgeons at our medical partner, African Mission Healthcare Foundation, can help. On May 9th, Joyline will undergo a fracture repair procedure, called an open reduction and internal fixation, at AIC Kapsowar Hospital. The treatment will repair her fractured femur, and enable her to live a pain-free life. Now, African Mission Healthcare Foundation is requesting $1,145 to fund this procedure. Joyline says: "I feel so much pain, and the worst of it all is that I cannot walk. I am so uncomfortable when I see my mother helping me do things that I could do on my own. Kindly help me so that I may be able to go back to school and study well, as this is my final year in primary school."
Jayden is a preschooler from Haiti. Jayden lives with his parents, who are both schoolteachers, and older brother in a small city in the mountains of central Haiti. He likes to draw and is learning to read. Jayden has a cardiac condition called atrial septal defect and ventricular septal defect. Two holes exist in his heart, one between the two upper chambers and another between the two lower chambers. Blood leaks through these holes, straining his heart and making it difficult for him to obtain oxygen. Because the surgery he needs is not available in Haiti, Jayden will fly to Dominican Republic to receive treatment. On April 28th, he will undergo cardiac surgery, during which surgeons will use patches to close the holes in his heart so that blood can flow normally. Our medical partner Haiti Cardiac Alliance is also contributing $9,000 to pay for surgery, but Jayden and his family still need help covering 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 Jayden overseas. Jayden's mother shared, "Our family has been very frightened for our son's health so we were so happy to get the news that he could have this surgery!"
Daniel is a 10-year-old student from Ethiopia. He is in second grade and loves school. His favorite subject is English. He also loves playing football and games with friends, eating fruits and eggs with injera. He is the fifth child in the family with four older brothers. Both parents are daily laborers on a farm and get income by sharing the profit during harvest with the landowner. They use the income to feed the family and also sell some of the produce to buy other goods for the house. During the rainy season, they engage in other labor work such as chopping wood, gardening and delivery of different goods. Even though their family income is sufficient to support the basic needs of their family, it is a challenge to afford Daniel's surgery. Daniel was born with hypospadias, a congenital disease that causes urinary dysfunction. Without treatment, he will continue to experience uncomfortable symptoms. Earlier he had two surgeries with Bethany Kids Myungsung Christian Medical Centre (BKMCM). For the third surgery, he had to wait for four years. The wait made him drop out of school and has affected his mental wellbeing. Fortunately, Daniel is now scheduled to undergo corrective surgery on February 28th. Our medical partner, African Mission Healthcare Foundation, is requesting $1,293 to cover the total cost of his procedure and care. Daniel's dad said “I will be happy if my son completely heals and becomes free from shame. I am eager to send him back to school.”
Marion is a 6-year-old student from the highlands of Elgeyo Marakwet county in Kenya. She is the second born in a family of three girls and currently attending preschool near her family home. Her parents are small-scale potato farmers. One day Marion's mother went to the river to fetch water. While she was gone, her children were sitting near an open fireplace at home making breakfast. Unfortunately, Marion's dress caught fire on the open flame, and as a result, she sustained severe burns on her back, abdomen and thighs. It has been difficult for her to walk, and the wounds are causing extreme discomfort. She especially needs a third surgery to treat the severity of her burns contractures. Despite Marion's parents having medical insurance, due to previous surgeries that she has had to treat the injuries, the insurance (a monthly subscription) has run its course and is no longer an option. Her parents do not have the funds to pay for Marion's surgery and need support. Fortunately, our medical partner, African Mission Healthcare (AMH), is helping Marion receive treatment. On January 25th, surgeons at their care center will perform a burn contracture release surgery that will allow her to walk with greater ease and resume her normal life at home and school. Now, she and her family are requesting $1,478 to help fund this procedure. Marion's mother says, “I am really looking forward to seeing my daughter live and walk in a normal way. I worked hard to pay for insurance coverage, but unfortunately, it cannot fund the upcoming procedure. I am disappointed, but I will not lose hope. Kindly help her.”
Chit Htun is a 21-year-old man from Burma who lives with his mother, two sisters and a brother. His mother is a homemaker, while Chit Htun and his siblings are students. They are supported financially by two aunties and Chit Htun's former teacher. Chit Htun was born with spina bifida as well as hydrocephalus. When Chit Htun was just over a month old, he had a shunt inserted in his brain to control hydrocephalus. In October 202, Chit Htun fell down the stairs in his home and hit his head during the fall. Since that time, he has been experiencing headaches and dizziness with occasional loss of consciousness. Chit Htun's mother brought him to a hospital in Yangon, where he received a CT scans showing that the original shunt was in place. A second shunt was inserted to help with the loss of consciousness, but the headaches and dizziness continued to be a problem. In October 2022, Chit Htun had a seizure, accompanied by nausea and vomiting. Chit Htun's mother brought him to Mae Sot Hospital, where he received a CT scan on November 28th, 2022 with the help of Burma Children Medical Fund (BCMF). The doctor diagnosed Chit Htun with severe chronic hydrocephalus and suspected shunt malfunction. BCMF is now fundraising $1,500 to help cover the cost of surgery to replace Chit Htun's current shunt. Chit Htun's mother shared, "My son and I have been in Mae Sot for the past two months and we are homesick already. I hope that he will receive surgery soon and recover from his symptoms."
Kenenitu is a young child from Ethiopia. She is a beautiful baby who loves playing with other children. She developed bowel obstruction and an emergency colostomy surgery was done at our medical partner's care center BKMCM. The condition and care has been challenging for Kenenitu and her mother who has been affected psychologically. Kenenitu's mother is a single mom with four children. Her brother stepped in to help raise the children as her husband has left without support. Before giving birth to Kenenitu, her mother used to make injera, an Ethiopian cuisine, for a living. Currently, she is not working. The family received logistical support from an NGO to arrive at the hospital and Kenenitu's mother is staying at another NGO in Addis Ababa for medical follow-up and accommodation. Due to their financial situation, the family cannot afford the medical bills for Kenenitu's treatment. Kenenitu's mother has struggled emotionally with her daughter's condition. She said, "I wondered what was going to happen to her. I used to cry a lot and I was not in my normal mental condition. But when I heard that she could be treated, my hope was restored and I felt better." Kenenitu was born with an anorectal malformation, a congenital abnormality that leads to a complete or partial intestinal blockage. She needs to undergo a series of procedures to eliminate bowel dysfunction. Kenenitu is scheduled to undergo surgery to correct her condition on December 20th. Our medical partner, African Mission Healthcare Foundation, is requesting $1,500 to cover the total cost of Kenenitu's procedure and care. After her recovery, Kenenitu will no longer experience bowel dysfunction or be at risk of developing health complications in the future. Kenenitu's mother said, "After receiving treatment, I hope she will start making stool... I want to take her to school and educate her."
Samuel is a 21-year-old talkative young man. He is the second born in a family of five children. His father passed away when he was four years old, so his mother had to raise him and his siblings by herself. She does jobs on tea farms to provide for the family. When Samuel was two years old, his abdomen started to swell, which was very painful for him. His mother took him to the hospital and he was given some medication and sent back home. The medication did not work as expected. He was then taken to a different hospital for examination. He was given more medication and after some time he seemed to be better. The stomachache did not go away completely, however. Samuel and his mother shared that over the years, he has had stomachaches and gotten used to taking pain medication. In 2017 when Samuel was in high school, the pain worsened and his abdomen started to swell again. He had to leave school as a result. His mother took him to a hospital in Meru where he was admitted for three months. While in the hospital, scans and a biopsy were done to determine what the problem was. He was given a colostomy, where the end of the colon is brought through an opening in the abdominal wall, in order to pass stool. This surgery is often performed to bypass bowel malformations, but colostomies are usually temporary and may call for closure. In Samuel's case, his colostomy requires closure in order to restore bowel function and prevent future complications. At that time, his doctors did not manage to treat him and referred him to BethanyKids Hospital in 2018. On arrival, he was examined and admitted, as he was not in good condition. After more scans and tests, he was ultimately diagnosed with Hirschsprung’s disease. Since then, Samuel has undergone several surgeries with the aim of trying to better his condition. The first surgery failed, but the second was successful. He is now scheduled to undergo his last surgery to close the colostomy so that he can pass stool on his own again and live a more active life. Earlier in his treatment, Samuel's parents had enrolled in the national health insurance program (NHIF), which helped them pay for most of his hospital bills. BethanyKids also chipped in on occasion to help with some of the bills. Unfortunately, for his last surgery, NHIF has rejected the request since he is beyond the age to be covered by his mother’s insurance. Our medical partner, African Mission Healthcare Foundation, is helping him to undergo treatment and needs $1,084 to cover the cost of a colostomy closure for Samuel. The surgery is scheduled to take place on November 11th and, once completed, will hopefully allow him to live more comfortably and confidently. Samuel’s Mother says, “For years now, I have been very worried about my son, but God has seen us through.”
Noah is a young boy from Ngarenanyuki, a small village in the rural parts of Arusha, Tanzania. He is a member of a big family with seven siblings. His father is a livestock keeper and at their home, the young children are responsible for helping around with light house chores. In 2021, Noah was in the kitchen with some of his siblings, and he accidentally fell into a pot of boiling water. He was badly burnt on his left side of the elbow near the chest. His parents provided first aid to Noah, because they live in a remote area, and it was hard for them to get to the nearest hospital. Noah’s wounds healed eventually, but left him with a burn scar contracture. The contractures tighten the skin around the burn area, and it is difficult to move his arm. Noah came to our center during a medical camp and was assessed to find out if he was fit for the required treatment to help with the burn scar contracture. Noah's parents cannot afford treatment and are appealing for help. Fortunately, our medical partner, African Mission Healthcare Foundation, is helping Noah receive treatment. On October 12th, surgeons at their care center will perform a burn contracture release surgery to release the tightening and help him move his hand easily. Now, he needs help to fund this $874 procedure. Noah’s mother says, "I was worried that that my boy will grow up with that deformity but with what I have seen here, he is going to be better.”
Meet Venesa, a beautiful two year old girl. She was born at home with a swelling at the lower part of her back, and with legs that were not straight like other babies their family knew. The day after she was born, Venesa's parents took her to the hospital, where she was diagnosed with spina bifida and clubfoot. The family was advised to wait until Venesa turned nine months old, before having her undergo the surgery that she needs. Although surgery was deemed urgent, when Venesa was finally old enough, her parents couldn't afford to pay for it. Then, about a year ago, Venesa was diagnosed with hydrocephalus. Venesa's mom shared that shortly after this last diagnosis, Venesa's father abandoned the family and is not involved in helping support them any more. Venesa's mother used to work at a salon, but after Venesa's birth, she has been unable to work. They are now living with Venesa's grandmother, who does what she can to help. Without surgery for her spina bifida, Venesa risks paralysis of her lower limbs, infection of the exposed nerve tissue, and developmental delays. Our medical partner, African Mission Healthcare Foundation, is requesting $1,151 to cover the cost of Venesa's spina bifida closure surgery. The procedure is scheduled to take place on September 14th, at BethanyKids Kijabe Hospital. This procedure will hopefully spare Venesa from the risks associated with her condition, allowing her to experience a strong and healthy life. Venesa’s mother says: “Since she was born, I have no peace knowing that I can’t afford her treatment.”
Naw Ywa is a 29-year-old woman who lives with her husband, sister-in-law, and three nieces in a refugee camp in Thailand. Naw Ywa is a homemaker, and she weaves and sells traditional Karen clothing in her spare time. Her husband also works as a homemaker and cares for his sister, who has a mobility impairment. Naw Ywa's three nieces all currently attend school in the refugee camp. This past March, Naw Ywa began to experience severe pain in her left pelvic area. This pain was accompanied by fatigue, dizziness, and trouble breathing. Although she did seek medical attention at the hospital in the refugee camp, she was only given painkillers, which temporarily alleviated her symptoms. After a few months of repeatedly being readmitted to the hospital without fully treating her condition, a doctor referred Naw Ywa to our medical partner's care center, Mae Sariang Hospital (MSH). On July 6th, she was brought to MSH and received an ultrasound. Her doctor diagnosed her with adenomyosis, a condition that occurs when the tissue that typically lines the uterus grows into the muscular wall of the uterus. She was also diagnosed with a five cm large myoma, which is a tumor that develops in or around the uterus. Her doctor has advised that she undergo a hysterectomy to remove her uterus and alleviate her symptoms. Our medical partner, Burma Children Medical Fund, is requesting $1,500 to fund Naw Ywa’s total abdominal hysterectomy. The procedure is scheduled to take place on August 17th. Once completed, she will hopefully be able to live more comfortably and confidently. Naw Ywa shares, “Me and my husband want to have children, but we agreed with the doctor’s plan. I do not want to experience this pain anymore, and my husband also does not want to see me in pain.”
Nancy is a bright and social 12-year-old student from Tanzania. She is the youngest in a family of three children. Her and her siblings are being raised by their grandparents with the help of amazing well-wishers, since their grandparents are older and appreciate the extra help. Nancy currently attends primary school, and her favorite subjects include Swahili, mathematics, and social studies! She is very friendly and loves to play netball with her schoolmates. However, playing is becoming increasingly difficult due to her condition. Nancy has clubfoot of the left foot. Clubfoot is a condition where the foot is twisted out of shape, which causes difficulty walking and even wearing shoes. Fortunately, Nancy and her family traveled to visit our medical partner's care center, Arusha Lutheran Medical Centre. There, surgeons will perform clubfoot repair surgery on July 15th. Our medical partner, African Mission Healthcare Foundation, is requesting $935 to fund Nancy's clubfoot repair. After treatment, she will be able to walk easily. Her grandmother says, "Nancy and her siblings have been in my care since they were babies. We struggle to raise them. That's why well-wishers help. Unfortunately, they can’t help her with her treatment. Please help us."
Naw Mu is a 44-year-old mother of two children from Burma. She lives with her daughter and son. Her daughter goes to school, while her son stays home with her. Naw Mu used to work as a day laborer, but stopped working last year when her health began to decline. Since then, her sister, who works as a pastor, has supported the family. In the summer of 2018, Naw Mu was tying sheafs of freshly harvested paddy when she experienced a sudden shooting pain in her abdomen and chest, along with other uncomfortable symptoms. From then on, she experienced abdominal pain whenever she worked hard or lifted something heavy. For the next four years, Naw Mu visited many clinics and hospitals, and was finally diagnosed with an umbilical hernia and high blood pressure. She experiences dizziness, nausea, and abdominal and joint pain. She also has little appetite, and has difficulty sleeping or sitting for long periods of time. Fortunately, our medical partner, Burma Children Medical Fund (BCMF), is helping Naw Mu access treatment. On April 8th, she will undergo hernia repair surgery at BCMF's care center. Now, she needs help raising $991 to fund her procedure and care. After recovery, hopefully her symptoms will subside and she can live comfortably. Naw Mu shared, "I was so happy when I heard that I have donors who could assist with the cost of my surgery! I really want to say thank you to the donors and everyone who helped me search for a donor."