Solomon joined Watsi on November 29th, 2017. One year ago, Solomon joined our Universal Fund, supporting life-changing treatments for a new Watsi patient every month. Solomon's most recent donation supported Loveness, a future doctor from Tanzania, to find clubfoot treatment so she can walk easily and go after her dreams.
Solomon has funded healthcare for 22 patients in 8 countries.
Solomon has funded healthcare for 22 patients in 8 countries.
Loveness is a charming, friendly and smart girl who is currently in the 8th grade. She is a charismatic girl who makes friends easily. Loveness wishes to be a doctor in the future, and she is already working hard towards fulfilling her dreams. Her best subjects are mathematics, science, biology, and physics. She says English as a subject is giving her a hard time, but she is determined to keep improving. She enjoys drawing and painting in her spare time. Loveness lost her mother when she was just two years old. After her mother passed away, her aunt on her mother’s side decided to take Loveness and raise her as her own daughter because, she shared, the father had a hard time managing by himself. Loveness has clubfoot of her right foot. Clubfoot is a condition in which the foot is twisted out of shape. This causes difficulty walking and even wearing shoes. Fortunately, Loveness traveled to visit our medical partner's care center, Arusha Lutheran Medical Centre. There, surgeons will perform clubfoot repair surgery on June 7th. Our medical partner, African Mission Healthcare Foundation, is requesting $935 to fund Loveness's clubfoot repair. After treatment, she will be able to walk easily. Loveness says, “I wish I could have my foot treated so that I can walk normally.”
Gordon is a six year old boy, living with his parents and two younger siblings in a one roomed house in the Korogocho area of the capital city. His mother is a homemaker, while his father works as a vendor. Gordon was born with multiple birth conditions, including spina bifida, and hydrocephalus, as well as bilateral clubfoot. Currently, he cannot stand or walk - or wear shoes - and he has to crawl every time he wants to move about. At a visit to a mobile health clinic, it was determined that Gordon needs surgery to correct his feet. His family cannot afford the estimated hospital bill, and is requesting help to cover the costs so he can get the care he needs. Fortunately, Gordon's family traveled to our medical partner's care center, AIC Cure International Hospital. There, surgeons will perform clubfoot repair surgery on May 30th. Our medical partner, African Mission Healthcare, is requesting $1,286 to fund Gordon's surgery and care. After treatment, Gordon should be able to put on shoes, to stand, and to walk. “I would request the donors to help my son undergo surgery. My desire is to see him grow up like other children,” Gordon’s mother told 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."
Aljahnie is a four-year-old boy from the Philippines. He loves to play with toy cars, to sing nursery rhymes, and to listen to songs. His mother is a stay-at-home mom, and his father is a jeepney driver. Despite working hard, they are unable to finance his medical needs. Aljahnie was born with an anorectal malformation, a congenital abnormality that leads to a complete or partial intestinal blockage. He needs to undergo a series of procedures to eliminate bowel dysfunction. Aljahnie is scheduled to undergo surgery to correct his condition on March 17th. Our medical partner, World Surgical Foundation Philippines, is requesting $1,279 to cover the total cost of Aljahnie's procedure and care. After his recovery, Aljahnie will no longer experience bowel dysfunction or be at risk of developing health complications in the future. "By the grace of God, and extra caution, we hope that his condition will be much better after this treatment. We are very grateful to World Surgical Foundation and WATSI for helping us," shared Aljahnie’s mother.
Naw Eh is a 18-year-old woman from who lives with her family in a refugee camp in Thailand. Naw Eh moved to the refugee camp in 2019 from across the Burma border with hope to continue her education as her village only offered primary school. In 2020, Naw Eh met and married her husband in the refugee camp. Unable to work currently, every month, Naw Eh's household receives 770 baht (approx. 26 USD) to meet their daily needs. In her free time, Naw Eh likes to embroider traditional Karen clothes which she sells to earn more for their family. Naw Eh is currently expecting her second child, and doctors recommend that she deliver via a caesarean section (C-section) as Naw Eh was diagnosed with eclampsia. Eclampsia is a rare, but serious condition where high blood pressure results in seizures during pregnancy. The doctors at Mae Sariang Hospital believe a C-section will ensure the safety of both mother and child. Our medical partner, Burma Children Medical Fund, is helping Naw Eh undergo a C-section on February 10th. This procedure will cost $1,500, and Naw Eh is seeking support to fund this potentially life saving surgery for her and her baby. Naw Eh said: “I stopped weaving and embroidering clothes because my stomach is getting bigger making it hard to do. I am excited to have my second baby.”
Vicheka is the eldest of two children in her family and loves her younger sister who is three years old. Their family lives in Preah Vihear near the Thai border of Cambodia. Her father is a soldier and her mother is a potato farmer. At school, she is fond of math and Khmer literature and would like to be a teacher when she is older. She likes reading books, painting, playing with her little sister, and taking walks with her parents. When Vicheka was five, she was diagnosed with scoliosis of the spine—a sideways curvature of the spine that most often is diagnosed in adolescents. She has uneven shoulders, a bump in her lower back, difficulty standing up straight, and shortness of breath. It has become difficult for her to breathe, she tires easily, and she is having difficulty walking. This can be very difficult for young girls, they are often hidden at home because other children make fun of the way they look. A neighbor told her parents about our medical partner Children's Surgical Centre, so they traveled over 10 hours for a diagnosis and surgery. Surgeons plan to put in expanding rods along her spine. The expanding rods will allow her to grow and keep her spine from curving further, which could cause her more health problems if left untreated. Their family needs $1,500 for the surgery, which will cover medications, implants, and post-operative care. Vicheka said, "I hope the doctors can fix my spine so I can play with my friends and my back will be straight. I want to continue in school but it is hard for me to keep up, and I miss school."
Mu is a 17-year-old boy who lives with his sister in Mae Sot, Thailand. Before that, he lived with his parents, one older sister, two younger brothers and one younger sister in a refugee camp. His sister works at a non-governmental organisation helping others in need. Around mid-August, Mu woke up one morning with pain in his left knee. At first he thought that the pain would go away on its own and that it was nothing serious. However, when the pain remained a few days later, he told his sister about it. His sister bought him a type of Burmese pain reliever balm to apply on his knee. He applied the balm for a week, but he did not feel any better. When he and his sister noticed that his left knee had become slightly swollen his sister called their father. Mu’s father told them that it could be an ulcer and suggested that they go to a hospital or buy him pain medication to reduce swelling. His sister bought the medication their father had suggested at a pharmacy, and Mu took it for a week. However, he did not feel better, and the swelling did not decrease. Mu was able to have an MRI at Chiang Mai Hospital and now the doctor recommends he undergo surgery to remove a tumor on his left knee. Mu sought treatment through our medical partner, Burma Children Medical Fund and is now scheduled to undergo mass removal surgery on December 17th. He is requesting $1,500 to cover the total cost of his procedure and care which will enable him to get off of using crutches and back to feeling well again. Mu said, "After I heard from the doctor that my leg does not need to be amputated, I feel so happy."
Petro is a young student and the last born to his mother, who has six children. Petro is a bright student and is currently in the second year of his primary school education. Petro was diagnosed with a condition called bilateral genu varus, in which his legs bow outward at the knee. This condition is typically caused by an excessive accumulation of fluoride in the bones, which often stems from contaminated drinking water. As a result, he experiences pain and discomfort after walking for a while. Fortunately, on November 18th, Petro will undergo corrective surgery with our medical partner, African Mission Healthcare (AMH). This treatment will help restore Petro's mobility and allow him to participate in various activities, as well as significantly decrease his risk of future complications. AMH is requesting $880 to fund Petro's procedure. Petro shared, "I would like to be able to walk without difficulty and be able to play with my friends."
Malaso is a six-month-old baby girl and the youngest child in a family of three children. Her mother stays home with the children and her father is the sole breadwinner of their family. He sells maize and beans to provide for the family. A few days after Malaso was born, she was diagnosed with an anorectal malformation. She cannot pass stool and needs a needs a colostomy, or a procedure where the end of the colon is brought through an opening in the abdominal wall. Fortunately, our medical partner, African Mission Healthcare (AMH), is helping Malaso to receive treatment. On October 14th, she will undergo a colostomy at AMH's care center. Once complete, Malaso will hopefully be able to live more comfortably and confidently. Now, she and her family need help raising $1,152 to fund her procedure and care. Malaso’s father shared, "it has been hard for us to raise the transportation fees to the hospital for her treatment. It was a big blow for us financially when she developed a complication during her first surgery."
Samiri is a four-year-old boy and the only child of his single mother. His father is married to another woman and has two other children. Samiri's mother provides for their family through her work as a tailor. Samiri has not started school yet, but his mother would like to enroll him in kindergarten next year. Her hope is that Samiri's condition will be treated before he joins school. Samiri has been diagnosed with bilateral Genu Varus, which means that his legs are angled inwards at the knees. This condition is typically caused by an excessive accumulation of fluoride in the bones, which often stems from contaminated drinking water. As a result, Samiri has difficulty walking. Our medical partner, African Mission Healthcare (AMH), is requesting $880 to fund corrective surgery for Samiri. The procedure is scheduled to take place on September 14th. Treatment will hopefully restore Samiri's mobility, allowing him to participate in a variety of activities and greatly decreasing his risk of future complications. Samiri’s mother shared, "I can never find the money needed to cover my son’s treatment cost. I am struggling to even put food on the table for my son. Please help him."
Shallet is a humble and jovial three-year-old girl. She's the third child born in a family of four children and her parents are teachers. Shallet has hydrocephalus, spina bifida, and clubfoot of both feet. She has visited local hospitals since birth for treatments, and began casting for clubfoot when she was four weeks old. Her condition causes her difficulty walking and even wearing shoes. Fortunately, Shallet traveled to visit our medical partner, African Mission Healthcare (AMH), for treatment. At AMH's care center, surgeons will perform clubfoot repair surgery on August 18th and now, AMH is requesting $1,286 to fund Shallet's clubfoot repair. Her parents shared that they hope that the treatment will be of great impact to Shallet because she will be able to wear shoes and walk with ease. Shallet's father shared, “we have high hopes for Shallet and it is our joy to see her excel in life and become an independent person like other girls in the society.”
Stuwart is a playful and friendly boy and the only child so far in his family. He is currently in the first grade and he loves counting numbers and drawing. Stuwart’s father works as a bodaboda taxi driver to be able to support and care for his family. They shared that his income is not much but it helps them make ends meet. Stuwart was diagnosed with genu valgus. His legs bow inward so that his knees touch and rub against each other when he walks. This condition is typically caused by an excessive accumulation of fluoride in the bones, which often stems from contaminated drinking water. As a result, he is having a hard time walking and is experiencing pain. Our medical partner, African Mission Healthcare, is requesting $880 to fund corrective surgery for Stuwart. The procedure is scheduled to take place on July 15th. Treatment will hopefully restore Stuwart's mobility, allow him to participate in a variety of activities, and greatly decrease his risk of future complications. Stuwart’s mother says "We've tried to seek treatment for our son but all our efforts have not been successful despite trying to get national insurance. We are either to pay with what we don't have or wait for one year. Please help."