Manivanna joined Watsi on August 15th, 2016. Six years ago, Manivanna joined our Universal Fund, supporting life-changing treatments for a new Watsi patient every month. Manivanna's most recent donation supported Yoon, a beautiful 12-year-old girl from Burma, to fund an Achilles tendon lengthening procedure so that she can walk again.
Manivanna has funded healthcare for 71 patients in 11 countries.
Manivanna has funded healthcare for 71 patients in 11 countries.
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.”
John is a young student from Haiti who lives with his mother and two older brothers in a neighborhood of Port-au-Prince. He already loves going to kindergarten and enjoys playing with puzzles. John has a cardiac condition called double outlet right ventricle meaning the major arteries connect to the heart in an abnormal location making it difficult for blood to properly flow through his body. Unfortunately the treatment John needs to heal is not available anywhere in Haiti. So, John is flying to the Cayman Islands to receive cardiac surgery. On May 25th, surgeons will detach the arteries from John's heart and reconnect them in their anatomically correct locations. Have a Heart Cayman is contributing $17,000 to pay for this surgery. Our medical partner, Haiti Cardiac Alliance, needs $1,500 to help John's family cover labs, medicines, and follow-up appointments. It also supports passport obtainment and the social workers from Haiti Cardiac Alliance who will accompany John's family overseas. John's mother shared, "Our family all looks forward to our son having a more normal life after this surgery!"
Rehiwilzahra is a sweet toddler from Haiti. She lives in Port-au-Prince with her mother, father, and three older siblings. Rehiwilzahra likes watching cartoons and playing with her older siblings. Rehiwilzahra has a cardiac condition called Tetralogy of Fallot. This heart condition involves several related heart defects including a hole between the two lower chambers of the heart, and a muscular blockage of one of the valves. These defects prevent blood from circulating properly through the lungs leaving Rehiwilzahra weak and short of breath. The surgery Rehiwilzahra needs to heal is not available in Haiti, so she will need to fly to the Dominican Republic to undergo cardiac surgery to close the hole in her heart with a patch and remove the blockage from her valve. Our medical partner, Haiti Cardiac Alliance is helping Rehiwilzahra's family raise $1,500 to cover the cost of labs, medicines, and follow-up appointments. This amount also supports passport obtainment and the social workers to accompany Rehiwilzahra's family overseas. Rehiwilzahra's mother shared, "We have been praying for a long time for a solution to our daughter's heart problem. We are very thankful to everyone who is helping her!"
Khoem is a loving grandmother and a widow with two sons, two daughters, and several grandchildren. Her husband passed away several years ago, so she lives with her youngest daughter, who works in a local factory and supports her mother. Over the past several years, her greatest joy is playing with her grandchildren when they come to visit. Due to her age, she mostly stays home and listens to the radio. Earlier this month, Khoem tripped in her house and fell, fracturing her left hip. Although she experienced a lot of pain and was not able to walk, she did not seek any medical help because she was worried she could not pay. A relative visited her and suggested she go to Children's Surgical Centre (CSC) for diagnosis and treatment. She is in constant pain and cannot walk so is using a wheelchair to get around. Fortunately, Khoem took her relatives advice and came to CSC. There surgeons can perform a surgery to relieve Khoem of her pain and allow her to walk more easily again. Her treatment is scheduled for March 15th, and Khoem needs help raising $1,087 to pay for this procedure. "I hope that I can walk without pain, and play with my grandchildren again," shared Khoem.
Yousos is a 26-year-old rice farmer who is married with has a four-year-old son and an eight-month-old son. Yousos enjoys reading and playing chess. In May 2019, Yousos was in a motor vehicle accident that caused a right hip fracture. Yousos sought treatment at a local hospital and was diagnosed with avascular necrosis. Yousos was also seen by a Khmer traditional healer, but his hip pain has persisted. Now Yousos's hip pain is so great, he can no longer walk. Fortunately, a neighbor told Yousos about our medical partner, Children's Surgical Centre (CSC). At CSC, surgeons can perform a total hip replacement to relieve Yousos of his pain and allow him to walk easily. CSC is helping Yousos raise the $1,087 to cover the cost of the procedure scheduled for February 16th. Yousos is now hopeful to be more active and feel well again. He shared, "I hope I can walk easily again without pain."
Margaret is a 41-year-old who works jobs she can find in her neighborhood. She hails from Baringo County in Kenya and is married with 8 children aged between 26 and three years old. Together with her husband, they work on their farm and other people's farms to earn a living. They also get their school fees for their kids from this work. Their family lives in a grass-thatched house. Fifteen years ago, Margaret began to experience troubling symptoms, including a neck swelling that has continuously grown over the years. Before she was seen by our medical partner's doctors, Margaret had tried to seek medication from different hospitals but she could not receive treatment because of financial strain. She opted for herbal treatments, which did not improve her condition either. Her thyroid condition has affected her general well-being and she cannot carry out her day-to-day duties normally since she gets tired easily. This has affected her daily income and support for her family. Margaret attended one of the free medical camps held at Kapsowar Hospital and after examination by the doctors, an ultrasound was done. She was diagnosed with a non-toxic multinodular goiter. The doctor recommended surgery, but Margaret is unable to raise the required funds. Our medical partner, African Mission Healthcare Foundation, is helping Margaret receive treatment. She is scheduled to undergo a thyroidectomy on January 13th at our medical partner's care center. Surgeons will remove all or part of her thyroid gland. This procedure will cost $936, and she and her family need help raising money. Margaret says: "I really look forward to getting well and going back to normal so that I can work like before and support my husband in providing for our family.”
Yasin is a 9-year-old student and the third born in a family of five children. Yasin is a social, talkative, and playful boy despite his challenges in walking due to his clubfoot condition. Yasin loves math and English. When asked if there are any sports, he loves he said “I love football, but my friends play better than me because of my feet, I cannot run as fast as them. So, I lose most of the time.” Yasin’s father sells vegetables at a local market and their income is not enough to care for the family and pay for Yasin’s needed treatment cost. Yasin has clubfoot of both his feet. Clubfoot is a condition in which the foot is twisted out of shape. This causes difficulty walking and even wearing shoes. Fortunately, Yasin traveled to visit our medical partner's care center, Arusha Lutheran Medical Centre. There, surgeons will perform clubfoot repair surgery on December 14th. Our medical partner, African Mission Healthcare Foundation, is requesting $935 to fund Yasin's clubfoot repair. After treatment, He will be able to walk easily and wear shoes. Yasin’s class teacher says “I felt I had to do something because it made me very sad seeing Yasin walking around school with no shoes on. It was even worse when I realized that he also went to a pit latrine toilet with no shoes on something that is a danger to his health. Please help him.”
Joven is a 14-month-old boy from Haiti who is very loved by his family. Joven 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, Joven has been experiencing growth in his head and without treatment, Joven will experience severe physical and developmental delays. Our medical partner, Project Medishare, is requesting $897 to cover the cost of surgery for Joven at Hospital Bernard Mevs that will treat his hydrocephalus. This is the only site in the country where this care is currently available and the procedure is scheduled to take place on November 19th. This critical treatment will drain the excess fluid from Joven's brain to reduce intracranial pressure and greatly improve his quality of life. With proper treatment, Joven will hopefully develop into a strong, healthy young boy. Joven's mom states, "I have been so worried ever since I learned of his diagnosis. The first time I began to have hope was when I heard WATSI may be able to help Joven have surgery."
Kolongo is a 17-year-old student and the oldest child in a family of six children. He is currently in class five in school and his best subjects are Swahili and math. Kolongo is hard-working both at school and home. He helps his parents with farm work when he is not at school. Kolongo’s parents are small-scale farmers of maize, cassava, and sorghum. They depend entirely on what they harvest for food and his father also seeks day laboring jobs to supplement the family's income. Kolongo was diagnosed with right genu valgus, which means that his right leg is bowing inward 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 of his condition, walking to school and other daily activities are difficult. Fortunately, our medical partner, African Mission Healthcare (AMH), is helping Kolongo to receive treatment. On October 8th, he will undergo corrective surgery at AMH's care center. Treatment will hopefully restore Kolongo's mobility, allowing him to participate in a variety of activities and greatly decreasing his risk of future complications. Now, AMH is requesting $880 to fund his procedure and care. Kolongo shared, "walking long distances is a challenge and carrying out my daily life activities, like working on the farm and carrying anything heavy causes me pain. I will be happy if I have my leg corrected."
Nehemia is a nine-year-old child from Tanzania and the fourth born in a family of five children. She is currently in kindergarten and she loves singing the vowels. Nehemia's parents keep livestock for a living and sell the milk. Once in a while, they also sell a goat to make additional money. Nehemia has clubfoot of her left foot. Clubfoot is a condition in which the foot is twisted out of shape. This causes difficulty walking and even wearing shoes. Fortunately, Nehemia traveled to visit our medical partner, African Mission Healthcare (AMH), to receive treatment. On September 14th, surgeons at AMH's care center will perform clubfoot repair surgery. Now, AMH is requesting $935 to fund Nehemia's clubfoot repair. After treatment, she will be able to walk easily. Nehemia’s father shared, "every day when she gets home from school she complains of pain and you can easily see she is trying not to put pressure on the foot due to fear of pain. Please help my daughter."
Elsa is a 9-year-old boy from Ethiopia. He loves to play football with his dad and other kids. He is the first born in a family of three. His father is a daily laborer and his mother takes care of their house and family. Elsa and his family live in a rented house. Their family shared with us that Elsa does not go to school because his father hides him from the community for fear of gossip and stigma due to his birth condition. His parents are highly affected psychologically as a result of his affliction. His father is planning to send him to school in September after his surgery and recovery. Elsa was born with hypospadias, a congenital abnormality. Without treatment, he will continue to experience uncomfortable symptoms and will be at risk of infertility. Elsa had his first stage of hypospadias repair surgery in January and is now planned for a second stage surgery. He will be healthy and active after this treatment. Elsa is scheduled to undergo corrective surgery on August 31st. Our medical partner, African Mission Healthcare Foundation, is requesting $1,293 to cover the total cost of his procedure and care. His father said, “I hope my child goes to school after the treatment. I hope he will mingle and play with other children and that will make him happy, break his isolation, and resolve the tension in his mind. If God wills he will be a doctor.”
Srey Pov is a 22-year-old factory worker from Cambodia. She has two brothers and two sisters. Srey Pov has been married for three years and her husband is a tractor driver. Together, they have one son. In March, Srey Pov was in a motor vehicle accident that caused paralysis of her left arm. She has been diagnosed with a brachial plexus injury. The brachial plexus is a nerve network that transmits signals from the spine to the shoulder, arm, and hand. Injuries to this nerve network can result in loss of function and sensation. She is unable to lift her left arm and she cannot work. Our medical partner, Children's Surgical Center (CSC), is helping Srey Pov receive treatment. She traveled to CSC's care center where, on June 14th, she will undergo brachial plexus repair surgery. After recovery, she will be able to use her arm again. Now, she needs help to fund this $696 procedure. Srey Pov shared, "I hope I can use my arm again so I can return to work at the garment factory and do my housework."