Zaimah joined Watsi on March 12th, 2013. Five years ago, Zaimah joined our Universal Fund, supporting life-changing treatments for a new Watsi patient every month. Zaimah's most recent donation supported Seladin, five-month-old girl from Ethiopia, to fund a anorectal malformation surgery.
Zaimah has funded healthcare for 61 patients in 12 countries.
Zaimah has funded healthcare for 61 patients in 12 countries.
Teltila is a lively five-month-old girl from Ethiopia and a sibling to an older brother and sister. She is sociable, loves to play with her mom, and enjoys it when her mom talks to her. Her dad is physically impaired and unable to move around easily. He sells candies and some sweets on the street for a living and her mom is a housewife raising their three kids. His income is not enough to maintain the family but fortunately, they are supported by a foundation in their town that works with people with impairments. Teltila was born with a birth condition called anorectal malformation, a congenital abnormality that leads to a complete or partial intestinal blockage causing pain and complications. She developed bowel obstruction because of her condition and an emergency colostomy, one of the series of procedures needed to eliminate the condition, was done for her at our medical partner's care center, BethanyKids Myungsung Christian Medical Centre (BKMCM). She has had multiple issues with her colostomy care and associated complications and as a result, she continues to feel significant discomfort. According to her mother, Teltila had her first surgery when she was 45-days-old and unfortunately, the second surgery was delayed due to finances. The money they saved could only cover doctor reviews and some level of surgical fees. After getting an appointment, her bag was stolen with all the money and documents at a bus stop. Teltila's mother was devastated and did not know what to do. She heard of a charitable organization that supports the poor and went there to share her story. Teltila is scheduled to undergo surgery to correct her condition on August 12th. Our medical partner, African Mission Healthcare Foundation, is requesting $1,500 to cover the total cost of Teltila's procedure and care. After her recovery, she will no longer experience bowel dysfunction or be at risk of developing health complications in the future. Teltila's mother says, "I am now so thankful. I lost all I had and I just received it back through you all. I hope my daughter will be treated."
Prince is a three-year-old boy from Kenya and the fifth born in a family of six children. Prince's mother works as a vendor and separated from Prince's father after he was born. Prince has an abnormal gait and limps when he walks. His mother shared that he has had the condition since birth and feels it may have started when, unfortunately, the doctor dropped Prince during her Caesarian delivery. Fortunately, our medical partner, African Mission Healthcare (AMH), is helping Prince receive treatment. He is scheduled to undergo a proximal fibular osteotomy on June 14th at AMH's care center. After surgery, his gait will improve and he will be able to walk to school and continue with his studies. Now, their family needs help raising $1,224 to fund the procedure. Prince's mother shared, “I am appealing for help from well-wishers, I would like to see my son walking well like other children and continuing with life normally."
Joana is a 50-year-old primary school teacher from Malawi. She teaches a class of more than 80 children. She shared that she loves teaching because it makes her feel young and energetic. Joana is also a mother of two children of her own, ages 29 and 27. In March 2021, Joana visited a local clinic for a routine check-up and was diagnosed with a uterine mass. A total abdominal hysterectomy, or a procedure where both the uterus and cervix are removed, was recommended as treatment. If her condition is not treated, Joana is at risk of becoming severely anemic. After the surgery, it is expected that Joana will no longer experience the uncomfortable symptoms associated with her condition. Fortunately, our medical partner, African Mission Healthcare (AMH), is helping Joana to receive treatment. On June 5th, surgeons at AMH's care center will perform a hysterectomy. Now, Joana needs help to fund this $1,363 procedure. Joana shared, “I will soon be a grandmother and I want to be in good health so I can play with my grandchildren the way I play with learners at school. I appreciate your support to have this uterine mass removed."
Phat is a 40-year-old factory worker from Cambodia. She has one son and one daughter. Phat works in a garment factory in the Kompong Cham province. In her free time, Phat enjoys cooking food for her children at home. In May 2013, Phat fell hard on the ground while walking and injured her ankle. She has felt consistent right ankle pain since that accident. Over time, it has worsened, and in the last year her ankle has become very stiff. She cannot walk well and is in pain. Fortunately, surgeons at our medical partner, Children's Surgical Centre, can help. On March 31st, Phat will undergo a fracture repair procedure, which will cost $465. With this procedure, she will be able to walk again without pain. Phat shared, "I hope after the surgery I am in less pain and the wound heals quickly so I can return to working at the factory and caring for my children." Phat's husband also shared, "I do worry about my wife's ankle, and I hope that after surgery she has no more pain."
Sabato is a 3-year-old boy and the only child of his father who is unwell and raising him alone. As a result, Sabato was left in the care of his grandparents. His grandparents are elderly and depend entirely on small-scale farming. They shared that at their age, raising Sabato was not easy, but through the help of their other children, they are able to make ends meet. Sabato was diagnosed with bilateral genu varus, or knock knees. When Sabato reached two years of age, his grandparents noticed his legs were curving outwards, but they thought it was normal rickets that he would outgrow with time. The condition Sabato has is typically caused by an excessive accumulation of fluoride in the bones, which often stems from contaminated drinking water. Due to his condition, Sabato struggles to walk, to play with his fellow children, and use the bathroom comfortably. Our medical partner, African Mission Healthcare, is requesting $880 to fund corrective surgery for Sabato. The procedure is scheduled to take place on April 20th. Treatment will hopefully restore Sabato's mobility, allow him to participate in a variety of activities, and greatly decrease his risk of future complications. Sabato’s aunt shared, "I really wanted to help my nephew after seeing how much he was suffering, but didn’t expect that the treatment cost would be this expensive. I have no source of income, and his father is dependent on our parents who are also old. Please help to correct my nephew's legs."
Daw Mya is a 59-year-old woman from Burma. She lives with her daughter, granddaughter, son, daughter-in-law, and grandson in Yangon, Burma. Daw Mya is currently too ill to work, but her daughter works as a seamstress in a factory. Her granddaughter goes to school, her son is a taxi driver, her daughter-in-law looks after their son at home. Her daughter and her son both help look after Daw Mya and try to support her as best they can. Daw Mya was diagnosed with a heart condition that involves a malformation of the mitral valve, the valve between the left atrium and left ventricle. This valve controls the flow of blood, but certain conditions may cause blood to flow backward or the valve to narrow. Currently, Daw Mya feels tired and experiences heart palpitations with chest pain. She has no appetite and cannot sleep well at night, and both of her legs are swollen. Our medical partner, Burma Children Medical Fund, is requesting $1,500 to fund a mitral valve replacement for Daw Mya. The treatment is scheduled to take place on February 21st and, once completed, will hopefully allow her to live more comfortably. Daw Mya said, “I want to get better soon so that I can help my family. I want to help them because my daughter-in-law is always looking after me and her child [my grandson], so she cannot work. If I can look after the household chores and take care of the family, they can go to work and earn more income for our family. I cannot go anywhere because of my condition. They always take care of me and they spend too much of their money on me.”
Jue is a 25-year-old woman who lives with her family in a village in Hmawbi Township, Yangon Division, Burma. Her parents are housekeepers, and her youngest brother is a first-year university student who has been seeking work. Jue used to run a beauty salon, but had to stop working four months ago when her health deteriorated. In her free time, Jue likes to watch the news and videos relating to her work at the beauty salon. She also likes to read books and wants to write a book of her own someday. In August 2020, Jue felt pains in her stomach and chest. She would also experience difficulty breathing sometimes, and she would feel tired when she walked for a longer period of time. Jue went to the clinic in her village, where she received oral medication, but she did not feel better after taking it. She returned to the clinic several times over the course of two months, but her condition continued to worsen – the chest pain, difficulty breathing and feeling of fatigue happened more often. Jue decided to go to another clinic in North Okkala Township in Yangon in November 2020. At the clinic, the doctor listened to her heart with a stethoscope, and informed her that she has a congenital heart condition. The doctor recommended she receive a blood test, an echocardiogram (echo) and an electrocardiogram (ecg) at a hospital. After visiting a hospital to receive those tests, the doctor there told her that she was born with a hole in her heart and that she might need to receive surgery at the general hospital. However, the cost of surgery was too high. Luckily, Jue crossed paths with another former patient and was referred to Watsi's Medical Partner Burma Children Medical Fund (BCMF) to seek assistance with accessing treatment. Fortunately, surgeons at our medical partner can help. On January 24th, U Win will undergo an atrial septal defect closure procedure. Once recovered, her quality of life will significantly improve and she will be able to return to working at her beauty salon. Now, our medical partner, Burma Children Medical Fund, is requesting $1,500 to fund this procedure. Jue shared, “I want to get better as quickly as possible and go back to work. I’m worried about my younger brother. He doesn’t have a job, and he needs to graduate from university. I’m also worried about Covid-19 because nobody has a job right now.”
Khaing is a 27-year-old woman from Thailand. She lives with her husband and a three-year-old son in a village in Tak Province. Originally from Karen State, Burma, they moved to their current home three years ago in search of better job opportunities. Her husband is a day laborer and she is homemaker. Ten years ago, Khaing started feeling like her nose was blocked and that she could not breathe well. She also had a runny nose and saw a small mass in her nostril while looking at her reflection in the mirror. At the time, Khaing did not go to see a doctor because she could not afford to pay for treatment, and she thought that she would feel better over time. However, four years ago she noticed that the mass had grown. Khaing went to her local hospital in Burma, where the doctor confirmed she had a mass in her nostril and gave her medication for a week. She did not go back to her follow-up appointment as she had run out of money. She then tried to treat herself with traditional medicine unsuccessfully as the mass continued to increase in size. In the beginning of May 2020, Khaing developed a severe headache and pain in her nose. The area around her nose also became swollen. She went to Mae Tao Clinic for treatment, where the medic found large masses in both of her nasal cavities. She was then taken to Mae Sot Hospital (MSH) for further investigation. At MSH, she received an x-ray of her nose and the doctor told her that the masses were large and surrounded by a lot of pus. After a CT scan, the doctor diagnosed her with a nasal polyp and scheduled her for surgery on December 28th, 2020. Currently, the area around her nose is swollen and painful. Her nostrils feel itchy, her nose is blocked, and has to breathe through her mouth. She still has a headache, though since she received pain medication from the doctor at MSH, this has been less severe. Fortunately, surgeons at our medical partner can help. On December 28th, Khaing will undergo an endoscopic sinus surgery. Once recovered, she will be able to breathe normally again and her quality of life will significantly improve. Now, our medical partner, Burma Children Medical Fund, is requesting $1,500 to fund this procedure. Khaing shared, "I really want to have surgery and feel better. I am not scared because I believe that the surgery will help me be free from headaches and breathe well again."
Byamugisha is an Ugandan subsistence farmer who mostly grows tomatoes, green papers, and cabbages to earn a living. He is a father to five children: two boys and three girls who are still at school. He says he also rears domestic animals like pigs, goats, and chickens. He operates the farm together with his wife and children. Their family lives in a muddy uncemented semi-permanent house. Byamugisha came in presenting with a bilateral inguinal swelling that he has had for almost one year. He says he feels severe pain when walking long distances, when he stands for long hours, and during other activities. He shared that he can no longer do cultivation, which is his only source of income, due to his condition. This has made him have a poor quality of life and if not treated, his condition may result in worse compilations like strangulated hernia or possibly cause intestinal obstruction. Fortunately, on April 28th, he will undergo hernia repair surgery at our medical partner's care center. Our partner, African Mission Healthcare Foundation, is requesting $219 to fund Byamugisha's surgery. Once completed, this procedure will hopefully allow him to live more comfortably and confidently. Byamugisha says, “I hope that my surgery will enable me to regain my health once again so that I can continue with farming to support my family.”
Beatrice is a young student from Kenya. She is a calm girl and the seventh born in a family of eight children. Her family hails from Mokoyon village in West Pokot County. Beatrice's father is a farmer while her mother is a housewife. They live in a one roomed grass thatched house in their village. Beatrice 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, Beatrice traveled to visit our medical partner's care center, AIC Cure International Hospital. There, surgeons will perform clubfoot repair surgery on November 23th. Our medical partner, African Mission Healthcare Foundation, is requesting $1,286 to fund Beatrice's clubfoot repair. After treatment, she will be able to walk easily, play, and wear shoes like the other children she knows. “We are requesting for support so that her foot can be corrected and she can continue with her normal life,” Julius, Beatrice’s father told us.
Teresiah is a teenage girl from Kenya who has special needs. She was born into a family of 3 girls and hails from a very humble background. Her studies Limuru Cheshire Home were partially sponsored by a compassionate organization. Since she left school last year, the organization has helped her family settle in a small two-roomed iron-built house, which is a real milestone. Her dad has a health condition that requires surgery but it has been postponed several times due to funds. Her dad cannot do heavy manual jobs and so he mostly remains at home with Teresiah while her mother goes to search for casual work. Teresiah has clubfoot that has rendered her walking difficult. She was reviewed by specialists at Cure International Hospital and surgery is recommended. The surgery will be of great impact as she will finally be able to walk comfortably and help her parents at more home. She will be able to be more independent as she grows. Fortunately, Teresiah traveled to visit our medical partner's care center, AIC Cure International Hospital. There, surgeons will perform clubfoot repair surgery on October 12th. Our medical partner, African Mission Healthcare Foundation, is requesting $1,286 to fund Teresiah's clubfoot repair. After treatment, she will be able to walk easily. “Any assistance accorded to our daughter will be highly appreciated. God bless you," Teresiah’s mom told us.
Megan is a 3-month old baby girl from Tanzania, and the only child to her single mother. Megan was born with clubfoot and spina bifida, which contributed to her acquiring hydrocephalus. Megan’s father left their family when her mother was five months pregnant and they lost any contact with him. Megan's grandmother, who was also a single mom after her husband passed away at a young age, depends on selling second-hand clothes. Her income is very limited to be able to provide for her children and be able to afford school fees. Due to this, Megan's mother was not able to continue with her studies due to financial challenges and joined her mother in selling second hand clothes. Megan 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, Megan has been experiencing an increasing head circumference. Without treatment, Megan will experience severe physical and developmental delays. Our medical partner, African Mission Healthcare Foundation, is requesting $1,300 to cover the cost of surgery for Megan that will treat her hydrocephalus. The procedure is scheduled to take place on September 21st and will drain the excess fluid from Megan's brain. This will reduce intracranial pressure and greatly improve her quality of life. With proper treatment, Megan will hopefully develop into a strong, healthy young girl. Megan’s mother says, “I have no one to run to for help and support, all my relatives have told me they can no longer support us in any way and yet my daughter is suffering. Please help save my daughter.”