Vijay joined Watsi on July 29th, 2013. Four years ago, Vijay became the 1715th member to automatically support a new Watsi patient every month. Since then, 4,743 more people have become monthly donors! Vijay's most recent donation supported Emmanuel, a 1-year-old baby boy from Kenya, to fund congenital anorectal malformation surgery.
Vijay has funded healthcare for 62 patients in 11 countries.
Emmanuel is a small baby boy from Kenya. Emmanuel’s father is a casual laborer in Kayole and sometimes goes out his way to carry luggage for people so that he can provide for his family of two children. Because of the extra care Emmanuel needs, his mother is not able to go look for work. Emmanuel 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. Emmanuel is scheduled to undergo surgery to correct his condition on August 27th. Our medical partner, African Mission Healthcare Foundation, is requesting $1,393 to cover the total cost of Emmanuel's procedure and care. After his recovery, Emmanuel will no longer experience bowel dysfunction or be at risk of developing health complications in the future. Emmanuel’s mother says, “I am very hopeful that our son will be treated.”
Alex is a 22-month-old boy from Tanzania. He is the youngest of two children. His parents depend entirely on small-scale farming for a living. Alex’s father decided to travel to neighboring Kenya to seek small jobs in order to supplement the little harvest they are able to currently get from their farm. Alex was born with spina bifida, a type of neural tube defect in which the spine does not properly close around the spinal cord. Without treatment, Alex is at risk of lower-limb paralysis, infection of the exposed nervous tissue, development of tethered cord syndrome, and possible developmental delays. Our medical partner, African Mission Healthcare Foundation, is requesting $1,063 to cover the cost of Alex's spina bifida closure surgery. The procedure is scheduled to take place on June 15th. This procedure will hopefully protect Alex from the risks associated with his condition, allowing him to grow and develop along a healthy trajectory. Alex's mother says, “I will be very happy to see my son walk by himself like his sibling. Please help us as the cost is too high for us to afford."
Win is a 49-year-old woman from Burma. She lives with her husband and four sons. Two of her sons are distant learners at university while her husband and two other sons work as masons. However, her husband had to stop working to look after the housework when she was no longer able to do so. Win was diagnosed with a heart condition that involves a malformation of her 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, Win feels tired, has no appetite, cannot sleep well nor walk longer distances. She also has a headache, chest pains, and tingling and numbness in her extremities. Our medical partner, Burma Children Medical Fund, is requesting $1,500 to fund a mitral valve replacement for Win. The treatment is scheduled to take place on March 11th and, once completed, will hopefully allow her to live more comfortably. Win said, “When I recover from my illness, I will go back to doing the housework so that my husband can also go back to work.’’
Rose is a 40-year-old woman. She is married and was blessed with six children, two sons and four daughters. Rose and her husband are not financially stable. Her husband is a Khat farmer while Rose is a small-scale farmer who plants maize and beans for home use. She sells the rest for additional income. Last year, Rose began to experience swelling in her abdomen. An x-ray revealed that she has an epigastric hernia which needs to be repaired. She explained that she cannot afford the hospital bill now because her husband's Khat business is heavily affected by the COVID-19 pandemic. Fortunately our medical partner, African Mission Healthcare, can help. They are asking for $768 to fund the cost of her surgery. Rose shared, "I am pleading for help."
Pheanith is a 19-year-old construction worker from Cambodia. Phearith and his wife have been married for two years and they have one young son. Everyday Phearith and his family go for a walk in the evening. He also likes playing football, listening to music on his phone. Two years ago, Pheanith injured the big toe on his left foot when a heavy object fell on it. He received treatment at a local hospital, but his wound did not heal. He received a second round of treatment at a local hospital two months later, but it was once again botched. The wound has become infected, and the infection is spreading through his foot. It is difficult for him to walk, and he experiences pain throughout his leg. He cannot currently work. When Pheanith learned about our medical partner, Children's Surgical Centre, he traveled for four hours seeking treatment. On May 12th, surgeons at CSC will perform a skin graft procedure to to heal his chronic wound, and help him to walk more easily again. Now, Pheanith needs help to fund this $474 procedure. Phearith said, "I want so much to finally heal this wound and walk again. My family cannot do well if I cannot work and make money, so I am excited for the surgery."
Catherine is a 17-year-old student from Tanzania, the youngest in her family of three children. She is currently in Form Four and hoping to graduate secondary school this year. She is a shy but bright young girl. Catherine’s father is a construction worker and her mother owns a shop at their home where she sells day-to-day household stuff. Catherine 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, Catherine has been experiencing headaches for the past two weeks continuously. She was originally taken to the hospital and was tested for a UTI and malaria but found to have nothing wrong. Her headaches got more severe, followed by vomiting and irritability and could not control her urination. Her family was told to do a CT scan test but the surgeons were not satisfied with the results and needed to do an MRI. The MRI showed that there is build up of CSF fluids causing pressure in her brain and the doctors shared that Catherine needs surgery as soon as possible. Without treatment, Catherine will experience severe physical and developmental delays. Our medical partner, African Mission Healthcare Foundation, is requesting $1,238 to cover the cost of surgery for Catherine to treat her hydrocephalus. The procedure is scheduled to take place on April 29th and will drain the excess fluid from Catherine's brain. This will reduce intracranial pressure and greatly improve her quality of life. With proper treatment, Catherine will hopefully develop into a strong, healthy young girl. Catherine says, “I would really like to get better and continue with school. Please help me get well.”
Abdiaziz is a child from Ethiopia. He is a beautiful baby boy. Abdiaziz has two brothers and a sister and he loves to play with his mom. Abdiaziz is exclusively breastfeeding. His father is an English teacher in a language school with a limited income while his mother is a house wife. They live in a rented house and Abdiaziz’s father's income is only enough for their basic needs. Abdiaziz 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. Abdiaziz is scheduled to undergo surgery to correct his condition on February 6th. Our medical partner, African Mission Healthcare Foundation, is requesting $1,500 to cover the total cost of Abdiaziz's procedure and care. After his recovery, Abdiaziz will no longer experience bowel dysfunction or be at risk of developing health complications in the future. Abdiaziz's mom said “I hope my child will heal completely after the coming surgeries. I believe he will lead a bright future and a quality life.”
Philomena was diagnosed with ARM at birth. With this condition, the little one was found to lack an anal opening and instead was passing stool through her vagina. A few hours after birth, Philomena, one in a set of twins, was noted to have a distended abdomen. The doctor quickly checked on the baby and discovered she lacked an anal opening. To keep Philomena from getting a fistula, the doctors put in a colostomy at three days. Philomena’s parents paid for this through some family savings they had. When they left for home, Philomena’s twin sister developed a persistent cough which was later found to be a hole in the heart. "I have never felt this drained ever in my life. Since I gave birth I am always in hospitals with either one of my two babies,” says Philomena’s mother. Due to lack of finances, Philomena’s parents shared their plight with their church members and one of them advised that they visit Watsi Partner Care Center BethanyKids Hospital. At BethanyKids a surgery to create an anal opening has been recommended. If not treated, Philomena will not lead a normal life and will be forced to use a colostomy for life. The surgery is a cost Philomena’s parents cannot bear. Philomena’s father is a carpenter while her mother closed her grocery store to tend to the children. Together they have five children with three currently in school. With very limited income and having exhausted their savings, Philomena’s parents are not able to raise the funds needed. They had defaulted on paying the national health insurance premiums as they could not keep up, but they’ve been advised to try to maintain this coverage in the future given their family's health needs. “Please help us. It is quite a stressful time for us but we believe we will come from it as victors,” says Philomena’s mother.
Witness is a student from Tanzania who is the first born child in a family of four children. She is smart, intelligent, and very hard working girl. Witness has completed her form four education and is currently waiting for her results to be able to join form five and six. She wishes to be a laboratory technician when she completes her studies and be able to support her parents and siblings. Witness’ father used to work as foreman at a construction site but after the project matured he has not been able to get any other job thus he is now forced to seek any casual day jobs to be able to support his family. The mother sells vegetables and the little income she gets she helps her husband to support her family. Witness was diagnosed with right genu varus. Her leg is bowed so that her knees cannot 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, she has difficulty walking. Our medical partner, African Mission Healthcare, is requesting $838 to fund corrective surgery for Witness. The procedure is scheduled to take place on January 24th. Treatment will hopefully restore Witness's mobility, allow her to participate in a variety of activities, and greatly decrease her risk of future complications. Witness says, “My secondary education has been really challenging for me due to my leg’s condition. If you can help correct my leg I would be able to continue with my further studies with ease without all this challenges I am going through.”
Robdu is a beautiful and playful baby girl from Ethiopia. She was born with an anorectal malformation, a birth defect where a child has an imperforate anus or they have no opening in their anus. She developed bowel obstruction because of the condition and an emergency colostomy was done. She has also had multiple issues with her colostomy care, requiring constant hospital visits. She is planned for PSARP in our facility to correct the congenital defect. Robdu and her two brothers live with their parents in Ethiopia. Her father relies on subsistence farming to make ends meet while her mother is a housewife. They do not have funds required for the surgery and so appeal for financial assistance. Robdu is scheduled to undergo surgery to correct her condition on December 31st. Our medical partner, African Mission Healthcare Foundation, is requesting $1,500 to cover the total cost of Robdu's procedure and care. After her recovery, Robdu will no longer experience bowel dysfunction or be at risk of developing health complications in the future. Her dad said, “I hope she will get well. And it is my dream to educate her and see her achieving so big in her life.”
Iqram is a young boy from Tanzania. Iqram is a two-year-old boy, the only child to his parents, who struggles to stretch his right hand due to a burn scar contractures. The playful boy was playing with his friends when he went back to his mother's house and by accident, fell on hot milk sustaining burns on his right side, especially his right hand. He spent a month in the hospital where the wounds were nursed and successfully healed. However, his right elbow skin healed with contractures. The contractures restrain Iqram's ability to fully stretch and use his hand. The family has not been able to raise funds for a contracture release surgery, but their hope for help remains. Iqram's father is a casual labourer at a factory and his mother a housewife. Their income is little to meet the treatment cost. They hope to have Iqram's hand released and be able to use it with ease especially when he joins the school. Iqram's aunt referred them to our facility when she learnt of an outreach program and upon review, he had contracture release recommended. Iqram's parents appeal for financial assistance Fortunately, our medical partner, African Mission Healthcare Foundation, is helping Iqram receive treatment. On September 27th, surgeons at their care center will perform a burn contracture release surgery to The surgery will allow Iqram to fully stretch his hand, restoring ability to utilize it. Now, he needs help to fund this $832 procedure. Iqram’s mother says, “My son’s life will be very challenging if he not able to have his hand corrected please help him."
On August 13th, after classes, Michale was playing with his friend at school. While fooling around, Michale’s friend poked him in the right eye. Right away, Michale’s eye began to hurt and his eye became watery. Eventually, he could no longer open his right eye. When he told a teacher about this, the teacher called his mother. His mother then took him back home before bringing him to Mae Tao Clinic (MTC) in Thailand, on 15th August 2019. Unfortunately, that day was a full moon Buddhist holiday in Thailand. Therefor he had to wait till the next day to have his eye examined by a medic. After checking his eye the following day, the medic gave him an ointment for his eye and painkillers. On August 20th, he was referred to Mae So Hospital for further assessment. At the hospital, the ophthalmologist checked his eye, diagnosed him corneal perforation and informed him that he will likely have to remove his right eye and referred him to Chiang Mai Hospital (CMH) for further treatment. After he came back from the hospital, Michale told the MTC medic about what the doctor had said and how he could not afford to seek further treatment in Chiang Mai. Therefore, the MTC medic referred him to Burma Children Medical Fund (BCMF) for assistance in accessing further treatment. Michale says, “I would like to become an engineer, so I would like to study engineering when I graduate from high school.”