Anton joined Watsi on April 8th, 2014. Seven years ago, Anton joined our Universal Fund, supporting life-changing treatments for a new Watsi patient every month. Anton's most recent donation traveled 8,700 miles to support Nurat, a three-week-old baby from Tanzania, to fund spine surgery to grow up healthily.
Anton has funded healthcare for 85 patients in 11 countries.
Anton has funded healthcare for 85 patients in 11 countries.
Nurat is a three-week old baby from Tanzania. She is the first child of her young parents at a local hospital in Manyara. Nurat’s mother still lives at her parents’ home while her father lives at a rented house. Before Nurat's birth, her mother sold flowers and cooking pots to earn a living and her father has a small kiosk selling domestic items such as sugar, salt, bread. Nurat was born with spina bifida that puts her at risk of lower-limb paralysis, infection, and possible developmental delays. Our medical partner, African Mission Healthcare Foundation, is requesting $1,015 to cover the cost of Nurat's spina bifida closure surgery. The procedure is scheduled to take place on June 23rd. This procedure will hopefully spare Nurat from the risks associated with his condition, instead allowing her to grow and develop into a healthy girl . Nuru’s mother hopes the best for her child, "Am still in shock and unsettled due to my daughter’s conditions. I was informed that both conditions could be corrected but we are not in a position to afford any of the treatment costs. Please help save my daughter I don’t know what to do."
Grace is a one-month-old baby girl and the youngest in a family of three children. Both of her parents are small scale farmers, mainly producing maize and vegetables for their food. Her father also seeks other work as a casual laborer, like working on other farms or fetching water to sell to other villages, to supplement the family's income. Grace 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, Grace is at risk of lower limb paralysis, infection of the exposed nerve tissue, development of tethered cord syndrome, and possible developmental delays. Our medical partner, African Mission Healthcare (AMH), is requesting $1,015 to cover the cost of Grace's spina bifida closure surgery. The procedure is scheduled to take place on June 4th, and will hopefully help prevent some of the risks associated with her condition, allowing her to grow and develop along a healthy trajectory. Grace’s mother shared, "the cost of surgery is too high for us to afford, please help us."
Emmanuel is a newborn baby and the second child in his family. His mother used to sell maize in a market near their home before she gave birth to Emmanuel. After giving birth, she hasn't yet returned to her business since she has been taking care of Emmanuel. They shared that his father works on a construction site and the daily work is hard to come by. Since birth, Emmanuel has had a left inguinal hernia. If not treated, the hernia may result in intestinal tissue damage or even death. Fortunately, on May 8th, he will undergo repair surgery at our medical partner's care center. Our medical partner, African Mission Healthcare Foundation, is requesting $444 to fund Emmanuel's surgery. Once completed, this procedure will hopefully allow him to live more comfortably. Emmanuel’s mother says, “As a family, it is very hard for us to raise money for Emmanuel’s surgery due to our poor financial capabilities. Any financial help offered to us will be highly appreciated.”
Htoo is a 6-year-old boy from Thailand. He lives with his parents, brother and two sisters in a refugee camp on the border of Thailand and Burma. Htoo and his siblings were born in the refugee camp. Htoo’s mother is a homemaker, while Htoo’s older brother and sisters go to primary school and Htoo attends kindergarten. His father used to work as a day labourer, but has been unemployed since the pandemic began. Currently, they have no income and receive some financial support for their daily expenses. Luckily, Htoo's family receives free basic healthcare and education in the camp. In late October 2020, Htoo was diagnosed with an inguinal hernia. If he stands up for a short period of time, or walks, the right side of his private area will swell. Around twice a week, Htoo shares with his parents that this area is hurting him and he feels uncomfortable. Fortunately, on April 8th, he will undergo hernia repair surgery at Mae Sot General Hospital, our medical partner's care center. Our medical partner, Burma Children Medical Fund, is requesting $1,500 to fund Htoo's hernia repair surgery. The procedure is scheduled to take place on April 8th and, once completed, will hopefully allow him to live more comfortably. Htoo's father shared, “Most of the time, my son is very active and playful. He will only rest when he complains about the pain.”
Pascalina is a 38-year-old mother of seven. She is a farmer and loves looking after her children, who are all in school. Pascalina was married, but her husband passed away in 2009, so she has been taking care of her family on her own ever since. Now, her brother occasionally provides financial support to her family for school fees and other basic needs. When she was 18 years old, Pascalina sustained a burn and was taken to a hospital nearby. Her wounds healed, but she developed a contracture on her right hand, which makes it hard for her to carry out her day-to-day duties normally. It has been difficult for her to look after her children with this contracture, and she has been relying on her left hand as a result. Fortunately, our medical partner, African Mission Healthcare, is helping Pascalina receive treatment. On March 4th, surgeons at their care center will perform a burn contracture release surgery to help restore mobility to her right hand. Now, she needs help to fund this $874 procedure. Pascalina shared, "Please help me have this surgery because it will enable me to work and carry out my daily life activities with ease, especially taking care of my children.”
Myo is a 16-year-old boy from Burma. He lives with his parents and four brothers in northern Rakhine State. Myo is a student in grade nine and his four brothers also go to school. However, they have been unable to study since the Covid-19 pandemic shut all schools. Myo’s parents are day laborers, and their family's combined income is just enough to cover their daily expenses since Myo and his brothers’ schooling is free. To survive with limited income, they forage for vegetables and fish. If they fall ill, they use traditional medicine, which is more affordable then going to a clinic or a hospital. Myo was diagnosed with a heart condition that involves a malformation of the mitral valve, which is 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, Myo cannot walk long distances or climb stairs because of his tiredness. Sometimes, he cannot breathe very well. Our medical partner, Burma Children Medical Fund, is requesting $1,500 to fund a mitral valve replacement for Myo. The treatment is scheduled to take place on February 7th and, once completed, will hopefully allow him to live more comfortably. Myo shared, “I am worried about my health and I feel sorry for my parents. Because of my health problems, my father had to work more days to earn more money. Also, my mother cannot work because she accompanies me and has to take care of me. I hope my school will reopen soon so that I can go back to school. One day I hope that I can become a teacher. I want to teach because there are not enough teachers in my village.”
James is a very playful and jovial boy. He loves to play with his friends and, his grandmother shared, they would play with anything because toys are hard to come by. One day James and his friends found a calabash and chose to play with it. While they were playing, one of them took the calabash and threw it to James. The calabash hit James at his right hip and he fell down. He struggled to stand up and immediately started limping and crying out of pain. He was rushed home to his grandmother where she took him to a nearby facility. James was given some pain medication and then sent home. His grandmother shared that a few days down the line his situation was not getting any better and he could not walk. James's grandmother sourced some funds and brought him to Kijabe Hospital for examination. Upon review, the doctor requested scans to develop a treatment plan, but due to lack of money to pay for the scan, his grandmother decided to go back home and look for money. While at home, it was took her a long time to raise the required amount for the scans. One day their church pastor visited to check on how they are adapting to life after the death of James’s mother. During the visit, he noticed that James was barely moving. He was concerned and asked his grandmother what was wrong. James's grandmother explained what happened and the current situation they are in. The pastor brought James back to Kijabe Hospital for the scans. When the doctor reviewed the scans, they immediately admitted James as an emergency case and a surgery was done helping to save his leg. During a regular clinic follow-up yesterday, his doctor noticed that the wound was oozing and was concerned about an infection. An x-ray was done and showed that his leg again needs emergency surgery to treat his condition. James is the youngest of four children. His father separated with his mother, and left James and his siblings to his mother. A few years later, James's mother died and his grandmother has taken full responsibility of the four children. To earn a living, his grandmother does laundry and ploughs farms for their neighbors. She does not have another source of income. James's first surgery was supported by Friends of Kijabe Hospital, but his grandmother is appealing for financial help for the surgery that is now needed for James. James’ grandmother shared, “At home after the first surgery, I was very happy to see James slowly trying to play with his friends again. Those were happy moments that I never thought James would experience again. I am requesting for financial help to put back a smile on his face."
Meet Diana: a 17-year-old bright, social, and jovial girl at our partner's clinic in Voi, Kenya. Diana is the second born in a family of three children. Their family hails from Sofia village in Taita Taveta county and her single mother is a small business lady. Diana was born healthy, however, when she was seven months old, her mother noticed her condition when she started crawling. She could not stand or walk, and her left part of the body was weak. It is then that Diana's mom learned that she has a condition known as Hemiplegic CP, causing paralysis of one side of the body. Diana's left hand is greatly affected and she cannot hold things or engage in household duties like washing clothes and dishes. Her desire is to have her hand straight and functional so that she can be independent and do her own things at home and in her future. Diana's mother is unable to raise the estimated cost of $1,224 and has requested for support for her daughter's surgery. “I would like to request for support so that my hand can function well and I can help my mother at home. If my hand functioned normally, I will be happy,” Diana told us.
Kabula is the fifth born child in her family and was born with Spina Bifida. Her parents were referred to a more advanced hospital for treatment but they could not afford to travel to there or the cost of treatment that would be needed. They returned home tried to raise money but months kept passing by and they still could not afford it. Kabula kept getting sick every now and then with fever and vomiting, and her family took her to the nearby clinic where they were given medications. Kabula's parents separated two months ago, her mom shared, as Kabula's father was blaming her mom for giving birth to a child with Hydrocephalus. He also felt he could not afford any treatment for her with his living as a subsistence farmer, so Kabula's mother has been caring for her alone. Kabula's mother has now returned back to her parent's house to live. Kabula has been scheduled for Spina Bifida repair surgery and a VPS insertion and her mother is requesting financial support. She said, “I have been left with no support from my husband due to our child’s condition. Please help save her life.”
Johnson is a 2-month-old baby boy from Tanzania. He is the last born in a family of three children and was born with a left clubfoot. His condition is causing worry for his parents. They tried to seek doctor's advice from a local hospital and were referred to Watsi's Medical Partner Care Center ALMC/Plaster House. Johnson has been diagnosed with a left positional clubfoot which needs manipulation and casting to correct his foot so that he does not grow up disabled. If this condition is not treated Johnson will have difficulty learning to stand and walk when the time comes. He will also not be able to wear normal shoes and walking will always be difficult for him. Johnson’s father works as bodaboda taxi driver to be able to care for and support his family. They also practice small-scale farming where they grow crops for their own family. Their income is not enough to pay for their basic needs and still afford their son’s treatment cost so they are asking for help. Fortunately, Johnson's family traveled to visit our medical partner's care center where surgeons will perform clubfoot repair surgery on October 9th. Our medical partner, African Mission Healthcare Foundation, is requesting $890 to fund Johnson's clubfoot repair. After treatment, he will be able to walk easily when he grows up and develop like any other child. Johnson’s mother shared, “We wouldn’t want our son to grow up disabled. Please help us we since we are unable to afford the treatment cost as our income is not enough.”
Johnson is an 8-month baby boy from Tanzania. Johnson, the last born child in a family of four, and already is a very active and friendly little boy. Johnson's parents are both subsistence farmers. Johnson was born in a local hospital where his parents were informed that his spine was not fully formed, thus resulting in a condition known as spinal bifida. Because Johnson's condition was not severe, they were informed that he wouldn’t need treatment and that it would close on its own. As their family continued to attend clinics they were told to wait till Johnson gets to five months old for him to have any kind of treatment. At five months they took him to hospital for the treatment but the cost was too high for them to afford and they had to return home. As time went by, Johnson's mother saw that his condition could end up complicated if he didn’t get treatment soon and end up greatly affecting Johnson later in life. She decided to seek treatment. She went to Mt Meru and was referred to Watsi's Medical Partner Care Center ALMC for more help. Johnson 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, Johnson 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 $1,015 to cover the cost of Johnson's spina bifida closure surgery. The procedure is scheduled to take place on September 7th. This procedure will hopefully spare Johnson from the risks associated with his condition, instead allowing him to grow and develop along a healthy trajectory. Johnson’s mother says, “We are concerned if our son does not get his spine corrected, it might affect his ability to walk. Please help my son.”
Samphors is a 27 years business woman from Cambodia. She and her husband have been married for four years and have one son. They work together on their business, selling drinks, and take turns looking after their son. Samphors likes riding her bike, cooking for her family, and tailoring fun outfits for her son. In 2018, Samphors had an ear infection. This infection caused the tympanic membrane, or the ear drum, in her left ear to perforate. For this reason, Samphors experiences hearing loss, tinnitus, discharge, and constant mild pain. She cannot communicate clearly with others, and must take time to clean the discharge every other day. Samphors traveled to our medical partner's care center to receive treatment. On August 6th, she will undergo a myringoplasty procedure in her left ear. During this procedure, surgeons will close the perforation. Our medical partner, Children's Surgical Centre, is requesting $464 to fund this procedure. This covers medications, supplies, and inpatient care. Samphors shared, "I hope that after this surgery I can stop spending money on medicines and get rid of my ear pain and discharge, so I can live comfortably with my family and enjoy life."