Anton has funded healthcare for 76 patients in 11 countries.
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."
Nay Kaw is an 11-year-old student from Burma. He lives with his parents, two older brothers and two younger sisters. He is currently in first grade since he left monkhood last year. His father is a farmer and his mother is a homemaker who looks after his youngest sister at home, the other sister is also a student like Nay Kaw. Nay Kaw, along with his two brothers, help with household chores and in his free time, he likes to play cane ball and hunt. Since birth, Nay Kaw has a had a mass on his right wrist. When he turned three years old, the mass increased in size but was still not painful. But by the time he was ten years old, the mass increased in size again, and became swollen and painful. His mother took him to a traditional healer but the medicine he received did not help. Fortunately our medical partner, Burma Children Medical Fund, can help. He is now scheduled to undergo mass removal surgery on July 9th. This surgery will relieve him of his pain and discomfort. He needs your help to cover the $1,500 cost of his procedure and care. Nay Kaw shared, “I would like to be a teacher because I would like to teach children like my friends who are not able to go to school to study.”
Rin is a 49-year-old rice farmer from Cambodia. He and his wife have been married for 20 years, and have two children together. His wife works in a factory, and his children are all in school. He works long hours, and raises chickens for additional income. He enjoys cooking for his family in his free time. Rin had a work accident and has an open fracture on left forearm. He went to a local hospital for an open reduction internal fixation and skin graft, but the surgery did not help him feel better. He has now come to Watsi's Medical Partner CSC because the fracture is still impacting him in a challenging way. He cannot use his fingers and has pain when he tries to work with this hand. One year ago, he was dragged under a vehicle and fractured his left forearm. He went to a local hospital and was operated on, but the fracture did not heal properly. He still experiences chronic pain from his injury, and he cannot move his hand. His family has lost their primary source of income since he cannot work, and he is worried about being able to support them. Fortunately, surgeons at our medical partner, Children's Surgical Centre, can help. On June 3rd, Rin will undergo a fracture repair procedure, which will cost $465. After the surgery, he will be able move his wrist and hand, and return to work. Rin said, "I am proud of my work and I want to work so I can support my family. My hand is in pain all the time, but I really hope that this surgery is enough for me to keep working."
Minea is 12-year-old 4th grade student. Her favorite subject in school is Khmer literature, and she hopes to be a teacher when she grows up. In her free time she enjoys exercising for good health, reading books, and watching cartoons on TV. She has one older sister; together they like to cook fried rice with chicken. Five years ago, Minea's spine curvature became noticeably worse at around 20 degrees. For a time she was using a back brace but it did not improve her condition in the long term. In recent months her scoliosis has advanced to a 45 degree angle. Her family is concerned that her condition will prohibit her from attending school and make her self conscious about her appearance. She has difficulty in sleeping, sitting, standing, or walking, and she feels uncomfortable with her appearance. Minea's mother said "I hope that the doctors will help my daughter improve her quality of life, and that she will be able to be happy and confident."
Muslim is a 2-year-old child from Ethiopia. He is a beautiful baby boy who loves sweets and rice. He also loves to play with a ball. Muslim has one brother and one sister. He loves to play with his mom and siblings. His father is a farmer and his income is very limited and insufficient for the family’s daily needs. He also does hard labor work to support the family. His mom is a housewife and she raises her children full time. Muslim 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. Muslim is scheduled to undergo surgery to correct his condition on May 5th. Our medical partner, African Mission Healthcare Foundation, is requesting $1,500 to cover the total cost of Muslim's procedure and care. After his recovery, Muslim will no longer experience bowel dysfunction or be at risk of developing health complications in the future. Muslim’s mom said, “I hope he will be operated and heal completely.”
Toeur is the sixth of seven children in his family, including four brothers and three sisters. He likes to stay home and help around the house and cook, as well as watch television and listen to music. Toeur was born with a hump on his spine and, at the age of two, he fell down the stairs and has since had a curve in his spine. He has pain in his right knee and experiences paraparesis, where he has partial paralysis in his legs and requires crutches when he walks. He cannot do any heavy work and stays near his house most days. Spinal surgery will correct Toeur's spine position and relieve his symptoms. He will be able to walk comfortably again, and will be able to take on daily activities with greater ease. He shared, "My family worries about my pain a lot, and they hope that I will be able to work again and help provide for the family. I hope that my spine will be straight and will no longer have a curve, and I won't have anymore pain in my knee so I can return to work."
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.”
Yabesera is a young boy from Ethiopia. Yabsira has a twin sister named Tseganesh. They both are cute toddlers and Yabsira loves to play with his sister Tseganesh. They have an older brother too. Yabsira’s dad is a shoe-shiner with limited income while his mom is a housewife and takes care of their babies at home. Yabesera was born with hypospadias, a congenital abnormality that causes urinary dysfunction. Without treatment, he will continue to experience uncomfortable symptoms and will be at risk of infertility. Unfortunately, he contracted measles last year and could not undergo surgery. His mother brought him to our facility and requested to proceed with the surgery now and the family appeals for financial help. Fortunately, Yabesera is scheduled to undergo corrective surgery on January 14th. Our medical partner, African Mission Healthcare Foundation, is requesting $1,231 to cover the total cost of his procedure and care. Yabsira’s mom said, “We can’t afford the medical bill. I used to wash clothes for income but once the children were born, I had to take care of them. We are living by the income of my husband only and it is very limited to maintain the family’s needs. The community helps us by giving food and milk for our babies. But still, they are nutritionally badly affected. They didn’t start walking as a result of it. We came here by the support of an organization. We are here with the hope of getting treatment for our boy.”
Saitabu is a one-month-old baby from Kenya who has congenital spina bifida and hydrocephalus. Saitabu gets frequent fevers and vomiting due to the condition. He requires urgent surgery but the family was not able to raise funds needed. Saitabu's parents are peasant livestock keepers. They are not able to meet daily needs and those of their baby's cost of surgery. Saitabau 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, Saitabau has been experiencing An increasing head circumference. Without treatment, Saitabau 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 Saitabau that will treat his hydrocephalus. The procedure will drain the excess fluid from Saitabau's brain. This will reduce intracranial pressure and greatly improve his quality of life. With proper treatment, Saitabau will hopefully develop into a strong, healthy young boy. Saitabau’s mother says, “Please help my son we can’t afford his treatment cost and he really needs this.”
Lameck is a child from Tanzania. Lameck is a fifth born child in a family of five children, he is a shy little boy and likes to keep to himself. His parents are subsistence farmers who earn very little and can barely support their family. Lameck 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, Lameck traveled to visit our medical partner's care center, Arusha Lutheran Medical Centre. There, surgeons will perform clubfoot repair surgery on September 10th. Our medical partner, African Mission Healthcare Foundation, is requesting $890 to fund Lameck's clubfoot repair. After treatment, he will be able to walk easily with no pain and difficulty. Lameck’s father says, “Please help my son get the treatment he needs so he may be able to walk without difficulty.”