Adrian has funded healthcare for 76 patients in 14 countries.
Ruth is a 15-year-old from Kenya who has special needs. She is a student at Limuru Cheshire Home (a center for girls with physical/mental disabilities) and was admitted to the institute in 2019. She was born into a family of two, being the firstborn followed by a brother who lives with her aunt. Her mother, who was a single mom, died when Ruth and her brother were young. This led to the two being separated and since Ruth is more vulnerable, she was left under the care of their grandmother. Together they live in a two-roomed house and they depend on the local community for upkeep. Life has become more difficult now that Ruth's grandmother cannot move around even for firewood since she has to ensure Ruth’s safety. Ruth has clubfoot that makes her walking extremely difficult. Last year she was brought to Watsi's Medical Partner Care Center CURE Hospital, where she was recommended for surgery. Since her grandmother cannot afford the treatment, her surgery has not yet taken place. The surgery would highly enhance Ruth's mobility as well as improve her self-esteem and ability to socialize with her peers. Fortunately, surgeons at our partner hospital will perform clubfoot repair surgery on October 12th. Our medical partner, African Mission Healthcare Foundation, is requesting $1,286 to fund Ruth's clubfoot repair. After treatment, she will be able to walk easily. “I will appreciate any kind of support give to make my granddaughter walk comfortably,” Ruth’s grandmother told us.
Lay is a 45-year-old man from Burma. He lives with his family in a village in Karen State. His wife is a homemaker while his son and daughter-in-law work as a day laborers. He also used to work as a day laborer before he stopped two months ago due to his loss of vision in his left eye. He has blurred vision and sometimes he also feels dizzy. When the doctor checked his left eye, he was diagnosed with a cataract as well as glaucoma. Our medical partner, Burma Children Medical Fund, is requesting $1,500 to fund lens replacement surgery for Lay. On March 17th, doctors will perform a lens replacement, during which they will remove Lay's natural lens and replace with an intraocular lens implant in his eye. After recovery, he will be able to see clearly. Now, he needs help to fund this $1,500 procedure. Lay said, "Now I am happy that I will receive surgery with the help of donors. Thank you everyone for helping me and I pray for you all with all my heart. I know this surgery will return my vision and will be a great benefit for my family if it will allow me to go back to work.”
Joseph is a two-month-old baby boy from Tanzania. He is the last born of his mother who has eight children. His father is polygamous with two wives, Joseph's mother being the first wife. The second wife has five children making a family of fourteen children. Four children in the family have been able to join school but the rest have not had a chance to attend yet. Joseph's older siblings who do not go to school help their parents to look after their cattle of five cows and five goats. Both parents depend on small-scale farming of maize, beans, and vegetable for their food and they are able to sell a goat once in a while to be able to get money to buy other commodities. Joseph 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, Joseph 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, is requesting $1,015 to cover the cost of Joseph's spina bifida closure surgery. The procedure is scheduled to take place on August 10th and will hopefully spare Joseph from the risks associated with his condition, instead allowing him to grow and develop along a healthy trajectory. Joseph’s mother shared, “The money needed to pay our son’s surgery cost is too high for us to afford, kindly help us.”
Veronica is a 12-month-old girl from Kenya. Veronica’s mother was a stay at home mother but now prepares and sells mandazi (pastries) while her father who used to farm now is a laborer in construction sites in order to make ends meet. Being the third born in a family of five, Veronica’s parents are not able to raise enough to pay for her treatment. Veronica underwent a colostomy, in which the end of the colon is brought through an opening in the abdominal wall. This surgery is often performed to bypass bowel malformations, but colostomies are usually temporary and may call for closure. In Veronica's case, her colostomy requires closure in order to restore bowel function and prevent future complications. Our medical partner, African Mission Healthcare Foundation, is requesting $650 to cover the cost of a colostomy closure for Veronica. The surgery is scheduled to take place on July 13th and, once completed, will hopefully allow her to live more comfortably and confidently. Veronica’s mother says, “Being Veronica’s last surgery, I’m looking forward to see her well.”
Daw Ei is a 48-year-old woman from Burma. She lives with her husband, mother, two daughters, son, and daughter-in-law in Yangon. Her husband is a security guard, her mother is retired, and her daughter-in-law is a homemaker. Her eldest daughter works in a factory, her other daughter is a student, and her son works as a mason. Daw Ei used to work as a shop vender herself but had to stop three years ago due to her health problem. Daw Ei 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 Ei suffers from chest pains, feels tired and cannot walk long distances. Sometimes, she has no appetite. Our medical partner, Burma Children Medical Fund, is requesting $1,500 to fund a mitral valve replacement for Daw Ei. The treatment is scheduled to take place on June 14th and, once completed, will hopefully allow her to live more comfortably. Daw Ei said, “I’m worried about my health problem. Also, I’ve spent all my money on [seeking] treatment and I had to borrow 300,000 kyat (approx. 300 USD) from my daughter’s friend. I want to be cured.”
Bernard is a driver from Kenya. Bernard is a father of 8 children from his two wives. He lives in a rental house and is the main breadwinner in the family. He does not have national insurance nor did he own the vehicle he drove when the road accident occurred. Bernard is a driver in the public transport system, commonly referred to as matatus. On 12th of February 2020, John was involved in a grisly road accident that left 22 people with various injuries. According to Bernard, the oncoming vehicle was overlapping at high speed at a place that is increasingly becoming a blackspot. Bernard and the other patients were brought to Watsi's medical partner care center and immediately started receiving treatment. Bernard had a nail implant on his left femur and a right foot closed reduction and percutaneous pinning that morning. He has been recovering and is planned for a second surgery to correct the acetabular open reduction and internal fixation (ORIF). He is in chronic pain and is not able to move from his bed. Fortunately, surgeons at our medical partner can help. On February 19th, Bernard will undergo a fracture repair procedure called an ORIF. This treatment will help Bernard heal well and be able to walk and eventually work again. Now, our medical partner, African Mission Healthcare Foundation, is requesting $1,042 to fund this procedure. Bernard says, “I am appealing for help to have the surgery. My family is not able to raise the funds needed. I am however hopeful that soon I will be able to walk.”
Peter is an eight-year-old boy from Kenya. He is outgoing and a bit cheeky. The family of six children relies on their mother’s limited income from peasant farming and their father’s goat slaughtering wage work he gets from time to time. Peter was diagnosed with cryptorchidism, a condition in which the testicles remains undescended. If left untreated, Peter has an increased risk of developing hernias, testicular cancer, and fertility problems in the future. Peter will be receiving assistance from our medical partner, African Mission Healthcare Foundation (AMHF). Fortunately, he is scheduled to undergo corrective surgery on February 17th. AMHF is requesting $535 to cover the total cost of his procedure and care. “I want to be a driver when I grow up,” says Peter.
Tin is a 20-year-old from Burma. He lives in a nunnery with his mother and aunt, who are nuns, in a village in Katha Township. Tin became a monk 13 years ago when his father passed away. His mother then became a nun. Tin left monkhood two months ago, when he became very ill. He is now unable to work, and he is looked after by his mother. However, sometimes when he feels better, he teaches Buddhist theology to boys from a nearby monastery. As his mother is a nun, she has no income except for whatever she is given during weekly alms collections. Usually she receives dried food staples such as rice in addition to money. Currently, Tin feels tried if he has to walk for a while and if he has to use stairs. Tin was born with ventricular septal defect, a cardiac condition in which a hole exists between the two lower chambers of the heart. Blood leaks through this hole without first passing through his lungs to obtain oxygen, leaving him sick and short of breath. Tin is scheduled to undergo heart surgery on March 15th to correct the condition and improve his quality of life. Our medical partner, Burma Children Medical Fund, is requesting $1,500 to cover the total cost of Tin's procedure and care. Tin said, “Sometimes I have chest pain and when I have them, I have difficulty breathing.”
Naw Htee is a 30-year-old woman from Thailand. In 2006, Naw Htee and her family fled from Karen State, Burma to Thailand because there were conflicts between the armed groups and the country's military in their village. She now lives in a refugee camp with her family. In 2010, Naw Htee felt a severe toothache while she and her parents were visiting her village in Burma. She went to the nearest local clinic, where she had her molar teeth extracted. After the procedure, Naw Htee was in extreme pain; she could not even open her mouth as she used to. She was told that pain after tooth extraction is normal and that the pain will be diminished if she takes painkillers. Naw Htee tolerated the pain and hoped for the pain to be gone. Since then, Naw Htee could barely open her mouth. Naw Htee was too afraid to tell about her condition to anyone. She carried this burden for almost 9 years, until she decided to seek help. She then visited the clinic in the refugee camp. After trying oral medication and since her condition remained the same, she was referred to Mae Sariang General Hospital (MSGH) in July 2019. There, she received an x-ray, and the doctor diagnosed her with Ankylosis of the Temporamandibular joint [TMJ], stiffness of a joint due to abnormal adhesion and rigidity of the bones of the joint of jaw. She was then referred on to Chiang Mai Hospital (CMH) as MSGH does not have capacity to treat her condition. Once at CMH, the doctor told Naw Htee that she needs to undergo a special x-ray prior to receiving treatment. Doctors want Naw Htee to undergo a CT scan, a procedure in which x-ray images taken from several angles are combined to produce cross-sectional images of the body. This scan will hopefully help doctors diagnose her condition and formulate an appropriate treatment plan. Our medical partner, Burma Children Medical Fund, is requesting $469 to cover the cost of Naw Htee's CT scan and care, scheduled for February 5th. Naw Htee mentioned, “I wanted to be a healthy, strong and supportive mother, even without the support of their father.”
Joe is a 12-year-old student from Thailand. He moved to Mae Sot in early 2019, in search for better education. He now lives at a boarding house while studying at a migrant learning center. Joe noticed his blurred vision since he was five years old. Although he told his parents about it, his parents thought it was not that serious; they just told him that his eye sight will get better with time. As Joe did not experience any pain, aside from blurry vision, Joe stopped complaining about his problem to his parents. Joe continue to have a blurred vision, especially in his left eye. After he moved to Mae Sot, he told his uncle about his eye sight. His uncle made arrangements for him to meet with a medic, who later found that Joe has a cataract on his left eye and that it needs to be fixed in order for Joe to regain a clear vision in his left eye. Our medical partner, Burma Children Medical Fund, is requesting $1,500 to fund lens replacement surgery for Joe. On December 10th, doctors will perform a lens replacement, during which they will remove Joe's natural lenses and replace them with an intraocular lens implant in each eye. After recovery, he will be able to see clearly. Now, he needs help to fund this $1,500 procedure. Joe said, “I don’t know yet of what I want to be in the future, but all I’m looking forward to is to ride a bicycle and play with my friends without any difficulty seeing.”
Maria is a beautiful four month old baby from Tanzania who came to our hospital when she just five days old. She is the last born child in a family of five children. Maria was born at home through the help of midwives. This was because the nearest clinic was a long distance from home and Maria’s father was not at home. Soon the midwives informed Maria’s mother that their daughter had a problem with her back and head. This brought panic to her mother and without money, they had to wait for her husband to return. When Maria’s father arrived and saw her condition he had some money with him from selling two of their goats. They depend solely on livestock keeping and small scale farming for their living. The family took her to our ALMC hospital where she was diagnosed with Spina Bifida, hydrocephalus and encephalocele. She has received surgery for Spinal Bifida to save her from getting an infection on the spine that could lead her not to be able to walk or lead to death. She now needs another surgery to help correct the hydrocephalus condition. Her parents are asking for help. Our medical partner, African Mission Healthcare Foundation, is requesting $1,238 to cover the cost of surgery for Maria that will treat her hydrocephalus. The procedure is scheduled to take place on December 10th and will drain the excess fluid from Maria's brain. This will reduce intracranial pressure and greatly improve her quality of life. With proper treatment, Maria will hopefully develop into a strong, healthy young girl.
Clifterson was born with a heart condition called double outlet right ventricle, in which the aorta connects to the heart in a different place than it normally does. This prevents the heart from pumping oxygen-rich blood to his body, leaving him sick and short of breath. If untreated, it would be fatal. Clifterson lives in a rural area of southwest Haiti with his mother who is a farmer. Clifferson's mother says, "I am so happy to know that there is a chance for my child to become healthy!"