Andrew joined Watsi on November 15th, 2015. Six years ago, Andrew joined our Universal Fund, supporting life-changing treatments for a new Watsi patient every month. Andrew's most recent donation supported Natalia, a 13 year old girl from Bolivia, to fund heart surgery.
Andrew has funded healthcare for 73 patients in 12 countries.
Andrew has funded healthcare for 73 patients in 12 countries.
Natalia, who is 13 years old, lives in the mountains above La Paz with her parents and two younger brothers. Natalia was born with a cardiac condition called atrial septal defect, in which a hole exists between the two upper chambers of her heart. Because of this hole, blood leaks out without passing through the chambers of her heart to gather oxygen, leaving Natalia weak and short of breath. Fortunately, Natalia's family sought care through our medical partner, Haiti Cardiac Alliance, and Natalia is now scheduled for corrective surgery on January 17th, at Hospital del Niño Dr. Ovidio Aliaga Uría. During the surgery, doctors will sew a patch over the hole in Natalia's heart, enabling her to live a healthy life. Another organization Gift of Life International has contributed $3,000 and our medical partner is seeking your help to fund the remaining $1,500 needed for this life-saving procedure. Natalia said: "I am looking forward to this surgery so that I can go to school without feeling tired."
Erick is a 10-year old boy, and the oldest of four siblings. He and his family live in Tanzania, where Erick particularly enjoys studying Kiswahili, civics and mathematics, with an eye towards becoming a businessman when he grows up. When he isn't studying, he is out playing with his friends, or helping to do chores around the house. Erick's parents work as farmers, an occupation that has proved increasingly daunting, in light of the drought that has lasted for three years already. Erick has been diagnosed with a right clubfoot. A surgery he underwent previously caused his right leg to be slightly twisted downward and inward, making it difficult and painful for him to walk long distances. He requires another procedure to help correct his right leg, but his parents are unable to afford the medical bill, and are appealing for help. Fortunately, Erick sought assistance from our medical partner, African Mission Healthcare Foundation, at Arusha Lutheran Medical Centre. It is there, on December 15th, that surgeons will perform clubfoot repair surgery, which will enable Erick to walk more easily, to continue with his studies, and to pursue his dreams, without having to contend with his clubfoot. Now Erick's family needs your help to fund his procedure, which will cost $935. Erick says: "I feel like it will be hard for me to achieve my dreams with my current foot condition. I appeal for your support."
Hnin is a determined 5-year-old girl from Burma. In her free time, she likes to draw pictures. Hnin lives with her grandmother and brother in Mon State. She goes to kindergarten, her brother goes to primary school, and her grandmother is a washerwoman. Hnin's parents, who work as day laborers in Thailand, also send them money every month to help support basic needs. Hnin was born with club foot of her left leg. With the help of Burma Children Medical Fund (BCMF), she underwent casting at Mawlawmyine Christian Leprosy Hospital (MCLH) to straighten her foot. Hnin's family was told to bring her back when she was five years old as she would need another surgery to fully correct her clubfoot. Currently, Hnin still has a cast on her left leg. When she walks, she walks on the side of her left foot. Because of this, she cannot play on the playground or keep up with her friends. Without treatment, Hnin's condition will continue to cause her discomfort and will further limit her movement. Our medical partner, Burma Children Medical Fund, is requesting $1,500 to cover the cost of surgery for Hnin, which is scheduled to take place on November 18th. This procedure will elongate her Achilles tendon, allowing increased motion at the ankle joint. Hnin said, “My left leg is so heavy with the cast, but I am not scared to have the operation on my leg. I want to have surgery."
Teresiah is a quiet but social mother of three children, who lives with her family in Kenya. She is a small-scale farmer while her husband works as a casual laborer. Teresiah's children are all in school and she has big hopes for their future. Teresiah started experiencing severe epigastric pains intermittently. She has visited many hospitals without much success. Finally, at Nazareth Hospital, an ultrasound scan examination was done, and it showed that Teresiah has Cholelithiasis - gall stones. In addition to the severe pain she is experiencing, Teresiah might also develop complications like inflammation of the pancreas, gall bladder, or gall bladder obstruction. The surgeons advised that she needs to undergo surgery to treat her condition. Teresiah is not in a position to fund her treatment and she therefore requests for help. She needs $788 to fund her surgery. Teresiah says, "Having kids in school and not being able to take care of them is very difficult. I humbly ask for assistance and medical attention. I want to take care of my family and return to my regular life."
Naima is a smiley and playful baby girl from Ethiopia. She loves to breastfeed and play with her seven older siblings and her mother. Her dad is a retired driver and the community elder, and her mother stays home to care for the children. Because Naima's father has no source of income, their older children support them financially. Naima was born with an anorectal malformation, a congenital abnormality that leads to a complete or partial intestinal blockage. She needs to undergo a series of procedures to eliminate bowel dysfunction. Naima developed bowel obstruction because of her condition and an emergency colostomy was done. She has had multiple issues with her colostomy care and associated complications. As a result, she cannot make stool in a typical way. Her parents have been very troubled because of her condition and are asking for support. Naima is scheduled to undergo surgery to correct her condition on September 22nd. Our medical partner, African Mission Healthcare Foundation, is requesting $1,500 to cover the total cost of Naima's procedure and care. After her recovery, Naima will no longer experience bowel dysfunction or be at risk of developing health complications in the future. Naima's father says, “I hope my child will get the treatment and heal. Once she finishes her treatment, I hope she will be relieved from her pain and suffering and lead a healthy life.”
Eliana is a friendly and talkative young girl from Tanzania. She is the firstborn child in a family of three. Her parents both work as small-scale farmers, and they depend entirely on what they harvest for their daily living. When Eliana was two years old, her parents noticed that her left leg was swelling up and that she would limp when walking. They initially thought she had fallen and hurt herself, so they took her to a local dispensary, where she was prescribed pain relieving medication. Eliana was eventually diagnosed with genu valgus, which is a malalignment of the knees. This condition is typically caused by an excessive accumulation of fluoride in the bones, which often stems from contaminated drinking water. As a result, Eliana struggles to stand and cannot walk more than four steps without either experiencing pain or falling down. This has resulted in her having to crawl most of the time in order to move from one place to another. In 2020, Eliana had corrective osteotomy surgery, which fortunately helped correct her legs to a point where she can now enjoy walking and playing with other children. However, she requires a second-stage procedure in order to remove her implant so her condition can heal entirely. Our medical partner, African Mission Healthcare, is requesting $880 to fund corrective surgery for Eliana. The procedure is scheduled to take place on August 11th. Treatment will allow Eliana's legs to completely heal, fully restoring her mobility, and greatly decreasing her risk of future complications. Eliana’s grandmother says, “The first surgery my granddaughter got helped ease her walking. I believe this next surgery will make her legs even better.’’
Faith is a beautiful four-month-old baby from Kenya. She is the youngest of two children. To support their family, her mother is a stay-at-home mom, and her father herds and sells cattle. Faith was born at home with several congenital conditions. Her parents took her to a nearby facility for examination, where she was diagnosed with spina bifida, hydrocephalus, and clubfoot. They were referred to another facility where a medical device, called a shunt, was used to help treat the hydrocephalus, draining the excess fluid from her brain. On discharge, the hospital referred her and her family to our medical partner's care center, BethanyKids Kijabe Hospital, where Faith was examined and scheduled for spina bifida repair surgery. Spina bifida is a type of neural tube defect in which the spine does not properly close around the spinal cord. Without treatment, Faith 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 $1,151 to cover the cost of Faith's spina bifida closure surgery. The surgery is scheduled to take place on July 13th. This procedure will hopefully spare Faith from the risks associated with her condition, instead allowing her to grow and develop along a healthy trajectory. Faith’s father says, “When I saw the problems that my child has, I was worried that she would never receive treatment. I am hopeful she will receive treatment with your help.”
Nimo is a 3 year old girl, living with her grandmother in Ethiopia. When she was just a few months old, Nimo's parents gave her to her grandmother, as with four other children already at home and Nimo's medical condition, they were unable to take care of Nimo. Nimo's grandmother, who has a small business, was already supporting four other people, so she shared that it is hard for them to survive from day to day. Nimo was born with a congenital malformation, that led to a blockage in her intestines. At first, when Nimo began to show signs of this condition, her family didn't have the funds to take her to the hospital. By the time someone provided funds so that Nimo could get to the hospital, she was weak and underweight from malnourishment. An emergency colostomy was performed, and over time, Nimo gained strength, and is now able to run and play with her friends. However, she still has multiple issues that require medical attention and additional surgery to help her fully heal. Nimo is scheduled to undergo surgery to correct her condition on July 5th, at BethanyKids Myungsung Christian Medical Centre. Our medical partner, African Mission Healthcare, is requesting $1,500 to cover the total cost of Nimo's procedure and care. After her recovery, Nimo will no longer experience bowel dysfunction, or be at risk of developing related health complications in the future. Nimo's grandmother says: “When she heals, I will go to my home and celebrate with my family. ”
Thay is a one-year-old girl from Burma. She lives with her parents, grandfather, three sisters and a brother in a village. Thay's mother looks after her and her brother at home, her grandfather is retired, and her sisters go to school. Thay's father works as a porter, but has has difficulty finding work for over a month. With the increasing number of internally displaced people settling in their village due to the humanitarian crisis, there are now many individuals competing for the same work. When Thay was around eight months old, her parents noticed that her head was increasing in size. As a result, Thay cannot yet sit up or crawl. She is only able to turn her head, and will cry if she cannot see her parents. Thay was recently diagnosed with hydrocephalus, which has causes fluid to build up in her brain. Without immediate surgery to alleviate the intracranial pressure, Thay is at risk of developing severe, potentially fatal medical complications. Our medical partner, Burma Children Medical Fund, is requesting $1,500 to fund the insertion of a ventriculoperitoneal shunt for Thay, which will drain the fluid that has accumulated in her brain. The procedure is scheduled to take place on May 20th and, once completed, will greatly improve Thay's quality of life as she grows up. Thay's father said, "I am thankful to every organisation and everyone for supporting my daughter’s treatment cost. Because of you, I believe that my daughter will receive surgery and be healthy and live a normal life after treatment."
Juvens is a sweet 2-year-old boy from Haiti. Juvens is his parent's first child. His parents have been happy to see Juvens starting to play, but his condition makes it difficult for him to control his head and his body. Juvens has been diagnosed with hydrocephalus, a condition in which cerebrospinal fluid accumulates in the brain increasing intracranial pressure. Without treatment, Juvens will experience severe physical and developmental delays. Our medical partner, Project Medishare, is requesting $957 to cover the cost of surgery for Juvens at Hospital Bernard Mevs that will treat his hydrocephalus. This is the only site in the country where this care is currently available and the procedure is scheduled to take place on April 19th. This critical treatment will place a shunt to drain the excess fluid from Juvens's brain to reduce intracranial pressure and greatly improve his quality of life. With proper treatment, Juvens will hopefully develop into a strong, healthy young boy. Juvens's family is hopeful that the surgery will allow him to be able to walk and talk and be able to play as he grows.
Evaline is a nine-month-old baby girl, who is the youngest of two in her family. Evaline and her parents come from a Maasai community, who are largely livestock keepers. They mostly live in remote regions where they can find water and pasture for their livestock. Living in such an environment makes it difficult to access healthcare, so it is common that mothers neither go to a clinic during pregnancy nor deliver at a hospital. Most mothers deliver at home with the help of midwives. Evaline was born with clubfoot of her left foot. Clubfoot is a condition in which the foot is twisted out of shape. This causes difficulty walking and even wearing shoes. Fortunately, Evaline's parents traveled to our medical partner's care center, Arusha Lutheran Medical Centre. There, surgeons performed clubfoot repair surgery on March 22nd. Our medical partner, African Mission Healthcare Foundation, is requesting $935 to fund Evaline's clubfoot repair. After treatment and recovery, she can learn to walk, run, and play like other children when the time comes. This will be especially helpful when she is school age and needs to walk longer distances to attend school,\. Evaline’s mother says, "Help my daughter, it hurts seeing her foot like this."
K is a 46-year-old homemaker from Burma. K lives with her husband, son and two daughters in a refugee camp. K and her husband are small scale vegetable farmers. K's eldest daughter is a nurse in the refugee camp's hospital, while her other daughter and son are students. In her free time, K enjoys cleaning her house and weaving traditional Karen shirts. K has a cataract in her left eye that causes blurred vision. K's challenged vision has prevented her from weaving, and causes her to walk slowly so she does not get injured. Our medical partner, Burma Children Medical Fund, is requesting $1,500 to help fund K's lens replacement surgery on February 16th. After recovery, K will be able to see clearly again. K shared, "After surgery, when I can see again, I hope to go back to weaving and helping with all the household chores.”