Patrick joined Watsi on July 17th, 2014. Eight years ago, Patrick joined our Universal Fund, supporting life-changing treatments for a new Watsi patient every month. Patrick's most recent donation traveled 8,500 miles to support Esther, a brilliant seven-year-old girl from Kenya, to fund surgery so she can walk more easily.
Patrick has funded healthcare for 107 patients in 13 countries.
Patrick has funded healthcare for 107 patients in 13 countries.
Esther is a young girl from Kenya. She likes reading books and enjoys going to school. Her family lives in a rural village, and she is the youngest in her family. Esther's mother is a business woman, while her father is a laborer on construction sites. Esther's right foot is affected by clubfoot, a condition in which the foot is twisted out of shape. This causes difficulty walking and even wearing shoes. She was born with hemiplegic CP, which means the right side of her body is weakened. Her condition has greatly impacted Esther and has made it difficult for her to engage with her peers at school. Earlier Esther was taken to a hospital, where she was given an orthosis to help correct her condition without surgery, however, she hasn't received treatment since then. Fortunately, Esther now traveled to visit our medical partner's care center, AIC Cure International Hospital. There, surgeons will perform clubfoot repair surgery on January 16th. Our medical partner, African Mission Healthcare Foundation, is requesting $1,286 to fund Esther's surgery. After treatment, she will be able to walk more easily and proceed with her studies uninterrupted. Esther’s mother says, “I am appealing for your financial help so that my daughter can walk well like other girls.”
Jayden is an adorable 1-month-old baby from Kenya. He has two older siblings. His mother works as a hairdresser but currently stays home caring for Jayden, while his father works as a casual laborer at construction sites. The family shared that they do not have the insurance coverage to cover Jayden’s surgery needs and request assistance. Jayden 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, Jayden is at risk of lower-limb paralysis, exposed nervous tissue infection, tethered cord syndrome development, and possible developmental delays. Jayden will undergo spina bifida closure surgery on December 13th. This procedure will help Jayden grow up healthy and without any risks associated with this condition. Our medical partner, African Mission Healthcare Foundation, is requesting $1,151 to cover the cost of Jayden’s spina bifida closure surgery. Jayden’s mother says: “We have never seen such a condition in our family, and it is very hard to explain to people. We are hopeful that he will be treated soon.”
Samuel is a 21-year-old talkative young man. He is the second born in a family of five children. His father passed away when he was four years old, so his mother had to raise him and his siblings by herself. She does jobs on tea farms to provide for the family. When Samuel was two years old, his abdomen started to swell, which was very painful for him. His mother took him to the hospital and he was given some medication and sent back home. The medication did not work as expected. He was then taken to a different hospital for examination. He was given more medication and after some time he seemed to be better. The stomachache did not go away completely, however. Samuel and his mother shared that over the years, he has had stomachaches and gotten used to taking pain medication. In 2017 when Samuel was in high school, the pain worsened and his abdomen started to swell again. He had to leave school as a result. His mother took him to a hospital in Meru where he was admitted for three months. While in the hospital, scans and a biopsy were done to determine what the problem was. He was given a colostomy, where the end of the colon is brought through an opening in the abdominal wall, in order to pass stool. This surgery is often performed to bypass bowel malformations, but colostomies are usually temporary and may call for closure. In Samuel's case, his colostomy requires closure in order to restore bowel function and prevent future complications. At that time, his doctors did not manage to treat him and referred him to BethanyKids Hospital in 2018. On arrival, he was examined and admitted, as he was not in good condition. After more scans and tests, he was ultimately diagnosed with Hirschsprung’s disease. Since then, Samuel has undergone several surgeries with the aim of trying to better his condition. The first surgery failed, but the second was successful. He is now scheduled to undergo his last surgery to close the colostomy so that he can pass stool on his own again and live a more active life. Earlier in his treatment, Samuel's parents had enrolled in the national health insurance program (NHIF), which helped them pay for most of his hospital bills. BethanyKids also chipped in on occasion to help with some of the bills. Unfortunately, for his last surgery, NHIF has rejected the request since he is beyond the age to be covered by his mother’s insurance. Our medical partner, African Mission Healthcare Foundation, is helping him to undergo treatment and needs $1,084 to cover the cost of a colostomy closure for Samuel. The surgery is scheduled to take place on November 11th and, once completed, will hopefully allow him to live more comfortably and confidently. Samuel’s Mother says, “For years now, I have been very worried about my son, but God has seen us through.”
Thet is a 35 year old husband and father, who lives with his wife, son and in-laws in Mon State in Burma. Both Thet and his wife work in his uncle's grocery store, while his in laws are farmers. When he isn't working, Thet enjoys spending time with his son and reading. In November 2018, Thet started to experience tiredness when working, and frequent headaches. He also had a rapid heartbeat, and he couldn't sleep well. He went to a hospital in Mawlamyine, where he was referred to a different hospital in Yangon for further treatment. At the hospital in Yangon, Thet was diagnosed with mitral valve regurgitation and stenosis, which would require surgery to correct. Thet was sent home with medications to manage his condition. In March 2022, Thet went back to the hospital in Yangon, because of continuing fatigue, headaches, coughing and fever. The doctor told him they would contact him to schedule his surgery in May, but Thet never heard back from the hospital. When Thet told his neighbor about this, his neighbor gave him the phone number of a heart patient who had been helped by our medical partner, Burma Children Medical Fund (BCMF). Thet followed up, and thanks to the assistance of Burma Children Medical Fund, he is finally scheduled for surgery to replace the valve in his heart on October 13th, at Pun Hlaing Hospital. Now Thet needs your help to fund the $1,500 to cover the cost of this surgery. "I have sold all my jewelry to pay for the cost of traveling to the hospital. I feel less stressed since I met the BCMF staff,” said Thet.
Cho is a 23-year-old woman from Thailand, living with her husband, son and her husband’s cousin in a refugee camp, in Mae Hong Son Province. Her husband works as a medic at the hospital in the refugee camp, and her husband’s cousin goes to school. Cho is a homemaker, and looks after her son. In her free time, Cho loves to play with her son, while on Saturdays, she likes to attend church. Cho is currently expecting her second child. At a recent antenatal visit, Cho's doctors told her that she would need to give birth via Caesarean section, due to complications she experienced when giving birth to her son. A C-section offers the best opportunity for a safe and healthy outcome for both Cho and her new baby. Our medical partner, Burma Children Medical Fund, is helping Cho access the care that she needs. On September 8th, Cho will undergo a Caesarean section at Mae Sariang Hospital. Burma Children Medical Fund is seeking $1,500 to fund this procedure and ensure a safe delivery. “I want to work as a teacher in the future again, when my children are old enough to go to school,” Cho said.
Penlope is a 42-year-old mother of three children, with all her children in school. She does farming together with her husband and what they earn helps to meet their day to day needs. Penlope is expecting a new baby and has been having antenatal care at Nyakibale Hospital. At her last visit, the medical team has recommended she delivery via cesarian section to ensure a safe delivery. She is not able to raise the funds needed for surgery and appeals for help. Penlope shared: “I hope to deliver well this time, in safe hands, and I expect all to be well with your support.”
Mi is a 58-year-old mother from Thailand. She lives with her husband and her three daughters. She supports her family by working as a homemaker. Her husband does not work because he is ill. Her eldest daughter is an accountant, her second eldest daughter is a homemaker, and her youngest daughter does not work because she is attending school. Some of Mi's favorite activities include cleaning her house and growing vegetables in her garden. In February, Mi started experiencing pain in her left breast. After examining the area, she noticed a small mass. Over time, the mass increased in size and the pain worsened. She currently still experiences pain in her left breast. Although she takes medication, it only alleviates her pain temporarily. Because of this, she cannot cook or clean, and her daughter has had to take over the household chores. Fortunately, Mi sought treatment through our medical partner, Burma Children Medical Fund. She is now scheduled to undergo mass removal surgery on July 12th. She is requesting $1,500 to cover the total cost of her procedure and care. Mi shares, “I want to get better soon. Then my second eldest daughter can find work so that we can pay back our debt. I want to live happily with my family for the rest of my life.”
Meet Tessy, a beautiful 4-year-old girl, living in Kenya. In March 2022, Tessy and several of her family members were involved in an accident. Her grandparents and an uncle did not survive this event, and Tessy's parents and her sister - and Tessy herself - were all hospitalized with traumatic injuries. Her parents and her sister have all since recovered. Tessy sustained injuries to her head, chest, hand and legs, and she remained in the Intensive Care Unit of the hospital for several months. While Tessy has a visible deformity of her left arm and her right thigh, her doctors shared that her overall progress since the accident is impressive. Some of her fractures are healing well, but the fracture of her right femur requires surgical intervention. Fortunately, our medical partner, African Mission Healthcare Foundation, is here to help Tessy access the care that she needs. On June 10th, Tessy will undergo an open reduction and internal fixation at AIC Kijabe Hospital. African Mission Healthcare Foundation is seeking $1,500 to fund this procedure, without which Tessy would find it difficult to walk, and would live in chronic pain. Tessy’s father says: “Her condition has greatly improved. She was in the ICU for almost two months and responded well to treatment. She needs the surgery to help with the healing and to be able to walk again.”
Hla is a 40-year-old woman living with her husband and adopted daughter in a refugee camp on the Thai-Burma border. Hla and her family fled their village in Burma, due to fighting in the area. In January, Hla learned that she was pregnant for the first time after ten years of marriage. Then in March, Hla had to flee with her husband and daughter due to the fighting near her village. They moved in with her uncle, who lives in a refugee camp. Once there, she sought prenatal care at a clinic in the camp, where she was told that she had a breech baby, which would require a Caesarean section in order for her baby to be delivered safely. The C-section is scheduled for May 11th at nearby Mae Sot Hospital (MSH). When Hla told a friend that she does not have the money to pay for her hospital stay, her friend referred her to our medical partner, Burma Children Medical Fund (BCMF), for help with paying for her care. Currently, Hla is eight months pregnant and is worried about her condition and the health of her baby. Burma Children Medical Fund is seeking $1,500 to cover the costs of Hla's treatment, and for the safe delivery of her baby. Hla said, "I was very worried when I heard that I will need an expensive C-section. I could not think of anyone to help pay for my surgery, and I felt stressed about giving birth through a C-section. After I heard from BCMF staff that donors could help pay for my surgery, I started to feel so much more relaxed and less worried. I still worry about my baby being born healthy."
Demetria is a peanut-butter maker from the Philippines. Demetria was diagnosed with cholecystitis 10 years ago and advised by her doctor to undergo surgery, but due to financial constraints, she opted to self-medicate using herbal medicines. This served as a temporary relief to her symptoms, but now these have worsened over time, and during the past 2 weeks, she started experiencing intolerable pain and difficulty keeping food down. With age and her worsening symptoms, Demetria is not capable of earning income to support her medical treatment. She shared that she and her husband rely on their granddaughter who works as an online tutor, to support their daily needs. Fortunately, Demetria was referred to our medical partner and is now scheduled to undergo surgery to correct her condition on April 7th. Our medical partner, World Surgical Foundation Philippines, is requesting $1,253 to cover the total cost of her procedure and care. After her recovery, Demetria will no longer experience severe pain in her abdomen or be at risk of other complications in the future. “Once the surgery is done, I hope to go back to doing my small peanut butter-making business so I can help sustain our daily needs like I used to before," Demetria shared. "Thank you so much WSFP and Watsi for all your help,” she added.
Margaret arrived at the hospital with visible yellow eyes and prolonged discomforts that is causing her worries. The medical team has scheduled her for a binary reconstruction to help heal her condition. As a mother of three, she has been visiting different faculties for medical care since 2009. These frequent visits have depleted her family's resources and exhausted her health coverage. Margaret's husband is a Boda-Boda taxi driver, but the income he earns goes to rent and other basics for their family. Margaret told us, "My eyes are turning yellow and they making me very uncomfortable and scared. I need this surgery to help me get well.”
Irene is a beautiful baby girl and the only child in her family. Irene's mother is young and was still in school when she was born, so they are living with her grandmother. Her grandmother sells charcoal to earn a living and it is hard for them to make ends meet each month. Irene has been diagnosed with hydrocephalus, a condition in which excess fluid accumulates in the brain and increases intracranial pressure. When Irene was one month old, her mother noticed that her head was increasing in size. She took her to a nearby facility for examination, and was then referred to another facility who admitted her for a few days; however despite medication, her condition did not change. Irene was discharged and sent home, but a few days later she developed a fever so her mother took her back to the previous facility. After another examination, Irene was finally referred to our medical partner's care center, BethanyKids Hospital. Irene’s mother did not have the funds to cover their transport to BethanyKids, but with help from medical staff they were able to make it to the hospital with a social workers accompaniment. On arrival, Irene was booked for a shunt insertion surgery to help treat her condition. Without treatment, Irene will experience severe physical and developmental delays. Our medical partner, African Mission Healthcare, is requesting $720 to cover the cost of Irene's surgery to treat her hydrocephalus. The procedure is scheduled to take place on February 9th, during which surgeons will drain the excess fluid from Irene's brain to reduce the pressure inside her head. This will greatly improve her quality of life, and allow her to develop into a strong, healthy young girl. Irene’s mother says, “It is a difficult moment for us for the past few months and we did not know if she will be treated as we do not have funds for the surgery.”