Lorenz joined Watsi on June 6th, 2015. Two years ago, Lorenz joined our Universal Fund, supporting life-changing treatments for a new Watsi patient every month. Lorenz's most recent donation traveled 1,600 miles to support Nath, a 21-year-old from Cambodia, to fund brachial plexus repair surgery to heal his arm.
Lorenz has funded healthcare for 69 patients in 12 countries.
Lorenz has funded healthcare for 69 patients in 12 countries.
Nath is a 21-year-old with three brothers and one sister. Nath's father works as a tuk-tuk taxi driver, and his mother sells traditional Khmer noodles. Nath works in a water purification factory and enjoys playing games, watching TV, and reading books in his free time. In February, Nath was in a motor vehicle accident that caused his right hip to dislocate, and he also suffered trauma to his left shoulder and neck. His family took him to a clinic for treatment following the accident. While his hip has healed, Nath is still unable to move his left shoulder and arm. Upon review, Nath was diagnosed with a brachial plexus injury on his left side. The brachial plexus is a nerve network that transmits signals from the spine to the shoulder, arm, and hand. Injuries to this nerve network can result in loss of function and sensation. Currently, Nath cannot lift his left arm, which means he cannot work. Fortunately, Nath traveled to our medical partner's care center to receive treatment, as this is the only center in the country where the treatment he needs is available. On June 9th, Nath will undergo brachial plexus repair surgery. After recovery, he will be able to use his arm again. Our medical partner, Children's Surgical Centre (CSC), is requesting $709 to fund this procedure. Nath says, "I hope my arm heals and I can use it again so I can regain strength and return to work."
Gordon is a six year old boy, living with his parents and two younger siblings in a one roomed house in the Korogocho area of the capital city. His mother is a homemaker, while his father works as a vendor. Gordon was born with multiple birth conditions, including spina bifida, and hydrocephalus, as well as bilateral clubfoot. Currently, he cannot stand or walk - or wear shoes - and he has to crawl every time he wants to move about. At a visit to a mobile health clinic, it was determined that Gordon needs surgery to correct his feet. His family cannot afford the estimated hospital bill, and is requesting help to cover the costs so he can get the care he needs. Fortunately, Gordon's family traveled to our medical partner's care center, AIC Cure International Hospital. There, surgeons will perform clubfoot repair surgery on May 30th. Our medical partner, African Mission Healthcare, is requesting $1,286 to fund Gordon's surgery and care. After treatment, Gordon should be able to put on shoes, to stand, and to walk. “I would request the donors to help my son undergo surgery. My desire is to see him grow up like other children,” Gordon’s mother told us.
U Chit is a 42-year-old husband and father from Burma. He lives with his in-laws, wife and son. His father-in-law works as a day laborer, while his wife and his mother-in-law are homemakers. U Chit used to work with his father-in-law, and also as a motorcycle taxi driver for extra income. However, he stopped working in January when his health worsened. When schools reopen, his son will begin kindergarten. A little over a year ago, U Chit began experiencing dizziness, fatigue, tightness in his chest and difficulty breathing when he exerted himself. A month later, he visited a local clinic where he was diagnosed with high blood pressure. However, in December 2021, U Chit lost a lot of weight and experienced night sweats in addition to his other symptoms. He was diagnosed with aortic valve regurgitation, mitral valve regurgitation and tricuspid valve regurgitation, and was placed on a waiting list to receive surgery. Because his condition is severe, the doctor recommended that he undergo surgery as soon as possible. Fortunately, our medical partner, Burma Children Medical Fund (BCMF), is helping U Chit access treatment. On April 8th, he will undergo mitral valve replacement surgery at BCMF's care center. After recovery, his symptoms should improve. Now, he needs help raising $1,500 to fund his procedure and care. U Chit shared, "I gave up and I was ready to die before. There are a lot of heart patients waiting to receiving surgery. Since I heard that I could have surgery with the help of donors, I feel like there is hope that I will survive. I have to look after my family because my son is still young. I will always remember everything the donors did for me."
Lionel is a charming five-month-old baby from Colombia. He was born near the northern coast and his parents are from Venezuela. After he was born, they moved to Medellin due to his father's job. Lionel was born with clubfoot of his right foot. Clubfoot is a condition in which the foot is twisted out of shape. This causes difficulty walking and wearing shoes as he grows older. Fortunately, Lionel's family traveled to visit our Medical Partner Clínica Noel where they can offer life-changing treatment. There, surgeons will perform clubfoot repair surgery on March 22nd. Our medical partner is requesting $1,422 to fund Lionel's clubfoot repair. After treatment, he will be able to learn how to walk and live a fully active life ahead. His father said: "I hope my little champion can get his surgery, I pray for his wellbeing. I just want his feet to be normal and hope to see him walking like any other child."
Florvencia is an eight-month-old girl from Haiti. She has an older brother and her father supports their family as a taxi driver. Florvencia has been diagnosed with hydrocephalus, a condition in which excess cerebrospinal fluid accumulates in the brain and increases intracranial pressure. As a result of her condition, Florvencia has been experiencing a rapidly growing head circumference. Without treatment, Florvencia will experience severe physical and developmental delays. Our medical partner, Project Medishare, is requesting $957 to cover the cost of surgery for Florvencia at Hospital Bernard Mevs that will treat her hydrocephalus. This is the only site in the country where this care is currently available and the procedure is scheduled to take place on February 17th. This critical treatment will place a shunt to drain the excess fluid from Florvencia's brain to reduce intracranial pressure and greatly improve her quality of life. With proper treatment, Florvencia will hopefully develop into a strong, healthy young girl. The family shared how grateful and happy they are to have this opportunity for surgery for their little girl.
Vicheka is the eldest of two children in her family and loves her younger sister who is three years old. Their family lives in Preah Vihear near the Thai border of Cambodia. Her father is a soldier and her mother is a potato farmer. At school, she is fond of math and Khmer literature and would like to be a teacher when she is older. She likes reading books, painting, playing with her little sister, and taking walks with her parents. When Vicheka was five, she was diagnosed with scoliosis of the spine—a sideways curvature of the spine that most often is diagnosed in adolescents. She has uneven shoulders, a bump in her lower back, difficulty standing up straight, and shortness of breath. It has become difficult for her to breathe, she tires easily, and she is having difficulty walking. This can be very difficult for young girls, they are often hidden at home because other children make fun of the way they look. A neighbor told her parents about our medical partner Children's Surgical Centre, so they traveled over 10 hours for a diagnosis and surgery. Surgeons plan to put in expanding rods along her spine. The expanding rods will allow her to grow and keep her spine from curving further, which could cause her more health problems if left untreated. Their family needs $1,500 for the surgery, which will cover medications, implants, and post-operative care. Vicheka said, "I hope the doctors can fix my spine so I can play with my friends and my back will be straight. I want to continue in school but it is hard for me to keep up, and I miss school."
Mu lives with her four nieces and nephew in a refugee camp along the Thai/Burma border region. One of her nieces is a medic, the other a teacher, and the two youngest go to school with her nephew. Mu is unemployed and in her free time she enjoys gardening and reading the Bible. In 2019, Mu started to suffer from abdominal pain, back pain, and exhaustion. When she touched her lower abdomen, she could feel a mass. After the International Rescue Committee (IRC) helped her undergo medical investigations at multiple hospitals, she was diagnosed with bilateral endometriosis cysts and was told she has cysts outside of her uterus. Although she needed surgery, she was told she would have to wait because all surgeries had stopped due to the outbreak of COVID-19 in Thailand. In September, she had an ultrasound which showed that she had one new cyst. The doctor said she would need surgery soon but Mu could not go back to Mae Sot Hospital for the next few months because more COVID-19 cases in the refugee camp caused a lockdown. When she was finally able to go to the hospital this month, doctors have scheduled her for surgery to remove her cysts. With Mu unable to pay for the procedure, IRC referred her to our medical partner Burma Children Medical Fund for financial assistance to raise $1,500 that is needed for her treatment. "I felt like half of my worries disappeared when I heard that I could have surgery with the support of donors," said Mu. "I have waited so long to receive surgery and my condition is so painful. I would like to say thank you so much to everyone who is helping me."
Marian is a seven-year-old student and the youngest child of three children in her family. Her mother is a housewife, while her father is a small-scale farmer. Marian has clubfoot of the right foot, a condition in which the foot is twisted out of shape. This causes difficulty walking and even wearing shoes. Marian tiptoes when she walks, has difficulty walking for long distances, and often falls. Fortunately, our medical partner, African Mission Healthcare (AMH), is helping Marian receive treatment. On November 22nd, she will undergo clubfoot repair surgery at AMH's care center. After treatment, she will be able to walk well, run, and play with her peers in school. Now, AMH is requesting $1,286 to fund Marian's procedure and care. Marian's mother shared, "I would love to see my daughter walking like other girls, and any support to make her surgery possible will be highly appreciated by our family."
Taraja is a charming five-year-old girl from Southwestern Tanzania and the oldest child in her family. Taraja has not started school yet, but her parents hope that once her condition is treated, she can enroll in kindergarten. Taraja’s parents grow maize, vegetables, and sorghum for a living. They get most of their food from their farm and her father also takes casual laboring jobs, like working on other peoples’ farms and carrying luggage, to supplement the family's income. Taraja has clubfoot of both feet. Clubfoot is a condition in which the foot is twisted out of shape causing difficulty walking and even wearing shoes. Fortunately, our medical partner, African Mission Healthcare (AMH), is helping Taraja receive treatment. On October 8th, Taraja will undergo clubfoot repair surgery at AMH's care center. After treatment, she will be able to walk easily and wear shoes. Now, AMH is requesting $935 to fund Taraja's procedure and care. Taraja’s mother shared, "it was very strange to see our daughter’s feet in this position. We tried to find treatment for her but we were advised to go to a big hospital, something we couldn’t afford to do. Please help us if it’s possible."
Nin is a 27-year-old rainy day farmer from Cambodia. He has 3 older sibling. Nin shared that he enjoys playing volleyball, football, fishing, and plays chess with his friends. In July 2021, Nin was in a motor vehicle accident that caused a mandible injury and paralysis of his shoulder. After the accident, he had his mandible fixed at a local government hospital. He was also diagnosed with a brachial plexus injury on his right side. The brachial plexus is a nerve network that transmits signals from the spine to the shoulder, arm, and hand. Injuries to this nerve network can result in loss of function and sensation. Nin still has no shoulder abduction, no elbow or wrist flexion, and has no sensation at the level of his forearm. Nin needs nerve reconstruction surgery to repair the injured nerves. Nin traveled to our medical partner's care center to receive treatment. On September 6th, he will undergo a brachial plexus repair surgery. After recovery, he will be able to use his arm and hand again. Our medical partner, Children's Surgical Centre, is requesting $696 to fund this procedure. Nin hopes that he can use his hand again as soon as possible.
Suraiya is a young three-year-old girl and the last born child in a family of two. Her parents depend on small scale farming of maize and vegetables to feed their family and they sell the surplus to make ends meet. Suraiya's mother also sells food at a local food joint commonly known as Mama Ntilie to supplement their income. Suraiya was diagnosed with bilateral genu varus. She is currently having a hard time walking due to her legs bending outwardly. Her mother noticed the condition when Suraiya learned to stand and walk. They tried to seek treatment for her at the district hospital but the cost was too high for them to afford. They were advised to get national health insurance for her but due to financial challenges, they could not afford to get the insurance. During a medical outreach program organized by Plaster House, Suraiya's parents were advised to take her to ALMC Hospital for review. Her condition is typically caused by an excessive accumulation of fluoride in the bones, which often stems from contaminated drinking water. Over the years Suraiya's legs have worsened making walking more difficult and painful for her. Suraiya and her family are appealing for help for her to be treated. Our medical partner, African Mission Healthcare, is requesting $880 to fund corrective surgery for Suraiya. The procedure is scheduled to take place on August 19th. Treatment will hopefully restore Suraiya's mobility, allow her to participate in a variety of activities, and greatly decrease her risk of future complications. Suraiya’s mother says, "Money to cover our daughter’s treatment cost has been our biggest challenge because the cost is too high for us to afford. Please help treat our daughter.”
Dora is a teenager studying in class six and her best subjects are English and Swahili. Once she completes her studies, Dora has dreams to become a teacher. At home, she is the seventh oldest of her mother's eleven children. Dora's father has three wives, so Dora has twenty siblings total. Dora likes helping her mother with home chores, such as washing dishes and keeping their home clean. Dora's parents are small scale farmers of maize and vegetable, and they also have a few cattle that they depend on for milk. Dora was diagnosed with left genu valgus, a condition typically caused by an excessive accumulation of fluoride in the bones, which often stems from contaminated drinking water. As a result, her left leg is bowed so that her knees touch, thus making walking difficult. Dora has to walk forty minutes one way to and from school everyday, so this condition poses a significant barrier to Dora continuing her education and pursuing her aspirations. Our medical partner, African Mission Healthcare (AMH), is requesting $880 to fund corrective surgery for Dora. The procedure is scheduled to take place on July 15th. Treatment will hopefully restore Dora's mobility, allow her to participate in a variety of activities, and greatly decrease her risk of future complications. Dora shares her current condition, "When I walk to school my leg pains so much there are days I am unable to put weight on the leg especially when it’s cold. Please help me."