Linda joined Watsi on October 4th, 2015. Six years ago, Linda joined our Universal Fund, supporting life-changing treatments for a new Watsi patient every month. Linda's most recent donation supported Rose, a beautiful 7-month-old baby from Haiti, to fund surgery that will help her to grow up healthy and strong.
Linda has funded healthcare for 76 patients in 12 countries.
Linda has funded healthcare for 76 patients in 12 countries.
Rose is a 7-month-old baby from Haiti. She lives with her father and grandmother, and they shared that she loves to smile and play with her family! Rose has been diagnosed with hydrocephalus, a condition in which excess cerebrospinal fluid accumulates in the brain and increases intracranial pressure. As a result, Rose has been experiencing an increasing head circumference. Without treatment, Rose will experience severe physical and developmental delays. Our medical partner, Project Medishare, is helping Rose receive treatment at Hospital Bernard Mevs, the only site in Haiti where the treatment she needs is available. On May 27th, Rose will undergo surgery to drain the excess fluid from her brain to reduce intracranial pressure and improve her quality of life. With this treatment, Rose will hopefully develop into a strong, healthy young girl. Project Medishare is requesting $897 to cover the cost of her surgery. Rose's father shared that he hopes for a healthy life for Rose in the future.
Vania is a hardworking 14-year-old student from Haiti. She lives in an urban area of the island nation's capital, Port-au-Prince, with her parents and three younger brothers. She enjoys studying, especially science and literature. Unfortunately, Vania has not been able to attend school for two years because of her heart condition. She suffered from rheumatic fever early in her childhood. The illness damaged one of the four valves in her heart, leaving her with a condition called rheumatic mitral regurgitation. Her heart cannot pump blood adequately through her body, which leaves her weak and short of breath. The good news is that surgery can help. Vania will fly to the Cayman Islands to receive treatment. On May 16th, surgeons will remove her damaged valve and implant an artificial valve in its place. Another organization, Have a Heart Cayman, is contributing $17,000 to pay for the procedure. But Vania's family also needs help to fund other medical and travel costs, which is where our Watsi donors come in. They are raising $1,500 to cover lab work and medicine for Vania, along with checkup and followup appointments. It also will help pay for her to get a passport and support social workers from our medical partner, Haiti Cardiac Alliance, who will accompany Vania and her family overseas. Vania says, "I am looking forward to this surgery so that I can feel more normal and go back to school."
Feven is a beautiful 7-month-old baby girl from Ethiopia. She has two older brothers and five sisters. She loves to play with her mom. Her dad is a farmer and he works hard, but his income is not enough to maintain the family so his brother often helps. All their children are in school and Feven's mom sometimes is able to sell items at the market. Feven was born with a birth defect called anorectal malformation. She developed bowel obstruction because of her condition and had an emergency colostomy surgery. Her parents shared that they are highly affected psychologically and are sad and worried about their baby. Feven now needs a follow up surgery to help her eliminate bowel dysfunction. She is scheduled to undergo surgery to correct her condition on March 22nd. Our medical partner, African Mission Healthcare, is requesting $1,500 to cover the total cost of her procedure and care. After her recovery, Feven will no longer experience bowel dysfunction or be at risk of developing related health complications in the future. Her mom shared, “We were so worried. But thank God he gave us this opportunity.”
Myo Myint is a 34-year-old woman who is married with two sons and a daughter. Myo Myint, her husband, and her oldest son work as day laborers, but since April 2020, they have had difficulty finding work due to COVID-19. She proudly shared that her younger son and daughter are both students. In her free time, Myo Myint likes to listen to the news on the radio and walk around to collect sticks and branches that she uses for her cooking. Myo Myint has been experiencing difficulty with her vision in her right eye. She can only read for a few minutes before her eye begins to hurt and her vision becomes doubled. She visited a local hospital, where the doctor determined she has a cataract in her right eye and recommended lens replacement surgery. Our medical partner, Burma Children Medical Fund (BCMF), is helping Myo Myint receive treatment. On March 1st, doctors will perform a lens replacement, during which they will remove Myo Myint's natural lenses and replace them with an intraocular lens implant in each eye. After recovery, she will be able to see clearly. BCMF is requesting $1,500 to help fund this procedure. Myo Myint shared, "I want to see clearly and find extra money to support my children to finish their education."
Heavenlight is a 14-year-old girl and the second-born child in a family of seven children. Heavenlight was going to join advance grades in school this January, but she had to stop attending school because she is having difficulty walking to and from school every day. Heavenlight loves biology, physics, and chemistry and wishes to be a doctor when she grows up. She is worried this dream might be lost if she does not have her leg treated. Heavenlight was diagnosed with genu valgus. This condition causes her legs to bow inward so that her knees 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, Heavenlight has difficulty walking. Our medical partner, African Mission Healthcare, is requesting $880 to fund corrective surgery for Heavenlight. The procedure is scheduled to take place on January 13th. Treatment will hopefully restore Heavenlight's mobility, allowing him to participate in a variety of activities, and greatly decrease his risk of future complications. Heavenlight shared, “I am ready to miss a few months of class just to have my leg corrected because it is painful and I struggle a lot walking to school."
Gideon is four years old and the last-born in his family of six children. He is a playful, charming, friendly, and happy boy. Gideon comes from the southern highlands of Tanzania close to Katavi National Park. Gideon has not yet started school, but his father says when he gets to be six years old, he will enroll him. Most children in this region join school starting at the age of six due to the long distance they must walk to school. Parents must wait for their children to grow strong enough to walk to and from school before enrolling them. Gideon’s parents are small-scale farmers of maize, beans, and vegetables and only sell a few of their harvests to get money to buy other basics for their family. Gideon has been diagnosed with bilateral genu valgus, where his legs bow inward so that they 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, he experiences pain and discomfort. Our medical partner, African Mission Healthcare, is requesting $880 to fund corrective surgery for Gideon. The procedure is scheduled to take place on January 4th. Treatment will hopefully restore Gideon's mobility, allow him to participate in a variety of activities, including school in the future, and greatly decrease his risk of future complications. Gideon’s father says “My son walks with a gait and falls down a lot. He also complains of pain after a long day of play.”
Marvens is a student from Haiti. He lives with his parents and three siblings in a neighborhood of Port-au-Prince. He enjoys going to school and would like to continue to university and study business in the future. Marvens has a cardiac condition called atrial septal defect. A hole exists between the two upper chambers of his heart. Marvens will fly to Dominican Republic to receive treatment as it is not available within Haiti. On November 26th, he will undergo cardiac surgery, during which surgeons will sew a patch over the hole in his heart so that blood can no longer leak through. Our medical partner, Haiti Cardiac Alliance, is contributing $8000 to help pay for surgery. Marvens's family also needs help to fund the costs of surgery prep. The $1,500 bill covers labs, medicines, and checkup and followup appointments. It also supports passport obtainment and the social workers from our medical partner, Haiti Cardiac Alliance, who will accompany Marvens's family overseas. Marvens wanted to share: "I would like to say thank you to everyone who is helping to heal my heart so that I can be normal and healthy."
Edrian is an active and talkative 4-year-old boy. He is the youngest in a family of three children. Both of his parents work as teachers, and one of his parents secured a new job recently which they are feeling optimistic about. A few months after Edrian was born, his mother noticed a birth condition. She consulted with his father, and they decided to raise funds to take Edrian to a local hospital. After examination, Edrian was diagnosed with left undescended testes, and surgery was done to address this condition. However, his surgery was unsuccessful and the doctors referred their family to our medical partner’s care center, BethanyKids Kijabe Hospital (BKKH) for additional care. At BKKH, Edrian was diagnosed with cryptorchidism, a condition in which one or both of the testicles remains undescended. If left untreated, Edrian has an increased risk of developing hernias, testicular cancer, and fertility problems in the future. Fortunately, Edrian will be receiving assistance from our medical partner, African Mission Healthcare Foundation (AMHF), and will undergo corrective surgery on November 1st. AMHF is requesting $646 to cover the total cost of his procedure and care. Edrian’s mother shared, “It has been a long and stressful journey for us since he was diagnosed with the condition, but we are still hopeful that all will be well.”
Nehemia is a nine-year-old child from Tanzania and the fourth born in a family of five children. She is currently in kindergarten and she loves singing the vowels. Nehemia's parents keep livestock for a living and sell the milk. Once in a while, they also sell a goat to make additional money. Nehemia has 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, Nehemia traveled to visit our medical partner, African Mission Healthcare (AMH), to receive treatment. On September 14th, surgeons at AMH's care center will perform clubfoot repair surgery. Now, AMH is requesting $935 to fund Nehemia's clubfoot repair. After treatment, she will be able to walk easily. Nehemia’s father shared, "every day when she gets home from school she complains of pain and you can easily see she is trying not to put pressure on the foot due to fear of pain. Please help my daughter."
Vedastus is a two-year-old boy and the only child of his young parents. He's a friendly boy who is currently having a hard time walking because his legs bow outwards. Vedastus' mother works at a local food joint as a cook. Her income is not much, but enables her to support and care for her son. Vedastus' father is still in college studying, which leaves Vedastus' mother as the only parent with an income. Vedastus was diagnosed with fluorosis - genu varus, where his legs bowing outwards so that his knees do not 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, Vedastus cannot walk well and he is in pain. Our medical partner, African Mission Healthcare, is requesting $880 to fund corrective surgery for Vedastus. The procedure is scheduled to take place on September 2nd. Treatment will hopefully restore Vedastus's mobility, allow him to participate in a variety of activities, and greatly decrease his risk of future complications. Vedastus’s mother says "I am the only person working to be able to provide for our son. The father of my son is still studying and my income is not enough to care for Vedastus and afford his treatment cost. Please help us, he needs treatment for his leg because he is struggling to walk.”
Maria Jose is a cute and intelligent baby from Colombia. She lives with her single mother, Sandra, and her godmother and aunt. Sandra only has good wishes for her daughter, and works really hard to see her baby happy. Maria Jose has clubfoot on both feet, a condition in which the foot is twisted out of shape. This will cause difficulty walking and even wearing shoes in the future. Fortunately, Maria Jose's family traveled to visit our medical partner, Clínica Noel. There, surgeons will perform clubfoot repair surgery on August 31th. Our partner is requesting $1,500 to fund Maria Jose's bilateral clubfoot repair. After treatment, she will be able to crawl, walk and run with ease. Sandra shares her hopes for Maria Jose's development, "I really wish to see her grow as a normal child, and enjoy every step of her life. After the surgery I deeply want to see her crawl, walk, run, and play with other kids."
Jesca is a hardworking, friendly, and sociable girl who loves music and singing in the choir at church. She's an 18-year-old teenager, born as the third child in a family of nine. Jesca was only able to study until seventh grade because she was experiencing mobility issues due to clubfoot, making going to school particularly challenging. Jesca's father tried to encourage his daughter to continue with school by discussing with her the the importance of education. However, Jesca was too concerned about going to secondary school, which is located even further away and thereby posing an even bigger challenge for her. Jesca has clubfoot on her left foot. Clubfoot is a condition in which the foot is twisted out of shape, causing difficulty walking and even wearing shoes. Fortunately, Jesca has now traveled to visit our medical partner's care center, Arusha Lutheran Medical Centre. There, surgeons will perform a clubfoot repair surgery on June 29th, and requests support of $935 for her treatment costs. After treatment, Jesca will be able to walk normally and is hopeful for a better life ahead. Jesca describes her previous decisions about school with regret but turns an optimistic outlook for her future: "If it wasn’t for my foot I would have probably continued with school and maybe today I would be in a better position. I am now working but my foot is still limiting my work. Please help me have my foot corrected."