Carolyn joined Watsi on March 12th, 2013. 1,771 other people also joined Watsi on that day! Carolyn's most recent donation traveled 8,400 miles to support Evaline, a smart young girl from Tanzania, to fund reparative surgery on her leg to allow her to walk with ease.
Carolyn has funded healthcare for 136 patients in 15 countries.
Carolyn has funded healthcare for 136 patients in 15 countries.
Evaline is a charming, smart seven-year-old girl. She knows a lot a fun facts! Evaline is being raised by her grandmother, after her father was upset when she was born with a birth condition impacting her left leg. Her mother decided to have Evaline grow up in the care of her grandmother out of fear of discrimination. Evaline thinks of her grandmother as her own mother and they are very close. Evaline’s grandparents are small-scale farmers who depend entirely on what they harvest for their food. They are able to make small amounts of money by selling vegetables. Evaline was born with a condition on her left leg called amniotic banding and left clubfoot. She has undergone treatment for clubfoot but is in need of care for her amniotic banding condition. As a result, she has a hard time walking and carrying out daily life activities. Fortunately, our medical partner, African Mission Healthcare, is helping Evaline to receive the life changing treatment she needs. On March 2nd, surgeons at their care center, Arusha Lutheran Medical Centre, will perform corrective surgery on her left leg, which will allow her to walk more easily. Evaline and her grandparents needs help to fund this $639 procedure. Evaline’s grandmother says,"This far my granddaughter has gotten through your treatment is a miracle."
Colleta is a 26-year-old woman who works at a small boutique in Nairobi. She is married and has two children, who are four-years-old and five-months-old. Colleta and her family currently live in the capital city, but they plan to relocate to Colleta’s hometown soon. Colletta and her family were involved in a serious car accident last month. Her parents and brother passed away, and her husband and two children were seriously injured and admitted to the ICU. Although her husband’s condition has stabilized, Colleta’s kids are in critical condition and under pediatric intensive care. Colletta sustained a fracture to her right pelvic bones. As a result, she experiences severe pain and cannot sit, turn her body, or feed herself. Fortunately, surgeons at our medical partner, African Mission Healthcare (AMH), can help Colletta receive treatment. On April 28th, she will undergo a fracture repair procedure, called an open reduction and internal fixation, that will allow her to sit and walk again. AMH is requesting $979 to fund this procedure. Colleta shared, “I am in pain and cannot even turn or sit. I am also sad that I lost my parents and my brother. My kids and husband are in critical care and still in ICU. I feel confused and heartbroken.”
Ko Ko is a three-year-old boy who lives with his parents and his siblings. His father and oldest brother are agricultural day labourers while his mother looks after him. Ko Ko enjoys playing with his toys and playing football with his brothers. He also enjoys watching movies on his mother's phone. When Ko Ko was one year old, his mother noticed a small white spot on his right pupil. She did not know what had caused the spot, but did not think it was serious. In December, Ko Ko’s mother asked him to give her a cup of water, but when he stood up he called out that he could not see where the water was, while trying to feel his way with his hands. Currently, Ko Ko is only able to recognize light. He needs his mother to guide him, and help him with tasks such as eating and showering Doctors want Ko Ko to undergo a CT scan. This scan will hopefully help doctors diagnose his condition and formulate an appropriate treatment plan. Our medical partner, Burma Children Medical Fund, is requesting $414 to cover the cost of Ko Ko's CT scan and care, scheduled for February 3rd. Ko Ko's mother said: "As a mother, I worry about him and I want to give him everything so that his vision can return, but I do not have money to pay for his treatment. Thank you so much for your kindness and for helping my son. May the goodness you have shown us return to you and may you be successful.”
Daw Khin is a 45-year-old woman from Burma. She lives with her parents, who are retired and supported by Daw Khin's sister, who earns an income from renting out their land. Daw Khin used to work as a teacher before her condition made it difficult for her to continue teaching her students. Around June 2020, Daw Khin began to feel very tired and experienced heart palpitations. She shared that it felt like she could not breathe while teaching. Because these episodes happened infrequently, she did not seek treatment at the time; however, in December 2020, her condition worsened, and she went to a local hospital. After receiving an electrocardiogram, doctors determined she has an enlarged heart and an abnormal heartbeat and prescribed medication to help Daw Khin feel better. Since Daw Khin's symptoms continued, her sister brought her to a cardiologist in April 2021. Upon review, Daw Khin's condition was diagnosed as an atrial septal defect, a birth condition in which there is a hole in the wall that divides the upper chambers of the heart. The cardiologist informed her that she would need surgery, but the cost was too high for Daw Khin's family, so they returned home with medications. Daw Khin currently experiences headaches, difficulty sleeping, and fatigue and heart palpitations when talking or walking short distances. Fortunately, a friend visited Daw Khin in June and told her about our medical partner, Burma Children Medical Fund (BCMF). Daw Khin contacted BCMF and learned that BCMF will be able to help her finally heal. On February 6th, she will undergo an atrial septal defect (ASD) closure. BCMF is requesting $1,500 to help fund her procedure. Daw Khin shared, "I would like to teach all my students again in the future. I like teaching students."
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."
Melany is a joyful six-year-old girl from Colombia. She lives with her great-grandmother as he mother left when she was two years old. Melany loves to play with her "nana", and laughs a lot. Melany was born with Cerebral Palsy, and her great grandmother has been incredibly supportive in her treatment through the years, ensuring that she has the best possible prognosis. Due to her condition, Melany experiences recurrent hip dislocation and requires corrective surgery to help her walk. Fortunately, our medical partner, Clínica Noel, is helping Melany receive treatment. On February 14th, she will undergo corrective surgery, and, now, she and her family need help raising $1,362 to fund her procedure and care. Melany's great-grandmother shared, "my biggest motivation is seeing her walk by herself, or at least depend a little less on me. I'm afraid to die and leave her alone in a world where she only has me and her uncle."
Nita is a 31-year-old seller of Khmer beverages. She has a 6-year-old daughter. Her husband works for a company in the capital city of Phnom Penh in Cambodia. When not caring for her family, she likes to exercise, read books, and listen to music. A year ago, a mass started growing on Nita's right mandible, which she originally thought was a wisdom tooth. She visited a local hospital for a biopsy, and she was diagnosed with a low-grade mucoepidermoid carcinoma. She experiences pain and discomfort. She is scared she will be permanently disfigured or might die. When Nita learned about our medical partner, Children's Surgical Centre, she traveled for two hours seeking treatment. On December 6th, surgeons at CSC will perform a mandibulectomy and extensive facial reconstruction to to rid her body of the tumour and avoid permanent disfigurement. Now, she needs help to fund this $657 procedure. She is hopeful that the tumor will be removed and she will quickly heal.
Srey Nath is a bright young student who loves to read books and wants to be a teacher when she grows up. She has two older brothers and lives with her parents who are rainy day rice farmers. They also grow vegetables and keep cows and chickens to feed their family and make extra money at the local market. Over the past several years, Srey Nath's back has curved which limits her movement and lung expansion. She has trouble standing up straight or walking, and is easily winded when she is active due to difficulty expanding her lungs. She shared that she feels embarrassed with her friends and very shy about how her back looks. She loves school but doesn't want to attend now because of the abnormal curvature of her spine, and the chronic pain it causes. Srey Nath's neighbors told her family to visit our medical partner, Children's Surgical Centre for a diagnosis and treatment. Surgeons have diagnosed her with scoliosis of the thoracic spine. She needs expanding rods in her back to straighten her spine as she grows to avoid any further medical problems. Srey Nath and her parents traveled two and a half hours to seek treatment and need help raising $1,500 for this specialty surgery. Srey Nath's mother said: "My daughter needs this surgery to grow normally and become a teacher. I hope we can raise the money so she can fulfill her dream someday."
Mark Gabriel is a two-year-old boy from the Philippines. He loves singing the alphabet and Twinkle Twinkle Little Star. He is the oldest son of his parents. His father works as a call center agent, while his mother is a stay-at-home mom. Mark Gabriel was born with a birth condition that leads to a complete or partial intestinal blockage. He needed to undergo a series of procedures to eliminate bowel dysfunction. Fortunately, our medical partner, World Surgical Foundation Philippines, is helping Mark Gabriel receive treatment. On December 8th, he will undergo colostomy closure surgery to correct his condition. After his recovery, Mark Gabriel will no longer experience bowel dysfunction or be at risk of developing health complications in the future. Now, World Surgical Foundation Philippines is requesting $1,279 to cover the total cost of Mark Gabriel's procedure and care. Mark Gabriel's mother shared, "after his surgery, we hope that he will live a life without carrying a colostomy bag."
Saray is a 16-year-old construction worker from Cambodia. His parents are rice farmers, and he has an older brother and an older sister. When he is not working, he enjoys playing football, volleyball and games on his phone. He also likes to sing with his friends. Four months ago, while playing football, Saray fell on his shoulder and a mass appeared and grew quickly. A biopsy revealed that he has osteosarcoma of the shoulder, a rare type of bone cancer in which cancerous cells produce irregular bone. Although osteosarcoma is rare, it is the most common childhood bone cancer. He cannot move his shoulder and experiences persistent bone pain. Fortunately, a CT scan revealed that cancer has not yet spread. This diagnosis is very difficult for a young man with his whole life ahead of him. When Saray's parents learned about our medical partner, Children's Surgical Centre (CSC), they traveled there to see a specialist. On December 8th, surgeons at CSC will perform a shoulder disarticulation procedure, during which they will separate his entire arm from the shoulder joint. This procedure will remove the mass, avoid metastasis, and allow Saray to seek further treatment. Now, he and his family need help raising $446 to fund his procedure and care. Saray shared that he hopes that cancer will not reappear after the mass is gone, and he can be without pain.
Mu is a 17-year-old boy who lives with his sister in Mae Sot, Thailand. Before that, he lived with his parents, one older sister, two younger brothers and one younger sister in a refugee camp. His sister works at a non-governmental organisation helping others in need. Around mid-August, Mu woke up one morning with pain in his left knee. At first he thought that the pain would go away on its own and that it was nothing serious. However, when the pain remained a few days later, he told his sister about it. His sister bought him a type of Burmese pain reliever balm to apply on his knee. He applied the balm for a week, but he did not feel any better. When he and his sister noticed that his left knee had become slightly swollen his sister called their father. Mu’s father told them that it could be an ulcer and suggested that they go to a hospital or buy him pain medication to reduce swelling. His sister bought the medication their father had suggested at a pharmacy, and Mu took it for a week. However, he did not feel better, and the swelling did not decrease. Mu was able to have an MRI at Chiang Mai Hospital and now the doctor recommends he undergo surgery to remove a tumor on his left knee. Mu sought treatment through our medical partner, Burma Children Medical Fund and is now scheduled to undergo mass removal surgery on December 17th. He is requesting $1,500 to cover the total cost of his procedure and care which will enable him to get off of using crutches and back to feeling well again. Mu said, "After I heard from the doctor that my leg does not need to be amputated, I feel so happy."
Naw Khu is a 25-year-old woman from Burma. She lives with her parents and two brothers in a village. Naw Khu is a homemaker, while the rest of her family works as farmers growing beans and nuts on their land. Unfortunately, due to the pandemic and the Burmese military takeover, Naw Khu's family has had difficulty selling their crops. In early September 2021, Naw Khu started to experience edema in her whole body, and especially in her face, legs, and hands. Her abdomen has also become enlarged and she has experienced a loss of appetite. She has had abnormal bleeding and feels tired when walking long distances. At night, she often has a fever and has difficulty sleeping. Our medical partner, Burma Children Medical Fund (BCMF), is helping Naw Khu receive treatment. On December 9th, she will undergo a CT scan, or 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. Now, Naw Khu needs help raising $414 to cover the cost of Naw Khu's CT scan and care. Naw Khu shared, "sometimes I want to give up, but I feel bad for my mother. She tries very hard to help me. She spends all her time with me. I feel sorry for her."