Carolyn joined Watsi on March 12th, 2013. 1,770 other people also joined Watsi on that day! Carolyn's most recent donation traveled 7,400 miles to support Sathya, a 4 year old boy from Cambodia, to fund ear surgery.
Carolyn has funded healthcare for 190 patients in 18 countries.
Carolyn has funded healthcare for 190 patients in 18 countries.
Sathya is a charming, 4-year-old boy, living in Cambodia with his parents and younger sister. At home, he enjoys painting and drawing, and his favorite foods are Cambodian soup and fried eggs. Yesterday, Sathya was playing at home with a small object. His mother saw him stick a small, round, green item into his ear, and then realized, too late, that it had become stuck. Sathya is scared, and he also has pain in his right ear. Sathya's family sought help from the doctors at our medical partner, Children's Surgical Centre. On January 10th, surgeons at Kien Khleang National Rehabilitation Centre will remove the object from Sathya's ear. Now, Sathya and his family need help to raise $273 to fund this procedure. Sathya's mother said: "I hope after removing this from my son's ear, he is not in pain anymore."
Saw Myo is a 14-year-old from Burma. He lives with his grandparents, parents, two sisters, and brother. His grandparents are retired. His father farms paddy and rubber trees on their land, while his mother is a homemaker. Saw Myo and his siblings are all in school, but Saw Myo recently had to stop attending due to a medical condition. Saw Myo has had a lump on his lower spinal cord since he was nine years old due to an injury from a slingshot. He received medicinal ointment from a traditional healer that helped with the stiffness and prevented further growth. However, Saw Myo fell off his bicycle a few years later, and the lump grew in size. His family took him to several clinics, and an X-ray indicated a potential spinal cord problem. The doctors recommended a computerized tomography (CT) scan, but due to COVID-19 policies, Saw Myo could not receive the scan. His parents continued to try and help Saw Myo receive treatment but learned that his condition could not be treated locally. Saw Myo's mother then contacted a neighbor who worked as a medic at a clinic in Burma and began raising money for his care. The doctors want Saw Myo to undergo an MRI, which is an imaging procedure that uses magnetic fields and radio waves to produce images of bodily organs. This scan will help doctors diagnose his condition and formulate an appropriate treatment plan. Our medical partner, Burma Children Medical Fund (BCMF), is helping Saw Myo receive this treatment. On November 15th, he will undergo an MRI. BCMF requests $814 to cover the cost of Saw Myo's MRI procedure and care. Saw Myo's mother said: “We have been so worried since we saw the mass increasing in size. It was tiring to seek treatment in Burma, and we now have borrowed a lot of money without Saw Myo having received treatment."
Darika is 11 years old, and lives in Phnom Penh City, Cambodia with her parents and her two younger brothers. She attends grade seven in public school, and her favorite subject is Khmer literature. When she grows up, she would like to be a doctor. At home, she enjoys writing stories and reading books to her brothers. Darika has genou valgum or knock knees. It is a knee misalignment that turns her knees inward. Additionally, her left leg is shorter than her right leg. This causes her to limp, and if she walks for too long, her legs become painful. She shared that she feels embarrassed by how her legs look, and doesn't want other children to make fun of her. Darika needs to under go a procedure using metal plates to realign her legs, while lengthening the bones in her left leg. With the aid of our medical partner, Children's Surgical Centre, Darika is now scheduled for surgery at Kien Khleang National Rehabilitation Centre, on December 12th. Darika and her family need your help to pay for this procedure, which will cost $469. The surgery, and physical therapy afterwards, will enable Darika to walk without pain. Darika's mother said: "I hope my daughter's legs will be straight, and she will be able to be like other children, and not be in pain anymore."
Meet Zipporah, who is almost three years old. She has four siblings and lives with them and her parents in Nairobi County in Kenya. Zipporah was healthy at birth. However, when she was about one year old, her mother noticed a swelling in her right thigh, which appeared to affect her mobility. Subsequently, Zipporah was diagnosed with Coxa vara, a deformity of the hip, which causes a shortening of the leg. As a result of her condition, Zipporah limps and experiences pain in her hip. With the help of our medical partner, African Mission Healthcare Foundation, Zipporah is now scheduled to undergo surgery to correct her deformity on February 27th, at AIC Cure International Hospital. This procedure, which will cost $1,224, will prevent further deterioration of her condition. Zipporah and her parents need help to fund the costs of this life-changing surgery. “We would like to request support from well-wishers to help my daughter undergo surgery so that she can resume walking well like other children and enroll in school.” Zipporah’s mother told us.
Meet Nafissa. She is a 25-year old woman who shared that she tends to be very shy and reserved. She lives with her parents and her young child in an area of Burkina Faso where conflict is currently impacting their lives deeply. When she was a child, Nafissa developed a painful growth on the left side of her chin. This swelling in her lower jawbone affected her ability to eat, and was determined to be a benign tumor that needed to be removed. Her parents were able to secure the funds to send Nafissa to a hospital in Togo, where she could be treated at no cost to her family. The growth was removed, and for several years, Nafissa did well. However, the growth recurred, and in the middle of last year, Nafissa returned to Togo, where the second growth was excised. This time, however, the surgeon determined that her whole jawbone would also need to be removed. As the doctor in Togo did not have the necessary training to perform the surgery that Nafissa needed, he referred her to a physician with our medical partner, African Mission Healthcare. Miraculously, Nafissa is now scheduled for a major jaw surgery with the leading team at AIC Kijabe Hospital in Kenya. As Nafissa's husband abandoned her because of her condition, and provides no support to Nafissa or their child, Nafissa and her parents are looking to you to help fund the $1,500 procedure, which will finally relieve Nafissa of the pain and symptoms that result from the tumor. Nafissa says: “It pains me that I have to stay at home with no friends. Making it worse, I cannot work to provide for my child.”
Sophea is an 18-year-old student from Cambodia. She lives at home with her parents and two siblings. Her dad is a rice farmer and her mom cares for the children at home. Sophea spends most of her free time reading and studying. She enjoys spending time with her family and going to school. Sophea was born with club feet, a condition in which the feet are turned in and under, making it difficult to walk and balance. Currently, Sophea uses a wheelchair to help her get around. Sophea's family traveled an hour and a half to visit our medical partner, Children’s Surgical Centre (CSC), so she could undergo clubfoot treatment. On February 15th, surgeons will perform bilateral tendon Achilles lengthening (TAL) and casting. Surgery and physiotherapy will improve her mobility. The procedure will cost $572. Sophea said, “I hope I will look better after surgery and walk someday.”
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."
Marion is a 6-year-old student from the highlands of Elgeyo Marakwet county in Kenya. She is the second born in a family of three girls and currently attending preschool near her family home. Her parents are small-scale potato farmers. One day Marion's mother went to the river to fetch water. While she was gone, her children were sitting near an open fireplace at home making breakfast. Unfortunately, Marion's dress caught fire on the open flame, and as a result, she sustained severe burns on her back, abdomen and thighs. It has been difficult for her to walk, and the wounds are causing extreme discomfort. She especially needs a third surgery to treat the severity of her burns contractures. Despite Marion's parents having medical insurance, due to previous surgeries that she has had to treat the injuries, the insurance (a monthly subscription) has run its course and is no longer an option. Her parents do not have the funds to pay for Marion's surgery and need support. Fortunately, our medical partner, African Mission Healthcare (AMH), is helping Marion receive treatment. On January 25th, surgeons at their care center will perform a burn contracture release surgery that will allow her to walk with greater ease and resume her normal life at home and school. Now, she and her family are requesting $1,478 to help fund this procedure. Marion's mother says, “I am really looking forward to seeing my daughter live and walk in a normal way. I worked hard to pay for insurance coverage, but unfortunately, it cannot fund the upcoming procedure. I am disappointed, but I will not lose hope. Kindly help her.”
Valentina is a beautiful 2-year-old girl from Bolivia. She lives in La Paz with her parents, who are a teacher and a homemaker respectively, and two older siblings. Valentina was born with a cardiac condition called atrial septal defect, in which a hole exists between the two upper chambers of her heart. As a result blood leaks through this hole, leaving her weak and short of breath. Our medical partner HCA is helping Valentina access life-saving cardiac treatment so she can grow up healthy. During surgery, doctors will use a patch to close the hole so that blood can no longer leak through it. Her family is raising $1,500 to support her surgery and care. Valentina's mother shared: "Our family is very thankful that Valentina can have this opportunity for her heart to be healed."
Khine is a 17-year-old girl from Burma. She lives with her mother, her older sister, and her uncle's family. She works as a domestic worker. Three months ago, she started to feel dizzy and have headaches. She had a CT scan at Mae Sot Hospital, which indicated she might have a brain tumor. Shine experiences headaches, dizziness, and sometimes vomits. She has also had seizures multiple times and weakness in her limbs. She has little appetite and has lost weight. Gradually, she is losing her ability to speak. Khine sought treatment through our medical partner, Burma Children Medical Fund. She is now scheduled to undergo surgery to remove the tumor on February 3rd. She is requesting $1,500 to cover the total cost of her procedure and care. Her uncle said, "Although I am a man, I have cried for my niece. I even thought about selling one of my organs (for money), one of my kidneys perhaps, because we cannot afford to treat her. Thank you to all the donors for helping my niece. After she is treated, I want her to have a happy family, with a husband and children. I cannot wait to see my niece happy."
Meet Gianna, a lovely, four year old girl from Kenya. Gianna lives with her grandmother, while her mother works at a local hotel, and her father is a casual laborer on construction sites. Gianna was born with Osteogenesis imperfecta, also known as brittle bone disease. A child born with this condition has soft bones that break easily. Gianna has never walked, and lives in near constant pain. When she did try to walk using support, she fractured some bones. Our medical partner, African Mission Healthcare Foundation, is here to help Gianna access the care that she needs. On January 16th Gianna will undergo a procedure at AIC Cure International Hospital, that will provide greater support for Gianna's bones, and which may even enable her to gain sufficient strength to walk. Gianna's family is seeking your support to fund the $1,224 needed to pay for the surgery. Gianna's grandmother said: "Gianna has never walked, and my desire is to see her walk like other children. Your financial support to help her undergo surgery will be greatly appreciated."
Meet Night, a jovial and playful five year old girl. Night lives with her parents and two younger siblings in a traditional home in Kenya. Her father works selling second hand clothing, while her mother stays home to take care of the children. Shortly after she was born, Night's parents realized that something seemed wrong. They brought Night to a health facility in Turkana County where they lived, and were referred on to BethanyKids Hospital. There she was diagnosed with hydrocephalus, which meant that fluid was collecting in her head. Surgery was performed, and a shunt was placed to continuously drain the fluid from Night's head. A year later, however, Night's head began to increase in size, and she developed weakness on the right side of her body. The doctors at the local health facility urged Night's parents to take her back to BethanyKids Hospital for additional treatment, but Night's parents didn't have enough money to do this. With the help of our medical partner, African Mission Healthcare Foundation, Night is now scheduled to undergo a craniotomy on January 5th at BethanyKids Kijabe Hospital, when surgeons will drain excess fluids from Night's brain. Night's father is providing as much of a co-pay as possible for this procedure, but the family needs your help to raise the remaining $1,500 required to cover all of the costs of Night's surgery and care. Night’s father said: “Night is not able to communicate well because of her condition. This surgery will help her to be able to speak.”