Amelia joined Watsi on December 2nd, 2015. Four years ago, Amelia joined our Universal Fund, supporting life-changing treatments for a new Watsi patient every month. Amelia's most recent donation supported Jefferson, a 3-month-old baby boy from Haiti, to fund surgery for hydrocephalus.
Amelia has funded healthcare for 50 patients in 9 countries.
Amelia has funded healthcare for 50 patients in 9 countries.
Jefferson is a three-month-old baby boy from Haiti. He lives with his parents and one older brother. Jefferson has been diagnosed with hydrocephalus, a condition in which excess cerebrospinal fluid accumulates in the brain, increasing intracranial pressure. As a result of his condition, the circumference of Jefferson's head has been increasing in size. Without treatment, Jefferson will experience severe physical and developmental delays. Our medical partner, Project Medishare, is requesting $897 to cover the cost of surgery at Hospital Bernard Mevs, which will treat Jefferson's 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 14th. During surgery, excess fluid will be drained from Jefferson's brain, reducing the intracranial pressure, and greatly improving his quality of life. With proper treatment, Jefferson should develop into a strong and healthy young boy. The family is looking forward to Jefferson growing up happy and healthy.
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.”
Sue is a 25-year-old woman living with her husband, mother and child in a camp for internally displaced people and refugees in Thailand. Both Sue and her husband are unemployed, and the family depends upon the rations that they receive from the organizations that support the camp. Five months ago Sue noticed that her abdomen was swelling. At first she thought that she might be pregnant, but other symptoms started to emerge. She was able to receive an ultrasound at the hospital, which showed that there is a large tumor growing on her ovary. As the tumor may prove to be cancerous, the doctors told Sue that she would need to have both of her ovaries and her uterus surgically removed. Sue sought treatment through our medical partner, Burma Children Medical Fund, and she is now scheduled to undergo mass removal surgery on December 23rd at Maharaj Nakorn Chiang Mai Hospital. Her family is seeking $1,500 to cover the cost of her procedure and care. Sue said: "I wish my condition will get better so that I can spend more time with my daughter and mother, and my husband in the future." Her husband also shared: "I feel pity on my wife when I see she is in pain and cannot sleep. I am stressed about her condition, but now I feel released of worry when I heard that she is going to receive surgery soon. Thank you to Burma Children Medical Fund and all the donors for helping my wife."
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.”
Ma Win is an 18-year-old girl who lives with her parents, sister and brother-in-law in Yangon, Burma. Ma Win’s sister works at a clothing factory, while her brother-in-law works as a day laborer. Her parents are homemakers. Before Ma Win's current illness, she also worked at a factory. When Ma Win was four years old, she experienced a bout of high fever, and was brought to the local clinic. She received an injection, and the doctor informed her parents that she was born with a heart problem. However, she was too young at the time for corrective surgery. Instead, she was sent home with medication, and appeared to be doing well until this past year. In April, Ma Win began experiencing chest pains, high fever and difficulty breathing. She went to a clinic, and received an x-ray and an echocardiogram. After the doctor checked her results, she was diagnosed with an opening between two major blood vessels leading from the heart. The doctor told her and her family that she would need to have surgery. When Ma Win explained to the doctor that her family could not afford to pay for the surgery, she was referred to the abbot of a local monastery, who provided the family with information about our medical partner, Burma Children Medical Fund. Now Ma Win is scheduled for cardiac surgery on October 23rd at Pun Hlaing Hospital. After she has recovered, she should no longer experience chest pains or difficulty breathing, and she won't have to worry any longer about her condition. She will also be able to return to work, which will help ease her family's financial burdens. Now she needs your help to raise $1,500 to cover the cost of her procedure. Ma Win said: “I am scared to receive surgery, but my mother tries to encourage me. However, I am very happy that I will be able to receive treatment with your help. I would like to say thank you so much to all the donors.”
Naima is a smiley and playful baby girl from Ethiopia. She loves to breastfeed and play with her seven older siblings and her mother. Her dad is a retired driver and the community elder, and her mother stays home to care for the children. Because Naima's father has no source of income, their older children support them financially. Naima was born with an anorectal malformation, a congenital abnormality that leads to a complete or partial intestinal blockage. She needs to undergo a series of procedures to eliminate bowel dysfunction. Naima developed bowel obstruction because of her condition and an emergency colostomy was done. She has had multiple issues with her colostomy care and associated complications. As a result, she cannot make stool in a typical way. Her parents have been very troubled because of her condition and are asking for support. Naima is scheduled to undergo surgery to correct her condition on September 22nd. Our medical partner, African Mission Healthcare Foundation, is requesting $1,500 to cover the total cost of Naima's procedure and care. After her recovery, Naima will no longer experience bowel dysfunction or be at risk of developing health complications in the future. Naima's father says, “I hope my child will get the treatment and heal. Once she finishes her treatment, I hope she will be relieved from her pain and suffering and lead a healthy life.”
Kidus is a five-month-old baby from Ethiopia who is his parents' first child. Some of his favorite activities include breast feeding and playing with his mother. His parents are both students and farmers. They earn their income by selling fruits from their farm; however, the weather in their area is very sunny and their land is dry, which makes their harvest limited. Kidus was born with an anorectal malformation, a congenital condition that leads to a complete or partial intestinal blockage. He needs to undergo a series of procedures to eliminate bowel dysfunction. Kidus recently underwent a colostomy, an intestinal procedure that inserts a colostomy bag. His parents share that paying for this surgery was very difficult. They had to borrow the money from individual loaners, and it has been difficult for them to repay it. In the middle of these challenging times, they heard about our medical partner, African Mission Healthcare Foundation, and their care center, BethanyKids Myungsung Christian Medical Centre. Kidus's parents decided to seek financial assistance so he could complete the series of surgeries he needs. Kidus is now scheduled to undergo surgery to correct his condition on August 17th. Our medical partner is requesting $1,500 to cover the total cost of Kidus's procedure and care. After his recovery, Kidus will no longer experience bowel dysfunction and will be able to live more comfortably and confidently. Kidus's dad says, “We were happy that we got this opportunity. We hope that our child will get the treatment and make stool just like other people.”
Kwan is a 17-year-old boy who enjoys watching TV and learning Mandarin online during his free time. Although he is originally from Burma, he lives with his parents, two brothers, and both of his grandmothers in a village in Thailand. They moved to Thailand about five years ago in search of safer living conditions. Both of Kwan’s grandmothers are retired, and his father is unable to work due to being ill. His mother and older brother support their family by working as day laborers. Kwan and his younger brother both attend a local migrant school, where Kwan is a 10th grade student. In September of 2017, Kwan broke his left forearm while playing basketball with his friends. He was referred to Burma Children Medical Fund (BCMF) for financial assistance accessing treatment, and he underwent surgery to insert a steel rod into his left forearm at their medical care center, Mae Sot Hospital (MSH). Following surgery, doctors told Kwan that the steel rod would need to be removed a year after surgery. However, he was not scheduled for an appointment to remove the rod, and he was not told why it needed to be removed. Initially, this did not seem like an issue since Kwan regained movement in his fingers, was able to move his arm more comfortably, and was able to help his mother with household chores. Since he was not in pain and his family did not have enough money to pay for the procedure, Kwan was not brought back to MSH to have the rod removed. However, he began working as an agricultural day laborer in 2020 when his studies were moved online due to the outbreak of COVID-19. He began to experience pain in the area where the rod was located when carrying anything even slightly heavy. Due to financial constraints and a fear of being arrested for traveling to the clinic without documentation because of an increase in main road checkpoints, Kwan kept his pain a secret. However, he eventually sought medical attention at MSH after the pain progressed. There, a doctor confirmed that his arm had healed well and the rod needed to be removed. Fortunately, our medical partner, Burma Children Medical Fund is helping Kwan receive treatment. On July 27th, doctors will perform rod removal surgery. This procedure will cost $1,500, and Kwan and his family need your support. He mentions that after he recovers from surgery, he wants to find work as a day laborer. He wants to help his family earn more money so his mother no longer has to do hard labor. His mother says, “I don’t know what to say, but in our heart, we are so thankful to the donors for helping Kwan with his first, as well as this second, surgery. We will never forget this help for the rest of our lives.”
Kasaine is an 8-year-old boy, living with his family in a mud and grass thatched house in Southern Kenya. Kasaine's father is a farmer and a herder, while his mother stays home to take care of their family. Kasaine was born with a condition known as Rt hemiplegic CP, which means that his right side is weak, affecting his mobility, and the use of his hand. He tiptoes when he walks, and is able to walk only short distances. Kasaine also has clubfoot of his right foot, which causes his foot to be twisted, making it even more difficult for him to walk or to wear shoes. Fortunately, Kasaine's family traveled to visit our medical partner's care center, AIC Cure International Hospital. There, surgeons will perform clubfoot repair surgery on June 20th. Our medical partner, African Mission Healthcare Foundation, is requesting $1,286 to fund Kasaine's clubfoot repair. After treatment, he'll be able to walk much more easily, play with friends, and continue with his education. “My prayer is to see my son walking normally like other children.” Kasaine's mother told us.
Rayvan is a 1 month old baby boy living with his parents and three siblings in Kenya. Rayvan's mother used to plough her neighbors' farms, while his father herds cattle and ploughs farms to earn a living for their family. Rayvan parents shared that he was born at home because they could not afford to pay for his delivery at a hospital. After his birth, his mother noticed that Rayvan had a large swelling on the lower part of his back. She immediately took him to a nearby hospital to be examined. Rayvan was given some medication, and sent back home. After using the medication for a few weeks, there was no change in his condition. His mother shared her concerns about Rayvan with her friends, and one of them referred her to our medical partner's care center BethanyKids Hospital in Kijabe. On arrival, he was examined and diagnosed with spina bifida, a condition that requires surgical intervention to heal. Without surgery, Rayvan is at risk of developing paralysis of his lower limbs, infection of the exposed nervous tissue, and possible developmental delays. His parents do not have health insurance, and are unable to pay for the surgery he needs. Our medical partner, African Mission Healthcare, is requesting $1,151 to cover the cost of Rayvan's spina bifida closure surgery, which is scheduled to take place on May 18th at BethanyKids Hospital. This procedure will hopefully spare Rayvan from the risks associated with his condition, and enable him to grow up strong and healthy. Rayvan’s mother says: “I have never seen such a condition before and I was very much worried about my child. Now I’m happy to hear that he can get treated. The sad part is that I cannot afford the treatment but I believe that God will make a way.”
Catherine works hard to care for her two children. She currently lives with her partner who works different part-time jobs to help make ends meet for their family. A month ago, Catherine began experiencing abdominal pain. She got checked at her local health center and was advised to undergo an ultrasound. The test showed that she is suffering from Cholecystolithiasis, a condition where there are one or more gallstones in her gallbladder. Their family already finds it hard to sustain their day-to-day needs, so didn't know where to find the money for her needed surgery. Fortunately, a health center worker knew about our partner care facility, the Our Lady of Peace Hospital, and was able to reach out to World Surgical Foundation Philippines and Watsi for support. Catherine 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 Catherine's procedure and care. After her recovery, Catherine will no longer experience severe abdominal pain or be at risk of developing severe health complications in the future. “My maintenance medicine costs more than our daily meal budget. I’m grateful to WSFP and WATSI for helping us. Aside from the fact that I’ll be free from pain, I can now take good care of my children,” she shared.
Cali is a two-year-old girl from the Philippines. She loves to watch TV, and play with her siblings and cousins. Her mother takes care of her and her siblings while her father is a tricycle driver. The family’s income provides for their basic necessities but is not enough to cover Cali's medical treatment. Cali was born with an anorectal malformation, a congenital abnormality that leads to a complete or partial intestinal blockage. She needs to undergo a series of procedures to eliminate bowel dysfunction and is scheduled to undergo surgery on March 23rd. Our medical partner, World Surgical Foundation Philippines, is requesting $1,279 to cover the total cost of Cali's procedure and care. After her recovery, Cali will no longer experience bowel dysfunction or be at risk of developing health complications in the future. “Nowadays, you'll find bullies everywhere, and we have been worried that growing up, her condition might affect her ability to interact with others. So thank you, WSFP and Watsi, for helping us. We are hopeful that if the [colostomy] closure is done, she’ll be able to live a normal life, without worrying about her appearance and what others might say about her, ” Cali's mother shared.