Susan joined Watsi on December 19th, 2014. Twelve months ago, Susan joined our Universal Fund, supporting life-changing treatments for a new Watsi patient every month. Susan's most recent donation traveled 4,000 miles to support Gideon, a special young man from Kenya, to fund hernia repair.
Susan has funded healthcare for 253 patients in 13 countries.
Susan has funded healthcare for 253 patients in 13 countries.
Gideon, who was born with intellectual disabilities, lives in and attends a special school in Eldoret town. Gideon likes being in school and he likes drawing during his free time. His parents live in the village and it’s been a long time since Gideon has seen them, so he is looking forward to seeing them when he gets treated. Gideon came to the hospital after having a swelling in a sensitive area for more than two years. He reports that it was gradual on the onset but worsened with time. Gideon was brought to the hospital by one of his relatives after they were told of Gideon's condition. Before they came to Kapsowar Hospital, they had tried many other hospitals, but every time they were asked to pay huge amounts of money for treatment, which they cannot afford. Gideon has an appointment for a hydrocelectomy surgery to repair the double hernia bulges. He has been experiencing severe discomfort in the affected area and a mild headache, and feels ashamed walking around due to the swelling. Currently, Gideon is under the care and support of the Samaritans, but they don’t have money to pay for his surgery, only for room and board. They are asking anyone reading this story to support Gideon so he can undergo a successful surgery for recovery. Gideon is a happy young man who looks forward to seeing his parents soon. His uncle says, “I will be happy to see him without the swelling. He deserves to live a happy and healthy life like others.”
Dylan is a little baby from Colombia who is the firstborn of his family. Dylan's father is 20 years old and works at a furniture factory while his 18-year-old mother is at home with her newborn. Dylan enjoys listening to music. With his beautiful eyes, he already attracts the affection of all around him. Dylan was born with 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. Dylan's family traveled to visit our medical partner, Clínica Noel. There, surgeons will perform clubfoot repair surgery on August 26th. Clínica Noel is requesting $1,500 to fund Dylan's bilateral clubfoot repair. After treatment, he will be able to crawl, walk, and run as he grows up. His mother shares,"I would love to see him run and play as a normal kid." His father tells us of his grand hopes for young Dylan's future, "I would love to see him playing soccer and to celebrate with him when he becomes a champion."
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."
Gift is curious, charming, and social two-year-old boy. He's the second born child in a family of three children. Both of his parents are small scale farmers who grow maize, beans, and vegetables for their food. They also go out to seek other work, such as helping on other farms, to earn an income. Gift has clubfoot of his right foot. Clubfoot is a condition in which the foot is twisted out of shape. This causes difficulty walking and even wearing shoes. Fortunately, our medical partner, African Mission Healthcare (AMH), is helping Gift receive treatment. On July 13th, surgeons at AMH's care center will perform clubfoot repair surgery. Now, AMH is requesting $935 to fund Gift's procedure. After treatment, Gift will be able to walk and wear shoes. Gift’s mother shared, "I know my son will be very happy to be able to wear shoes and walk in a normal way. Please help him have this treatment."
Susan is a seven-year-old girl in the first grade and the second child in her family. Unfortunately, Susan was involved in a grisly road traffic accident when a vehicle lost control on March 8th, 2021. Five children and the teachers were hit, and one child unfortunately passed away. Susan survived despite sustaining fractures on her right hand and leg. She was brought to our medical partner's care center, Nazareth Hospital, and had a fracture repair surgery on her hand and leg. One week ago the plates were removed. Susan's hand has healed well but she has started having severe pain on her leg. When Susan's parents brought her back to the hospital, a X-Ray showed the fracture has reoccurred, and the surgeon recommended a repeat surgery. Without treatment, Susan will continue experiencing the pain, she may never be able to use her leg again, or her leg may eventually heal with a deformity. Fortunately, the surgeons at Nazareth can help. On July 1st, Susan is scheduled to undergo a fracture repair procedure, called an open reduction and internal fixation. Afterward, Susan will freed from pain and will be able to use her leg to walk to school and play again. Susan’s father works temporarily as a welder and her mother is a housewife. Their income is limited and their health insurance can no longer cover for another surgery after supporting the previous one. Therefore, our medical partner, African Mission Healthcare Foundation (AMH), is requesting $1,049 to fund this procedure for Susan. “We thank God that our child is alive as one child died during the accident. We are hoping her surgery can be successful so that we can see her happy again and not in pain. We plead for her surgery sponsorship, ” Susan’s father wishes for her daughter's full recovery.
Nuriya is 2-year-old toddler from Ethiopia who loves his mom and dad very much and always wants to be with them. Nuriya enjoys chatting and playing with his parents. Now he also has a three-month-old baby sister. His parents are working hard to raise them both. They shared that they went through a lot as a previous immigrant in Saudi Arabia and their family now decided to stay in their home country to raise a family and support it from their homeland. Nuriya's grandparents gave his parents a small piece of land that they are now farming. However, the fruit that they farm is only enough to maintain the daily needs of the family. Nuriya was born with hypospadias, a congenital abnormality that causes urinary dysfunction. Without treatment, he will continue to experience uncomfortable symptoms and will be at risk of infertility. Fortunately, Nuriya is scheduled to undergo corrective surgery on July 6th. Our medical partner, African Mission Healthcare Foundation, is requesting $1,293 to cover the total cost of his procedure and care. Nuriya was also born with another birth condition that Watsi donors supported for treatment and his family is tremendously grateful for support. Nuriya's mother is inspired by the care he is receiving, “I hope he will be a doctor in the future. Just as the doctor who treated him and changed his health in the past, I want him to grow and treat so many kids with sickness and disability.”
Lim is a brave, seven-year-old girl. She has three older sisters, and her parents make and sell palm sugar. In school, Lim is currently in second grade and enjoys to read books. At home, she likes to play with her dolls and draw pictures with her sisters. Two months ago, Lim developed a chalazion, or inflamed cyst, in her right eye, causing her itchiness, irritation, and tearing. This makes it difficult for her to see clearly and study at school. Lim traveled for one hour and a half with her father to seek treatment from our medical partner, Children's Surgical Centre (CSC). On June 17th, surgeons will remove the cyst through a chalazion excision procedure. After recovery, Lim's symptoms should improve. She needs help raising $187 to fund this procedure. Lim is optimistic, "I hope my eye is better and comfortable as soon as possible so I can do well in school and not worry about my eye."
Munyantwari is an 18-year-old student from Uganda. He completed his secondary education and is waiting for the examination results so as to continue with the rest of his education. Munantwari lost his mother in 2018 and currently lives with his father and six siblings. His siblings are all in school, making it a major struggle for his father to meet all their expenses. The father trades in second-hand clothes to make ends meet. During Muyantwari's free time, he enjoys spending time with family. Six months ago, Munyantwari began to experience troubling symptoms, including abdominal pains. When he came to Rushoroza Hospital due to severe pain, he was diagnosed with appendicitis and had surgery recommended to prevent the symptoms from getting worse. The condition limits his work output at home, especially when doing domestic chores. However, with the struggles the father is going through, Munyantwari is afraid the cost might be too high for them to afford. Our medical partner, African Mission Healthcare Foundation, is helping Munyantwari receive treatment. He is scheduled to undergo a curative laporotomy on June 10th at our medical partner's care center. This procedure will cost $284, and Munyantwari and his family need your support. Munyantwari shared, “I pray for a successful surgery. I hope to resume and proceed with education comfortably for a better future.”
Israel is a one-year-old baby from Colombia who loves animals. His mother came to Colombia from Venezuela to seek better opportunities, where she fell in love with a Colombian man who became Israel's father. Israel loves to play with cars and his dog. Even though he doesn't speak a lot yet, he is constantly looking for a phone to call his grandmother. Israel was born with polydactyly of both feet. This means that he has an extra toe on each foot, which prevents him from wearing shoes and walking normally. On August 17th, surgeons from our medical partner will perform a polydactyly repair procedure to remove the extra digits. Our medical partner, Clínica Noel, is requesting $799 to fund this procedure. After surgery, Israel will be able to start wearing shoes and learn to walk and run. His mother offered advice for other mothers in a similar situation to stay hopeful: “The only thing that worried me was to know if he was going to be able to walk normally and wear shoes. I would tell a mother whose son was just diagnosed with polydactyly to just calm down and let the doctors help her, fortunately, this is not a complex pathology and the treatment already exists.”
Srey Ka is a nine-year-old, third grade student. She lives with her parents and her two siblings. Her parents are construction workers. Srey Ka enjoys writing at school, especially creating stories about other students. Outside of school, she likes to play sports with her friends. One month ago, due to a traumatic injury, Srey Ka developed a cataract in her left eye, causing blurry vision and tearing. She has difficulty seeing things clearly, recognizing faces, and going anywhere outside. When Srey Ka's family learned about our medical partner, Children's Surgical Centre (CSC), she traveled for two hours with her mother to seek treatment. On June 15th, doctors will perform a phacoemulsification cataract surgery and an intraocular lens implant in her left eye. After recovery, Srey Ka will be able to see clearly. Now, her family needs help to fund this $229 procedure. Srey Ka wishes for recovery: "I hope I can easily play sports with my friends again, and see my teacher easily in school."
Guadalupe is an one-year-old baby from Colombia. She is an only child, so she is regarded as the little princess of the family, which consists of her mother, grandma, and uncle. She is already sympathetic and friendly, and loves to play with stuffed toys and with other kids. Guadalupe has clubfoot on her right foot. Clubfoot is a condition in which the foot is twisted out of shape. This causes difficulty walking and even wearing shoes. Fortunately, Guadalupe's family traveled to visit our medical partner, Clínica Noel, where they can offer treatment. There, surgeons will perform clubfoot repair surgery on August 13th. Our medical partner is requesting $1,422 to fund Guadalupe's clubfoot repair. After treatment, she will be able to start walking and running without pain. Her mother shares a story and her hopes for Guadalupe, "I would really love to see her walk and run normally, she is not the first person with this condition in our whole family, I have a cousin who received treatment when he was 8 years old and it was really hard to see him asking why he couldn't run like the other kids."
Marilyn is a 10-month-old baby girl from a small town in Colombia. She lives with her mother, grandmother, three aunts and one uncle, who is a farmer. Marilyn has clubfoot, a condition in which her foot is twisted out of shape. This causes difficulty walking and even wearing shoes. Fortunately, Marilyn's family traveled to visit our medical partner, Clínica Noel, where surgeons will perform clubfoot repair surgery on July 26th. Now, Clínica Noel is requesting $1,422 to fund Marilyn's life-changing procedure. After treatment, she will be able to start walking and running after her dreams as she grows. Her mother shared, "my biggest dream is for her to get well soon, to see her walking and running as a normal child, with no pain or anything."