William's Story

William joined Watsi on November 6th, 2014. Nine years ago, William joined our Universal Fund, supporting life-changing treatments for a new Watsi patient every month. William's most recent donation traveled 8,500 miles to support Charles, a future doctor from Kenya, to fund corrective surgery.

Impact

William has funded healthcare for 101 patients in 13 countries.

Patients funded by William

Alazar is a sweet boy from Ethiopia. He is the seventh child in his family. Five of the children are girls and two are boys. He loves to sing songs, go to church, try martial arts, and drink juice. His dad is diabetic and his condition causes him to faint often. He has government health insurance and gets treatment in a local government hospital. Because of his condition, Alazar's dad cannot work. His mom makes traditional bread and sells it on the street to feed her children. She makes her bread by firewood and this makes it hard for her to always have the smoke of the wood making the bread. She is the only one who works for income in their family, but her older children help with housework. They bring water from the spring carrying it on their back. She proudly sends all her children to school. Alazar underwent an earlier colostomy, in which the end of the colon is brought through an opening in the abdominal wall. This surgery is often performed to bypass bowel malformations, but colostomies are usually temporary and may call for closure. In Alazar's case, his colostomy requires closure in order to restore bowel function and prevent future complications. Our medical partner, African Mission Healthcare Foundation, is requesting $1,009 to cover the cost of a colostomy closure for Alazar. The surgery is scheduled to take place on January 9th and, once completed, will hopefully allow him to live more comfortably and confidently. Alazar's mom said: “After he gets the treatment and heals I will praise my Lord. I will tell everyone who knows me about the hand of God. I did ask God ‘to heal my baby. You gave me this child; don’t take it away from me. I always cry and pray.’ I hope God has heard my prayer leading me to you. I will go to my church and testify what God did to all community in the church.”

$431raised
$578to go

Linah, a baby girl from Arusha, was born with clubfoot, a condition characterized by the foot being twisted out of shape. To provide her with an opportunity for a healthy and active life, medical intervention is necessary. Unfortunately, her parents, who are self-employed, are unable to shoulder the financial weight of her treatment. Linah's mother earns a living by selling vegetables at the local market, while her father supports the family through small-scale farming. Despite their modest income, they are determined to provide the best possible future for their children. Linah has an older brother who is just one year old, and her parents are acutely aware of the potential lifelong consequences of untreated clubfoot. They believe that pursuing early treatment will allow Linah to grow up without enduring any disabilities or the social impact. Her father's personal experience influenced the decision to bring Linah to our medical partner's care center: Plaster House. He was also once treated at the facility, and the positive outcome of his treatment has instilled confidence in their family regarding Plaster House's expertise and commitment to providing quality care. Linah's mother wishes to see her daughter receive the same level of treatment and care that her spouse received in the past. However, due to the family's limited financial resources, they cannot afford the costs associated with Linah's treatment. Thankfully, Linah had the opportunity to visit Arusha Lutheran Medical Centre, our medical partner's care center. On June 13th, skilled surgeons will perform a clubfoot repair surgery for her. Our medical partner is seeking $935 to cover the costs of Linah's treatment. Following the intervention, she will be able to lead a rewarding life without the burdens imposed by clubfoot. Linah’s mother says, "I wish for my daughter to get good care and the best treatment that will give her a chance to live a life free from disability."

$935raised
Fully funded

Juan, an 11-month-old boy from Bolivia, lives with his mother and five older siblings in a neighborhood in the mountains above La Paz. Juan was born with a cardiac condition called ventricular septal defect, in which a hole exists between the two lower chambers of his heart. Blood leaks through this hole without passing through his lungs to obtain oxygen, leaving him weak and making it difficult for him to gain weight. To address Juan's condition, congenital heart surgery is the only viable treatment option. Skilled doctors at Hospital del Niño Dr. Ovidio Aliaga Uría will perform the surgery by closing the hole in his heart using a patch. However, due to Juan's low weight, the surgeons have determined that it is unsafe to proceed with the procedure. As a result, he will be hospitalized for several weeks before the surgery to receive proper nutritional support, enabling him to gain weight and prepare for the operation. Our medical partner, Haiti Cardiac Alliance, is actively seeking your generous support to raise $1,500 to support Juan's cardiac care. Your contribution will play a vital role in enabling Juan to receive the life-changing congenital heart surgery he urgently requires. By partnering with Haiti Cardiac Alliance and making a financial contribution, you can make a significant difference in Juan's life and overall well-being. Juan's mother shared, "I am very hopeful that after this surgery, my son will gain appetite and start growing and gaining weight more normally!"

$1,500raised
Fully funded

Anastazia is a nine-year-old student from Tanzania. She has seven siblings and lives in the heart of Serengeti, a beautiful area in Tanzania, home to some of the most breathtaking wildlife on the planet. Her father is a small-scale farmer who relies on subsistence agriculture to provide for his family. From a very young age, Anastazia's legs started bowing, making it difficult to walk, run, or play like other children her age. Her parents noticed the problem and did everything they could to find a solution, including visiting local doctors and healers, but nothing worked. Unfortunately, they could not afford to take her to a hospital in the city, which was too far away. As a result, Anastazia was forced to live with her condition and learned to adapt to it. She walks to school with her siblings, but with some difficulty and discomfort. Fortunately, Anastazia was able to reach our medical partner, African Mission Healthcare (AMH), where she was diagnosed with Acquired bilateral genu varus. Her legs bow outward so that her knees do not touch. This condition is typically caused by an excessive accumulation of fluoride in the bones, often stemming from contaminated drinking water. AMH is requesting $880 to fund corrective surgery for Anastazia. The procedure is scheduled to take place on April 17th, and the treatment will hopefully restore Anastazia's mobility. This will allow her to participate in various activities and greatly decrease her risk of future complications. Anastazia says, “I wish to be able to walk to school with my siblings without having to endure so much pain.”

$880raised
Fully funded