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Aaron Nir

Aaron's Story

Aaron joined Watsi on March 1st, 2026. 21 other people also joined Watsi on that day! Aaron's most recent donation supported Rayvan, a three-year-old from Tanzania, to fund mobility-restoring surgery.

Impact

Aaron has funded healthcare for 9 patients in 4 countries.

Patients funded by Aaron

Moses is a 10-year-old boy from Kenya. He is the youngest of two children. His mother is single and unemployed, but she runs a small salon to earn income. According to his mother, life has not been easy for her as a single parent. Her firstborn had a baby while still in school, and the child has had ongoing health challenges due to congenital abnormalities, resulting in frequent hospital visits. Moses, on the other hand, has generally been healthy and is currently in Grade Five. He is described as a well-behaved and bright student who performs well in school. About two months ago, while bathing him, his mother noticed a small swelling in the left inguinal region. She decided to bring him to our medical partner's care center, Nazareth Hospital, where an ultrasound scan was performed. Moses was diagnosed with cryptorchidism, a condition in which one or both of the testicles remain undescended. If left untreated, Moses has an increased risk of developing hernias, testicular cancer, and fertility problems in the future. Moses will be receiving assistance from our medical partner, African Mission Healthcare (AMH). Fortunately, he is scheduled to undergo corrective surgery on January 19th. AMHF is requesting $483 to cover the total cost of his procedure and care. "I hope I am not too late to bring my son for treatment, but I hope to get help and have him operated on so that he may not have problems when he grows up. I appreciate your support," said Moses' mother.

$483raised
Fully funded

Divyana is a cheerful eight-year-old boy from Ethiopia. He loves playing football and spending time with his friends and younger brother. He lives in Sekota, and they travelled approximately 870 kilometers to seek treatment, a journey that took three days. His mother is a dedicated housewife, while his father works as an agricultural officer in a government institution. Together, his parents work hard to support their family and meet their children’s needs. Divyana's mother discovered his condition at birth and was immediately overwhelmed with frustration and panic. Questions raced through her mind, she says, “What is wrong with him? Is it my fault? How can I help my child?” Fear and stress consumed her, but her instinct to protect him never wavered. She began seeking information about his condition, choosing not to share too much with him to safeguard his emotional well-being. To prevent potential teasing or stigma, she instructed him to isolate himself whenever he went to the bathroom, warning him that other children might ridicule him if they saw him. She repeated this often, worried about how his condition might affect his social life and learning, especially since hypospadias is uncommon in their community. Divyana frequently compared himself to his younger brother and asked his mother why he was different. These moments left her feeling helpless, with no answers, only tears. One day, while visiting a relative in Addis Ababa who was undergoing orthopedic treatment, Divyana ’s mother heard about several successful cases being treated at the facility. Curious and hopeful, she began asking questions, but without revealing her son’s condition. Eventually, she received the contact information for the field patient coordinator at our medical partner's care center, BethanyKids Myungsung Christian Medical Centre. Doctors confirmed that Divyana was born with hypospadias, a condition that causes urinary dysfunction. Without treatment, he will continue to experience uncomfortable symptoms and will be at risk of future complications. Fortunately, Divyana is scheduled to undergo corrective surgery on November 20th. Our medical partner, African Mission Healthcare, is requesting $1,293 to cover the cost of his procedure and care. Divyana's mother said, "I wish my child were very healthy, and I am thrilled to get this opportunity."

$1,293raised
Fully funded

Peter is a 10-year-old boy from Tanzania. He is the third born among seven children, raised by loving parents who survive through small-scale farming. From the day Peter was born, something was different about his feet. His parents noticed that both of his feet bent inward, making it difficult for him to balance and walk normally. As the years passed, the condition worsened. Walking long distances—something every child in his village must do daily—became painful and exhausting for him. Despite this, He is a joyful boy with a bright smile, loved by his family and admired by his friends. He enjoys going to school, playing with other children, and dreaming big, just like any other child. But his condition has started to limit him more each year. He can no longer walk comfortably to school, and running or playing with his friends is now too painful to bear. Peter’s family tried their best to seek help, but with limited financial resources and no specialized services nearby, they were left with few options. Peter has clubfoot, a condition in which the foot is twisted out of shape. The tissues connecting the muscle to the bones are shorter than usual, and this causes difficulty walking and even wearing shoes. Fortunately, Peter's family traveled to visit our medical partner's care center, Kafika House. Surgeons will begin clubfoot treatment on December 16th. Our medical partner, African Mission Healthcare, is requesting $1,119 to fund Peter's clubfoot repair. After treatment, Peter has a chance to receive the life-changing treatment that will not only relieve his daily pain but also give him a chance to walk, run, and go to school without limitations. Peter says, "I wish that I wouldn't feel any pain walking to school and playing with my friends."

$1,119raised
Fully funded