Mark A CarltonUNIVERSAL FUND MEMBER

Mark's Story

Mark joined Watsi on November 23rd, 2016. Four years ago, Mark joined our Universal Fund, supporting life-changing treatments for a new Watsi patient every month. Mark's most recent donation supported Phanna, a factory worker from Cambodia, to fund surgery to restore his mobility.

Impact

Mark has funded healthcare for 51 patients in 10 countries.

Patients funded by Mark

Phanna is a 26-year-old factory worker from Cambodia. He lives in Kampong Thom Province with his widowed mother, who is a rice farmer. He is the second child of four siblings, and his siblings all work as factory workers. In his free time, he enjoys playing volleyball with his friends in the village. In April 2026, Phanna was involved in a serious motorcycle and truck collision while traveling to his hometown. He has been diagnosed with a brachial plexus injury on his left side, causing paralysis in his left arm. The brachial plexus is a nerve network that transmits signals from the spine to the shoulder, arm, and hand. Injuries to this nerve network can result in loss of function and sensation. He is unable to lift his arm, bend his elbow, or move his wrist normally. This makes it difficult for him to perform daily activities independently and prevents him from returning to his job as a factory worker. Phanna traveled to our medical partner's care center, Kien Khleang National Rehabilitation Centre, to receive treatment. This is the only center in the whole country where this treatment is available. On July 16th, he will undergo a brachial plexus repair surgery. After recovery, the procedure is expected to help him regain movement in his shoulder and elbow, improve his arm function, regain independence, and return to work. Our medical partner, Children's Surgical Centre, is asking for help to fund this procedure. Phanna's family can contribute $50, but needs help raising $687 more. Phanna said, “Since the accident, I have not been able to use my left arm, and it has changed every part of my life. I hope this surgery will help me regain movement so I can return to work, take care of myself, and live more independently. I am grateful for the chance to receive this treatment.”

$155raised
$532to go

Tennyson is a playful 11-year-old boy from Kenya. He is currently in grade 3 and loves drawing and playing with friends. His father is a construction worker, while his mother is a home maker. Tennyson has clubfoot of right foot, a condition in which the foot is twisted out of shape. Tennyson was also born with a hearing impairment. His mother first noticed that his right foot was bending when he was three years old. “He struggled to walk and would often complain of pain, and as he grew, it only got worse,” she recalls. They sought help at a nearby hospital but were informed that the condition could not be treated there. With no clear solution, they returned home. As time passed, the condition worsened. The pain increased, Tennyson's foot began to swell, and walking became more difficult. Eventually, Tennyson had to stop going to school because he could no longer walk. One of his teachers grew concerned and reached out to the family. After learning about Tennyson’s condition, the teacher informed his mother about a mobile clinic by AIC CURE Hospital, where Tennyson could undergo a review. At the clinic, Tennyson was assessed and scheduled for serial casting and a clubfoot surgery. He has been undergoing the casting and is now ready for the repair surgery, which has been scheduled for May 25th. Our medical partner, African Mission Healthcare, is requesting $1,286 to fund Tennyson's clubfoot repair. After treatment, his foot will gradually straighten and restore his ability to walk. Tennyson's mother says: “I am praying that his foot will be straightened, so that he can walk without pain, go back to school, and live like other children.”

$836raised
$450to go

Hikma is a charming 20-month-old girl who lives with her parents and older brother in Ethiopia. Her parents were small-scale farmers until they were displaced due to war in their area. Now, her mother is a dedicated home maker, and her father works as a daily laborer. As with many other displaced families, it has been difficult for them to afford their daily necessities. Hikma was born with an anorectal malformation, a congenital condition that can lead to a complete or partial intestinal blockage. However, the symptoms were not obvious until she was around one year old. Her mother was deeply distressed by what she observed and immediately informed Hikma’s grandmother, who then began seeking for medical assistance. To avoid social stigma, however, the family tried to keep Hikma’s condition private. Eventually, the grandmother came across a Catholic missionary organization, which connected the family with a field coordinator of our medical partner's care center, BethanyKids Myungsung Christian Medical Centre (BKMCM). With the support of relatives and the Catholic missionaries, Hikma's family raised funds to travel to Addis Ababa. Upon arrival at the hospital, doctors explained that Hikma would need a series of surgeries to eliminate bowel dysfunction. The family was relieved and encouraged to hear that Hikma could be helped. Presently, Hikma has already undergone the first surgery, a colostomy creation, and recovered well. Now, Hikma needs support for her second surgery, which will occur on April 20th. Our medical partner, African Mission Healthcare Foundation, is requesting $1,500 to cover the total cost of Hikma's procedure and care. After her recovery, Hikma will no longer experience bowel dysfunction or be at risk of developing health complications in the future. Hikma’s mother said, “I would like to thank you sincerely for your support and the services you provided. Thank you again. I truly hope my child will grow up to be a wonderful woman.”

$1,500raised
Fully funded

Michael is a 10-year-old student from Kenya. When his mother was pregnant with him, she went through a very hard time. She had married into a different tribe, and this brought her a lot of pain. “I was rejected because I was seen as a foreigner,” she said quietly. “This made my pregnancy very difficult. Then my only son was born with clubfoot, and life felt too heavy to bear.” Clubfoot is a condition where one or both feet turn inward, affecting the bones and muscles. Michael lived with this condition on both of his feet for almost ten years without treatment. As he grew older, walking became painful and tiring. “My feet are very sensitive,” Michael said. “I cannot walk without my slip-on shoes. I want to walk fast or even run, but I cannot.” Many times, he leaned on walls for support while watching other children walk and play freely. His mother's pain grew deeper when her in-laws rejected her and her husband, saying their child was cursed. Michael’s father supported them at that time. But after everything they went through, they stopped looking for treatment, and Michael grew up with the condition. Even so, they still hoped that one day things would change. In 2025, that hope came back when they moved to a new village. A neighbor told Michael's mom about CURE Children’s Hospital of Kenya. Fortunately, Michael traveled to visit our medical partner's care center, AIC Cure International Hospital. At the clinic, the doctors examined Michael and quickly scheduled him for surgery. There, surgeons will perform clubfoot repair surgery on March 25th. While Michael is scheduled for surgery, his family cannot afford it. Our medical partner, African Mission Healthcare, is requesting $1,286 to fund Michael's clubfoot repair. After treatment, he will be able to walk easily and attend school without disruptions. "I am looking forward to getting better so that I can continue with my studies and engage with my friends in playing football," Michael told us.

$1,286raised
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