Gilles PoupardinUNIVERSAL FUND MEMBER
Gilles' Story

Gilles joined Watsi on January 31st, 2018. Five years ago, Gilles joined our Universal Fund, supporting life-changing treatments for a new Watsi patient every month. Gilles' most recent donation supported Phorp, a young man from Cambodia, to fund surgery for nerve damage to his left arm.

Impact

Gilles has funded healthcare for 73 patients in 11 countries.

Patients funded by Gilles

Phorp is a 21-year-old rice farmer from Cambodia. He lives at home with his parents and 18-year-old brother. His family also works as rice farmers in Siem Reap province. At home, in his free time, Phorp loves to play volleyball. In August, Phorp was in a motorbike accident and fell on his left shoulder. He sustained multiple injuries, including lacerations and paralysis of his left arm due to nerve damage. He visited the local provincial hospital for stitches for the lacerations, but he did not receive care for the nerve damage. Phorp has been diagnosed with a brachial plexus injury on his left side. 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. There has been no improvement in his arm over the last several months. Currently, he cannot use his hand and, consequently, cannot work outside in the rice paddies with his family. Fortunately, Phorp traveled to our medical partner's care center for treatment. This is the only center in the country where this treatment is available. On November 3rd, he will undergo a brachial plexus repair surgery. After recovery, he should be able to use his arm once again. Our medical partner, Children's Surgical Centre (CSC), is requesting $709 to fund this procedure. Phorp contributed $100 to his care. Phorp said, "After surgery, I hope that I can lift my shoulder and arm and be able to work."

$709raised
Fully funded

Hassan is an only child whose parents separated before he was born. Prior to his birth, Hassan's mother worked alongside his grandmother, doing farm work to earn income. After Hassan was born, his mother had to stop working so she could take care of him. Hassan was diagnosed with spina bifida at birth, a condition that occurs when a developing baby's spinal cord fails to develop or close properly while in the womb. Hassan had a swelling on his back that was open and leaking. He was admitted in hospital for a few days while his mother was taught how to dress the wound. An MRI and a CT scan were done and he was scheduled for surgery weeks later. While home, his mother continued with the wound dressings as instructed until the leaking stopped. During one of the post-natal clinics, Hassan and his mother were referred to our medical partner's care center, BethanyKids, for treatment. Upon arrival at BethanyKids, Hassan was examined and was additionally diagnosed with hydrocephalus, a build up of fluids in the brain. He was then scheduled for a spina bifida repair surgery, and the mother was told that once he recovered, he would be scheduled for a shunt insertion surgery. Due to financial challenges and a loss of income for Hassan's mother, the family is unable to meet the medical expenses. Without treatment, Hassan is at risk of lower-limb paralysis, infection of the exposed nervous tissue, development of tethered cord syndrome, and possible developmental delays. Fortunately, our medical partner, African Mission Healthcare, is helping Hassan receive treatment. On March 15th, surgeons at BethanyKids will conduct a spina bifida closure surgery to promote Hassan's healthy growth and development. Now, Hassan's family needs help to fund this $1,151 procedure. Hassan’s mother says, “A while back, I had already given up on Hassan's treatment. Because the community had never seen such a condition, I was told that I would always get children who have different medical conditions. After coming to this facility, I realized that this was not the case. My hopes were raised again and now I’m looking forward to the best outcome in Hassan’s treatment.”

$370raised
$781to go

Jecinta is a delightful 4-year-old girl from Kenya. She is playful and jovial. Born with a birth condition her journey began at Kiambu Hospital, where dedicated healthcare professionals initiated a treatment plan to address the condition. She was prescribed braces as part of her comprehensive care to correct her clubfeet. With the support of her mother, she embarked on a hopeful journey towards improved mobility and a future filled with possibilities. The braces played a role in maintaining the corrections achieved through casting and other interventions. However, along the way, and because of the hardships, Jecinta, like many children, faced challenges in using the braces. Unfortunately, she lost to follow-up at Kiambu Hospital, and the regular monitoring and follow-up appointments ended. Over more than a year with no follow-up, Jecintas deformity recurred. Currently she tiptoes as she walks and feels pain. Fortunately, Jecinta and her mother traveled to visit our medical partner's care center, AIC Cure International Hospital. Our medical partner, African Mission Healthcare, is requesting $1,286 to fund Jecinta's clubfoot repair. After treatment, she be able to walk well, with no pain and discomfort. Her self-esteem will also improve, and she will continue with her education without any hardship. “I will appreciate if consider my daughter to undergo surgery so that she can stand on her feet and walk confidently like other children,” Glory, Jecinta’s mother, told us.

$1,286raised
Fully funded