Charles MathisonMONTHLY DONOR
Charles' Story

Charles joined Watsi on June 22nd, 2020. Two years ago, Charles joined our Universal Fund, supporting life-changing treatments for a new Watsi patient every month. Charles' most recent donation traveled 8,200 miles to support Danilo, a 40-year-old construction worker and tricycle driver from Philippines, to fund a cholecystectomy and hernia repair so he can live comfortably.

Impact

Charles has funded healthcare for 36 patients in 9 countries.

All patients funded by Charles

Samuel is a 21-year-old talkative young man. He is the second born in a family of five children. His father passed away when he was four years old, so his mother had to raise him and his siblings by herself. She does jobs on tea farms to provide for the family. When Samuel was two years old, his abdomen started to swell, which was very painful for him. His mother took him to the hospital and he was given some medication and sent back home. The medication did not work as expected. He was then taken to a different hospital for examination. He was given more medication and after some time he seemed to be better. The stomachache did not go away completely, however. Samuel and his mother shared that over the years, he has had stomachaches and gotten used to taking pain medication. In 2017 when Samuel was in high school, the pain worsened and his abdomen started to swell again. He had to leave school as a result. His mother took him to a hospital in Meru where he was admitted for three months. While in the hospital, scans and a biopsy were done to determine what the problem was. He was given a colostomy, where the end of the colon is brought through an opening in the abdominal wall, in order to pass stool. This surgery is often performed to bypass bowel malformations, but colostomies are usually temporary and may call for closure. In Samuel's case, his colostomy requires closure in order to restore bowel function and prevent future complications. At that time, his doctors did not manage to treat him and referred him to BethanyKids Hospital in 2018. On arrival, he was examined and admitted, as he was not in good condition. After more scans and tests, he was ultimately diagnosed with Hirschsprung’s disease. Since then, Samuel has undergone several surgeries with the aim of trying to better his condition. The first surgery failed, but the second was successful. He is now scheduled to undergo his last surgery to close the colostomy so that he can pass stool on his own again and live a more active life. Earlier in his treatment, Samuel's parents had enrolled in the national health insurance program (NHIF), which helped them pay for most of his hospital bills. BethanyKids also chipped in on occasion to help with some of the bills. Unfortunately, for his last surgery, NHIF has rejected the request since he is beyond the age to be covered by his mother’s insurance. Our medical partner, African Mission Healthcare Foundation, is helping him to undergo treatment and needs $1,084 to cover the cost of a colostomy closure for Samuel. The surgery is scheduled to take place on November 11th and, once completed, will hopefully allow him to live more comfortably and confidently. Samuel’s Mother says, “For years now, I have been very worried about my son, but God has seen us through.”

74%funded
$812raised
$271to go

Son is a 21-year-old mother of two. She and her husband have two sons - one is four years old and the other is one year old. Both she and her husband are construction workers. When not working outside on construction sites, she is a busy mother caring and cooking for her active children. Four months ago, on the way home from work, Son was in a motor vehicle collision. She injured her left shoulder and received a hard blow to the face, fracturing her left orbital bones. Her family took her to a government hospital to repair the bones surrounding her eye. The traumatic injury also damaged the muscle and nerve function of her shoulder, which was not repaired. This is a devastating injury for their young family, as it can cause a significant loss of function and ability to perform tasks of daily living. Son has been diagnosed with a brachial plexus injury on her 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. She has pain and is unable to lift her left arm. She cannot work in construction or manage her household, which has also been very hard for her husband. Son traveled to our medical partner's care center to receive treatment. This is the only center in the whole country where this treatment is available. On October 17th, she will undergo a brachial plexus repair surgery. After recovery, she hopes that her arm will be functional and she can work, do housework, and care for her children. Our medical partner, Children's Surgical Centre, is requesting $709 to fund this procedure. She says: "After surgery, I hope I can use my left arm. This treatment will help me in the future to return to work."

73%funded
$519raised
$190to go

Jayden is a sweet baby and the last born in a family of 5 children. His parents separated before he was born and his mother does laundry for neighbors to provide for the family. Shortly after Jayden was born, his mother noticed a large swelling on his back. She did not have the money to take him to a doctor at the time but, when he was seven months old, she took him to the hospital where Jayden was examined and was sent to another facility for a scan. Unfortunately, the scan was not done because Jayden's mother could not raise the required amount of money. She shared her plight with her boss who got in touch with one of the ambassadors from BethanyKids hospital in their village. The ambassador reached out to her the following day and helped bring Jayden to the hospital. Upon examination, he was diagnosed with spina bifida and urgent surgery was recommended. Spina bifida is a type of neural tube defect in which the spine does not properly close around the spinal cord. Without treatment, Jayden is at risk of lower-limb paralysis, infection of the exposed nervous tissue, development of tethered cord syndrome, and possible developmental delays. Our medical partner, African Mission Healthcare, is requesting $1,151 to cover the cost of Jayden's spina bifida closure surgery. The procedure is scheduled to take place on June 21. This procedure will hopefully spare Jayden from the risks associated with his condition, instead allowing him to grow and develop along a healthy trajectory. Jayden’s mother says, “I have been praying for a long time for Jayden’s healing and I now believe that he will be treated.”

$1,151raised
Fully funded