Patricia BreechMONTHLY DONOR
Patricia's Story

Patricia joined Watsi on March 17th, 2017. Six years ago, Patricia joined our Universal Fund, supporting life-changing treatments for a new Watsi patient every month. Patricia's most recent donation supported Bela, an 18-month-old girl from Philippines, to fund surgery for a birth condition.

Impact

Patricia has funded healthcare for 72 patients in 12 countries.

All patients funded by Patricia

Dennis is the first born in a family of four children. When he finished high school, he was reluctant to join college because of his condition. He currently is not able to work because he gets easily tired and cannot carry heavy loads. He joined college just recently but has been out of school for the past two months. Now that he is at home, he helps his mother who picks tea for a living. He does not have a health insurance coverage and cannot raise the required amount of money to cater for his hospital bill. In 2019 while he was sitting for his national school exams, Dennis experienced sharp pain in his esophagus. He took a glass of water, and the pain went away for a few weeks. The pain used to occur roughly two times in a month and a glass of water would help a lot. Late last year, the pain worsened. He was not in a position to swallow food. He went to a herbalist and was given some medication to use for some time. When the dose was over, the pain was still persistent, and he still could not swallow food normally. He was then referred to Kijabe Hospital by a friend where he was examined and given some medication to use. He didn't feel better and decided to go back to the herbalist for different medication but there was no change. Later he finally returned to Kijabe Hospital and scans and tests revealed that he has Achalasia. He is scheduled for a heller's myotomy which is a curative laparotomy surgery for his condition. Now he needs $1,074 to pay for the surgery. Dennis says, "I feel very sad. If I was healthy, I would be able to work well and be comfortable with myself.”

58%funded
$629raised
$445to go

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

Meet Venesa, a beautiful two year old girl. She was born at home with a swelling at the lower part of her back, and with legs that were not straight like other babies their family knew. The day after she was born, Venesa's parents took her to the hospital, where she was diagnosed with spina bifida and clubfoot. The family was advised to wait until Venesa turned nine months old, before having her undergo the surgery that she needs. Although surgery was deemed urgent, when Venesa was finally old enough, her parents couldn't afford to pay for it. Then, about a year ago, Venesa was diagnosed with hydrocephalus. Venesa's mom shared that shortly after this last diagnosis, Venesa's father abandoned the family and is not involved in helping support them any more. Venesa's mother used to work at a salon, but after Venesa's birth, she has been unable to work. They are now living with Venesa's grandmother, who does what she can to help. Without surgery for her spina bifida, Venesa risks paralysis of her lower limbs, infection of the exposed nerve tissue, and developmental delays. Our medical partner, African Mission Healthcare Foundation, is requesting $1,151 to cover the cost of Venesa's spina bifida closure surgery. The procedure is scheduled to take place on September 14th, at BethanyKids Kijabe Hospital. This procedure will hopefully spare Venesa from the risks associated with her condition, allowing her to experience a strong and healthy life. Venesa’s mother says: “Since she was born, I have no peace knowing that I can’t afford her treatment.”

76%funded
$877raised
$274to go

Elinipa is a beautiful two-year-old girl. She is an incredibly friendly child who loves to play with her five older siblings. At birth, she was a healthy child. It wasn't until she was learning to walk however, that her mother noticed that her legs were slightly curved, yet even so they did not seek treatment assuming it was a minor problem that she would outgrow. Elinipa has now been diagnosed with bilateral valgus, which is a condition caused by an excessive accumulation of fluoride in the bones, which often stems from contaminated drinking water. As a result of her condition, Elinipa's legs bow inward to the point that her knees touch. This makes walking persistently more difficult as she continues to grow. Through our medical partner's outreach program her parents learned that their daughter needs surgery to correct her legs. Elinipa's parents are small scale famers who depend entirely on what they harvest to make a living. As a result, their income is not enough to afford to take Elinipa to the hospital to treat her condition. Our medical partner, African Mission Healthcare, is requesting $880 to fund corrective surgery for Elinipa. The procedure is scheduled to take place on May 13th at our medical partner's care center, Arusha Lutheran Medical Centre. With this treatment Elinipa's mobility will hopefully be restored, thus allowing her to participate in a variety of activities, and greatly decreasing her risk of future complications. Elinipa’s father says, “I am worried with how her legs continue to bend inward. Please help us.”

$880raised
Fully funded