Patricia BreechUNIVERSAL FUND MEMBER
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 Priscillah, a 61-year-old farmer from Kenya, to fund a thyroidectomy.

Impact

Patricia has funded healthcare for 76 patients in 12 countries.

patients you have funded

Aung, who is 25 years old, lives with his mother, brother and two sisters in Burma. His mother is retired, and his brother is a security guard. One of his sisters works at a bicycle factory, while the other one works for a local company. Aung is currently unemployed because of his poor health. In October 2022, Aung fell ill and developed a persistent cough. He went to a charity hospital, where he was told that he had a heart infection. After he was treated with injected antibiotics, the doctor told him that he needed an echocardiogram, because he might have a heart condition due to the infection. After the echo was completed, he was diagnosed with mitral valve regurgitation, and he was referred to a cardiologist in Yangon. Aung went to see the cardiologist, who told him that he would need surgery, which he could not afford. On December 25, 2022, both of Aung's legs and his arms became swollen, and he was unable to sleep. He went to a private hospital, where it was determined that he would need surgery as soon as possible. Currently, Aung feels extremely fatigued, experiences chest pains, and has difficulty breathing. Sometimes, his legs and his arms become swollen, and he cannot sleep well at night. Our medical partner, Burma Children Medical Fund, is requesting $1,500 for the mitral valve replacement surgery that Aung needs. The procedure is currently scheduled to take place on April 2nd, at Pun Hlaing Hospital. "In the future, I want to work as a taxi driver, because I believe that I could easily earn money doing this [in the city]," said Aung.

$792raised
$708to go

Daw Nan is a 64-year-old woman from Myanmar. She lives with her husband in a village in Karen State. Her husband is retired and she occasionally works as an agricultural day laborer. She also grows cashews in her garden and sells what she harvests once a year. Sometimes, her daughter, who works in Thailand, sends her pocket money. In her free time, she likes to go to the temple and meditate. Currently, she can only perceive light with her right eye and the vision in her left eye is starting to blur. She cannot see people's faces with her right eye, and her left eye is sensitive to light. Because of her poor vision, she can only walk slowly because she is worried that she will trip and fall. She also feels stressed about her vision problem, and she has lost weight and has little appetite. Our medical partner, Burma Children Medical Fund, is requesting $1,500 to fund lens replacement surgery for Daw Nan. On February 10th, doctors will perform a lens replacement, during which they will remove Daw Nan's natural lenses and replace them with an intraocular lens implant in each eye. After recovery, she will be able to see clearly. Now, she needs help to fund this $1,500 procedure. Daw Nan said, "Since the vision in my right eye worsened and I noticed that the vision in my left eye is worsening, I feel stressed at all times. I cannot work properly as my [left] eye hurts and waters when it is bright outside. I feel sad. Even though I eat, I have a poor appetite and I have lost weight. I will be very happy if I can see again after my surgery."

$865raised
$635to go

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.”

$1,074raised
Fully funded

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.”

$1,084raised
Fully funded

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.”

$1,151raised
Fully funded