Profile 132x132 boris profile sep 2013 closer medium

Boris Jabes

MONTHLY DONOR

United States

Boris' Story

Boris joined Watsi on September 8th, 2014. Six years ago, Boris joined our Universal Fund, supporting life-changing treatments for a new Watsi patient every month. Boris' most recent donation traveled 8,700 miles to support Mgosi, a baby from Tanzania, to fund clubfoot treatment.

Impact

Boris has funded healthcare for 72 patients in 12 countries.

All patients funded by Boris

Mgosi

Mgosi is a 17-month-old baby girl from Tanzania. She is a beautiful, friendly, and playful girl. She is the last born to her mother, who has three children, and shared that Mgosi's father is polygamous with three wives and a total of twelve children. Mgosi was born with a right clubfoot that has made her not able to learn how to walk until now. Mgosi was born at home with the help of a midwife and her parents were informed about her condition and advised to seek treatment for her. Due to financial challenges, they have not been able to do so. Both of her parents are small-scale farmers and sell a small amount of their harvest in order to buy other basic commodities. Our medical partner's outreach team visited their village and Mgosi’s parents got to hear about ALMC Hospital and The Plaster House. They decided to seek help for her. Mgosi has been diagnosed with right clubfoot and an umbilical hernia, which both need to be corrected. For her clubfoot, she will start with manipulation and casting to help corrected her foot enabling her to be able to walk like her age mates and save her from the challenges she is going through at the moment. Thereafter, she will be able to have her umbilical hernia corrected. Mgosi's family traveled to visit our medical partner's care center, Arusha Lutheran Medical Centre where surgeons will perform clubfoot repair surgery on October 9th. Our medical partner, African Mission Healthcare Foundation, is requesting $935 to fund Mgosi's clubfoot repair. After treatment, she will be able to ambulate with ease. Mgosi’s mother shared, “I would love to see my daughter walk like other children of her age please help my daughter. The cost is too high for us to afford it.”

62% funded

62%funded
$585raised
$350to go
Simon

Simon is a 3-month old baby boy from Tanzania and the only child to his parents. He was born healthy but when he was two months old he started having fevers and vomiting. His parents tried to seek treatment for him but the medication he was using only helped reduce the fevers. Soon his parents noticed his head was increasing in size and his general health became very poor due to the regular vomiting. His parents depend on small-scale farming for a living and their income is not always enough to get them by. Due to financial challenges, Simon's parents could not afford to take him to a referral hospital in time, hence his condition worsened. Through ALMC Hospital's outreach program, they learned about Simon's condition and the need for him to get treatment. Simon has been diagnosed with hydrocephalus which is putting him in danger of brain damage due to the pressure building up in his head, causing him not to be able to feed well and regular fevers. His parents cannot afford the treatment cost and are asking for help. Simon has been diagnosed with hydrocephalus, a condition in which excess cerebrospinal fluid accumulates in the brain and increases intracranial pressure. As a result of his condition, Simon has been experiencing increasing head circumference, fevers and vomiting. Without treatment, Simon will experience severe physical and developmental delays. Our medical partner, African Mission Healthcare Foundation, is requesting $1,300 to cover the cost of surgery for Simon that will treat his hydrocephalus. The procedure is scheduled to take place on September 7th and will drain the excess fluid from Simon's brain. This will reduce intracranial pressure and greatly improve his quality of life. With proper treatment, Simon will hopefully develop into a strong, healthy young boy. Simon’s mother says, “My son’s head keeps increasing in size and his general health deteriorates as days go by, we are unable to afford the treatment cost. Please help us.”

79% funded

79%funded
$1,028raised
$272to go
Khin

Khin is a 39-year-old woman who lives with her family in Hpa-An Township, Karen State, Burma. Both her children are in preschool. She and her husband are subsistence farmers, growing rice during the rainy season on rented land. The rest of the year, her husband collects leaves used to make roofs, works as a daily labourer or collects branches to sell. Khin was born with a scar the size of an ant bite on her upper lip. Her parents thought that it would disappear or heal on its own but the scar developed into a growth and increased in size. Her parents passed away when she was young and after that she went to live with her brother’s family. By the time she was around 20 years old, the growth had become large and soft, covering the area between her upper lips and her nose. When the pain became unbearable in 2005, her uncle dropped her off at Mae Tao Clinic (MTC) in Thailand, a free clinic close to where her uncle used to work. At this point, the growth had become so large that dragged her upper lip down and extended into her nostrils. At MTC, she was seen by doctors and medics, before she was diagnosed with a hemangioma. At this point, the growth had worsened, and she was bleeding from her lips. In April 2006, Khin went to Chiang Mai Hospital and had the hemangioma removed surgically. The growth later has returned. Overtime, the hemangioma has increased in size and become hard. It has now expanded into Khin’s nostrils, especially her left nostril, which causes her to have difficulty breathing at times. She feels uncomfortable but is not in pain. Sometimes she also feels like she has a blood clot in her nostrils during her nosebleeds. Because the nosebleed can start at any time and can last anywhere from 10 to 20 minutes, her life revolves around managing her nosebleeds. She is unable to work or sleep properly, and if she is about to have a nosebleed, she is unable to eat. The nosebleeds have also affected her ability to earn an income for her children and continues to impact her social life. “When I socialise, I do not feel comfortable and some people think I have a disease that I can infect them with,” said Khin. “So, I hope to get better after surgery, and I hope I will no longer have nosebleeds. I don’t want to bleed, and I want to socialise with my friends and family happily. [Right now] my friends won’t even touch me.”

100% funded

$1,500raised
Fully funded