Hef's Story

Hef joined Watsi on June 5th, 2021. Two years ago, Hef joined our Universal Fund, supporting life-changing treatments for a new Watsi patient every month. Hef's most recent donation supported John, a 6 year old boy from Kenya, to fund hearing treatment.

Impact

Hef has funded healthcare for 30 patients in 8 countries.

Patients funded by Hef

Sephania is a baby from Simanjiro, Arusha in Tanzania. He lives among the Maasai people. He comes from a large family of six siblings, raised by a single mother. His father died shortly after he was born, and his mother depends on her brothers, who are cattle breeders. They help provide basic needs for the family since his mother does not work and has no means to earn a living. Sephania was born with both his legs twisted inward and downward. His mother was informed that there was treatment for the condition. She could not afford transport money at the time and had to wait for almost 2 years before she was able to collect enough money to travel to a medical center. She arrived at our center with an escort, who helped her translate as she only speaks Maasai. After a brief assessment with our team, we set up a treatment plan for Sephania, starting with a series of castings. Sephania has clubfoot on both feet. Clubfoot is a condition in which the foot is twisted out of shape. This causes difficulty walking and even wearing shoes. Fortunately, Sephania traveled to visit our medical partner's care center, Arusha Lutheran Medical Centre. There, surgeons will perform clubfoot repair surgery on May 12th. Our medical partner, African Mission Healthcare Foundation, is requesting $935 to fund Sephania's clubfoot repair. After treatment, he will be able to walk easily. Sephania’s mother says, "It has taken a while to be able to come for treatment. I hope my son will get treatment that will help with his foot’s condition."

$435raised
$500to go

Meet Nafissa. She is a 25-year old woman who shared that she tends to be very shy and reserved. She lives with her parents and her young child in an area of Burkina Faso where conflict is currently impacting their lives deeply. When she was a child, Nafissa developed a painful growth on the left side of her chin. This swelling in her lower jawbone affected her ability to eat, and was determined to be a benign tumor that needed to be removed. Her parents were able to secure the funds to send Nafissa to a hospital in Togo, where she could be treated at no cost to her family. The growth was removed, and for several years, Nafissa did well. However, the growth recurred, and in the middle of last year, Nafissa returned to Togo, where the second growth was excised. This time, however, the surgeon determined that her whole jawbone would also need to be removed. As the doctor in Togo did not have the necessary training to perform the surgery that Nafissa needed, he referred her to a physician with our medical partner, African Mission Healthcare. Miraculously, Nafissa is now scheduled for a major jaw surgery with the leading team at AIC Kijabe Hospital in Kenya. As Nafissa's husband abandoned her because of her condition, and provides no support to Nafissa or their child, Nafissa and her parents are looking to you to help fund the $1,500 procedure, which will finally relieve Nafissa of the pain and symptoms that result from the tumor. Nafissa says: “It pains me that I have to stay at home with no friends. Making it worse, I cannot work to provide for my child.”

$1,500raised
Fully funded

Boramey is an adorable 2-year-old toddler from Cambodia. She has an older sister, who is seven and in the 1st grade, and an older brother, who is four and not in school yet. Her father works as a driver for a construction company, and her mother sells groceries at a local market. Boramey's favorite activities include playing with the other children in her neighborhood and snacking on bread. When Boramey was born, she experienced an injury called shoulder dystocia, which occurs when one or both of a baby's shoulders become stuck inside the pelvis during childbirth. As a result, the nerves responsible for providing feeling and movement in her shoulder and arm were stretched. Boramey cannot move her left arm and has no shoulder abduction or elbow or wrist flexion. She 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. Our medical partner's care center is the only center in Cambodia where the treatment Boramey needs is available. On January 3rd, she will undergo a brachial plexus repair surgery. Our medical partner, Children's Surgical Centre (CSC), is requesting $709 to fund this procedure. Boramey's parents were able to gather $100 to contribute to her care. Boramey's mother said: "I hope the doctors can fix her arm so she can use it like other children and be able to go to school when she is old enough."

$709raised
Fully funded

Su is 10-year-old girl who lives in Thailand. Both of her parents work for a community based organization helping others in their area. In her free time, Su likes to draw pictures and play with her friends. Su was born with clubfeet and a dislocated hip. She received corrective surgery in Chiang Mai with the help of our medical partner BCMF after she was born. During her last visit to the hospital when she was young, the doctor told her mother that they only had to return to the hospital when she outgrew her clubfeet correction shoes. However, her parents could never bring her back. In additional to financial constraints, their legal documents expired, and later when they had legal documents, they could not go to Chiang Mai due to covid-19 travel restrictions. In June 2022, Su started to experience pain in her right foot whenever she walked more than 10 minutes. She also experienced pain in her right hip for the first time when she walked. The doctor at Mae Sot Hospital diagnosed her with a dislocated hip and referred her to the larger hospital Chiang Mai for further treatment. In October an MRI was performed for Su and it was determined that she may need two surgeries: one for hrt hip and another for her clubfeet condition. The first surgery is for a hip replacement and the doctor scheduled her for surgery on November 25th so she can be out of pain as quickly as possible. Her family needs $1500 for her hip replacement surgery. Su's father said, "I am hopeful for my daughter to receive surgery soon. After surgery, I hope that she will be able to walk like other children and she will not be shy when she grows up. Now, when she goes to school, some of her friends tease her that she cannot walk properly like other children."

$1,500raised
Fully funded