Spencer joined Watsi on January 2nd, 2021. Four months ago, Spencer joined our Universal Fund, supporting life-changing treatments for a new Watsi patient every month. Spencer's most recent donation supported Amos, a three-year-old from Kenya, to fund surgery for a birth condition so he can walk well.
Spencer has funded healthcare for 5 patients in 3 countries.
Amos is a three-year-old boy and the third born in a family of four children. Amos’s father works at construction sites while his mother works at home to take care of their home and family. Amos was born with a condition known as Blount's disease, or bowing of both legs. The condition has greatly affected his mobility and he cannot walk for a long distances or stand. He is almost school-aged, but unfortunately cannot attend school because of the severity of his condition. Fortunately, our medical partner, African Mission Healthcare (AMH) is helping Amos to receive treatment. Amos is scheduled to undergo surgery on May 9th. Now, AMH is requesting $1,224 to fund Amos's procedure. After the surgery, he will be able to walk well, stand for long periods of time, and even begin school! Amos's father shared, “my desire as a parent is to see my son walking like other children. Any support will be highly appreciated."
Sary is a 49-year-old security guard who has proudly been married for 32 years. Together they have three sons and two daughters. Sary lives with his wife, who is a farmer, and their children. He does not have a lot of free time, but when he does he shared that he enjoys being with his children and listening to the radio. In June of 2020, Sary was in a motor vehicle accident that caused paralysis of his right shoulder. He has been diagnosed with a brachial plexus injury on his right 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. Sary is unable to lift his arm and he can't work. Sary traveled to our medical partner's care center to receive treatment. On March 16th, he will undergo a brachial plexus repair surgery. After recovery, he will be able to use his arm again. Our medical partner, Children's Surgical Centre, is requesting $696 to fund this procedure. Sary was hopeful about his treatment and shared, "I hope I can be back to work as soon as possible."
In late January, the Muinde family from Kenya was blessed with their firstborn child, a daughter they named Emmaculate. Emmaculate's mother works in a mobile money shop and Emmaculate's father has a small electronics shop. They live in a small rented house in Nakuru, and are able to use their income to cover most of their family's basic needs. They learned that Emmaculate was born with a rare form of craniosynostosis, which meant that her eyes were not fully formed and her pupil was not visible in both of her eyes. A few days after her birth, Emmaculate was reviewed at her local clinic, and the doctor referred Emmaculate to a nearby facility for further examination. Ultimately, Emmaculate was seen by the doctors at our Medical Partner Care Center BethanyKids Kijabe Hospital (BKKH). On March 1st, Emmaculate will undergo a craniotomy in order to release the pressure in her brain. However, Emmaculate’s parents are not able to cover the amount needed for her surgery. Emmaculate’s father says, “When I was told about my child’s condition and the treatment required, my heart sank as we could not afford any of this treatment. As a family, we are requesting financial help.”
Scholastica is a 6-month-old baby girl from Tanzania. She is the last born in a family of six children. Scholastica was born a healthy child but, at four months of age, her mother noticed her head was growing very fast and she was not able to support it. They could not afford the cost of seeking care at the regional hospital at the time. Scholastica's parents are small scale farmers and work hard to make ends meet with their income. Eventually, they were able to get some money from relatives and took her back to the regional hospital. There, Scholastica was diagnosed with hydrocephalus, a condition in which excess cerebrospinal fluid accumulates in the brain and increases intracranial pressure. Without treatment, Scholastica will experience severe physical and developmental delays. Unfortunately, she was not able to get an appointment at the regional hospital for a long time. As time went on, Scholastica's condition grew worse. Her head increased in size and her eyes began rolling down. Though they were concerned, her parents could not raise money to seek an alternative hospital for care. Eventually, their friend referred them to our medical partner's care center, ALMC Plaster House. Their friends and neighbours supported them with bus fare for the two-day journey to the hospital. Now, she is scheduled for an ETV surgery to treat her condition, and the family appeals for financial support for this procedure. Our medical partner, African Mission Healthcare Foundation, is requesting $1,300 to cover the cost of ETV surgery for Scholastica that will treat her hydrocephalus. The procedure is scheduled to take place on January 25th and will drain the excess fluid from Scholastica's brain. This will reduce intracranial pressure and greatly improve her quality of life. It will also reduce the likelihood of severe fevers, vomiting, and potential brain damage. With proper treatment, Scholastica will hopefully develop into a strong, healthy young girl. Scholastica’s mother shared, "We travelled for two days because we were told there is hope for my daughter to get help. Please help save her.”
Phearin is a 24-year-old from Cambodia. He has three older brothers who are all married. When he is not working, Phearin enjoys playing football, listening to music, playing games on his phone, and meeting up with his friends in the evening. In August, Phearin was in a motor vehicle accident that caused a clavicle fracture and paralysis of his right arm. His family took him to a private clinic where the fracture was treated. He has been diagnosed with a brachial plexus injury on his right 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. He is unable to lift his arm and he cannot work. Phearin traveled to our medical partner's care center to receive treatment. On December 9th, he will undergo a brachial plexus repair surgery. After recovery, he will be able to use his arm again. Our medical partner, Children's Surgical Centre, is requesting $696 to fund this procedure. Phearin said, "I really hope I can regain use of my arm so I can return to working as soon as possible."