Sarah RothwellUNIVERSAL FUND MEMBER
Sarah's Story

Sarah joined Watsi on March 12th, 2013. Nine years ago, Sarah joined our Universal Fund, supporting life-changing treatments for a new Watsi patient every month. Sarah's most recent donation traveled 1,900 miles to support Keina, a four-year-old girl from Haiti, to fund life changing heart surgery.

Impact

Sarah has funded healthcare for 118 patients in 11 countries.

Patients funded by Sarah

Lourdez is a mother of three from the Philippines. Currently, her family depends on the income of their second child, who works as a call center agent. Lourdez shared that this income is not enough for the family's expenses and hopes that, after her treatment, she will be able to work and help earn money to support her family. Seven months ago, Lourdez began to experience troubling symptoms, including unbearable stomach pain that lasted for hours. She immediately consulted with a doctor. However, she knows her family cannot afford the cost of surgery, so she had to look for other treatment options. Fortunately, a friend brought her to one of our care centers, where the doctors advised Lourdez to undergo a cholecystectomy, the surgical removal of the gallbladder. If left untreated, her symptoms will continue to worsen and put her at risk for further health complications in the future. After seeking treatment through our medical partner, World Surgical Foundation Philippines (WSFP), Lourdez is scheduled to undergo a cholecystectomy on December 13th. The Philippine Health Insurance Corporation is supporting a portion of the cost of the procedure. WSFP is requesting $1,128 to cover the remaining cost of her surgery and care. Lourdez said, "This treatment will be a great help, not just for me but for my family. We have no other means of funding my surgery. As a basic earner, my daughter's income is often not enough for our family's needs and expenses. The free surgery would be a blessing and an opportunity for me to help my daughter earn for the family."

$557raised
$571to go

Vanila is a 17-year-old girl. She comes from a sizable family that includes five siblings, with her being the second-to-last born. She is a student and recently completed her secondary education with the hope of going further in her education. Her parents work as farmers, relying on their harvest for sustenance. Additionally, her father engages in casual day-to-day jobs to supplement their income. Three of Vanila’s siblings are independent and working, and they occasionally assist their parents in covering household expenses. Vanila’s journey began when, as a baby, her parents noticed both of her legs twisting inward and downward. Unfortunately, financial constraints prevented them from addressing her medical needs. In September 2023, Vanilla’s family learned about Kafika house, and the services offered. They visited, and she was diagnosed with bilateral clubfoot, a condition that significantly limited her mobility. With both legs affected, she commenced treatment for her left foot first, starting with manipulation and casting. In October 2023, she underwent surgery, and her treatment progressed well, showing positive results. Currently, Vanila is on the verge of beginning treatment for her right foot. She will undergo a similar process to correct the defect in her right foot. The team will begin clubfoot treatment for Vanila on December 29th. Our medical partner, African Mission Healthcare, is requesting $935 to fund Vanila's clubfoot repair. After treatment, her mobility will significantly improve. Vanilla says: “I’m looking forward to the day that I will be walking comfortably.”

$935raised
Fully funded

Four year old Neserian lives with his family in a village in the Manyara region of Tanzania. The family has long depended upon agriculture and livestock keeping to sustain them. However, climate change has shadowed their agricultural activities, rendering them increasingly unreliable. Consequently, Neserian’s father has turned to selling cattle to support his household. But drought has led to the cattle being unable to feed properly, so that they fetch considerably less money at the market. Neserian's father works hard to meet the needs of his family. In October 2022, Neserian was alone at home, when he ventured too close to an open flame. His clothing caught fire, and he suffered burns to his right elbow and wrist. The neighbors came to his aid, and when his mother returned home, she brought him to a local hospital for care. Neserian remained at the hospital for a month. Despite the care that he received, Neserian has only a limited range of motion of his right arm. Sadly, the local hospital lacks the resources to address this. Neserian and his father traveled for nine hours to consult with doctors from our medical partner's care center the Plaster House NGO. After a thorough assessment, it was determined that Neserian would need to undergo a Z-plasty procedure, to release his right axilla and elbow, along with a full thickness skin graft on his right hand. The pinky on his right hand will need to be amputated. The surgical procedures are set for August 15th but the cost of treatment is beyond the means of Neserian's family, prompting them to appeal for your assistance in covering the $1,088 needed for Neserian's care. After he has healed completely, Neserian will be able to use his hand, and lead a full life, free from disability. Neserian’s father says: “We wish for him to be able to use his hand because he is about to start school, and we are worried it will be hard for him as his right hand is the one affected.”

$1,088raised
Fully funded

Mabasa is a four-year-old child from Tanzania. Like any other child, he is filled with dreams, curiosity, and a boundless spirit. He comes from a mid-sized family with five siblings. However, his journey has taken an unexpected turn that threatens to overshadow his bright future. Born to hardworking farming parents, Mabasa was a healthy and joyful baby. Yet, at age two, he began to experience a troubling transformation that has left his family deeply concerned. Mabasa’s parents, dedicated farmers who work relentlessly to provide for their family, noticed something amiss when their son’s legs started to bend as he took his first steps. This struck them with concern and fear. The condition worsened as months passed, casting a shadow of uncertainty over their child’s future. Mabasa was diagnosed with left genu valgus. Colloquially known as "knock-knee," genu valgum is a condition in which the knees bend inward, and can cause pain, difficulty walking, and arthritis. Mabasa's left leg has curved inward, affecting his mobility. To their dismay, the doctors could find no apparent cause for Mabasa’s condition and suggested a healthy nutrition regimen and medications to improve his overall health. Mabasa’s parents followed these recommendations, but despite their unwavering efforts, there was no sign of improvement. Our medical partner, African Mission Healthcare, is requesting $880 to fund corrective surgery for Mabasa. The procedure is scheduled to take place on September 14th. Treatment will hopefully restore Mabasa's mobility, allowing him to participate in a variety of activities, and greatly decrease his risk of future complications. Mabasa’s father says, “I wish for my son to have a bright future and that this condition won’t be a problem in the future.”

$880raised
Fully funded