Katrina CrisostomoUNIVERSAL FUND MEMBER
Katrina's Story

Katrina joined Watsi on April 22nd, 2016. Seven years ago, Katrina joined our Universal Fund, supporting life-changing treatments for a new Watsi patient every month. Katrina's most recent donation supported Mohammed, a 3-year-old boy from Kenya, to fund clubfoot repair surgery and care.

Impact

Katrina has funded healthcare for 111 patients in 12 countries.

Patients funded by Katrina

Hassan is an only child whose parents separated before he was born. Prior to his birth, Hassan's mother worked alongside his grandmother, doing farm work to earn income. After Hassan was born, his mother had to stop working so she could take care of him. Hassan was diagnosed with spina bifida at birth, a condition that occurs when a developing baby's spinal cord fails to develop or close properly while in the womb. Hassan had a swelling on his back that was open and leaking. He was admitted in hospital for a few days while his mother was taught how to dress the wound. An MRI and a CT scan were done and he was scheduled for surgery weeks later. While home, his mother continued with the wound dressings as instructed until the leaking stopped. During one of the post-natal clinics, Hassan and his mother were referred to our medical partner's care center, BethanyKids, for treatment. Upon arrival at BethanyKids, Hassan was examined and was additionally diagnosed with hydrocephalus, a build up of fluids in the brain. He was then scheduled for a spina bifida repair surgery, and the mother was told that once he recovered, he would be scheduled for a shunt insertion surgery. Due to financial challenges and a loss of income for Hassan's mother, the family is unable to meet the medical expenses. Without treatment, Hassan is at risk of lower-limb paralysis, infection of the exposed nervous tissue, development of tethered cord syndrome, and possible developmental delays. Fortunately, our medical partner, African Mission Healthcare, is helping Hassan receive treatment. On March 15th, surgeons at BethanyKids will conduct a spina bifida closure surgery to promote Hassan's healthy growth and development. Now, Hassan's family needs help to fund this $1,151 procedure. Hassan’s mother says, “A while back, I had already given up on Hassan's treatment. Because the community had never seen such a condition, I was told that I would always get children who have different medical conditions. After coming to this facility, I realized that this was not the case. My hopes were raised again and now I’m looking forward to the best outcome in Hassan’s treatment.”

$370raised
$781to go

Nay is a 31-year-old man from Burma. He lives with his mother, two sisters, two brothers-in-law, two nephews, and two nieces in a village in Karen State along the Burma border. Nay works in Thailand as a day laborer, spending one week working in Mae Sot and then returning for two days to his village. Nay’s mother is retired and one of his sisters is a homemaker, taking care of her children. The other sister and two brothers-in-law are day laborers on a farm in Karen State. They also grow vegetables for family consumption. His nephews and one niece go to school. Their monthly income is enough for basic needs and they make an effort to pay for basic health care. In his free time, Nay enjoys helping in his community and fixing electronic items. In July 2023, Nay began to experience blurred vision in his right eye. He has intermittent pain and discharge. These symptoms have made it increasingly difficult for him to see clearly. Nay feels uncomfortable seeing only with his left eye and feels sad and depressed about his condition. Nay was diagnosed with retinal detachment, a condition in which the retina pulls away from the supportive tissue in the eye, resulting in vision loss. If left untreated, he could lose vision entirely in the right eye. Nay is scheduled to undergo surgery to reattach his retina on January 18th. Our medical partner, Burma Children Medical Fund, is requesting $1,500 to cover the cost of this procedure and care. After the surgery, Nay's vision will hopefully be restored, and he will resume his daily activities comfortably. Nay said “I was stuck and hopeless while the doctor was telling me that I would need a surgery. I don’t even know how to explain about my health problem to my family. I worry they will feel so sad and worry about me. I am unhappy and feel tired emotionally. After learning that I have donors who will help me paying for my treatment in Chiang Mai, I feel like my hope has returned and I'm wishing my vision would repair and I'll be able to continue my career in the future."

$1,020raised
$480to go

Jecinta is a delightful 4-year-old girl from Kenya. She is playful and jovial. Born with a birth condition her journey began at Kiambu Hospital, where dedicated healthcare professionals initiated a treatment plan to address the condition. She was prescribed braces as part of her comprehensive care to correct her clubfeet. With the support of her mother, she embarked on a hopeful journey towards improved mobility and a future filled with possibilities. The braces played a role in maintaining the corrections achieved through casting and other interventions. However, along the way, and because of the hardships, Jecinta, like many children, faced challenges in using the braces. Unfortunately, she lost to follow-up at Kiambu Hospital, and the regular monitoring and follow-up appointments ended. Over more than a year with no follow-up, Jecintas deformity recurred. Currently she tiptoes as she walks and feels pain. Fortunately, Jecinta and her mother traveled to visit our medical partner's care center, AIC Cure International Hospital. Our medical partner, African Mission Healthcare, is requesting $1,286 to fund Jecinta's clubfoot repair. After treatment, she be able to walk well, with no pain and discomfort. Her self-esteem will also improve, and she will continue with her education without any hardship. “I will appreciate if consider my daughter to undergo surgery so that she can stand on her feet and walk confidently like other children,” Glory, Jecinta’s mother, told us.

$1,286raised
Fully funded

Alven is a hardworking father from Philippines. He is a single father, acting as both parents to his daughter. He has been separated from his wife for 18 years and lives with his siblings. Alven is a maintenance worker and shared that he is known to be a "workaholic". One year ago, Alven began to experience troubling symptoms, including extreme abdominal and back pain. The pain was so extreme, he could not go to work two days a week which has affected his income. In April, he went for a check-up at Ospital ng Paranaque, a general surgery hospital. Alven was diagnosed with gallstones, hardened deposits of digestive fluid that can form in the gallbladder. Alven has been advised to undergo a cholecystectomy, the surgical removal of the gallbladder. If left untreated, his symptoms will continue to worsen and put him at risk for further health complications in the future. After seeking treatment through our medical partner, World Surgical Foundation Philippines (WSFP), Alven is scheduled to undergo a cholecystectomy on November 11. A portion of the cost of the procedure is being supported by the Philippine Health Insurance Corporation, and WSFP is raising the remaining $1128 to cover the cost of Alven's surgery and care. Alven told us: "This assistance is a big help to me because my income is only enough to support my daughter and is not sufficient to support my surgery. Your help means a lot to me and my family. I hope that you continue to help others because I am truly blessed to be one of your beneficiaries."

$1,128raised
Fully funded

Siek Meng is a 15-year-old who resides in the Prey Veng province of Cambodia with her parents and two younger brothers. Her parents make a living as rice farmers, and when Siek Meng returns home from school, she helps care for her siblings. During her free time, she enjoys learning English by watching English-language films and television shows. She aspires to pursue higher education in the capital of Phnom Penh and study medicine in the future. Around the age of 6, Siek Meng and her parents noticed something concerning about her back. However, they postponed seeking treatment until two years later due to the high cost of treatment and not considering it essential at that time. Unfortunately, the condition has since deteriorated, and she has been diagnosed with scoliosis, a deformity of the spine. In the past year, Siek Meng has experienced increased difficulty breathing as her rib cage presses on her lungs. Additionally, she occasionally feels numbness in her legs caused by her vertebrae compressing nerves. Thankfully, Siek Meng and her father undertook a challenging journey of two and a half hours to reach our medical partner, Children's Surgical Centre (CSC), seeking assistance for her disability. The medical team at CSC plans to perform a spinal fusion with implants on August 2nd, which requires financial support as the operation costs $1500. This amount will cover radiology, medications, surgery, and post-operative physiotherapy care. CSC is requesting $1500 to help fund this procedure for Siek Meng. Siek Meng shared, "I am feeling embarrassed about my back and I want to not have chest pain anymore. I hope after surgery I can go back to school and be able to walk around my village more easily."

$1,500raised
Fully funded

Kaung is a 2-year-old baby boy who lives in Burma with his grandmother, uncle, aunt, and five-month-old cousin. His grandmother is retired, his uncle is a motorbike taxi driver and his aunt is a homemaker. Kaung was born with a condition called Congenital Hydrocephalus. Congenital Hydrocephalus is caused by a brain malformation or birth condition that causes excessive cerebrospinal fluid to accumulate in brain cavities. Cerebrospinal fluid is a clear, colorless liquid that surrounds the brain and spinal cord, protecting them from injury. It carries nutrients to the brain and spinal cord and takes away waste. In a healthy person, the amount of this fluid produced by the brain is absorbed by the body. In hydrocephalus, the fluid fails to drain and accumulates, leading to pressure on the brain. Kaung's symptoms include intensifying nasal congestion and coughing with mucus. Additionally, his head is gradually increasing in size as the fluid continues to put pressure on his brain. The condition is most often treated by inserting a shunt. The shunt diverts excess cerebrospinal fluid (CSF) from the brain to another part of the body where the fluid can be reabsorbed. Kaung's family visited a doctor when he was born to address the issue. At the time, the doctor advised the family to seek further treatment. However, Kaung was never brought to a hospital or clinic due to the financial difficulties of the family. Fortunately, Kaung was able to meet with our medical partner, Burma Children Medical Fund (BCMF). With the help of BCMF and Watsi, Kaung received a CT scan at Mae Sot General Hospital. The doctor was able to diagnose his condition and scheduled Kaung to undergo surgery immediately. Kaung is scheduled for surgery on May 26th. Kaung's aunt said, "My nephew becomes cuter by the day, and he is always smiling. I tried to save money to treat him, but I could not. But now, we are so happy to have met you all at BCMF. We are happy to know that Kaung will have the opportunity to get treated because of your support.”

$1,500raised
Fully funded