Ruwan Randeniya
Ruwan's Story

Ruwan joined Watsi on March 10th, 2015. 17 other people also joined Watsi on that day! Ruwan's most recent donation traveled 8,200 miles to support Baluku, a fisherman from Uganda, for hernia repair surgery.


Ruwan has funded healthcare for 19 patients in 13 countries.

Patients funded by Ruwan

Snow is a ten-year-old Burmese girl who lives in a refugee camp with her parents and older sisters. For the past eight years they have lived in the camp. Snow's family moved to the camp as they didn’t own their own home or land, and they were living with Snow’s grandmother and other members of the extended family. This situation influenced their decision to migrate to the refugee camp in Thailand. Snow and her family would like to relocate to a third country but they are uncertain whether the opportunity will present. In the camp, Snow’s mother does laundry for others for a small income. Previously her father worked as a carpenter but is unable to work now because of hemorrhoids. Their monthly income is insufficient for daily expenses, savings or health care expenses. Living in the camp, they receive food rations which offset the burden. At times the family has to borrow small amounts of money, which they repay when they can. Snow and her two sisters attend school. Symptoms first appeared with Snow when she was seven-years-old. She had severe pain in her abdomen when she was just sitting, and she was uncomfortable walking. After an examination at the camp's medical clinic, she was diagnosed with rectal polyps. On January 28th, the surgeon excised a rectal polyp. Snow’s mother didn’t receive information from the hospital regarding Snow’s diagnosis or treatment due to the language barrier. Snow was symptom-free for eight months but she had to return to the clinic on several occasions with the same symptoms. She was finally given a diagnosis of juvenile polyposis - marked by frequent recurrence of polyps in the colon and rectum with third degree internal hemorrhoids. $1500 will cover the cost of Snow's surgery to remove the additional polyps she now has. Although she is still going to school, Snow is unable to engage in active play and her appetite and sleep patterns have been disturbed. She likes to play with her dog and she enjoys singing and listening to music. "I would like to be a singer when I am older," Snow said. Let's help make it possible!

Fully funded

"I am unhappy that I have right ear pain, and it is difficult to communicate with other people," shares Sao, a 39-year-old wife and mother. She works as a cook and cares for her parents in her home in Cambodia. “For two years, Sao has experienced discharge from her right ear every day as well as hearing loss,” our medical partner, Children’s Surgical Centre (CSC), tells us. “She has been treated with antibiotics at another hospital, but her condition did not improve.” Doctors at CSC have discovered a cholesteatoma—an abnormal skin growth located behind the eardrum—in Sao’s right ear. A cholesteatoma initially develops as a cyst after chronic ear infections or perforation of the eardrum. Over time, the cyst sheds layers of old skin that collect within the ear. Without treatment, a cholesteatoma can grow large enough to cause hearing loss, dizziness, or facial paralysis. Treatment for Sao is a mastoidectomy, a surgical procedure in which doctors remove the diseased cells in the hollow, air-filled spaces in the skull behind the ears. The cells—known as mastoid air cells—are diseased as a result of the chronic ear infections that spread to the skull structures near Sao’s right ear. Doctors will also remove the cholesteatoma that has grown behind her right eardrum. $809 pays for surgery for Sao as well as two hearing tests, one night in the hospital, one day of inpatient post-operative care, and three outpatient follow-up visits in the month following surgery. “Sao’s ear discharge and pain will stop after the surgery,” says CSC. Sao’s uncle, who accompanied her to the appointment at CSC, looks forward to a successful procedure for his niece. "I hope after the operation is done, Sao's ear discharge will stop, and she can have good hearing and health,” he shares.

Fully funded

Mayda, a 10-year-old girl from Guatemala, is the fourth of seven children. "Mayda's father works as a farm hand, harvesting coffee on their neighbor's plantation," our medical partner, Wuqu’ Kawoq (WK), tells us. “Mayda’s mother cooks, cleans, takes care of the children, and helps harvest coffee.” Two years ago, Mayda underwent successful surgery for a heart murmur, which was funded by Watsi. Recently, she was also diagnosed with epilepsy. Mayda was doing well until last December. "She came home one day from school with a note from the school nurse saying that she had a seizure that lasted several minutes,” WK explains. “She had lost consciousness and did not remember anything. Since then she has had two more seizures at home." Because of these seizures and the resulting symptoms, Mayda has been unable to attend school. With $967, Mayda can receive the medical care and anticonvulsant medications that she requires for a healthier life. She will receive a brain MRI and other diagnostic workup for preliminary testing. She will also receive anti-epileptic medication to control her spastic episodes and to improve her mobility and independence. With treatment, “Mayda will gain control of her body,” WK continues. “This will increase her quality of life and put her on track to receive the education she deserves and live a healthy and productive life.” "We want her to grow well and be healthy,” Mayda’s parents share. “She has already been through so much with her surgery and now her seizures. We just want her to get better."

Fully funded

Joshua is an eight-month-old baby boy who lives with his parents and older brother in Guatemala. His older brother loves playing with Joshua whenever he can. Our medical partner, Wuqu’ Kawoq (WK), tells us, “Joshua was born with Noonan syndrome, which is a congenital disorder that can lead to a plethora of physical and mental defects, including various heart murmurs, restrictive lung function, gastrointestinal issues and difficulty feeding, motor delays, learning disabilities, cryptorchidism, bleeding disorders, severe joint and skeletal pain, and neurological defects.” “Joshua has obvious physical deformations and cryptorchidism (an undescended testicle), but overall, he is a happy, calm child,” WK continues. “He currently has issues eating and could benefit from supplementation, as well as from physical therapies to help his muscular development.” Joshua’s father works as a grain trader to support the family, while his mother tends to the household. Joshua’s brother has a condition that required surgery by specialist, leaving very little money to pay for Joshua’s care. For $1,385, Joshua can undergo a thorough diagnostic work-up, which, WK explains, will “identify other potentially dangerous conditions Joshua may have, and allow us to coordinate critical care before it is too late.” Funding also covers the cost of treatment, therapy, and a case manager to help Joshua’s family manage his appointments and monitor his progress. “Therapy will help him to develop strength and be able to move more easily,” says WK. “This will increase his quality of life as he grows and ensure he can have the best future possible.” “We just want what is best for our boys,” shares Joshua’s father.

Fully funded