Ryan P CarneyMONTHLY DONOR
Ryan's Story

Ryan joined Watsi on December 23rd, 2014. Eight years ago, Ryan joined our Universal Fund, supporting life-changing treatments for a new Watsi patient every month. Ryan's most recent donation traveled 8,300 miles to support Hnin, a determined 5-year-old girl from Burma, to fund surgery to regain mobility and walk more easily.

Impact

Ryan has funded healthcare for 98 patients in 13 countries.

All patients funded by Ryan

Nimo is a 3 year old girl, living with her grandmother in Ethiopia. When she was just a few months old, Nimo's parents gave her to her grandmother, as with four other children already at home and Nimo's medical condition, they were unable to take care of Nimo. Nimo's grandmother, who has a small business, was already supporting four other people, so she shared that it is hard for them to survive from day to day. Nimo was born with a congenital malformation, that led to a blockage in her intestines. At first, when Nimo began to show signs of this condition, her family didn't have the funds to take her to the hospital. By the time someone provided funds so that Nimo could get to the hospital, she was weak and underweight from malnourishment. An emergency colostomy was performed, and over time, Nimo gained strength, and is now able to run and play with her friends. However, she still has multiple issues that require medical attention and additional surgery to help her fully heal. Nimo is scheduled to undergo surgery to correct her condition on July 5th, at BethanyKids Myungsung Christian Medical Centre. Our medical partner, African Mission Healthcare, is requesting $1,500 to cover the total cost of Nimo's procedure and care. After her recovery, Nimo will no longer experience bowel dysfunction, or be at risk of developing related health complications in the future. Nimo's grandmother says: “When she heals, I will go to my home and celebrate with my family. ”

$1,500raised
Fully funded

Thay is a one-year-old girl from Burma. She lives with her parents, grandfather, three sisters and a brother in a village. Thay's mother looks after her and her brother at home, her grandfather is retired, and her sisters go to school. Thay's father works as a porter, but has has difficulty finding work for over a month. With the increasing number of internally displaced people settling in their village due to the humanitarian crisis, there are now many individuals competing for the same work. When Thay was around eight months old, her parents noticed that her head was increasing in size. As a result, Thay cannot yet sit up or crawl. She is only able to turn her head, and will cry if she cannot see her parents. Thay was recently diagnosed with hydrocephalus, which has causes fluid to build up in her brain. Without immediate surgery to alleviate the intracranial pressure, Thay is at risk of developing severe, potentially fatal medical complications. Our medical partner, Burma Children Medical Fund, is requesting $1,500 to fund the insertion of a ventriculoperitoneal shunt for Thay, which will drain the fluid that has accumulated in her brain. The procedure is scheduled to take place on May 20th and, once completed, will greatly improve Thay's quality of life as she grows up. Thay's father said, "I am thankful to every organisation and everyone for supporting my daughter’s treatment cost. Because of you, I believe that my daughter will receive surgery and be healthy and live a normal life after treatment."

$1,500raised
Fully funded

Gatguon is an 8-week-old baby girl from a remote area of South Sudan. The civil war in South Sudan has made it difficult for many to access healthcare and treatment, including Gatguon's family. Gatguon was born with swelling in the back of her head. Upon referral to Old Fangak Clinic, the doctor diagnosed Gatguon with spina bifida, a type of neural tube defect in which the spine does not properly close around the spinal cord. Without treatment, Gatguon is at risk of lower-limb paralysis, infection of the exposed nervous tissue, development of tethered cord syndrome, and possible developmental delays. Gatguon urgently needs spina bifida repair surgery to correct the condition and reduce risk of infection. Unfortunately, this treatment is not available for her in South Sudan. Dr Jill Seaman and her team at Old Fangak Clinic facilitated Gatguon’s travel to Kenya – a long and difficult journey for a sick baby. Now, doctors at our medical partner's care center in Kenya will perform the surgery she needs. Gatguon’s parents have two kids. Her mother is a stay-at-home mom and her father is a vegetable farmer. They are hopeful that baby Gatguon will be treated and that they will continue taking care of her and loving her unconditionally. Our medical partner, African Mission Healthcare, is helping Gatguon's family raise $1,151 to cover the cost of spina bifida closure surgery. The procedure is scheduled to take place on April 20th and will hopefully spare Gatguon of further complications and allow her to grow and develop along a healthy trajectory. Gatguon’s mother shared, “We hope that our child will be treated.”

$1,151raised
Fully funded