Savinay NangaliaMONTHLY DONOR
Savinay's Story

Savinay joined Watsi on September 19th, 2016. Six years ago, Savinay joined our Universal Fund, supporting life-changing treatments for a new Watsi patient every month. Savinay's most recent donation supported Thu Zar, a 21-year-old woman from Thailand, to fund surgery to remove a large tumor.

Impact

Savinay has funded healthcare for 58 patients in 11 countries.

All patients funded by Savinay

Thu Zar is a 21-year-old woman who lives with her parents, three sisters, and three nieces in Mae Sot near the Thailand-Burma border. Her family moved from Shan State in Burma to Thailand in 2008 in search of better opportunities. She used to work at a logistics company until two weeks ago when she quit due to her condition. Her parents run a small shop from their home, and her oldest sister is a cleaner at a restaurant. One of her other sister’s is unemployed and her third sister as well as her three nieces all go to school. In 2015, Thu Zar felt a small mobile mass in her chest. She did not feel any pain at the time and forgot about the mass. In 2019, she attended a workshop about reproductive health at her school, run by Mae Tao Clinic (MTC). During the workshop she remembered the mass and later when she was alone, she checked to see if it was still there. She felt the mass and thought that it had increased in size, but she did not experience any pain. The next day, she told the workshop trainer about the mass. The trainer told her to go to MTC for treatment. However, Thu Zar decided she did not want to take time off from school to go to the clinic, since she thought the mass was not causing her any pain or discomfort. Now, Thu Zar's condition has worsened and causes her great pain. She can only sleep on her back, because if she sleeps in any other position she experiences immense pain. Thu Zar sought treatment through our medical partner, Burma Children Medical Fund. She is now scheduled to undergo mass removal surgery on June 9th to heal her condition. She is raising $1,500 to cover the total cost of her procedure and care. Thu Zar is very worried about her health and told us, "I feel very sad and depressed with this condition."

64%funded
$973raised
$527to go

Pascalina is a beautiful five-year-old girl. She's is the second-born in a family of three children, and is always notably friendly to those around her. Both of Pascalina's parents are small scale farmers, while her father also seeks out casual laboring jobs to further help earn a living. Pascalina was born as a healthy child, however when she reached one and a half her parents became concerned. At that age they had expected her to be able to stand up and walk, yet she could not. Pascalina was diagnosed with bilateral genu valgus. This is a condition typically caused by an excessive accumulation of fluoride in the bones, which often stems from contaminated drinking water. As a result, Pascalina couldn't stand or walk, as her legs were too weak. Her parents tried seeking treatment for her and used medication, but nothing seemed to help. By the time Pascalina had turned three, despite her feeble ability to stand and walk for a short distances at a time, her parents began to notice that her legs were bent inward forming knocking knees. Last year they visited a local hospital in their village seeking treatment, however were then advised to go to a referral hospital that her parents could not afford. A year later, having not received any treatment, Pascalina’s legs had become so impacted that she was unable to walk or stand without crying due to the pain she felt. A local priest advised her parents to seek care at The Plaster House, in Arusha, Tanzania. There, through internal funding, Pascalina was able to have surgery on both legs to help correct them. However, given the severity of her condition, the first surgery was not enough to fully correct her legs. As a result, she needs another surgery to complete her treatment and her parents are asking for help to fund her care. Our medical partner, African Mission Healthcare, is requesting $880 for corrective surgery for Pascalina. The procedure is scheduled to take place on February 11th. With treatment, Pascalina's mobility will hopefully be restored, which will allow her to walk without pain, and play with her siblings and friends like normal. Her risk of having future complications will decrease as well. Pascalina's mother says, "We could not afford treatment for a long time, but since the first surgery, she has improved. We wish to see her continue improving and be like any other normal child."

$880raised
Fully funded

Leakhen is a bright and hardworking 12-year-old girl. She and her brother live with their parents, who are rainy day farmers, in Takeo province in Cambodia. Leakhen enjoys playing with her brother, reading books, and doing homework. When she grows up, Leakhen would like to be a teacher. Leakhen was born with congenital scoliosis. Congenital scoliosis is the presence of an abnormal curvature of the spine. The curvature causes the spinal column to bend left or right. Leakhen is not able to stand up straight or expand her lungs, which causes her frequent fatigue and chronic pain. Because of the stress that scoliosis places on the vital organs of adolescents and their ability to grow, active treatment is required. If not corrected, she could experience progressive weakness, numbness, or a loss of coordination. Leakhen is embarrassed to go places because of her condition. She has had two previous surgical procedures, and surgeons have determined that she needs a revision of her spinal rod to help her heal. Leakhen and her family traveled to our medical partner’s care center to receive treatment. On September 17th, she will undergo a revision of her spinal rod. During this procedure, surgeons will implant and expand a rod to allow her to continue to grow normally. Our medical partner, Children’s Surgical Centre, is requesting $1,500 to fund this procedure. This covers medications, supplies, and inpatient care. This support will help her feel confident and be active like other children her age. Leakhen said, "I hope that my spine will look better and I can play with other children."

$1,500raised
Fully funded

Lemayan is a young three year old boy and the last born child to his mother of five. His father has two wives and a total of seven children in their family. Lemayan's parents are livestock keepers who depend on the sale of milk for their livelihood and once in a while, they are able to sell cattle, however their income is limited. Lemayan was diagnosed with Bilateral Varus. He is having difficulty walking and has pain when he stands or walks for a short distance. His mother noticed the condition when he learned to stand and walk. It began as a slight curve, but over the years the curve has increased significantly. His condition is typically caused by an excessive accumulation of fluoride in the bones, which often stems from contaminated drinking water. As a result, it has led to Lemayan not wanting to stand or walk by himself, thus forcing the mother to carry him on her back most of the time. Through a visit of doctors to their village, his parents learned that he could get treated at Watsi's medical partner's care center. Lemayan's parents cannot afford the treatment cost and are asking for help. Our medical partner, African Mission Healthcare, is requesting $880 to fund corrective surgery for Lemayan. The procedure is scheduled to take place on August 19th. Treatment will hopefully restore Lemayan's mobility, allow him to participate in all kinds of activities, and greatly decrease his risk of future complications. Lemayan's mother says, “It was a slight curve back then when he learnt to stand but over the years the curve has increased significantly and now he is scared of walking. Please help.”

$880raised
Fully funded