Serdar Yildirim
Serdar's Story

Serdar joined Watsi on April 28th, 2015. 15 other people also joined Watsi on that day! Serdar's most recent donation traveled 8,500 miles to support Precious, a baby from Kenya, to fund hernia surgery.

Impact

Serdar has funded healthcare for 25 patients in 9 countries.

Patients funded by Serdar

Tin was born via normal delivery at Mae Tao Clinic (MTC) in Thailand on July 16th, 2016. After her birth, doctors discovered that she has a large teratoma—a benign tumor that contains cells that can grow hair, teeth, or nails—protruding from her groin. The teratoma is about half the baby’s body size. Baby Tin is able to urinate and pass waste, but her breathing is labored, and her heartbeat has lowered slightly because her body is under the strain of having to pump blood and oxygen in and out of the large teratoma. Since two months before Tin's birth, her mother has been living at Social Action for Women (SAW), an organization in Mae Sot, Thailand, that helps women in need. When she arrived at SAW, she traveled to MTC with a medic who works at the clinic because she thought she had a mass in her abdomen. There, she learned that she was seven months pregnant. She did not know that Tin had a large growth on her body until she was born. Tin will need surgery to remove the teratoma so that she can grow and develop normally. Unfortunately, Tin's mother has no income and no family support. She receives a small stipend from SAW to cover minor expenses, and she sleeps and eats for free at SAW’s safe house. MTC referred Tin to Burma Children Medical Fund (BCMF) for surgical care. $1500 pays for surgery to remove the teratoma from Tin's body as well as transportation to and from the hospital, pre- and post-surgical consults, and 40 days of hospital care, including lab tests, imaging, medicine, and food for Tin and her mother. Let's help fund surgery for Baby Tin!

$1,500raised
Fully funded

Walter, who is 10 years old, has been having seizures his whole life. He has also undergone a stroke and severe developmental delays that is likely due to an infection that he had as an infant. His body wastes several hundred calories each day having seizures, which are now much more under control than before, and this problem is complicated by the fact that his parents can't afford to give him the high-calorie and high-protein foods that he needs. Walter lives with his parents and older sister, who is his primary caregiver since his parents both work. His father works half day as a school janitor, and the other half of the day as a day laborer harvesting corn and squash. His mother works as a weaver, making traditional textiles to sell to help cover Walterr's medical costs. Even though they both want the best for their son, they lack the resources to give him the high-calorie food supplements and micronutrients he needs in order to gain weight and overcome his acute malnutrition. The few foods his parents can buy for him are hard for him to chew and swallow, making it impossible for him to gain weight. He has fallen into acute malnutrition, and his body is weak. He is at greater risk of getting sick, and diarrhea, respiratory illness and fevers can be life threatening for him in his weakened state. Growth monitoring, micronutrients and food supplementation will help Walter recover from malnutrition--saving his life now and putting him on track to live a better life in the future. He will gain weight, his immune system will grow stronger with the increased caloric intake, preventing him from having any life-threatening situations with diarrhea and fevers. This will further increase his appetite and help him use the extra calories to develop mentally instead of those calories being wasted on getting over frequent illnesses. His parents will receive the support they need to feel empowered to give Walter the diet he needs to grow and develop healthily. Intervention now will prevent the future devastating effects of malnutrition, and give Walter the chance to live a healthy and productive life, finish school, get a good job, and escape the cycle of malnutrition and poverty that made him sick in the first place. His sister shares, "I want for my brother to gain weight. I don't want for my brother to suffer."

$512raised
Fully funded

Meet Olivia, a 15-month-old girl from Guatemala who has recently been diagnosed with acute malnutrition. "Olivia's height and weight are over two standard deviations below normal, meaning she is not getting the food she needs to grow," our medical partner, Wuqu Kawoq' (WK), reports. "Her immune system has also been weakened by her poor diet." Acute malnutrition is characterized by the lack of proper nutrients, proteins, and calories needed to grow. It weakens the immune system and often causes diarrhea, coughs, and fevers. If not treated, Olivia will have an increased risk of developing chronic disease later in life and could experience developmental delays. "Treating her now will have a large impact," WK details. "She will likely be able to reach developmental milestones just like healthy kids her age, setting her up for a successful life instead of one filled with malnutrition and poverty." Olivia's father works as a farmer, and is unable to afford the treatment that his daughter needs because of the volatile seasonality of his income. The treatment will cost $512 and will allow Olivia to receive growth monitoring, micronutrients, deworming medication, and food supplementation. Olivia's parents will also receive nutrition lessons to teach them what, when, and how to feed her a proper diet that will help her grow up healthy. Olivia loves to play with her older sister and her mother is excited for her to receive treatment. "I would like for my daughter to be healthy, and to not get sick anymore," she shares.

$512raised
Fully funded

At 19 months old, Kanakate is an active little girl who loves talking, running, and taking walks with her parents near their home in Ethiopia. “Kanakate was born with a birth defect called anorectal malformation,” our medical partner, African Mission Healthcare Foundation (AMHF), tells us. “Children with this defect have an imperforate anus, or they have no opening where the anus should have been. As a result, Kanakate cannot pass stool in the normal way.” Treatment for an anorectal malformation typically involves three surgical procedures. In the first procedure—a colostomy—doctors pull an end of the colon through a cut in the abdominal wall and suture it in place to create an opening for passing stool. This is followed by an anorectoplasty to create an anal opening and then, two or three months later, a colostomy closure. Kanakate underwent an emergency colostomy after she developed a bowel obstruction. Currently, “Kanakate has multiple issues with her colostomy care and associated complications from the colostomy,” explains AMHF. Because of these issues, the next steps in her care—anorectoplasty and colostomy closure—are more urgent. Kanakate’s parents, who work as farmers, have been unable to afford the care that she needs. “We have no money to cover our child's hospital bill. And that is really worrying us,” shares her father. In addition, the social stigma associated with Kanakate’s condition has been challenging for the family. $1,500 covers the costs of the final two surgical procedures and inpatient care, including labs, imaging, pain medicine, and antibiotics. After surgery, “Kanakate will be able to pass stool in a normal way,” says AMHF. “We hope that our daughter will get treatment and be well after all these months of waiting for treatment,” says Kanakate’s father.

$1,500raised
Fully funded