Tabreez VerjeeMONTHLY DONOR
Tabreez's Story

Tabreez joined Watsi on April 10th, 2015. Seven years ago, Tabreez joined our Universal Fund, supporting life-changing treatments for a new Watsi patient every month. Tabreez's most recent donation traveled 8,800 miles to support Nan, a farmer from Cambodia, to fund fracture repair.

Impact

Tabreez has funded healthcare for 24 patients in 11 countries.

All patients funded by Tabreez

Elvis, an 18-year-old boy from Guatemala, started to get seizures when he was eight years old. Now he gets about one seizure every week, and they are often severe--he has had to be hospitalized following many of his seizures. He has not been able to study because of his mother's fear of him having a seizure during class, and also because his mother cannot afford to pay for both his treatment and his education, forcing her to choose to pay for his medications. Elvis is the youngest of three children. He was raised by a single mother who is incredibly hard working and strong, and who wakes up at dawn every morning to wash the neighbors' clothes, helping her to earn a few dollars per day. Elvis and his mother have tried to seek out treatment in Guatemala City, but since they live in a rural, mountainous community that is far away from the city, they have not been able to afford to continue traveling several hours for each appointment, and have run out of money to pay for medications. Elvis loves to sing along to Christian ballads on the radio, and his faith has helped him stay strong through his health problems. For $967, treatment will be possible for Elvis. This treatment will give him access to the medications he needs to get his seizures under control. He will undergo comprehensive diagnostic work to determine the cause of his seizures and see if he has any other related conditions. His mother will not have to live in fear of her son having a seizure, and she will no longer have to choose between sending him to school and paying for treatment. This will give Elvis the chance to be a normal teenager, go back to school, and his mother will be able to feel secure that his condition is more stable. "I want my son to stop suffering. Every time he has a seizure he suffers, and I suffer with him. I want him to study and become a great professional," shares Elvis's mother.

$967raised
Fully funded

Sela is an eight-month-old baby girl from Cambodia. Sela is living with syndactyly--she has webbed fingers and an extra digit on her left hand. Due to these abnormalities, it has been very difficult for Stela to use her hand. Thus, she and her mother traveled three hours to seek the help of our medical partner, Children’s Surgical Centre (CSC). Under normal conditions, the webbing dissolves, leaving five independent digits on every extremity. With syndactyly, on the other hand, the degradation of the tissue between fingers or toes is left incomplete during gestation and, in a few cases, like Sela’s, the webbing also covers an extra digit wedged in between. This specific situation, known as “polysyndactyly,” is a very rare occurrence, but when treated early in life it does not present lasting complications. However, if left unaddressed, Sela will lose significant functionality in her left hand. For $321, Sela will undergo a syndactyly repair, which will include a release to separate her fingers and a procedure to remove her extra digit. She will have also receive a skin graft to help heal her remaining digits. The funds will also cover supplies, inpatient care for ten days, and follow up visits for up to one year after the procedure. Because of the skin graft, this operation can be slightly more complicated than other surgeries, but CSC’s medical team says that the benefits of surgery (releasing Sela’s digits and allowing her to live a comfortable life) outweigh the minor risks. Sela’s parents are grateful and eager to have her surgery done. “I hope my daughter will have a normal hand like other people after surgery,” shares Sela’s mother.

$321raised
Fully funded