V

Vijay Mariadassou

MONTHLY DONOR

Vijay's Story

Vijay joined Watsi on July 29th, 2013. Five years ago, Vijay joined our Universal Fund, supporting life-changing treatments for a new Watsi patient every month. Vijay's most recent donation supported Akankwatsa, a small-scale farmer from Uganda, to fund a hysterectomy.

Impact

Vijay has funded healthcare for 66 patients in 11 countries.

All patients funded by Vijay

Myint

Myint is a 52-year-old father from Burma. He lives with his wife, two sons and daughter. Myint used to work as a construction manager, and his wife is a homemaker. In his free time, Myint likes to search for building design ideas on Facebook and likes to read books. He also enjoys helping a charity group that drives patients to hospitals in an ambulance. Myint was diagnosed with a heart condition that involves a malformation of the mitral valve, which is the valve between the left atrium and left ventricle that controls the flow of blood. Malformations of this sort may cause blood to flow backward, or cause the valve to narrow. Currently, Myint has difficulty breathing and chest pains. He cannot sleep well at night and has to take medication to help him fall asleep. He also feels tired when he talks for a long time. Myint needs a mitral valve replacement surgery to improve his quality of life. Since April 2020, he has been unable to work due to his poor health. When his eldest son's university classes did not resume this year, his son found work as a truck driver to make additional money. However, due to government imposed COVID-19 restrictions, his work ceased around August. Myint's family now lives off of their savings and borrow money when needed. They are appealing for financial help for Myint's health. Our medical partner, Burma Children Medical Fund, is requesting $1,500 to fund a mitral valve replacement for Myint. The treatment is scheduled to take place on October 25th and, once completed, will hopefully allow him to live more comfortably. Myint shared, “After I have recovered fully, I will go back to work. But if I cannot do that same job anymore, I will look for something else that I can do. I will save money for my family’s future. I want my daughter and my sons to successfully complete their studies.”

100% funded

$1,500raised
Fully funded
Catherine

Catherine is a 17-year-old student from Tanzania, the youngest in her family of three children. She is currently in Form Four and hoping to graduate secondary school this year. She is a shy but bright young girl. Catherine’s father is a construction worker and her mother owns a shop at their home where she sells day-to-day household stuff. Catherine has been diagnosed with hydrocephalus, a condition in which excess cerebrospinal fluid accumulates in the brain and increases intracranial pressure. As a result of her condition, Catherine has been experiencing headaches for the past two weeks continuously. She was originally taken to the hospital and was tested for a UTI and malaria but found to have nothing wrong. Her headaches got more severe, followed by vomiting and irritability and could not control her urination. Her family was told to do a CT scan test but the surgeons were not satisfied with the results and needed to do an MRI. The MRI showed that there is build up of CSF fluids causing pressure in her brain and the doctors shared that Catherine needs surgery as soon as possible. Without treatment, Catherine will experience severe physical and developmental delays. Our medical partner, African Mission Healthcare Foundation, is requesting $1,238 to cover the cost of surgery for Catherine to treat her hydrocephalus. The procedure is scheduled to take place on April 29th and will drain the excess fluid from Catherine's brain. This will reduce intracranial pressure and greatly improve her quality of life. With proper treatment, Catherine will hopefully develop into a strong, healthy young girl. Catherine says, “I would really like to get better and continue with school. Please help me get well.”

100% funded

$1,238raised
Fully funded
Philomena

Philomena was diagnosed with ARM at birth. With this condition, the little one was found to lack an anal opening and instead was passing stool through her vagina. A few hours after birth, Philomena, one in a set of twins, was noted to have a distended abdomen. The doctor quickly checked on the baby and discovered she lacked an anal opening. To keep Philomena from getting a fistula, the doctors put in a colostomy at three days. Philomena’s parents paid for this through some family savings they had. When they left for home, Philomena’s twin sister developed a persistent cough which was later found to be a hole in the heart. "I have never felt this drained ever in my life. Since I gave birth I am always in hospitals with either one of my two babies,” says Philomena’s mother. Due to lack of finances, Philomena’s parents shared their plight with their church members and one of them advised that they visit Watsi Partner Care Center BethanyKids Hospital. At BethanyKids a surgery to create an anal opening has been recommended. If not treated, Philomena will not lead a normal life and will be forced to use a colostomy for life. The surgery is a cost Philomena’s parents cannot bear. Philomena’s father is a carpenter while her mother closed her grocery store to tend to the children. Together they have five children with three currently in school. With very limited income and having exhausted their savings, Philomena’s parents are not able to raise the funds needed. They had defaulted on paying the national health insurance premiums as they could not keep up, but they’ve been advised to try to maintain this coverage in the future given their family's health needs. “Please help us. It is quite a stressful time for us but we believe we will come from it as victors,” says Philomena’s mother.

100% funded

$708raised
Fully funded