K

Kantideep Thota

MONTHLY DONOR

United Kingdom   •   Born on February 10

Kantideep's Story

Kantideep joined Watsi on February 22nd, 2014. Five years ago, Kantideep joined our Universal Fund, supporting life-changing treatments for a new Watsi patient every month. Kantideep's most recent donation traveled 4,200 miles to support Turyakira, a 27-year-old nursing student from Uganda, to fund a thyroidectomy.

Impact

Kantideep has funded healthcare for 51 patients in 13 countries.

All patients funded by Kantideep

Myo

Myo is a 16-year-old boy from Burma. He lives with his parents and four brothers in northern Rakhine State. Myo is a student in grade nine and his four brothers also go to school. However, they have been unable to study since the Covid-19 pandemic shut all schools. Myo’s parents are day laborers, and their family's combined income is just enough to cover their daily expenses since Myo and his brothers’ schooling is free. To survive with limited income, they forage for vegetables and fish. If they fall ill, they use traditional medicine, which is more affordable then going to a clinic or a hospital. Myo 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. This valve controls the flow of blood, but certain conditions may cause blood to flow backward or the valve to narrow. Currently, Myo cannot walk long distances or climb stairs because of his tiredness. Sometimes, he cannot breathe very well. Our medical partner, Burma Children Medical Fund, is requesting $1,500 to fund a mitral valve replacement for Myo. The treatment is scheduled to take place on February 7th and, once completed, will hopefully allow him to live more comfortably. Myo shared, “I am worried about my health and I feel sorry for my parents. Because of my health problems, my father had to work more days to earn more money. Also, my mother cannot work because she accompanies me and has to take care of me. I hope my school will reopen soon so that I can go back to school. One day I hope that I can become a teacher. I want to teach because there are not enough teachers in my village.”

95% funded

95%funded
$1,425raised
$75to go
Nay Kaw

Nay Kaw is an 11-year-old boy from Burma. He lives with his parents, two older brothers and two younger sisters in a village in Karen State. Nay Kaw and his sister are both students. He is a grade one student since leaving the monkhood last year. His father is a farmer. Nay Kaw was born with a small mass on his right wrist. Once Nay Kaw's mother was able to save up and send him to Mae Tao Clinic for treatment in Thailand, Nay Kaw had the mass surgically removed in July at Mae Sot Hospital. After surgery, the biopsy revealed that the mass was caused by a hemangioma. As a result of this, the doctor referred him for further treatment in nearby Chiang Mai. Since his surgery, the pain in his wrist has decreased. However, if something touches his right wrist or if he has to carry something heavy in his right hand, he is in a lot of pain. Doctors want Nay Kaw to undergo an MRI, an imaging procedure that uses magnetic fields and radio waves to produce images of bodily organs. This scan will hopefully help doctors diagnose his condition and formulate an appropriate treatment plan. Our medical partner, Burma Children Medical Fund, is requesting $814 to cover the cost of Nay Kaw's MRI and care, scheduled for October 8th. "I want my right hand to be normal and I do not want to have an unusually large wrist," he said. "If the pain in my hand decreases, I will help my mother with the housework. If my hand will be without pain and I will be able to play with my friends at school, I will be happy with my friends again. In the future I will go school and become a good person."

100% funded

$814raised
Fully funded
Johnson

Johnson is an 8-month baby boy from Tanzania. Johnson, the last born child in a family of four, and already is a very active and friendly little boy. Johnson's parents are both subsistence farmers. Johnson was born in a local hospital where his parents were informed that his spine was not fully formed, thus resulting in a condition known as spinal bifida. Because Johnson's condition was not severe, they were informed that he wouldn’t need treatment and that it would close on its own. As their family continued to attend clinics they were told to wait till Johnson gets to five months old for him to have any kind of treatment. At five months they took him to hospital for the treatment but the cost was too high for them to afford and they had to return home. As time went by, Johnson's mother saw that his condition could end up complicated if he didn’t get treatment soon and end up greatly affecting Johnson later in life. She decided to seek treatment. She went to Mt Meru and was referred to Watsi's Medical Partner Care Center ALMC for more help.  Johnson was born with spina bifida, a type of neural tube defect in which the spine does not properly close around the spinal cord. Without treatment, Johnson is at risk of lower-limb paralysis, infection of the exposed nervous tissue, development of tethered cord syndrome, and possible developmental delays. Our medical partner, African Mission Healthcare Foundation, is requesting $1,015 to cover the cost of Johnson's spina bifida closure surgery. The procedure is scheduled to take place on September 7th. This procedure will hopefully spare Johnson from the risks associated with his condition, instead allowing him to grow and develop along a healthy trajectory. Johnson’s mother says, “We are concerned if our son does not get his spine corrected, it might affect his ability to walk. Please help my son.”

100% funded

$1,015raised
Fully funded