Deepthi KulkarniUNIVERSAL FUND MEMBER
Deepthi's Story

Deepthi joined Watsi on September 24th, 2016. Seven years ago, Deepthi joined our Universal Fund, supporting life-changing treatments for a new Watsi patient every month. Deepthi's most recent donation supported Robert, a 7-year-old boy from Kenya, to fund spinal surgery.

Impact

Deepthi has funded healthcare for 80 patients in 10 countries.

Patients funded by Deepthi

Hapyness is a charming 9-month-old girl, born to hardworking farmers in the remote village of Igot, in the Ulanga district of Tanzania. Her family's daily life revolves around the cultivation of maize and millet, which not only sustains their meals, but also provides a modest income for the family’s necessities. Unfortunately, her father, who is advancing in age, cannot work extended hours, so her mother toils diligently on the farm, to ensure they yield bountiful harvests. Hapyness was born with a clubfoot, a condition in which the foot is abnormally twisted, making it difficult for her to crawl and eventuall to walk. At the time of her birth, the nurse in attendance recommended immediate medical attention. However, locating such specialized care in their isolated village proved to be impossible. After months of searching, Hapyness' father crossed paths with a young boy who had had a clubfoot which had been successfully treated, and he was able to provide Hapyness' father with the information he had been seeking. As a result of this meeting, Hapyness' parents brought her to the Plaster House, where her treatment will begin on October 6th. Our medical partner, African Mission Healthcare Foundation, is requesting $935 to fund Hapyness' clubfoot repair. After treatment, she will be able to crawl and to walk comfortably as she grows. Hapyness’s mother says: “I am glad there is a chance for my daughter to get treatment. I hope she doesn't have to live with this disability for the rest of her life.”

$935raised
Fully funded

John is a 2-month-old baby from Tanzania. He resides in a modest home with his parents and two siblings. His mother is a devoted stay-at-home mother, while his father works as a carpenter. His father’s income is enough to cover the family’s basic needs. After John's birth, the doctors realized he was born with a congenital condition and advised his mother to seek specialized care. His right foot was twisted inward and downward. They started him on casting at the hospital for three weeks, hoping it might help him heal. However, it became apparent that his condition was more complex and would require surgical intervention as the only viable option to give John a chance at a more mobile and fulfilling life. However, the financial burden proved to be overwhelming for John’s family. Living on a modest income, they could not afford the surgical treatment cost. They had to make a hard decision to stop their son’s treatment. Sometime after discontinuing their son’s treatment, John’s mother learned about our medical partner the Plaster House and the services it provides. Fueled by love and hope for her son, she sought assistance from the center. John underwent a comprehensive wellness assessment; however, the family cannot raise money for his treatment and is appealing for financial assistance. John has clubfoot on his right foot. Clubfoot is a condition in which the foot is twisted out of shape. This causes difficulty walking and even wearing shoes. The Plaster House team will begin clubfoot treatment on September 19. Our medical partner, African Mission Healthcare, is requesting $935 to fund John's clubfoot repair. After treatment and as he grows he will be able to walk comfortably, wear shoes, enjoy playtime with his peers, and reassure his parents that their son is free from disability. John’s mother says: “I hope my son’s treatment will be smooth and he will turn out okay after his treatment.”

$935raised
Fully funded

Six-year-old Tay lives with her mother, sister, and brother in a village in Shan State in Burma. Tay's mother is a teacher. When Tay was three years old, she was frequently ill with a rapid heartbeat and fingertips that would turn blue. Her mother brought her to a nearby hospital, where the doctor told them that Tay had congenital heart disease and would need to be treated in Yangon. However, due to the Covid-19 pandemic, Tay's mother did not feel it was safe to take Tay to Yangon. When she turned five, Tay's symptoms worsened, and her mother brought her to a hospital in Yangon in August 2022. At the hospital, Tay was diagnosed with an atrial septal defect, and her mother was told that Tay would require surgery- which the family could not afford to pay for. Fortunately, Tay's aunt referred her to our medical partner, Burma Children Medical Fund, for help. Now Tay is scheduled to undergo atrial septal defect closure at Pun Hlaing Hospital on May 13th. As Tay is becoming progressively more ill- with episodes of rapid breathing and weight loss due to a lack of appetite- this procedure is critical for her health and well-being. Burma Children Medical Fund is seeking $1,500 to cover the cost of Tay's care. “When I learned that my daughter [Tay] needs surgery, I felt very sad and I cried because I cannot afford to pay for her surgery. But when I learned that the organization [BCMF] will support the cost of my daughter’s surgery, I felt very happy and thankful to all the donors and that organization. I want to see her healthy,” said Tay's mother.

$1,500raised
Fully funded