Aditi's Story

Aditi joined Watsi on November 1st, 2017. Six years ago, Aditi joined our Universal Fund, supporting life-changing treatments for a new Watsi patient every month. Aditi's most recent donation traveled 4,500 miles to support Hassan, a five-month-old infant from Kenya, to fund spina bifida surgery.


Aditi has funded healthcare for 82 patients in 9 countries.

Patients funded by Aditi

Hassan is an only child whose parents separated before he was born. Prior to his birth, Hassan's mother worked alongside his grandmother, doing farm work to earn income. After Hassan was born, his mother had to stop working so she could take care of him. Hassan was diagnosed with spina bifida at birth, a condition that occurs when a developing baby's spinal cord fails to develop or close properly while in the womb. Hassan had a swelling on his back that was open and leaking. He was admitted in hospital for a few days while his mother was taught how to dress the wound. An MRI and a CT scan were done and he was scheduled for surgery weeks later. While home, his mother continued with the wound dressings as instructed until the leaking stopped. During one of the post-natal clinics, Hassan and his mother were referred to our medical partner's care center, BethanyKids, for treatment. Upon arrival at BethanyKids, Hassan was examined and was additionally diagnosed with hydrocephalus, a build up of fluids in the brain. He was then scheduled for a spina bifida repair surgery, and the mother was told that once he recovered, he would be scheduled for a shunt insertion surgery. Due to financial challenges and a loss of income for Hassan's mother, the family is unable to meet the medical expenses. Without treatment, Hassan is at risk of lower-limb paralysis, infection of the exposed nervous tissue, development of tethered cord syndrome, and possible developmental delays. Fortunately, our medical partner, African Mission Healthcare, is helping Hassan receive treatment. On March 15th, surgeons at BethanyKids will conduct a spina bifida closure surgery to promote Hassan's healthy growth and development. Now, Hassan's family needs help to fund this $1,151 procedure. Hassan’s mother says, “A while back, I had already given up on Hassan's treatment. Because the community had never seen such a condition, I was told that I would always get children who have different medical conditions. After coming to this facility, I realized that this was not the case. My hopes were raised again and now I’m looking forward to the best outcome in Hassan’s treatment.”

$596to go

Elizabeth, who is seven months old, lives with her parents and two older brothers in a small house in Haiti, that they share with other relatives. Both of her parents are farmers. Elizabeth has a cardiac condition called atrioventricular septal defect. A large hole exists in the center of her heart, which affects all four of the heart's chambers. Blood leaks through this hole without passing through her lungs to obtain oxygen, leaving Elizabeth weak and unable to gain weight. Elizabeth will fly to the Dominican Republic to receive treatment. As she is too small and weak to undergo major surgery to completely correct her condition, on April 9th she will have a procedure, during which the doctors at Hospital CEDIMAT will implant a shunt, that will allow oxygenated blood to circulate through her body. This will stabilize Elizabeth's condition so that she can continue to grow and gain weight until she can more safely undergo a complete repair in several years. While another organization is contributing money to pay for Elizabeth's surgery, our medical partner, International Cardiac Alliance, is seeking your help to fund the $1,500 needed to cover the costs of Elizabeth's pre and post-operative care and for the documents and travel costs for Elizabeth, her family, and the social workers that will accompany the family. Elizabeth's mother said: "Our daughter's heart condition has been very stressful for our family, and we are very thankful to know that there may be a way to solve it!"

$101to go

Amare is a brave, social young boy who is smart and good at communicating. He hails from Ethiopia and loves to play with his friends. He shared that he loves innovating new things - like making a tuk tuk and a mobile toy with metal wire and wood. Amare loves to study and read books. He also loves to help his mom at home with cleaning and making stew and coffee. Amare is the third child of his parents. His mom lost ten children, both in her womb and after they were born. She was heartbroken when she conceived Amare as she thought that he wouldn’t grow up. When Amare's mother gave birth to him, she was traveling by foot to a marketplace and she gave birth on the road. She shared that she saw he had a wound and was scared that he would die. She took him to Sekota hospital. The doctor told her that the disease was curable by surgery and that he would live with care. He referred them to another hospital and she brought Amare there when he was a seven month-old baby. She was informed that he was too young for the complex procedure. She brought him again when he was two years-old. She got the same response, to come back when he is older. Then, Amare's mother lost hope in modern medicine. She told us that she started to go to church and apply holy water to her baby. But his condition stayed with him. She got sad and, in her words, "left it all to God". Both mom and dad are traditional farmers. They harvest once in a year because they get rain only in one season. They couldn’t use irrigation since there was no river near their field. They travel for thirty minutes to get underground spring water for drinking and cooking. They have one cow for their milk consumption. For these reasons, they can’t afford the medical bills for their son. Amare was born with a congenital anomaly called bladder exstrophy. That is an abnormally open bladder from the front. His bladder is open to the air, which results in leaking urine directly to his abdomen. He has suffered from pain from the irritation of the bladder, infection & smell from the continuous urinary leakage. Mom is very much worried and concerned because of his condition. His required treatment is called a mainz pouch procedure which is diverting his urination to another opening & making a pouch bladder from bowel. His surgery is scheduled for March 7th. His family needs help raising the $1,500 to fund the surgery. Amare said, “My friends from school and the neighborhood say I smell. I felt bad about it and tried to stay away from my friends. I like playing with my friends but nowadays what I prefer is to study at home alone. Or to be with my mother and help her with work.” Amare's mom said, “My neighbors talk, so when there is holiday party at home I let him stay at the outside kitchen. If there is clean cloth, he [can] change and mingle in the party but mostly he stays away. Amare said to me ‘If I couldn’t get treatment and heal while you are alive I will never heal and survive.' Because I don’t have any hope with my siblings and relatives. This hurt me a lot. I feel like I don’t have power to heal him or to provide him medical treatment."

Fully funded

Recheal is a 20-year-old from Kenya. She is studying in secondary school but has been unable to attend school for the last three months due to her condition. Recheal is the sixth born in a family of eleven children. Her parents are small-scale farmers, growing maize and beans for their family’s home use. Recheal does not have medical coverage, and her parents had to sell cattle and maize to raise Ksh 120,000.00 ($783) to cover her initial surgery costs. Recheal needs to undergo urgent surgery, and her family is requesting financial assistance. Recheal has been diagnosed with an abdominal bile leak that is causing her discomfort and pain. Her doctors have recommended surgery to ease the pain and enable her to resume her studies. She first experienced painful stomach swelling in August 2023. She visited a local health center and was treated for worms, which relieved her of pain for a while, but it recurred with time. She then visited our medical partner’s hospital for review. At the beginning of November, she received a CT scan that showed a liver cyst that required surgery. She underwent a laparotomy to remove the cyst on November 23rd. Four days later, the doctors identified a bile leakage that needed to be rectified. She is now scheduled for emergency surgery on November 28th to fix the fatal condition. African Mission Healthcare (AMH) is requesting $1,074 to fund this surgery. Recheal said, “I have missed school for three months now. This procedure will help ease stomach pain and enable me to return to school.”

Fully funded

Simwenda is a three-year-old boy from Tanzania. He resides in a village in the Mpanda district. His parents, hardworking farmers, work daily to provide for their family’s subsistence needs. Simwenda was born with a clubfoot - a birth abnormality in which the foot is twisted out of shape or position. The tissues connecting the muscles to the bone (tendons) are shorter than usual, causing the foot to twist and making walking and wearing shoes difficult. Simwenda’s parents, with limited resources and no access to medical insurance, could only watch their son’s condition worsen for three years. It broke their hearts to see him suffer. The nearest hospital could not provide the treatment he needed. Simwenda’s parents shared their son’s story with their community, hoping for help and learned that services would be available at the Plaster House, a care center of our medical partner, African Mission Healthcare (AMH). However, Simwenda's parents encountered a significant obstacle in obtaining care: transportation costs. Their village is hundreds of miles from Arusha, where the medical care center is located. Simwenda’s family organized a fundraising event to raise money for the transportation and additional expenses of the journey. Upon Simwenda’s arrival at the center, he received a warm welcome. The medical team will begin clubfoot treatment on September 15. AMH is requesting $935 to fund Simwenda's clubfoot repair. After treatment, he will be able to walk with less struggle. Simwende’s mother says: “Despite our financial situations, we have tried so hard to get him treatment. I hope this time around our son has a chance to get treatment.”

Fully funded

Abnet, a precious 9-month-old baby girl from Ethiopia, has captured our hearts with her beauty and spirit. She is the only child of her young 20-year-old parents. Her father works alongside his own father as a coffee farmer, while her mother lovingly tends to their home. Despite not having had the opportunity for formal education, they pour their efforts into providing for their family through the limited farming they do, though it yields barely enough to sustain them. From the very beginning, Abnet's parents demonstrated their determination to seek medical care for their daughter, even in the face of financial challenges. Abnet was born with a congenital anorectal malformation, a condition that disrupts bowel function due to a partial or complete blockage of the intestines. In order to alleviate her suffering and restore her health, she must undergo a series of intricate procedures. Their family initially went to a government hospital, where they were referred to another medical facility. Sadly, their hopes were dashed as they were asked to return two years later. Recognizing the worsening state of Abnet's health, they reached out to a local social worker, sharing their child's condition. Fortunately, the social worker was able to introduce them to our medical partner, African Mission Healthcare (AMH). Abnet underwent a thorough evaluation leading to a recommendation for the necessary surgery. Abnet is now scheduled for surgery on August 15th. AMH is requesting $1500 to help fund her procedure. Following her successful recovery, Abnet will be a healthy little girl, able to resume normal activities. Abnet's mother shared, "When we first learned of our daughter's condition, a sense of worry and helplessness engulfed us. The path forward seemed uncertain and daunting. Despite the challenges we faced, we relentlessly pursued treatment for our beloved child. Though previous avenues turned us away, the administrative office introduced us to this lifeline of support. We embraced it with hope, and it has brought us to this moment, filled with gratitude and anticipation."

Fully funded