Kantideep joined Watsi on February 22nd, 2014. Four years ago, Kantideep became the 1909th member to automatically support a new Watsi patient every month. Since then, 4,563 more people have become monthly donors! Kantideep's most recent donation traveled 4,800 miles to support Johnson, a baby boy from Tanzania, to fund spina bifida treatment.
Kantideep has funded healthcare for 43 patients in 11 countries.
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.”
Navin is a 9-year-old student from Cambodia. His parents are farmers, and he has three brothers and one sister. He is in the third grade at school and his favorite subject is math. He likes going on walks with his parents, reading science books, and watching TV. He wants to be a police officer when he grows up. When he was four-years-old, Navin received a poorly administered injection, causing a flexion contracture of his right knee. He is unable to fully straighten his knee. When Navin learned about our medical partner, Children's Surgical Centre, he and his family traveled for three hours seeking treatment. On August 5th, surgeons at CSC will perform a quadricepsplasty procedure of his right leg so that he will able to straighten his knee easily and walk without trouble. Now, Navin needs help to fund this $430 procedure. Navin's father shared, "I will be glad to see my son walk easily and grow up strong so that he can be a policeman like he wants."
Nay Kaw is an 11-year-old student from Burma. He lives with his parents, two older brothers and two younger sisters. He is currently in first grade since he left monkhood last year. His father is a farmer and his mother is a homemaker who looks after his youngest sister at home, the other sister is also a student like Nay Kaw. Nay Kaw, along with his two brothers, help with household chores and in his free time, he likes to play cane ball and hunt. Since birth, Nay Kaw has a had a mass on his right wrist. When he turned three years old, the mass increased in size but was still not painful. But by the time he was ten years old, the mass increased in size again, and became swollen and painful. His mother took him to a traditional healer but the medicine he received did not help. Fortunately our medical partner, Burma Children Medical Fund, can help. He is now scheduled to undergo mass removal surgery on July 9th. This surgery will relieve him of his pain and discomfort. He needs your help to cover the $1,500 cost of his procedure and care. Nay Kaw shared, “I would like to be a teacher because I would like to teach children like my friends who are not able to go to school to study.”
Pheap is an eight-year-old primary school student from Cambodia. His parents are farmers, and he is the oldest of three siblings. He practices reading everyday so that he can do well in school, but he doesn't yet know what he wants to be when he grows up. He loves to eat fried noodles at lunchtime. When he was four years old, he got a fever and was treated at a private clinic. The doctors there determined he had bone tuberculosis and performed an osteotomy to remove part of his left femur. His left leg is now shorter than his right. Pheap has trouble will physical activities such as running or bike riding, feeling pain and weakness in his left leg. His condition also affects his self confidence when interacting with other children. Fortunately, surgeons at our medical partner, Children's Surgical Centre, can help. On June 3rd, Pheap will undergo a procedure on his left leg, which will cost $465. After recovering, his leg will experience less pain and will be prepared for lengthening. Pheap said, "I hope that my leg will be less painful after surgery, and I hope that soon I will be able to run normally."
Gift is 6-month-old baby from Kenya. We met Gift at Watsi's Partner Care Center with her mother Silvia. She was sleepy and looked tired after traveling for over 6 hours from their home just to get a doctor's check-up. She is youngest in their family of two kids. Her mother is a housewife, while her father is a farmer and a casual laborer in construction sites. Gift has clubfoot of both feet. She has been on casting since birth and tenotomy was done when she was two months old however the deformity has never corrected. Clubfoot is a condition in which the foot is twisted out of shape. This causes difficulty walking and even wearing shoes as she grows up. Fortunately, Gift traveled to visit our medical partner's care center, AIC Cure International Hospital. There, surgeons will perform clubfoot repair surgery on May 11th. Our medical partner, African Mission Healthcare Foundation, is requesting $1,224 to fund Gift's clubfoot repair. After treatment, the bones will realign so that her feet can face in the right direction and she will be able to put on shoes and walk uprightly when she is older. “My joy would be to see my daughter walking well like other children and I would request you to help my daughter undergo surgery,” Gift’s mother told us.
Cyrus is a businessman from Kenya and the father of four children. He sells second-hand clothes to make a living. His wife takes up small jobs to complement his income. He was involved in a road accident as a pillion passenger while rushing home to avoid trouble with the police during the current COVID-19 curfew in the country. While riding a motorcycle, they lost control as they were trying to avoid hitting a pedestrian. He suffered a closed femur fracture and was rushed to the hospital. He is in pain and cannot walk. Fortunately, surgeons at our medical partner can help. On April 7th, Cyrus will undergo a fracture repair procedure, called an open reduction and internal fixation. This procedure will help him walk easily again. Now, our medical partner, African Mission Healthcare Foundation, is requesting $1,451 to fund this procedure. Cyrus says, “I am in great pain and worried of the financial cost required. Kindly help me. I look forward to continue providing for my children.”
Lazaru was diagnosed with an anorectal malformation a day after birth. This is a condition where Lazaru was born without an anal opening. While changing his diapers, his mother noticed that Lazaru had not passed stool since he was born. His abdomen was distended and he was quite irritable. A closer look confirmed that their son lacked an anal opening. This was unheard of and discreetly, his parents rushed him to the nearest hospital. Lazaru was further referred and a colostomy put in place when he was three days old. A second surgery would be needed later on to create an anal opening. The funds they had were exhausted and thus could not afford to pay for the subsequent surgery. A previous Watsi beneficiary from their village advised them to visit BethanyKids Hospital where they could get assistance. With hopes high, they set out. The creation of an anal opening is needed without which, Lazaru risks scarring at the colostomy site due to occasional leakages and infection. Lazaru lives with his parents and elder brother in a one-room traditional house in the Rift Valley region of Kenya. His parents are subsistence farmers and own a few goats. His family was also advised to apply for national health insurance to support future needs, which they did not know was possible. They are appealing for help towards their son’s surgical care. “A friend told us that we would get help from here and we are happy even for the warm reception,” says Lazaru’s mother.
Jane works as a house help in western Kenya and has struggled with her hearing for the past 5 years. The hearing loss started when she had Quinine medication administered. The gradual hearing loss has affected her social lifestyle and most of the time she misses out on conversations. Jane has not been to any hospital previously. She was referred to our facility where an audiometry test was done and hearing loss diagnosis made. Her small income of $30 per month is all she earns to care for her late sister’s children. Jane requires $929 for the hearing aids. She appeals for financial assistance. Jane says, “My hope is to be able to socially converse with people without having to ask them to repeat what they said."
Ezra is a four-year-old from Tanzania who is the first born to a family of three children. His parents are small scale farmers who depend on what they harvest for their daily living. Ezra has clubfoot of both feet. Clubfoot is a condition in which the foot is twisted out of shape. This causes difficulty walking and even wearing shoes. Fortunately, Ezra traveled to visit our medical partner's care center, Arusha Lutheran Medical Centre. There, surgeons will perform clubfoot repair surgery on January 7th. Our medical partner, African Mission Healthcare Foundation, is requesting $890 to fund Ezra's clubfoot repair. After treatment, he will be able to walk easily. Ezra’s mother says, “We had no idea that our son’s condition was treatable but through education and seeing other children who had similar condition getting treatment, this has given us hope but our biggest challenge now is that we can’t afford the treatment cost please help us.”
Myat is a two-month-old boy who lives with his family in Hpa-An Town, Karen State, Burma. His father passed away when his mother was two months pregnant with him. Myat’s mother is a homemaker and she takes care of him at home. All of his sister and brothers are students. Myat’s grandfather drives a tricycle taxi. On 6 June 2019, Myat was born without any complications at HGH. Since he was born, his mother noticed that he has been passing white coloured stools, but she did not do anything about it because she thought it was normal. When he was just over a month old, his mother noticed that Myat’s navel was bigger than normal. His mother then took him to HGH. The doctor examined his navel and told his mother not to worry too much and he also told her come back if it becomes bigger. A few days later, Myat’s mother noticed that his navel has become bigger and his mother took him to the hospital again. The doctor again took a look at Myat’s navel and advised his mother to take him to a hospital in Yangon for treatment. However, Myat’s mother did not have money to go to Yangon. On 6 September 2019 Myat received an X-ray at Mae Sot Hospital (MSH) and was given a diagnosis of a bulging navel and biliary atresia, a childhood disease of the liver in which one or more bile ducts are abnormally narrow, blocked, or absent. Currently, Myat still passes white coloured stools. He also has a bulging navel which never goes away. His mother is very much worried for him, especially that she just learned about his liver disease. Myat’s mother said, “I would like him to be like other children. I feel bad for him but at the same time happy that an organization Burma Children Medical Fund will help him for his treatment.”
Aloyce is a student from Tanzania. He is nineteen years old young man and the last born child in a family of three children. Aloyce only had the chance to study up to class seven. Due to financial challenges, he couldn’t continue with his studies and fulfill his dream of becoming an engineer. He stayed home helping his parents in their small scale farming to make himself productive and support his parents. Eventually a relative came in and offered to take him to Dar es Salaam and teach him welding work so that he could be able to make a living for himself. Aloyce has been diagnosed with hydrocephalus, a condition in which excess cerebrospinal fluid accumulates in the brain and increases intracranial pressure. As a result of his condition, Aloyce has been experiencing seizures and fainting. Without treatment, Aloyce 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 Aloyce that will treat his hydrocephalus. The procedure is scheduled to take place on October 15th and will drain the excess fluid from Aloyce's brain. This will reduce intracranial pressure and greatly improve his quality of life. With proper treatment, Aloyce will hopefully develop into a strong, healthy young boy. Aloyce says, “People look at me differently now due to this condition please help me get this treatment so that I can be able to resume my training and normal life activities again.”
Jean is a mother of two from Haiti. She lives in a small city in southern Haiti with her husband and two young boys. Jean has a cardiac condition called rheumatic mitral regurgitation. One of the four valves in her heart has been severely damaged due to a rheumatic fever she suffered several years ago. Jean will fly to the United States to receive treatment. On September 11th, she will undergo cardiac surgery, during which surgeons will remove her damaged valve and implant an artificial replacement. Another organization, The Heart Hospital Baylor Plano, is contributing $35,000 to pay for surgery. Jean's family also needs help to fund the costs of surgery prep. The $1,500 bill covers labs, medicines, and checkup and followup appointments. It also supports passport obtainment and the social workers from our medical partner, Haiti Cardiac Alliance, who will accompany Jean's family overseas. "I am looking forward to this surgery so that I can play with my children and take care of them."