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, 4,010 more people have become monthly donors! Kantideep's most recent donation traveled 4,500 miles to support Gift, a baby from Kenya, to fund mobility-restoring clubfoot treatment.
Kantideep has funded healthcare for 39 patients in 11 countries.
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."
Mary struggles with ambulation due to a spinal complication she is having. This has been the struggle for the past 12 months and continues to strain her daily life. Mary complained of fatigue and back pain in October of 2018 and sought treatment in a nearby hospital and was given no conclusive diagnosis. She was then referred to a more advanced facility and came to Kijabe. Mary had MRI and X-ray imaging done and was diagnosed with TB of the spine. Her surgeon recommended spinal decompression and fusion surgery to correct the condition. If not treated, Mary will continue experiencing much pain and ambulation struggles. Mary is a mother of 4 children and together, they live in her parent's house. Mary used to sell second-hand clothes but stopped in October when she could not bear the persistent fatigue and pain. Currently, her needs and those of her children are met by her relatives. She is not able to raise the full amount required for surgery.
Zawadi is a baby from Tanzania. For seven months, Zawadi has been experiencing difficulty breathing and swallowing. Zawadi was recently diagnosed with enlarged tonsils, which, if not treated, will cause her symptoms to persist and possibly intensify over time. Our medical partner, African Mission Healthcare Foundation, is requesting $633 to fund a tonsillectomy for Zawadi, which is scheduled to take place on July 18. Surgeons will remove her tonsils, hopefully relieving Zawadi of her symptoms and helping her live more comfortably. Zawadi’s mother says, “We didn’t know our daughter’s problem was treatable we happy to hear she could be treated and be ok, but the cost is too high for us to afford please help us.”
Wycliff is a student from Kenya. He has clubfoot of his right foot. Clubfoot is a condition in which the foot is twisted out of shape. This causes difficulty walking and even wearing shoes. Fortunately, Wycliff traveled to visit our medical partner's care center, AIC Cure International Hospital. There, surgeons will perform clubfoot repair surgery on June 28. Our medical partner, African Mission Healthcare Foundation, is requesting $1,224 to fund Wycliff's clubfoot repair. After treatment, he will be able to walk easily.
Kibet is a baby from Kenya. His parents are farmers, relying on seasonal rains for their maize plantation. Kibet 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, Kibet has been experiencing a rapid increase in head circumference. Without treatment, Kibet will experience severe physical and developmental delays. Our medical partner, African Mission Healthcare Foundation, is requesting $685 to cover the cost of surgery for Kibet that will treat his hydrocephalus. The procedure is scheduled to take place on August 9 and will drain the excess fluid from Kibet's brain. This will reduce intracranial pressure and greatly improve his quality of life. With proper treatment, Kibet will hopefully develop into a strong, healthy young boy. Kibet’s mother says, “My hope is to have my son treated. He is my only child and would wish to see him lead a normal life."