Akhil joined Watsi on June 29th, 2015. 22 other people also joined Watsi on that day! Akhil's most recent donation supported Milka, a 48-year-old mother from Kenya, to fund a mastectomy to prevent her cancer from spreading.
Akhil has funded healthcare for 48 patients in 10 countries.
Akhil has funded healthcare for 48 patients in 10 countries.
Milka is a 48-year-old woman. She is the mother of three children, between 6 and 26 years. She works harvesting tea at a tea plantation, while her husband gets jobs working at construction sites. Their income is not enough to pay for life-saving surgery, and they do not have medical coverage. Milka woke up one morning at the beginning of February this past year and discovered a lump in her right breast. It was painless at first, but later became painful. She went to a clinic in her local area, but was referred to a bigger facility that offers cancer care. She came to Kijabe Hospital this month where she had an ultrasound, mammogram, and a core biopsy that revealed cancer. Milka has been diagnosed with breast cancer. Without treatment, the cancer may spread to other organs. Doctors recommend a mastectomy, a surgery to remove breast tissue, to rid her body of breast cancer and to prevent the cancer from metastasizing, or spreading. Our medical partner, African Mission Healthcare Foundation, is requesting $1110 to cover the cost of a mastectomy for Milka. The procedure is scheduled to take place on November 8th. After treatment, Milka will hopefully return to a cancer-free life. Milka says, "I might be scared that I am losing my breast, but I know it is important to stop the cancer.”
Shellden is a sweet two-year-old and the youngest-born child in her family. Her family lives in an informal settlement in Kenya's capital city of Nairobi. Shellden's mother is a homemaker, while her father is a laborer working in construction sites. Last year, Shellden's mother noticed a sudden bowing of her legs when she started to stand and take her first steps to walk. Her mother took her to a local hospital, where she has continued with follow-up visits over the past year. However, since there has been no improvement so far, her mother was referred to the care center at our medical partner, African Mission Healthcare (AMH), for the treatment Shellden needs to heal. On February 28th, Shellden will undergo corrective surgery that will allow her to walk without difficulty and be able to easily attend school once she is old enough. AMH is requesting $1,224 to fund Shellden's procedure. Shellden's mother shared, "At the moment, we don’t have work and are unable to pay for national insurance because of our current economic status. Any support will be highly appreciated."
Gideon is four years old and the last-born in his family of six children. He is a playful, charming, friendly, and happy boy. Gideon comes from the southern highlands of Tanzania close to Katavi National Park. Gideon has not yet started school, but his father says when he gets to be six years old, he will enroll him. Most children in this region join school starting at the age of six due to the long distance they must walk to school. Parents must wait for their children to grow strong enough to walk to and from school before enrolling them. Gideon’s parents are small-scale farmers of maize, beans, and vegetables and only sell a few of their harvests to get money to buy other basics for their family. Gideon has been diagnosed with bilateral genu valgus, where his legs bow inward so that they touch. This condition is typically caused by an excessive accumulation of fluoride in the bones, which often stems from contaminated drinking water. As a result, he experiences pain and discomfort. Our medical partner, African Mission Healthcare, is requesting $880 to fund corrective surgery for Gideon. The procedure is scheduled to take place on January 4th. Treatment will hopefully restore Gideon's mobility, allow him to participate in a variety of activities, including school in the future, and greatly decrease his risk of future complications. Gideon’s father says “My son walks with a gait and falls down a lot. He also complains of pain after a long day of play.”
Srey Nath is a bright young student who loves to read books and wants to be a teacher when she grows up. She has two older brothers and lives with her parents who are rainy day rice farmers. They also grow vegetables and keep cows and chickens to feed their family and make extra money at the local market. Over the past several years, Srey Nath's back has curved which limits her movement and lung expansion. She has trouble standing up straight or walking, and is easily winded when she is active due to difficulty expanding her lungs. She shared that she feels embarrassed with her friends and very shy about how her back looks. She loves school but doesn't want to attend now because of the abnormal curvature of her spine, and the chronic pain it causes. Srey Nath's neighbors told her family to visit our medical partner, Children's Surgical Centre for a diagnosis and treatment. Surgeons have diagnosed her with scoliosis of the thoracic spine. She needs expanding rods in her back to straighten her spine as she grows to avoid any further medical problems. Srey Nath and her parents traveled two and a half hours to seek treatment and need help raising $1,500 for this specialty surgery. Srey Nath's mother said: "My daughter needs this surgery to grow normally and become a teacher. I hope we can raise the money so she can fulfill her dream someday."
Thida is a five-year-old child and her father is a blacksmith while her mother is a seller in the market. One of the things she likes to do when she is not in school is telling jokes to her mother :) For the past year, Thida has had difficulty swallowing. She does not sleep well at night because she cannot breathe well. Her parents are concerned because it is hard for her to concentrate in school when she doesn't sleep well. As a result, Thida often feels poorly and misses school. When Thida's parents learned about our medical partner, Children’s Surgical Centre, she traveled for four hours with her mother hoping for treatment. On March 30th, doctors will perform a tonsillectomy. After recovery, she will be able to breathe better and sleep more restfully at night. Now, Thida needs help to fund this $241 procedure. Thida's mother shared, “I hope after surgery that my daughter can breathe and swallow better than before. She often misses school, and she wants an education."
Sumeya is a baby girl from Ethiopia who loves music. She also loves sweets and playing with her mom. She is her parents' first child, and her mom is a housewife while her dad is a teacher in a mosque. They all live together in his parents’ house, who help support them with their basic needs. Sumeya was born with an anorectal malformation, a congenital abnormality that leads to a complete or partial intestinal blockage. She needs to undergo a series of procedures to eliminate bowel dysfunction. Sumeya is scheduled to undergo surgery to correct her condition on April 20th. Our medical partner, African Mission Healthcare Foundation, is requesting $1,500 to cover the total cost of Sumeya's procedure and care. After her recovery, Sumeya will no longer experience bowel dysfunction or be at risk of developing serious health complications in the future. Her mom said “ It is my hope that my baby will heal and get in to school.”
Patrick has clubfoot of both feet. Clubfoot is a condition in which the foot is twisted out of shape, and it causes difficulty walking and even wearing shoes. After he was born, his parents visited the nearest dispensary in their village to take him for treatment, where he was referred to a bigger hospital that would have more resources to treat him. Because Patrick's parents are small scale farmers with minimal income, they decided to return home and save up money so that they could take him to a proper hospital to have his feet corrected. Through a neighbor, Patrick's parents got to know about Watsi's Partner ALMC Plaster House and decided to come and seek treatment for Patrick. Patrick needs to start manipulation and casting, which will help correct his feet. If Patrick does not get this treatment, his learning-to-walk process will be very challenging. It will take a long time for him to be able to stand and walk, and it may be painful. He will not be able to wear normal shoes like other children, and could potentially experience discrimination due to his disability. Fortunately, Patrick traveled to visit our medical partner's care center, Arusha Lutheran Medical Centre. There, surgeons will perform clubfoot repair surgery and begin his treatment on January 15th. Our medical partner, African Mission Healthcare Foundation, is requesting $935 to fund Patrick's clubfoot repair. After treatment as he grows, he will be able to walk and play with ease. Patrick’s mother shared, "We wish our son to have his feet corrected but the treatment cost is too high for us to afford. Please help our son.”
Anitha is a beautiful six-year-old child from Tanzania. She is the only child to her mother, who is a single parent. Her mother shared that Anitha's father left their family when Anitha was a baby and Anitha herself has never met him. Her mother helps her aunt in a small vegetable garden, where they grow tomatoes and sell them an open market. Whatever they can earn is what they use for their basic needs. Anitha has clubfoot of both her feet. Clubfoot is a condition in which the foot is twisted out of shape. This causes difficulty with walking and even wearing shoes. Fortunately, Anitha traveled to visit our medical partner's care center, Arusha Lutheran Medical Centre. There, surgeons will perform clubfoot repair surgery on January 5th. Our medical partner, African Mission Healthcare Foundation, is requesting $935 to fund Anitha's clubfoot repair. After treatment, she will be able to walk more easily and play with her friends. Anitha’s mother shared, “All I wish for my daughter is to see her walk normally so that she can pursue her studies and have a better life.”
Collins is a young boy from the northeastern slopes of Mt Kenya in Meru County, Kenya. He is 5 years old and is the firstborn in a family of two children. His mother is a housewife, while his father is a mason. Collins was born with clubfoot. Clubfoot is a condition in which the foot is twisted out of shape. Since birth, he has had serial casting treatment, but his condition has yet to improve. Both his mother and his sibling also have neglected clubfoot conditions. Collins has difficulty with walking and wearing shoes, and is unable to play with other kids. In January 2020, he was able to undergo a left posterior medial release (PMR) with Watsi support, and his foot has corrected well. As a result of the surgery, he is able to wear his left shoe and his walking has improved. However, his right foot is still deformed and requires surgery for him to be able to walk comfortably and confidently on both feet. Fortunately, Collins' family traveled back to our medical partner's care center, AIC Cure International Hospital. There, surgeons will perform clubfoot repair surgery on his right foot on January 11th. Our medical partner, African Mission Healthcare Foundation, is requesting $1,286 to fund Collins's clubfoot repair. This surgery will be very impactful for Collins because he will be able to walk, play, and enjoy life like other children. His mother is grateful for the support for his first surgery, and again appeals for support for this procedure as their income level is not high enough to afford his needed care. Collins' mother shared, “I would like to thank CURE Hospital and AMH-Watsi who made possible my son’s first surgery. May the almighty God bless you. I continue to plead for support for the planned surgery on his right foot so that he can fully walk without any difficulty.”
Kelvin is a 13-year-old boy from from Nyeri County in Central Kenya. He is a humble and calm child, and the 4th born in a family of six children. His mother is a farmer, while his father passed on 6 years ago after a long illness. At school, Kelvin is in Class 3 at Karangi Primary School. His teacher says he is a bright boy and performs well in class. Kelvin is actually supposed to be in Class 8 but, because of the condition of his feet, he has not been able to advance in his education as quickly. Kelvin was born with bilateral clubfoot, which was neglected and not treated earlier on. Clubfoot is a condition in which the foot is twisted out of shape, and causes difficulty walking and even wearing shoes. Though he was taken to a hospital in the area to seek treatment, he could not initially undergo surgery due to lack of money. Now, Kelvin faces difficulty as he walks because his feet knock each other and causes him to fall every time. Unfortunately, this has affected his self-esteem when he sees other people playing and he cannot join. In March 2020, Kelvin underwent left triple arthrodesis surgery supported by Watsi donors and the procedure corrected his foot perfectly. Now, he is scheduled to undergo a right triple arthrodesis, a surgery to correct his right foot so he can walk well with both feet. Fortunately, Kelvin traveled back to visit our medical partner's care center, AIC Cure International Hospital. There, surgeons will perform clubfoot repair surgery on him on January 11th. Our medical partner, African Mission Healthcare Foundation, is requesting $1,286 to fund Kelvin's clubfoot repair. This surgery will be very impactful as he will be able to wear both shoes, walk well, and play with friends. Kelvin will also be able to continue with his studies without any hindrances. His mother asks for support for his second surgery. Kelvin's mother shared, “We are grateful to God for the support we received from Cure Hospital through the Watsi donors. I have seen great improvement with my son and am looking forward to seeing him walking like other children. God bless you and continue with the good work you do of helping needy families to have surgery. God bless you."
Simon is a child from Tanzania. He is the second born child to a family of four children. Simon’s parents depend on small scale farming of maize, beans and cassavas for their living. Simon 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, Simon has been experiencing an increasing head circumference and inter-cranial pressure. Without treatment, Simon will experience severe physical and developmental delays. Our medical partner, African Mission Healthcare Foundation, is requesting $728 to cover the cost of surgery for Simon that will treat his hydrocephalus. The procedure is scheduled to take place on September 2nd and will drain the excess fluid from Simon's brain. This will reduce intracranial pressure and greatly improve his quality of life. With proper treatment, Simon will hopefully develop into a strong, healthy young boy. Simon’s mother says, “My son was doing so well after the surgery but now he is going through a lot of pain, he can’t eat well please help my son.”
Mbondo is a nursery school pupil and likes reading and drawing. He also likes playing with other children and sometimes he says that his friends imitate him as he walks. Mbondo hails from Tulimani village in Makueni County. He is an orphan and lives with his grandparents. His mother passed 3 years ago as a result of an accident along Makutano junction Machakos road while his father passed 2 years later after a long illness. Mbondo was born with a condition known as knock knees, the grandmother did not notice the condition at an early stage until recently when he noticed the knees knocking each other and he was limping as he walks. Mbondo's grandparents who are taking care of him are farmers and mostly depend on their children for daily bread cannot afford to pay even a quarter of the estimated bill and thus requested for support.