Mehryar joined Watsi on September 19th, 2016. Six years ago, Mehryar joined our Universal Fund, supporting life-changing treatments for a new Watsi patient every month. Mehryar's most recent donation supported Loveness, a future doctor from Tanzania, to find clubfoot treatment so she can walk easily and go after her dreams.
Mehryar has funded healthcare for 80 patients in 11 countries.
Mehryar has funded healthcare for 80 patients in 11 countries.
Loveness is a charming, friendly and smart girl who is currently in the 8th grade. She is a charismatic girl who makes friends easily. Loveness wishes to be a doctor in the future, and she is already working hard towards fulfilling her dreams. Her best subjects are mathematics, science, biology, and physics. She says English as a subject is giving her a hard time, but she is determined to keep improving. She enjoys drawing and painting in her spare time. Loveness lost her mother when she was just two years old. After her mother passed away, her aunt on her mother’s side decided to take Loveness and raise her as her own daughter because, she shared, the father had a hard time managing by himself. Loveness has clubfoot of her right foot. Clubfoot is a condition in which the foot is twisted out of shape. This causes difficulty walking and even wearing shoes. Fortunately, Loveness traveled to visit our medical partner's care center, Arusha Lutheran Medical Centre. There, surgeons will perform clubfoot repair surgery on June 7th. Our medical partner, African Mission Healthcare Foundation, is requesting $935 to fund Loveness's clubfoot repair. After treatment, she will be able to walk easily. Loveness says, “I wish I could have my foot treated so that I can walk normally.”
Isaac is a 12-year-old student and the eldest in a family of two children. Isaac's mom shared that she is raising her children on her own after their father left when her youngest was diagnosed with rickets. Isaac’s mother does laundry for neighbors to be able to provide for the family. Last year, Isaac started having stomach pain. Issac's mother took him to a nearby hospital, where he was examined and diagnosed with ulcers. Issac's mother then brought him to our medical center's care center, Bethany Kids Hospital where Issac was diagnosed with cryptorchidism. If left untreated, Isaac has an increased risk of developing hernias, testicular cancer, and fertility problems. Fortunately, he is scheduled to undergo corrective surgery on May 11th. Our medical partner African Mission Healthcare is requesting $646 to cover the total cost of his procedure and care. Isaac’s mother shared, “I am very worried for my son now that I know what will happen if the surgery is not done. I’m praying and hoping that God will make it happen.”
Philip is a charming, friendly, and talkative three-year-old boy, and the youngest child in a family of six children. Philip's family has experienced financial challenges, and they are supported by their church. Philip does not attend school yet, but some of his siblings have their education are sponsored and are doing well in school. Philip has been diagnosed with bilateral genu valgus, a condition in which the knees angle inward and touch one another when the legs are straightened. The condition is typically caused by an excessive accumulation of fluoride in the bones, which often stems from contaminated drinking water. As a result, he has difficulty walking. Fortunately, our medical partner, African Mission Healthcare (AMH), is helping Philip receive medical treatment. On April 8th, he will undergo corrective surgery at AMH's care center. Treatment will hopefully restore Philip's mobility, allowing him to attend school, participate in a variety of activities, and greatly decreasing his risk of future complications. Philip’s mother shared, "please help my son, he is struggling to walk."
Aljahnie is a four-year-old boy from the Philippines. He loves to play with toy cars, to sing nursery rhymes, and to listen to songs. His mother is a stay-at-home mom, and his father is a jeepney driver. Despite working hard, they are unable to finance his medical needs. Aljahnie was born with an anorectal malformation, a congenital abnormality that leads to a complete or partial intestinal blockage. He needs to undergo a series of procedures to eliminate bowel dysfunction. Aljahnie is scheduled to undergo surgery to correct his condition on March 17th. Our medical partner, World Surgical Foundation Philippines, is requesting $1,279 to cover the total cost of Aljahnie's procedure and care. After his recovery, Aljahnie will no longer experience bowel dysfunction or be at risk of developing health complications in the future. "By the grace of God, and extra caution, we hope that his condition will be much better after this treatment. We are very grateful to World Surgical Foundation and WATSI for helping us," shared Aljahnie’s mother.
Makara is a 14-year-old seventh grade student. He is the youngest in his family, and has two brothers and four sisters. His parents are rice farmers, and they also raise chickens and cows. In his free time, Makara enjoys playing football with his friends. His favorite meal is kari soup and Coca-Cola. In the future, he wants to be a lawyer. When he was three years old, Makara was burned by a fire on his right hand. Burn scar contractures have developed on his index, middle, and ring fingers, tightening the skin near the burns. He has limited use of the fingers on his right hand. When Makara's family learned about our medical partner, Children's Surgical Centre (CSC), he traveled for six and a half hours seeking treatment. On February 11th, surgeons at CSC will perform a burn contracture release surgery to help him use his right hand easily again. Now, he needs help to fund this $477 procedure. Makara shared, "I really hope my hand heals and I can use it normally."
Ray is a 2-year-old boy who lives with his four brothers and parents in a refugee camp. His siblings go to school and his mother weaves traditional Karen skirts for sale at their home. Unfortunately, his father has been unable to leave the refugee camp to search for work since August 2021, due to local COVID-19 restrictions. When Ray was eight months old, his mother noticed a worrying swelling. She brought him to the hospital in the refugee camp, where a medic examined Ray and advised his mother to come back if it increased in size. In July 2021, his parents brought him back to the hospital for a medical examination and he was referred to Mae Sariang Hospital for further treatment. With the help of the organization Malteser International (MI) staff, Ray and his mother were brought to the hospital, where a doctor examined Ray and diagnosed him with an inguinal hernia. Ray has little appetite and cries frequently, and the pain he feels often causes him to wake up during sleep. After completing a physical examination, the doctor scheduled him to be admitted to the hospital on January 12th so he can receive hernia repair surgery the following day. As Ray’s family cannot afford to pay for surgery, MI staff referred him to our medical partner, Burma Children Medical Fund, for assistance accessing treatment. This procedure will cost $1,486, and Ray and his family need help raising money. Ray's mother shared, “I will send Ray to school when he is older and I want him to become a doctor because I want my son to help the community and other families."
Ngasungui is a five-month-old baby girl and the youngest child in a family of five children. Her parents have five cows and five goats, and they make a living selling milk to their neighbors. Ngasungui was born with 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. A visiting doctor referred Ngasungai's parents to our medical partner's care center for treatment. Fortunately, Ngasunguii and her parents traveled to visit our medical partner's care center, Arusha Lutheran Medical Centre. On December 17th, surgeons there will perform clubfoot repair surgery. Now, our medical partner, African Mission Healthcare (AMH), is requesting $935 to fund Ngasungui's procedure and care. After treatment, she will be able to walk easily and her self esteem will not be affected by her condition. Ngasungui’s mother shared, "I pray that my child gets this treatment and everything goes well. I want her to live and grow without disability."
Razack is a 1-year-old baby boy and the first child in his small growing family. He's a very charming and friendly little boy. Razack's parents are subsistence farmers who farm maize, sunflower,s and beans. They are not able to afford the medical treatment that Razack needs. Razack has clubfoot of his left foot. Clubfoot is a condition in which the foot is twisted out of shape. This causes difficulty walking and even wearing shoes. Fortunately, Razack traveled to visit our medical partner's care center, Arusha Lutheran Medical Centre. There, surgeons will perform clubfoot repair surgery on November 18th. Our medical partner, African Mission Healthcare Foundation, is requesting $935 to fund Razack's clubfoot repair. After treatment, he will be able to walk easily. Razack’s mother says, “Please help my son get this treatment so he can be able to walk properly. He tries to walk but you can see the difficulty as he is walking.”
Emmanuel is young boy from Kenya. He is shy, but a very active boy. Emmanuel's father ploughs at his neighbor's homes and sometimes does construction work to earn a living for their family. His mother does laundry and house chores to help provide for their family too. They do not earn a lot of money, and haven't been able to raise money to afford Emmanuel’s surgery. Emmanuel has been diagnosed with a condition called cryptorchidism. If left untreated, Emmanuel has an increased risk of developing hernias, testicular cancer, and fertility problems in the future. Emmanuel will be receiving assistance from our medical partner, African Mission Healthcare (AMH). Fortunately, he is scheduled to undergo corrective surgery on October 14th. AMH is requesting $646 to cover the total cost of his procedure and care. Emmanuel’s father says, “As a family, it will be a great joy for us when Emmanuel is treated.”
Leakhen is a bright and hardworking 12-year-old girl. She and her brother live with their parents, who are rainy day farmers, in Takeo province in Cambodia. Leakhen enjoys playing with her brother, reading books, and doing homework. When she grows up, Leakhen would like to be a teacher. Leakhen was born with congenital scoliosis. Congenital scoliosis is the presence of an abnormal curvature of the spine. The curvature causes the spinal column to bend left or right. Leakhen is not able to stand up straight or expand her lungs, which causes her frequent fatigue and chronic pain. Because of the stress that scoliosis places on the vital organs of adolescents and their ability to grow, active treatment is required. If not corrected, she could experience progressive weakness, numbness, or a loss of coordination. Leakhen is embarrassed to go places because of her condition. She has had two previous surgical procedures, and surgeons have determined that she needs a revision of her spinal rod to help her heal. Leakhen and her family traveled to our medical partner’s care center to receive treatment. On September 17th, she will undergo a revision of her spinal rod. During this procedure, surgeons will implant and expand a rod to allow her to continue to grow normally. Our medical partner, Children’s Surgical Centre, is requesting $1,500 to fund this procedure. This covers medications, supplies, and inpatient care. This support will help her feel confident and be active like other children her age. Leakhen said, "I hope that my spine will look better and I can play with other children."
Lemayan is a young three year old boy and the last born child to his mother of five. His father has two wives and a total of seven children in their family. Lemayan's parents are livestock keepers who depend on the sale of milk for their livelihood and once in a while, they are able to sell cattle, however their income is limited. Lemayan was diagnosed with Bilateral Varus. He is having difficulty walking and has pain when he stands or walks for a short distance. His mother noticed the condition when he learned to stand and walk. It began as a slight curve, but over the years the curve has increased significantly. His condition is typically caused by an excessive accumulation of fluoride in the bones, which often stems from contaminated drinking water. As a result, it has led to Lemayan not wanting to stand or walk by himself, thus forcing the mother to carry him on her back most of the time. Through a visit of doctors to their village, his parents learned that he could get treated at Watsi's medical partner's care center. Lemayan's parents cannot afford the treatment cost and are asking for help. Our medical partner, African Mission Healthcare, is requesting $880 to fund corrective surgery for Lemayan. The procedure is scheduled to take place on August 19th. Treatment will hopefully restore Lemayan's mobility, allow him to participate in all kinds of activities, and greatly decrease his risk of future complications. Lemayan's mother says, “It was a slight curve back then when he learnt to stand but over the years the curve has increased significantly and now he is scared of walking. Please help.”
Bright is a very charming, friendly, and playful 2-year-old boy. He's his mother's only child. Bright's mother works at a shop as salesperson while his father owns a small liquor shop. The two parents live separately and his mother is single, though his father does try to provide for his son when he is able. Bright was diagnosed with genu varus, a condition typically caused by an excessive accumulation of fluoride in the bones, which often stems from contaminated drinking water. As a result, Bright's legs bow outward so that his knees do not touch. He has having difficulty walking and experiences pain when he walks for a short distance. Our medical partner, African Mission Healthcare (AMH), is requesting $880 to fund corrective surgery for Bright. The procedure is scheduled to take place on July 15th. Treatment will hopefully restore Bright's mobility, allow him to participate in a variety of activities, and greatly decrease his risk of future complications. Bright’s mother shares, "My son falls down when walking and needs to be supported most of the time, his age mates are running about but not my son, please help."