Matthew has funded healthcare for 69 patients in 11 countries.
Kheav is an 85-year old traditional Khmer healer from Cambodia. She enjoys listening to the monks pray on the radio and spending time with her family. One year ago, Kheav developed a cataract in her left eye, causing her blurry vision. She has difficulty seeing things clearly, recognizing faces, and going anywhere outside. When Kheav learned about our medical partner, Children's Surgical Centre, she traveled for one and a half hours seeking treatment. Doctors will perform a small incision cataract surgery and an intraocular lens implant in her left eye. After recovery, she will be able to see clearly. Now, she needs help to fund this $211 procedure. Kheav shared, "I hope that I will be able to see clearly so I can recognize my relatives' faces and can go outside easily again."
Megan is a 3-month old baby girl from Tanzania, and the only child to her single mother. Megan was born with clubfoot and spina bifida, which contributed to her acquiring hydrocephalus. Megan’s father left their family when her mother was five months pregnant and they lost any contact with him. Megan's grandmother, who was also a single mom after her husband passed away at a young age, depends on selling second-hand clothes. Her income is very limited to be able to provide for her children and be able to afford school fees. Due to this, Megan's mother was not able to continue with her studies due to financial challenges and joined her mother in selling second hand clothes. Megan has been diagnosed with hydrocephalus, a condition in which excess cerebrospinal fluid accumulates in the brain and increases intracranial pressure. As a result of her condition, Megan has been experiencing an increasing head circumference. Without treatment, Megan will experience severe physical and developmental delays. Our medical partner, African Mission Healthcare Foundation, is requesting $1,300 to cover the cost of surgery for Megan that will treat her hydrocephalus. The procedure is scheduled to take place on September 21st and will drain the excess fluid from Megan's brain. This will reduce intracranial pressure and greatly improve her quality of life. With proper treatment, Megan will hopefully develop into a strong, healthy young girl. Megan’s mother says, “I have no one to run to for help and support, all my relatives have told me they can no longer support us in any way and yet my daughter is suffering. Please help save my daughter.”
Elizabeth is a young student from Kenya. She is a class 6 pupil and enjoys reading and playing with her friends. Elizabeth is the youngest in a family of four. Her mother is a single parent and supports the family through farming. Elizabeth 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, Elizabeth traveled to visit our medical partner's care center, AIC Cure International Hospital. There, surgeons will perform clubfoot repair surgery on August 18. Our medical partner, African Mission Healthcare Foundation, is requesting $1,286 to fund Elizabeth's clubfoot repair. After treatment, she will be able to walk well and wear shoes to school. “My prayer is that Elizabeth will one day walk well like other girls and continue with her normal life. Please help her walk comfortably,” Elizabeth's mother shared with us.
Edwin is a fifteen year old boy from Kenya. He was brought by his mother to a medical camp organized by our partner hospital, Cure International. He is in the eighth grade and very bright. His mother is a housewife while the father is a mason. Edwin was born with a condition known as hemiplegia, a weakness that results from damage to the part of the brain that controls muscle movements. This damage may occur before, during or shortly after birth. Therefore, the entire left side of his body is weak and he cannot see with his left eye. He is currently not able to walk and he keeps falling. The condition is worsening and lowering his self-esteem which is affecting his schoolwork. He is an aspiring engineer but is worried that the condition will hinder him from achieving his goals. Fortunately, our medical partner, African Mission Healthcare, can help. They are now requesting your help to fund this $1,224 surgery that will repair a congenital foot deformity. “My prayer is for my son to receive help, undergo the surgery, and continue with his life like other children. I would love to see him healthy and able to pursue his dream. I would greatly appreciate any kind of help,” Edwin’s mother shared.
Esther is a small-scale farmer who has two children and also takes care of her sister's four children because her sister unfortunately passed away. She is now the sole provider of six children and pays for their school fees all by herself. They live together in a 2 bedroom house. Esther started to experience abdominal pain 3 years ago. Due to the severity of the pain, she recently visited our medical partner's care facility. She will undergo surgery for her acute appendicitis. Now, our medical partner, African Mission Healthcare, is requesting $646 to cover the cost of Esther's curative laparatomy. This surgery will hopefully relieve her pain and enable her to live life more comfortably and confidently. "I would really appreciate treatment because I am the sole breadwinner for my family," shared Esther.
The world welcomed a new baby boy, he has not yet been named, so goes by baby of Hawa Hassan. He is a first-born child to his mother who moved to Arusha, Tanzania four years ago looking for work. She was able to find work locally and has been earning income as a housemaid for two years now. Baby of Hawa was born in the hospital and was directly referred to Watsi's Medical Partner Care Center ALMC when the doctors noticed he had a birth defect. At ALMC Hospital, he was admitted to the NICU and his mother was informed that her baby needed surgery as soon as possible to correct this birth defect. His mother could not afford surgery for her son for she does not earn enough to be able to afford the treatment. His father is a shop keeper and he is also not able to afford his son’s needed surgery, they had just enough savings for their baby’s birth costs. This surgery will enable Hawa's baby to be able to pass stool normally, if not treated this condition will cause discomfort for the baby as he cannot pass stool, and he may stop feeding properly. If not treated, his condition may even result in death. Hawa shared, “Please help my son get this treatment so that he can continue to feed well, I am worried about him. He looks very sick and discomforted.”
Lay is a 45-year-old man from Burma. He lives with his family in a village in Karen State. His wife is a homemaker while his son and daughter-in-law work as a day laborers. He also used to work as a day laborer before he stopped two months ago due to his loss of vision in his left eye. He has blurred vision and sometimes he also feels dizzy. When the doctor checked his left eye, he was diagnosed with a cataract as well as glaucoma. Our medical partner, Burma Children Medical Fund, is requesting $1,500 to fund lens replacement surgery for Lay. On March 17th, doctors will perform a lens replacement, during which they will remove Lay's natural lens and replace with an intraocular lens implant in his eye. After recovery, he will be able to see clearly. Now, he needs help to fund this $1,500 procedure. Lay said, "Now I am happy that I will receive surgery with the help of donors. Thank you everyone for helping me and I pray for you all with all my heart. I know this surgery will return my vision and will be a great benefit for my family if it will allow me to go back to work.”
Nisriya is a young beautiful and playful girl from Ethiopia. Nisriya is the second-born girl in a family of three girls. She comes from a peasant family where her father is the sole breadwinner of the family. He is a casual labourer who relies on daily wages to make ends meet. Her mother is a housewife who delivered her third child in September 2019. Nisriya 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. She had a colostomy done but it is currently giving her multiple issues. She faces stigma from society forcing her parents to hide her from the public realm. If not treated, she will be at risk of infections in the colostomy area and continue suffering discrimination. After her recovery, Nisriya will no longer experience bowel dysfunction or be at risk of developing health complications in the future. Nisriya is scheduled to undergo surgery to correct her condition on November 14th. Our medical partner, African Mission Healthcare Foundation, is requesting $1,500 to cover the total cost of Nisriya's procedure and care. Her dad said, “It is my hope that my child will get successful surgery and I hope when she heal completely she will go to school. And I hope I will get her a good school working hard since she loves education."
Nuriya is a cute child from Ethiopia. Nuriya's mother was in Saudi Arabia for four years doing domestic work and her employers did not pay her during this time. She asked for her salary several times but they refused to pay her. Finally she decided to go home and they send her home without her payment. Nuriya’s father was also immigrant in Saudi Arabia for eight years. He went to Saudi Arabia illegally by sea and was caught and deported back to Ethiopia several times but he kept using his savings to go back. Once Nuriya’s parents were back in Ethiopia, they decided to stay and start a family. Their families have decided to help them and accommodate them until they find work. Nuriya’s father has not found work and now he plans to buy oxen and start farming. Nuriya 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. Nuriya is scheduled to undergo surgery to correct his condition on October 07. Our medical partner, African Mission Healthcare Foundation, is requesting $1,500 to cover the total cost of Nuriya's procedure and care. After his recovery, Nuriya will no longer experience bowel dysfunction or be at risk of developing health complications in the future. Nuriya’s mother said “We can’t afford the medical bill. We are here through the support of another organization. We are living under the support of our relatives. Nuriya’s colostomy operation was done by the government. I believe the child will get better soon."
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.
Peter is a young student from Kenya. For three years, Peter has had an inguinal hernia. This condition causes him pain and discomfort. Fortunately, on August 7, he will undergo repair surgery at our medical partner's care center. Our medical partner, African Mission Healthcare Foundation, is requesting $423 to fund Peter's surgery. Once completed, this procedure will hopefully allow him to live more comfortably. “I want to be an engineer when I grow up," says Peter.
Meki is a child from Kenya. Since birth, Meki has been experiencing difficulty breathing. Frequent illness has caused his parents to worry and spend their little earnings on medication. He was recently diagnosed with enlarged tonsils and adenoids, which are the soft tissue behind the nasal cavity. Without treatment, this condition will cause Meki's symptoms to persist and possibly even intensify. Our medical partner, African Mission Healthcare Foundation, is requesting $779 to fund an adenotonsillectomy for Meki, which is scheduled to take place on July 9. Surgeons will remove his tonsils and adenoids, hopefully relieving Meki of his symptoms and helping him live more comfortably. Meki’s mother says, “My hope is to have my son treated and being able to breathe. Please help me."