Malorie joined Watsi on July 21st, 2016. Six years ago, Malorie joined our Universal Fund, supporting life-changing treatments for a new Watsi patient every month. Malorie's most recent donation supported Dar, a 21-day-old baby girl from Burma, to fund a colostomy so she can grow up healthy.
Malorie has funded healthcare for 71 patients in 13 countries.
Malorie has funded healthcare for 71 patients in 13 countries.
Dar is a 21-day-old baby girl who lives with her parents and her brother in a village in the border area of Karen State in Burma. Dar was born at home with the help of a traditional birth attendant. Two days after she was born, Dar's mother noticed a problem when Dar was passing stool. She told Dar’s father to call a medic from the clinic to their home. The medic realized that Dar was born with a anorectal condition and shared with Dar’s mother that baby Dar would urgently need surgery to receive a colostomy. Dar’s parents are subsistence farmers who grow rice and raise chickens. They also forage for vegetables in the jungle and go fishing when they want to eat fish. To purchase staples that they cannot produce such as salt and oil, Dar’s father works as an agricultural day labourer during the rainy season. However, since the rainy season has not yet begun, they currently have no income. However, their daily needs are fulfilled from living off the land. If they are sick and need to seek treatment, they go to the free clinic in their village run by Burma Medical Association (BMA). Fortunately our medical partner Burma Children Medical Fund is helping Dar's family access the medical care she needs. They need help raising $1,500 to fund the treatment she needs. “We had to borrow money so far for Dar’s treatment and my husband cannot work,” said Dar’s mother. “I want to send my baby to school until she graduates so that she can become educated. I want this for her future because I only went to school until grade four. After she completes her studies, she can become whatever she wants one day.”
Rehiwilzahra is a sweet toddler from Haiti. She lives in Port-au-Prince with her mother, father, and three older siblings. Rehiwilzahra likes watching cartoons and playing with her older siblings. Rehiwilzahra has a cardiac condition called Tetralogy of Fallot. This heart condition involves several related heart defects including a hole between the two lower chambers of the heart, and a muscular blockage of one of the valves. These defects prevent blood from circulating properly through the lungs leaving Rehiwilzahra weak and short of breath. The surgery Rehiwilzahra needs to heal is not available in Haiti, so she will need to fly to the Dominican Republic to undergo cardiac surgery to close the hole in her heart with a patch and remove the blockage from her valve. Our medical partner, Haiti Cardiac Alliance is helping Rehiwilzahra's family raise $1,500 to cover the cost of labs, medicines, and follow-up appointments. This amount also supports passport obtainment and the social workers to accompany Rehiwilzahra's family overseas. Rehiwilzahra's mother shared, "We have been praying for a long time for a solution to our daughter's heart problem. We are very thankful to everyone who is helping her!"
James is is a 43-year-old man who is married with two children. James and his wife are casual laborers taking any job available, which means their income is limited and inconsistent. James was brought in on a stretcher by his wife and brother. His wife shared that they have had a very difficult life recently. James has been bedridden following a fall and broken leg as they could not afford the cost of his treatment. Fortunately a neighbor intervened and now he is seeking help. Our medical partner's team will perform a fracture repair to heal his leg and they also plan to follow up to assess if he has weakened bones. If not treated James may never be able to walk again and his leg may heal with deformity. Our medical partner, African Mission Healthcare, is raising $1,049 to fund this procedure. “I have been at home at the mercy of God. At least my neighbor directed us to Nazareth Hospital. I hope I can get help so that hopefully I can walk again,” said James quietly.
Keysha is a bright 12-year-old who lives on a small farm in northwest Haiti with her parents and four siblings. She really likes going to school and helping to take care of her family's animals. Keysha was born with a hole between the two upper chambers of her heart; blood leaks through this hole without passing through her lungs to obtain oxygen, leaving her weak and fatigued. During her upcoming surgery, doctors will use a catheter probe to plug the hole in Keysha's heart with a device so that blood can no longer leak through it. With this treatment, she can finally have a healthier life ahead. Keysha is hopeful to have more energy and feel healthy after her surgery. She shared, "I am looking forward to this surgery so that I can walk to my friends' houses to visit them without getting tired."
Ravuth is a bright student in the 4th grade. He's the youngest in his family and has three older siblings. When not studying, Ravuth likes to play football, watch TV and play games with his friends from school. Six weeks ago, Ravuth had a severe ear infection. This infection caused a cholesteatoma, or an abnormal skin growth, to develop in the middle ear behind the ear drum. Ravuth now experiences ear discharge, pain, fevers, and hearing loss. It is difficult to listen and he feels shy because he doesn't understand the conversation. He has frequently been absent from class and his mother is worried that he might be held back in school. Ravuth's family traveled to our medical partner's care center to receive treatment. On January 18th, he will undergo a mastoidectomy procedure in his left ear. During this procedure, ENT surgeons will remove the cholesteatoma. Our medical partner, Children's Surgical Centre, is requesting $925 to fund this procedure. This covers medications, supplies, and inpatient care. Ravuth said: "I hope my hearing will improve and I can go back to school!"
Lazaro is a social and friendly 15-year-old student and the third born child in a family of nine children. His parents are small-scale farmers and livestock keepers. He is currently in class five, and his best subjects in school are social studies and mathematics. Lazaro was born with clubfoot of both feet, a condition in which the feet are twisted out of shape. This causes difficulty walking and even wearing shoes. Despite his condition, he tries to keep active and loves to play football. Fortunately, our medical partner, African Mission Healthcare (AMH), is helping Lazaro receive treatment. On December 17th, he will undergo clubfoot repair surgery at AMH's care center. After treatment, he will be able to run and play with friends more easily. Now, AMH is requesting $935 to fund Lazaro's procedure and care. Lazaro shared, "I would love to have normal feet like my siblings and friends. I will be so happy if it can be possible."
Scovian is a quiet 6-year-old student and the firstborn in a family of two. She was brought to our clinic by her grandmother who takes care of her. She shared that Scovian's mother is a hawker in a town near her home while her father left the family because of her birth condition. Scovian has clubfoot of both feet. The condition has seriously affected her mobility. Balancing and maintaining her posture is a challenge. Clubfoot is a condition in which the foot is twisted out of shape. This causes difficulty walking and even wearing shoes. Scovian is stigmatized due to this condition in the village and at school. At school, Scovian is often mocked by other pupils. Due to that, her grandmother escorts her to school every day. Fortunately, Scovian traveled to visit our medical partner's care center, AIC Cure International Hospital. There, surgeons will perform clubfoot repair surgery on November 22nd. Our medical partner, African Mission Healthcare, is requesting $1,286 to fund Scovian's clubfoot repair. After treatment, her self-esteem will be boosted, she will be able to put on shoes, walk well, and engage with friends. Also, she will be able to continue with her studies well. Scovian's grandmother says, “If the surgery is done and is successful, I will be grateful to God.”
U Ghwe is a 70-year-old man who lives with his wife and granddaughter in Burma. His wife is ill and not able to look after household chores most of the time. His granddaughter is a student in grade 12, but since her school is closed right now, she looks after the household chores. U Ghwe is a weaver and primarily makes bamboo baskets used to carry materials for construction. The family also fishes and raises chickens. Four years ago, U Ghwe had a stroke which left the muscles in his right foot very stiff. Although he can walk, he cannot wear sandals comfortably and instead goes barefoot. About a month ago, while cutting bamboo for weaving, he felt something bite the sole of his right foot. When he got home that evening, his foot was painful, itchy, red and swollen. Unfortunately, he did not have money to seek treatment at a clinic and eventually, the wound developed into an abscess filled with pus. A family member finally recommended that he visit our medical partner's care center for further examination and treatment. After examination, a doctor diagnosed him with an ulcer and told him that he has diabetes. The doctor shared with him that any injury U Ghwe sustains will not heal easily. His doctor has recommended surgery to clean the ulcer and help it to heal. Our medical partner, Burma Children Medical Fund (BCMF), is helping U Ghwe receive the recommended treatment. On October 7th, he will undergo a wound debridement procedure at BCMF's care center to help his wound heal. Now, he needs help raising $694 to fund his procedure and care. U Ghwe shared, "I do not know how long my daughter will not be able to [give] me money. Today, my daughter called me and said that my son-in-law will need to have surgery so she cannot send me money. I am the only one who can earn an income, so if I do not feel better, I will not be able to work. I am interested in working with wood. If was younger, I would learn and become a carpenter but now I feel I am too old."
Arahufu is a two-year-old boy who loves football. He is the youngest child in a family of five children. Aruhufu's father works as a ‘manamba’, where his job is to call passengers onto a bus at the bus stop. When he manages to fill all the sits in the bus, he is then given some money. Arahufu was diagnosed with bilateral genu varus, a condition in which his legs bow outward. 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 has difficulty walking and running. Our medical partner, African Mission Healthcare (AMH), is requesting $880 to fund corrective surgery for Arahufu. The procedure is scheduled to take place on September 14th. Treatment will hopefully restore Arahufu's mobility, allowing him to participate in a variety of activities, and greatly decreasing his risk of future complications. Arahufu’s mother shared, “I can never find the money needed to cover my son’s treatment cost. I am struggling to even put food on the table. Please help him.”
Meshack is a young baby and the third born in a family of three children. His mother sells groceries in a local market and his father is a mechanic. His parents work hard to earn a humble income, just enough to provide for the family. Meshack was born a healthy and happy baby. However, a few days later, his mother noticed that he was not passing urine properly. His parents took him to a nearby hospital for examination where he was diagnosed with hypospadias, a congenital abnormality that causes urinary dysfunction. Without treatment, he will continue to experience uncomfortable symptoms and will be at risk of infertility. The doctor referred Meshack to visit BethanyKids Hospital once he turned 7 months old. Once they visited the hospital, he was scheduled to undergo a hypospadias repair surgery. Fortunately, Meshack is scheduled to undergo corrective surgery on August 19th. Our medical partner, African Mission Healthcare Foundation, is requesting $847 to cover the total cost of his procedure and care. Meshack’s mother shared, “It is hard for us to even think of raising any money as we cannot afford it, please help us. Thank you for your support.”
Hul is a 21-year-old motorcycle mechanic. He has two brothers and one sister. Hul's parents work as farmers. In March, Hul fell hard and damaged his left shoulder. He has been diagnosed with a brachial plexus injury on his left side. The brachial plexus is a nerve network that transmits signals from the spine to the shoulder, arm, and hand. Injuries to this nerve network can result in loss of function and sensation. He has no shoulder abduction or elbow flexion, and can not move his fingers. He is unable to work. Hul traveled to our medical partner's care center to receive treatment. On July 14th, he will undergo a brachial plexus repair surgery. After recovery, he will be able to use his left arm again. Our medical partner, Children's Surgical Centre, is requesting $696 to fund this procedure. Hul said, "I hope I can regain use of my left arm and hand so I can work again to support myself."
Guadalupe is an one-year-old baby from Colombia. She is an only child, so she is regarded as the little princess of the family, which consists of her mother, grandma, and uncle. She is already sympathetic and friendly, and loves to play with stuffed toys and with other kids. Guadalupe has clubfoot on 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, Guadalupe's family traveled to visit our medical partner, Clínica Noel, where they can offer treatment. There, surgeons will perform clubfoot repair surgery on August 13th. Our medical partner is requesting $1,422 to fund Guadalupe's clubfoot repair. After treatment, she will be able to start walking and running without pain. Her mother shares a story and her hopes for Guadalupe, "I would really love to see her walk and run normally, she is not the first person with this condition in our whole family, I have a cousin who received treatment when he was 8 years old and it was really hard to see him asking why he couldn't run like the other kids."