Daniel joined Watsi on September 8th, 2014. Seven years ago, Daniel joined our Universal Fund, supporting life-changing treatments for a new Watsi patient every month. Daniel's most recent donation traveled 8,800 miles to support Samrach, a factory worker and loving father of two from Cambodia, to fund nerve surgery to help him use his arm following a road accident.
Daniel has funded healthcare for 76 patients in 12 countries.
Daniel has funded healthcare for 76 patients in 12 countries.
Samrach is a 27-year-old clothing factory worker. He's is married with two small children. His daughter is six years old and just starting the first grade, and his son is nine months old. His wife is also a factory worker in their province. He likes to play with his children and listen to music. Ten months ago, on his way home from the factory, Samrach was in a motorcycle crash. He suffered fractures of the femur, clavicle, forearm, and multiple other injuries. He lost his left leg below the knee due to the trauma injury, and spent three months in a provincial hospital. A local taxi driver told him about the specialty care at our medical partner Children's Surgical Center (CSC). Doctors have diagnosed him 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 cannot lift his left shoulder, bend his elbow, or use his hand. He feels unwell and shared that he often feels very depressed that he cannot work or support his family. Samrach traveled to our medical partner's care center to receive treatment. On January 6th, he will undergo a brachial plexus repair surgery. After recovery, he hopes to regain the use of his arm so he can find work in the factory again. Our medical partner is requesting $696 to fund this life-changing procedure. Samrach said: "I hope this surgery will work for me, and I can start working again to have money to feed my children and make sure they go to school."
Sheila is a 13-year-old bright and outgoing girl. She is a partial orphan who lives with a guardian that helped to rescue her from a difficult situation growing up. Sheila lives at a special place alongside 10 other children who come from a similar background. Her guardian says that Sheila's clubfoot condition limits her from her potential. Sheila was born with clubfoot and the condition has affected her mobility and lowered her self-esteem in a way that she cannot connect with her peers. Her guardian and family are not financially able to support the surgery and are appealing for financial assistance. Fortunately, Sheila traveled to visit our medical partner's care center, AIC Cure International Hospital. There, surgeons will perform clubfoot repair surgery on December 6th. Our medical partner, African Mission Healthcare Foundation, is requesting $1,286 to fund Sheila's clubfoot repair. After treatment, Sheila will be able to easily interact with her peers and have a high self-esteem. Her guardian says, “I would very much appreciate the support that may be provided for Sheila's care. She will be able to explore her full potential.”
Jhonatan Mercado is a creative four-year-old from Venezuela. A year ago his family moved to Medellin in Colombia seeking for a better future for their kids. Jhonatan is an older brother in a family of two children, his little brother is one year old. Jhonatan he loves to play with his mom with Legos. He already loves soccer too. Jhonatan Mercado 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, Jhonatan Mercado's family traveled to visit our Medical Partner Clínica Noel. There, surgeons will perform clubfoot repair surgery on December 20th. Our medical partner, Clínica Noel, is requesting $1500 to fund Jhonatan Mercado's bilateral clubfoot repair. After treatment, he will be able to walk without pain or further complications. His mother said "We are really glad that finally we found help, we have been in different treatments since he was 6 months old but now we have a lot of faith in this procedure and in Doctor Miguel."
Nin is a 27-year-old rainy day farmer from Cambodia. He has 3 older sibling. Nin shared that he enjoys playing volleyball, football, fishing, and plays chess with his friends. In July 2021, Nin was in a motor vehicle accident that caused a mandible injury and paralysis of his shoulder. After the accident, he had his mandible fixed at a local government hospital. He was also diagnosed with a brachial plexus injury on his right 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. Nin still has no shoulder abduction, no elbow or wrist flexion, and has no sensation at the level of his forearm. Nin needs nerve reconstruction surgery to repair the injured nerves. Nin traveled to our medical partner's care center to receive treatment. On September 6th, he will undergo a brachial plexus repair surgery. After recovery, he will be able to use his arm and hand again. Our medical partner, Children's Surgical Centre, is requesting $696 to fund this procedure. Nin hopes that he can use his hand again as soon as possible.
Duncan is a 28 year old man who is currently single and unable to work due to his condition. Duncan experienced trauma in early 2010 after a road traffic accident that caused spine injury and hearing loss. At the time of the accident, Duncan had a loss of consciousness, memory loss, and was even paraplegic at one point. He also had tinnitus in his right ear but with earlier support from Watsi donors, he got a hearing aid fitted and can now communicate well. Duncan now walks on a crutch, however, his pain worsens with movement, and radiates to his lower limbs. Because of his condition, Duncan has been in and out of hospitals. He is supposed to visit the hospital regularly. For convenience, he currently lives with his relatives nearby in Nairobi. His parents are elderly farmers in his ancestral home in Kisii in rural Kenya. Duncan is currently struggling to walk. An MRI exam identified canal stenosis and bone degeneration, so doctors have recommended surgery. He is scheduled for L4/5, L5/S1 Decompression, and Spine Fusion to avert chances of being immobile for the rest of his life. The hospital is requesting $1,500 to perform his surgery and his health insurance coverage will not cover this care. He currently relies on well-wishers to pay for his medical bills. Duncan told us, “I cannot walk well without support. I am also in pain and very uncomfortable. I hope to get better soon.”
Sam Oeun is a 41-year-old bus driver. He is married and has one son and two daughters. His wife is a food seller. At home, Sam Oeun enjoys watching boxing on TV. Two years ago, Sam Oeun developed a pterygium in his left eye, causing him burning, itchiness, and discomfort with his appearance. Pterygiums are non-cancerous growths of the conjunctiva, a mucous layer that lubricates the eye. The growths occur when the conjunctiva is exposed to excessive sun damage and the cells grow abnormally over the pupil. When Sam Oeun learned about our medical partner, Children's Surgical Centre (CSC), he traveled there hoping for treatment. Sam Oeun needs a surgical procedure to remove the abnormal growth and replace it with a conjunctival graft to prevent recurrence. The total cost of his procedure is $216. This covers medications, supplies, and inpatient care for two days. The procedure is scheduled for June 16th. Sam Oeun shared, "I hope after surgery my eye feels comfortable so I can go back to work and not worry about my eye anymore."
Nurat is a three-week old baby from Tanzania. She is the first child of her young parents at a local hospital in Manyara. Nurat’s mother still lives at her parents’ home while her father lives at a rented house. Before Nurat's birth, her mother sold flowers and cooking pots to earn a living and her father has a small kiosk selling domestic items such as sugar, salt, bread. Nurat was born with spina bifida that puts her at risk of lower-limb paralysis, infection, and possible developmental delays. Our medical partner, African Mission Healthcare Foundation, is requesting $1,015 to cover the cost of Nurat's spina bifida closure surgery. The procedure is scheduled to take place on June 23rd. This procedure will hopefully spare Nurat from the risks associated with his condition, instead allowing her to grow and develop into a healthy girl . Nuru’s mother hopes the best for her child, "Am still in shock and unsettled due to my daughter’s conditions. I was informed that both conditions could be corrected but we are not in a position to afford any of the treatment costs. Please help save my daughter I don’t know what to do."
Olivia is a 3-year-old girl who lives with her parents in a small city in the north central part of Haiti. Her father works in a local hospital and her mother is a homemaker. She is their only child. Olivia has a cardiac condition called Tetralogy of Fallot. This condition involves several related defects, including a hole between two chambers of the heart and a muscular blockage of one of the valves. Olivia will fly to Cayman Islands to receive treatment. On June 4th, she will undergo cardiac surgery, during which doctors will close the hole in her heart with a patch, and dissect the blockage of her valve. Another organization, Haiti Cardiac Alliance, is contributing $18,000 to pay for surgery. Olivia'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 Olivia's family overseas. From father: "Our family will pray for everyone who is helping to save our daughter's life."
Juma is a 15-year-old boy and the youngest of nine children born to his mother. He is an intelligent boy who completed primary school with good marks, but unfortunately, his father couldn't afford to send him to secondary school. Juma stays home and helps his mother work on the farm where they grow maize, vegetables, and cassava. Juma's dream is to become a teacher. Since childhood, Juma has had a right inguinal hernia that causes him pain. Our medical partner, African Mission Healthcare (AMH), is helping Juma receive treatment. On May 4th, he will undergo hernia repair surgery at AMH's care center. Now, AMH is requesting $566 to fund Juma's surgery. Once completed, this procedure will hopefully allow him to live more comfortably and confidently. Juma shared, "please help me with this condition because as I grow older the pain keeps becoming worse which is a sign it's getting worse."
Htoo is a 6-year-old boy from Thailand. He lives with his parents, brother and two sisters in a refugee camp on the border of Thailand and Burma. Htoo and his siblings were born in the refugee camp. Htoo’s mother is a homemaker, while Htoo’s older brother and sisters go to primary school and Htoo attends kindergarten. His father used to work as a day labourer, but has been unemployed since the pandemic began. Currently, they have no income and receive some financial support for their daily expenses. Luckily, Htoo's family receives free basic healthcare and education in the camp. In late October 2020, Htoo was diagnosed with an inguinal hernia. If he stands up for a short period of time, or walks, the right side of his private area will swell. Around twice a week, Htoo shares with his parents that this area is hurting him and he feels uncomfortable. Fortunately, on April 8th, he will undergo hernia repair surgery at Mae Sot General Hospital, our medical partner's care center. Our medical partner, Burma Children Medical Fund, is requesting $1,500 to fund Htoo's hernia repair surgery. The procedure is scheduled to take place on April 8th and, once completed, will hopefully allow him to live more comfortably. Htoo's father shared, “Most of the time, my son is very active and playful. He will only rest when he complains about the pain.”
Daw Mya is a 59-year-old woman from Burma. She lives with her daughter, granddaughter, son, daughter-in-law, and grandson in Yangon, Burma. Daw Mya is currently too ill to work, but her daughter works as a seamstress in a factory. Her granddaughter goes to school, her son is a taxi driver, her daughter-in-law looks after their son at home. Her daughter and her son both help look after Daw Mya and try to support her as best they can. Daw Mya was diagnosed with a heart condition that involves a malformation of the mitral valve, the valve between the left atrium and left ventricle. This valve controls the flow of blood, but certain conditions may cause blood to flow backward or the valve to narrow. Currently, Daw Mya feels tired and experiences heart palpitations with chest pain. She has no appetite and cannot sleep well at night, and both of her legs are swollen. Our medical partner, Burma Children Medical Fund, is requesting $1,500 to fund a mitral valve replacement for Daw Mya. The treatment is scheduled to take place on February 21st and, once completed, will hopefully allow her to live more comfortably. Daw Mya said, “I want to get better soon so that I can help my family. I want to help them because my daughter-in-law is always looking after me and her child [my grandson], so she cannot work. If I can look after the household chores and take care of the family, they can go to work and earn more income for our family. I cannot go anywhere because of my condition. They always take care of me and they spend too much of their money on me.”
Myo is a 16-year-old boy from Burma. He lives with his parents and four brothers in northern Rakhine State. Myo is a student in grade nine and his four brothers also go to school. However, they have been unable to study since the Covid-19 pandemic shut all schools. Myo’s parents are day laborers, and their family's combined income is just enough to cover their daily expenses since Myo and his brothers’ schooling is free. To survive with limited income, they forage for vegetables and fish. If they fall ill, they use traditional medicine, which is more affordable then going to a clinic or a hospital. Myo was diagnosed with a heart condition that involves a malformation of the mitral valve, which is the valve between the left atrium and left ventricle. This valve controls the flow of blood, but certain conditions may cause blood to flow backward or the valve to narrow. Currently, Myo cannot walk long distances or climb stairs because of his tiredness. Sometimes, he cannot breathe very well. Our medical partner, Burma Children Medical Fund, is requesting $1,500 to fund a mitral valve replacement for Myo. The treatment is scheduled to take place on February 7th and, once completed, will hopefully allow him to live more comfortably. Myo shared, “I am worried about my health and I feel sorry for my parents. Because of my health problems, my father had to work more days to earn more money. Also, my mother cannot work because she accompanies me and has to take care of me. I hope my school will reopen soon so that I can go back to school. One day I hope that I can become a teacher. I want to teach because there are not enough teachers in my village.”