Nick joined Watsi on September 19th, 2016. Five years ago, Nick joined our Universal Fund, supporting life-changing treatments for a new Watsi patient every month. Nick's most recent donation supported U Nyan, a 62-year-old man from Burma, to fund treatment for a painful abscess on his elbow.
Nick has funded healthcare for 64 patients in 12 countries.
Nick has funded healthcare for 64 patients in 12 countries.
U Nyan is a 62-year-old man who lives with his wife in Mon State, Burma. He used to work as a tricycle taxi driver as well as a day labourer but since he had stroke around three months ago, he stopped working. His wife also had a stroke and cannot work. They have a daughter who works across the border in Bangkok, and she sends them some money every three or four months. However, the amount that her daughter sends is not enough for U Nyan and his wife for their daily expenses and they shared that, occasionally, their neighbor also gives them food. Recently, U Nyan noticed a small lump on his left elbow, which rapidly became enlarged and painful. Currently, U Nyan is in a lot of pain and cannot sleep. After seeking treatment at various clinics and hospitals, U Nyan was finally referred to Mawlamyine Christian Leprosy Hospital (MCLH) where he was diagnosed with an abscess around his left elbow joint and scheduled for surgery on May 9th. When he told the doctor that he could not afford to pay for his surgery, the doctor referred him to our medical partner Burma Children Medical Fund for financial assistance accessing surgery. He has already borrowed about $350 so far to help with his diagnosis and treatment, and people in his community have pitched in to support him financially. Our medical partner is helping him raise $760 for his surgery. “After surgery I want to go home and look after my wife. I want to listen to sermons, meditate and do good deeds,” shared U Nyan.
Demetria is a peanut-butter maker from the Philippines. Demetria was diagnosed with cholecystitis 10 years ago and advised by her doctor to undergo surgery, but due to financial constraints, she opted to self-medicate using herbal medicines. This served as a temporary relief to her symptoms, but now these have worsened over time, and during the past 2 weeks, she started experiencing intolerable pain and difficulty keeping food down. With age and her worsening symptoms, Demetria is not capable of earning income to support her medical treatment. She shared that she and her husband rely on their granddaughter who works as an online tutor, to support their daily needs. Fortunately, Demetria was referred to our medical partner and is now scheduled to undergo surgery to correct her condition on April 7th. Our medical partner, World Surgical Foundation Philippines, is requesting $1,253 to cover the total cost of her procedure and care. After her recovery, Demetria will no longer experience severe pain in her abdomen or be at risk of other complications in the future. “Once the surgery is done, I hope to go back to doing my small peanut butter-making business so I can help sustain our daily needs like I used to before," Demetria shared. "Thank you so much WSFP and Watsi for all your help,” she added.
Cali is a two-year-old girl from the Philippines. She loves to watch TV, and play with her siblings and cousins. Her mother takes care of her and her siblings while her father is a tricycle driver. The family’s income provides for their basic necessities but is not enough to cover Cali's medical treatment. Cali 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 and is scheduled to undergo surgery on March 23rd. Our medical partner, World Surgical Foundation Philippines, is requesting $1,279 to cover the total cost of Cali's procedure and care. After her recovery, Cali will no longer experience bowel dysfunction or be at risk of developing health complications in the future. “Nowadays, you'll find bullies everywhere, and we have been worried that growing up, her condition might affect her ability to interact with others. So thank you, WSFP and Watsi, for helping us. We are hopeful that if the [colostomy] closure is done, she’ll be able to live a normal life, without worrying about her appearance and what others might say about her, ” Cali's mother shared.
Edmond is a playful eight-year-old boy. He is the second born child in a family of four children. Sadly, his father passed away in 2021 after a short illness. His mother works as a sweeper in a supermarket to provide for the family. The family lives in a two-room home. Recently, Edmond fell while playing at school and injured his left arm. He was brought to a local hospital where he had an x-ray and was told that he had dislocated his elbow. However, he received a second opinion at our medical partner's care center and was diagnosed with a left supracondylar fracture. He needs urgent surgery to treat his injury so he can heal properly. Fortunately, our medical partner, African Mission Healthcare (AMH), is helping Edmond receive treatment. On February 8th, he will undergo surgery to repair the fracture. This will ensure that his hand heals well and that he can use it fully in the future. Now, their family needs help raising $852 to fund his procedure and care. Edmond's mother shared, "I dream of getting my family out of poverty. I am trying to look for a better job so that I can care for my children. Unfortunately, my son's arm is now fractured. I am worried about his future if he is not treated."
Ezra is a very talkative and active boy. He would like to be a truck driver when he grows up. He's in grade five and the last born in a family of five children. A few years ago, his father fell into a deep hole he was digging and broke both of his legs. He has been recovering well but he is still unable to work. His mother, who is the sole breadwinner of the family does farming, ploughs farms, and does laundry for their neighbors to provide for the family. The family can not raise the required funds to cater for Ezra’s surgery. Ezra was born 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. Fortunately, Ezra is scheduled to undergo corrective surgery on October 19th. Our medical partner, African Mission Healthcare Foundation, is requesting $847 to cover the total cost of his procedure and care. Ezra’s mother says, “I was really worried that my son will not get treated but now at least I’m very hopeful that he will.”
Ndaanya is a five-year-old boy and the youngest child in a family of three children. His mother is not married and works as a farmer to support her family growing maize, sunflowers, groundnuts and vegetables. Ndaanya 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, Ndaanya traveled to visit our medical partner, African Mission Healthcare (AMH), to receive treatment. On September 14th, surgeons at AMH's care center will perform clubfoot repair surgery. Now, AMH is requesting $935 to fund Ndaanya's clubfoot repair. After treatment, he will be able to walk easily and start schooling. Ndaanya’s mother shared, "I had lost hope... I knew this problem could only be corrected when he was a small baby and because his treatment was not successful I thought he would live with this disability for the rest of his life. I will be so happy and grateful if you help correct my son’s feet.”
Shallet is a humble and jovial three-year-old girl. She's the third child born in a family of four children and her parents are teachers. Shallet has hydrocephalus, spina bifida, and clubfoot of both feet. She has visited local hospitals since birth for treatments, and began casting for clubfoot when she was four weeks old. Her condition causes her difficulty walking and even wearing shoes. Fortunately, Shallet traveled to visit our medical partner, African Mission Healthcare (AMH), for treatment. At AMH's care center, surgeons will perform clubfoot repair surgery on August 18th and now, AMH is requesting $1,286 to fund Shallet's clubfoot repair. Her parents shared that they hope that the treatment will be of great impact to Shallet because she will be able to wear shoes and walk with ease. Shallet's father shared, “we have high hopes for Shallet and it is our joy to see her excel in life and become an independent person like other girls in the society.”
Dylan is a little baby from Colombia who is the firstborn of his family. Dylan's father is 20 years old and works at a furniture factory while his 18-year-old mother is at home with her newborn. Dylan enjoys listening to music. With his beautiful eyes, he already attracts the affection of all around him. Dylan was born with clubfoot on both feet, a condition in which the foot is twisted out of shape. This will cause difficulty walking and even wearing shoes in the future. Dylan's family traveled to visit our medical partner, Clínica Noel. There, surgeons will perform clubfoot repair surgery on August 26th. Clínica Noel is requesting $1,500 to fund Dylan's bilateral clubfoot repair. After treatment, he will be able to crawl, walk, and run as he grows up. His mother shares,"I would love to see him run and play as a normal kid." His father tells us of his grand hopes for young Dylan's future, "I would love to see him playing soccer and to celebrate with him when he becomes a champion."
Paulo is a 5-year-old boy boy and the third born in a family of five siblings. He is yet to start formal schooling and his father has been taking him out with him grazing their cattle. His parents are livestock keepers from a pastoralist community. Paulo was diagnosed with bilateral genu valgus, or knock knees. His parents noted that he would complain of fatigue after walking for a shorter distance. They also started noting changes in how his legs looked, as they started bowing inward so his knees 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, Paulo is not able to sustain lengthy walks. His relative referred them to a local dispensary providing health services, where a team from Watsi's medical partner's care center was conducting outreach. Paulo was reviewed and had surgery recommended to heal his condition. However, his family is not able to raise the cost of surgery required and thus appeals for help. Our medical partner, African Mission Healthcare, is requesting $880 to fund corrective surgery for Paulo. The procedure is scheduled to take place on June 10th. Treatment will hopefully restore Paulo's mobility, allow him to participate in a variety of activities, and greatly decrease his risk of future complications. Paulo’s father shared, "Please help my son; his legs are really bad and we cannot afford the treatment cost. Thank you for your support."
Vivian is a fifth-grade student and the eldest of two children in her family. Vivian is a friendly and a hard working girl both at school and at home. She loves to help her mother with house chores and enjoys learning new things. In 2019, Vivian was involved in a fire accident which has left her with burns and contracture on her right side. As a result, her range of movement is limited and it is difficult for her to use her right side of her body freely. Fortunately, our medical partner, African Mission Healthcare, is helping Vivian receive treatment. On May 11th, surgeons will perform a skin graft procedure to repair her injury and increase mobility on that side of her body. Now, Vivian's family needs help to fund this $747 procedure. Vivian’s mother shared, "After her first surgery, she could use her arm well but over the year it has started contracting again. She has been scheduled for another surgery which we cannot afford. Please help."
Lomnyak is a 5-year-old boy and the fourth born child in a family of five children. Lomnyaki and his siblings live with their mother, as their father left and doesn't offer support. His mother does not currently work as she is taking care of their family and she shared how challenging it was as they do not have livestock nor a place to farm. They are doing their best to get through a challenging living situation. Lomnyak was born with spina bifida, a type of neural tube defect in which the spine does not properly close around the spinal cord. Without treatment, Lomnyak is at risk of lower-limb paralysis, infection of the exposed nervous tissue, development of tethered cord syndrome, and possible developmental delays. Our medical partner, African Mission Healthcare Foundation, is requesting $1,015 to cover the cost of Lomnyak's spina bifida closure surgery. The procedure is scheduled to take place on April 19th. This procedure will hopefully spare Lomnyak from the risks associated with his condition, instead allowing him to grow and develop along a healthy trajectory. Lomnyak’s mother shared, "I didn’t know that this condition was life-threatening but I suspected it to be the cause of my son not being able to stand nor walk. Please help him get this surgery."
Fidelica is a third grade student from Haiti. She is an only child and enjoys learning to play piano and guitar. Fidelica has a cardiac condition called atrial septal defect, which means a large hole exists between the two upper chambers of her heart. This condition may have serious risk factors for heart failure or stroke. In order to receive treatment, Fidelica must fly from Haiti to the Dominican Republic. On March 15th, she will undergo cardiac surgery, as surgeons will use a patch to close the hole in her heart. Another organization, Gift of Life International, is contributing $5,000 to pay for her surgery. However, Fidelica's family needs help raising an additional $1,500 to fund related costs such as labs, medicines, and follow-up appointments. This funding will also help the family cover travel costs for the procedure, such as obtaining a passport and having social workers from our medical partner, Haiti Cardiac Alliance, accompany Fidelica's family overseas. Fidelica's mother says, "I am excited for this surgery so that I can let my daughter run and play with other children!"