Daniel joined Watsi on March 12th, 2013. Six years ago, Daniel joined our Universal Fund, supporting life-changing treatments for a new Watsi patient every month. Daniel's most recent donation traveled 3,100 miles to support Katweensly, a 16 year old student from Haiti, to fund prep and travel for heart surgery.
Daniel has funded healthcare for 120 patients in 16 countries.
Daniel has funded healthcare for 120 patients in 16 countries.
Meet Katweensly, a 16 year old student, living with her mother and siblings in a small town in Haiti, near the border with the Dominican Republic. Katweensly, who is a junior in high school, particularly enjoys her math and science classes. As a young child, Katweensly suffered a bout of rheumatic fever, which damaged one of the four valves in her heart. As a result, her heart cannot pump blood efficiently through her body, leaving her feeling weak and short of breath. Thanks to the help of our medical partner, Haiti Cardiac Alliance, Katweensly is scheduled to travel to the Dominican Republic for surgery, which is scheduled for November 10th, at Hospital CEDIMAT. There, doctors will first try to repair the damaged valve. If they are unable to do this, they will implant an artificial valve. Another organization, Mitral Foundation, is helping supporting the cost of the surgery, but Katweensly's family needs an additional $1,500 to pay for lab tests, medicines, and follow up appointments that are a part of her overall treatment. In addition, support will help cover the travel costs and ensure a social worker from Haiti Cardiac Alliance can support the family during treatment in the Dominican Republic. Katweensly said: "I am feeling very happy to finally have the chance to have my heart repaired after waiting for so long."
Meet Su, a 10-year-old girl, living with her mother in Thailand. Because her parents are no longer together, Su sometimes also goes and stays with her father. Both of her parents work for local community organizations. When Su has free time, she enjoys drawing pictures, and playing with her friends. Su was born with clubfeet and a dislocated hip. After her birth, she received corrective surgery in Chiang Mai, with the help of our medical partner, BCMF. During her last visit to the hospital after her surgery, the doctor told her mother that she would need to bring Su back to the hospital after she had outgrown the special, corrective shoes she wore for her clubfeet. Due to financial constraints, issues with documentation, and the Covid pandemic, Su's parents were never able to bring her back to the hospital. In June 2022, Su started to experience pain in her right foot, whenever she walked for longer than 10 minutes. And, for the first time, she also began to feel pain in her right hip when she walked. The doctor at Mae Sot Hospital diagnosed her with a dislocated hip, and referred her to Chiang Mai for further treatment. Doctors in Chiang Mai want Su to undergo an MRI, which will help them to reach a definitive diagnosis, and to formulate a plan of treatment. Our medical partner, Burma Children Medical Fund, is requesting your help to cover the $814 cost of Su's MRI and care, scheduled for October 18th, at Maharaj Nakorn Chiang Mai Hospital. "I want my daughter to become a doctor in the future so that she can help others who also suffer from clubfeet," said Su's mother.
Prisla is a charming and social 5-year-old girl. She is an only child born who loves to play with other children. Prisla's parents separated when she was around two years old and she has been raised by her father with the help of her grandparents and uncles. The father is a small-scale famer who also does casual jobs to get money to support her upbringing. At two years old, Prisla was severely burned when she accidentally dipped her hands in a pot of boiling water. Prisla was never taken to hospital and instead treated with traditional medication at home. Prisla is now having difficulty using her hands in daily life activities due to her contracted fingers. Prisla has been scheduled for surgery to start correcting the right-hand fingers. Fortunately, our medical partner, African Mission Healthcare Foundation (AMH), is helping Prisla receive treatment. On May 12th, surgeons at their care center will perform a burn contracture release surgery to help her finally straighten her fingers. AMH is requesting $639 to fund this life-altering procedure. Prisla’s uncle, who brought her for care, shared, “Her father cannot afford to take her to hospital, please help get her fingers corrected.”
Sophea is married to a security guard, and they have two active sons who are six and four years old. Sophea sells vegetables at a local market to help support her family. She enjoys cooking, reading books, and taking care of her children. In October 2021, she was in a traffic accident that resulted in several fractures and road burns. Her fractures have since healed, but she developed a burn contracture and a joint dislocation, impeding her ability to use two of her fingers. Now she is unable to carry things, and it is painful whenever she tries to straighten her fingers. Fortunately, our medical partner, Children's Surgical Centre, can help. Surgeons plan to release the contracture and repair the dislocation, and apply a skin graft to her fingers. This will improve the mobility and stability of the fingers on her hand so she can get back to doing all she needs to each day. Sophea needs help to pay the cost of the $487 surgery, which will include hospitalization, medications, and post-operative rehabilitation. Sophea shared, "I hope my fingers will be able to function after my operation. I will be able to use my hand, and not have pain. This will help me to care for my family and work hard."
Linda is a two-month-old baby girl. She was born in a public hospital in Mai Mahiu town where her mother was living with a friend. At birth, she was diagnosed with spina bifida. Her mother was referred to another facility more familiar with this diagnosis, and upon further examination referred Linda to our medical partner's care center BethanyKids Hospital for treatment. On arrival at the hospital, Linda was found to be in critical condition and had to be admitted and put on medication. She stayed in the hospital for more than two weeks. When she got better, she was discharged home and scheduled to undergo spina bifida repair surgery with support from Watsi. Last week, Linda reported back to the hospital for her surgery, but arrived with a fever. She was admitted to the High Dependency Unit. While in hospital, she was diagnosed with hydrocephalus, or a build-up of fluids in the cavities of the brain, which required urgent surgical intervention. The spina bifida surgery was postponed to a later date while she recovers from the shunt insertion surgery to heal her hydrocephalus. Linda is the youngest in a family of three children. Her father left the family one month before she was born. He used to do casual jobs and had not been supportive. During the last few months before Linda was born, her mother was very sick and lost her job as a security guard, thus losing the family's only source of income. Having come from Uganda, they did not have many people to help them. Her Ugandan friend heard of her suffering and offered to accommodate her as she was pregnant. Since then, this friend has been facilitating their hospital transport and helping with financial support as much as possible. Linda’s mother cannot raise any money to pay for her daughter’s surgery and is appealing for support. Hydrocephalus is a condition in which excess cerebrospinal fluid accumulates in the brain and increases intracranial pressure. Without treatment, Linda will experience severe physical and developmental delays. Our medical partner, African Mission Healthcare Foundation, is requesting $720 to cover the cost of surgery for Linda to treat her hydrocephalus. The procedure is scheduled to take place on September 14th, and will drain the excess fluid from Linda's brain. This will reduce intracranial pressure and greatly improve her quality of life. With proper treatment, Linda will hopefully develop into a strong, healthy young girl. Linda’s mother says, “I am still confused with all that is going on, and I hope that she will be okay.”
Faith is a very cheerful and friendly 9-year-old student from Kenya. She is the youngest in her family. Her father works as a casual laborer, and her mother works as a vegetable vendor. Her mother shares that she is limited in seeking more job opportunities due to her daughter's required care. Faith was born with hemiplegic cerebral palsy, a condition that results from damage to the part of the brain that controls muscle movements. She also has clubfoot of her right foot. Clubfoot is a condition in which the foot is twisted out of shape. This causes difficulty walking and wearing shoes. Faith is currently unable to stand and walk on her own, but she can sit comfortably. Her parents have visited different hospitals in search of treatment for her without success. Fortunately, Faith recently traveled to visit our medical partner's care center, AIC Cure International Hospital. There, surgeons will perform clubfoot repair surgery on August 22nd. Our medical partner, African Mission Healthcare Foundation (AMHF), is requesting $1,286 to fund Faith's clubfoot repair. After treatment, she will hopefully be able to stand and walk without support. Her parents will also be able to seek more job opportunities to further provide for their family. Faith's mother shares, "We are not in a position to raise the estimated hospital bill. We are seeking help from AMHF for my daughter to undergo surgery. God will bless you."
Jeremy is a beautiful five-year-old boy from Kenya who has autism. To support their family, his mother manages their home and cares for her children, and his father currently works as a mechanic. His parents share that their income is just enough to sustain the basic needs of their family of six. On July 7th, Jeremy was playing with his brother when he fell and broke his leg. An X-ray scan showed that he has a fracture of his femur bone on his right leg. Since the incident, he has been experiencing severe pain. Fortunately, surgeons at our medical partner, African Mission Healthcare Foundation, can help. On July 12th, Jeremy will undergo a fracture repair procedure, called an open reduction and internal fixation. This procedure will allow his injury to heal and help him walk again. Now, our medical partner is requesting $1,049 to fund this procedure. Jeremy’s mother expressed, “I am desperate and worried...I am pleading for assistance so that soon he can be treated. I thank God in advance."
Brian is a 12 year old boy living with his parents and three older siblings. His father is a motorcycle taxi driver earning a living whenever he can from the limited work, while his mother stays at home to care for the children. When Brian was about nine months old, his parents noticed that he had general body weakness. He was diagnosed with rickets and additional medical conditions, which have caused a delay in many of his milestones as he continues to grow. Brian's physical coordination is limited, and he suffers from a profound hearing loss, for which his doctors have recommended hearing aids. But hearing aids are too expensive for his family to afford, so Brian currently attends a special school, which can accommodate his hearing loss. The doctors have assured Brian's parents that with hearing aids, Brian would be able to attend an ordinary school near their home. Our medical partner, African Mission Healthcare, is requesting $1,171 to cover the costs of the hearing aids and the fitting, which is scheduled to take place on June 17th at AIC Kijabe Hospital. With his hearing restored, Brian will be able to attend a regular school, and to interact more fully with the world around him. Brian's father says: “Brian is unable to pick up voices and this is affecting his studies. He shifted to a special school because of his condition. His doctors say that he can hear well if fitted with hearing aids. If he gets this medical attention, he can join his colleagues in a normal school.“
Minea is a sweet, nap-loving two-year-old boy. He is the first child in his family, and his parents work as rice farmers. They shared that Minea loves to play with toys and take a good nap, if not two, every day! Minea also loves to eat and cuddle with his parents. In December 2021, Minea and his mother were in a motorcycle accident that injured Minea's left shoulder. His parents took him to the local hospital for X-rays and care; however, his shoulder is still dislocated, meaning he cannot lift his arm or grasp objects with his hand. Minea 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. Minea's family brought him to our medical partner, Children's Surgical Centre (CSC), in February to undergo physiotherapy for his injury. Since there has been no improvement after three months of physiotherapy, CSC's specialty surgeons determined that Minea needs to undergo a nerve transfer surgery to heal. CSC is the only center in the whole country where this treatment is available, and, on April 21st, Minea will undergo surgery. His doctors shared that, after recovery, his nerve graft should regenerate so he can use his arm again. CSC is requesting $709 to fund this procedure. Minea's parents hope their child will have a successful surgery and he will be able to fully use his hand as he grows up.
Gatguon is an 8-week-old baby girl from a remote area of South Sudan. The civil war in South Sudan has made it difficult for many to access healthcare and treatment, including Gatguon's family. Gatguon was born with swelling in the back of her head. Upon referral to Old Fangak Clinic, the doctor diagnosed Gatguon with spina bifida, a type of neural tube defect in which the spine does not properly close around the spinal cord. Without treatment, Gatguon is at risk of lower-limb paralysis, infection of the exposed nervous tissue, development of tethered cord syndrome, and possible developmental delays. Gatguon urgently needs spina bifida repair surgery to correct the condition and reduce risk of infection. Unfortunately, this treatment is not available for her in South Sudan. Dr Jill Seaman and her team at Old Fangak Clinic facilitated Gatguon’s travel to Kenya – a long and difficult journey for a sick baby. Now, doctors at our medical partner's care center in Kenya will perform the surgery she needs. Gatguon’s parents have two kids. Her mother is a stay-at-home mom and her father is a vegetable farmer. They are hopeful that baby Gatguon will be treated and that they will continue taking care of her and loving her unconditionally. Our medical partner, African Mission Healthcare, is helping Gatguon's family raise $1,151 to cover the cost of spina bifida closure surgery. The procedure is scheduled to take place on April 20th and will hopefully spare Gatguon of further complications and allow her to grow and develop along a healthy trajectory. Gatguon’s mother shared, “We hope that our child will be treated.”
Baraka is a beautiful, charming 3-month-old baby boy and the youngest in a family of three children. Baraka’s father works for a construction company. His mother was selling vegetables by the roadside until the government forced her to close her stall. Baraka has clubfoot on both feet. Clubfoot is a condition in which the foot is twisted, causing difficulty walking and even wearing shoes. Fortunately, Baraka's family traveled to visit our medical partner's care center, Arusha Lutheran Medical Centre. There, surgeons performed clubfoot repair surgery on March 11th. Our medical partner, African Mission Healthcare Foundation, is requesting $935 to fund Baraka's surgery. After treatment, he will be able to walk and play just like other kids as he gets older. Baraka’s mother says, “I want my baby to grow up a normal child without a disability. Please help us so that he can have his feet corrected.”
Erlando is a playful three-year-old boy from the Philippines who loves to giggle and watch Tik Tok videos. Erlando was born with a congenital abnormality that leads to intestinal complications. This condition requires Erlando to go through a series of corrective procedures to eliminate the abnormality and reduce the risk of life-threatening complications. Erlando's parents sew uniforms for a living and work hard to earn enough to sustain their daily needs. Our medical partner, World Surgical Foundation Philippines, is helping Erlando's parents raise $1,279 to cover the total cost of Erlando's procedure and care. He is scheduled to undergo corrective surgery on February 16th and after his recovery, Erlando will be able to live a happier and healthier life. Erlando's mother shared," This surgery will be the biggest blessing our child will ever receive given our economic situation. It will be a such a relief to see him grow up healthy."