Daniel VivarelliMONTHLY DONOR
Daniel's Story

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.

Impact

Daniel has funded healthcare for 120 patients in 16 countries.

All patients funded by Daniel

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.

36%funded
$300raised
$514to go

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.”

$720raised
Fully funded

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.“

83%funded
$972raised
$199to go

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.

$709raised
Fully funded

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.”

$1,151raised
Fully funded