Charlotte Tom
Charlotte's Story

Charlotte joined Watsi on May 5th, 2014. 18 other people also joined Watsi on that day! Charlotte's most recent donation traveled 9,000 miles to support Issa, a farmer from Malawi, to fund prostate surgery.


Charlotte has funded healthcare for 27 patients in 8 countries.

All patients funded by Charlotte

Vincent is a 44-year-old man who lives with his wife and three children—ages two through eight—in a two-room rental house in Kenya. He used to work as a city council guard—commonly called council askaris—before he broke his right lower leg in a road accident in May 2007. After the accident, Vincent underwent a plating surgery to treat his broken leg. Five years later, he noted an area of swelling on his right leg. He sought medical attention for the swelling and learned that it was a cancerous tumor. Vincent started radiotherapy sessions in March 2013 at Kenyatta National Hospital. In 2015, after receiving a total of 24 radiotherapy sessions for his leg, Vincent came to Kijabe hospital with a wound on his right leg. Doctors performed an incisional biopsy and determined that Vincent has a wound ulcer that requires a skin graft and debridement. If not treated, Vincent is at risk of a severe infection, which may result in amputation of his leg. Vincent has not been able to work since the accident in 2007. House rent and other household expenses are met by his wife, who sells vegetables at a small green grocery. Given the family's financial situation, Vincent is unable to raise the amount of money needed for the treatment. $940 pays for the surgery that Vincent needs as well as 14 days of hospital care, including meals, pain medicine, antibiotics, and lab tests. Vincent's family and friends are contributing $156 to cover additional costs associated with his care. “I want to be treated and be able to provide for my family," shares Vincent. "My medical journey has been long, and I want to be able to start helping my family as I used to do."

Fully funded

Andrea is a five-month-old girl from Guatemala, who was born 13 weeks early because her mother had preeclampsia. She had to be on a ventilator the first two and a half months of her life. She has struggled to grow since then, and doctors have been puzzled with her case. First it was believed that she had sepsis, then lactose intolerance, but now her diagnosis is clearer. She has a rare genetic condition called Isovaleric Acidemia. This means that she cannot metabolize certain amino acids, meaning they accumulate in her body, reaching toxic levels. The public health care system in Guatemala in unequipped to handle her case, since her condition is so rare. If she does not receive treatment, she will likely pass away. Andrea is the youngest of two children. Her older brother, Diego, loves her a lot and often plays with her, showing her toys. Andrea's mother says that Andrea is a fighter--in her few months of life, she has spent half of it in intensive care, and has received 7 blood transfusions. Although her parents work hard to give her the best they can, her mother is unable to work because of Andrea, and her father cannot make enough money to purchase the extremely expensive formula that Andrea needs to consume to survive. This treatment, which costs $1016, will save Andrea's life. Right now, she is far too small for her age, and is struggling to gain weight. Not only will her physical strength improve with special formula, but her immune system will grow stronger, giving her body what it needs to fight off potentially-deadly sicknesses in her weakened state. Andrea's improvement will give her family hope that she can one day go to school, and be able to live with and manage her condition. "I hope that God allows the miracle of her recovery from this condition that she has," Andrea's mother shares. "I want her to be like a normal child her age, to be able to eat, go to parties with her friends, and not have restrictions."

Fully funded

Meet Rin! This two-year-old lives in Cambodia with her parents and two siblings. Children of her age often love to explore the world around them with their sense of touch, learning to pick up objects, play with toys, and eat on their own. But Rin is only able to do that tactile exploring with one of her hands. “When Rin was 6 months old, three fingers of her left hand were burned by hot water,” explains our medical partner, Children’s Surgical Centre (CSC). “The burn contracture that developed prevents full movement of that hand.” Contractures are the tightening and thickening of the skin or muscle surrounding a serious burn scar, and cannot heal without treatment. Rin needs to regain use of her hand so that she can eventually learn the many skills she will need to operate in the world independently. Fortunately, there is an operation that can make this possible. “Rin requires a release and skin graft surgery,” CSC says. In this two-part procedure, doctors will remove scar tissue from Rin’s burned hand, and replace the damaged skin with healthy skin from elsewhere on Rin’s body. “After the surgery she will regain the use of her left hand,” CSC reports. For $280, we can make this crucial operation happen for Rin. This sum will also cover the two-week hospital stay and ten days of physical therapy that the toddler will need to recover from her procedure. “I hope after surgery my daughter can use her hand properly again,” Rin’s mother shares. Let’s make that hope a reality.

Fully funded

"We would like to ask for help for the treatment of our son. We are greatly concerned for his future," share the parents of 14-month-old Archiel. Archiel lives with his family in the Philippines, and has been diagnosed with unilateral clubfoot. "Archiel cannot walk, he is only capable of rolling from left to right," shares our medical partner, International Care Ministries (ICM). "His mother observed that he has poor locomotive and speech development. This makes it hard for them to address his needs and keep him safe. One parent has to stay in the house and watch him all the time and that prevents his parents to work and sustain their family's needs." "Archiel gives his parents so much joy," ICM continues. "Though he cannot speak or walk, he manages to give happiness to his family by smiling and giggling when he is happy. Those simple moments are greatly cherished by the family. His parents are working together to supply for the needs of the family, but still, their income is not even enough for the needs of the children. That is why it is very hard for them to provide for his treatment." For $1,500, Archiel will receive treatment and surgery to correct his clubfoot. After surgery, "Archiel will be more comfortable in facing challenges in learning and development. As part of him is being treated, this can pave the way that other conditions can also be addressed. This surgery will also increase the quality of life of their family as it address the emotional needs, physical needs, and economic needs that is attached to his condition. With the surgery, he can now also start learning and developing his locomotive skills which will also hasten all other learning stages he has to face in his age," ICM adds. "We have been praying that our time to work for our family will be more than what we can do now," Archiel's parents add, "So the future of our children will be brighter. We also would like our life to become a testimony that God truly touches lives and hearts to help the poor like us. We would like to see Archiel grow, walk, go to school and fulfill whatever dream he has."

Fully funded