UNIVERSAL FUND MEMBERDesign & Dev, trying to help people who need it
United States • jeffescalante.com • Born on July 9th
Works at HashiCorp
Jeff joined Watsi on April 7th, 2013. Eight years ago, Jeff joined our Universal Fund, supporting life-changing treatments for a new Watsi patient every month. Jeff's most recent donation traveled 1,900 miles to support Stravensky, a future engineer from Haiti, to fund heart surgery.
Jeff has funded healthcare for 103 patients in 11 countries.
Jeff has funded healthcare for 103 patients in 11 countries.
Stravensky, who is 18 years old, and in his final year of high school, lives in Port-au-Prince in Haiti, with his parents and two sisters. He aspires to go on to university to study engineering. Stravensky was born with atrial septal defect, a cardiac condition, where a hole exists between the upper two chambers in his heart. Instead of circulating through his lungs and picking up oxygen, the blood leaks through the hole, leaving him weak and short of breath. Our medical partner, Haiti Cardiac Alliance, is seeking $1,500 to fund the costs of the surgery that Stravensky needs to repair his heart. The procedure, during which the hole will be repaired, is scheduled for February 1st, at Clinica Corominas. After this life changing operation, Stravensky should be able to live a healthy and comfortable life, and to pursue his ambitions without experiencing his current symptoms. From Stravensky: "I have been hoping to have my heart fixed ever since I was a small child - I can't believe it is finally happening!"
Kalyan, a 13-year-old seventh grader, lives with her mother and brother in Kandal province in Cambodia. She enjoys studying home economics and Khmer literature and would like to be a singer when she grows up. Kalyan was born with a spinal condition called listhesis, which is an unnaturally mobile vertebra that moves, leaves its normal position, and can cause different complaints when it compresses nerves and other vertebrae. Listhesis can be caused by a bone abnormality, trauma from an accident or injury, or result from a fracture or a tumor. Pinched nerves and chronic back pain are common symptoms of this condition, as is loss of flexibility and possible paralysis. Kalyan is frequently unable to attend school due to her condition. Fortunately, our medical partner, Children's Surgical Centre, can help. Specialty surgeons at Kien Khleang National Rehabilitation Centre can fuse her spine to avoid any further damage to Kalyan's back, while also alleviating her pain. Kalyan and her mother need your help to raise the $1,500 cost of the surgery, implants, hospitalization, and post-op medication. After recovery from the procedure, which is scheduled for February 7th, Kalyan's spine will be more stable, and she will be able to engage in all of the normal activities of a 13-year-old. Kalyan's mother shared: "I hope my daughter will no longer have pain and she can go back to school."
Ann is a 34-year-old widow and a mother of two children, ages 13 and 8 years old. She does odd jobs at a nearby small hotel; though she shared that her medical condition makes it hard to work. Ann started having epigastric pains in 2015 and has being treated intermittently for ulcers. She said that sometimes all her income goes to treatment, and yet she doesn’t get well. Recently, the pain became worse, and she was taken to different hospitals over the weekend before being brought to Nazareth Hospital, where she was admitted. A scan showed Cholelithiasis, and since she has severe pain on and off, the Surgeon recommended she should go for Cholecystectomy (surgical removal of the gall bladder) immediately. Unfortunately, her medical insurance (NHIF) did not approve her case, so she needs $788 to fund her surgery. If not treated, Ann will continue to experience the pain and may have complications like pancreatitis, blockage of the gall bladder with inflammation of the gall bladder. She is in severe pain already. “I am desperate, the doctor says I have to be operated on tomorrow but have no money to pay, and NHIF did not approve my application. Any support given, I will appreciate, at least to have my life back. I am the hope of my children who are still young,” said Ann quietly.
Su is 10-year-old girl who lives in Thailand. Both of her parents work for a community based organization helping others in their area. In her free time, Su likes to draw pictures and play with her friends. Su was born with clubfeet and a dislocated hip. She received corrective surgery in Chiang Mai with the help of our medical partner BCMF after she was born. During her last visit to the hospital when she was young, the doctor told her mother that they only had to return to the hospital when she outgrew her clubfeet correction shoes. However, her parents could never bring her back. In additional to financial constraints, their legal documents expired, and later when they had legal documents, they could not go to Chiang Mai due to covid-19 travel restrictions. In June 2022, Su started to experience pain in her right foot whenever she walked more than 10 minutes. She also experienced pain in her right hip for the first time when she walked. The doctor at Mae Sot Hospital diagnosed her with a dislocated hip and referred her to the larger hospital Chiang Mai for further treatment. In October an MRI was performed for Su and it was determined that she may need two surgeries: one for hrt hip and another for her clubfeet condition. The first surgery is for a hip replacement and the doctor scheduled her for surgery on November 25th so she can be out of pain as quickly as possible. Her family needs $1500 for her hip replacement surgery. Su's father said, "I am hopeful for my daughter to receive surgery soon. After surgery, I hope that she will be able to walk like other children and she will not be shy when she grows up. Now, when she goes to school, some of her friends tease her that she cannot walk properly like other children."
Saravandira is a 15-month-old infant from Haiti. She has one older brother and sister and lives with both of her parents. Saravandira has been diagnosed with hydrocephalus, a condition in which excess cerebrospinal fluid accumulates in the brain and increases intracranial pressure. As a result of her condition, Saravandira's head circumference has been increasing. Without treatment, Saravandira will experience severe physical and developmental delays. Our medical partner, Project Medishare, is requesting $897 to cover the cost of surgery for Saravandira at Hospital Bernard Mevs that will treat her hydrocephalus. This is the only site in the country where this care is currently available and the procedure is scheduled to take place on August 26th. This critical treatment will drain the excess fluid from Saravandira's brain to reduce intracranial pressure and greatly improve her quality of life. With proper treatment, Saravandira will hopefully develop into a strong, healthy young girl. The family hopes that she can grow up and be healthy enough to play with her brother and sister.
Joyce is a 52 year old, small-scale farmer. She relies on the proceeds from her small farm, and from the milk that she sells from the one cow that she and her husband own. Her husband is also a farmer, and together, they have five adult children. In October 2017, Joyce began to experience troubling symptoms, including pain in her neck - especially during swallowing - and difficulty in breathing. She went to a nearby health facility, and underwent several surgical procedures on her thyroid and esophagus, but her condition did not improve. In May of this year, Joyce presented at Kijabe Hospital with progressive difficulty in breathing. After she was evaluated and scans were done, Joyce was diagnosed with thyroid cancer. While she has an excellent prognosis, Joyce needs to be treated quickly, to prevent the cancer from spreading. Our medical partner, African Mission Healthcare Foundation, is helping Joyce access the care that she needs. She is scheduled to undergo a thyroidectomy on September 20th, at our medical partner's care center, AIC Kijabe Hospital. During this procedure, surgeons will remove all or part of Joyce's thyroid gland. This operation will cost $949, and she and her family need help raising money. Joyce says, “I am almost losing my voice. I have been through several hospitals seeking treatment. This cancer is threatening my life.”
Walendjina is an adorable two-year-old toddler from Haiti. She lives with her parents, who are both market vendors, and her two older siblings in a small village in the mountains of northwestern Haiti. Walendjina has Tetralogy of Fallot, a rare condition caused by a combination of four congenital heart conditions. These conditions include a hole between the two lower chambers of the heart and a muscular blockage of one of the valves. On August 15th, Walendjina will fly overseas to the Cayman Islands to receive treatment. During this cardiac procedure, surgeons will close the hole in her heart with a patch and remove the muscular blockage from her valve. A portion of the cost of Walendjina's treatment is being supported by Have a Heart Cayman, and our medical partner, Haiti Cardiac Alliance, is raising the remaining $1,500 to cover the cost of Walendjina's labs, medication, followup appointments, and travel fees for her and her family. Walendjina's father shares, "Our family has been very scared for our daughter's health ever since she was born. We will all be very glad to be able to stop worrying so much about her heart!"
Katelyn is an eight-year-old girl from Kenya. She is the middle child, with her older sibling being 11 years old and her younger sibling being two. Her father previously worked as a butcher in their hometown, but he has since stopped and currently does not have a source of income. Her mother is a homemaker and takes full-time care of the children. They all live together in a rental house. Katelyn was born with an ear condition, which has caused her to experience hearing loss. She eventually had to stop attending school due to her condition. She is currently unable to communicate with others despite her having some speech. Last month, Katelyn's parents took her to Kenyatta National hospital to receive medical care. After undergoing an audiogram scan, it was confirmed that Katelyn has moderate to profound hearing loss. Her doctor recommends that she receive hearing aids since this would help with her hearing and likely her speech as well. However, her family is not able to pay for them due to financial constraints. Fortunately, our medical partner, African Mission Healthcare Foundation, is helping Katelyn receive treatment on August 5th. Now, Katelyn's family needs help funding these $1,171 life-changing hearing aids. Katelyn's mother shares, “We didn’t know that she could not speak because she is unable to hear! Doctors have said that it’s possible for her to both hear and speak if she gets the aids.”
Elka is a 13-month-old baby who lives in Haiti with her parents. Both of her parents are hardworking vendors in their local market. Elka was born with a cardiac condition called patent ductus arteriosus, meaning blood leaks through a hole between two blood vessels located near her heart. This leaves her feeling weak and short of breath. Since the required treatment is not available in Haiti, our medical partner, Haiti Cardiac Alliance (HCA), is helping Elka travel to the Dominican Republic where she will be able to access the care she needs. On July 28th, she will undergo a procedure where doctors will use a catheter to plug the hole so blood can flow without issue through her body. Elka's family is looking to raise $1,500 to fund her necessary care, treatment, and travel. Elka also has a cleft lip and palate, so once her heart condition is treated, a team of doctors will soon be able to perform another surgery to repair this condition and help her have a healthier future and a full life ahead. Her mother says, "I am looking forward to my daughter growing up as a normal healthy child!"
Shantel is a 5-year-old cheerful girl from Elgeyo Marakwet County in western Kenya. Shantel is the eldest child in her family and lives with her grandmother in a semi-permanent house. Shantel's family grows maize on their small piece of land as their source of food along with casual jobs working on other farms and doing laundry to earn a living. Shantel recently visited AIC Kapsowar Hospital for an x-ray of an elbow fracture and a posterior splint for her right arm. She sustained the injury after falling from a tree while playing with other children. They visited another hospital near their home where she was stabilized with the splint, but was asked to wait to be seen by a surgeon. Shantel is right-handed and this injury has impacted her performance at school since she cannot write. An orthopedic surgeon determined that Shantel needed percutaneous pinning urgently to help restore the normal functioning of her limb and to be able to continue with her education. Our medical partner, African Mission Healthcare, is requesting $679 to cover Shantel's surgery on May 24th. Shantel's mother shared, "It hurts when my child needs help that I cannot offer her. Kindly help her so she may be able to go to school like other children.”
Shedrack is a 17-year-old teenager and the fourth born child in a family of seven. He had to drop out of school last year, but hopes to learn masonry at a local technical school so that he can work and make a living for himself. He is currently helping in looking after his family's cattle. His parents are small scale farmers, and his father also works as a night guard. His father shared that he can't yet afford to send Shedrack to the technical school. Shedrack was diagnosed with bilateral genu valgus. His legs bow inward at the knees. This condition is typically caused by an excessive accumulation of fluoride in the bones, which often stems from contaminated drinking water. As a result, he has had difficulty walking for four years now. His father says the problem started with a slight curve but over the years the curve has increased in size. Shedrack's aunt learned about Plaster House - a special site that provides a home to patients undergoing treatment at our medical partner's care center in Arusha, Tanzania. She informed Shedrack's father who brought him there seeking treatment. Unable to raise the funds needed for surgery, their family is asking for support. Our medical partner, African Mission Healthcare, is requesting $880 to fund corrective surgery for Shedrack. The procedure is scheduled to take place on May 6th. Treatment will hopefully restore Shedrack's mobility, allow him to participate in a variety of activities, and greatly decrease his risk of future complications. Shedrack says, “My legs hurt at the knees and carrying out daily life activities is now a big challenge.”
Margaret is a humble and quiet 13-year-old student, and the youngest child of three children in her family. She enjoys school, and reading in particular. Her mother works as a casual laborer at a flower farm in the area, and she is separated from Margaret's father. Margaret has clubfoot of both feet, a condition in which her feet are twisted out of shape. This causes her difficulty walking and even wearing shoes. Fortunately, our medical partner, African Mission Healthcare (AMH), is helping Margaret receive treatment. On April 11th, she will undergo clubfoot repair surgery at AMH's care center. After treatment, she will no longer use a wheelchair while in school, and she will be able to walk on her own. Now, Margaret and her family need help raising $1,286 to fund Margaret's procedure and care. Margaret's mother shared, "I will not be able to afford the estimated hospital bill despite my love for my daughter and my wish to see her walking on her feet. I request help for my daughter to undergo surgery and resume her normal life."