Emanuele joined Watsi on January 17th, 2022. 14 other people also joined Watsi on that day! Emanuele's most recent donation supported Abel, an 11-month-old baby boy from Bolivia, to fund heart surgery.
Emanuele has funded healthcare for 13 patients in 8 countries.
Emanuele has funded healthcare for 13 patients in 8 countries.
Abel, who is 11 months old, lives with his parents in La Paz. He is his parents' first child. Abel was born with a cardiac condition called ventricular septal defect. Because of this, a hole exists between the two lower chambers of his heart. Blood leaks through this hole without passing through Abel's lungs to obtain oxygen, leaving him weak and short of breath. Abel's parents sought the help of our medical partner, Haiti Cardiac Alliance, and now Abel is scheduled for surgery on January 16th, at Hospital del Niño Dr. Ovidio Aliaga Uria. During surgery, doctors will sew the hole shut, so that blood will no longer leak out. This procedure should enable Abel to grow into a healthy young boy. Abel's mother said: "Our family is praying that our son will be strong and healthy after this surgery!"
Kenenitu is a young child from Ethiopia. She is a beautiful baby who loves playing with other children. She developed bowel obstruction and an emergency colostomy surgery was done at our medical partner's care center BKMCM. The condition and care has been challenging for Kenenitu and her mother who has been affected psychologically. Kenenitu's mother is a single mom with four children. Her brother stepped in to help raise the children as her husband has left without support. Before giving birth to Kenenitu, her mother used to make injera, an Ethiopian cuisine, for a living. Currently, she is not working. The family received logistical support from an NGO to arrive at the hospital and Kenenitu's mother is staying at another NGO in Addis Ababa for medical follow-up and accommodation. Due to their financial situation, the family cannot afford the medical bills for Kenenitu's treatment. Kenenitu's mother has struggled emotionally with her daughter's condition. She said, "I wondered what was going to happen to her. I used to cry a lot and I was not in my normal mental condition. But when I heard that she could be treated, my hope was restored and I felt better." Kenenitu 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. Kenenitu is scheduled to undergo surgery to correct her condition on December 20th. Our medical partner, African Mission Healthcare Foundation, is requesting $1,500 to cover the total cost of Kenenitu's procedure and care. After her recovery, Kenenitu will no longer experience bowel dysfunction or be at risk of developing health complications in the future. Kenenitu's mother said, "After receiving treatment, I hope she will start making stool... I want to take her to school and educate her."
Emmanuel is a 17-year-old student from Haiti who hopes to become a doctor. He lives with his aunt and uncle in a neighborhood of Port-au-Prince so that he can more easily attend school, as his parents live in the countryside. Emmanuel has a cardiac condition called rheumatic mitral regurgitation, which means one of his heart valves was severely damaged from an infection he experienced in early childhood. In 2017, Emmanuel underwent heart surgery to repair his existing valve. This surgery stabilized his heart for several years, but the valve remains unable to pump blood adequately throughout his body. Emmanuel needs to undergo a second surgery to replace the valve with a prosthetic heart valve. Emmanuel will fly to the Dominican Republic to receive treatment, as this surgery is unavailable in Haiti. On November 10th, he will undergo cardiac surgery, during which surgeons will remove the damaged heart valve and implant a replacement valve. An organization called Mitral Foundation is contributing $8,000 to pay for help pay for surgery. Emmanuel's family also needs help to fund the costs of surgery prep. The $1,500 bill covers labs, medicines, and check-up and follow-up appointments. It also supports passport obtainment and the social workers from our medical partner, Haiti Cardiac Alliance, who will accompany Emmanuel's family overseas. Emmanuel shared, "I am looking forward to growing stronger and having much more energy after my surgery!"
Hsa is an 18-year-old living with his parents, three brothers and a sister, in Burma. Two of his siblings are still in school, while the remainder of his family work as subsistence farmers. Hsa, however, is currently unemployed, and enjoys playing various sports with his friends. Hsa has cataracts in both of his eyes, making it difficult for him to see clearly. Thanks to assistance from our medical partner, Burma Children Medical Fund, Hsa is scheduled for cataract surgery on October 11th, at Maharaj Nakorn Chiang Mai Hospital. During the surgery, doctors will replace Hsa's own lenses with intraocular implants, enabling Hsa to live a more independent life. Now, Hsa needs your help to fund this $1,500 procedure. Hsa said: "I wish to see again so that I can look after myself. Then my family will no longer need to assist me with everything."
Nu is a 57-year-old woman from Thailand. She lives with her husband and two sons in a refugee camp. Her sons go to school. She and her husband raise chickens and grow vegetables both for their own consumption and for sale. She has cataracts and her vision is blurry. She is often worried that she might slip and fall due to her poor vision, and she has to walk slowly and carefully. Sometimes, she will have a headache and a stiff neck. Since her vision has become blurry, she can no longer read, which she shared she especially likes to do to read the Bible or the lyrics for new hymns. Our medical partner, Burma Children Medical Fund, is requesting $1,500 to fund lens replacement surgery for Nu. On September 15th, doctors will perform a lens replacement, during which they will remove Nu's natural lenses and replace them with an intraocular lens implant in each eye. After recovery, she will be able to see clearly. Now, she needs help to fund this $1,500 procedure. “When I go to church, I feel sad because I cannot participate, like reading passages from the Bible," she shared.
Shee is a bright and caring 12-year-old girl from Thailand who likes to play the piano, listen to music, and help her caregiver garden with her friends. She lives with 30 students, including her younger brother, in the dormitory of Has Thoo Lei Learning Centre. She is currently in fifth grade, and her brother is in third grade. Both her and her brother's dormitory fees, including food and accommodations, are funded by a Christian nonprofit organization called Compassion Thailand. Both of her parents currently live in Burma and work as subsistence farmers. Her father also works as a day laborer. Shee's parents support her and her brother with their school fees and pocket money. For the past two years, Shee has dealt with femoral hernias. As a result of her condition, she experiences pain in her right groin, as well as pain and discomfort when she sits for a long period of time. When she plays with her friends or is active, the bulge increases in size. Her condition has progressively worsened, and she has had to miss school frequently as a result. Fortunately, she will undergo hernia repair surgery at Mae Sot General Hospital, our medical partner's care center. Our medical partner, Burma Children Medical Fund, is requesting $1,500 to fund Shee's hernia repair surgery. The procedure is scheduled to take place on August 22nd. Once completed, she will hopefully be able to live more comfortably. Shee says, “I want to become a nurse when I grow up one day and help people in my community who are sick and need my help.”
Abigael is a bright seven-year-old from Kenya. She is the firstborn in a family of two children. Her mother is a single mom who works to support her family by doing a variety of work on other people’s farms. Abigael attends school, and one of her favorite ways to spend time is playing with her friends, both at school and at home. Abigael was born with clubfoot on her left foot. Clubfoot is a condition in which the foot is twisted out of shape. This causes difficulty walking and even wearing shoes. Abigael's mother noticed the condition and took her to the nearest hospital when she was two weeks old. She underwent a series of casting there; however, over time, her clubfoot became progressively worse rather than improving. Fortunately, Abigael and her family traveled to our medical partner's care center, AIC Cure International Hospital, to seek treatment. There, surgeons will perform clubfoot repair surgery on July 12th. Our medical partner, African Mission Healthcare Foundation, is requesting $1,286 to fund Abigael's clubfoot repair. After treatment, she will be able to put on shoes, walk comfortably, play with her friends freely, and continue with her education uninterrupted. Abigael’s mom shares, “I request support for my daughter's clubfoot to be corrected so that she can be able to put on her shoes and walk like other children.”
Meet Tessy, a beautiful 4-year-old girl, living in Kenya. In March 2022, Tessy and several of her family members were involved in an accident. Her grandparents and an uncle did not survive this event, and Tessy's parents and her sister - and Tessy herself - were all hospitalized with traumatic injuries. Her parents and her sister have all since recovered. Tessy sustained injuries to her head, chest, hand and legs, and she remained in the Intensive Care Unit of the hospital for several months. While Tessy has a visible deformity of her left arm and her right thigh, her doctors shared that her overall progress since the accident is impressive. Some of her fractures are healing well, but the fracture of her right femur requires surgical intervention. Fortunately, our medical partner, African Mission Healthcare Foundation, is here to help Tessy access the care that she needs. On June 10th, Tessy will undergo an open reduction and internal fixation at AIC Kijabe Hospital. African Mission Healthcare Foundation is seeking $1,500 to fund this procedure, without which Tessy would find it difficult to walk, and would live in chronic pain. Tessy’s father says: “Her condition has greatly improved. She was in the ICU for almost two months and responded well to treatment. She needs the surgery to help with the healing and to be able to walk again.”
Agrey is a five-month-old baby boy, and the first child born to his parents. Agrey was born with spina bifida and bilateral clubfoot. Agrey's father, who is a truck driver at a local sand quarry, was able to find enough money to take Agrey to a referral hospital for assessment of his spina bifida. But their family could not afford to pay for the surgery necessary to correct this condition, which put Agrey at risk of losing the ability to use his lower limbs, and endangering his life in the event of a serious infection. They were referred to the Plaster House for help, and through Watsi funding, Agrey had his spina bifida corrected. Agrey's bilateral clubfoot also means that both of his feet are twisted out of shape, which would make it difficult for Agrey to walk when he gets older. Fortunately, Agrey's family brought him to Arusha Lutheran Medical Centre, our care partner's health center. There, surgeons will perform clubfoot repair surgery on May 13th. Our medical partner, African Mission Healthcare, is requesting $935 to fund this procedure and his care. After treatment, Agrey's feet will be straightened and he will be able to wear shoes and to walk easily as he grows up. Agrey’s mother says: “My son has had his first surgery of his back and it was successful. He now needs to start treatment for his feet. Thank you for your help.”
Meet Mercy, a 7-year-old jovial and calm girl. Our medical partner met Mercy at Cure Hospital's satellite clinic in Matuu, Kenya when she arrived with her mother. Mercy is a second grade student who is very bright and likes to study. Her mother is a homemaker while her father works on a tea farm whenever he can get small jobs there. Mercy has clubfoot of both of her feet. Clubfoot is a condition in which the foot is twisted out of shape. This causes difficulty walking and even wearing shoes. Fortunately, Mercy's family was referred to our medical partner's care center, AIC Cure International Hospital. There, surgeons will perform clubfoot repair surgery on April 11th. Our medical partner, African Mission Healthcare Foundation, is requesting $1,286 to fund Mercy's clubfoot repair. After treatment, she will be able to walk, play and run like other kids she knows. “As a mother, I will be so happy seeing my child walking like other children,” Mercy’s mother told us.
SokChea is a 57-year-old farmer. She and her husband farm their ancestral land; they have seven children who are all married and help them with the farming. She enjoys spending time with the family and cooking for her grandchildren. When SokChea was about ten years old, she developed chronic ear discharge from both ears. Sometimes she would experience headaches, dizziness, and ringing in her ears. The infection she had caused the tympanic membrane, or the ear drum, in both ears to perforate. Now she cannot communicate clearly with others because it is hard for her to hear. She shared that this feels embarrassing for her so she shies away from speaking with strangers. Also, the medications she has used are costly for the family. SokChea traveled to our medical partner's care center to receive treatment. On March 10th, she will undergo a myringoplasty procedure in both ears. During this procedure, surgeons will close the perforations. Our medical partner, Children's Surgical Centre, is requesting $913 to fund this procedure. This covers medications, supplies, and inpatient care. "I hope that my hearing will improve and I won't have to spend money to keep buying ear drops," SokChea told us.
Pascalina is a beautiful five-year-old girl. She's is the second-born in a family of three children, and is always notably friendly to those around her. Both of Pascalina's parents are small scale farmers, while her father also seeks out casual laboring jobs to further help earn a living. Pascalina was born as a healthy child, however when she reached one and a half her parents became concerned. At that age they had expected her to be able to stand up and walk, yet she could not. Pascalina was diagnosed with bilateral genu valgus. This is a condition typically caused by an excessive accumulation of fluoride in the bones, which often stems from contaminated drinking water. As a result, Pascalina couldn't stand or walk, as her legs were too weak. Her parents tried seeking treatment for her and used medication, but nothing seemed to help. By the time Pascalina had turned three, despite her feeble ability to stand and walk for a short distances at a time, her parents began to notice that her legs were bent inward forming knocking knees. Last year they visited a local hospital in their village seeking treatment, however were then advised to go to a referral hospital that her parents could not afford. A year later, having not received any treatment, Pascalina’s legs had become so impacted that she was unable to walk or stand without crying due to the pain she felt. A local priest advised her parents to seek care at The Plaster House, in Arusha, Tanzania. There, through internal funding, Pascalina was able to have surgery on both legs to help correct them. However, given the severity of her condition, the first surgery was not enough to fully correct her legs. As a result, she needs another surgery to complete her treatment and her parents are asking for help to fund her care. Our medical partner, African Mission Healthcare, is requesting $880 for corrective surgery for Pascalina. The procedure is scheduled to take place on February 11th. With treatment, Pascalina's mobility will hopefully be restored, which will allow her to walk without pain, and play with her siblings and friends like normal. Her risk of having future complications will decrease as well. Pascalina's mother says, "We could not afford treatment for a long time, but since the first surgery, she has improved. We wish to see her continue improving and be like any other normal child."