Sierra joined Watsi on December 8th, 2014. 20 other people also joined Watsi on that day! Sierra's most recent donation traveled 8,700 miles to support Glory, a 16-year-old aspiring newscaster from Tanzania, to fund surgery so she can use her hand again.
Sierra has funded healthcare for 71 patients in 12 countries.
Sierra has funded healthcare for 71 patients in 12 countries.
Glory lives with her grandmother in the village to attend school, while her four younger siblings live with her parents in the city. She is currently in form four and would like to be newscaster when she completes her studies. Last December, Glory developed an infection on her right hand. This affected her studies to some extent, but she was determined to go to school to complete her final year. However, the wound has now contracted as it healed, making her unable to straighten her fingers. This injury has made it difficult to hold a pen well enough to write, but she has continued her studies as best as she can. Glory's family learned that she needs surgery to heal her condition and to be able to fully use her hand in the future. Her father could not afford the cost of the surgery out of his wages earned in his construction job. But, when he heard about the visiting plastic surgery team over the radio, he decided to seek help. Now, African Mission Healthcare is seeking support to fund her surgery, which will allow her better mobility in her hand. Glory says, “It was hard for me to accept that my finger would need to be amputated but the surgeons have assured me that it will help me use my other fingers better making carrying out daily activities easier than now. Especially in my studies.”
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."
Moses is a 15-year-old and the 2nd born in a family of 5 children. He hails from a village in Migori County, Kenya and both of his parents have physical disabilities. They live in a two-roomed traditional mud house in the village. Moses is sponsored in school by an organization known as Maranatha Faith Assembly (MFA) and is in the fifth grade. His teacher reports that he is very bright and a promising student and once his condition is corrected, he can excel greatly in life. Moses has clubfoot of his right foot. Clubfoot is a condition in which the foot is twisted out of shape. This causes difficulty walking and even wearing shoes. Moses was born with bilateral clubfoot, which has greatly affected his mobility. He underwent surgery on his left foot in 2019 and has healed well. Now he needs treatment for his other foot too. Fortunately, Moses traveled to visit our medical partner's care center, AIC Cure International Hospital. There, surgeons will perform clubfoot repair surgery on January 10th. Our medical partner, African Mission Healthcare, is requesting $1,286 to fund Moses's clubfoot repair. After treatment, he will be able to walk and run well, play with friends and continue with his education uninterrupted. Moses says, “ I would love to walk and play football just like my friends.”
Mark Gabriel is a two-year-old boy from the Philippines. He loves singing the alphabet and Twinkle Twinkle Little Star. He is the oldest son of his parents. His father works as a call center agent, while his mother is a stay-at-home mom. Mark Gabriel was born with a birth condition that leads to a complete or partial intestinal blockage. He needed to undergo a series of procedures to eliminate bowel dysfunction. Fortunately, our medical partner, World Surgical Foundation Philippines, is helping Mark Gabriel receive treatment. On December 8th, he will undergo colostomy closure surgery to correct his condition. After his recovery, Mark Gabriel will no longer experience bowel dysfunction or be at risk of developing health complications in the future. Now, World Surgical Foundation Philippines is requesting $1,279 to cover the total cost of Mark Gabriel's procedure and care. Mark Gabriel's mother shared, "after his surgery, we hope that he will live a life without carrying a colostomy bag."
Dortensley is a 14-month-old baby from Haiti who is loved and cared for by his mother. Dortensley has been diagnosed with hydrocephalus, a condition in which excess cerebrospinal fluid accumulates in the brain and increases pressure within the skull. As a result of his condition, Dortensley's head grew beyond his expected development and he experiences seizures. Without treatment, Dortensley will experience severe physical and developmental delays. On November 9th, Dortensley will undergo surgery at the care center of our medical partner, Project Medishare. Surgeons will place a shunt to drain the excess fluid from Dortensley's brain to reduce intracranial pressure and greatly improve his quality of life. Upon recovery, Dortensley should develop into a strong, healthy young boy. Project Medishare is currently the only site in the country to offer this critical care and is requesting $957 to help fund Dortensley's procedure. Dortensley's mother shared that she could not afford surgery for her child, but is now feeling hopeful. She said: "There is a God after all. God bless everyone that is helping my child."
Elia is a three-year-old boy and the youngest child in a family of three children. Eli's mother sells sugar, salt, tea leaves and kerosene to people in her village to provide for the family. Elia has clubfoot of his right foot. Clubfoot is a condition in which the foot is twisted out of shape causing difficulty walking and even wearing shoes. Due to financial challenges, his parents have never been able to seek treatment for their son. Fortunately, our medical partner, African Mission Healthcare (AMH) is helping Elia receive treatment. He traveled to visit AMH's care center after a passerby who saw him struggling to walk recommended the place to their family with hopes he could be treated. On October 8th, surgeons will perform clubfoot repair surgery. After treatment, Elia will be able to walk easily. Now, AMH is requesting $935 to fund Elia's procedure and care. Elia’s mother shared, "I am struggling alone to find food for my children. Getting the money need to cover the treatment cost is not something I can afford."
Nakoyai is a 13-year-old student and the second-born child in a family of five children and lives with her parents who keep livestock for a living. Nakoyai was involved in a motorbike accident while walking to school. This left her with acquired valgus of her left foot, in which the joint of the toe closest to the ankle is bent upwards, while the others are bent downwards. She has difficulty walking and was admitted to a local hospital for almost one year, throughout which her parents spent their savings and sold most of their cattle to pay the hospital bills. Nakoyai dropped out of school after her discharge from hospital because she was no longer able to walk to her school, which was quite far from her home. One year later, she received a scholarship to join a boarding school and was brought to our medical partner's care center seeking treatment. Our medical partner, African Mission Healthcare (AMH), is requesting $880 to fund corrective surgery for Nakoyai. Treatment will hopefully restore Nakoyai's mobility, allowing her to participate in a variety of activities and greatly reducing her risk of future complications. The procedure is scheduled to take place on September 10th. Nakoyai shared, "I feel pain when I walk and I cannot play most of the sports at school because of my leg. I will be happy if my leg could be treated so that I can walk around and play like my friends.”
Evaline is a charming seven-year-old girl. She is being raised by her grandmother, while her mother is married and lives in a different part of the country. Evaline’s grandparents are small scale farmers. They harvest their own food and sell vegetables for extra income. Evaline was born with clubfoot of her left foot. Clubfoot is a condition in which the foot is twisted out of shape. She experiences difficulty walking and carrying out daily activities. Her grandmother has not yet enrolled her in school for fear of discrimination. Fortunately, our medical partner, African Mission Healthcare (AMH), is helping Evaline to receive treatment. She traveled to visit AMH's care center where surgeons will perform clubfoot repair surgery on August 10th. Now, AMH is requesting $935 to fund Evaline's surgery. With successful treatment, she will be able to walk easily and is excited to enroll in school. Evaline’s family member shared, "this condition made her father deny her but I would be glad to see her treated and grow up as a normal child."
Gift is curious, charming, and social two-year-old boy. He's the second born child in a family of three children. Both of his parents are small scale farmers who grow maize, beans, and vegetables for their food. They also go out to seek other work, such as helping on other farms, to earn an income. Gift has clubfoot of his right foot. Clubfoot is a condition in which the foot is twisted out of shape. This causes difficulty walking and even wearing shoes. Fortunately, our medical partner, African Mission Healthcare (AMH), is helping Gift receive treatment. On July 13th, surgeons at AMH's care center will perform clubfoot repair surgery. Now, AMH is requesting $935 to fund Gift's procedure. After treatment, Gift will be able to walk and wear shoes. Gift’s mother shared, "I know my son will be very happy to be able to wear shoes and walk in a normal way. Please help him have this treatment."
Ku is a seven-year-old boy who lives with his parents and two younger sisters in a refugee camp in Northern Thailand. Ku's mother weaves shirts that she sells, and Ku's father helps weave, too. Ku is a primary school student, while one of his sisters is in nursing school, and his youngest sister is too young to go to school. On June 6th, Ku and two of his friends were playing in a tamarind tree when they all fell out of the tree. Ku injured his left arm in the fall and his father carried him to the camp hospital for an exam. The medic there told Ku's father that his elbow might be broken. After they bandaged his arm, Ku visited another hospital for an x-ray and was diagnosed with a left elbow fracture. Ku is in pain and cannot bend his arm or lift anything. With the help of our medical partner, Burma Children Medical Fund (BCMF), Ku will undergo surgery to reset his fractured bones and ensure proper healing. The procedure is scheduled for June 9th and will cost $1,500. After surgery, Ku will no longer be in pain and he will be able to go back to school. He will regain full mobility in his arm. Ku's father shared, "Ku is an active boy who loves school and reading a lot. He always says that he wants to become a health worker to look after his family and others when he grows up. I want him to recover and go back to school soon."
Isaac is a 23-year-old from Kenya who works as a manual laborer, loading and off-loading sand in the Maai Mahiu area. His father passed away while he was young, and he has been living with his mother and sister. A few weeks ago, during work, Issac slipped into a ditch and broke his right femur. His colleagues came to help him and brought him to Kijabe hospital. It is difficult for Isaac to walk, and he is in chronic pain. Fortunately, surgeons at our medical partner can help. On May 11th, Isaac will undergo a fracture repair procedure, which will help him walk easily again. Now, our medical partner, African Mission Healthcare Foundation, is requesting $1,500 to fund this procedure so he can walk again. Isaac shared, “I am in pain and can’t walk without support. I am out of options since I cannot afford the cost of the treatment.”
Netsanet is a 5-month-old baby girl from Ethiopia. She has seven siblings and loves to play with all of them along with her mom and dad. Netsanet's dad is a traditional farmer. He has no land of his own, but farms another person's land and shares the fruit with the owner. He also does labor work in his free time to earn more for their family. Most of the kids in the house attend school, but the oldest ones have also started working to support their family. Netsanet 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 and reduce the risk of serious complications. Netsanet is scheduled to undergo surgery to correct her condition on April 13th. Our medical partner, African Mission Healthcare Foundation, is requesting $1,500 to cover the total cost of Netsanet's procedure and care. After her recovery, Netsanet will no longer experience bowel dysfunction or be at risk of developing health complications in the future. Netsanet's dad shared, “After receiving this treatment, I hope my baby will be able to use the bathroom comfortably.”