217 Patients Funded
$38651 Total Donated
Team Teespring is all about enabling access. We believe that everyone with an idea should have access to a market. We believe that everyone with a passion should have access to a product that shows it.
In the same vein, we believe that everyone should have access to healthcare, so that they can enhance our world by doing the things they love. That's why we created the Teespring Watsi Team. Together we aim to spread entrepreneurship, passion, and health to every corner of this globe!
Let's put some smiles on some faces!
Naw Ree is a 49-year-old woman from Thailand. Naw Ree has lived by herself in a refugee camp in northern Thailand since 2009. As a camp resident, Naw Ree receives 243 baht (approx. $8 USD) each month from an organization that supports refugee camp residents. She also works as a maternal and child health worker, receiving 900 baht (approx. $30 USD) per month. Naw Ree raises chickens and grows vegetables. Despite receiving free health care services in the camp, Naw Ree is struggling to make ends meet. On December 16th, 2020, Naw Ree went to see a woman who had recently given birth, to remind her about vaccinating her baby on time. After sitting and talking to the woman in her home, Naw Ree stood up to leave but felt light headed and fell. She put out her left hand to stop her fall, and hurt her left arm. She went to the hospital in the camp, run by Malteser International [MI] Thailand, and received pain medication and her arm was put into a sling. The next day, she was referred to Mae Seriang General Hospital for further treatment. At the hospital she received x-rays and the doctor told her that she had fractured one of the bones in her left forearm. She was then referred to Chiang Mai Hospital for further treatment, but her transfer was delayed for over two weeks due to an outbreak in COVID-19 cases in northern Thailand. Since Naw Ree lives by herself, she has to cook, wash her clothes, and feed her chickens without anyone's help, a difficult feat with her broken arm. Currently, she is in pain but has no fever. She can only fall asleep if she takes pain medication. With the help of our medical partner, Burma Children Medical Fund, Naw Ree will undergo surgery to reset her fractured bones and ensure proper healing. The procedure is scheduled for January 6th and will cost $1,500. After surgery, Naw Ree will no longer be in pain. She will be able to go back to work as a health worker and she will be able to complete her household chores without pain or discomfort. Naw Ree shared, "My greatest wish is that I recover and that I may be able to use my left arm again."
Dany is 29-years-old. She is married and her husband is a farmer. Together they have one son. When Dany's not caring for her very active child, she likes to go through Facebook and watch TV. For the past ten years, she has had consistent right ear discharge and pain. When she was a child, she had surgery for an abscess near her right ear. This infection caused a cholesteatoma, or an abnormal skin growth, to develop in the middle ear behind the ear drum. For this reason, Dany experiences hearing loss and ear discharge. It is difficult for her to hear or communicate with others. Dany traveled to our medical partner's care center to receive treatment. On January 14th, she will undergo a mastoidectomy procedure in her right ear. During this procedure, ENT surgeons will remove the cholesteatoma. Our medical partner, Children's Surgical Centre, is requesting $925 to fund this procedure. This covers medications, supplies, and inpatient care. "I really hope that after the operation my ear will be better, the hearing will be normal, the ear discharge and pain will all be gone," Dany said.
Naw Kwee Moo is a 54-year-old woman from the Karen region in Burma, who lives with her husband and their family in a refugee camp. Of her children, three daughters and three sons still live in the refugee camp along with them near the Thai-Burma border. Naw Kwee is a homemaker and her husband is currently too ill to work. Five of their children go to school in the camp, four other children have moved away, and her second oldest son graduated from a post-secondary program in May 2020. He worked as an agricultural day laborer at a nearby Thai village until mid-December 2020. Due to Covid-19 travel restrictions, he was no longer allowed to leave the camp. Naw Kwe’s household receives a monthly cash card to purchase basic rations. Although they receive free education and basic health care in the camp, they shared how hard it is to make ends meet. Starting four years ago, Naw Kwee often went to the camp’s hospital run by Malteser International (MI) Thailand to receive treatment for urinary tract infections (UTI). Most of the time, she would feel better after taking medication, but she was no longer able to work as an agricultural day laborer because of her pain. Over the next few years, she was diagnosed with chronic UTI. “I think my condition was caused from consuming dirty water,” she said. “When I worked as a day laborer, we had no access to clean water.” Naw Kwee received antibiotics through an intravenous (IV) line at the camp’s hospital. When her condition did not improve, a doctor at the camp’s hospital referred her again to Mae Sariang Hospital in March 2020. There she received a urine test and an x-ray of her kidneys, ureters and bladder. She was finally diagnosed with a right kidney stone. After multiple visits, the doctor at Mae Sariang Hospital referred her to Chiang Mai Hospital (CMH) for further treatment. However, Naw Kwee could not travel to CMH for a while due to travel restrictions after the outbreak of Covid-19. Finally, last June medical staff from her camp were able to bring Naw Kwee to Chiang Mai. During her appointment, the doctor scheduled her to undergo an intravenous pyelogram on July 16th, 2020. After she received a diagnostic test, she returned to CMH for her follow-up appointment on November 19th, 2020. During her appointment, she received more tests and it was at her next appointment Naw Kwee was told she needed to undergo multiple rounds of laser treatment to break up the stone in her kidney. She received her first round of laser treatment on February 11th, 2021. Two days later, she developed a fever and could only pass a bit of urine. She also started to experience severe back pain and other troubling symptoms. MI staff took her back to the hospital where she received an ultrasound. The nurse shared with her that after her laser treatment, the stones had broken up and many of them where now stuck in her ureter, creating a blockage. She now needs emergency surgery to remove the stones. Our Medical Partner Burma Children Medical Fund is seeking $1,500 to support her surgery and finally relieve her of her painful condition.
Sinuon is a bright 9-year-old girl. She has one younger brother, who is 6 years old and in grade one. Her mother works as a factory worker, while her father is a construction worker. In Sinuon's free time, she likes to read books, do homework from school, play with toys with her brother, watch TV and go outside with her parents. Sinuon has a condition called congenital torticollis, where she was born with a strained neck position due to a tight, short neck muscle. Doctors are not sure why children are born with this condition, but it is not an uncommon one. Sinuon's family was referred to Children's Surgical Centre by other non-governmental hospital staff who recognized that she needed specialty care. Currently, Sinuon is unable to move her neck significantly, and the appearance of her neck makes her feel more self-conscious. Fortunately, Sinuon is scheduled to undergo a contracture release surgery on her neck on February 2nd. Our medical partner, Children's Surgical Centre, is requesting $454 to cover the total cost of her procedure and care. Once recovered, she will be able to move her neck more freely and feel more comfortable with her appearance. Sinuon shared, "I hope that I will feel better and have more easy movement of my neck after surgery."
Haruna is a 10-year-old student from Tanzania. Haruna is the fourth born child in a family of five children. He is currently in Class Five, and his best subjects are mathematics and social studies. Haruna is a big lover of football, which his father says he picked at an early age. Unfortunately, a few months ago, his father has had to stop him from playing football due to the level of deformity in his legs and risk of getting a fracture. Haruna was diagnosed with genu varus. His legs bow outwards at the knee so that they do not touch. 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 difficulty walking for a distance and he is no longer able to play football, the sport he loves. The procedure Haruna needs is costly for his family. Haruna's parents are small-scale farmers of maize, beans and tobacco. They are able to get their food from the harvest of maize and vegetable and some little money from selling tobacco harvest. Now, they are appealing for financial support for Haruna's cost of care. Our medical partner, African Mission Healthcare, is requesting $880 to fund corrective surgery for Haruna. The procedure is scheduled to take place on December 3rd. Treatment will hopefully restore Haruna's mobility, allow him to participate in a variety of activities, and greatly decrease his risk of future complications. Haruna shared, “I would like to be able to walk well and play like my friends. Please help me get this treatment."
Nay Kaw is an 11-year-old boy from Burma. He lives with his parents, two older brothers and two younger sisters in a village in Karen State. Nay Kaw and his sister are both students. He is a grade one student since leaving the monkhood last year. His father is a farmer. Nay Kaw was born with a small mass on his right wrist. Once Nay Kaw's mother was able to save up and send him to Mae Tao Clinic for treatment in Thailand, Nay Kaw had the mass surgically removed in July at Mae Sot Hospital. After surgery, the biopsy revealed that the mass was caused by a hemangioma. As a result of this, the doctor referred him for further treatment in nearby Chiang Mai. Since his surgery, the pain in his wrist has decreased. However, if something touches his right wrist or if he has to carry something heavy in his right hand, he is in a lot of pain. Doctors want Nay Kaw to undergo an MRI, an imaging procedure that uses magnetic fields and radio waves to produce images of bodily organs. This scan will hopefully help doctors diagnose his condition and formulate an appropriate treatment plan. Our medical partner, Burma Children Medical Fund, is requesting $814 to cover the cost of Nay Kaw's MRI and care, scheduled for October 8th. "I want my right hand to be normal and I do not want to have an unusually large wrist," he said. "If the pain in my hand decreases, I will help my mother with the housework. If my hand will be without pain and I will be able to play with my friends at school, I will be happy with my friends again. In the future I will go school and become a good person."
Chamroeurn is a 25-year-old factory worker from Cambodia. He is the son of farmers and has two brothers and one sister. He works in a factory where stone is processed for construction. In his free time he enjoys playing football, listening to music, playing games on his phone, and helping his family around the house. In April, Chamroeurn sustained a workplace injury on his left hand while he was operating a large machine. He first sought help from a private clinic three months ago but their treatment attempts were unsuccessful. He cannot use his hand and is in a lot of pain. Fortunately, surgeons at our medical partner, Children's Surgical Centre, can help. On July 14, Chamroeurn will undergo a fracture repair procedure, which will cost $465. This procedure will heal his injured hand and allow him to regain full use. "I hope after surgery my hand will feel well and I can use it again at work. Since this injury I have not been able to earn money to support my family," shared Chamroeurn.
Susana is a 62-year-old farmer from Kenya. She is a talkative and happy grandmother who lives in along the Kerio Valley. Susana is a mother of four and is a subsistence farmer in the upcountry. She plants millet and sorghum in her small farm along the valley to meet her daily needs. She lives in a mud house with her husband. She shared that her four children did not finish school due to lack of money and are in the village doing casual jobs like working in hotels, while her two daughters are married. Susana was well until the Sunday, August 9th when she accidentally fell and injured her left hip. She is currently in pain and unable to walk. Fortunately, surgeons at our medical partner can help. On August 13th, Susana will undergo a fracture repair procedure, called an open reduction and internal fixation. This procedure will help her walk again. Now, our medical partner, African Mission Healthcare Foundation, is requesting $1,016 to fund this procedure. Susana shared, “I want to get back on my feet and resume my normal duties of farming and taking care of my husband."
Salmani is a six-month-old baby from Tanzania and the second born in his family. His parents live in Arusha where they are both subsistence farmers. Salmani was born healthy, but at the age of three months, Salmani’s mother observed that his head size looked abnormal. His neck was not as strong as a 3-month-old, and she felt his other body parts were somewhat weak. As a result of his condition, Salmani has been experiencing an increasing head circumference and inability to sit on his own. His mother took him to Mount Meru Hospital and they referred their family to Watsi's Medical Partner Care Center ALMC Hospital for treatment. She decided she had to wait to go because they could not afford to proceed with Salmani's treatment, doctor’s visits, or the tests required. Later on, they heard about Watsi's ALMC-The Plaster House program and how children with disabilities are able to be supported. Salmani's parents wish to see him be able to sit, walk one day, and also to see his head size return back to normal. Salmani has been diagnosed with hydrocephalus, a condition in which excess cerebrospinal fluid accumulates in the brain and increases intracranial pressure. Without treatment, Salmani will experience severe physical and developmental delays. Our medical partner, African Mission Healthcare Foundation, is requesting $1,300 to cover the cost of surgery for Salmani that will treat his hydrocephalus. The procedure is scheduled to take place on December 14th and will drain the excess fluid from Salmani's brain. This will reduce intracranial pressure and greatly improve his quality of life. With proper treatment, Salmani will hopefully develop into a strong, healthy young boy. Salmani’s mother shared, “Please help my son get this treatment so that we can save his life and he can be able to play like other children.”
Esther is a small-scale farmer from Kenya. She used to work in her small village farm for subsistence and her husband worked as a chef in a city restaurant. However, with the closure of businesses currently due to COVID, they have limited finances. Two years ago, Esther has been experiencing lower abdominal pain, back pain and fatigue. She has been diagnosed with a swollen abdominopelvic mass. She needs to undergo a hysterectomy, a procedure in which surgeons will remove her uterus. Our medical partner, African Mission Healthcare Foundation, is requesting $832 to fund Esther's surgery. On June 12th, she will undergo gynecological surgery at our medical partner's care center. Once recovered, Esther will be able to resume her daily activities free of pain. Esther shared hopefully, “My desire is to be treated and regain back my strength.”
Vireak is an 18-year-old student. He is the elder brother to two younger sisters. Both of Vireak's parents work in construction. In his free time, Vireak enjoys reading books, exercising, listening to music, and helping his family with cooking and taking care of his younger sisters. Vireak has been diagnosed with lumbar scoliosis. He has a curved spine causing back pain and has difficulty walking and sitting. On November 12th, surgeons at the Children's Surgical Centre (CSC) will perform an orthopedic repair surgery on Vireak to alleviate his scoliosis pain. Our medical partner is requesting $1,500 to fund his spinal surgery. Once recovered, his quality of life will significantly improve and he will be able to return to life as normal. Vireak shared, "I hope after my surgery my back gets better and I can have a straight spine and be free of discomfort."
Johnson is an 8-month baby boy from Tanzania. Johnson, the last born child in a family of four, and already is a very active and friendly little boy. Johnson's parents are both subsistence farmers. Johnson was born in a local hospital where his parents were informed that his spine was not fully formed, thus resulting in a condition known as spinal bifida. Because Johnson's condition was not severe, they were informed that he wouldn’t need treatment and that it would close on its own. As their family continued to attend clinics they were told to wait till Johnson gets to five months old for him to have any kind of treatment. At five months they took him to hospital for the treatment but the cost was too high for them to afford and they had to return home. As time went by, Johnson's mother saw that his condition could end up complicated if he didn’t get treatment soon and end up greatly affecting Johnson later in life. She decided to seek treatment. She went to Mt Meru and was referred to Watsi's Medical Partner Care Center ALMC for more help. Johnson was born with spina bifida, a type of neural tube defect in which the spine does not properly close around the spinal cord. Without treatment, Johnson is at risk of lower-limb paralysis, infection of the exposed nervous tissue, development of tethered cord syndrome, and possible developmental delays. Our medical partner, African Mission Healthcare Foundation, is requesting $1,015 to cover the cost of Johnson's spina bifida closure surgery. The procedure is scheduled to take place on September 7th. This procedure will hopefully spare Johnson from the risks associated with his condition, instead allowing him to grow and develop along a healthy trajectory. Johnson’s mother says, “We are concerned if our son does not get his spine corrected, it might affect his ability to walk. Please help my son.”