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Success! Haysam from Tanzania raised $880 to fund surgery to restore his mobility.

Haysam
100%
  • $880 raised, $0 to go
$880
raised
$0
to go
Fully funded
Haysam's treatment was fully funded on July 4, 2022.

Photo of Haysam post-operation

July 18, 2022

Haysam underwent surgery to restore his mobility.

Haysam had a successful surgery that has helped his ability to walk! His family is relieved that Haysam will be able to lead an active, full, and happy childhood.

Haysam’s mother says “Thank you for your kindness, help, and support. God bless you all.”

Haysam had a successful surgery that has helped his ability to walk! His family is relieved that Haysam will be able to lead an active, full...

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June 22, 2022

Haysam is a 2-year-old boy who told us that his favorite playmate is his older brother! Haysam’s father drives a school bus, and he shared that this provides for his family’s needs but is insufficient to also cover Haysam’s medical treatment costs.

Haysam was diagnosed with acquired left valgus, which means his leg curves outward. This condition is typically caused by an excessive accumulation of fluoride in the bones, which often stems from contaminated drinking water. As a result, Haysam walks with a limp. His parents have taken Haysam to different hospitals for treatment, but they were told he would grow out of the condition in time. However, over the last few months, his walking has become more challenging, and he becomes easily exhausted when walking.

Haysam’s family was able to visit our medical partner, African Mission Healthcare (AMH), for review and treatment. On June 24th, Haysam will undergo surgery to help restore his mobility, allow him to participate in various activities, and significantly decrease his risk of future complications. AMH is requesting $880 to fund this procedure.

Haysam’s mother says, “When my son walks, people ask me what is wrong with his legs because you can see clearly, that he limps when walking. I need your help to get my son treated.”

Haysam is a 2-year-old boy who told us that his favorite playmate is his older brother! Haysam’s father drives a school bus, and he shared t...

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Haysam's Timeline

  • June 22, 2022
    PROFILE SUBMITTED

    Haysam was submitted by Edward Mugane, Impact Assessment Coordinator at African Mission Healthcare.

  • June 23, 2022
    PROFILE PUBLISHED

    Haysam's profile was published to start raising funds.

  • June 24, 2022
    TREATMENT OCCURRED

    Haysam received treatment at Arusha Lutheran Medical Centre (ALMC) in Tanzania. Medical partners often provide care to patients accepted by Watsi before those patients are fully funded, operating under the guarantee that the cost of care will be paid for by donors.

  • July 4, 2022
    FULLY FUNDED

    Haysam's treatment was fully funded.

  • July 18, 2022
    TREATMENT UPDATE

    Haysam's treatment was successful. Read the update.

Funded by 7 donors

Funded by 7 donors

Treatment
Fluorosis - Genu Valgus / Varus
  • Cost Breakdown
  • Diagnosis
  • Procedure
On average, it costs $880 for Haysam's treatment
Hospital Fees
$831
Medical Staff
$15
Medication
$11
Supplies
$0
Labs
$23
  • Symptoms
  • Impact on patient's life
  • Cultural or regional significance

​What kinds of symptoms do patients experience before receiving treatment?

Patients with genu valgum (or "knock-knees") have knees that bend inward and cause an abnormal walking gait. Patients with genu varum (or bowleggedness) have knees that bend outward and cause knee or hip pain and reduced range of motion in the hips.

​What is the impact on patients’ lives of living with these conditions?

The patient's mobility is hindered, which can prevent the patient from making a living through physical labor. The patient may also develop arthritis later in life.

What cultural or regional factors affect the treatment of these conditions?

In the United States, supplemental fluoride is added to the water to improve dental health. However, in areas of northern Tanzania, there is too much naturally-occurring fluoride in the water, which causes bone curvature.

  • Process
  • Impact on patient's life
  • Risks and side-effects
  • Accessibility
  • Alternatives

What does the treatment process look like?

After surgery, the patient will stay in the hospital for 4-5 days. During this time, the surgical wound will be monitored for swelling and infection. The patient will complete physiotherapy to help him or her walk or move the limbs. A series of X-rays will be performed over several months to monitor the healing process.

What is the impact of this treatment on the patient’s life?

The bones and joints will be aligned, and long-term disability will be prevented.

What potential side effects or risks come with this treatment?

This procedure is not risky, but it is time-consuming. The rehabilitation process can take several months.

How accessible is treatment in the area? What is the typical journey like for a patient to receive care?

Care is not easily accessible. Most patients live in remote, rural areas and are identified through mobile outreach. The pediatric surgical program at Arusha Lutheran Medical Centre was started to meet the large burden of pediatric disability in the region.

What are the alternatives to this treatment?

There are no alternatives. Although some cases can heal on their own, the patients submitted to Watsi require dedicated treatment.

Meet another patient you can support

100% of your donation funds life-changing surgery.

Su

Meet Su, a 10-year-old girl, living with her mother in Thailand. Because her parents are no longer together, Su sometimes also goes and stays with her father. Both of her parents work for local community organizations. When Su has free time, she enjoys drawing pictures, and playing with her friends. Su was born with clubfeet and a dislocated hip. After her birth, she received corrective surgery in Chiang Mai, with the help of our medical partner, BCMF. During her last visit to the hospital after her surgery, the doctor told her mother that she would need to bring Su back to the hospital after she had outgrown the special, corrective shoes she wore for her clubfeet. Due to financial constraints, issues with documentation, and the Covid pandemic, Su's parents were never able to bring her back to the hospital. In June 2022, Su started to experience pain in her right foot, whenever she walked for longer than 10 minutes. And, for the first time, she also began to feel pain in her right hip when she walked. The doctor at Mae Sot Hospital diagnosed her with a dislocated hip, and referred her to Chiang Mai for further treatment. Doctors in Chiang Mai want Su to undergo an MRI, which will help them to reach a definitive diagnosis, and to formulate a plan of treatment. Our medical partner, Burma Children Medical Fund, is requesting your help to cover the $814 cost of Su's MRI and care, scheduled for October 18th, at Maharaj Nakorn Chiang Mai Hospital. "I want my daughter to become a doctor in the future so that she can help others who also suffer from clubfeet," said Su's mother.

65% funded

65%funded
$535raised
$279to go
Samuel

Samuel is a 21-year-old talkative young man. He is the second born in a family of five children. His father passed away when he was four years old, so his mother had to raise him and his siblings by herself. She does jobs on tea farms to provide for the family. When Samuel was two years old, his abdomen started to swell, which was very painful for him. His mother took him to the hospital and he was given some medication and sent back home. The medication did not work as expected. He was then taken to a different hospital for examination. He was given more medication and after some time he seemed to be better. The stomachache did not go away completely, however. Samuel and his mother shared that over the years, he has had stomachaches and gotten used to taking pain medication. In 2017 when Samuel was in high school, the pain worsened and his abdomen started to swell again. He had to leave school as a result. His mother took him to a hospital in Meru where he was admitted for three months. While in the hospital, scans and a biopsy were done to determine what the problem was. He was given a colostomy, where the end of the colon is brought through an opening in the abdominal wall, in order to pass stool. This surgery is often performed to bypass bowel malformations, but colostomies are usually temporary and may call for closure. In Samuel's case, his colostomy requires closure in order to restore bowel function and prevent future complications. At that time, his doctors did not manage to treat him and referred him to BethanyKids Hospital in 2018. On arrival, he was examined and admitted, as he was not in good condition. After more scans and tests, he was ultimately diagnosed with Hirschsprung’s disease. Since then, Samuel has undergone several surgeries with the aim of trying to better his condition. The first surgery failed, but the second was successful. He is now scheduled to undergo his last surgery to close the colostomy so that he can pass stool on his own again and live a more active life. Earlier in his treatment, Samuel's parents had enrolled in the national health insurance program (NHIF), which helped them pay for most of his hospital bills. BethanyKids also chipped in on occasion to help with some of the bills. Unfortunately, for his last surgery, NHIF has rejected the request since he is beyond the age to be covered by his mother’s insurance. Our medical partner, African Mission Healthcare Foundation, is helping him to undergo treatment and needs $1,084 to cover the cost of a colostomy closure for Samuel. The surgery is scheduled to take place on November 11th and, once completed, will hopefully allow him to live more comfortably and confidently. Samuel’s Mother says, “For years now, I have been very worried about my son, but God has seen us through.”

74% funded

74%funded
$812raised
$271to go

Meet another patient you can support

100% of your donation funds life-changing surgery.

Su

Meet Su, a 10-year-old girl, living with her mother in Thailand. Because her parents are no longer together, Su sometimes also goes and stays with her father. Both of her parents work for local community organizations. When Su has free time, she enjoys drawing pictures, and playing with her friends. Su was born with clubfeet and a dislocated hip. After her birth, she received corrective surgery in Chiang Mai, with the help of our medical partner, BCMF. During her last visit to the hospital after her surgery, the doctor told her mother that she would need to bring Su back to the hospital after she had outgrown the special, corrective shoes she wore for her clubfeet. Due to financial constraints, issues with documentation, and the Covid pandemic, Su's parents were never able to bring her back to the hospital. In June 2022, Su started to experience pain in her right foot, whenever she walked for longer than 10 minutes. And, for the first time, she also began to feel pain in her right hip when she walked. The doctor at Mae Sot Hospital diagnosed her with a dislocated hip, and referred her to Chiang Mai for further treatment. Doctors in Chiang Mai want Su to undergo an MRI, which will help them to reach a definitive diagnosis, and to formulate a plan of treatment. Our medical partner, Burma Children Medical Fund, is requesting your help to cover the $814 cost of Su's MRI and care, scheduled for October 18th, at Maharaj Nakorn Chiang Mai Hospital. "I want my daughter to become a doctor in the future so that she can help others who also suffer from clubfeet," said Su's mother.

65% funded

65%funded
$535raised
$279to go