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Success! Nchambi from Tanzania raised $880 to fund corrective leg surgery so she can restore her mobility and return to school.

Nchambi
100%
  • $880 raised, $0 to go
$880
raised
$0
to go
Fully funded
Nchambi's treatment was fully funded on November 29, 2022.
July 4, 2022

Nchambi is a bright and creative 8-year-old student. She is the fifth born in a family of seven children from her mother. She is currently in class six, but she unfortunately had to stop her studies to seek treatment for her condition. Some of her favorite subjects in school are arts and crafts, social studies, and mathematics.

Nchambi was diagnosed with left genu varus, meaning her left leg is bent at the knee, making it difficult to walk. This condition is typically caused by an excessive accumulation of fluoride in the bones, which often stems from contaminated drinking water. As a result, she struggles with walking to school and carrying out her daily life activities, such as helping her mother with small home chores like cleaning cloths, washing plates, and sweeping. They shared that fetching water is now something she cannot do at all due to her leg condition. Recently, every morning before school, Nchambi has had to wake up extra early to prepare because it takes her a long time to make the one-kilometer walk to her school.

Our medical partner, African Mission Healthcare, is requesting $880 to fund corrective surgery for Nchambi. The procedure is scheduled to take place on July 5th. Treatment will hopefully restore Nchambi’s mobility, allowing her to participate in a variety of activities and greatly decrease her risk of future complications.

Nchambi shares, “I can’t catch up with my friends when walking to school because I am slow. I can’t walk as fast as them because of my leg.”

Nchambi is a bright and creative 8-year-old student. She is the fifth born in a family of seven children from her mother. She is currently i...

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Nchambi's Timeline

  • July 4, 2022
    PROFILE SUBMITTED

    Nchambi was submitted by Joan Kadagaya, Curative Medical Support Program-Partner Representative at African Mission Healthcare.

  • July 8, 2022
    PROFILE PUBLISHED

    Nchambi's profile was published to start raising funds.

  • July 12, 2022
    TREATMENT SCHEDULED

    Nchambi was scheduled to receive 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.

  • November 29, 2022
    FULLY FUNDED

    Nchambi's treatment was fully funded.

  • TODAY
    AWAITING UPDATE

    Awaiting Nchambi's treatment update from African Mission Healthcare.

Funded by 11 donors

Funded by 11 donors

Treatment
Fluorosis - Genu Valgus / Varus
  • Cost Breakdown
  • Diagnosis
  • Procedure
On average, it costs $880 for Nchambi'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.

Emily

Emily is a newborn baby from Kenya. She is the third born in a family of three children. Her mother is a stay-at-home mum to help raise their kids and their family relies on their father's to provide for their needs. Her father does small-scale farming and other casual jobs like ploughing farms for people. Emily 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, Emily has been experiencing an increasing head circumference since she was two months old. Her parents thought it would stop and she would grow healthier, but it did not. Her parents took Emily to a hospital in Narok town where she was examined and immediately referred to Bethanykids hospital's specialist team for treatment. On arrival, she was examined, diagnosed with hydrocephalus and sent for a scan. The family did not have money to cater for the CT scan and opted to go back home and have the scan done when they got money. Luckily, a neighbor lent them money for the CT scan, which was done, and they were able to bring back the results. She is now scheduled for surgery as soon as possible to protect her brain from being damaged by the excess fluid in the head. Without treatment, Emily will experience severe physical and developmental delays. Her family does not have medical insurance coverage and cannot raise the required amount of money to cater for the hospital bill. Our medical partner, African Mission Healthcare Foundation, is requesting $720 to cover the cost of surgery for Emily that will treat her hydrocephalus. The procedure is scheduled to take place on November 2nd and will drain the excess fluid from Emily's brain. This will reduce intracranial pressure and greatly improve her quality of life. With proper treatment, Emily will hopefully develop into a strong, healthy young girl. Emily’s father says, “I always try to see things from a positive side, and I know that God will avail the required healing for our daughter.”

22% funded

22%funded
$160raised
$560to go

Meet another patient you can support

100% of your donation funds life-changing surgery.

Emily

Emily is a newborn baby from Kenya. She is the third born in a family of three children. Her mother is a stay-at-home mum to help raise their kids and their family relies on their father's to provide for their needs. Her father does small-scale farming and other casual jobs like ploughing farms for people. Emily 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, Emily has been experiencing an increasing head circumference since she was two months old. Her parents thought it would stop and she would grow healthier, but it did not. Her parents took Emily to a hospital in Narok town where she was examined and immediately referred to Bethanykids hospital's specialist team for treatment. On arrival, she was examined, diagnosed with hydrocephalus and sent for a scan. The family did not have money to cater for the CT scan and opted to go back home and have the scan done when they got money. Luckily, a neighbor lent them money for the CT scan, which was done, and they were able to bring back the results. She is now scheduled for surgery as soon as possible to protect her brain from being damaged by the excess fluid in the head. Without treatment, Emily will experience severe physical and developmental delays. Her family does not have medical insurance coverage and cannot raise the required amount of money to cater for the hospital bill. Our medical partner, African Mission Healthcare Foundation, is requesting $720 to cover the cost of surgery for Emily that will treat her hydrocephalus. The procedure is scheduled to take place on November 2nd and will drain the excess fluid from Emily's brain. This will reduce intracranial pressure and greatly improve her quality of life. With proper treatment, Emily will hopefully develop into a strong, healthy young girl. Emily’s father says, “I always try to see things from a positive side, and I know that God will avail the required healing for our daughter.”

22% funded

22%funded
$160raised
$560to go