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Success! Sefania from Tanzania raised $890 to fund clubfoot repair.

  • $890 raised, $0 to go
to go
Fully funded
Sefania's treatment was fully funded on June 11, 2020.

Photo of Sefania post-operation

January 13, 2020

Sefania underwent clubfoot repair.

Sefania’s manipulation and casting clubfoot treatment is going well. This treatment is to help correct the position of his feet which make it hard for him to wear shoes, walk, and carry out his daily life activities. Through this treatment, he is able to walk like other normal children without challenges. He has been scheduled to have a final surgery to complete the treatment in February by the clubfoot specialist who will be having a clinic camp.

Sefania says, “Am happy now that my feet are being corrected, I will be able to walk normally and even play football without having to struggle due to my feet being deformed. Thank you.’’

Sefania’s manipulation and casting clubfoot treatment is going well. This treatment is to help correct the position of his feet which make i...

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December 8, 2019

Meet Sefania, a class four pupil who loves playing football. He is confident to be as good as Ronaldo in football. Unfortunately, his feet limit him from being the best player! He has bilateral clubfoot, a condition that affects the positioning of his feet. This makes it hard for him to walk or run. Despite the condition, Sefania enjoys playing football with his friends. He was reviewed in our facility and surgery to correct the deformity recommended. However, his parents are not able to raise the funds needed for the surgery. With the right surgery. Sefania will be able to walk with ease and less fatigue. He will enjoy playing football with his friends.

Sefania is the second born in a family of three children. His parents are small scale farmers, relying on subsistence output to meet their daily needs. They are not able to provide for their family and save some more for their child’s surgery. They appeal for help.

Fortunately, Sefania traveled to visit our medical partner’s care center, Arusha Lutheran Medical Centre. There, surgeons will perform clubfoot repair surgery on December 09. Our medical partner, African Mission Healthcare Foundation, is requesting $890 to fund Sefania’s clubfoot repair. After treatment, He will be able to walk easily.

Sefania says, “I would be so happy if I could walk like my friends and not have to struggle to have them help me.”

Meet Sefania, a class four pupil who loves playing football. He is confident to be as good as Ronaldo in football. Unfortunately, his feet l...

Read more

Sefania's Timeline

  • December 8, 2019

    Sefania was submitted by Robert Kariuki, Process Coordinator at African Mission Healthcare, our medical partner in Tanzania.

  • December 10, 2019

    Sefania's profile was published to start raising funds.

  • December 13, 2019

    Sefania received treatment at Arusha Lutheran Medical Centre (ALMC). 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.

  • January 13, 2020

    Sefania's treatment was successful. Read the update.

  • June 11, 2020

    Sefania's treatment was fully funded.

Funded by 18 donors

Funded by 18 donors

  • Cost Breakdown
  • Diagnosis
  • Procedure
On average, it costs $890 for Sefania's treatment
Hospital Fees
Medical Staff
  • Symptoms
  • Impact on patient's life
  • Cultural or regional significance

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

The foot is turned inward, often severely, at the ankle, and the arch of the foot is very high. Patients experience discomfort, and the affected leg may be shorter and smaller than the other.

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

These children have a difficult time walking and running. Years of trying to walk on a clubfoot will cause wounds and other skeletal problems, such as arthritis. Patients will have difficulty fitting in shoes and participating in normal play, school, and daily activities. Many Africans make their livings through manual labor, which can be difficult with an untreated clubfoot.

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

Incidence is 1/1,000 live births, or about 1,600 cases in Tanzania annually. This is roughly similar to rates in Western countries, though many cases may be missed. There is no known reason for its occurrence in this region.

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

What does the treatment process look like?

Patients will undergo a series of small operations, casting, and manipulations during their course of treatment. Patients will stay in the Plaster House, a rehabilitation center for children in Tanzania, for as long as their recovery takes.

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

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

What potential side effects or risks come with this treatment?

Clubfoot is very treatable. The surgery is minor and not risky.

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. If not treated, the condition will persist and will result in disability.

Meet another patient you can support

100% of your donation funds life-changing surgery.


Khaing is a 27-year-old woman from Thailand. She lives with her husband and a three-year-old son in a village in Mae Ramat District, Tak Province. Originally from Karen State, Burma, they moved to their current address three years ago in search of better job opportunities. Her husband is a day laborer and she is homemaker. Ten years ago, Khaing felt like her nose was blocked and that she could not breathe well. She also had a runny nose and saw a small mass in her nostril while looking at her reflection in the mirror. She did not go to see a doctor because she could not afford to pay for treatment. She also thought that she would feel better over time. However, four years ago she noticed that the mass had increased in size. She went to her local hospital in Karen State, Burma, where the doctor confirmed she has a mass in her nostril and gave her medication for a week. She did not go back to her follow-up appointment as she had run out of money. She then tried to treat herself with traditional medicine. However, this was unsuccessful as the mass continued to increase in size. In the beginning of May 2020, Khaing developed a severe headache and pain in her nose. The area around her nose also become swollen. She went to Mae Tao Clinic (MTC) on May 15, 2020 for treatment. The medic at MTC checked her nose with a flashlight and told her that she has a large mass in both of her nasal passages. She was then taken to Mae Sot Hospital (MSH) for further investigation. At MSH, she received an x-ray of her nose and the doctor told her that the masses are large and that they were infected. Khaing was told that she would need surgery to remove the masses as soon as possible. Before the surgery however, she would need to undergo a computerized tomography (CT) scan to confirm the diagnosis. Unable to pay for her CT scan nor her surgery, she went back to MTC to ask for help. The medic at MTC then referred Khaing to Burma Children Medical Fund for assistance accessing further treatment. Currently, the area around her nose is swollen and painful. She also feels like her nostrils are itchy. Her nose is blocked and has to breathe through her mouth. Although she still has a headache, the pain is now less severe because she received painkillers from the doctor at MSH. Doctors want Khaing to undergo a CT scan, a procedure in which x-ray images taken from several angles are combined to produce cross-sectional images of the body. This scan will hopefully help doctors diagnose her condition and formulate an appropriate treatment plan. Our medical partner, Burma Children Medical Fund, is requesting $414 to cover the cost of Khaing's CT scan and care, scheduled for August 21st. Khaing said, "I am depressed and I feel stressed about my condition. In the future, I want to work and support my parents. I also want my son to receive an education."

43% funded

$233to go

Meet another patient you can support

100% of your donation funds life-changing surgery.