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Success! Joyline from Kenya raised $1,286 to fund life-changing clubfoot treatment.

  • $1,286 raised, $0 to go
to go
Fully funded
Joyline's treatment was fully funded on December 28, 2021.

Photo of Joyline post-operation

January 4, 2022

Joyline underwent life-changing clubfoot treatment.

Joyline was admitted to the hospital and had a successful clubfoot surgery. Being her second surgery, this will be very impactful to her because both of her feet are now corrected and facing in the right direction. She will enjoy being able to wear shoes, walk properly, play with her friends, her self-esteem will improve and she’ll be able to continue with her studies like other children.

“I am extremely excited and grateful to God. As a family, we had lost hope but we can now put a smile on our faces as we see our daughter undergoing her 2nd surgery, which will fully correct her feet. God bless you and continue with the good work of helping needy patients,” Joyline’s father told us.

Joyline was admitted to the hospital and had a successful clubfoot surgery. Being her second surgery, this will be very impactful to her bec...

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November 15, 2021

Joyline is a humble 9-year-old girl. She’s the only child in her family and was born with a bilateral clubfoot condition. Her father is a farmer while her mother is a housewife. Together their family lives in a rural area of Kenya.

Joyline has clubfoot of both legs. Clubfoot is a condition in which the foot is twisted out of shape. This causes difficulty walking and even wearing shoes. Joyline cannot put on shoes, walk or play with her friends. Her situation makes her lead a lonely life as her father put it. She underwent foot surgery in 2020 and her condition was partially corrected. Joyline is now scheduled to undergo a corrective osteotomy surgery.

The family is not in a financial position to cater for the surgery and is appealing for financial assistance.

Fortunately, Joyline’s family traveled to visit our medical partner’s care center, AIC Cure International Hospital. There, surgeons will perform clubfoot repair surgery on November 22nd. Our medical partner, African Mission Healthcare Foundation, is requesting $1,286 to fund Joyline’s clubfoot repair. After treatment, Joyline will be able to put on both shoes, walk comfortably, play with other children and continue with her education uninterrupted.

Joyline’s father says, “Being our firstborn child, we would love to see her grow well, join school and excel in life. Any help to make her foot look and feel better would be highly appreciated.”

Joyline is a humble 9-year-old girl. She's the only child in her family and was born with a bilateral clubfoot condition. Her father is a fa...

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Joyline's Timeline

  • November 15, 2021

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

  • November 19, 2021

    Joyline's profile was published to start raising funds.

  • November 22, 2021

    Joyline received treatment at AIC Cure International Hospital in Kenya. 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.

  • December 28, 2021

    Joyline's treatment was fully funded.

  • January 4, 2022

    Joyline's treatment was successful. Read the update.

Funded by 19 donors

Funded by 19 donors

Club Foot Correction
  • Cost Breakdown
  • Diagnosis
  • Procedure
On average, it costs $1,286 for Joyline'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 in Kenya. 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.

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. AIC Cure International Hospital is one of the few pediatric orthopedic hospitals devoted to serving the physically disabled children of Kenya. Most parents bring their children from remote areas to seek treatment.

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.


Kwan is a sweet and charming one-year-old girl who loves to dance whenever she hears music! She also likes to play with coconut leaves and pretend she is cooking with them. She lives with her parents and four brothers in Thailand. Kwan’s family fled from Karen State, Burma in 2016 due to armed conflict in their area. Her two oldest brothers and her father all work as agricultural day laborers, her other two brothers currently attend school, and her mother works as a homemaker. Her parents share that their monthly income is enough for their basic day-to-day needs, and when they feel sick, they typically use traditional medicine to manage their symptoms. One year ago on March 1st, Kwan was born at Tha Song Yang Hospital. Immediately after birth, her mother noticed that she had a small lump between her eyes. The doctor diagnosed her with encephalocele, a condition that occurs when the neural tube does not close and causes a sac-like bulge with brain tissue and spinal fluid to poke through the skull. The mass is currently increasing in size and pressing on her nostrils. Doctors want Kwan 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 formulate an appropriate treatment plan. Our medical partner, Burma Children Medical Fund, is requesting $693 to cover the cost of Kwan's CT scan and care, which is scheduled for August 8th. Kwan's mother says, “I was so happy when I heard my daughter has donors who will help support her treatment. Every night I have prayed to God to help my daughter. I want to thank the organization and the donors so much for their kindness. I want my daughter to grow up the same as other people and go to school. I want her to become an educated person. I also want her to help poor communities.”

1% funded

$683to go

Meet another patient you can support

100% of your donation funds life-changing surgery.