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Collins is a young boy from Kenya who needs $1,286 to fund clubfoot repair surgery on his right foot.

Collins
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December 28, 2020

Collins is a young boy from the northeastern slopes of Mt Kenya in Meru County, Kenya. He is 5 years old and is the firstborn in a family of two children. His mother is a housewife, while his father is a mason.

Collins was born with clubfoot. Clubfoot is a condition in which the foot is twisted out of shape. Since birth, he has had serial casting treatment, but his condition has yet to improve. Both his mother and his sibling also have neglected clubfoot conditions. Collins has difficulty with walking and wearing shoes, and is unable to play with other kids.

In January 2020, he was able to undergo a left posterior medial release (PMR) with Watsi support, and his foot has corrected well. As a result of the surgery, he is able to wear his left shoe and his walking has improved. However, his right foot is still deformed and requires surgery for him to be able to walk comfortably and confidently on both feet.

Fortunately, Collins’ family traveled back to our medical partner’s care center, AIC Cure International Hospital. There, surgeons will perform clubfoot repair surgery on his right foot on January 11th. Our medical partner, African Mission Healthcare Foundation, is requesting $1,286 to fund Collins’s clubfoot repair. This surgery will be very impactful for Collins because he will be able to walk, play, and enjoy life like other children. His mother is grateful for the support for his first surgery, and again appeals for support for this procedure as their income level is not high enough to afford his needed care.

Collins’ mother shared, “I would like to thank CURE Hospital and AMH-Watsi who made possible my son’s first surgery. May the almighty God bless you. I continue to plead for support for the planned surgery on his right foot so that he can fully walk without any difficulty.”

Collins is a young boy from the northeastern slopes of Mt Kenya in Meru County, Kenya. He is 5 years old and is the firstborn in a family of...

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Collins's Timeline

  • December 28, 2020
    PROFILE SUBMITTED

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

  • January 03, 2021
    PROFILE PUBLISHED

    Collins's profile was published to start raising funds.

  • January 11, 2021
    TREATMENT SCHEDULED

    Collins was scheduled to receive treatment at AIC Cure International Hospital. 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.

  • TODAY
    AWAITING FUNDING

    Collins is currently raising funds for his treatment.

  • TBD
    AWAITING UPDATE

    Awaiting Collins's treatment update from African Mission Healthcare.

Funded by 39 donors

Treatment
Club Foot Correction
  • Cost Breakdown
  • Diagnosis
  • Procedure
On average, it costs $1,286 for Collins's treatment
Hospital Fees
$273
Medical Staff
$313
Medication
$179
Supplies
$396
Labs
$37
Radiology
$27
Other
$61
  • 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.

Rebecca

Rebecca is a 1-year-old girl from Tanzania. She is the last born in a family of two children and has started to grow into a strong and beautiful girl. Both of her parents depend on small scale farming to support their family. Rebecca was initially brought to the hospital by her parents seeking treatment to help correct her spina bifida condition. Spina bifida is a birth defect that occurs when the spine and spinal cord fail to form properly. This puts a child in danger of limb paralyses or death in case of a severe infection. At the time, Rebecca's parents could not afford the proposed surgery. Luckily, one of their friends advised them to seek help at our medical partner's care center, ALMC Plaster House. Through Watsi funding, Rebecca’s life was saved and she has been growing well since then. However, a few weeks ago, Rebecca's mother noticed her daughter's head was increasing in size at a very fast rate and she was complaining of headaches. Her parents had worked hard to save some money and got a health insurance card for their baby, so they decided to take her to the hospital to seek treatment. There, Rebecca was diagnosed with hydrocephalus, a condition in which excess cerebrospinal fluid accumulates in the brain and increases intracranial pressure. She needs to have an ETV surgery that will help relieve her of the pressure build-up, which would otherwise lead to brain damage. Unfortunately, their insurance has not matured enough to cover this kind of major surgery, so Rebecca's parents are appealing for financial support to help her. Our medical partner, African Mission Healthcare Foundation, is requesting $1,300 to cover the cost of surgery for Rebecca that will treat her hydrocephalus. The procedure is scheduled to take place on January 25th and will drain the excess fluid from Rebecca's brain. This will reduce intracranial pressure and greatly improve her quality of life. With proper treatment, Rebecca will hopefully develop into a strong, healthy young girl. Rebecca’s mother shared, “My daughter’s head is increasing in size and it is making her sick. She needs surgery but the insurance we got for her cannot cover the cost. Please help once more if it is possible because we don’t know where to run to for help besides all of you.”

92% funded

92%funded
$1,206raised
$94to go

Meet another patient you can support

100% of your donation funds life-changing surgery.

Rebecca

Rebecca is a 1-year-old girl from Tanzania. She is the last born in a family of two children and has started to grow into a strong and beautiful girl. Both of her parents depend on small scale farming to support their family. Rebecca was initially brought to the hospital by her parents seeking treatment to help correct her spina bifida condition. Spina bifida is a birth defect that occurs when the spine and spinal cord fail to form properly. This puts a child in danger of limb paralyses or death in case of a severe infection. At the time, Rebecca's parents could not afford the proposed surgery. Luckily, one of their friends advised them to seek help at our medical partner's care center, ALMC Plaster House. Through Watsi funding, Rebecca’s life was saved and she has been growing well since then. However, a few weeks ago, Rebecca's mother noticed her daughter's head was increasing in size at a very fast rate and she was complaining of headaches. Her parents had worked hard to save some money and got a health insurance card for their baby, so they decided to take her to the hospital to seek treatment. There, Rebecca was diagnosed with hydrocephalus, a condition in which excess cerebrospinal fluid accumulates in the brain and increases intracranial pressure. She needs to have an ETV surgery that will help relieve her of the pressure build-up, which would otherwise lead to brain damage. Unfortunately, their insurance has not matured enough to cover this kind of major surgery, so Rebecca's parents are appealing for financial support to help her. Our medical partner, African Mission Healthcare Foundation, is requesting $1,300 to cover the cost of surgery for Rebecca that will treat her hydrocephalus. The procedure is scheduled to take place on January 25th and will drain the excess fluid from Rebecca's brain. This will reduce intracranial pressure and greatly improve her quality of life. With proper treatment, Rebecca will hopefully develop into a strong, healthy young girl. Rebecca’s mother shared, “My daughter’s head is increasing in size and it is making her sick. She needs surgery but the insurance we got for her cannot cover the cost. Please help once more if it is possible because we don’t know where to run to for help besides all of you.”

92% funded

92%funded
$1,206raised
$94to go