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Success! Kabula from Tanzania raised $1,438 to fund spina bifida and hydrocephalus treatment.

Kabula
100%
  • $1,438 raised, $0 to go
$1,438
raised
$0
to go
Fully funded
Kabula's treatment was fully funded on December 25, 2020.

Photo of Kabula post-operation

December 26, 2020

Kabula underwent spina bifida and hydrocephalus treatment.

Kabula had successful surgery which helped repair the spinal bifida condition that was putting his life at risk. He also had a VPS insertion to relieve him of the pressure build-up that was being caused by fluid accumulating in his head. This surgery helped save him from brain damage and will help him get back to good health.

Kabula’s mother shared with a hopeful smile, “I see a lot of change and improvement in my son’s health. He is now starting to eat and no longer cries a lot due to the pain and suffering he was going through due to his head being big. I can’t pay you back, but only God can and bless you all. Thank you very much.”

Kabula had successful surgery which helped repair the spinal bifida condition that was putting his life at risk. He also had a VPS insertion...

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November 1, 2020

Kabula is the fifth born child in her family and was born with Spina Bifida. Her parents were referred to a more advanced hospital for treatment but they could not afford to travel to there or the cost of treatment that would be needed.

They returned home tried to raise money but months kept passing by and they still could not afford it. Kabula kept getting sick every now and then with fever and vomiting, and her family took her to the nearby clinic where they were given medications.

Kabula’s parents separated two months ago, her mom shared, as Kabula’s father was blaming her mom for giving birth to a child with Hydrocephalus. He also felt he could not afford any treatment for her with his living as a subsistence farmer, so Kabula’s mother has been caring for her alone.

Kabula’s mother has now returned back to her parent’s house to live. Kabula has been scheduled for Spina Bifida repair surgery and a VPS insertion and her mother is requesting financial support. She said, “I have been left with no support from my husband due to our child’s condition. Please help save her life.”

Kabula is the fifth born child in her family and was born with Spina Bifida. Her parents were referred to a more advanced hospital for treat...

Read more

Kabula's Timeline

  • November 1, 2020
    PROFILE SUBMITTED

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

  • November 2, 2020
    TREATMENT OCCURRED

    Kabula 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.

  • November 3, 2020
    PROFILE PUBLISHED

    Kabula's profile was published to start raising funds.

  • December 25, 2020
    FULLY FUNDED

    Kabula's treatment was fully funded.

  • December 26, 2020
    TREATMENT UPDATE

    Kabula's treatment was successful. Read the update.

Treatment
Myelomeningocoele w/ hydrocephalus
  • Cost Breakdown
  • Diagnosis
  • Procedure
On average, it costs $1,438 for Kabula's treatment
Hospital Fees
$1,095
Medical Staff
$15
Medication
$67
Supplies
$35
Labs
$157
Other
$69
  • Symptoms
  • Impact on patient's life
  • Cultural or regional significance

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

Symptoms of hydrocephalus include an enlarged head size, irritability, abnormal accumulation of cerebrospinal fluid in the brain, and increased intracranial pressure. Cognitive development can be affected, and damage to the optic nerve can cause blindness.

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

In young children, hydrocephalus affects brain development, cognition, and vision. In older children and adults, hydrocephalus also causes headaches.

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

The burden of infant hydrocephalus in East Africa is significant, with more than 6,000 new cases estimated per year. The majority are caused by neonatal infection and vitamin deficiency, and should thus be preventable. In East Africa, the single most common cause of hydrocephalus is infection, usually via neonatal meningitis or ventriculitis. Neonatal sepsis is common and is exacerbated by the lack of skilled perinatal care for the majority of births in Africa.

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

What does the treatment process look like?

Hydrocephalus patients are usually treated within a few days of arriving at the hospital. Fortunately, our medical partner can accept many patients who would otherwise go home if they could not afford the surgery cost. Treatment involves inserting a shunt into the brain to route cerebrospinal fluid to another part of the body. One month after surgery, the patient returns for a follow-up appointment.

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

This surgery is lifesaving. The patient will no longer be at risk of cognitive and vision damage. Surgical treatment for hydrocephalus can restore and maintain normal cerebrospinal fluid levels in the brain.

What potential side effects or risks come with this treatment?

This condition is treatable, though the outcome depends on how quickly the disease is identified and treated.

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

There are few quality care centers in the region. Hospitals lack adequate resources and expertise to treat this condition. With about one neurosurgeon per 10,000,000 people in East Africa, initial treatment for hydrocephalus is often unavailable.

What are the alternatives to this treatment?

Surgery is the only option.

Meet another patient you can support

100% of your donation funds life-changing surgery.

Naw Eh

Naw Eh is a 11-year-old girl who lives with her mother, five brother and two sisters in a refugee camp. She and her siblings study in the refugee camp while her mother weaves traditional indigenous Karen shirts to earn extra income for their household. In her free time, Naw Eh loves to play with her younger brother at home. Sometimes, she will play with her friends close to her house. She wants to be an English teacher at a primary school in the future. In late July 2021, Naw Eh went out to buy some snacks from a shop. On the way to the shop, she slipped and fell on the muddy road. When she fell she hurt her left leg. Since she was able to walk slowly, the medic in the camp did not think her leg was broken and only gave her pain medication. On 19 August 2021, Naw Eh lost her grip when she was sitting down in a chair and fell down. This time she could not stand up or walk. After a doctor at Mae Sariang Hospital diagnosed her with a fractured femur, she was referred to Chiang Mai Hospital for further treatment. At that hospital, the doctor told Naw Eh's brother that they want to do an MRI of her leg to check if she has any underlying conditions that caused her to break her femur so easily. With support from Watsi, the MRI was possible and now the surgeon has determined that surgery is required to help her leg heal properly. Currently, Naw Eh suffers from pain in her left leg and she cannot move or put weight on that leg. If she moves her leg, the pain increases. Her brother needs to help her use the bedpan as she cannot walk to the toilet. He also needs to help her get dressed. She is taking pain medication to help her sleep at night. She is worried that if her condition is not treated properly, she will never be able to walk again. She misses going to school and wants to continue her studies in grade four once her school reopens. With the help of our medical partner, Burma Children Medical Fund, Naw Eh will undergo surgery to reset her fractured bones and ensure proper healing. The procedure is scheduled for September 2nd and will cost $1,500. After surgery, Naw Eh will no longer experience pain in her leg and she will be able to get herself dress and be able to walk to the toilet. Naw Eh said, "I am worried that if I do not receive surgery and receive proper treatment, I will not be able to walk again."

85% funded

85%funded
$1,278raised
$222to go

Meet another patient you can support

100% of your donation funds life-changing surgery.

Naw Eh

Naw Eh is a 11-year-old girl who lives with her mother, five brother and two sisters in a refugee camp. She and her siblings study in the refugee camp while her mother weaves traditional indigenous Karen shirts to earn extra income for their household. In her free time, Naw Eh loves to play with her younger brother at home. Sometimes, she will play with her friends close to her house. She wants to be an English teacher at a primary school in the future. In late July 2021, Naw Eh went out to buy some snacks from a shop. On the way to the shop, she slipped and fell on the muddy road. When she fell she hurt her left leg. Since she was able to walk slowly, the medic in the camp did not think her leg was broken and only gave her pain medication. On 19 August 2021, Naw Eh lost her grip when she was sitting down in a chair and fell down. This time she could not stand up or walk. After a doctor at Mae Sariang Hospital diagnosed her with a fractured femur, she was referred to Chiang Mai Hospital for further treatment. At that hospital, the doctor told Naw Eh's brother that they want to do an MRI of her leg to check if she has any underlying conditions that caused her to break her femur so easily. With support from Watsi, the MRI was possible and now the surgeon has determined that surgery is required to help her leg heal properly. Currently, Naw Eh suffers from pain in her left leg and she cannot move or put weight on that leg. If she moves her leg, the pain increases. Her brother needs to help her use the bedpan as she cannot walk to the toilet. He also needs to help her get dressed. She is taking pain medication to help her sleep at night. She is worried that if her condition is not treated properly, she will never be able to walk again. She misses going to school and wants to continue her studies in grade four once her school reopens. With the help of our medical partner, Burma Children Medical Fund, Naw Eh will undergo surgery to reset her fractured bones and ensure proper healing. The procedure is scheduled for September 2nd and will cost $1,500. After surgery, Naw Eh will no longer experience pain in her leg and she will be able to get herself dress and be able to walk to the toilet. Naw Eh said, "I am worried that if I do not receive surgery and receive proper treatment, I will not be able to walk again."

85% funded

85%funded
$1,278raised
$222to go