Read our powered by our community 🙌 Check out our 🙌
Meet another patient

Watsi logo blueWatsi

Success! Saravandira from Haiti raised $897 to fund a procedure to drain excess fluid from her brain.

Saravandira
100%
  • $897 raised, $0 to go
$897
raised
$0
to go
Fully funded
Saravandira's treatment was fully funded on December 29, 2022.

Photo of Saravandira post-operation

January 20, 2023

Saravandira underwent a procedure to drain excess fluid from her brain.

Our medical partner shared that Saravandira had a successful surgery. This procedure will allow Saravandira to grow and develop without continued complications and worry from hydrocephalus.

Her family expressed their sincere gratitude to the people that made this surgery possible for their daughter!

Our medical partner shared that Saravandira had a successful surgery. This procedure will allow Saravandira to grow and develop without cont...

Read more
August 26, 2022

Saravandira is a 15-month-old infant from Haiti. She has one older brother and sister and lives with both of her parents.

Saravandira 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, Saravandira’s head circumference has been increasing. Without treatment, Saravandira will experience severe physical and developmental delays.

Our medical partner, Project Medishare, is requesting $897 to cover the cost of surgery for Saravandira at Hospital Bernard Mevs that will treat her hydrocephalus. This is the only site in the country where this care is currently available and the procedure is scheduled to take place on August 26th. This critical treatment will drain the excess fluid from Saravandira’s brain to reduce intracranial pressure and greatly improve her quality of life. With proper treatment, Saravandira will hopefully develop into a strong, healthy young girl.

The family hopes that she can grow up and be healthy enough to play with her brother and sister.

Saravandira is a 15-month-old infant from Haiti. She has one older brother and sister and lives with both of her parents. Saravandira ha...

Read more

Saravandira's Timeline

  • August 26, 2022
    PROFILE SUBMITTED

    Saravandira was submitted by Jennifer Rogers, Chief Nursing Officer at Project Medishare.

  • August 26, 2022
    TREATMENT OCCURRED

    Saravandira received treatment at Hospital Bernard Mevs in Haiti. 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.

  • August 29, 2022
    PROFILE PUBLISHED

    Saravandira's profile was published to start raising funds.

  • December 29, 2022
    FULLY FUNDED

    Saravandira's treatment was fully funded.

  • January 20, 2023
    TREATMENT UPDATE

    Saravandira's treatment was successful. Read the update.

Funded by 15 donors

Funded by 15 donors

Treatment
Hydrocephalus ETV
  • Cost Breakdown
  • Diagnosis
  • Procedure
On average, it costs $897 for Saravandira's treatment
Hospital Fees
$357
Medical Staff
$100
Medication
$80
Supplies
$0
Labs
$10
Radiology
$350
  • Symptoms
  • Impact on patient's life
  • Cultural or regional significance

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

Families usually notice this condition with their child as their head grows large. These children do not reach normal developmental milestones and become unable to hold their head up, sit on their own, or talk. Some children become very irritable and become unable to suck and swallow so getting enough nutrition becomes difficult.

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

Children living with hydrocephaly are living with some form of brain damage that progresses as they get older. This damage will prevent them from developing on a normal trajectory. They have trouble eating, being able to sit, stand and communicate. Often they develop seizures and often experience pain and irritability. If it remains untreated, this condition will lead to death.

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

There is a lot of fear and stigma toward these patients as their heads grow large. Families with children who have hydrocephalus have trouble finding caregivers and support because of this fear. Also it is a financial burden to care for these children because of medication for seizures and the extra care they require as they grow older.

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

What does the treatment process look like?

The treatment process involves a surgery to stop the extra fluid in the brain from accumulating and putting pressure on the brain. This is done by making a hole in part of the brain to drain the liquid (ETV). The patient usually spends one or two nights in the hospital and then goes home with a tiny incision in their head and abdomen.

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

This treatment is the only thing that will save the patient’s life. This treatment will prevent further brain damage. If it is caught early it allows the child to grow and develop fully. If it is caught late, the patient can receive therapy to assist them to overcome the developmental difficulties caused by the damage already done to their brain.

What potential side effects or risks come with this treatment?

The main complication caused by this surgery is simply that is does not work. In this case the child is given another surgery and a shunt is placed.

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

There is only one hospital in the country that performs surgeries for children with hydrocephaly. This hospital is in Port au Prince, Haiti. Children that live in the North or South of the country have to travel very far for clinic visits and surgery. This requires spending all day or several days on public transport to reach the hospital.

What are the alternatives to this treatment?

There are no current alternatives this treatment. If the brain damage is too far advanced then palliative care to treat the child’s pain and support the family is the only other option.

Meet another patient you can support

100% of your donation funds life-changing surgery.

Heng

Heng is a 16-year-old student from Cambodia in the 11th grade. His father is a roof builder and his mother stays at home. He has two older sisters who live at home, but have finished school and work outside of the home. In his free time, Heng enjoys reading books, exercising, fishing, and listening to music. At school, he likes math and would like to go into Information Technology. In June 2022, Heng was in a motorcycle collision where he fractured his right shoulder, femur, and hand, as well as both clavicles and several facial bones. His family took him to a local government hospital for surgery, but five months later, he still cannot move his right shoulder, elbow, wrist, or fingers. He has been diagnosed with a brachial plexus injury on his right side. The brachial plexus is a nerve network that transmits signals from the spine to the shoulder, arm, and hand. Injuries to this nerve network can result in loss of function and sensation. Heng has difficulty with daily tasks, feels poorly, and has stopped going to school due to his injury. Fortunately, our medical partner, Children's Surgical Centre (CSC), is helping Heng receive treatment. He traveled to CSC's care center, the only center in Cambodia where the required treatment is available. On November 14th, he will undergo a brachial plexus repair surgery. After recovery, he hopes to move his shoulder and use his hand. Now, he needs help raising $709 to fund his procedure and care. Heng's mother shared, "we hope Heng will recover and use his shoulder and arm again after surgery."

36% funded

36%funded
$258raised
$451to go

Meet another patient you can support

100% of your donation funds life-changing surgery.