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Kervensley from Haiti raised $957 to fund neurosurgery to help him grow up healthy.

  • $957 raised, $0 to go
to go
Fully funded
Kervensley's treatment was fully funded on March 21, 2022.
April 15, 2022

Kervensley underwent neurosurgery but later had complications.

We just received an update from our medical partner that we wanted to share with you. Kervensley’s surgery went well and the doctors were able to place a shunt to help drain excess fluid from his brain. After recovering he was in the pediatric unit at the hospital and the medical team had to treat him for an emergency cardiac arrest. He recovered and was transferred to the pediatric intensive care unit, but sadly he had another cardiac event and passed away. Our thoughts are with his family during this difficult moment. They are grateful for all the support to try to help their son.

We just received an update from our medical partner that we wanted to share with you. Kervensley's surgery went well and the doctors were ab...

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March 7, 2022

Kervensley is a 6-month-old baby boy from Haiti. Kervensley is the firstborn child in his family and he brings his parents a great deal of joy. Kervensley has been diagnosed with hydrocephalus, a condition in which excess cerebrospinal fluid accumulates in the brain and increases intracranial pressure. Without treatment, Kervensley will experience severe physical and developmental delays.

Our medical partner, Project Medishare, is assisting Kervensley’s parents in raising $957 to cover the cost of surgery for Kervensley at Hospital Bernard Mevs. This is the only site in the country where this care is currently available and the procedure is scheduled to take place on March 7th. This critical treatment will drain the excess fluid from Kervensley’s brain to reduce intracranial pressure. With proper treatment, Kervensley will hopefully develop into a strong, healthy young boy.

Kervensley’s parents are hopeful to see their son be able to walk, talk, and play with other children as he grows older.

Kervensley is a 6-month-old baby boy from Haiti. Kervensley is the firstborn child in his family and he brings his parents a great deal of j...

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Kervensley's Timeline

  • March 7, 2022

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

  • March 10, 2022

    Kervensley 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.

  • March 11, 2022

    Kervensley's profile was published to start raising funds.

  • March 21, 2022

    Kervensley's treatment was fully funded.

  • April 15, 2022

    We received an update on Kervensley. Read the update.

Funded by 7 donors

Funded by 7 donors

Hydrocephalus VPS
  • Cost Breakdown
  • Diagnosis
  • Procedure
On average, it costs $957 for Kervensley'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?

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 putting a small tube in the brain that drains the fluid into the abdomen (VP shunt). 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?

In some children the shunt that drains the fluid into the abdomen can become blocked or infected. In these cases the shunt is removed, the infection is treated, and the shunt is replaced.

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.


Seint, who is 34 years old, lives with her parents and her aunt in Ayeyarwaddy Division in Burma. Her parents and her aunt make and sell mats from their home. When Seint was 13-years old, she noticed she started to easily tire, experienced heart palpitations, and had barely enough energy to play with her friends. Her mother took her to a nearby clinic, where the doctor examined her and told them that she had congenital heart disease. The doctor gave Seint medication, which she used together with traditional medicine. Both helped her to feel better. In November 2022, Seint felt extremely tired and experienced heart palpitations while she was completing physical exercises with her students. She also had difficulty breathing, and her vision became blurred. Her mother took her to a clinic, where she received medications which helped her to feel better. A few days later, however, she started to experience pain in her back whenever she felt tired. She also started to have difficulty breathing again, and had heart palpitations. Her mother brought her to a hospital in Yangon, where she received an echocardiogram that allowed the doctor to diagnose her with atrial septal defect. After additional testing, the doctor scheduled her to undergo urgent heart surgery at Pun Hlaing Hospital. Our medical partner, Burma Children Medical Fund, is seeking $1,500 to fund Seint's surgery, which will allow her to regain her health, and to live symptom free. Seint said: "I would like to recover as soon as possible. In the future, I will continue to work as a teacher. I love teaching students and wearing our school uniform proudly."

33% funded

$1,005to go

Meet another patient you can support

100% of your donation funds life-changing surgery.