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Success! Daissa from Haiti raised $957 to fund life-saving hydrocephalus treatment.

Daissa
100%
  • $957 raised, $0 to go
$957
raised
$0
to go
Fully funded
Daissa's treatment was fully funded on May 4, 2022.

Photo of Daissa post-operation

May 11, 2022

Daissa underwent life-saving hydrocephalus treatment.

Our medical partner just shared great news that Daissa’s surgery went well to treat her hydrocephalus condition. The surgery will allow her the chance to grow and develop along a much healthier trajectory.

Daissa’s mother is relieved and grateful for the chance this surgery has given her little girl.

Our medical partner just shared great news that Daissa's surgery went well to treat her hydrocephalus condition. The surgery will allow her ...

Read more
March 30, 2022

Daissa is a 2-month-old baby from Haiti. She has brothers and sisters and lives with her mom.

Daissa 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, Daissa has been experiencing an increasing head circumference. Without treatment, Daissa will experience severe physical and developmental delays.

Our medical partner, Project Medishare, is requesting $957 to cover the cost of surgery for Daissa 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 March 31st. This critical treatment will place a shunt to drain the excess fluid from Daissa’s brain to reduce intracranial pressure and greatly improve her quality of life. With proper treatment, Daissa will hopefully develop into a strong, healthy young girl.

Her mom is hopeful that with treatment Daissa can grow up healthy like other children.

Daissa is a 2-month-old baby from Haiti. She has brothers and sisters and lives with her mom. Daissa has been diagnosed with hydrocephal...

Read more

Daissa's Timeline

  • March 30, 2022
    PROFILE SUBMITTED

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

  • March 31, 2022
    TREATMENT OCCURRED

    Daissa 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.

  • April 1, 2022
    PROFILE PUBLISHED

    Daissa's profile was published to start raising funds.

  • May 4, 2022
    FULLY FUNDED

    Daissa's treatment was fully funded.

  • May 11, 2022
    TREATMENT UPDATE

    Daissa's treatment was successful. Read the update.

Funded by 1 donor

Profile 48x48 589fbadd efcd 4457 b1c0 38cd87c88a22

Funded by 1 donor

Profile 48x48 589fbadd efcd 4457 b1c0 38cd87c88a22
Treatment
Hydrocephalus VPS
  • Cost Breakdown
  • Diagnosis
  • Procedure
On average, it costs $957 for Daissa's treatment
Hospital Fees
$357
Medical Staff
$100
Medication
$80
Supplies
$60
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 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.

Buradina

Buradina is a 65-year-old small scale farmer who lives with her husband. Together they have four children who are now grown and starting families of their own. Two months ago, Buradina stepped on a thorn that pierced one of the toes on her left foot. She pulled it out using her hand, but part of it remained in the toe. Her daughter tried to remove the thorn, but was also unable to do so. Buradina's foot started to swell, and so she was taken to the hospital. While at the hospital for treatment - which ultimately was unsuccessful - Buradina was diagnosed with diabetes. Fortunately she traveled to our medical partner's care center Rushoroza Hospital where her diabetes was stabilized. As the original wound on her toe hadn't healed, the infection now spread to her foot. The doctors have worked with Buradina to make the best medical plan and an amputation of her leg below the knee is now the only option for Buradina as her foot is septic, which can be life threatening. Our medical partner, African Mission Healthcare, is requesting $255 to fund Buradina's surgery, which is scheduled for June 3rd at Rushoroza Hospital. Once completed, this procedure should allow her to live more comfortably. After recovering, Buradina is most looking forward to being able to work around the house, since she may no longer be able to work on the farm. Buradina says: “I am in pain and my condition is worsening. My family cannot afford the surgery and my only hope to live a better life is through surgery. I hope and pray that I may be considered for treatment.”

0% funded

0%funded
$0raised
$255to go

Meet another patient you can support

100% of your donation funds life-changing surgery.