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Jean Emile from Haiti raised $1,500 to fund prep for cardiac surgery.

Jean Emile
100%
  • $1,500 raised, $0 to go
$1,500
raised
$0
to go
Fully funded
Jean Emile's treatment was fully funded on May 1, 2018.
June 26, 2018

Jean Emile received partial treatment.

After arrival at the hospital, Jean Emile underwent a cardiac catheterization, which revealed a much greater risk to attempting surgery than was previously understood based on echocardiogram alone. Based on this new information, the hospital decided not to proceed with surgery and instead asked Haiti Cardiac Alliance to pursue placement at another overseas center that specializes in Jean Emile’s specific condition. Thankfully, another hospital agreed to accept his case and Jean Emile will be traveling again later this year for another attempt to treat his condition.

After arrival at the hospital, Jean Emile underwent a cardiac catheterization, which revealed a much greater risk to attempting surgery than...

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March 30, 2018

Jean Emile is a preschooler from Haiti. He lives with his mother, father, and two brothers in a neighborhood of Port-au-Prince. He has been attending preschool, and likes playing with cars and action figures.

Jean Emile has a cardiac condition called large ventricular septal defect. A hole exists between the two lower chambers of his heart. Blood leaks through this hole without first passing through the lungs to obtain oxygen, leaving him sick and short of breath.

Jean Emile will fly to Cayman Islands to receive treatment. On April 6, he will undergo cardiac surgery, during which surgeons will sew a patch over the hole so blood can no longer leak through it. Another organization, Health City Cayman Islands, is contributing $17,000 to pay for surgery.

Jean Emile’s family also needs help to fund the costs of surgery prep. The $1,500 bill covers labs, medicines, and checkup and followup appointments. It also supports passport obtainment and the social workers from our medical partner, Haiti Cardiac Alliance, who will accompany Jean Emile’s family overseas.

His mother says, “I have been praying for years that my son could have this surgery. I am very excited the time has arrived!”

Jean Emile is a preschooler from Haiti. He lives with his mother, father, and two brothers in a neighborhood of Port-au-Prince. He has been ...

Read more

Jean Emile's Timeline

  • March 30, 2018
    PROFILE SUBMITTED

    Jean Emile was submitted by Owen Robinson, Executive Director at Haiti Cardiac Alliance.

  • April 2, 2018
    PROFILE PUBLISHED

    Jean Emile's profile was published to start raising funds.

  • April 6, 2018
    TREATMENT SCHEDULED

    Jean Emile was scheduled to receive treatment at Health City Cayman Islands in Cayman Islands. 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.

  • May 1, 2018
    FULLY FUNDED

    Jean Emile's treatment was fully funded.

  • June 26, 2018
    TREATMENT UPDATE

    Jean Emile's treatment was started but not completed. Read the update.

Treatment
Overseas Prep and Transportation
  • Cost Breakdown
  • Diagnosis
  • Procedure
On average, it costs $1,980 for Jean Emile's treatment
Subsidies fund $480 and Watsi raises the remaining $1,500
Hospital Fees
$0
Medical Staff
$450
Medication
$360
Supplies
$0
Travel
$900
Labs
$180
Other
$90
  • Symptoms
  • Impact on patient's life
  • Cultural or regional significance

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

When a hole exists in the heart, a physician can hear a buzzing noise, or murmur, in the child's chest as blood passes through the hole at high velocity. The child's parents might notice that their son or daughter cannot keep up with other children in daily activities. In severe cases, the lack of oxygen in the bloodstream can lead to dramatic symptoms, such as blue lips and tongue, clubbed fingers and toes, and heart failure. The patients treated by Haiti Cardiac Alliance tend to fall into two categories. They are either born with some type of hole or defect in the heart, or they develop valve disease as a result of an untreated strep throat infection (rheumatic fever). Patients with rheumatic valve disease experience swelling of the abdomen and extremities, as the heart tries to circulate blood through the body despite the valve's dysfunction.

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

Virtually all of the conditions treated at Haiti Cardiac Alliance will eventually lead to death without surgery, the majority of them within one to two years. In the meantime, patients experience heart failure as their hearts struggle to compensate for the presence of leaks or other defects. In most conditions, the heart becomes fatigued, limiting the child's ability to be active, go to school, and participate in daily life.

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

Families in Haiti often have complex cultural mechanisms for understanding cardiac illnesses and their causes, sometimes involving voudou or other religious belief systems. Nevertheless, the overwhelming majority of Haitian families in our medical partner's program also engage with the medical explanations and treatment of these conditions. Parents are willing and cooperative participants in their child's treatment.

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

What does the treatment process look like?

The patient is first referred to our medical partner, Haiti Cardiac Alliance (HCA), by a pediatrician or another medical practitioner who detects symptoms that might be cardiac in nature. HCA staff then perform an echocardiogram to diagnose the cardiac condition. If surgery is required, the child joins a triaged waitlist to be placed for surgery with partner hospitals. It can sometimes take 6-12 months to move through this waitlist. During this period, HCA provides periodic cardiac checkups, changing the patient's triage position as appropriate. The child and his/her guardian then travel to the hospital with an HCA social worker. Typically, the child spends 4-5 days in or near the hospital prior to surgery for testing and examinations. After surgery, he or she spends several more days as an inpatient prior to being discharged. When the child is strong enough to travel, usually after several more weeks, he/she returns home to Haiti. HCA provides regular cardiac checkups for at least five years postoperatively before the final discharge from their program.

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

These treatments are almost always life-saving in nature. These cardiac conditions are not survivable over the long-term without surgery. Within weeks after surgery, the patient should notice a difference in energy level. Many patients also undergo a growth spurt and/or gain significant weight after a surgery.

What potential side effects or risks come with this treatment?

The risk of death during or shortly after an open-heart surgical procedure is about 3%. Other risks, though rare, include stroke and post-operative infection. In a small percentage of cases, the material used to patch the hole "blows," and a follow-up surgery is necessary to re-patch the defect.

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

Patients come to Haiti Cardiac Alliance (HCA) from the entirety of Haiti. This can involve three days of travel in buses, pickup trucks, or even on horseback. There is no cardiac surgery of any kind available in Haiti outside of the HCA treatment network.

What are the alternatives to this treatment?

In general, patients are treated with medications to prevent heart failure until they are ready to travel. Patients may also seek care from traditional healers, who may use liquids and powders derived from local plants and roots.

Meet another patient you can support

100% of your donation funds life-changing surgery.

Kidus

Kidus is a cute and playful little boy. He loves playing with toys and football with other children. His favorite food is Shiro (Ethiopian staple food) and meat. He also loves watching cartoons and is good at observing and imitating some characters from cartoon shows. He is the only child in the family. His dad is a tailor, employed at a local tailor shop. His father uses the little income to provide food for their family and pay rent. Kidus was born with a congenital anomaly called bladder exstrophy and he underwent surgery at BethanyKids with Watsi's support in 2021 to heal this condition. He was also born with a congenital anomaly called epispadias and has an inguinal hernia. Now he is scheduled for epispadias and right inguinal hernia repair. Epispadias impacts his ability to urinate and puts him at risk of future complications. Kidus is now much more playful than beforeand his family can see how intelligent he is. His family also shared how very much better psychologically they feel after his first treatment. But they are still worried about his urinary condition. He is now scheduled for the two surgeries that will take place simultaneously, and his family needs financial support. Kidus' father said, “Kidus means the world to me. To see him completely well will bring me so much joy. I want him to have a great personality with a kind heart; just like the amazing people helping him recover and become healthy. I really hope that he becomes a doctor in the future and helps those who are in need.”

0% funded

0%funded
$0raised
$1,040to go

Meet another patient you can support

100% of your donation funds life-changing surgery.