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Success! Andy from Bolivia raised $1,500 to fund cardiac surgery to patch a hole in his heart, so that he can grow strong and breathe easily.

Andy
100%
  • $1,500 raised, $0 to go
$1,500
raised
$0
to go
Fully funded
Andy's treatment was fully funded on March 1, 2023.

Photo of Andy post-operation

March 12, 2023

Andy underwent cardiac surgery to patch a hole in his heart.

Andy underwent a successful surgery to patch a hole in his heart. His doctors expect a full recovery enabling him to live an active life with no further symptoms from his heart condition.

Andy told us: “I am excited to be able to run and play with my friends from now on!”

Andy underwent a successful surgery to patch a hole in his heart. His doctors expect a full recovery enabling him to live an active life wit...

Read more
November 28, 2022

Andy lives in a neighborhood of La Paz with his parents and younger sister; he is in the fifth grade and likes playing video games and spending time with his friends and family.

Andy was born with a heart condition called ventricular septal defect: a hole exists between the two lower chambers of his heart, and blood leaks through this hole without passing through his lungs to obtain oxygen, leaving him weak and short of breath. During surgery, doctors will sew a patch over this hole to close it. His surgery costs $1,500, and Andy’s family needs help to pay for it.

Andy’s mother said, “Our family is very hopeful that after this surgery Andy will have more energy and will grow bigger and stronger!”

Andy lives in a neighborhood of La Paz with his parents and younger sister; he is in the fifth grade and likes playing video games and spend...

Read more

Andy's Timeline

  • November 28, 2022
    PROFILE SUBMITTED

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

  • November 29, 2022
    TREATMENT OCCURRED

    Andy received treatment at Hospital del Niño Dr. Ovidio Aliaga Uría in Bolivia. 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 29, 2022
    PROFILE PUBLISHED

    Andy's profile was published to start raising funds.

  • March 1, 2023
    FULLY FUNDED

    Andy's treatment was fully funded.

  • March 12, 2023
    TREATMENT UPDATE

    Andy's treatment was successful. Read the update.

Treatment
Congenital Cardiac Surgery
  • Cost Breakdown
  • Diagnosis
  • Procedure
On average, it costs $4,000 for Andy's treatment
Subsidies fund $2,500 and Watsi raises the remaining $1,500
Hospital Fees
$3,000
Medical Staff
$300
Medication
$100
Supplies
$0
Travel
$600
  • 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. Parents might notice that their child 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.

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

Most congenital cardiac conditions will eventually lead to death without surgery, often within a period of months or years depending on severity. 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?

Pediatric open-heart surgery has only been made available in Bolivia in recent years. Most families are unfamiliar with the concept of open-heart surgery and are at first quite reluctant to allow their child to undergo this care. Indigenous belief systems in Bolivia can at times contribute to a family's reluctance to proceed with surgery, and must be addressed through thoughtful conversation and social accompaniment of each family.

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

What does the treatment process look like?

The child's cardiac symptoms are usually first detected by their local pediatrician, who then refers the child to the nearest pediatric cardiologist for exam and diagnosis. Once diagnosed, HCA works with the local cardiologist and the surgical team in La Paz to ensure that the child is enrolled on the waiting list for surgery at the hospital, and works directly with the family to facilitate their transportation to La Paz, often from very long distances, and to support them socially and logistically after arrival. The child then undergoes surgery and recovers for about a week in La Paz before returning home to their community. HCA then coordinates with the child's pediatric cardiologist to ensure high-quality, long-term follow-up care, and provides financial support for medications and doctor visits as needed.

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

These treatments are almost always life-saving in nature as the cardiac conditions are not survivable over the long-term without surgery. Within weeks after surgery, the patient should already 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 will separate from the edges of the hole, 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?

For families without private-sector insurance, the cardiac surgery program in La Paz is the only year-round surgical program in Bolivia capable of treating children who need open-heart surgery. Children come to this program from throughout Bolivia; many families live in extremely remote and mountainous areas that can require several days of overland travel to reach La Paz. For patients who live more than 8-10 hours away by road, HCA arranges for families to come by plane from the nearest commercial airport to their home.

What are the alternatives to this treatment?

In general, patients are treated with medications to prevent heart failure until they are able to obtain their surgeries. 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.

Dollores

Dollores is a hardworking 59-year-old woman from Philippines. She was an English as a Second Language (ESL) teacher, and then worked as a call center agent. Unfortunately, in October 2022, she was dismissed from her job due to being medically unfit. Now, she lives with her daughter and family, and the sole breadwinner is her son-in-law, who works in finance. In June 2022, Dollores noticed a mass on her right breast. At her initial examination, she was told that the mass was benign, but in a follow-up biopsy, she was diagnosed with breast cancer. Without treatment, the cancer may spread to other organs. A mastectomy, or a surgery to remove breast tissue, has been recommended to remove the cancer and prevent it from metastasizing. Fortunately, our medical partner, World Surgical Foundation Philippines (WSFP), is helping Dollores receive treatment. On January 7th, she will undergo a mastectomy at WSFP's care center. After treatment, Dollores will hopefully return to a cancer-free life. A portion of the cost of her treatment is being supported by the Philippine Health Insurance Corporation. Dollores needs help raising $1,058 to cover the remaining cost of her procedure and care. Dollores shared tearfully, "your help brings relief to my heart and mind. This will ease my worries, especially about the medical bill. I believe that there's a reason why you're saving me, and that's for me to continue with my life. Thank you, WATSI and World Surgical Foundation Philippines! I hope to give back the help that you've given me."

34% funded

34%funded
$368raised
$690to go
Samuel

Samuel is a 21-year-old talkative young man. He is the second born in a family of five children. His father passed away when he was four years old, so his mother had to raise him and his siblings by herself. She does jobs on tea farms to provide for the family. When Samuel was two years old, his abdomen started to swell, which was very painful for him. His mother took him to the hospital and he was given some medication and sent back home. The medication did not work as expected. He was then taken to a different hospital for examination. He was given more medication and after some time he seemed to be better. The stomachache did not go away completely, however. Samuel and his mother shared that over the years, he has had stomachaches and gotten used to taking pain medication. In 2017 when Samuel was in high school, the pain worsened and his abdomen started to swell again. He had to leave school as a result. His mother took him to a hospital in Meru where he was admitted for three months. While in the hospital, scans and a biopsy were done to determine what the problem was. He was given a colostomy, where the end of the colon is brought through an opening in the abdominal wall, in order to pass stool. This surgery is often performed to bypass bowel malformations, but colostomies are usually temporary and may call for closure. In Samuel's case, his colostomy requires closure in order to restore bowel function and prevent future complications. At that time, his doctors did not manage to treat him and referred him to BethanyKids Hospital in 2018. On arrival, he was examined and admitted, as he was not in good condition. After more scans and tests, he was ultimately diagnosed with Hirschsprung’s disease. Since then, Samuel has undergone several surgeries with the aim of trying to better his condition. The first surgery failed, but the second was successful. He is now scheduled to undergo his last surgery to close the colostomy so that he can pass stool on his own again and live a more active life. Earlier in his treatment, Samuel's parents had enrolled in the national health insurance program (NHIF), which helped them pay for most of his hospital bills. BethanyKids also chipped in on occasion to help with some of the bills. Unfortunately, for his last surgery, NHIF has rejected the request since he is beyond the age to be covered by his mother’s insurance. Our medical partner, African Mission Healthcare Foundation, is helping him to undergo treatment and needs $1,084 to cover the cost of a colostomy closure for Samuel. The surgery is scheduled to take place on November 11th and, once completed, will hopefully allow him to live more comfortably and confidently. Samuel’s Mother says, “For years now, I have been very worried about my son, but God has seen us through.”

82% funded

82%funded
$893raised
$190to go

Meet another patient you can support

100% of your donation funds life-changing surgery.