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Success! Luis from Guatemala raised $1,500 to fund corrective surgery.

Luis
100%
  • $1,500 raised, $0 to go
$1,500
raised
$0
to go
Fully funded
Luis's treatment was fully funded on February 1, 2018.

Photo of Luis post-operation

December 15, 2017

Luis underwent corrective surgery.

Luis underwent a successful surgery to correct his cryptorchidism. He has recovered from surgery and is back at home, safe and healthy under the care of his mother.

Luis’s mother says, “Thank you so much for the great help you have given us in the operation for my son. Thankfully the doctor says that everything is well and that his surgery went well. May God bless every one of you who made this possible.”

Luis underwent a successful surgery to correct his cryptorchidism. He has recovered from surgery and is back at home, safe and healthy under...

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October 5, 2017

Luis is young boy from Guatemala. Luis has a genetic syndrome called cri-du-chat, which causes cognitive and motor delays, among other symptoms. Luis is beloved by his entire family—he loves to play and sing with his older brother, and his mother works incessantly to care for Luis provide the best for him so that he can live happily.

Luis needs to undergo surgery to treat cryptorchidism. Cryptorchidism—or undescended testicles—is a condition commonly found in young boys who were born prematurely, as Luis was. In order to treat this condition, he will undergo a simple surgery that relocates the undescended testicle into its proper position. If left untreated, Luis could be at risk for a variety of reproductive illnesses in the future, including inguinal hernia, infertility, and testicular cancer.

On October 5, Luis will undergo a procedure called an orchidopexy, which is surgery to move an undescended testicle into the scrotum and permanently fix it there. $1,500 will pay for his laboratory testing, medication, travel, and accompaniment. This treatment will lessen Luis’s chances of developing complications later in life.

Luis’s mother says, “Thank you so much for this support. I will fight with everything I have for my son to have a better life.”

Luis is young boy from Guatemala. Luis has a genetic syndrome called cri-du-chat, which causes cognitive and motor delays, among other sympt...

Read more

Luis's Timeline

  • October 5, 2017
    PROFILE SUBMITTED

    Luis was submitted by Hannah Shryer, Complex Care Coordinator/Research Intern at Wuqu’ Kawoq, our medical partner in Guatemala.

  • October 05, 2017
    TREATMENT OCCURRED

    Luis received treatment at Hospital San Juan de Dios Guatemala. 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.

  • October 05, 2017
    PROFILE PUBLISHED

    Luis's profile was published to start raising funds.

  • December 15, 2017
    TREATMENT UPDATE

    Luis's treatment was successful. Read the update.

  • February 01, 2018
    FULLY FUNDED

    Luis's treatment was fully funded.

Treatment
Orchidopexy
  • Cost Breakdown
  • Diagnosis
  • Procedure
On average, it costs $1,766 for Luis's treatment
Subsidies fund $266 and Watsi raises the remaining $1,500
Hospital Fees
$374
Medical Staff
$0
Medication
$14
Supplies
$0
Travel
$667
Labs
$57
Other
$654
  • Symptoms
  • Impact on patient's life
  • Cultural or regional significance

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

Cryptorchidism occurs when the testicle has not moved into the scrotum before birth. Sometimes, this corrects itself within the first several months of life. However, if it does not, the treatment is a simple surgery to reposition the testicle into the scrotum.

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

To develop and function normally, testicles need to move to a slightly cooler temperature than normal body temperature. If this does not occur, the male may experience fertility issues, including low sperm count and poor sperm quality, as well as higher rates of testicular cancer. Also, they are at high risk for testicular torsion, when the spermatic cord twists and cuts off the blood supply to the testicle. Limitation in blood supply to the testicle may result in the need to remove the testicle. Cryptorchidism may lead to an inguinal hernia, which is when the opening between the inguinal canal and abdomen loosens to allow part of the intestines to move into the groin area. This causes extreme pain and discomfort.

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

Cryptorchidism occurs all over the world. It is especially common in premature males with an incidence rate of roughly 30%. Only 3% of full term infant males are born with cryptorchidism. However, for the majority of both premature and full term infants, the testicle descends on its own during the first year of life, leading to a true incidence rate of roughly 1%. The main difference in Guatemala is the lack of access to necessary surgical interventions to correct cryptorchidism. Individuals may have this condition for several years until they develop effects, such as an inguinal hernia, that are so painful that the need for treatment cannot be ignored.

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

What does the treatment process look like?

The treatment for cryptorchidism is surgery, during which the surgeon places the testicle into the scrotum and stitches it into place. If the patient has an inguinal hernia due to the undescended testicle(s), it may be corrected during this surgery as well. It is either an open or laparoscopic surgery and generally requires one day in the hospital post-op.

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

This treatment allows the boy to live a normal childhood and adult life. He will no longer be at high risk of infertility or testicular cancer. He will not experience the extreme discomfort and pain of the inguinal hernia or pressure against the pubic bone.

What potential side effects or risks come with this treatment?

This condition is very treatable. This is a one-time surgery which, in the majority of cases, permanently addresses this condition. Risks are uncommon, but include excessive bleeding, severe pain, infection, and adverse reaction to anesthesia.

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

Most of the national hospitals have surgeons who can perform this procedure. In fact, our medical partner often uses these surgeons perform procedures for patients. The catch is that the hospitals and other institutions who perform these procedures may say they are free but then make up the cost of the procedure by charging patients for other — often unreasonable — things. Therefore, most of the time, patients still cannot afford to have the procedure done. Our medical partner works with patients to pay for the necessary preoperative testing and subsidize surgical fees, transportation, and lodging, so that patients can get on with their lives.

What are the alternatives to this treatment?

The alternative for most patients is simply to forgo treatment and hope for the best.

Meet another patient you can support

100% of your donation funds life-changing surgery.

Meet another patient you can support

100% of your donation funds life-changing surgery.