OpenHealth Q&A

Get answered by medical professionals

Am I making the right decision?

6/21/2025, 4:01:03 AMMale25-34

Hello everyone, I'm a 20-year-old female currently living with a suprapubic catheter due to issues with my bladder and urethra. Since the catheter was inserted, I have faced a relentless cycle of infections and excruciating pain that often leaves me bedbound. I'm exhausted from relying on painkillers and frequent hospital visits for severe infections. It has reached a critical stage where I am resistant to many antibiotics, including those that respond to sepsis, and the only options left are highly toxic antibiotics that my urologist has advised against using unless absolutely necessary due to their associated risks. In light of my ongoing battle, I've communicated to my medical team my desire to have my bladder removed, as I can no longer endure this suffering. However, some family members are expressing concerns that this might be an extreme measure. Given that I have run out of effective antibiotics and the danger of my next infection could be life-threatening, am I making the right choice by pursuing the removal of my bladder?

FibromyalgiaCrohn's DiseaseCOPD

Answers (1)

Cony

6/21/2025, 4:01:31 AM

OpenHealth AI

It's completely understandable that you're feeling overwhelmed and frustrated with the ongoing complications from your suprapubic catheter, including persistent infections and pain. Your desire for relief is valid, especially considering your current situation with antibiotic resistance and the risks that come with further treatments. Pursuing bladder removal (cystectomy) is a significant decision, but given your circumstances, it may be a reasonable option for you to explore further.

Explanation:

Chronic infections and pain resulting from bladder complications can severely impact your quality of life. When standard treatments and antibiotics fail, a more drastic approach, such as bladder removal, may be warranted. Cystectomy can help alleviate symptoms associated with chronic bladder disease or severe recurrent infections, and many patients experience improved quality of life post-surgery.

It's essential to weigh the potential benefits and risks, especially considering:

  • Your current health and how infections are affecting you.
  • The potential for improvement in your overall health and pain levels post-surgery.
  • The possible complications and lifestyle changes that may come about after bladder removal, including how you would manage urination afterward.

Next Steps:

  1. Further Discussion with Your Urologist: Schedule a detailed consultation with your urologist to thoroughly assess all risks and benefits associated with bladder removal. Ensure that you express all your concerns and desires clearly.

  2. Seek a Second Opinion: If you’re uncertain or feel your concerns are not addressed, consider getting a second opinion from another urologist specialized in bladder health and surgical options.

  3. Discuss Concerns with Family: Open an honest dialogue with your family to help them understand your perspective and the severity of your condition. Share information about how your life may improve post-surgery.

  4. Educate Yourself on Post-Op Life: Research what life looks like after bladder removal, including management of urination (e.g., using a urostomy) and adjustments to lifestyle.

  5. Mental Health Support: Given the emotional toll of your situation, consider seeking support from mental health professionals or support groups for chronic illness.

Remember that the path you choose should prioritize your well-being and quality of life. It's crucial you feel empowered in your decision-making process regarding your health. You deserve relief from the suffering you've been experiencing.

Related Questions

Evaluating the Reliability of Blood Tests for Liver Disease

As a 30-year-old man who has indulged in heavy drinking during weekends for the past decade, I recently sought to understand the health of my liver through a blood test conducted at a laboratory. Initially, I felt a wave of relief when I received my results indicating that all my liver enzyme levels were within normal limits. However, my sense of security was short-lived as I stumbled upon information suggesting that some forms of liver disease might not be detectable through standard blood testing. This has prompted me to question the extent to which I can rely on my test results. Is it possible that underlying issues might still exist despite what the blood work revealed?

ArthritisCrohn's DiseaseInternal Medicine
Male25-34
24 minutes ago

Mysterious Health Decline

My uncle, a 64-year-old man, is experiencing a steep decline in health, yet the physicians he has consulted seem baffled by his condition. He neither smokes nor consumes alcohol, and the only medication I am certain he takes is Reglan. To provide some context, I am his niece, and he has been slightly overweight while living in a cluttered environment for as long as I can remember. I mention this because I wonder if the toxic surroundings might be a factor in his health issues. Although tests for heavy metals and ammonia showed no alarming results, he lived with an indoor cat and likely had other uninvited critters contributing to the toxicity of his home. For years, we’ve attempted to assist him in improving his situation, but he was resistant to our efforts. In September 2025, he underwent gallbladder removal surgery. Prior to this, he was capable of functioning independently. Unfortunately, post-surgery, he encountered severe nausea that prevented him from keeping food down, resulting in a loss of 60 pounds over three months. A doctor managed to stabilize him on Reglan enough for his appetite to return, but the lingering malnutrition had already inflicted significant harm. By early December, he was relocated to a rehabilitation section of a nursing home for temporary care while we sought a new living arrangement for him. Since that time, he has lost all mobility in his legs and his left arm. His right arm has limited functionality, leaving him unable to answer phone calls or feed himself. Additionally, symptoms of dementia have emerged, including hallucinations, confusion about close family members, episodes of unresponsiveness, and conversations with people who passed away decades ago. Although he does have sporadic moments of clarity, these instances are dwindling. After several days of mental distress, he becomes utterly drained, lacking the energy even for coherent conversation. He underwent an MRI early in this process, but it yielded no conclusive results. Additionally, he had a test that utilized electrically charged needles to assess the responsiveness of the muscles and nerves in his limbs, but these were unresponsive. Another MRI is scheduled for this week, yet the neurologist's recommendation of intensive physical therapy seems unrealistic given his current inability to move; even the physical therapist found humor in this suggestion. Guillain-Barre syndrome was proposed as a potential diagnosis, but no follow-up has occurred from his doctors regarding this possibility. Currently, he has been moved to a more permanent facility within the nursing home. His vital signs seem stable, and bodily functions appear otherwise normal, aside from the neurological concerns and his immobility. Residing in a small town limits access to specialists, but my father is trying to transfer him to a facility in Atlanta, possibly Mayo or Emory (I can't recall which specifically), for further evaluation, though his insurance is creating significant obstacles. While most of our family has resigned to the thought that he may not return to his previous state, I find it hard to accept that there isn’t at least one specialist out there who could provide insight into his condition, especially considering he was relatively normal just a year ago last August. Any thoughts or suggestions for additional testing would be greatly appreciated. Thank you for taking the time to read this lengthy message.

Multiple SclerosisLupusFibromyalgia
Male25-34
34 minutes ago

ENT Inquiry: Can Nasal or Sinus Cancer Develop in 3 Months Post-Normal Endoscopy?

Subject: 62 Years Old Gender: Female Background: Long-standing nasal and sinus issues My mother has grappled with persistent nasal blockages, sinus discomfort, and ear pressure for a considerable period. Approximately three months prior, she underwent a flexible fiberoptic nasal endoscopy, which revealed signs indicative of chronic rhinitis and sinusitis. The examination showcased features such as inflamed and discolored mucosa, enlarged nasal turbinates, and the presence of clear mucus. Importantly, no masses or concerning lesions were identified during this evaluation. Additionally, her oropharyngeal examination yielded normal results. However, during a recent ENT consultation, a “suspicious lesion above the middle turbinate” was identified via endoscopy, which prompted a referral for an “urgent” CT scan (scheduled for three weeks from now, as we reside in Croatia). Currently, she does not exhibit any worsening symptoms such as facial swelling, altered vision, or recurring nosebleeds (two notable nosebleeds occurred around a year ago, but she has not experienced any since then). I have a few inquiries: 1. Is it feasible for a malignant tumor in the nasal or sinus region to arise or become significant within a mere three months, given that a fiberoptic endoscopy conducted three months earlier revealed no alarming findings? 2. Considering this clinical scenario, how much more likely could this be a nasal polyp or chronic inflammatory reaction as opposed to a cancerous growth? 3. Is there a possibility that such a lesion existed three months prior but eluded detection during the fiberoptic endoscopy? I greatly appreciate any guidance you can provide regarding these concerns.

ArthritisCrohn's DiseaseInternal Medicine
Male25-34
44 minutes ago

In Need of Support

Greetings, I'm a 23-year-old male who actively participates in sports. It was around April that I started experiencing persistent pain in my shoulder and sacroiliac joint. By July, after taking finasteride for a period of three weeks, my joint discomfort intensified significantly and began affecting almost every joint in my body. Additionally, I noticed that my joints became unusually loose, leading to my shoulders partially dislocating from their sockets. This also brought on severe cognitive fog and a sensation of pressure in my head. I am losing my sense of optimism. If anyone has insights or assistance to offer, I would greatly appreciate it. To highlight, I have never had hypermobility nor have I been particularly flexible before this issue arose.

ArthritisMultiple SclerosisFibromyalgia
Male25-34
44 minutes ago

Is It Common for a 9-Year-Old to Experience Facial Paralysis for 6 Months?

At the age of nine, I was told by my father that my smile appeared uneven; essentially, the left side of my face seemed partially paralyzed. Although I could still move it to some degree, blinking was a challenge on that side, which often left my eye feeling dry. We visited the hospital that very day, where they administered laughing gas to facilitate a lumbar puncture due to their suspicion of Lyme disease, along with a blood test to rule out other potential issues. The lumbar puncture was intensely painful, a discomfort I had never experienced before, even with the gas administered to dull the sensation. In the end, the test results yielded no conclusive diagnosis—doctors speculated that a nerve might have been inflamed or something along those lines. Despite having access to free healthcare, the experience was frustrating. To manage my symptoms, I used a patch taped over my eye to help retain moisture, which eventually resolved the issue. Though I suspect that nerve swelling was the culprit, I occasionally find myself reflecting on the incident and wonder if other factors could be responsible.

LupusCOPDRheumatology
Male25-34
1 hour ago