Row 86272

Row ID: 86272 | Dataset Entry | Axioma AXP Content Repository

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This page contains data entry 86272 from the Axioma AXP content repository. The structured data below represents the complete record for this entry.

I'm in the process of trying to find out what I have going on. Many of the symptoms overlap with IBS...or cancer, from what I've read. More from the cancer than IBS; there's some major differences that don't apply to iBS.

I was made to do physical therapy for pelvic floor issues. I'm 3 months in with no progress, my symptoms are worsening, nothing they've had me do has helped.

But this is my only option. They wouldn't test anything, and still won't. My bf is becoming concerned the amount of agony I end up in is going to cause me to have a heart attack or organ failure. I have lost my voice many times from wailing in agony that I cannot alleviate. I cannot go to the bathroom like normal and it often contains large amounts of mucus, sometimes being *mostly* mucus.

No one will fucking help me. No blood in the stool, no problem, it seems. No one will even check if it's cancer. My dad died younger than I am currently, of cancer, but fuck me.

I don't even have an alternative for thr physical therapy not working. They just appealed my insurance to extend it. Some of the exercises actually cause the pain, sweats, discomfort, rock feeling deep inside that's been plaguing me since lockdown. And they're getting longer, initially being like 5 minutes of the horrible sensation, now having reached upwards of 40 minutes straight.

Imagine the worst diarrhea/constipation feeling you've ever felt, combined, with pain, and add on not being able to actually go to the bathroom any time it occurs, lasting for 40 minutes. They actually couldn't release me one day because it jacks my heart rate up so high; I had to wait until it went down. They didn't look into it any further other than to acknowledge my heart rate was nearly 200 for a few minutes. They didn't really acknowledge when I said this is what happens every time, that its doing this sometimes 11 times in a 24 hour period.

I've started to come to terms that this is likely going to kill me before I ever even know what it is. I'm only 33. At the current rate of severity, I will be stuck in permanent agony within the next year. As is, I wake up 7+ times a night and spend several hours a day writhing in pain on my couch, punching my lower back to try and reduce the internal pain. At this present moment, my voice is half gone from the last few days of wailing.

**Can't say it's us missing it when we can't even get tested for it.**

I've begged and cried for help. I'm jumping through all their hoops. They've *seen* one of the alarming effects themselves, to the point that I couldn't leave until it stopped. No one will test me for anything; not even a blood test. They only caught the heart rate because they take blood pressure and whatnot before all appointments. Last time, they didn't even do that. I just went in and started their exercises.

I can't even get anything for relief. A toradol shot for a different issue let me have 5 days agony-free. Didn't help what I got it for, but it helped this issue...they won't let me have toradol shots for this. Even though it gives me 5 days of sleep and living like a normal person. I'm not even worthy of the one thing thats helped me.

**Don't blame people suffering from these issues when doctors refuse to help us.**

FieldValue
text I'm in the process of trying to find out what I have going on. Many of the symptoms overlap with IBS...or cancer, from what I've read. More from the cancer than IBS; there's some major differences that don't apply to iBS. I was made to do physical therapy for pelvic floor issues. I'm 3 months in with no progress, my symptoms are worsening, nothing they've had me do has helped. But this is my only option. They wouldn't test anything, and still won't. My bf is becoming concerned the amount of ag…
label r/health
dataType comment
communityName r/Health
datetime 2024-05-24
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Raw Record

{
  "text": "I'm in the process of trying to find out what I have going on. Many of the symptoms overlap with IBS...or cancer, from what I've read. More from the cancer than IBS; there's some major differences that don't apply to iBS.\n\nI was made to do physical therapy for pelvic floor issues. I'm 3 months in with no progress, my symptoms are worsening, nothing they've had me do has helped.\n\nBut this is my only option. They wouldn't test anything, and still won't. My bf is becoming concerned the amount of agony I end up in is going to cause me to have a heart attack or organ failure. I have lost my voice many times from wailing in agony that I cannot alleviate. I cannot go to the bathroom like normal and it often contains large amounts of mucus, sometimes being *mostly* mucus.\n\nNo one will fucking help me. No blood in the stool, no problem, it seems. No one will even check if it's cancer. My dad died younger than I am currently, of cancer, but fuck me. \n\nI don't even have an alternative for thr physical therapy not working. They just appealed my insurance to extend it. Some of the exercises actually cause the pain, sweats, discomfort, rock feeling deep inside that's been plaguing me since lockdown. And they're getting longer, initially being like 5 minutes of the horrible sensation, now having reached upwards of 40 minutes straight. \n\nImagine the worst diarrhea/constipation feeling you've ever felt, combined, with pain, and add on not being able to actually go to the bathroom any time it occurs, lasting for 40 minutes. They actually couldn't release me one day because it jacks my heart rate up so high; I had to wait until it went down. They didn't look into it any further other than to acknowledge my heart rate was nearly 200 for a few minutes. They didn't really acknowledge when I said this is what happens every time, that its doing this sometimes 11 times in a 24 hour period. \n\nI've started to come to terms that this is likely going to kill me before I ever even know what it is. I'm only 33. At the current rate of severity, I will be stuck in permanent agony within the next year. As is, I wake up 7+ times a night and spend several hours a day writhing in pain on my couch, punching my lower back to try and reduce the internal pain. At this present moment, my voice is half gone from the last few days of wailing.\n\n**Can't say it's us missing it when we can't even get tested for it.**\n\n I've begged and cried for help. I'm jumping through all their hoops. They've *seen* one of the alarming effects themselves, to the point that I couldn't leave until it stopped. No one will test me for anything; not even a blood test. They only caught the heart rate because they take blood pressure and whatnot before all appointments. Last time, they didn't even do that. I just went in and started their exercises.\n\nI can't even get anything for relief. A toradol shot for a different issue let me have 5 days agony-free. Didn't help what I got it for, but it helped this issue...they won't let me have toradol shots for this. Even though it gives me 5 days of sleep and living like a normal person. I'm not even worthy of the one thing thats helped me.\n\n**Don't blame people suffering from these issues when doctors refuse to help us.**",
  "label": "r/health",
  "dataType": "comment",
  "communityName": "r/Health",
  "datetime": "2024-05-24",
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}
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