Anyone have abdominal pain with an indwelling urinary catheter?
Anybody here an indwelling urinary catheter?....
My "Foley" catherter is exchanged each month by myself, which the VA allows (I'm an Air Force veteran).
I flush it daily with a saline solution. If not flushed routinely, it plugs within a couple weeks.
My problem...
I'm awakened each night by lower abdominal pain after sleeping only 4 or 5 hours. I'd put pain level at about 5 on a scale of 1-10.
It's only a problem at night. Once I'm up and moving around the pain disappears, or falls to less than level 1 within 5 or 10 minutes.
However, any time I push against my lower abdomen it's quite painful... about level 5.
In the past six months, the VA has scanned with ultrasound, Xrays, MRI, and recently "CT of the abdomen and pelvis with intravenous constrast."
The results of this latest test being that my liver, kisneys, prostate, and intestines are functioning normally.
Seems to me that rules out everything else but my bladder as the pain source.
The CT exam mentions "The bladder wall demonstrates diffuse bladder wall thickening and prominence of the superficial vascular structures sugesting inflammation."
The "...suggesting inflammation." part leads me to think that is the most likely source of pain. Perhaps there's an infection.
If so, what can be done?
Doctors at the VA hospital in Madison, Wisconsin seem to be baffled by the source... weird!
Anybody here also having a similar problem?
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You might want to consider a Caster oil pack put on your stomach.
Look up Barbara Oneill. Shes holistic, disingenuously ostricized, yet highly intelligent, profusely well read and effective with many remedies.
Search her with gut/abdominal issues.
Contrary to the criticism, shes outstanding and knows the bodys ways of healing itself.
Have you tried food allergy testing? After years of ulcers esophagitis, Linx surgery etc. turned out I was allergic to most foods I was eating. Had Linx removed and now if I avoid the foods I feel better!
I am cramping in abdomen A LOT more and very very painful. I'm female so I know too much about cramps from onset of puberty, I wanted to curl up and die, 3 days every stinkin month. Gave birth c-section of twins, they gave me petocin, afterwards to help make my uterus cramp, mine was stuck in "open " mode and I was hemorrhaging orange size clots.
Severe cramping is also a sign of a potential intestinal obstruction forming.
Any ideas on how to tell what is causing my severe cramps and how to know if I should go to doctor would be very much appreciated.
I have chronic 💩💩 issues, longggggg term. The severe cramping started about a year ago with a partial small bowel obstruction forming. I DO NOT want to go to the doctor, only as last resort.
I'm in diarrhea mode now, nothing new for me, and it doesn't mean I don't have any impactions. Cramps are wrapping around my left side to mid-lower back. I am nauseous for no apparent reasons throughout my life, but the nausea is picking up too. I've not eaten any new food, no new medication. I'm nibble on crackers and small sips of 7-UP. Water makes me more nauseous. HELP thanx ShelleyW
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1 ReactionWow. You have had a lot to deal with. So sorry. Have you gone to a gi Dr. Had any gi testing?barium swallow? Ph impedance testing? Motility testing? If I was in your position even though you don’t want to do to Dr. I would 100 percent go see a gi Dr! Give you peace of mind as well as a diagnosis. 😊
Also a ct scan? Or Cta scan? They sound necessary. At this point.
graceym1,
Yes, I have had all the tests you mentioned. I was with the same GI for 17 years: celiac biopsy, CIC, chronic idiopathic constipation, fecal impactions, small bowel partial obstructions, 2 resolved by me quit eating solids, using meal replacement protein shakes (my daughter is very knowledgeable about which is best for me, or I never would have used them). The 3rd one landed me in ER, ICU, gastric nasal tube for 3 days. Then 3 anal blockages that required digital removal, by me. So, I still don't eat a lot of solid foods, and I have to take miralax every day.
I don't ever believe that a Dr. can give me peace of mind. Just the thought of it makes me break down sobbing or LOL. I have had CT's, MRI's, biopsies, x-rays every 1-2 months, always showing I have heavy fecal load in large intestines, I guess that means I am quite literally full of 💩💩. Thanx, for your suggestions. Shelley
You have certainly been through alot. I’m sorry. I’m glad you have a knowledgeable daughter that helps you! Have you been to nyu or Columbia Presbyterian in nyc? Or Mayo Clinic? UVA? What are drs saying you have exactly? And why can’t they fix it?
graceym1,
My parathyroid glands are over worked and under paid, 😱, I have slightly elevated calcium, has been trending up for 5+- years. I had secondary HPTH diagnosed in 2008, due to malabsorption... I have severely damaged villi in my intestines due to lifelong celiac disease, I didn't know it, because I am have been asymptomatic or have the opposite symptoms. This is also a surgery like yours... I could wait, and continue with a declining QoL, or get it done. My body systems are overwhelmed, with several problems, it has no fight left, so every time I turn around I get a different, more weird and serious diagnosis. I, like the other's will want to know what your decision is. Good luck. ShelleyW
In my experience Miralax gives me a lot of gas and cramping, I switched to colace
Are you constipated even with daily Miralax? The dose can be adjusted upward quite a bit to get the right amount. I have been taking Miralax mixed with Metamucil in a 3/4:1/4 ratio. The metamucil adds some bulk to the stool helping it move along. I use generics for both. I wonder if you have a redundant (extra long and loopy). That makes too much water be absorbed from the stool resulting in consipation. Sometimes surgery to remove some colon is advised. I assume you are on a celiac diet? I have a similar problem with CC and it’s miserable. So sorry you’re dealing with this! I have times where I get so blocked up i take 8 caps of miralax over 2-3 hrs and that clears it. It’s like doing a colonoscopy prep mini style.
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