It seems my lifelong IBS is worse than usual. Any tips from fellow sufferers? Do you up prednisone during an attack? The endocrinologist suggested upping prednisone when feeling unwell.
Managing IBS and PMR: It seems my lifelong IBS is... - PMRGCAuk
Managing IBS and PMR
If it is the IBS that is causing the discomfort taking more pred is unlikely to help.
‘“A study was conducted that examined the use of prednisolone, a corticosteroid medication that helps control inflammation, in treating IBS. However, no significant reduction in IBS symptoms was found in people who took prednisolone”
Im not taking it for the IBS pain per se; I get good help from ginger tea. I feel extremely unwell during it and worry about the IBS stress.
As I understand it you are saying you are feeling extremely unwell and stressed from the IBS?? Have you asked your doctor for any advice?
Last night I ate a delicious helping of spicy chili; normally I like spicy food but I think this time it turned in me. I have regular exams. My gastro, as good as he is, never really talked about IBS other than they can see the spasticity with the colonoscopy. I’ve had multiple abdominal surgeries for other reasons..
I am a retired nurse anesthetist and realize it’s mainly self care. However with tapering and adrenal insufficiency I was wondering if anyone else had increasing issues with IBS.
We need differentiate between irritable bowel syndrome IBS and inflammatory bowel disease IBD. The latter can be autoimmune; the former is functional- our “wiring”. On colonoscopy one can see the intestine clamp down in a spasm as the doctor is trying to pass his instrument. I have seen this and this is my case. There were times when I had extreme abdominal pain from emotional upset. I was in so much pain once that I couldn’t drive my car and asked to go to the hospital in an ambulance. They took a CAT scan; all they saw was a cramped intestine. The standard treatment is emotional support and avoid food triggers to these spasms. These can vary from person to person.
I am sorry I am getting muddled. I thought you were asking whether you should increase your pred dose??
I just was wondering about other PMR sufferers with IBS and what they did with an IBS flare regarding prednisone. My endocrinologist suggested doubling the pred dose during an illness. I did not mean upping the taper program dose. I actually took an extra 5mgm one time only on the day I felt terrible. I think it helped my general feeling.
I assume he said it on the basis of Sick Day Rules?
healthunlocked.com/pmrgcauk...
I’m in the US.
If you read the attachment on PMRPro’s post it explains what Sick Day Rules are. ie double the dose for a short time if you are ill enough to have to stay in bed.
Oh; that’s the same advice I got then. We just don’t call it the “Sick Day Rule”.
I was in such spasm I stayed on my daybed. Does a daybed count?— haha
There is probably a thin grey line between a day bed and actually collapsing onto your normal bed and not wanting to move.
Have you thought about trying Buscopan? It’s used for IBS, and you can buy Over the counter. Usually one to two tablets three times a day. Check with your pharmacist for any interactions with current meds. I hope that helps.
Sangu1,
Buscopan (scopolamine) has been banned in the US otc because a certain number of users had a cancer like markers in their blood. I am familiar with the drug in my anesthesia practice. It is used to dry the mouth and prevent post operative nausea.
It is also used transdermally behind the ear for motion sickness prophylacticly.
I personally did not like using it because patients woke up in delirium.
It is indeed an antispasmotic but at my age I cannot afford confusion.
Peppermint tea and ginger tea work well. With this severe attack I didn’t have the peppermint tea on hand- until hubby was dispensed to the store.
so I have been diagnosed with IBS since my 30s, Im now 73, I would have sudden onsets of diarrhea, through the years, that changed this past DEC, to where I was having problems with cramping, pressure, and passing hard bits of stool, saw my GP, he did ultrasounds, told me to start taking metamucil daily, said, only showed spasms in ultrasound, then sent me for catscan, same verdict, so I didn,t understand why the change in my bowel habits, except I said, I had tried to taper from 5 mgs of pred, to 4 back starting in Nov, and did the dead slow taper, seemed I had been doing ok at 5 , bloodwork at that time was ok, had been on 5 for many mos. at any rate, still am having that issue, but somewhat better with metamucil, although have to move bowels several times a day, like from 4 to 6 times, so the end all conclusion from my GP was, just "spasms" ?? so what is the difference then from IBS and inflammatory bowel disease, ?
Inflammatory bowel disease can be autoimmune in nature while IBS - used to be called spastic colon- means just that. The bowel is “wired” such that it spasms more easily from various triggers, including emotional issues. With inflammatory bowel disease (IBD) the bowel is inflamed while with IBS no inflammation is found - just a bowel in “knots”.
There is a website called help for ibs with helpful suggestions to manage it.
Hi, I suffer from both PMR and Ulcerative Colitis.. I did find that being on Prednisolone for my PMR did lessen the problem with Colitis somewhat. I did however have a flare up of my Colitis last year during lockdown but brought it back under control by increasing my Pentasa (Ulcerative Colitis medication) rather than a Pred increase.
I have IBS and I cannot eat anything spicy, if I did I would be in agony for days. Since eliminating spicy foods it has been much better. I don't eat anything that has garlic in or peppers of any kind either, tomatoes can also set mine off so I try to avoid them too.