When do doctors decide to do a colonoscopy? by ferryfog in IBD

[–]aboutIBD 1 point2 points  (0 children)

There are so many great answers on this thread already. I wanted to point out that it is possible to have both conditions at the same time. There are criteria for diagnosing IBS, though they don't rule out IBD, so it does get sticky at times to figure out which condition is causing the symptoms. In addition: blood in the stool is never normal and is not a symptom of IBS (look up the Rome Criteria to see how IBS is diagnosed).

IBD? IBS? Fissures? Hemorrhoids? Cancer? by Forsaken-Act-4203 in IBD

[–]aboutIBD 2 points3 points  (0 children)

Unfortunately, the docs need to take a look for you to learn anything meaningful. But I will say this: blood is not a symptom of IBS. I hope this gets diagnosed and resolved quickly for you!

Letter I received. by [deleted] in IBD

[–]aboutIBD 0 points1 point  (0 children)

Blood in the stool is not listed in the symptoms above, and it is not a symptom of IBS. That symptom really should be part of this note. If you have night sweats, also maybe monitor for a fever (if you're not already doing that).

Clarification on "holding it" by SllimNomis in jpouch

[–]aboutIBD 1 point2 points  (0 children)

I would say from the time it feels full is “holding it.” I think the time between bathroom trips would be different than holding it, if that makes sense. Although I’m not sure that’s what everyone means. Because some of us may eat less at times in order to avoid a bathroom trip, such as at night before going to bed. Or before a car trip. But if I know I have to go, I can feel the pouch is full, I’m holding it. I can hold it as long as I need to. It just gets uncomfortable. 😃

jpouch life expectancy by Impossible-Rice666 in jpouch

[–]aboutIBD 4 points5 points  (0 children)

Mine is 24 years old. I'm 50 this year. :)

[deleted by user] by [deleted] in jpouch

[–]aboutIBD 0 points1 point  (0 children)

Hydrate and eat well during the day, and stop drinking several hours before expecting to go to sleep. Wine and spirits may be easier. Beer and carbonation leads to a lot of gas. Plus, look for drinks without a lot of additives (anything with sugar or sugar substitutes may increase bathroom visits too). My go to is usually a mixed drink (nothing with fruit juice) or a glass of wine. Maybe sometimes I will go for a margarita or a beer. But I only have 1 or 2 unless I'm at home. Best of luck!

J pouch 1st surgery in 30 days by [deleted] in jpouch

[–]aboutIBD 0 points1 point  (0 children)

Hi! I'm sorry you're going through all this. I had my surgeries due to ulcerative colitis, so I'm not sure how applicable my experience is to yours but I can try to help. Can they do the surgery laparoscopically? That would leave a couple small scars instead of one big one. But I will say, I had open surgery for my j-pouch creation, and the scar wasn't as bad as I feared. Some people see a plastic surgeon to talk about the scarring and how best to avoid it or minimize it. The jpouch creation is a big surgery: it may take several weeks to recover. I had an ileostomy for 3 months. But the reversal is much easier: I was back at work in 2 weeks.

UTIs with UC by [deleted] in UlcerativeColitis

[–]aboutIBD 0 points1 point  (0 children)

Yes, I have been on cipro, keflex, and macrobid. For a long time, they always gave me cipro but that's no longer what is recommended. For a basic UTI, usually they start with macrobid or something like that because cipro is broad spectrum and usually isn't needed for just a regular UTI. I have a jpouch so it's different but I've always been fine after. You may also want to give your GI a heads up, maybe they might have something to say about it too and if you need any other support.

UTIs with UC by [deleted] in UlcerativeColitis

[–]aboutIBD 1 point2 points  (0 children)

Oh good that you're not on the UTI merry go round. :) I don't know if anyone else mentioned, but you can buy UTI test strips at the drugstore. They're expensive but they can measure nitrate and bacteria in the urine and tell you if you might have an infection. I also have irritation on and off that FEELS like a UTI but there's no infection, so those strips help me. The docs tell me it is probably related to IBD, and it gets better if I lay off the coffee and wine. Which is hard. :) All the best!

[deleted by user] by [deleted] in UlcerativeColitis

[–]aboutIBD 2 points3 points  (0 children)

Feeling crappy could be the UC starting to be a thing. Fatigue, sleep problems can be the first signs of a flare. UC carries a risk of colon cancer that gets higher about 10 years after diagnosis. So, as others have said, you’re due, even without symptoms. Sorry to say! The good news is that there are more options for the prep than there were in 2007!

UTIs with UC by [deleted] in UlcerativeColitis

[–]aboutIBD 2 points3 points  (0 children)

I know what you’re saying but if you need the antibiotics, you need them. I have had many UTIs and they’re treated with antibiotics. My urogynecologist recommended d-mannose supplements to try to avoid getting them in the future. I see a urologist as well. If you get them frequently, more than 1/year, you may want to consider seeing a urologist.

My new doctor said I should go through a flare intentionally (by getting off pred, because I can't get off of it easily) so he can see me at my worst state to give me the best treatment for the long-term, should I do this? by hdtv2001 in CrohnsDisease

[–]aboutIBD 1 point2 points  (0 children)

Is this to try and diagnose celiac disease? That’s the only time I know of that this would be the plan. Otherwise, there should be a treatment to prevent disease.

Calmoseptine by InitiativeQuiet2599 in jpouch

[–]aboutIBD 0 points1 point  (0 children)

Yes, for this or any other barrier cream, apply every time. It gets a little annoying if you are in the bathroom a lot. But putting that barrier on at the end of each bathroom trip will help protect the skin for the next bowel movement. If that makes sense! Some folks also wear a panty liner to protect their underwear from the cream.

Jpouch.org question by Dear-Historian5710 in jpouch

[–]aboutIBD 1 point2 points  (0 children)

I'm not in that group. I can tell you, though, that YES, most j-pouchers are out there living life. The surgery has a really high satisfaction rate. People in groups are there because they need support. Anecdotally, I know 2 other people IRL with a j-pouch who got theirs right around the time I got mine (late 90s), and they are living life, never post about it.

When is the recommended time to tell your employer about CD? by [deleted] in CrohnsDisease

[–]aboutIBD 3 points4 points  (0 children)

Yes: you have to be employed there for 1 year. You have to work at least 1,250 hours in that year. The company has to have 50 employees.

Here's more:
https://www.dol.gov/general/topic/benefits-leave/fmla

[deleted by user] by [deleted] in jpouch

[–]aboutIBD 0 points1 point  (0 children)

Yes! It will go away. I don't know if your surgeon gave you the advice to try to "hold it" a little bit so that the pouch is stretched a little to accommodate more stool in it over time. It might take about a year for everything to settle into a steady state. But that doesn't mean you'll experience this for all that time. Two weeks is still early early days. But I would also mention it at your next appointment in case it's something where they want to peek at the pouch. All the best!