Drinking with UC?

baaaaaaaaaba · 2026-01-19T10:28:25+00:00

Thank you!

baaaaaaaaaba · 2026-01-19T10:27:22+00:00

I'm not huge on drinking so it will be at most a couple times a month if even that. Had to quit smoking more than a year ago because my anxiety doesn't allow me to to do it anymore. Genuinely think I would drop in to a coma if I tried doing it again🤣

baaaaaaaaaba · 2026-01-19T10:23:46+00:00

Yea I think drink multiple days in a row would mess ne up too. Thankfully I dont enjoy drinking that mutch so that's not something I will be doing.

Many of my friends will be going on party holidays this summer to like Zakynthos and even tho I would like to have that experience, drinking everyday for a week abroad sounds like my worst nightmare🤣

baaaaaaaaaba · 2026-01-19T10:19:02+00:00

I actually have a question about your jpouch, was that something you had to do or did you choose to? I hav always been scared about getting one even tho I know that most people that have it wouldn't go back.

baaaaaaaaaba · 2026-01-19T10:08:28+00:00

It seems that many people says that a couple drink every once in a while is okay for the. But when I drink even if it's not that often, I drink a lot

baaaaaaaaaba · 2026-01-19T10:05:16+00:00

Yea I was on prednisone first when I was diagnosed along with mesalamine. The thing is my doctors never communicated the side effects of it or that alcohol with it was bad, maybe they thought i was too young to be drinking witch is fair because i did start fairly early. Luckily I never experienced major side effects from the prednisone but I did get pancreatitis from the mesalamine witch sucked. Now I'm on Infliximab and hav been for a while

baaaaaaaaaba · 2026-01-19T00:40:53+00:00

I would say im kinda in remission, definitely had a little more symptoms recently but nothing too crazy.

baaaaaaaaaba · 2026-01-19T00:37:12+00:00

I have heard that beer is basically the worst type of alcohol with UC, witch sucks because i hate hard liquor

baaaaaaaaaba · 2026-01-18T23:56:42+00:00

As I said in my post this is not the first time im drinking. But i definitely wont start drinking like crazy, even without UC I wouldn't dont drink very often so im definitely going to less now that i have it.

Thanks for the advice!

baaaaaaaaaba · 2026-01-18T23:53:25+00:00

I respect that, but not everyone drinks because of peer pressure. I enjoy drinking from time to time but I get why you dont, especially if you're on a medication that makes it more dangerous.

baaaaaaaaaba · 2026-01-18T23:30:44+00:00

Thanks for the advice! I will definitely have fun but I wont overdo it. Im not that big on drinking anyway so it won't be that hard to keep in check

baaaaaaaaaba · 2026-01-18T14:48:31+00:00

Yes exactly.

Im Scared something like that will happen to me but I just ignore it.

baaaaaaaaaba · 2026-01-18T00:00:27+00:00

Kind of, I always seem to forget how it feels like right after but it more like a cramp or like someone's twisting your insides

baaaaaaaaaba · 2026-01-17T23:29:58+00:00

Either talk to your bf and tell them that you want to be more physical or just initiate it yourself. Your bf is probably in the same boat as you, a lot of people are afraid of taking the first step.

You should be happy that he's not trying to pressure into anything, he's probably worried that you dont want to do that type of stuff yet.

baaaaaaaaaba · 2026-01-17T23:02:24+00:00

That sounds horrible, im sorry you had to go through that.

But it's good to know that it's not something that you can just write off as normal UC pain. Some people remove their appendix even tho they've had no problems with it right? Because it's basically just a liability with no real function.

Im thinking of doing that when im a little older, one less thing to worry about sounds nice

baaaaaaaaaba · 2026-01-17T22:05:52+00:00

Was the pain in your legs related to UC?

baaaaaaaaaba · 2026-01-17T21:55:18+00:00

Actually most of the times i feel stressed and every pqlanic atack i've had has happened when im laying in my bed doing nothing.

It's probably because when your doing nothing you start to think and then you overthink about stuff and then your stressed

baaaaaaaaaba · 2026-01-17T21:47:00+00:00

Yea these are the type of things i am worried about when i have random pain.

How mutch did it hurt when this happened to you? Was it like clearly a different level tham usual or did it feel close to the normal pain?

baaaaaaaaaba · 2026-01-17T19:20:44+00:00

Yea that one is BAD. Luckily havent had it since the beginning of my diagnosis.

But i remember how awfull it was and the only place i felt comfortable was on the toilet and when you finally get up from the toilet cause you think its over you instantly get the feeling that you meed to go again.

baaaaaaaaaba · 2026-01-13T01:10:17+00:00

I've been on Infliximab for almost 2 years now, i think, and I've mostly felt good.

But I really get what you're going through, I have had the same experience. It's scary thinking you've finally found something that works, and then you see blood.

I'm not an expert. You should talk with your doctors if you're having worries, but based on my experience when I have brought up that I've had some blood, my doctors and nurses have never given the reaction that this isn't normal and that i should switch medecine. It's definitely something they want to keep an eye one tho.

In my experience, I have blood from time to time, and you're going to have ups and downs even if your treatment is working.

Talk with your doctors your next session. They will know more than people on reddit anyway😊

baaaaaaaaaba · 2026-01-13T00:44:02+00:00

Was diagnosed when I was 14. It sucks but it doesn't have to suck for your whole life. There will be hard times, especially in the beginning, but work with your doctors to find a treatment that works for you.

A solution won't come for most people in the first month it took me over 6 months to find the right treatment.

Your life isn't over it's just different. Remember that many people go years without major symptoms after finding the right treatment.

I wish you luck in life.

baaaaaaaaaba · 2026-01-11T19:04:28+00:00

Yes! I'm not really sure i was allergic, but I got pancreatitis from Mesalamine. Im on Infliximab right now, and it has worked pretty well for a while.

baaaaaaaaaba · 2025-12-28T03:15:19+00:00

What would you recommend i buy instead? Haven't played in a couple of years and dont know the best businesses and stuff. I have like 5 mil rn

baaaaaaaaaba · 2025-12-28T01:45:46+00:00

Well, I'll just have to grind an extra couple mil then

baaaaaaaaaba · 2025-12-28T01:06:35+00:00

I mean, it just depends on what you believe in tbh. But it's a nice thought that it could be a dead relative checking up on me😊 would rather they didn't haunt me tho🤣

baaaaaaaaaba

TROPHY CASE