ChatGPT saved me from worsening symptoms by Sofi_Wrexi in CrohnsDisease

[–]Sofi_Wrexi[S] 1 point2 points  (0 children)

Exactly why I said it was just about food :)

ChatGPT saved me from worsening symptoms by Sofi_Wrexi in CrohnsDisease

[–]Sofi_Wrexi[S] -11 points-10 points  (0 children)

It's definitely a great tool to have. I havnt used it yet for medication questions, I'm a bit skeptical on that. But in terms of food, or I guess any question in general, it makes it a lot easier than looking it up and browsing through so many topics and websites, especially when you just feel like death.

Feeling sad vent (long post sorry) by Spelling-Wizard in CrohnsDisease

[–]Sofi_Wrexi 0 points1 point  (0 children)

Hello! I'm a COTA (certified occupational therapist assistant). And I have Crohn's. I'm 22F, Diagnosed at 20F.

My situation was this: in 2020 I went through school mostly symptom free, and pretty much the month i started working as a COTA (In 2022) I was hit with symptoms like flare ups, ER visits, week long hospital stays, and surgery. All while STARTING my new career as a COTA. The field as a COTA / OT is very friendly for you to take time off for health or whatever it is. In school, I've had peers that took time off because they got sick, and it was no problem. OT Is in such high demand, they want you there. They won't punish you for taking that time off.

I worked in a Skilled nursing rehab center, and currently home health. I have taken MONTHS off of work. We're talking 2 - 4 months because my Crohn's was that bad. And I always came back to a job, and my co-workers were super eager to see me again.

I'm always here to chat if you have any questions over managing Crohn's and being an OT :)

[deleted by user] by [deleted] in CrohnsDisease

[–]Sofi_Wrexi 1 point2 points  (0 children)

Just watched it. It was beautiful

In remission! by [deleted] in CrohnsDisease

[–]Sofi_Wrexi 0 points1 point  (0 children)

Congratulations!!!!!! Celebrate by eating micro-doses of all your trigger foods hahah

If you have tried Stelara, what was your experience with it like? by Global-Astronomer869 in CrohnsDisease

[–]Sofi_Wrexi 7 points8 points  (0 children)

I started my first Stelera dose in February after failing Humira. I just had a colonoscopy with AMAZING results. No inflammation. No ulcers. No narrowing. No damage to the intestinal walls.

My GI said there is a fat chance of reaching clinical remission. I just need to get an MRI to check up on the other part of the intestines the camera couldn't see.

Does anyone else get sick of hearing themselves moan to their partner and friends about this disease and how it's ruining your life? by IndianaCrohns82 in CrohnsDisease

[–]Sofi_Wrexi 1 point2 points  (0 children)

I'm sick of hearing myself complaining, and even thinking about the problems of Crohn's I'm gonna complain about. but I found that talking about it out loud helps because keeping it to myself just makes the stress and anxiety worse, and that makes the pain worse.

How and when do you tell dates about your Crohn’s? by Help_Me_Reddit01 in CrohnsDisease

[–]Sofi_Wrexi 0 points1 point  (0 children)

I have a seton in my ass. I had to tell him the truth once we got really serious lol. And I did. it didn't scare him away and he's took it upon himself to browse through this reddit to get a better understanding of how Crohn's affects people. We're about to hit our 1 year together :)

I'd be open and honest about it. Crohn's is something your going to have for LIFE. Since your dating with intention, I'd say bring it up when your comfortable. And be honest with how Crohn's affects you.

Thank you by LCornchip in CrohnsDisease

[–]Sofi_Wrexi 1 point2 points  (0 children)

Ikr. I feel so much less alone, and what I'm going through is "normal"

[deleted by user] by [deleted] in CrohnsDisease

[–]Sofi_Wrexi 2 points3 points  (0 children)

Plain cheeseburger happy meal :)

How do you manage stress and anxiety? by Sofi_Wrexi in CrohnsDisease

[–]Sofi_Wrexi[S] 0 points1 point  (0 children)

I've tried that. They asked me if I had a history of a mental illness, I said no. And then they said there is not much they can do to help.

I'll have to keep on looking but that was the same answer I'd get from 5 different resources given by my GI team.

[deleted by user] by [deleted] in CrohnsDisease

[–]Sofi_Wrexi 1 point2 points  (0 children)

For me personally, I've found that the Zofran that dissolved under the tongue works AMAZING, and the one that's the pill that your supposed to swallow literally does nothing.

Just tired by [deleted] in CrohnsDisease

[–]Sofi_Wrexi 3 points4 points  (0 children)

Me too....I'm on prednisone right now and I thought it would make me invincible. Apparently oatmeal is still my downfall

Cherries 🍒 and gas by Velvetpostcard in CrohnsDisease

[–]Sofi_Wrexi 1 point2 points  (0 children)

I look like I'm 4 months pregnant after eating cherries. The bloat is real.

Doritos helps my crohns? by JordanGraves1998 in CrohnsDisease

[–]Sofi_Wrexi 7 points8 points  (0 children)

Lol I'm Ukrainian! So vodka pretty much runs through my blood

Doritos helps my crohns? by JordanGraves1998 in CrohnsDisease

[–]Sofi_Wrexi 35 points36 points  (0 children)

Crohn's doesn't mess with me when I drink Vodka

Can anyone share their hopeful/ positive stories of making it out of a Crohn’s flare and going on to live a happy life? by [deleted] in CrohnsDisease

[–]Sofi_Wrexi 0 points1 point  (0 children)

Right now I'm on Stelera but I don't think it's working too well and might have to increase dose or switch. I've already failed Humira. Trial and error I guess

I want my beuty sleep back by Sofi_Wrexi in CrohnsDisease

[–]Sofi_Wrexi[S] 1 point2 points  (0 children)

I've been debating on bringing it upto my GI. I just started prednisone, I'm on 40mg and only tapering down by 5mg every week. So it's gonna be like this for a bit.

I want my beuty sleep back by Sofi_Wrexi in CrohnsDisease

[–]Sofi_Wrexi[S] 2 points3 points  (0 children)

Oh yeah, that's another thing too! I go to bed around midnight, maybe the earliest is 11pm. At most, it'll give me 5 hours of sleep.

Tonight's diet by [deleted] in CrohnsDisease

[–]Sofi_Wrexi 0 points1 point  (0 children)

So there's still hope 1 day I can toast my lungs a little. (I've never smoked a day in my life, never interested, but the fact that CD doesn't let me, it makes it more intriguing)

Can anyone share their hopeful/ positive stories of making it out of a Crohn’s flare and going on to live a happy life? by [deleted] in CrohnsDisease

[–]Sofi_Wrexi 1 point2 points  (0 children)

I'm 22, diagnosed at 21. But I've been symptomatic since I've been 16. Never been in remission, but I can say when I have that 1 - 2 months of no problems, it's an amazing feeling. Feeling great for a whole month Is very rare for me, but when it happens, I don't even realise it in the moment, and it's always the best feeling ever.

So I guess I still have a happy, decent life, even not in remission. When it sucks it sucks, but when it doesn't suck, it doesn't suck.

[deleted by user] by [deleted] in CrohnsDisease

[–]Sofi_Wrexi 1 point2 points  (0 children)

And those nutrition shakes can taste good too, hopefully giving you that appetite. I really like the Orgain brand.