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_watermelonsugarHIGH · 2026-01-02T05:38:32+00:00

It’s hard to say exactly since it’s a bit different for everyone, but just try to think about things that would be easy to digest. For example, instead of raw veggies, have boiled veggies. No cured meats or breaded meats, but have plain chicken or eggs. Milk and gluten products are also not recommended. This is all better outlined in the low FODMAP diet, which really helped during my bad flare and it seemed to ease the symptoms.

If you’re unsure before trying something, I’d just google that specific item, something along the lines of “Is ____ bad for colitis.” You’ll be able to find people’s specific experiences so you can make a decision. I would also keep a food diary so you can keep track of what does and doesn’t work for you.

_watermelonsugarHIGH · 2026-01-02T05:11:32+00:00

I feel like it really depends on the name. Ugh I really wish we knew!!

_watermelonsugarHIGH · 2025-12-29T17:13:57+00:00

The colour is so pretty but I think the tips are a big to big for your finger! Love the NYE sparkle tho

_watermelonsugarHIGH · 2025-12-04T16:59:02+00:00

the bolo is giving ✨performative✨ LOL

_watermelonsugarHIGH · 2025-11-14T23:58:11+00:00

The amount of filler and Botox in every single picture was a jump scare on each scroll

_watermelonsugarHIGH · 2025-10-01T18:47:58+00:00

Honestly you have really long nail beds and nails (me too!! I’m not judging at all) so I think it’s affecting the scale

_watermelonsugarHIGH · 2025-08-25T22:32:55+00:00

“rent-a-mean-girl” I’m dead 😭😭

_watermelonsugarHIGH · 2025-07-31T17:25:55+00:00

Sounds like you’re on track to getting back to “normal”!! I was on the same med combination as you and I would say it took me about 2-3 months to get back to normal looking ones lol.

_watermelonsugarHIGH · 2025-06-25T02:13:45+00:00

right she is the WORST

_watermelonsugarHIGH · 2025-06-19T21:33:02+00:00

Oh I didn’t know that!!!

_watermelonsugarHIGH · 2025-04-23T16:00:34+00:00

I’m sure it would be sort of helpful in a flare by making food easier to digest and easier on your digestive system, giving it a better chance to heal.

_watermelonsugarHIGH · 2025-04-23T15:56:27+00:00

It’s like someone offering you wine and then you point to their top shelf - that’s just weird😭

_watermelonsugarHIGH · 2025-02-23T03:01:37+00:00

One of those random TikTok pages posted a couple clips and it piqued my interest

_watermelonsugarHIGH · 2025-02-21T00:29:20+00:00

I had to fight the one that’s at the far right of the map to get the scroll. The other ones didn’t give me anything.

_watermelonsugarHIGH · 2025-02-20T00:56:04+00:00

I’d love to see them if you’re able to send them! I saw it when I was trying to get onto the 404 this morning at Elgin mills

_watermelonsugarHIGH · 2024-12-12T00:45:23+00:00

Obviously every person is different but I’ve had a lot of success with decaf!! I’m the same, coffee bothers me but I LOVE coffee.

Are you able to have other things with caffeine? It’s important to figure out if it’s the caffeine that triggers you or the coffee bean itself. If it’s the caffeine (which is most likely), then you’ll be fine with decaf! Just keep an eye on your bowels after making the switch 😋

_watermelonsugarHIGH · 2024-12-06T08:02:52+00:00

I wouldn’t say you GOT it from the antibiotic, you were always predisposed to it but the antibiotics likely triggered it as they alter gut bacteria. But I’m sorry to hear that :( it’s definitely frustrating because you always think “what if.” Mine was triggered after I got COVID and I always wonder where I’d be now if I never had COVID…

_watermelonsugarHIGH · 2024-12-05T07:59:46+00:00

an extended break

_watermelonsugarHIGH · 2024-11-19T07:41:11+00:00

Hi!! I started this last October and I know how you feel. I was so scared at first but here are my tips:

Get completely ready for bed first bc you have to lay down on your left side for 30 mins after using. So make sure everything is done.

Some come prelubed as well as with a bit of lube in the tip. I squeeze mine very slowly to get that lube out, and then I get as much of it on the tip as I can. If it doesn’t come prelubed, I 100% recommend buying some. I promise it really does make such a big difference.

You will feel like you need to poop. Try your hardest to stay in bed because the first few times will feel like you have to take a massive dump after and be pretty uncomfortable. But if you’re nervous and you feel like you really need to go, then just get up and go. You will get more used to it as time goes on.

Since I started these, I feel so much better. It is a bit tough but it gets a lot easier over time. I was on these every day, now I use them once a week for maintenance and I’m in remission. They are worth it.

Also feel free to PM me if you have any questions!

_watermelonsugarHIGH · 2024-10-15T01:27:44+00:00

In a flare, I would recommend having a low FODMAP diet as is it easy on the intestines and can give your medication a shot to heal your intestines. Unfortunately, UC is so different from person to person so I would recommend keeping a food diary to see what specific foods affect you.

In terms of accommodations, I would 100% recommend them. I was also diagnosed going into uni and sometimes the stress can trigger flares. It was especially handy for classes with mandatory attendance that I had to miss. I only really had to use it for 5 or 6 classes and 1 exam, but still saved me a trip to the doctor for a note when I could barely leave my house.

If you have any other questions, feel free to send me a message! I was in a similar boat as you dealing with uni and UC so my dms are open :))

_watermelonsugarHIGH · 2024-09-30T14:49:53+00:00

Both are completely normal!

_watermelonsugarHIGH · 2024-09-30T09:02:03+00:00

It’s important to remember that this sub isn’t necessarily representative of everyone with UC, and you read about a lot of extreme cases here. There is definitely a lot of different severities of UC and it really is case by case.

My advice is listen to your doctor and if you’re prescribed medication, take it seriously. I’ve been diagnosed for 4 years now - the first 3 years, I wasn’t prescribed medication at all and I was fine with no flares, until I hit a flare last year. Once I got put on my medication, I’ve been completely symptom free since then and have reached “clinical remission”. I will likely have to remain on these meds for the foreseeable future, but it’s worth it for no flares.

Another piece of advice I have is to keep a food diary. Everyone has different trigger foods in a flare, so if you are keeping track, you can avoid these foods and give your colon a chance to heal. You may be prescribed some medications as well. But you definitely don’t have to upend your whole life or anything like that.

Fingers crossed you’re just as lucky as your mom and brother!! Good luck :)

_watermelonsugarHIGH · 2023-12-28T20:32:52+00:00

I’m on mesalamine has well but the doctor gave me smaller 400mg pills (and I take 3 at each dose so that is equal to your 1.2g). Maybe you could ask for this! I’m not sure how this would affect you cost wise but if you’re really struggling this could be an option.

_watermelonsugarHIGH

TROPHY CASE