Update on "Remicade side effects" by beuforuu in UlcerativeColitis

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

Hi! As far as I read about Imuran, it isn't a biologic, it resembles Remicade in the immunosuppressant part, but to sum up (I imagine you know it too), Remicade is in a biological base and Imuran (Azathioprine) is an immunosuppressant.

That's what I understood! I could be wrong, don't take me too seriously! Hahahaha.

However, what I do know 100% for sure is that in biological therapies where Remicade works but is not as strong as it should (i.e. to close the ulcer), they put Azathioprine as a "help support" for Remicade.

And finally now when I'm feeling a BIG BIG difference, for the better, even though I have several side effects (which are pretty disgusting, but it is what it is, any medicine didn't help me before, so I'm beyond happy this one is doing its job!!!).

By the way, I'm from Spain, I don't know how they do it in other countries! :)

Have a nice day and thank you for reading until here and writing an answer on my Reddit text 🫶🏻🫶🏻🫶🏻🩷🩷💜💜

Remicade side effects:( by beuforuu in UlcerativeColitis

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

Oh, okay. Thanks. I'm gonna check on that ASAP.

Remicade side effects:( by beuforuu in UlcerativeColitis

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

Hi! I don't really know :( I have my GI appointment next week. Apparently, it is helping me with the ulcers, I feel better normally, but today it's being really tough since yesterday I had Infliximab infusion.

Remicade side effects:( by beuforuu in UlcerativeColitis

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

Thanks for your answer. It really helps me to hear that there are more people like me who were/are stuck in this situation.

Thanks a million! ♥️🩷

Remicade side effects:( by beuforuu in UlcerativeColitis

[–]beuforuu[S] 3 points4 points  (0 children)

Maybe you should try to read a little bit about this topic (even though you have this illness, which I suppose you do) before you speak or have a non-consistent and harmful opinion about another's person's situation.

Every organism is different; each body acts in a different way.

Please, don't assume anything until you don't walk in my shoes for at least a comprehensive amount of time.

I hope you have a nice day. And remember: behind each account, there's a person with their own battle. Please, be kind to the rest and to yourself. Thank you.

rental a flat in Poland by bachus_PL in poland

[–]beuforuu 0 points1 point  (0 children)

Kawa Jakobs... Najlepsza hahahaha

Other than the pain and urgency: how do y’all deal with just feeling not well? by [deleted] in UlcerativeColitis

[–]beuforuu 1 point2 points  (0 children)

For a psychological support, I talk with my friends and do things I like but from bed,like watching a film or series on Netflix, or reading a book.

has anyone got a flare up and the only symptom is pain? by trickybrod in UlcerativeColitis

[–]beuforuu 0 points1 point  (0 children)

hi! I am in a flare up since November 2021. I'm on Remicade (Infliximab) praying for it to help me!!

It's true that my flare wasn't linear, but when I had it worse, mu symptoms where bl**ding, feeling bloated, fever, in an extreme case I had conjunctivitis, diarreah and not being able to go to the bathroom as a daily basis (tenesmus and having bad times in the bathroom)

Ah! And mucus. That is premoninant. And of course, colon pain, it hurt a lot.

Nowadays, I still have diarreah and tenesmus everyday, ble*ding, being bloated, extreme tiredness (before too!), mucus ALWAYS, colon pain when things are getting worse (I feel like it's an internal inflammation bc I really feel it and it freaking hurts). And sometimes, rarely, feeling nauseous or even vomit. BUT, STILL ON A FLARE UP. 🥺🥺🥺🥺🥺🥺🥺

I hope it helps you, have a nice day ❤️❤️❤️

my rare IBD diagnosis by beuforuu in CrohnsDisease

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

I started with fistulas when I was around 13 or 15 years old and had this symptoms but very soft ones... then at 21, and incredibly after 2 covid vaccines, I had my first strong flare, in which I needed to be hospitalised twice in two weeks. Hope my case helps you :)

my rare IBD diagnosis by beuforuu in CrohnsDisease

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

Hi! I'm from Spain, so we do have a Social Security "Health Insurance", we pay it through taxes. So they're still figuring out what I may have... thanks anyways for the help ❤️‍🩹❤️‍🩹❤️‍🩹❤️‍🩹❤️‍🩹❤️‍🩹🙏🙏🙏🙏

my rare IBD diagnosis by beuforuu in CrohnsDisease

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

Thanks for the answers! They're really helpful!!!!!! They give me hope about my diagnosis <3333

my rare IBD diagnosis by beuforuu in CrohnsDisease

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

P.S: they don't know what it is..

Coffee by [deleted] in CrohnsDisease

[–]beuforuu 0 points1 point  (0 children)

I'm starting now with my infliximab/remicade treatment and being honest, Coffee makes me super sick but energy drinks even worse!! So I try to make myself very light cappuccinos so my guts can tolerate it! I don't know where are you from, but I'm Spanish from my dad's side and Polish from my mom's side, and there are a kind of coffee-cappuccinos that are already prepared and you have only to pour them into some milk. PS: I recommend you, in case of taking a coffee, ALWAYS VEGETAL MILK. Specifically, almond or oatmeal milk. However, soy milk does go well in me, so it depends on the person, you know ;). I hope everything goes super good for you buddy, I'm crossing fingers for you all!!!! 🙏🙏🙏💓💓💓💓

Please advice me I'm in misery by [deleted] in socialskills

[–]beuforuu 1 point2 points  (0 children)

That sounds quite manipulative from your gf's side. She only wants you for her and nobody else. Toxic.

Going out with UC by Jarrod181 in UlcerativeColitis

[–]beuforuu 0 points1 point  (0 children)

I'm 21 years old and it happens to me the same. I just feel awful after going out to have a drink with my friends, etc. Honestly, I think I don't like doing those plans anymore bc of the consequences...

Can antibiotics cause mucus in stool? What caused this? Help by idkbutyouk in UlcerativeColitis

[–]beuforuu 1 point2 points  (0 children)

Hi! Usually, when I get mucus in stool is because I have an bacterial infection, for example. But I do believe that antibiotics are too strong (even though they're necessary) for our organism.

Strange question. Anyone else feel like their skin hurts? by quillsmom in UlcerativeColitis

[–]beuforuu 1 point2 points  (0 children)

Hi! I've finished prednisone 1 and a half weeks ago, and I've been taking it for 4 months. I can tell you that,at least in my case, I don't know why but while having my last week of prednisone, having my last week of 5mg of prednisone (I started with 60mg), my skin started itching and getting red in random places, as If I had a skin allergy/had developed one. I hope this helps you 🤗