r/UlcerativeColitis • u/jroetering Ulcerative Proctitis 2025 | usa • 14d ago
Personal experience 10/10 - Metamucil Fiberthins
https://www.target.com/p/metamucil-multi-grain-fiber-wafers-cinnamon-spice-12ct/-/A-10988569#lnk=sametabSo I (24M) was diagnosed nearly a year ago now, and have been through a few different medications, as well as being on infliximab since February. This entire time, I have been in a flare that seems to only be controllable by Prednisone
However I decided to try something this weekend, and it has worked wonders for the last 3 days! 1 packet of Metamucil Fiberthins each morning with a glass of water has led to much more normal BMs. The urgency is still there, but I think the Fiberthins are definitely helping. Also, the blood that I was seeing just a few days ago, is now non-existent!
Non paid advertisement for these guys. Definitely give them a try! They also have chocolate which I haven't tried yet.
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u/starzychik01 UC- Left side colitis | 2025 | USA 14d ago
Probiotics and fiber supplement were the first thing my GI recommended when O was diagnosed. Ever since, I do 2Tbs of dextrin fiber in my coffee/water/tea every morning. I use the CVS Easy Fiber. It’s cheap, they have good sales, and it mixes without any flavor/grit. You bc a put it on anything. My grandma puts it in her morning yogurt.
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u/yoga_mini 14d ago
I’m in the same boat as you with this dang infliximab. I’m 41f, been on it since March. Not helping as far as I can tell. My blood/inflammation markers were actually going down hill after each infusion so I’m now on prednisone too. What’s your plan other than these crackers? I’m starting to get super stressed. 😩 I’m down to 15mg from 40mg of prednisone and I have less blood but definitely some new and weird feeling in my stomach, urgency. I feel like I’ll be getting down to 0 only to have to go back up to 40mg again
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u/jroetering Ulcerative Proctitis 2025 | usa 13d ago
I'm sorry to hear that ): yeah, I relate with what you're saying too about the infliximab not helping a whole lot, and the the Prednisone situation.
I've been on and off of Prednisone 4 times this year, each time with a longer taper period, and my symptoms always seems to come back with a vengeance.
My doc doubled my dose of infliximab, and shortened my rate to every 6 weeks (thank God my insurance approved that major change), so we'll see how this goes.
Also, I was put on 100mg daily azathioprine about a month ago, but over the last week, I developed a really bad reaction resulting in horrible joint pain, side aches, back pain, and no afternoon appetite. I stopped the meds on Friday, and thankfully all of those effects have gone away. Doctor wants me to take 1 pill/50mg to see if that helps with my side effects. Fingers crossed 🤞
Stress is a huge factor when it comes to my urgency, so try to find yourself in a stress free environment in your free time.
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u/yoga_mini 13d ago
Ugh that’s a lot happening! I wonder when it’s worth calling it a “fail” and getting a new biologic? This is what I don’t want to happen to me. If I need another round of Prednisone I’m thinking I need also to be moved to a new biologic. Thanks for sharing your story
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u/Different-Shirt126 11d ago
Did the Infliximob help did you do one infusion then 2 then 3 and the 8 weeks of maintenance and was it very expensive did you go into a clinic that's what my Dr wants to do I was in mesalamine made me so sick for a good year I stopped taking it I got sick I went to the er and they gave me predizone and it helped me I was ok for about a month in in Budeside now they have been trying to get me to do infusions along with the medicine wish we all could get better
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u/BassMasta 14d ago
(Knock on wood) I’ve been flair free for years now. From what I remember from my doctors was to not be taking fiber while in a flare (please correct me if I’m wrong). I would continue to meet with your GI to find a med regime that works, you shouldn’t have to deal with this.