this post was submitted on 13 Jun 2023
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Crohn's and Ulcerative Colitis

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This is a support group for people with Crohn's Disease and Ulcerative Colitis, and their familes.

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  3. If you are unsure, see Rule 1 and 2

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[–] JigglySackles 5 points 1 year ago (1 children)

Worst thing about prednisone for me is the taste. I don't get why it can't have even the slightest coating on it to keep that nasty bitter taste out my mouth. I don't have chron's though.I've heard it's awful. I'm guessing they give you prednisone with some regularity?

[–] MorganCS 1 points 1 year ago (1 children)

Seriously! Nastiest taste ever. If you take it with some peanut butter (or any nut butter I guess), it really seems to cut down on it.

I have Ulcerative Colitis, and whenever I have a major flare, I end up on prednisone for anywhere from 3 months at the shortest, to 1 year (8 pills a day) for the longest.

And then there's the weight gain.... Thanks for responding!

[–] JigglySackles 2 points 1 year ago

Ugh that sounds awful. The side effects of prednisone are no fun to deal with either. My boss was in it for an extended time and got the rounded moon face from it. Peanut butter is a good idea, I'll try that next time. Thanks for the idea!

[–] jamescodesthings 1 points 1 year ago (1 children)

What do you mean "your family doesn't want to be around you because you're angrily working at 4am on the pred"!?

Sucks, it has kept me alive so many times but my dad and my other half know to warn people when I'm on it. I go a bit batshit.

[–] MorganCS 1 points 1 year ago

Bless my wife for putting up with me during a flare. Angry to crying and back in 30 minutes.