I had a really bad flare up of UC in Feb no tablets work...
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I had a really bad flare up of UC in Feb no tablets worked. I was addmitted to hospital and had IV steroids for a week. This got things under control. Since then I have been on 20mg pred daily when I try to reduce things flare up again. Im having lots of side effects. My moods are all over the place I have gained a stone in weight and Im developing a hump at the top of my back which is slowly getting bigger and my face is all puffy. I have been told that these things should go when I come off the pred. Has anyone else had these side effects?
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0 likes, 4 replies
Guest
Posted
Are you following a saltless diet? I was warned about the possible side effects of the drug and stuck religiously to the diet. As a result I only experienced the mood swings but that was OK as most of the time I was quite cheerful. My weight actually went down (no salt!) not up.
I hope you will find a way to reduce the side effects
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Guest
Posted
cheers
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Guest
Posted
I have been on Prednisolone since I had a flare up of UC in September. I was addmitted to hospital for two weeks but refused steroids by IV. I am now down to 5mg a day and I belive I should be off them by end of this month. My UC has been up and down and my bloods have never been right since.
I have put around a stone on in weight but my face has never bloated but my belly has big time. My moods have also been bad but people around me have been very supportive. My Dr wants me off them now to see if the new medication I have been taking is working and as from another reply above steroids do hide a lot of things.
I have been told my weight will go down when i stop them but I will have to follow a diet for a little while. I did find that each time I reduced the steroids the effects got smaller so hopefully when you are able to reduce yours things should pick up.
Good Luck
:o
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Guest
Posted
I also have UC. I was put on Prednisolone when I was 10. I gained a lot of weight and everytime they tried to reduce my medication I had a flare up.
I was then put Mercaptopurine which, touch wood, has kept my condition under control. Doesn't make you put on. But the only thing is it's an un-licensed drug so I have to go to the hospital every four weeks to get a prescription.
Emma