i was diagnosed yesterday with uc
Posted , 6 users are following.
i have been prescribed asacol can anyone tell me what they are for .they have only beeen prescribed for two weeks. have been given no other imformation other than my biopsy will take two to four weeks tobring in a result,,,,,,what now...feel so alone
0 likes, 10 replies
jill18833 denise94793
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denise94793 jill18833
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sebtucknott denise94793
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Sorry to hear you've been diagnosed with UC. I've had UC for 7 years now. Yes it's not fun at times but actually it's changed me for the better and in a strange way I'm glad I have it now!
Things will get easier I promise. Seek help online is a great start, it really helps to speak to others that know what you're going through.
In terms of Asacol, its a non-steriodal anti inflammatory. In theory its meant to traval through your digestive system slowly releasing anti-inflammatory medicine where you have inflammation. Think of it a little bit like putting a cream on a rash.
I've been on Pentasa (the same form of drug, mesalasine) for the whole 7 years, it works quite well at making me less senstive to things.
It's isn't very strong though so some people don't always see amazing results from it but I feel they're expecting too much of it!
It's really worth look at things not just in medicine, my UC has been better than it's even been since massively changing my diet and lifestyle.
I hope that helps
Seb x
alison23639 denise94793
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There is a link on this site which gives lots of information on asacol https://patient.info/health/aminosalicylates
Basically its an anti inflamatory that will hopefully reduce your symptoms and get you in to remission.
Good luck and keep talking.
denise94793 alison23639
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alison23639 denise94793
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denise94793 alison23639
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alison23639 denise94793
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missey_woo denise94793
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millie1986 denise94793
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Please DO NOT feel alone.
This takes its tol on you physically & mentally.
I have never had asacol but it will be for inflammation in your system.
I was half diagnosed in January after a flexible sigmoidoscopy & was have a leaflet and like you felt like I was just to get on with it. I was devastated.
The crhones and colitis website is great I wouldn't bother too much with any other websites. It's such an unknown vowel disease and if one more person tells me I can't eat a curry I'll scream.
After my first appointment I was appointed an IBD nurse who was very full on and a bit extreme. I was terrified of her even though she was being nice she was just too intense.
Since then ive had numerous doctor and hospital appointmenta. The first time I was gave a suppositries I nearley had a heart attack. Now it's just a routine with medication. You must take it I feel better
I had my colonoscopy last week and it's literally almost confirmed its 100% uc bit waiting on biopsies.
The people on this forum are fantastic and I always feel like ive someone to talk to. Keep on top of your appointments make sure you attend them all.
I have said since January if u can get your head around what's going on inside that's half the battle!
Do you have anymore questions?
Stay strong. Millie, 29, female. X