does it get worse?

Hello, I was Dx with UC this past March and still seem to think I have somewhat mild symptoms...No D, just blood mucus and frequency in the a.m. with some mild cramping from time to time...Nothing too severe...I'm on medication now, and seem to be in remission, but we'll see for sure when I come off the prednisone...I do seem to be dependant on steroids...My question is, has anyone ever had mild symptoms and then it get worse? Does it spread as time goes on? I'm curious if I could be in for a rude awakening...I don't really worry about it getting worse or expect it to, but curious as to what I could possibly be in for in the future, as I do know everyone is very different...I read a lot on this forum and see that there are people in pretty bad shape, and thank God I don't have the severity as some of you all do...I guess I'm just hoping that my symptoms stay as they are and never get worse, BUT if they do get worse, I'll deal with it then...

Brandie

I was dx'd w/mild colitis 7 years ago and besides a few small flares have basically been fine, even when I am flaring, I can make it to the bathroom, its mostly just embarrasing when It's really loud and annoying when I stay with friends of friends who don't know and I have been holding it in for 5 hours praying I can get the bathroom and surrounding area by myself to let out the symphony of destruction (what it sounds like..gas puncuated by stools).

Right now I have changed meds a couple of times so I am still flaring on a scale of my 1 to 10, probably at a 5 or 6 today, but my 5 or 6 could be someone else's 1 or 2.

I am hoping this will get under control very quickly now w/the prednisone.  I did great on the 5ASA's but can no longer take them

When first Dx, I was maintained pretty well by just Rowasa, I could even get down to every other day, sometimes every three.  about 3-4 years ago sx's increased and had to go to Rowasa every day, then Dx w/IBS and other meds were added.  Every colonoscopy shows some increase in the disease, but not enough to freak me out.  Last year was the worst, why I can't tell you, couldn't stop catching a cold, had--not embellishing here--five flues throughout the year and in October of 06 had a major flare that ended me in the hospital for two weeks and out of work for five months and I'm still no where near where I was.  And you can see by my signature below all the lovely meds I currenlty have to take, long way from just Rowasa.  O.k., now here's the "positive" message for you: yes, things are a lot worse, but for some reason I don't have a fear about it (or the future), it is what it is.  If it get's worse than this I'll deal w/it somehow.  For the most part I'm TIRED (and frustrated) of the vigilance of my health, meds, etc.  I've posted some good "vents" on this forum on days I'm feeling fragile.  I think the best thing that came out of all this is that I really don't sweat the small stuff since this illness, or much, for the most part; I secretly laugh at some of the stuff I hear from people, "Can't sleep over which private school to send my kid to? Should I get botox? Do I look fat, I feel fat? I wish I had a bigger house, I hate my house????, I know I shouldn't have, but I spent 1700. on a LV bag, but I'm worth it: my mother-in-law (fill in the blank)...."  I guess, everyone has their own reality.  O.k, where am I going w/this, oh yeah, live in the moment, who knows what tomarrow will bring.  You may worry yourself sick over ten years from now and maybe five years from now somebody may have this all figured out and we will all be cured.  Who knows?

I have been reading everyone's post here and me being new, was just wondering, how do you all handle going to work, when a flare up happens, and I read that some of you are out of work for like 6 months, What do you tell your bosses???? or do you all keep quiet. I am on no medications at this time, I am waiting for what my doctor wants to do. because, he just diagnosed me as mild irritation in the entire colon and concerned might lead to chronic colitis. but I felt good all day, better then yesturday. I just wouldn't know how to handle this if I happen to get a flare up at work


Seahorse Lover

If you have specific questions, it's good to post a new topic, but I'll briefly answer about being out of work.  I've been at my current job for several years, so when I had a major flare and ended up in the hospital, my GI authorized state disability insurance, which gave me 67% of my current pay.  I'm still only working PT almost one year later, with a medical note signed by my GI--employers cannot fire you if a MD verifies medical illness.  I think the thing that saved me was I planned way ahead for the possibility my illness would get worse--I don't carry any debt, I don't live beyond my means, I have six months living expenses saved (I can hear the "that's impossible" but it can be done, believe me)--just good old-fashioned financial advice/planning.  As far as the working day to day stuff, I'm VERY lucky to work with compationate people that understand I'm challenged and when I'm at work, I give it my best.  Besides, there is something called American's with Disabilities--I know that there have been discussions before about whether UC is a disability, but I consider myself disabled with chronic conditions that do not allow me to function "normally."

I was diagnosed with UC in Nov of 2006. It was just in the rectum, with mild symptoms of pain and slight bleeding. The bowel movements became more frequent as I cldn't take measles as it gave me a pancreatitis and I'm allergic to sulphur. So the Dr's have bn at a loss as what to give me. Because of the frequency of my bowel motions I developed a thrombosis hemeroid which i had to get surgically removed as th epain was excrutiating. I then had really bad symptoms after the surgery. I then had to have a second surgery (because Dr's are Hacks) and now my UC i sunbearable I've likened the pain to no t passing painful stool. But to what I imagine will be what it is like to have a Baby and I'm not exaggerating I was loosing so much blood at 1 stage I cldn't get out of bed. Thats probably scared the crap out of you sorry. I am getting to a point which is that the worse my immune system gets the worse my UC gets. I'm now on only 3g of Entocort/budesonide I've only been taking it for 5 days now and I know once I stop my symptoms will be the same or

if I have to up the dosage I will probably get pancreatitis again. The only thing that works for me or was working b4 it got out of control was herbal remedies from a goo d naturopath also licorice and a green liquid called chlorophill which you get at health food stores mix with water and drink as many litres as you can handle. Good luck I'm sure I speak for everyone when i say i hope it doesn't get worse.