What are possible signs and symptoms of Ulcerative Colitis? You take ALOT of CRAPS, among other things
- Much more bowel movements per day compared to other people you know(2-3 times per day, not a big deal, 5-10 times per day consistently is a big deal)
- Consistently loose stools
- Loss of weight
- Low energy levels
- Waking up during the night to more bowel movements
- Bloody stools
- Using the restroom right after having a meal
- Running to the restroom and sitting down on the toilet JUST IN TIME
- Not wanting to be out in public for fear of not being near a restroom
- Being in your bathroom for 4-5 hours per day (man it was horrible)
- Cramps in your abdomen
- Enemia
- Night sweats
- Severe Headaches
- Dark urine
- Depression (often living with ulcerative colitis symptoms for a long amount of time can make anyone depressed)
- Fear of going out in public and having to use public restrooms
If you are reading this website and have any other ideas about symptoms to put down here, please fill out the form on this page and submit them on over. Who know’s you might really help someone out you don’t even know!
March 7, 2010 at 1:07 am
I have suffered digestive problems for some years and had food sensitivity diagnosed 8 years ago (yeast, dairy and tuna) but have since had irregular bowel movements , blood every time I go to the toilet and bloating and stomach pain, I recently had an endoscopy and 3 biopsy taken, the guy said it resembled colitis , but I have to wait for results.But (which I forgot to mention when I went for the test) the other thing that I have had for the last 2 years is a very sore tongue, which is cracked and coated white, I also often feel tired with headaches. Having looked at various sites re colitis and crohn’s I wonder if anybody else has had the tongue problem. I guess the digestive tract begins with the mouth?
BTW I really like your site
March 24, 2010 at 10:42 am
White coating on the tongue could be thrush. I had it once, I dissolved chewable vitamin C in my mouth and it was gone. Dunno about the cracking.
Much digestive difficulty is due to gut flora/fauna (I forget which is correct word) being overgrown, usually in response to too much carb in the diet. This is what causes GERD, too.
Look up: Leaky Gut Syndrome.
Visit: http://coolinginflammation.blogspot.com/2010/03/human-gut-flora-genes.html
August 18, 2011 at 12:29 pm
yes i have had that tongue problem i went to the hospital to see what it was and the doc told me it was from the steroids
February 22, 2012 at 4:34 pm
I remember how nasty that was, my doc also said it was from steroids…
November 18, 2010 at 2:25 am
I can relate to this on so many levels. My health ailments since childhood all seem to stem to UC. When I was young, I had constant ear infections, boils, and diarrhea. Then the doctors related it to my tonsillitis and had them removed. Then in my early teens, when I moved to Hawaii, I began to experience a rash on my body that would turn into blisters whenever I was out in the sun. They never knew what was the cause other than an allergy to ultraviolet light. In my twenties, it was severe depression which lead to a battle with alcohol, drugs, and one failed suicide attempt. When I went sober, I began to experience bloodied stool, excessive tiredness, mood swings, chronic arthritic pain, and bruises and cuts that wouldn’t heal properly made me wonder if this was because of my not depending on drugs or alcohol. It was years later when it was revealed to me that UC is an underlying variable.
I still have the fear of not going out much because of my bowel urgency but I make the most of it when I address it to the company I am with and then I relax better. I still am in Hawaii and while I cannot go out in direct sunlight for extensive periods of time; I’d rather be in “paradise” than to be somewhere else.
I have learned there are over 100 different symptoms of UC and it varies to each person. We just make the most of it and keep a sense of humour. Yes, it is hard at times but it does help bring peace of mind.
And finally, remember, build up your immune system!
June 18, 2011 at 12:14 am
dont forget nausea from the pain of going to the bathroom and also fevers. I have had uc now for 18 years, im 32.
February 26, 2012 at 11:46 am
Has anyone ever wondered what causes UC? We all have symptoms, but they are brought on by SOMETHING that causes our colon to react with mucous production, swelling, tenesmus, bleeding,etc. Drugs and supplements may help, but take a while to work.
Honestly, I believe my UC is brought on by stress. Doctors don’t want it to be that simple, so they deny stress is a cause. How may websites have you looked at that say “UC is not caused by stress.”? How many on this site subscribe to alternative therapy like yoga and meditation and say it works? I am living proof that stress caused my UC.
Are there ANY physicians or groups researching the CAUSE(S)?
If a cause was determined, then treatment would follow, but instead, we suffer in silence and denial, only hoping it will go away. Glad when it remisses, but stressed, sad, or angry upon its return. Let’s stop the cycle. I’m tired of this already and only a few days in. Does anyone know who we can lobby to do research?
February 26, 2012 at 5:27 pm
I completely agree with Wendy. I can point to stress in each of my major flares. Diagnosed in 1999, my job at the time was complete stress bath all the time. Last December I went into the hospital after almost 5 year remission (other than a few minor symptoms), and guess-a new job with stresses that were unmanageable put me there. Stress is the cause for my flares every time. Now I’m on immuran, asacol, and trying to retrain for a new career and the stress of this transition has me with symptoms again. I hope this doesn’t derail my chances to start over. And I am really taking care of myself-working out 4-5 times a week, running once or twice a week, no alcohol, minimal coffee, minimal processed foods or fast foods, lots of water and lots of good sleep. I know that stress triggers some reaction in my body that creates the flare and I wish I knew how to manage. Otherwise I am going to end up unemployable.
March 23, 2012 at 10:20 am
absolutely agree to stress. It does not matter what I eat, does not matter what medication i take…. stress/destress is the trigger!
March 26, 2012 at 9:58 am
I can relate. It seems like I have all these problems that seem unrelated to colitis, but really end up being related. Anyone ever have kidney stones? I was told kidney stones are due to colitis. Something about some of the fat that is supposed to come out in poop, doesn’t always for people with UC. It stays inside and then bonds with other things causing the stones. I had a 9mm stone stuck while trying to come out which was quite painful. I have more, and have passed quite a few.
And agree, with stress being the trigger.
May 16, 2012 at 5:09 pm
I’ve suffered with UC for over 20 years. I’ve flared under times of stress, and enjoyed complete remission for many months during times of major stress. Currently I’m flaring again (or maybe experiencing the same flare with a prednisone timeout), and I have drastically reduced my stress by changing jobs and outlook.
I can eat, drink anything during remission between flares. And during flares can eat next to nothing for months and still bleed (like now).
It makes no sense that I can fathom.
Best of luck, one and all.
May a toilet ALWAYs be within reach.
Eric