Diverticulitis/IBD :: Diverticular Bleeds Usually Stop On Their Own?
Oct 21, 2015
I have had diarrhea and rectal bleeding for a month and discomfort (but not pain) lower left side. I went to see my GP and she ordered blood and stool samples. A few days later I woke up in blood stained sheets and when I got up blood was running down my legs. I called 111 and was told to go straight to A&E. They kept me in all day on an IV drip as I was dehydrated with sluggish circulation and later discharged with antibiotics Co-Amoxiclav and a letter for my GP saying Diverticulitis/IBD?
Flexible sigmoidoscopy/colonoscopy/CT scan have been booked for 31 October. Despite the antibiotics, the diarrhea and bleeding continue and although I am drinking lots of water, I have a continually dry mouth. This is the first time I have ever experienced anything like this and am naturally very concerned. I don’t quite understand what is happening. Are the antibiotics to take away the inflammation? Will the bleeding continue until the inflammation is gone? I read somewhere that diverticular bleeds usually stop on their own. Is a month a long time for bleeding to continue? I am trying to be positive but feel very run down and 31 October seems like a long way away for the tests. Any advice please?
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I found out 6 months ago I had diverticular disease after a flair up of diverticulitis. I have recently had another flair up - a few days ago. Although it seems mild it is still fairly debilitating but doesn't seem as bad as first time. I don't know if I am experiencing day to day diverticular disease symptoms or diverticulitis? First attack had fever with it and feeling sick but this one is just pain and diarrhea and feeling really down. Can't eat except for liquids. Is this diverticulitis or diverticular disease and how do you know the difference? Is it to do with the fever being present or not? I am so worried as no real information has been given to me and I feel scared I won't be able to live a normal life with this. Can someone tell me the difference and should I be heading to the doctors as soon as i get a flair up or just put up with it until it gets worse? I have read so many scary things about it I don't know if I can cope.
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I'd love to know how long other people's flare-ups last on average. Have had D disease x 15 y. Had 3 attacks in past 6 wks. Urgh! I usually take antis & get up after 1 or 2 days, liquids only x 36hrs then soft foods x about a week, then gradually reintro fibre, seeds, pulses. Maybe I should stay on soft food more than a few days after 36h on liquids?? Opinions please! And btw its almost impossible to lose weight when this rotten condition dictates eating all the wrong stuff after an attack.. White flour pasta, mash..all those carbs! And stodge! Not helpful. Any ideas? Thanks. New to forum. Am 63 now & desperate to do anything to avoid surgery.
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I`ve been getting qite regularly dizzy spells where i need to sit down and start sweating and feeling ill. Then it just passes quite quickly. I`ve also been getting quite a lot of nose bleeds too.
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I have been suffering with pile for almost 5yrs now and have had no treatment. Recently noticed a something strange like a seed on my rectum.it itches and bleeds at times. This grows from the flesh that comes out as pile and goes back in. What can this be?
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I think I may have iron deficiency anemia my mom had it when she was younger and I have really bad nose bleeds in the middle of the night I have also fainted and I don't want to go to the doctor. Just wondering how dangerous could it be?
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I was Diagnosed last week with Diverticulitis, After 18 months of being in pain. The Doctor offered me surgery as soon as he told me I had Diverticulitis.
It's all confusing to me. so many different symptoms and different stories.
Can anyone tell me if I need to see my GP after being Diagnosed with Diverticulitis for antibiotics or anything else.
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My Mom suffered from Diverticulitis but she passed last year and her and I had never really discussed anything about it other than my sister or myself might eventually suffer from it because it could be hereditary. I have some questions that I would have asked my Mom but now I please need help since she’s gone. And I was too stressed and forgot to ask my GI these questions and he’s not reachable on the weekends. Thank you.
I’m a 47 year old Male. And I just started my Ciprofloxacin 500 mg (2 daily) & Metronidazole 500 mg (3 daily) yesterday. GI said to take the pills for a week to 10 days.
- How normally long before the more extreme burning sensations will begin to dissipate? 2-3 Days?
- How long should I stay on the liquid diet? The entire time while I’m taking the antibiotics?
- I bought Carnation, Boost & Ensure food drink supplements - Good idea?
- I also bought jello, pudding, chicken stock, red, white & blue popsicles, ginger ale, apple juice & plain yogurt - All good? Any other recommendations?
- How much water should I also be drinking daily?
- The Metronidazole seems to be awful. I have a metallic taste in my mouth, evening & morning headaches, stomach cramps & a nauseated feeling all the time. Is this normal?
- Any other suggestions or advice?
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I've had this condition for many years. Recent tests/scan show it's now extensive throughout the bowel. I've been given conflicting advice on appropriate diet and wondered whether anyone can provide more help? I've been taking fibre gel every other day for many years. Consultant insists this should continue.
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i have been told i have Diverticular disease, i have been given Mebeverine 135mg but have found they make no difference at all. I am so swollen and as they day goes on i look like i am pregnant. This has been like this for 7 months. I am so fed up and my left side is so uncomfortable. When i have a bath or shower you can see the left side swell.
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I went for my 2nd opinion today with another Gastroenterologist. The Surgeon had referred me.
He said he wants to do a gastroscopy and also a sigmoidoscopy. He also told me that one of the medications I have been taking for years for my hiatus hernia called Prevacid could cause diverticular colitis.
Has anyone had diverticular colitis?
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I was diagnosed with Diverticular Disease in Dec 2013 after 4 days in hospital and the Drs having no clue what was wrong. After having a CT scan they found the problem. I was 30yrs old and if I'm honest I was shocked. I felt this was an 'elderly' thing.
Since my diagnosis I have had 4 bouts of diverticulitis that I have dealt with myself. I take paracetamol and go on a liquid only diet for 4 days and until the symptoms go away. I had a sigmoid colonoscopy in April to see how much of my colon has these diverticula and the Dr said it was of medium severity at this point.
The only way I can describe the pain of a flare up is like having contractions, I've had 3 children and would take childbirth over this any day.
The point I'm trying to make is that I have found there is little or no support for people with this digestive disease. I read conflicting reports on what I should be eating to help live with this and its starting to take over my life. I run a business and have 3 children so I need to be able to manage this.
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I think that i have just had the shortest appointment time with a doctor.ever
Four minutes max. Told I had severe Diverticular Disease, to eat a high fibre diet, ,and to look on the internet if I wanted any more information, then he was out of the door, and that was it ,,except for a parting shot delivered in the corridor ""to come back if I had it again"
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It may seem a silly question but I would like to get fitter - take up running - in my fifties and just wondered does exercise help with DD or make it worse? Anyone out there exercises avidly? I feel so depressed since my diagnosis - like my life is over! I suppose this is a bit dramatic but anyone got advise on exercise?
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My mum was diagnosed with both colitis and diverticulitis, she was put on a (9mg) 2 month course of Budenofalk granules reduced to 1 week 6mg and then finally 1 week 3mg. The diarrhea and need to go to the toilet eased during this time, however she has now been of the medication and is back to having to rush to the toilet again, we are awaiting for a follow up appointment at the hospital but this isnt until next month, she visited her gp last week in the hope of some help/advice - they were only able to try and get the appointment pulled forward. She has lost just over 3 stone since November, and we are at our wits end as nothing she seems to eat/drink remains for long, within 30 minutes of having anything to eat she has to visit the loo. She has been taking the acidophilus 10 billion since the beginning of the year. Can anyone offer any advice is there others that are in this unfortunate situation, she feels like she is wasting away and a prisoner inside her own home.
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My breasts won't stop growing, how can i stop them, at the end of last year i was a 10DD/E (32DD-32DDD/F american sizing ) i'm now bulging out of a 10i (32J american )i can't go up a back size as a 10 is already loose..
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How can i stop smoking ? And what it's effect on body?
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long story short i have body acne and use to have a lot on my face but now its all mostly cleared up. My face still is red from the acne that was there. I started using aveeno .5% sylacic acid moisturizer. i now have an itchy face and few knew zits. Should i stop using it? I also use 5% benzoyl peroxide wash and on 40mg of accutane once a day.
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I always get the feeling I can't breath properly...I can but I get that feeling and it's getting worse as I get bigger....when in Labour with my first daughter I freaked out and couldn't breath 3 times. They called it a panic attack...? I'm starting to get really worried it will happen with this birth,but worse! And it's already happening . I calm down and take deep breaths but it is extremely scary!
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I'm so fed up! I don't see how my life can go from so good, to this complete isolation within a couple of weeks. I'm constantly anxious about my future, and what lies ahead for me. I feel so insecure, and feel like i'm living my life day by day, to survive. Citalopram is just making me tired at strange times of the day, i have NO motivation to do anything at all. I tried to see friends yesterday, but didn't enjoy it at all, i just wanted to be at home, this is not me? I feel like i've got someone else's personality.
Work is so hard, to just be in. I feel like there's no one there for me other than my Mum.
I seriously don't know how i'm going to get through this now. I'm so scared.
I'm seeing my counsellor later today, its the only thing thats keeping me going today.
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I have been on Mirt for about 5 weeks now.
I started on 30mg but the side effects are horrendous for me - it started with just a few aches, that gradually got worse by the day until every muscle in my body hurt (even my fingers and toes) and had put on almost a stone in weight. After 3wks on 30mg I had a follow up appointment with the Doctor, after mentioning all the problems I was having, he decreased my dose to 15mg and said a reduced dose would help with the side effects - it did for a few days, but the past week all of the above side effects have returned and are again getting worse each day.
I am going to stop taking them. Yes - I do feel I need something for my low moods - but my Doctor was reluctant to change the medication and the side effects are making me feel terrible physically.
So without the lectures of 'go back to your dr' etc etc, I am after some advice on how to stop taking this medication? Do I just stop? Do I lower my dose again, or take the dose every other day and over how long a time period?
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