Diverticular Disease :: Pain And Diet Management?
Jun 27, 2014
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'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 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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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 have an 8 year old who was diagnosed with Coeliac disease last May and has been following a gluten-free diet ever since. Her symptoms previously were pins and needles in hands and feet, mouth ulcers, calcium marks on teeth, bloating, aching joints and bones, and small pink spots on the face. She is also quite small for her age. Her symptoms have cleared up, However now and then she gets sick if we have problems with cross-contamination.
My problem is that she is still experiencing a degree of joint and bone pain. About 2 weeks ago was the last time she got sick because of cross contamination, but last night she couldn't sleep because of the pain. Is this normal - does anyone else experience this?
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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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I recently went on the Juice Plus diet and was told it didn't contain gluten even though it does contain Oats. Since starting the diet all my celiac symptoms have come back. Aching joints, swollen face and wrists and extreme tiredness. Has anyone else found this?
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I've just been diagnosed with Coeliacs disease and am finding it very stressful shopping so far. I am following the weight watchers diet as well but all the GF breads seem high in calories. Also I've had headaches for the last couple of days and feel like I'm in a world of my own. Could these be coz I've stopped all wheat or just coz I'm stressed. I've joined loads of groups online and have all the info but it seems like information overload.
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Basically I am 25 years old and as i've grown up I've noticed more and more that I was getting stomach cramps and bloating more and more often. It is very sporadic and I couldn't really say exactly what was causing it but I just thought it was normal. This was until the last 12 months when I started to think a bit more about it. I do a lot of exercise and play a lot of football. I was finding that I would get some form of cramp during a football game. Usually quite mild but sometimes worse. I also like to run and when training for a half marathon found that after a certain distance I would get pains. Almost every time after about 30-40 minutes running. It would normally be worse when running in the evenings. I started thinking about it and tried taking several things out of my diet. I am 95% certain I have a lactose intolerance as since cutting that out around 6 months ago I have seen an improvement. But I would still get pains.
This all resulted in me going Gluten Free and I finally experienced what it feels like to have a normal stomach. I was relaxed and could do whatever I wanted without any fear. So I decided for my own health I should get tested for celiacs disease and after 7 weeks of eating gluten again had the blood tests. Today I had the results and they have come back negative. I feel so deflated and just angry. What do I do now? I just feel like going back to Gluten Free and living like that self diagnosed. The weird thing I find with my disorder is it seems to be worse when i'm up and about. If me and my fiancee have gone out around town and have lunch it is often worse when walking around afterwards. I don't always get blinding pains either. It is often just severe constipation or stomach cramps just making me feel uncomfortable.
Really disheartening now and just want to know but can't carry on for much longer and really don't want to keep eating Gluten when I know I feel good when I don't. Any advise?
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I was switched from Nucynta 50mg to to Opana 5mg (OxyMorphone) by my Pain Mgt doctor and I have a total different experience. I don't know if they messed up or what, but here's the issue.
While I was on Nucynta, I would take it, and eventually feel the effects, i.e. the lightheadedness, the "high" feeling, and also the pain relief. The reason I was switched was that Nucynta gave me migraines. Bad enough where I got ill and had to run to bed with all lights off.
Onced I was switched to Opana 5mg, things were different. I took 3 last night, my very first dosage, and took the first. No effects, no pain relief, no "high" feeling, nothing. So, about a hour and fifteen minutes later, I took another one. Still nothing. So I wait again, same amount of time, took a third pill...... Nothing.
So, when I saw the doctor originally and was switched, I was told that Opana was an equivalent to the nucynta. So, if it's an equivalent, why did I go from 50mg to 5mg? I'm just curious. I know they are different drugs and probably manufacturers. Can anyone shed some light on this bizarre issue?
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I was in a car accident about a week ago and 4 days after the accident I started having pain on the left side of my ribs right under my breast when I take deep breathes, yawn, sneeze, ect. It a little swollen but doesn't hurt to touch. what could this be?
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Couple days ago I stepped out of bed and almost hit the floor as the excruciating pain shot through my calves. I have not exercised or done anything extreme. I have tried stretching and over-the-counter pain meds ..
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I have excruciating pain on my right side almost constantly and when I take a 1mg xanax, my pain goes away. Why is this? A Lot of people question this when I tell it but in all honesty it works. I wouldn't be telling it on here as telling it on here doesn't benefit me at all. I would just like to know why a xanax will stop my pain on my right side. Any ideas?
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I have asked to be removed from all pain medications as they were not helping at all and did not want to just keep increasing dosage. So my PM Dr. suggested i try Ativan or Diazepam before bed and also a muscle relaxant called Baclofen for spasms during the day (which i had been on in 2013) it did not work, but he insists on trying it over the Soma 350mg i had been on before the surgery.... any input
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I have been on 3 pills a day of norco 10/325, I want to slowly taper off. I need a plan that would be with no W/D's. I thought about starting a reduction of 1/2 a pill every week until I am free of the pills.
I also need to stop taking celexa, I am going to cut back 1/4 a week to iam off.
Will this work?
Or do I need to get suboxone and is that addicting.
Once off the pills, I don't know what I will do about my chronic pain.
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My dr. did a CT scan on my left side to see if I had sciatica as I had a lot of symptoms of it. It showed minimum damage to the nerve. I was not told what to do next? Should I get a follow up with what kind of specialist? Would a MRI show more information then the CT scan?
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will i have withdraws after taking suboxone 3 weeks? they put me back on pain meds because i having surgery soon
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I went to my Pm yesterday and let him know that I wanted off the methadone. So since I had to see the NP because it was considered an emergency visit they decided they were going to put me on the patch where you wear it for three day then take it off. So I asked about the side effect and after hearing them something in me panic and snapped and I said forget I want off of everything. So as off right now I am coming off of the methadone. I decided that with the scare of my heart and the new neurological problems they only way to know is if I come off of the meds. I am still on the Topamax he did not want to take me off of that because I have been on it for over a year and never had a problem. SO I am hoping in with 2 months we will know if it was the meds causing the neurological problems or the something else.
What made me snap was I was telling him that I wanted something for the muscle because I was having a lot of spasms and tightness and off of the methadone and he totally ignored me and said well we are going to give you something a lot strong and this should work since the methadone has not been working. It was as if he was not listening to me. He said to me you are going to Cleveland clinic (CCF) to be treated for the muscle so the will figure it out soon, I said yes but I do not get medicine from them because I have a contract with you. I don't know why he would not give me a muscle relaxer but I feel better knowing that I am coming off of the medicine for a while I just hope I can handle the pain long enough to see of it is neurological or a side effect from the methadone....
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.I had a C5-C7 disc fusion done 5 years ago that alleviated all of the pain in my neck and shoulders. What I am left with is a severe case of peripheral neuropathy. My feet and legs are numb to the touch but hypersensitive when I walk so I cannot go very long distances without the tingling burning throbbing pain. This pain is heightened at night when I go to sleep thanks mostly to the 300mg of Lyrica twice daily. I had an EMG nerve conductivity test performed which of course indicated severe neuropathy.
Now I am going to a neurologist who says I have to put up with the pain. I am going back on Monday to my neurosurgeon to ask for a lower MRI (never done) and I wanted a referral to PM because the pain is out of hand on 600mg of Lyrica daily. I have been on Oxycodone before and hated it and I do not like the stigma attached to these drugs so I thought I would ask my doctors to consider Methadone. What does everyone think? I know Methadone has its own stigma but is long acting and something I NEED right now and probably for good as I have had this neuropathy for 5 years.
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My 12 yr old son is experiencing no BM after 4 days of switching him to this GFDF diet ... Before he was IBS .... Not sure what to do
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I have suspected Piriformis Syndrome & SI Joint Dysfunction also causing sciatica, have also had some nerve pain in the back of my thigh, occasional calf cramps, foot cramps, and foot pain. Since my last Cortisol injection into my SI joint it has made everything horribly worse, I cannot sit now for very long without severe left foot pain that makes me feel nauseous it's so horrible. I have informed the consultant of this and am on a waiting list to go back and see him, this is the 2nd time the injections have caused me extra pain so have now lost faith in these and want to try alternatives.
My consultant previously wanted to put me on Amitriptyline but I have been on this before and was taken off it due to serious sedative side effects (even fell asleep eating in a restaurant) was on a small dose and still didn't improve with time. So I've read that Nortriptyline is an alternative with less side effects, can anyone advise if they have had less sedative side effects with this than Amitriptyline please?
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