Gallstones? Chronic Diarrhoea And Stomach Pain


Mar 21, 2016

Been sick since late September 2015. Have had on and off chronic diarrhoea pain in abdomen,back ribs area and occasionally feeling like a heart attack. That would disappear in a few hours.

I have had a colonoscopy, endoscopy, blood tests, fecal tests, ct scan and pancreas.

Specialist isn't booked till next month. I also basically eat only salad and meat these days.

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Chronic Pancreatitis? Tender Stomach, No Gallstones And Pain

So since 09 I have had incidents where I get pain in my upper abdomen. Usually it's shortly after a meal, but sometimes it does creep up on me a few hours post meal. It varies in severity and duration. In the beginning I only had it once/twice a year, but the pain was excruciating for 4-7 hours. Fast forward to 2011 I started having these incidents like every 4 months, but with less pain. In 2014 I had an incident every month, but pain again was less. Here in 2015, it seems to be going backwards. I have incidents every 2,5 months now and the pain is far from what it was in 09, but its still painful (its a dull squeezing kind of pain). Sometimes it will go away if I drink a smoothie containing ginger,lemon, beetroot and stuff like that. Other times I need to go for a walk. But then there are times when nothing but time helps. The only pattern I have been able to identify is, that if I am very hungry and eat some junk, then I MIGHT get it. Other than that, I have not been able to find any pattern to when I get them.

I fear it might be Chronic Pancreatitis. This worries me a great deal.

Stools have also been acting weird. Switching between brown/yellowish-brown in color and consistency is mainly normal, but also range between somewhat loose/normal/hard

My stomach is also somewhat tender to touch in the upper right side/middle. Feels sorta like how a black eye would. Nothing too painful at all, but still something I notice here and there, since I can sometimes feel it when I walk around. 

Two months ago I had my stomach looked at by a doctor performing a gastroscopy. He didn't find anything there. No ulcers. He also did an ultrasound of my gallbladder and apparently also my pancreas (Only thing he said was it looked good and that I had no gallstones).

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I am three weeks post op having had a full knee replacement. My recovery is going well and I'm not using crutches or a walking stick but am still in a lot of pain and having to take painkillers. My question is I have developed loose bowels only once a day at my normal time but it has been going on for over a week now, I have no bloating or abdominal pain with it. I can only take paracetamol as I'm allergic to codeine and Nurofen I felt might be causing the upset stomach but I haven't taken them for nearly a week now. Has anybody else suffered diarrhoea after a TKR? 

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Since December 2012 my sister has had severe pain in the left side of her stomach. The doctors have tested everything even when she was admitted into hospital, nothing was found on CT scans, MRI scans and no results from blood tests... She has just had a key hole operation to have a look inside and see what it is but they have said again there is nothing there.

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Is this a sign of labour? I'm booked in on Monday to have my c-section and finally meet my little girl but I started getting diarrhoea today?

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I've been having pains in my stomach since I was 14 and im 18 now and its gotten worse, when I have sex it hurts after sex it darts to hurt really bad that I can't move and it hard for me to breathe, every morning I use the bathroom below my belly button starts to hurt.. And when i am just hanging out and doing whatever at home or anything it just starts to hurt when i laugh it hurts, At first it was my right side just hurting now its my left side too, I've been going to the doctor, I thinks its my ovaries but no one see it but it feels like it alot, and i've taken an ultrasound and they didn't see anything, now I have to take an upper GI X-ray.. I went to the hospital cause this pain was so bad I couldn't get out of bed.. I don't know what this pain is and no one seem to find what it is either I don't know what to do, I can't take this pain anymore.

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Arthritis? Chronic Pain Syndrome?

Has anyone else been diagnosed with this condition? I shall explain! for 10yrs i've been told i had arthritis in my right hip and right hand giving me chronic pain, only to be seen by 5 different doctors due to a recent change in location and investigations i've now been told i have , mild osteoarthritis in my right hip and the joint between my thumb and index finger.

Not only that but all differnet 5 doctors have said it was different things. seeing my own doctor today, she said (or applied) that the pain might be in my head, then to turn round and say that she was certain that i had A chronic medical condition and what it was she was unsure of.

Is this Chronic pain syndrome another name for they havent a clue whats going on?

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Chronic Pain Following Total Hip Replacement

I had both hips replaced in Feb and Sept 2011. Prior to this I had many years of pain and a great deal of difficulty with medical fields trying to determine what was causing my pain. Anyway once it was decided to replace both hips I was happy they had at last found a cause and what I thought was a solution. My first his replaced was my right and this seemed to go okay, it was a total different story with my left. I have been in excruciating back and leg pain since, I cannot walk any distance or stand for any more than five minutes. I need to use a wheelchair if I go out and crutches also, I am stuck at home all day while my family go out to work - I am frustrated and feel useless.

My pain is across my lower back and generates down my legs, my last three toes on my right foot go numb constantly. The pain is tingling, numbness, sharp, deep pulsating pain and electric shock type pain. The more I try to do the worse the pain gets. I spend most of my time with my legs raised as this helps, the pain never goes away but does ease when resting. I have painkillers and muscle relaxants but they do not really help. My hip surgeon like most of the forums I have read told me my hips are fine according to the MRI scan. He then referred me to the Spinal consultant, after nearly a year of seeing the spinal people they have now turned round and said the pain is not coming from my back and there is nothing they can do to help. I asked them what I was supposed to do and they said they had no answers!! I have attended all the physio appointments and even did a three week intensive course along with hydrotherapy - nothing has made a difference.

I lost my job due to all this pain and I am now registered disabled. I had more mobility (although painful) prior to my surgery than I do now. It was nice to read that other people are going through what I am experiencing (although I would not wish this on anyone) it somehow makes me feel better.

I have had numerous cortisone injections in the hips, nerve block of the L4/5 nothing has worked for me post surgery. I had cortisone injection prior to my surgery and guess what it helped - work that one out. I am now being referred to the Pain Clinic (again) and Rheumatology as it was noticed on one visit to the hospital that I had a butterfly like redness on my face and they queried Lupus (still waiting for those appointments - surprise, surprise).

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Masturbation :: Stomach Pain On Ejaculation

About half a year ago I was masturbating and when I came I tried to hold it in to make the orgasm last longer. I ended up getting bad stomach pains, my stomach started heaving a few times and I felt sick for a few minutes. Since then I was unable to ejaculate fully without feeling sick. This went on for a couple of months where I kind of stopped myself ejaculating properly. During this time I visited my girlfriend in a different state...and I felt very anxious when ejaculating. There was even one point where my stomach started to heave when the tip of my penis was touched.

However when I got back I decided to just cum for real and just see what happened...eventually my stomach got used to it and I was ok and could cum normally. All was fine until last night when I came and the same thing happened again with my stomach and I felt ill for a couple of minutes after and my stomach hurt. I masturbated again tonight and the same thing happened. It's hard to explain but it's just this weird feeling in my stomach where I feel sick and faint whilst I'm cumming. Afterwards I feel fine.

I think most of it is physiological because I am such a bad hypochondriac and I do get anxious at the most stupid times. I looked up on google for anything it might be and there's nothing. Nothing to do with the prostate or anything...which I guess is a relief. But it's still an odd thing to have. Does anyone else get this way? Were you ever diagnosed with something or was it just something you just ignored and got better?

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Pregnant? Pain In Stomach After Anal Sex

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Ever since I was a little kid i've gotten those really intense stomach aches/cramps whenever i'm doing something special. When I was a kid I got them every single morning before school, I used to sit on the floor and almost cry because it hurt so badly but they always passed as soon as I got there. Nowadays I don't get them every time i'm going to school but every time i'm doing something special like going on a date with my boyfriend or travelling somewhere! I get so nauseous, I run to the bathroom several times and I can't eat for the entire day. It has been so bad I was on a date once and I couldn't eat, I had to force myself to and later run to the bathroom where I nearly threw up. I don't get nervous, at least I don't feel nervous.. but maybe that's it? I just think it's weird because I can be super excited about something but those stomach pains ruin everything..

Also lately i've had this weird burning sensation in my stomach, it gets worse when I eat spicy foods or drink coffee or anything else with lots of caffeine like energy drinks. I've never been sensitive to either before in my life. I've been a coffee drinker since age 5. Believe it or not..

But those burning stomach pains they have been there for maybe 2 or 3 months now.. everyday more or less. It's getting really annoying.

Any ideas what either of those things could be? Do I have a sensitive belly or something and how do I treat that?

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Prior to those two meds. I had an excruciating and unspeakable pains that waking me up in the middle of the nights lasted about 10 minutes or so. Furthermore, the pains made all over my body sweat like taking hot bath, because of excruciating and unspeakable pain. Those nights, I self-exercised stomping, and often back and forth legs on hard floor in trying to subside the pains.

However, despite maximum doses of two pain meds., I still have been experiencing 'stiffness' along with 'pain' on my legs, some mornings before getting up from the bed.

Is there any good meds. for me more to manage and first of all control muscle spasms and cramps on my both legs?

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Alternative To Opiates For Chronic Nerve Pain?

I live in the U.S. so the drug names may be different.  I have been taking hydrocodone (norco) 2 x 7.5 a day for over 2 years.  I had neck surgery in 2012 and within 6 mos the pain in my neck and left arm returned, along with the nerve pain in my arm.  After ruining my digestive system with ibuprofen ( I was taking at least 8 to 12, 200 mg each,  a day) I gave up and went to pain management for help. I had successful injections for low back pain a year or so before that, so I thought that is what they would want to do for this.  But the doctor said that it would not help, probably because of my surgery, I'm not sure now because its a distant foggy memory.  Anyway, the result was pills.  At first it was only 5 mg 2x a day.  Then he upped it within 2 mos to 7.5 mg. 2x a day. Since then I have read  a lot about opiates and know that it is very addictive.  I take it as prescribed but that means that I am just addicted to the prescribed dose.  I had surgery in September for my digestive problem that all started with the ibuprofen.  After the surgery they gave me Oxycodone.  Within 3 doses I started sweating and having a headache soon before my next dose was due.  I recognised this right away as a symptom of withdrawal.  I immediately stopped taking that and just suffered through the surgery pain with my "usual' med, hydrocodone.  Within a month, I started to realize that I have the same symptoms to a lesser degree with this med.  This can only mean that I am addicted to it.  When I went to my doctor for my usual appointment and med refill, I asked if there were any alternatives to Opiates.  I said I was uncomfortable taking this and wanted to find something else.  He said "Tylenol?, that's your only choice."  I was floored.  Well, I know tylenol can ruin your liver, so that wasn't even an option.  He then said, "the holidays are coming up, why don't WE wait until after that and rethink this".  Wow.  I was truly speechless.  So I took my scripts and left.  I did NOT make another appointment.  All that to ask this question.  Does anyone know if there is ANY option to opiates for chronic pain and permanent nerve pain?  If I do not take the med, my pain comes back, but the Nerve pain is the one that drives me back to take the pills.  Now it's in both arms and when the med starts to wear off they start to ache, then burning and tingling.  I have tried reducing the dose by taking half a pill, but all that does is make me count the hours to the next half pill. ugh. I want off this stuff and I know it can be done!  I have read several success stories right here.  Other symptoms I have are anxiety, depression, anger, constant waking up at night with the sweats.  I need support, answers, and a way to do this without losing my job,all my friends and my mind!!  

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Women Pelvic Pain :: Chronic Prostatitis

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