Chronic Pancreatitis? Tender Stomach, No Gallstones And Pain
Jan 5, 2016
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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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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I just got out of the hospital yesterday - was diagnosed with acute pancreatitis. I'll be following up with my primary care doc tomorrow. They ran all sorts of tests on me during my stay, but never mentioned that this may become a chronic thing. Does pancreatitis always have to become chronic? Do many people just have this one occurrence, then never again?
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I suffer with chronic pancreatitis since 2007 I have really bad anxiety and depression with it, my conditions were all caused by drinking way to much alcohol. I haven't had a single drop of alcohol for 2 years yet I've been admitted in hospital 4 times in them 2 years for my chronic pancreatitis. I live in the UK and I see a professor who deals with chronic pancreatitis once a year where I have a CT scan with contrast to see how my pancreas is, so far it seems to be holding its own but recently I am becoming more nausea everyday and vomiting everyday and its stopping me from eating. If i eat a small amount of any kind of food I'm instantly bloated all the time, I do smoke but I just haven't got it in me to stop smoking like the way I stopped alcohol because Iv'e been an alcoholic since 1994. I take medication everyday, propranolol for anxiety, omeprazole for acid in the stomach, vitamin b compound, and I also take tramadol 50mg when required because of my chronic pancreatitis pains I get everyday. At night i take pizotifen for my migraines and i take mirtazapine 30mg for my depression, I do really worry about my health and recently for the last month Iv'e been constantly vomiting everyday, I'm not eating as the smallest amount of food makes me feel bloated and gives me heartburn, but most of all I just haven't got no energy at all. Can someone help please as Iv'e asked my doctor for all kinds of things but he just says its due to your chronic pancreatitis, the last four weeks my days consist of coffee and smoking and so on, I can't eat and I'm feeling sick all of the time.
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I have gallstones but thanks by the grace of God I don't hafta have surgery I just need to follow up with a doc about getting them out so their not in no dangerous way right now I just need to act fast I was told not to wait to long because they can become serious and I don't want that but I do have the swelling of the stomach so I want to know as well is it the gallstones, I can sometimes feel a knot in my stomach and see it as well and I have a feeling is the gallstones...
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swollen neck glands are pretty common I know, but do many of you also get swelling in the groin area as well? This is new to me. I have not had a good week and earlier in the week I had swollen neck glands which I am familiar with, sore throat, aching muscles etc but today found a swelling in my groin which is tender and warm. Should I be worried?
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I was diagnosed with CP about a year ago. Since then I have quit alcohol, fatty foods, and exercising a lot. However, I noticed that although the pain had subsided, I was still getting this annoying pain from time to time. I finally got to know that coffee, coca cola, and a lot of tea during the day was causing the pain. Now I only drink one tea bag 3 times daily and the pain has gone. Hope this will help some of my friends with similar problem.on this forum.
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I'm not sure where to start. A lot has been going on in the past month. It all started when I started to feel like I had a couple of drinks when I had not. I was able to calm myself down because I thought I might be having some sort of anxiety attack. Long story short the symptoms did not go away. So I saw my doctor last week. With my vague answers to his questions he mentioned he wanted to do some further testing. Part of the testing was blood work and a 24 hour urine. That was last Wednesday. I had the blood draw on Thursday and turn my 24 hour urine and on Friday morning. It just so happened that I started my period on Friday. Its normal for me to feel a lot of lower back pain during my periods. this time is a little different. I started to feel the lower back pain then the pain moved to my upper abdomen on the left side. Then the pain moved to my lower right side of my back. now the pain is back on the left side of my upper abdomen. Of course everything that I have been reading leads to one thing... Pancreas. after calling my doctor my blood work has come back normal. However my urine test has not come back yet. They told me it could take up to a week. In the past this pain may have been here and it has gone away. But because of how much reading I have been doing on whyI have been feeling funny I've noticed the back pain and the abdomen pain a little more.
I have an appointment tomorrow afternoon. However I'm really scared.
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So DH has been taking the Aloe Vera juice for almost a week now and is feeling better now than he has for the last 6 months and I was wondering if anyone else was interested in trying it to see if it made any difference to their level of pain?
He drinks a 1 litre bottle over the course of about 3 days.
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I'm seventeen and I had sex with my boyfriend almost a week ago (this isn't our first time) and after we..did it. I had tender breast I couldn't even touch them they hurt that bad and he didn't touch them during the intercourse I also have had insanely sore sides to the point I have to hold my sides when going to the washroom because the pain is so bad , what is wrong..
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I have had issues with a frequent urination and a constant pressure on my bladder for over a year now. But since January of this year I have been experiencing extreme pain in my low low abdomen (like groin/cervix area). The pain also resides in my stomach and back. My ribs are sore to touch and I am constantly achy. I have been to the doctors who have done internal exams and say that everything LOOKS ok. I am 20 years old and my periods are regular. The pain is becoming a real problem and I'm becoming increasingly concerned. I have had ultrasounds on my pelvis and kidneys and they were fine. I've been put on meds to stabilise my bladder, but the gynaecologist won't see me for another 4 months. I know there is something further wrong with me - I can't understand why the pain keeps occurring. I don't enjoy having sex due to pain and a constant discomfort and pressure-like feeling. I'm starting to get very depressed as there is no diagnosis being made and all the tablets I am given do nothing.
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What could it be?
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I was diagnosed with shingles in my forehead and eye 6 weeks ago,( the worst kind!!) and after weeks of discomfort with eye and forehead re-infecting, watering eye, headaches , itching etc, I now feel better in myself and my vision is ok, but unfortunately I have had complications ands am left with such painful neuralgia, my head hurts just to touch it and my temple is so tender, I have been told that this can go on for months or longer.
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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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I just started reading about this and it really sounds like I may have this but I'm not sure. I have headaches sometimes that are awful and seem to start from my neck and back of my head. I see a chiropractor once a month and my x rays showed problems in c5 and c6 in my neck. I also have notalgia paresthetica which itches me too death sometimes in my right back shoulder. We figure it's caused from the c5 and c6 in my neck. I never sleep all through the night, always tossing and turning. And I feel fatigued ALL the time no matter how much rest I get. I had a blood test and my vitamin D is low. I can find "knots" on my back, usually I can find about 5 or 6 of them, even on my sides. I work a very physical and mentally stressful job and this causes me a lot of pain. When I am working usually mid day I will get a horrible sharp pain somewhere in my back and it just stops me. It's like someone taking a hot knife and stabbing me with it. It's hard for me to straighten myself up. My pain is in my mid and upper back, rarely ever in my lower back. I do get dizzy sometimes also and feel off balanced.
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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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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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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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i have rash on the penis (red dots) and they are not painful but have severe stomach pains. any idea what is it? medication?
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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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had anal sex with girlfriend .. now worried if she will get pregnant.
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