As a pancreatitis sufferer I found this threas really interesting.
My problems started September 2009. Suffering "stomach cramps" and was diagnosed with IBS, although no bowel difficulties! The medication I was put on didn't help and in November 2009 I almost collapsed at work and got rushed into A&E. I was in hospital for 10 days with pancreatitis, on a drip, doing lots of tests. They didn't find any gallstones and think I was suffering through my lifestyle choice, drinking, eating what I wanted (being so young, only 19 at the time, what I ate didn't really affect my waist!). They told me to quit drinking and take some medication and it will clear up. Whilst I was in hospital I was on paracetomol, which made things worse, realising I'm actually allergic to it! So came away from hospital having learnt something and a bag full of pills! I stayed off work and had the dullest Christmas of my life. My pains eased off but I wasn't completely pain free. Probably a day before new year I started suffering again real bad. I was due back at work a few days after new year- unfortunately never made it! I ended back in hospital with pancreatitis again. again no gsll bladder issues, so drip, pain killers, a week later they sent me on my way with morphine tablets. I started back at work mid-feb 2010. Still suffering pain a fair amount but managable. the hospital never once told me to stop drinking alcohol or change my diet. So I stopped drinking whilst I felt bad but eventually, around late march time (fed up of being 19 and not being allowed to drink) I started socially drinking again. Little bits of pain here and there, but nothing a few codeine couldn't solve!
My pains eventually pretty much disappeared around the September 2010 time, so a year of suffering!
Had a nice few months, forgot all about my recent troubles, had a nice christmas, started a new job etc!
Until the end of February!! I was suffering stomach (sort of right hand side under my ribs.... as before) pains in the week but thought I'd eaten something. I went away for a friends birthday and had quite a weekend on the ale. Sunday morning I woke up, being sick a lot and in agony! I was meant to drive 200 miles home in that state, lucky for me my partner can drive! So I got home ok and on the Monday went to the doctors and had a blood test and got pain killers. that night the emergency doctor rang and said my Amylase levels were 210 and my lipase levels were over 2000. Hence the pain! Definately pancreatitis, if the pain gets worse or become dehydrated i was to go into hospital. it took until the next morning and i was in hospital.
they pumped me full of vitamins and stuff and was on a drip for 2 days. luckily they only kept me in for 2 nights and came out on the 3rd march 2011. today it is 12th march and i am still in agony and have been sick a lot today. i've barely eaten since coming out of hospital and iv been drinking 4 litres of water a day.
really im looking for diet tips for low fat, what i can eat and what i should avoid?!
and also, is anyone who suffers from pancreatitis diabetic? or have a family history of diabetes? although i am not diabetic myself, my grandad was and i wonder if with it being the pancreas then there is some form of relation?
thanks
J x
We can now eat out like we use to. When he first came home all he could manage was about 3 spoons of soup at a meal.
We wish you well.
I always went to the hospital because of something else,for example: my Appendix, flew virus etc. But the always kept me longer because my blood results of my pancreas where very high. I'm also not in real pain, feels more like a stronger heartburn or pressure in my chest, when i'm eating. I don't drink anymore, and before that, i was not really drinking either.
I hope that forum gets active again, because it feels good to talk to people who go through the same, and know how hard it is that the doctors dont find anything. I kinda gave it up, I'm like i dont care anymore, I don't wanna be for the rest of my live on a diet I'm 27 years old, but it looks like i have to
Your mention of being on Amoxicillin rang a bell. My husband had just finished taking a course of Amoxicillin on the day of his attack. If you look it up you will see that is one of the side effects of it - causes pancreatitis. On his discharge paper the doctor noted that Cimetidine and Zocor are also probably causes of it too and had him discontinue taking them.
He has found that he can not eat much chocolate candy either. He now only drinks decaf coffee or tea when we eat out.
Had his second CT scan since leaving hospital in December and we will meet with the doctor tomorrow to discuss what it shows. His first one showed a psuedocyst and necrosis on the pancreas.
Thanks for all the stories and helpful tips. Just reading others experiences is helping me to learn to manage my own.
I am a 32 y.o. female. I had my gallbladder removed 16 years ago when I was 16. I have a strong female family history of gallbladder problems. My mom, sister, 2 aunts, grandma, several cousins have all had it removed at a young age, not obesity related either. I am 5'8, 175 pounds, so I am overweight. I am a frequent runner and triathlete. I run 12-20 miles per week.
I had my first (and hopefully last) pancreatitis attack 5-12-11. I had just eaten a bowl of cereal and drank a glass of chia seed water when the pain hit. Within 20 minutes, my husband called my EMT father to come and assess me. He was on call that night and made the call to transport me to the ER via ambulance. The pain was almost instant and increased in intensity until it was unbearable. The pain was localized directly midline below my sternum down to a few inches above my belly button. After an initial assessment they drew blood and took a urine sample. They then gave me Demerol via IV and the pain eased off a little, but still came in waves that intensified and then backed off. My labs came back with amylase level of 145 and lipase of 1225. They did an abdominal ultrasound, and everything looked unremarkable. They could not discover any cause of my attack.
I was discharged with instructions to not eat anything NPO for 3-4 days and then slowly re-introduce clear liquid diet and go from there. Luckily I had a dad who could give me IV bags twice a day and avoid being admitted to the hospital. He would text me in the morning and ask if I was ready for my "breakfast". The pain subsided and I managed it with Lortab 7.5 and IV's twice a day. I did take sips of water and PowerAde. Yesterday was the first day I tried eating anything. I had 1 cup of noodle soup broth for lunch and 1 cup for dinner. I snacked on 1 piece of bread through the whole day. I AM STARVING! :) Today is day 5 of eating pretty much nothing. Every time I think about eating, I'm reminded of the pain and I refrain. I'm so scared to eat anything at this point. They removed my IV line yesterday so now it is all on me to stay out of the hospital. Every twinge of pain, lack of urine, diarrhea makes me freak out. They drew labs yesterday and I am waiting for the results.
From what I've read, mine is a milder case. I want to keep it that way. I'm so concerned about what changes I need to make to my diet and how this will affect my running performance and abilities. I have a 10k in 2 weeks. I have a follow-up appointment with GI doc later this week.
Thanks for all the help! This was been a scary weekend.
Hi
I just spent 5 days in the hospital with AP. I had my gall bladder out in 1983, am a 50 year old female, slightly but not ridiculously overweight. I have had intermittent stomach problems for years, but never anything like this. My lipase was over 8,000 upon admission to the hospital. I had every ultrasound and CT they could do. When I left the hospital, I was given no instructions other then stay on a soft bland diet and no fats. I went away on vacation and had some horrible bouts of pain despiite being careful. Since I've been back I have been constantly nauseous, had stabbing pains, and lost twenty lbs in three weeks. I had an MRCP with nothing remarkable, and yesterday had an endoscopy. My GI doc is at a loss as to why I still have pain and am so nauseous since my labs are back to normal. I'm starting to think I'm going nuts, and I am staying on the no fat, no spice, bland, jello and broth diet. I just really don't know what to expect... Is this the normal recovery from pancreatitis?
Thanks for any insite...I am at a loss.
MK