Here are some things that help me:
Can't drink. Even a couple of drinks can put me down for a week.
A very hot shower or bath helps me a lot. I have a jacuzzy tub and often sleep in it. This has kept me from the ER several times.
Beef consumme, 0 fat.
Pritein juice smoothies.
Plain pasta.
I have just discovered K2O protein water. It has 5g protein, 5g fiber, 6g carbs and 0g fat. I have had no more problems from this than plain water, and it helps with the hunger.
When I feel a little better, Ensure Plus (generic) is a good meal. It has 350 calories 13g protien and 11g fat. You can live off of these if you can stand the fat.
This may be wrong: When I have a sudden attack with nausia and pain, I will force myself to vomit. I will drink a large amount water and repeat until my stomach is clean (clear fluid) and empty. Then I don't drink or eat anything for at least 12 hours. I think this helps. Any comments?? I am curious if anyone else has ideas on this.
When I am starved to the point of being dizzy and shaky, I will put a little brown sugar in my mouth and hold it there until dissolved. This restores blood sugar without putting anything in my stomach.
I am 47 and have 2 young boys. The pain often keeps me from going and doing things with them. I would rather be addicted to pain meds than be in so much pain I can't work, sleep or raise my kids.
Are all docs as conservative as mine? He only gives my one weeks worth of pain meds then tells me I am taking too much.
Since leaving, I have had a number of attacks. Twice, they were severe enough to leave me unable to work, sleep, eat, drink, or even move, but all I could do was self treat by not eating/drinking for a few days and taking over-the-counter pain meds.
It has been nine months and I am still hampered by this disease. I am a little relieved to see that even with the right medical care, I might still be suffering the same way I am now. I have cut out alcohol and many of my favorite foods, but I still seem to have a painful bout every few weeks or so, including my recent holiday vacation which was ruined.
I got online today hoping to find some sort of homeopathic remedies that might help me. Have any of you tried a special food/herb/root/etc. that has helped in recovery? Is there anything you can suggest for the pain (the ibuprofin just isn't cutting it)? Hot showers seem to be the only thing I have found that really helps; and even then it only aleviates the pain for a few hours. Are there any others out there that have tried to deal with this with minimal doctor treatment?
I've been in the hospital 4 times in the last 6 years for Acute Pancreatitis. I HATE jello and chicken broth any more and was searching for a better diet. Last January I had a Gastro doctor tell me to limit my fat intake to 20-30grams per day. The ADA standard recommended dietary allowance for fat is 65 grams per day...so it's pretty restrictive. I've made it my mission to find all the foods I can eat...binge on if I want and what doesn't work. I still don't have to watch my sugars/carbs (which is great since I LIVE for breads) but I miss buttered toast the most. I've managed to stay out of the hospital since last January. Haven't had a chocolate bar since then but have found subtitutes for most everything. Use applebutter for toast..you can really drench it. ( I choose bread that's 1 gram of fat per slice or less) I use bar-b-que sauce, Fat free sour cream or salsa for baked potatoes, I eat chocolate marshmallows or Miss Meringue cookies (which are primarly fat free) for binges. I have more trouble with sodas, coffee and big salads. Things that are harder to digest give me the most discomfort/pain. I try to limit to 30 grams max...if I go over..it hurts. Only once have I had a slight flare and I ate jello and sipped broth for a couple of days and it healed itself. Good luck. I've found trial and error works that best. (*hint..this sounds kind of gross..but I've found that if the fat in my diet is too high...my pee in the potty looks like I put a teaspoon of vegie oil on the water. Look for the oil slick. That means my body is flushing out the fat I can't process) It works for me. Only real problem is that my low fat diet (although it caused my bad cholesterol to drop from 242 to 168) my good cholesterol plummetted to 136. For women it should be over 150! The Niaspan they prescribe has horrible flushing side affects so I can't take it. That just means that all my fats need to be avocados, salmon oil/fish oil supplements, walnuts or almonds.
After a couple hours of pain and still waiting to be seen at the hospital - uncontrollable jerking movements of limbs started. Almost like someone having a mild seizure. I had no control over these - yet I'm told it was another hour or so before I was given pain relief.
Evenutally ambulanced to a differant hospital put on IV and morphine for pain. Diagnosois Acute Pancreatitis and Chole Cystitis (inflamed gallbladder) Cause unknown because I seldom drank alcohol. 3 months later still in pain although taking strong painkillers.
29 January CT scan showed growth/polyp in gallbladder. also possible duodenal ulcer (probably caused by so many painkillers on empty stomach) Pain had increased over a couple days prior to this and overnight of 29th had another'attack'. Jerky movements and pain. Could not go to local hospital becasue it has been hit byt a sickness bug!! My immune system could not cope with that!
My life seemed to end in October and still all movement hurts - even breathing! Weight loss 30lbs within 6 weeks. Constant nausea & sickness, almost no appetite - but I am afraid to eat in case 'That Pain' returns! Suggestions please for suitable but tasy diet? Did anyone else have these jerky movements of limbs?
Desperate in Devon....
poppyseed
Poppyseed
I saw a specialist and he ordered an ERCP, and found scar tissue at my bile duct (I had my galbladder removed 3 years ago, but kept having painful attacks).
Now I know it was pancreaitis all along after my surgery, and wish the other specialist & surgeon had diagnosed it earlier - the prior specialist said I had IBS two years ago. The surgeon said I had scar tissue and to live with it. Had both of them diagnosed me properly, I wouldn't be acute today. Grrrr.
Following the ERCP, I had pain from the procedure and it keeps reoccuring.
Prior to the ERCP the pain followed eating food, and was worse in the afternoon/evenings and is similar to a galbladder attack.
After the ERCP - I continue to have the same pain and tenderness that it feels like I just had the procedure done - it's been over a month, and I have cramping & pinching feeling in the morning and afternoon. Super tired. I am sick of being sick.....!
These posts are very helpful. And good to know we're all in this together. I think the emotional roller coaster is as hard on the insides as anything.
Hang in all. I am...
Here is the recipe for the potatoes, they are actually so good my husband likes them.
Chop up red skin potatoes with carrots, garlic, onions, red and green pepper. I add about 5 tablespoons of water and 4 of sugar free lemon juice. Bake in it the oven on 385 for 40 min with tin foil covering the pan. Then remve the tin foil and continue baking about 30 min or until soft.
This will help you not want to rip your torso off.