I had my gall bladder out over a year ago. Then immediately I got pregnant. I never had any trouble with diarrhea until just recently. Now, almost a year later, everytime I eat I get diarrhea so bad that I can barely make it to the bathroom. I have no idea what is going on. I can feel it rumbling in my stomach and i get intense cramping sometimes. What do you think it could be?
Some people that have had their gallbladders removed develop a condition in which excess bile in the intestinal tract causes diarrhea. This happened to my wife and FINALLY a physician's assistant asked her if she had ever tried Cholestyramine (a powder mix and cheaper) or Cholestid (pills and more expensive). It soaks up excess bile and helped her a lot. You do have to take it at times away from any other medications as it can "soak" them up as well so check with your doctor about this. Hope this helps.
I've taken it and it really helps when my diarrhea gets bad. I have had IBS for years and normally I control my diarrhea with opiates and Metamucil, but every once in a while, I have to go to the Cholestyramine. I also use Lomotil for it.
I'm Soar1's wife, the one with the history of chronic diarrhea. I have had just about every possible test and have tried almost all the drugs out there. For years, opiates helped the most, but I became tolerant of them. This past year, my motility went into warp drive and I have been virtually housebound for 8 of the 12 months. This last bout has gone on for 5 months straight. My doctors (I've seen several both locally and at a large university hospital) say I have a functional hypermotility problem of some sort, but they can't seem to slow it down. I have lost 20 pounds and am physically miserable. I do yoga and meditation every day, which helps me keep a positive attitude. I have also done accupuncture, counseling, therapy, biofeedback, etc. to try to control this, but to no avail.
One of the most perplexing problems is that my diarrhea is linked to severe sweating during the 2-3 episodes I have per day and night. When the sweating begins, so does the diarrhea and it continues until I am through. Right now I have this every morning, evening, and many times in the middle of the night. I do not sweat when I am not in this mode.
Cholestid/cholestyramine only work for a day or so. These drugs holds back the flood for a few hours, but not very long. Sorry to be so graphic, but that's the way it is.
Drugs like Hyoscamine (sp?), librax, etc. just slow it down enough to greatly prolong my agony.
My current specialist, at the large university hospital, won't even network with other physcians to gather information from them. He is probably too afraid to admit to anyone else in his profession that he is stymied by my problem. He says no "****" sights for physicans are available, which is really sad if this is true. My GI doctor here was very rude when I asked for a referral to the university, saying that I must think he was just a "country bumpkin doctor." He didn't understand my suffering because I am not him, his wife, or anyone close to him. I went to the university as it is supposed to be a research hospital and cutting edge, but like the Mayo Clinic, if they don't understand what to do, they tend to not want to deal with you.
I am hoping that someone out there can relate and give me some new ideas. I have kids and would like to be able to be part of their lives outside of the house. My husband is very supportive, for which I am grateful.
I have had IBS with the same type of diarrhea symptoms described by the other posters. I recently have had a surprising improvment in my symptoms. I started taking some chewable vitamin c tablets this fall as I never eat citrus products due to my GERD. I swear it seems like the vitamin c helps my diarrhea! I chew one 500mg tablet daily and as long as I remember to do that my symptoms are greatly improved. If I forget to take it for a few days, the diarrhea comes back. I never expected the vitamin c to have an effect on my IBS, but I swear it seems to be making a rather dramatic difference. Maybe its worth some of you giving it a try?
Ehlers-Danlos Syndrome Type 3
Severe DDD with multiple herniations and areas of stenosis, 16 affected disks!
C4-5 ACDF 2006
C3-6 ACDF 2013
Chronic Myofaschial Pain Syndrome
Check out Habba Syndrome. Been through this for years and just discovered-on the Discovery Channel,lol- that I almost certainly have this and not IBS. Never had any pain with mine, so always puzzeled the gastro guys. 4 trips to Intensive care and no answers from them, but I will ask the right questions this time.