Gastroparesis and gallbladder
Has anyone with gastroparesis also been diagnosed with slow gallbladder?
Interested in more discussions like this? Go to the Digestive Health Support Group.
Has anyone with gastroparesis also been diagnosed with slow gallbladder?
Interested in more discussions like this? Go to the Digestive Health Support Group.
Wow! Can I ask who your doctor is. They sound amazing! My doctor was like you should but were trying to get a second opinion?
I'm in Venice gastronomy, in Venice fl
Have you been tested for EPI?
No. What is EPI?
I had same symptoms for weeks. I already knew I had gastroparesis but was so sick couldn’t leave house because I was constantly in the bathroom. Finally stool tested for a battery of tests and was diagnosed with EPI- my pancreas was not producing enzymes. I am now on Creon and although I still have some issues it allows me to live a somewhat normal life. Good luck!
I had the same surgery you had for years ago because of acid reflux. They cut my esophagus and I was on a feeding tube for three months. Now I have Gastro paresis which I’m sure is due to the surgery. I had. I have extreme constipation because I can’t eat fiber. I, like you , am struggling to finding the right foods. It Is challenging
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1 ReactionI have Gastro paresis also due to a botched fundoplication surgery. Can you tell me something about the medicine they prescribed for you? I have not been prescribed anything except for constipation since I can’t eat fiber with Gastro paresis, the constipation is horrible.
I’m surprised you can eat fiber. I have Gastro paresis, and they have told me not to take any fiber because it takes too long to digest in the stomach. All the healthy things I used to eat are not good for gastroparesis because of that I have extreme constipation I think the best solution for me would be to go strictly on soft foods are soups.
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1 ReactionYes I eat fiber, because I also have mild chronic pancreatitis and mild gastroparsis, so Dr said its 2 different diets, so she said trial and error, so I've tried many different foods, and if I got a flare that food is off the list, if I feel fine then its safe, I tell you though in beginning of diagnoses, I could not eat fiber I would get pain and nausea, now I'm ok, you can't go by every thing you read online.
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1 ReactionReading up on gallbladders from a Cleveland Clinic post, and having IBS-C, wide-ranging food intolerances, and a redundant/slow colon, I would recommend focusing on the gallbladder issue and finding a specialist for that, as I sure don't have most of your issues and your gallbladder alone could account for just about every symptom you list, per my quick read of this Cleveland Clinic article (it is a great "gut" center like Mayo): https://my.clevelandclinic.org/health/diseases/23932-biliary-dyskinesia
Also, check out the specialties of the gastros on the Castle and Connally website. It is not an MD "pay to play" advertising platform, as you cannot "buy" your way onto its list and it is supposed to list the top 7% of MDs. See if your current gastro is on it. Find someone that specializes in gallbladders that does surgery in your region or at Mayo or Cleveland Clinic. Many gastros have sub-specialties. I would want an MD/surgeon with a gallbladder sub-specialty if possible. At least for a new opinion, no matter how much you love your current Gastro. You have been suffering with this for a long time.
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