Intestinal Metaplasia: What do you do to lower the risk of cancer?
Has anyone been diagnosed with intestinal metaplasia? What does your doctor recommend? I was just diagnosed and am very anxious about it because of the risk of cancer. Would like to hear your experience with it. Thank you.
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Welcome @kellbell8. Fellow member @evapa was in your exact situation about a year ago. I moved your post to this discussion that she started:
- Intestinal Metaplasia: What do you do to lower the risk of cancer? https://connect.mayoclinic.org/discussion/intestinal-metaplasia/
I did this so you can connect with Eva, @riflemanz64 @gastrogirl @jenatsky @laurarod @jillannw @callycamp @r400914 @sue225 and others sharing helpful information.
Kellbell, I can imagine you're concerned. Are you starting a list of questions you'd like to ask your doctor when you call on Monday?
Yes I have a long list of questions for my doctor. I'll be calling Monday to make an in-person appointment with him. Thanks so much for the connections and moving me to the discussion. I really appreciate it.
Thank you! I'm ordering that book today.
Thank you! Yes I have a very long list of questions.
wow! I'll have to ask my doctor about that. I've been on PPIs for years and am wondering what kind of roll they've played with my Metaplasia. I also have chronic gastritis and without PPIs I don't know how that would fare. If feels like a "darned if you do, darned if you don't" situation.
I also have chronic gastritis for years. Originally way back in 1997-99 I did take pantoloc but developed allergic reaction: horrible itching/rash. Then the same thing happened with h2 blockers. Anyway all these years I have struggled on with Gaviscon and liquid antacids. My family doc did not seem to know about this negative effect re acid supressing drugs and metaplasia.
There is something called sulcraflate which coats the lining of the stomach which the gastroenterologist also mentioned in his report. However, I suffer from horrid constipation and this is a major side effect of sulcraflate.
Basically I have a g.i. tract that I wouldnt wish on my worst enemy (well on second thought;)...
On a positive note it is so easy to stay slim!
I sure wish Drs. we’re all on the same page, one says this and another says this. My pharmacist said ppi’s are safe and only a small number of people get serious side effects. So who do I believe?
Thank you Sue, I need to asked my doctor as well. He just told me I need to be on PPI for life.
I was also just diagnosed with IM in my esophagus and stomach. My doctor called me and caught me off guard and now have a load of questions so will request a follow-up. Thank you all for the great advice and suggestions. Are there food, drinks, etc. that you know of that you should look towards for healing properties? I have had reflux for so long and thought I was good at avoiding all the trigger foods and yet I still got this diagnosis. I feel like I am going to have a small variety of foods to eat! I don't smoke or drink very often either. I read about ginger tea and lots of veggies, and whole grains. Do you avoid dairy as well? I also have a hiatal hernia and was on protonic for years but she just switched me to a time-released PPI and my reflux has been somewhat better.
Order the book "The Acid Watchers Diet". Lots of great information and recipes there. He speaks a lot on how to heal the esophagus. I've noticed a huge difference in my symptoms with the right diet and I don't feel deprived. I've also lost 10lbs which has helped with my hernia a lot.