Jump to content
  • Welcome to Celiac.com!

    You have found your celiac tribe! Join us and ask questions in our forum, share your story, and connect with others.




  • Celiac.com Sponsor (A1):



    Celiac.com Sponsor (A1-M):


  • Get Celiac.com Updates:
    Support Our Content
    eNewsletter
    Donate

Help! Does Pepto Slow Healing?


GFshay

Recommended Posts

GFshay Apprentice

I was CC'd on Thanksgiving after allowing a hostess to do her very best to cook gluten-free foods for me. Ever since then, I have had lots of pain in my upper and lower intestines (burning, throbbing & cramping), occasional D and nausea. I spent several days eating all my own, totally gluten-free foods which were easy on the stomach (rice, bananas, applesauce etc) with no real improvement. But I feel okay after I have sufficiently digested the food and if I fast for a while before my next meal. As soon as I eat, it all comes back again.

So I was trying to let my system do its thing on its own, with just some candied ginger, peppermints, and tea to help out. But finally I broke down after reading about the miracles of Pepto (which I used to live on), and started taking it. Immediately, I felt relief from nearly all the symptoms. The problem is, it's been a week since the CC (I wasn't even heavily glutened), and no improvement. The symptoms come back as soon as the pepto wears off.

Sorry for the long description...My question is: Is it possible that Pepto Bismol doesn't allow your body to heal itself on its own? Or should I keep taking it till the symptoms stop coming back? I'd try enzymes or probiotics but don't wanna mess with anything too much (I'm in grad school and need to get through the end of the semester).

Help!


Celiac.com Sponsor (A8):
Celiac.com Sponsor (A8):



Celiac.com Sponsor (A8-M):



emaegf Newbie

Are you sure it was CC? Since you have the same symptoms after eating gluten free foods it sounds more like food poisoning or gastritis.

You should get in to see your doctor as soon as possible for treatment so you don't miss more classes.

No Pepto doesn't affect your body from healing.

starrytrekchic Apprentice

It's common after you've been glutened for your body to get upset after every meal. For some people it only lasts a day or so, but for some it lasts up to two weeks. It can also depend on the amount of gluten you consumed.

Pepto-bismal may slow down your ability to get rid of the gluten. If you have diarrhea and have no other health concerns that diarrhea would complicate, it's better to get it out of your system as quickly as possible. However, after several days, the gluten should already be out--it's just a matter of your system calming down, in which case the pepto-bismal is fine.

GFshay Apprentice

Thanks for the input-- maybe it would help if I give you more info.

I didn't get really ill after Thanksgiving, but I just started feeling nauseous and had lots of cramping/bloating. I didn't have full-blown D and didn't vomit. So I don't think it was food poisoning and doesn't make me think the doctor would have much to say about it except to rest and take it easy, which I can't afford to do for another week or so.

I also didn't take Pepto to stop D... in fact, I didn't take anything except some Benadryl (which I heard can relax muscle cramping and reduce nausea) for several days after being exposed. I just allowed myself to feel the discomfort. But finally I was considering missing my last week of school and that's when I took Pepto (4-5 days after Thanksgiving). I've just been finding that it's very uncomfortable after eating, unless I take Pepto... but I hate depending on that.

So should I just keep taking it till the issues start to resolve? I've been trying to take it as infrequently as possible... which is about 3-4 pills per day (2 doses spread throughout the day). But is that bad?

Skylark Collaborator

You need to talk to a doctor about safety.

I doubt it would keep you from healing, and obviously you need to do what works to finish the quarter. I find Pepto tremendously helpful to deal with being glutened but I've never needed it for more than 4 or 5 days.

If it's always eating that hurts, I wonder if you would get relief from taking an acid blocker like Nexium for a time? That's another question for your doctor.

quincy Contributor

I was CC'd on Thanksgiving after allowing a hostess to do her very best to cook gluten-free foods for me. Ever since then, I have had lots of pain in my upper and lower intestines (burning, throbbing & cramping), occasional D and nausea. I spent several days eating all my own, totally gluten-free foods which were easy on the stomach (rice, bananas, applesauce etc) with no real improvement. But I feel okay after I have sufficiently digested the food and if I fast for a while before my next meal. As soon as I eat, it all comes back again.

So I was trying to let my system do its thing on its own, with just some candied ginger, peppermints, and tea to help out. But finally I broke down after reading about the miracles of Pepto (which I used to live on), and started taking it. Immediately, I felt relief from nearly all the symptoms. The problem is, it's been a week since the CC (I wasn't even heavily glutened), and no improvement. The symptoms come back as soon as the pepto wears off.

Sorry for the long description...My question is: Is it possible that Pepto Bismol doesn't allow your body to heal itself on its own? Or should I keep taking it till the symptoms stop coming back? I'd try enzymes or probiotics but don't wanna mess with anything too much (I'm in grad school and need to get through the end of the semester).

Help!

after my diagnosis in april of this year the main things that improved my healing was a good digestive enzyme, probiotics and something called GI Revive. you can order it online. also, stay away from dairy based on your level of intestinal damage. all dairy, including dairy in processed foods will cause you alot of distress. It seems I felt worse for the first month or 2 after the dx, so hang in there.

emaegf Newbie

Also you can try drinking Tonic Water sipping it throughout the day. I have talked with many who swear by it to reduce or prevent problems after getting glutened. Tonic Water contains quinine and helps relieve symptoms. Some even drink it after eating at a restaurant or any place outside their own home where they may get CC.


Celiac.com Sponsor (A8):
Celiac.com Sponsor (A8):



Celiac.com Sponsor (A8-M):



GFshay Apprentice

Thanks, those suggestions are great. I stopped the pepto 2 days ago and also cut out dairy. I'm feeling much better! I hate the idea of no dairy, but you're probably right that my amount of damage is too much for even the best Lactaid pills. I hope to return to it soon...

Tonic water, eh? That explains some of why I always felt better after having a vodka tonic. I just thought it was the alcohol relaxing my gut or something, but I'll have to try just the tonic. Thanks for the tip!

I've been looking into enzymes or probiotics but don't know what to try first. There are so many out there and I'm scared to make anything worse rather than better. Any suggestions for a newbie?

emaegf Newbie

When my stomach gets bad like yours has been my doc tells me to use a probiotic made for kids. It's easier on the system.

This is the one I use Open Original Shared Link

even though it states it may have milk residue I have never had a problem with it. Start with a 1/4 tsp once on day one then 1/4 tsp twicw a day on day 2 upto 1/4 tsp 3 times a day. When you first start taking it you may end up in the bathroom with D but that will go away in a few days. Your body has to get back to normal levels of good bugs in your system.

Archived

This topic is now archived and is closed to further replies.


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,899
    • Most Online (within 30 mins)
      7,748

    dcarter1682
    Newest Member
    dcarter1682
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.4k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Who's Online (See full list)

  • Upcoming Events

  • Posts

    • trents
      Welcome to the forum, @Judy M! Yes, he definitely needs to continue eating gluten until the day of the endoscopy. Not sure why the GI doc advised otherwise but it was a bum steer.  Celiac disease has a genetic component but also an "epigenetic" component. Let me explain. There are two main genes that have been identified as providing the "potential" to develop "active" celiac disease. We know them as HLA-DQ 2.5 (aka, HLA-DQ 2) and HLA-DQ8. Without one or both of these genes it is highly unlikely that a person will develop celiac disease at some point in their life. About 40% of the general population carry one or both of these two genes but only about 1% of the population develops active celiac disease. Thus, possessing the genetic potential for celiac disease is far less than deterministic. Most who have the potential never develop the disease. In order for the potential to develop celiac disease to turn into active celiac disease, some triggering stress event or events must "turn on" the latent genes. This triggering stress event can be a viral infection, some other medical event, or even prolonged psychological/emotional trauma. This part of the equation is difficult to quantify but this is the epigenetic dimension of the disease. Epigenetics has to do with the influence that environmental factors and things not coded into the DNA itself have to do in "turning on" susceptible genes. And this is why celiac disease can develop at any stage of life. Celiac disease is an autoimmune condition (not a food allergy) that causes inflammation in the lining of the small bowel. The ingestion of gluten causes the body to attack the cells of this lining which, over time, damages and destroys them, impairing the body's ability to absorb nutrients since this is the part of the intestinal track responsible for nutrient absorption and also causing numerous other food sensitivities such as dairy/lactose intolerance. There is another gluten-related disorder known as NCGS (Non Celiac Gluten Sensitivity or just, "gluten sensitivity") that is not autoimmune in nature and which does not damage the small bowel lining. However, NCGS shares many of the same symptoms with celiac disease such as gas, bloating, and diarrhea. It is also much more common than celiac disease. There is no test for NCGS so, because they share common symptoms, celiac disease must first be ruled out through formal testing for celiac disease. This is where your husband is right now. It should also be said that some experts believe NCGS can transition into celiac disease. I hope this helps.
    • Judy M
      My husband has had lactose intolerance for his entire life (he's 68 yo).  So, he's used to gastro issues. But for the past year he's been experiencing bouts of diarrhea that last for hours.  He finally went to his gastroenterologist ... several blood tests ruled out other maladies, but his celiac results are suspect.  He is scheduled for an endoscopy and colonoscopy in 2 weeks.  He was told to eat "gluten free" until the tests!!!  I, and he know nothing about this "diet" much less how to navigate his in daily life!! The more I read, the more my head is spinning.  So I guess I have 2 questions.  First, I read on this website that prior to testing, eat gluten so as not to compromise the testing!  Is that true? His primary care doctor told him to eat gluten free prior to testing!  I'm so confused.  Second, I read that celiac disease is genetic or caused by other ways such as surgery.  No family history but Gall bladder removal 7 years ago, maybe?  But how in God's name does something like this crop up and now is so awful he can't go a day without worrying.  He still works in Manhattan and considers himself lucky if he gets there without incident!  Advice from those who know would be appreciated!!!!!!!!!!!!
    • Scott Adams
      You've done an excellent job of meticulously tracking the rash's unpredictable behavior, from its symmetrical spread and stubborn scabbing to the potential triggers you've identified, like the asthma medication and dietary changes. It's particularly telling that the rash seems to flare with wheat consumption, even though your initial blood test was negative—as you've noted, being off wheat before a test can sometimes lead to a false negative, and your description of the other symptoms—joint pain, brain fog, stomach issues—is very compelling. The symmetry of the rash is a crucial detail that often points toward an internal cause, such as an autoimmune response or a systemic reaction, rather than just an external irritant like a plant or mites. I hope your doctor tomorrow takes the time to listen carefully to all of this evidence you've gathered and works with you to find some real answers and effective relief. Don't be discouraged if the rash fluctuates; your detailed history is the most valuable tool you have for getting an accurate diagnosis.
    • Scott Adams
      In this case the beer is excellent, but for those who are super sensitive it is likely better to go the full gluten-free beer route. Lakefront Brewery (another sponsor!) has good gluten-free beer made without any gluten ingredients.
    • trents
      Welcome to the forum, @catsrlife! Celiac disease can be diagnosed without committing to a full-blown "gluten challenge" if you get a skin biopsy done during an active outbreak of dermatitis herpetiformis, assuming that is what is causing the rash. There is no other known cause for dermatitis herpetiformis so it is definitive for celiac disease. You would need to find a dermatologist who is familiar with doing the biopsy correctly, however. The samples need to be taken next to the pustules, not on them . . . a mistake many dermatologists make when biopsying for dermatitis herpetiformis. 
×
×
  • Create New...

Important Information

NOTICE: This site places This site places cookies on your device (Cookie settings). on your device. Continued use is acceptance of our Terms of Use, and Privacy Policy.