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

Digestive Enzymes?


MissHaberdasher

Recommended Posts

MissHaberdasher Apprentice

Someone at the health food store told me to take enzymes to combat my stomach pain (4 weeks after a glutening). I was hesitant, but when I did research online (yes, very dangerous), I found this:

 

 

  • Low-grade inflammation in the digestive tract (such as that caused by “food allergies,” intestinal permeability, dysbiosis, parasitic infection, etc.) can lead to deficiencies in digestive enzymes.
  • Other symptoms that suggest you might have problems with digestive enzymes are:

    • Gas and bloating after meals
    • The sensation that you have food sitting in your stomach (a rock in your gut)
    • Feeling full after eating a few bites of food
    • An “oil slick” in the toilet bowl (undigested fat)

 

So far, two days in, it seems to be helping a bit, along with 1 or 2 ibuprofen per day to help with inflammation. After my last meal (which was mostly protein rich), I'm fairly nauseous, but yay, barely any pain!! What has been your experience with enzymes? Is there a certain food you'd recommend having with this? 

 

Sorry to keep harping on about my stomach pain after this one episode of gluten exposure, but, it has been a very long time since I was last glutened and the reaction has been pretty different from when I was new at this. Anything that messes with my favorite hobby, eating good food, stresses me out. I can't afford to lose much weight either.

 

With that being said, I could just see a doctor but my health insurance doesn't kick in until February and I am pretty nervous about finding a doctor that I can identify with, if that makes sense. 

 

Thank you all, I hope you know that this website is a huge comfort to me, especially when I feel so alone in a sea of people who have the super power of being able to digest anything.  <3 

 

 

 


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



Celiac.com Sponsor (A8-M):



1desperateladysaved Proficient

My functional medicine nurse told me that digestive enzymes help to break down food.  When there is villi damage, the villi can't do their job of telling the pancreas to fire.  They will heal, but in the meanwhile the enzymes can help sustain.

 

I like my enzymes.

 

D

KCG91 Enthusiast

I like mine! It looks to me like the 'problems with enzymes' could also apply to symptoms of a glutening, so maybe see how you feel taking them in a few weeks? 

I try to take them on an empty stomach and with a cold drink (hot drinks limit their effectiveness, it says on my bottle). Feel a lot brighter since taking them.

NoGlutenCooties Contributor

I take digestive enzymes with every meal and with any hard-to-digest snack (i.e. nuts, cheese).  They make a big difference for me.  Without them food will sometimes sit in my stomach for awhile and make me feel heavy, overly full, and generally sluggish.  I take them with the first bite of food.

I also take them when I take all of my other supplements in the morning, to help break those down as well.

moosemalibu Collaborator

I think I may be the only person that has said they cannot tell a difference by taking digestive enzymes. I bought a big bottle so I take them, but I can't feel a difference. But perhaps consistency is key? Keep at it.

1desperateladysaved Proficient

Perhaps you don't need them.  Maybe your villi do their job of telling your pancreas to fire, so you don't need them to help break down your food.  Maybe the kind you got didn't work for you.  These things do get pretty complicated to figure out at times.  I guess you will figure it out over time.

 

D

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,901
    • Most Online (within 30 mins)
      7,748

    tessycork47
    Newest Member
    tessycork47
    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)

    • There are no registered users currently online
  • 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.