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

Recently Diagnosed But No Reaction To Eating Gluten


Panda123

Recommended Posts

Panda123 Newbie

Hey everyone,

I'm an 18 year old male that was diagnosed with celiac disease two weeks ago. I'm a pretty active and outgoing person and I have no symptoms of celiac disease whatsoever. Except, I have been iron deficient for the last few years which led to an endoscopy (my diet is pretty healthy and balanced) and thus i was diagnosed with celiac disease.

Now, I've been eating gluten free for about 2 weeks now and i don't feel one bit different. My question is, how do i know if I'm doing this right? I've cut out all the gluten free foods but please note i still use the same utensils as my family (none of them eat gluten free). I just rinse them with hand prior to using even they have been already washed. Is this good enough to heal my intestines?

Again, I dont react at all to gluten but intestines's lining is flattened so I obviously have celiac disease.


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



Celiac.com Sponsor (A8-M):



MitziG Enthusiast

It is very common in the beginning to have no noticeable reaction to eating gluten. It is also common to begin reacting violently to it once you have been gluten-free for a few months. Until then, you just need to be very vigilant. Utensils should be fine as long as they are thoroughly washed. You need your own toaster, cutting board and colander. Plastic storage containers and utensils can hold gluten, so you should use new ones. Scratched teflon or enamel pans will also contaminate you- stainless steel is fine as long as it is washed thoroughly.

It isn't about just getting sick. You need to shut down the immune response to gluten, and as long as your body is exposed to even tiny ammounts, it will continue making antibodies, even if you don't feel sick.

Check out the newbie 101 topic for more detailed info on what changes to make.

And welcome to the boards!

nvsmom Community Regular

I don't know... I could be enough. It's a hard call when you have silent celiac to ensure you are contaminating your food. If you are sure that your vitamins, medications, sauces (soy, wochestershire, teriyaki, barbque) crackers and cereals are all gluten-free then you are probably doing enough.

I would check your iron levels and celiac blood panels in a few months to see if it's improving at all.

When I went gluten-free, my improvements were GI in nature as well as less frequent migraines. My energy didn't change a bit. I found out I was hypothyroid and that was holding my energy back. If low energy is an issue, and everything else is fine, you might want to have your TSH levels checked; Hashimoto's hypothyroidism occurs frequently along with celiac.

Best wishes.

Panda123 Newbie

It is very common in the beginning to have no noticeable reaction to eating gluten. It is also common to begin reacting violently to it once you have been gluten-free for a few months. Until then, you just need to be very vigilant. Utensils should be fine as long as they are thoroughly washed. You need your own toaster, cutting board and colander. Plastic storage containers and utensils can hold gluten, so you should use new ones. Scratched teflon or enamel pans will also contaminate you- stainless steel is fine as long as it is washed thoroughly.

It isn't about just getting sick. You need to shut down the immune response to gluten, and as long as your body is exposed to even tiny ammounts, it will continue making antibodies, even if you don't feel sick.

Check out the newbie 101 topic for more detailed info on what changes to make.

And welcome to the boards!

Wow that's a really good answer. Just what i was looking for! So I'll get my mum to get a new pan and cutting board for gluten free cooking. My parents are adamant that contamination of small particles of gluten won't do any harm (then again, they were adamant to not get a endoscopy too, and thought i was just fine). I have skimmed the 101 topic, sounds like a great read. Will read it thoroughly later today. But again, thanks a lot for that answer, really cleared up a lot of my doubts.

I don't know... I could be enough. It's a hard call when you have silent celiac to ensure you are contaminating your food. If you are sure that your vitamins, medications, sauces (soy, wochestershire, teriyaki, barbque) crackers and cereals are all gluten-free then you are probably doing enough.

I would check your iron levels and celiac blood panels in a few months to see if it's improving at all.

When I went gluten-free, my improvements were GI in nature as well as less frequent migraines. My energy didn't change a bit. I found out I was hypothyroid and that was holding my energy back. If low energy is an issue, and everything else is fine, you might want to have your TSH levels checked; Hashimoto's hypothyroidism occurs frequently along with celiac.

Best wishes.

Thanks for the answer. Yeah I strictly make sure everything i eat is gluten free.

On more question: As stated before, my iron and B12 levels are pretty darn low (cant remember the numbers right now). It's really bugging me because iron supplements cant help (as my intestines cant absorb any iron). Any rough estimate on how long would it be before i start to absorb iron properly?

LauraB0927 Apprentice

I had the exact same situation as you - no symptoms, could eat a bowl of pasta and not feel a thing. But I battled iron deficiency for years! After being gluten free for several months, NOW I have reactions to gluten. Most people seem to become more sensitive and have more reactions after being gluten free for a bit. My guess is that as the months go on you will definitely know if you've eaten or been exposed to it.

As other people said, get your lab work done again in 6 months and see if there are any changes. As long as you check all your labels, the antibodies should go down! And welcome to the forum! Ask lots of questions!!

TGK112 Contributor

I have had the same experience. What led me to being diagnosed was osteoporosis. I was shocked when I tested positive since I have never felt ill by eating gluten. It makes me a bit nervous - I feel that I am a very poor "barometer" - never knowing if I am accidentally eating gluten. I have just reached my 4 week mark. I am anxious to be tested again after 6 months to see if there has been any improvement. It's very difficult to know if I am truly gluten free.

cavernio Enthusiast

Tell your parents that celiac disease is an immune system response and remind them that the smallest of organisms, virii, are enough to make your immune system activate. A few virii in your body are miniscule compared to the amount of gluten in a crumb of bread. Also tell them that your doctor told you to avoid even the tiniest amount of gluten; even if they didn't, my GI did. Told me to have a new toaster, wash all the dishcloths and towels in hot water only, only use clean utensils cloths etc for any of my food, and don't take chances with a food I'm unsure about.

Also it's unclear to me if I get an sort of immediate gluten response yet. Initially I thought I didn't, but I'm not sure anymore. Although unlike you, I didn't feel very good prior to the dx.


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



Celiac.com Sponsor (A8-M):



MitziG Enthusiast

Your parents need to be educated. It isn't even just about celiac. If the auto-immune response is allowed to continue, you are likely to develop additional auto immune diseases, which they may understand are serious. Rheumatoid Arthritis, Lupus, Type 1 Diabetes, Multiple Sclerosis, Sjorens, Hashimotos, just to name a few. Auto immune diseases tend to cluster, and being celiac already raises your risk. It is important to doeverything you can to avoid that happening, even if you don't feel sick.

I recommend you print some info off the internet- your dr may not be a lot of help as many are kind of clueless about celiac. Celiac.com has great articles.

As for absorption- no one can tell you as everyone heals differently. But within 6 mos you will hopefully be significantly healed enough to be absorbing more. For some people it can take years. B12 can and should be taken sublingually- it absorbs better thru mucous membranes. You can get sublingual tablets at any drugstore. Same with Vit D which you didn't mention but tends to be low in the general population, even those without celiacs!

Pegleg84 Collaborator

Welcome to the forum, Panda.

I think you've probably caught your Celiac in very early stages, so that's really lucky! I had very low iron in my late teens, and looking back it was probably the first sign of the disease popping up. Probably if you hadn't been diagnosed and kept on eating gluten, you eventually would have gotten other symptoms.

That said, stick to the diet, do everything other posters have suggested, and you should hopefully see your iron levels going up in a few months. Unfortunately, you'll probably also start having reactions to accidental glutenings after you heal.

You should be thankful that you caught it early, and can heal without having to go through long years of suffering as many people do.

Good luck!

Peg

GottaSki Mentor

You've already had great advice.

Just wanted to add - if you do not start reacting to small amounts of gluten - I'd suggest repeating blood tests at 3 months, 6 months and then annually thereafter. My Celiac Doc had me tested at these intervals even though I had strong reactions to small amounts of gluten from the beginning.

Welcome to the site - keep asking questions - it is the best way to speed up the learning process.

archaeo in FL Apprentice

Panda123, these are all great suggestions. I don't know if I noticeably react, either, but I have noticed an improvement in my bowels. I'm looking forward to not having to take a ton of supplements.

My suggestion is to order some books, particularly "Real Life with Celiac Disease" and read up. That book, in particular, is good because the chapters are short and very focused and include case studies. The book is a compilation by a lot of medical professionals, and addresses a broad spectrum of topics.

It may be helpful for you to read the relevant chapters (another great thing about having short, focused chapters - I skipped the ones about kids, and being pregnant!) and then to mark them for your family to read. It's important for them to know how important it is for your health to eat gluten-free, so as not to develop other autoimmune disorders and to reduce your increased risk of some cancers. The book mentions that something as small as 1/50th of a slice of bread is enough to cause an antibody reaction (which sets off a chain reaction, it's not just a small, focused area). That may be important for them to know!

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,983
    • Most Online (within 30 mins)
      7,748

    Bryan s
    Newest Member
    Bryan s
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Scott Adams
      If you have DH you will likely also want to avoid iodine, which is common in seafoods and dairy products, as it can exacerbate symptoms in some people. This article may also be helpful as it offers various ways to relieve the itch--thanks for the tip about Dupixent, and I've added it to the article:  
    • Scott Adams
      I just want to clarify that what I posted is a category of research summaries we've done over the years, and nearly each one shows that there is definitely a connection to celiac disease and migraine headaches. The latest study said: "the study did indicate some potential causal associations between celiac disease and migraine with or without aura, as well as between migraine without aura and ulcerative colitis...this study did not find evidence of a shared genetic basis..." Anyway, there is definitely a connection, and you can go through more of the articles here if you're interested: https://www.celiac.com/celiac-disease/celiac-disease-amp-related-diseases-and-disorders/migraine-headaches-and-celiac-disease/
    • SusanJ
      Two months ago, I started taking Dupixent for dermatitis herpetiformis and it has completely cleared it up. I can't believe it! I have had a terrible painful, intensely itchy rash for over a year despite going fully gluten-free. See if your doctor will prescribe Dupixent. It can be expensive but I am getting it free. When the dermatitis herpetiformis was bad I could not do anything. I just lay in bed covered in ice packs to ease the pain/itching and using way too Clobetasol. Dapsone is also very good for dermatitis herpetiformis (and it is generic). It helped me and the results were immediate but it gave me severe anemia so the Dupixent is better for me. Not sure if it works for everyone. I cannot help with the cause of your stress but from experience I am sure the severe stress is making the celiac and dermatitis herpetiformis worse. Very difficult for you with having children to care for and you being so sick. Would this man be willing to see a family therapist with you? He may be angry at you or imagine that your illness is a psychosomatic excuse not to take care of him. A therapist might help even if he won't go with you. Also do you have any family that you could move in with (with the kids) for a short time to get away? A break may be good for you both.
    • knitty kitty
      @tiffanygosci, Thiamine deficiency is a thing in pregnancy for "normal" people, so it's exponentially more important for those with celiac disease and malabsorption issues. I studied nutrition before earning a degree in Microbiology because I was curious what the vitamins were doing inside the body.  See my blog.  Click on my name to go to my page, scroll to drop down menu "activities" and select blog.   So glad you're motivated to see the dietician!  We're always happy to help with questions.  Keep us posted on your progress! 
    • tiffanygosci
      Thank you for sharing all of this, Knitty Kitty! I did just want someone to share some commonality with. I did not know This one Deficiency was a thing and that it's common for Celiac Disease. It makes sense since this is a disorder that causes malabsorption. I will have to keep this in mind for my next appointments. You also just spurred me on to make that Dietician appointment. There's a lot of information online but I do need to see a professional. There is too much to juggle on my own with this condition.<3
×
×
  • 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.