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

I Have Glutening Symptoms...yay?


cavernio

Recommended Posts

cavernio Enthusiast

It's been a weird weekend because I had what I think I had a fairly immediate reaction to a food and I'm happy to know that I shouldn't be eating it. But I'm also sad because I want to eat it :-p

To start with when I first went gluten free after my blood test for a month or so, and then I went back on gluten for the biopsy, I didn't notice anything close to immediate. After a week or so I got more bloated, but that was it. Since then, I've never had a clear-cut reaction to anything until now.

It was nuts from bulk barn. I made a pecan crumb crust for a fruit tart and my tongue stung a little when I ate it, like I had mouth sores, even though I didn't have any. The rash on the back of my neck is the giveaway though. It's not too bad, but it's still there 24 hours later. I've never really had a rash like this before, only ever gotten a few bumps on my forearms in the past few years.

I also noticed a similar reaction in my mouth -actually it was much worse then- when I made a fake cheesecake from bulk barn cashews for new years. Burning mouth. But I had been having mouth sores for awhile before that, and it had lime juice and was pretty acidic.

I have also noticed that since my face has cleared up being gluten free, I get odd acne breakouts on it and my upper back/shoulders, but I've been very hesitant to think it could be gluten. I think that it likely is gluten now, but still have no real idea what the gluten is in. Well, that's not entirely true, I'm getting more concerned about eating at my parents, which is really s$#&ty. My parents and I have had a very angry relationship (or not a relationship) for many years, and we've come to a sort of peace where get together for dinner every week or so. My mom was very quick to take up cooking gluten free, and cooking's her thing, her way of showing she cares. But with the risk of CC in her house...ugh, this is really a relationship issue....why do things revolve around food so much and why is wheat so pervasive?!

Another possible gluten reaction I think I might get is just getting really tired and/or moody. Again, that's really hard to pinpoint, and the one time where it seemed like it had to be linked to eating at someone else's house I didn't notice any other reaction, like a burning mouth or rash or acne.

And then there's the everpresent pain in my hands and feet. It got really bad a couple weeks after the holidays were over, the holidays when I ate out a fair bit and made that cheesecake. And I just read that some specialists think neuropathy might be more sensitive to gluten than villi damage, or at least that's the only explanation that makes sense for people whose neurological problems don't get better or even get worse being gluten free.

Just venting some I guess. Probably should have put this is in the journal I can have in my profile or wherever it is. I guess I'm happy I still have some sort of radar for gluten now...wish it told me where exactly it came from while it caused the rash. Maybe write out 'nuts' on my skin.


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



Celiac.com Sponsor (A8-M):



rebeccanicole88 Rookie

I went totally off of gluten and for a while had no breakouts or sores. Then the mouth sores, rashes on my stomach, back, and neck came back. It was the stinging without the sores when I put chocolate covered almonds in my mouth. Kind of thinking it's either nuts or chocolate on top of the gluten. Thank you for sharing. Was wondering if someone else has experienced this before.

Em314 Explorer

why do things revolve around food so much and why is wheat so pervasive?!

Just wanted to say- I think this often as well. It blows.

cavernio Enthusiast

"It was the stinging without the sores when I put chocolate covered almonds in my mouth"

Well, I'm having a frustrating time finding any nuts that are gluten free. I've been buying the bulk barn ones that aren't roasted or anything, and although the label didn't say gluten free, they've been one of the few that didn't say may contain traces of or outright contain wheat. And they aren't next to the flours, only next to other nuts, but that's obviously not good enough and I should have been more cautious. I just haven't found any nuts in 3 grocery stores that don't say 'may contain wheat' right on them.

I may or may not have an issue with chocolate. I thought it was one of the things making my tongue dry, but dairy also does that to me and I've since found chocolate that has no traces of dairy too and it seems chocolate isn't causing issues anymore. I say 'seems like' because my tongue is often dry and I don't know how long a reaction to something would last.

In any case, I would first think that your chocolate covered almonds have traces of wheat on them before thinking it's chocolate. Most confections seem to.

  • 2 weeks later...
jhol Enthusiast

"It was the stinging without the sores when I put chocolate covered almonds in my mouth"

Well, I'm having a frustrating time finding any nuts that are gluten free. I've been buying the bulk barn ones that aren't roasted or anything, and although the label didn't say gluten free, they've been one of the few that didn't say may contain traces of or outright contain wheat. And they aren't next to the flours, only next to other nuts, but that's obviously not good enough and I should have been more cautious. I just haven't found any nuts in 3 grocery stores that don't say 'may contain wheat' right on them.

I may or may not have an issue with chocolate. I thought it was one of the things making my tongue dry, but dairy also does that to me and I've since found chocolate that has no traces of dairy too and it seems chocolate isn't causing issues anymore. I say 'seems like' because my tongue is often dry and I don't know how long a reaction to something would last.

In any case, I would first think that your chocolate covered almonds have traces of wheat on them before thinking it's chocolate. Most confections seem to.

hi cavernio

went gluten and dairy free for 3 days after a week of gluten and dairy light and thought i saw an improvement in the rash on my face and my palms seemed to have softened up. then went to my friends for tea - id taken something to eat but she,d made me cheese and onion pie - didnt have the heart to tell her i,d made changes to my diet - so i ate it. well 2 days later, palms are dry and cracked and face is all red and blotchy again!! :(

on another note i feel im gonna have a problem with nuts - ive given up chocolate already coz of acid reflux. i get a tingly feeling on my tongue and feel myself rubbing it backwards and forwards on my top teeth - drives me mad! and i must look like an idiot while im doing it lol. bought a nut free seed bar though and felt the same thing- so maybe i have a prob with seeds too :blink:

Archived

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

  • Get Celiac.com Updates:
    Support Celiac.com:
    Donate

  • Celiac.com Sponsor (A17):
    Celiac.com Sponsor (A17):





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - knitty kitty replied to Sarah Grace's topic in Related Issues & Disorders
      23

      Headaches / Migraines and Hypoglycaemia

    2. - trents replied to Sarah Grace's topic in Related Issues & Disorders
      23

      Headaches / Migraines and Hypoglycaemia

    3. - knitty kitty replied to Sarah Grace's topic in Related Issues & Disorders
      23

      Headaches / Migraines and Hypoglycaemia

    4. - Jmartes71 posted a topic in Coping with Celiac Disease
      0

      Related issues

    5. - trents replied to Sarah Grace's topic in Related Issues & Disorders
      23

      Headaches / Migraines and Hypoglycaemia


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,147
    • Most Online (within 30 mins)
      7,748

    rmr714
    Newest Member
    rmr714
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.5k
    • 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

    • knitty kitty
      Some people have difficulty processing tyrosine.  Cut out the nuts and cheese and see if there's any difference.  Everyone is different. This study shows that tyrosine can affect our brain with detrimental effects as we age. Neuro-Cognitive Effects of Acute Tyrosine Administration on Reactive and Proactive Response Inhibition in Healthy Older Adults https://pmc.ncbi.nlm.nih.gov/articles/PMC6084775/ "In conclusion, we show age-related effects of tyrosine administration especially on proactive, not reactive, response inhibition, accompanied by signal changes in dopamine-rich fronto-striatal brain regions. Specifically, we observed that tyrosine’s effect on brain and cognition became detrimental with increasing age, questioning the cognitive enhancing potential of tyrosine in healthy aging."
    • trents
      Nuts and cheese are not particularly high in tyrosine compared to many common foods most people eat nearly every day, particularly most meats and fish. I doubt that is the issue in and of itself, though nuts and cheese (particularly aged cheeses) can be a trigger for some migraine suffers for whatever reason. https://www.myfooddata.com/articles/high-tyrosine-foods.php
    • knitty kitty
      @Sarah Grace,  Thank you for the update!  It's so good to hear from you!  I'm glad Thiamine, B Complex and magnesium have helped you.  Yes, it's important to take all three together.    I had to quit eating cheese and nuts a long time ago because they triggered migraines in me, too.  They are high in tyrosine, an amino acid, found also in fermented foods like sauerkraut and red wine.   I found taking Tryptophan very helpful with migraines.  Tryptophan is a precursor of serotonin and people with migraines are often low in serotonin.  (Don't take tryptophan if you're taking an SSRI.)     This recent study shows tryptophan really helps. The association between dietary tryptophan intake and migraine https://pubmed.ncbi.nlm.nih.gov/31254181/   For immediate respite from a migraine, try smiling REALLY BIG, mouth closed, tongue pressed against roof of mouth, and crinkle up your eyes like you just heard or saw the funniest thing...  This causes an endorphin release in the brain.  Usually it's the funny event, then the endorphin release and then the smile.  Smiling first makes the endorphin center think it missed something and it catches up quickly by releasing endorphins after the big crinkle eyed smile.  Must make crinkly eyes with smile or it won't work.  If you do this too frequently within a short time frame (several hours), you can deplete your endorphins, but you'll make more in a couple of hours, so no worries. Get your thyroid checked, too.  Migraines are also seen in low thyroid function (Hashimoto's or hypothyroidism).  Celiac and thyroid problems go hand in hand.   Vitamin D helps, too.  Low Vitamin D is found in migraine.   I'm so glad you're doing better.  
    • Jmartes71
      Its been a complete nightmare dealing with all these health issues one thing after another and being told many different things.I am looking for a new primary care physician considering when I told my past doctor of 25 years I was diagnosed before any foods eliminated from my diet and now this year at age 54 no longer able to push considering Im always exhausted, leg pain , stomach,skin and eye issues,high blood pressure to name a few all worsen because I was a  school bus driver and few years until my immune system went to hell and was fired because of it.Im still struggling now, Im sibo positive and been told im not celiac and that I am.I have a hernia and dealing with menopause. Its exhausting and is causing depression because of non medical help. Today I saw another gastrointestinalist and he said everything im feeling doesn't add up to celiac disease since my ITg levels are normal so celiac disease is under control and it's something else. I for got I had Barrett's esophagus diagnosed in 2007 because recent doctors down played it just like my celiac disease. Im currently looking for a pcp in my area because it is affecting me personally and professionally. Im told since celiac looks under control it's IBS and I need to see a therapist to control it. Gastrointestinalist around here think only food consumption and if ITG looks normal its bit celiac disease it's something else. Is this right? This is what im being told. I want medical help but told its IBS.Im feel lost by " medical team "
    • trents
      My migraines generally have their onset during the early morning hours as well. Presently, I am under siege with them, having headaches all but two days so far this month. I have looked at all the things reported to be common triggers (foods, sleep patterns, weather patterns, stress, etc.). Every time I think I start to see a pattern it proves not to pan out in the long run. I'm not sure it's any one thing but may, instead, be a combination of things that coalesce at certain times. It's very frustrating. The medication (sumatriptan or "Imatrix") is effective and is the only thing that will quell the pain. NSAIDs, Tylenol, even hydrocodone doesn't touch it. But they only give you 9 does of sumatriptan a month. And it doesn't help that medical science doesn't really know what causes migraines. They know some things about it but the root cause is still a mystery.
×
×
  • 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.