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

Question About You Going gluten-free & The Effects


3groovygirls

Recommended Posts

3groovygirls Contributor

I have a question and I'll try to explain it right. Violet has Celiac, she has the gene for it, so obviously it comes from one of us, her parents. I haven't been tested and neither has my DH. However, I have my suspicions about it coming from my side of the family.

So here's my question. If you don't have Celiac (or don't know) has your tolerance of gluten changed at all? I'm not totally gluten-free, but I have cut out a TON of gluten. For instance we mostly eat gluten-free snacks (crackers, chips, etc) gluten-free pasta, gluten-free cereal. Basically I don't eat much gluten anymore by default. Now I'm finding that when I have something with gluten (beer in particular) it effects me HORRIBLY. Gas, bloating, diarrhea. It never used to. Is this common? If you go gluten-free, then when you eat it again does it bother *everyone* or would it just bother you if you might have Celiac or an intolerance towards it? My DH doesn't seem bothered by it, but I really am now. Do you think that's a sign that she gets it from me, or just a coincidence?

So I guess what I'm asking is, as a parent, once you cut out a lot of gluten, did you find YOUR tolerance for it went down even if you don't have Celiac? Or was it an indicator that maybe you should go get checked?

(BTW, I know I should get checked, but I've asked 2 Dr.s so far and none will test me b/c they say if I'm asymptomatic I don't need to be and "most cases are sporadic and not genetic". Basically both Dr.'s were totally wrong but I can't seem to find one who will and since I DO feel fine it hasn' been my top priority, KWIM?)


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



Celiac.com Sponsor (A8-M):



lizajane Rookie

i don't know if this will help, as I am the one diagnosed with celiac and THEN i took my kid off gluten. he had some classic signs of celiac in children and they ALL went away when i took him off gluten and they all come back when he is accidentally glutened.

BUT... i will say... you may not have noticed your own symptoms because you may have attributed them to something else and only noticed them now that you realize when you do or do not have gluten. my most serious symptom was fatigue- and foggy brain and irritability. it never ever occured to me that i had more gas than anyone else until it all went away when i stopped eating gluten! i never would have guessed that my near constant nausea was caused by celiac. i thought i was under stress or over-ate.

really, it doesn't matter if you have it or don't if it makes you feel bad to have it. if you don't eat it anymore and you feel better, then don't eat it anymore. the problem comes if you still eat it anyway. if you DO have celiac and you continue to eat gluten, you have a much higher risk of lymphoma. pretty good reason to either 1) never eat it or 2) get tested before you DO eat it!

mushroom Proficient

That is fairly classic for a celiac, to have a holiday from gluten and then feel much worse when they eat it again. It is the reason many of us are self-diagnosed. It would be too dreadful for us to even consider going back on gluten for the 2-3 months necessary for the testing to be accurate.

Kaycee Collaborator

Hi, what you describe has been the case for me. I went on a diet to loose weight a while back while still eating gluten. On the diet I wasn't eating much bread and or processed food, so not much gluten, and I felt quite good. My diarrhea eased off and I felt better, but the relief was only temporary. I am guessing my body was getting used to the lower gluten, but it wasn't being fooled as it wasn't long before the symptoms were all back. It was only after that, that I looked for answers and that is when I arrived at the conclusion it was gluten related. The doctor confirmed this with a diagnosis of coeliac, and that is when I started a gluten free diet.

Yes, if I slip up now, even with the minutest amount, I get very bloated, irritable, and the dreaded D, to name but a few symptoms. These are more symptoms than I realised I had before. I did not realise just how bloated I had been feeling. I guess at 48 years old, and having eaten gluten all my life, those annoying issues were just part of me and probably felt normal to me. Yes I do react quite differently to gluten now than I did before.

I am the only one diagnosed in my family. My mother is having issues with similar things, but her doctor says coeliac is not genetic and he doesn't feel she has enough symptoms to warrant being tested.

mushroom Proficient
My mother is having issues with similar things, but her doctor says coeliac is not genetic

What??? What rock did he crawl out from under?? Does your Mom believe this?? You need tp research on here and get information on paper for her to take to him. Studies with citations that he can't refute. He needs an education.

Kaycee Collaborator

Neroli, I would love to do what you say. But first of all I would need my mum and dad to believe there is a problem. I know it might sound a bit slack on my part, but I have discussed this exact thing with mum and dad. Mum goes as far to say, that my problems are similar to hers, but she is adamant that it could be the same disease. My father initially thought that it would be too hard for mum since she is in her late 70's. It doesn't help that I live in Northland and they in the south island.

I feel bad enough knowing I can't help, and that nothing I say will make a difference. I guess that is families for you, if I go on too much I get silenced, if I don't say anything, things stay the same. Vicious circle.

Cathy

mushroom Proficient

Well, Cathy, I can't say that I don't know how it is with families. My eldest sister and I are both gluten free and self-diagnosed, but she has a diagnosed celiac daughter; our middle sister refuses to even consider that she could have a problem even though I have seen multiple times grand evidence of similar symptoms to mine; she merely says, "I just get on with it," implying that we are making a big fuss about nothing. I just hope it does not rise up and bite her on the bum like it did me. :D

That being said, that doctor needs to be brought up short. Do you think you could mail or email the information to him since he is obviously too lazy to look it up himself?


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



Celiac.com Sponsor (A8-M):



ang1e0251 Contributor

It does seem to me that you also have a problem with gluten if you are reacting to it now. Some people want to think you "did it to yourself" because you restricted gluten foods. I disagree with this. I only eat pumpkin in the fall but it doesn't make me sick even though I haven't had any for 9 months. I usually only eat strawberries in warm weather when they are in season and again I don't react to those. Same with watermelon, cantalope, and mostly with turkey. If you're reacting to gluten, you have a problem with it. If it's an intolerance and not full out celiac disease, no test will show that.

Archived

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

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

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





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - Scott Adams replied to Roses8721's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      1

      gluten-free Oatmeal

    2. - knitty kitty replied to Jmartes71's topic in Related Issues & Disorders
      22

      My only proof

    3. - knitty kitty replied to Ginger38's topic in Related Issues & Disorders
      10

      Shingles - Could It Be Related to Gluten/ Celiac


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,561
    • Most Online (within 30 mins)
      7,748

    Valentino
    Newest Member
    Valentino
    Joined

  • Celiac.com Sponsor (A20):



  • Celiac.com Sponsor (A22):




  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m

  • Celiac.com Sponsor (A21):


  • Upcoming Events

  • Posts

    • Scott Adams
      Oats naturally contain a protein called avenin, which is similar to the gluten proteins found in wheat, barley, and rye. While avenin is generally considered safe for most people with celiac disease, some individuals, around 5-10% of celiacs, may also have sensitivity to avenin, leading to symptoms similar to gluten exposure. You may fall into this category, and eliminating them is the best way to figure this out. Some people substitute gluten-free quinoa flakes for oats if they want a hot cereal substitute. If you are interested in summaries of scientific publications on the topic of oats and celiac disease, we have an entire category dedicated to it which is here: https://www.celiac.com/celiac-disease/oats-and-celiac-disease-are-they-gluten-free/   
    • knitty kitty
    • knitty kitty
      Hi, @Ginger38, I've had shingles in the past.  I understand how miserable you're feeling.   Not only do i have the chickenpox virus lurking about, I also have the cold sore virus that occasionally flares with a huge cold sore on my lip when stressed or exposed to gluten.  The virus lives dormant in the nerves on the left side of my face.  It causes Bell's Palsy (resulting in drooling).  The cold sore virus is also in my eye.  My eye swells up and my vision is diminished permanently whenever I have a flare, so it's of the utmost importance to keep flares away and treat them immediately if they do happen so I don't lose any more vision.   I take the amino acid supplement L-Lysine.  Lysine messes with the replication of viruses, which helps the body fight them off.   I haven't had an outbreak for several years until this year when exceptionally stressed and contaminated, it flared up again. Lysine has been shown to be beneficial in suppression of viruses like the cold sore virus (a herpetic virus), the chickenpox virus (also a herpetic virus), as well as the HIV virus, and even the Covid virus.   I also take additional Thiamine in the form TTFD (tetrahydrofurfuryl disulfide) because Thiamine has antiviral properties as well.   For pain, a combination of Thiamine (like TTFD or Benfotiamine or Thiamine Hydrochloride), with B12 Cobalamine, and Pyridoxine B6 have been shown to have analgesic properties which relieve pain and neuropathy.    The combination of Thiamine B1, Pyridoxine B6 and Cobalamine B12 really does work to relieve pain.  I take it for back pain from crushed vertebrae in my back.  This combination also works on other pain and neuropathy.   I usually buy a supplement that combines all three and also Riboflavin B2 called EXPLUS online.  However, it's made in Japan and the price with the tariffs added makes it really expensive now.  But the combination of Thiamine B1, Pyridoxine B6 and B12 Cobalamine (and Riboflavin B2) still work even if taken separately.   I can't take Tylenol or ibuprofen because of stomach upsets.  But I can take the vitamin combination without side effects.  However, you can take the three vitamins at the same time as other pain relievers for added benefit.  The vitamins help other pain relievers work better. I hope you will try it.  Hopeful you'll feel better quickly. Interesting Reading: Thiamine, cobalamin, locally injected alone or combination for herpetic itching: a single-center randomized controlled trial https://pubmed.ncbi.nlm.nih.gov/23887347/ Mechanisms of action of vitamin B1 (thiamine), B6 (pyridoxine), and B12 (cobalamin) in pain: a narrative review https://pubmed.ncbi.nlm.nih.gov/35156556/ Analgesic and analgesia-potentiating action of B vitamins https://pubmed.ncbi.nlm.nih.gov/12799982/ A Narrative Review of Alternative Symptomatic Treatments for Herpes Simplex Virus https://pmc.ncbi.nlm.nih.gov/articles/PMC10301284/
    • Mari
      I think, after reading this, that you areso traumatized by not being able yo understand what your medical advisors have been  what medical conditions are that you would like to find a group of people who also feel traumatized who would agree with you and also support you. You are on a crusade much as the way the US Cabinet  official, the Health Director of our nation is in trying to change what he considers outdated and incorrect health advisories. He does not have the education, background or experience to be in the position he occupies and is not making beneficial decisions. That man suffered a terrible trauma early in his life when his father was assonated. We see now how he developed and worked himself into a powerful position.  Unless you are willing to take some advice or  are willing to use a few of the known methods of starting on a path to better health then not many of us on this Celiac Forum will be able to join you in a continuing series of complaints about medical advisors.    I am almost 90 years old. I am strictly gluten free. I use 2 herbs to help me stay as clear minded as possible. You are not wrong in complaining about medical practitioners. You might be more effective with a clearer mind, less anger and a more comfortable life if you would just try some of the suggestions offered by our fellow celiac volunteers.  
    • Jmartes71
      Thus has got to STOP , medical bit believing us! I literally went through 31 years thinking it was just a food allergy as its downplayed by medical if THEY weren't the ones who diagnosed us! Im positive for HLA-DQ2 which is first celiac patient per Iran and Turkey. Here in the States especially in Cali its why do you feel that way? Why do you think your celiac? Your not eating gluten so its something else.Medical caused me depression. I thought I was safe with my former pcp for 25 years considering i thought everything I went through and going through will be available when I get fired again for health. Health not write-ups my health always come back when you're better.Im not and being tossed away at no fault to my own other than shitty genes.I was denied disability because person said he didn't know how to classify me! I said Im celiac, i have ibs, hernia, sciatica, high blood pressure, in constant pain have skin and eye issues and menopause intensified everything. With that my celiac nightmare began to reprove my disregarded disease to a bunch of clowns who think they are my careteam when they said I didn't have...I feel Im still breathing so I can fight this so no body else has to deal with this nightmare. Starting over with " new care team" and waisting more time on why I think I am when diagnosed in 1994 before food eliminated from my diet. P.s everything i went through I did write to medical board, so pretty sure I will continue to have a hard time.
×
×
  • 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.