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

Is It Easy To Make The Connection?


Nen

Recommended Posts

Nen Explorer

I would think that if one has celiac or a gluten problem, wouldn't the symptoms come soon after ingesting the offending food? I suppose what I am getting at is, after years of eating gluten does the body just become basically "inflamed" to the point where it would be difficult to pin down gluten as a problem since you pretty much feel a base-line crappyness most of the time anyways?

I do feel cruddy on and off with health issues that I think I've just gotten so used to (especially in this past year with the lovely addition of headaches). I would say in this past year I have gone only one full week being able to truthfully say that I felt great. I will deliberately have days where I try to eat a lot of gluten containing foods (bread, pizza crust, cookies, more bread, etc) and I will feel just fine the rest of that day or even the next day, but not for long. So wouldn't all that gluten just stab me and make me keel over if I have a problem with gluten? Or is it more just an ongoing general health problems that are tougher to actually pin down because the body is so worn down anyways that there aren't any dramatic flareups?


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



Celiac.com Sponsor (A8-M):



cyberprof Enthusiast

Nen, some people can see a relationship (pre-diagnosis) between eating and feeling poor. Others, like me, don't a connection: I think most people are in this catagory. Yes, you are right that the body just becomes inflammed and even if it is a non-gluten day, you still feel bad from one or more of the following: Systemic damage to intestines, nerves, brain, joints etc.; the gluten doesn't leave the body in one day -takes 2-3 weeks perhaps; and lastly, low levels of vital nutrients, vitamins and even things like electrolytes etc.

I see from your signature that you first joined this forum in 2010. Have you ever given gluten-free a true 2-3 month trial to see if it helps?

Nen Explorer

Nen, some people can see a relationship (pre-diagnosis) between eating and feeling poor. Others, like me, don't a connection: I think most people are in this catagory. Yes, you are right that the body just becomes inflammed and even if it is a non-gluten day, you still feel bad from one or more of the following: Systemic damage to intestines, nerves, brain, joints etc.; the gluten doesn't leave the body in one day -takes 2-3 weeks perhaps; and lastly, low levels of vital nutrients, vitamins and even things like electrolytes etc.

I see from your signature that you first joined this forum in 2010. Have you ever given gluten-free a true 2-3 month trial to see if it helps?

Yeah I have been a member for awhile. I do lurk here from time to time. The thing is I'm not sure if I should just go with the gluten-free diet first, or get the nerve up to try to get tested first, which means convincing my doc. The thing is sometimes my symptoms seem to lighten up so much that they are just about not there (for very brief times like a few days maybe) and I think to myself "oh you're just being silly see? Now you are feeling ok so you're fine", then another round comes again of feeling cruddy that I have to push through. I still have worked through all this never taking a sick day, though I've dragged myself through many times. I keep going back and forth with myself in my head alternating between "really just get friggin tested!" and "don't be dramatic you're fine! Its probably not anything to do with gluten". Ugh.

cyberprof Enthusiast

Yeah I have been a member for awhile. I do lurk here from time to time. The thing is I'm not sure if I should just go with the gluten-free diet first, or get the nerve up to try to get tested first, which means convincing my doc. The thing is sometimes my symptoms seem to lighten up so much that they are just about not there (for very brief times like a few days maybe) and I think to myself "oh you're just being silly see? Now you are feeling ok so you're fine", then another round comes again of feeling cruddy that I have to push through. I still have worked through all this never taking a sick day, though I've dragged myself through many times. I keep going back and forth with myself in my head alternating between "really just get friggin tested!" and "don't be dramatic you're fine! Its probably not anything to do with gluten". Ugh.

Well, I don't suggest lying to your doc, but you could try not minimizing your symptoms. Tell him/her that you feel bad multiple times a day, often feel like missing work but struggle through anyway because you don't want to let your employer down etc. You might have to be insistent. I was undiagnosed for way too long (30+ years)and always told my docs how I felt and was told variations of "you're a hypocondriac" "you just have a sensitive stomach" "you have too much stress in your life" or my personal favorite "you would have no symptoms if you just lost weight." My point is, if they don't agree to test you, put your foot down and if they still won't, then go gluten-free anyway and see if it helps. Good luck!

love2travel Mentor

I think in your situation testing is crucial. Then if you have celiac you have all the proof you need to go strictly gluten free once and for all. When I was told I had celiac I didn't believe it. The only reason I found out was because my sister is gluten intolerant and I got tested. Talk about shock because I had no GI symptoms or anything I could relate to eating gluten whatsoever. When I went on my gluten challenge after being gluten free for four months I frankly enjoyed it because nothing happened to me at all. NOTHING. But I did not know at that time about the serious damage that was happening inside and that is what counts. After my biopsy there was no question (I didn't believe my bloodwork so my doctor made me get a biopsy to convince me!) and I have been strictly gluten free ever since. How do I keep motivated? I think of my future. I want to live a long and healthy life with my husband whom I adore. I don't want to develop celiac-related cancers or other illnesses.

So, if you need that extra motivation to take this seriously, get tested but know that unfortunately could show false negatives so the only answer is going gluten free.

MitziG Enthusiast

bingo. Baseline crappiness hit it on the head for me. In the beginning (as a child, I reacted fairly quickly..but doctors said it was just wheat and to remove wheat from my diet. Never mentioned gluten. As an adult, the immediate reactions were gone and I just randomly puked, had diarrhea and felt majorly fatigued all the time. Having been gluten-free for some time, now the immeciate reactions are back.

Nen Explorer

Thank you for the replies. I probably should just bite the bullet and get tested. That way I can know for (at least somewhat) sure or at least have something more to go on.

Are there percentages for the accuracy of the blood test? What I mean is is the percentage of false negatives high or is it low enough that the blood test can be a somewhat reliable barometer? Of course there are those who the blood test was negative, but the biopsy showed trouble. At the very least the blood test would be a start.

ETA: One other thing, I do have brief periods of feeling alright, like for a few days I'll realize my head isn't hardly hurting and I feel good, but it always comes right back again with one or a combination of any of these symptoms: (head pain, sinus problems, sore throat/glands, intestine issues, tired weak feeling, sore muscle/joints, tingling novicane feeling in various places, off balance spaced out feeling). These brief periods of feeling ok, can that still happen with celiac undiagnosed?


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



Celiac.com Sponsor (A8-M):



nvsmom Community Regular

Thank you for the replies. I probably should just bite the bullet and get tested. That way I can know for (at least somewhat) sure or at least have something more to go on.

Are there percentages for the accuracy of the blood test? What I mean is is the percentage of false negatives high or is it low enough that the blood test can be a somewhat reliable barometer? Of course there are those who the blood test was negative, but the biopsy showed trouble. At the very least the blood test would be a start.

ETA: One other thing, I do have brief periods of feeling alright, like for a few days I'll realize my head isn't hardly hurting and I feel good, but it always comes right back again with one or a combination of any of these symptoms: (head pain, sinus problems, sore throat/glands, intestine issues, tired weak feeling, sore muscle/joints, tingling novicane feeling in various places, off balance spaced out feeling). These brief periods of feeling ok, can that still happen with celiac undiagnosed?

I suspected celiac for a couple of years before I finally got tested. I'm one of those people who avoids doctors and believes in "toughing it out"... I now know that wasn't too smart on my part.

Anyway, I've had it my whole life and I too had periods where I felt worse or better. My symptoms were never debilitating. I played varsity sports (with stomach and head aches), worked 10+hours a day (who wouldn't feel tired right?), and had three kids (no wonder my back is bad and I get sore)... I could explain away all my symptoms because they were not always present, but while I did that I developed other autoimmune diseases, and did permanent injury to my body...

Bite the Bullet as soon as you can.

And yes, something like 25% of celiac's blood tests come up negative. That's why they often do the biopsy (but that can miss damaged areas too). You might want to get vitamin K, iron, calcium, folate and B12 levels checked too. Many celiac are low in those.

Good luck. :)

Nen Explorer

I suspected celiac for a couple of years before I finally got tested. I'm one of those people who avoids doctors and believes in "toughing it out"... I now know that wasn't too smart on my part.

Anyway, I've had it my whole life and I too had periods where I felt worse or better. My symptoms were never debilitating. I played varsity sports (with stomach and head aches), worked 10+hours a day (who wouldn't feel tired right?), and had three kids (no wonder my back is bad and I get sore)... I could explain away all my symptoms because they were not always present, but while I did that I developed other autoimmune diseases, and did permanent injury to my body...

Bite the Bullet as soon as you can.

And yes, something like 25% of celiac's blood tests come up negative. That's why they often do the biopsy (but that can miss damaged areas too). You might want to get vitamin K, iron, calcium, folate and B12 levels checked too. Many celiac are low in those.

Good luck. :)

Thanks for the reply. That is the thing with me too, the symptoms are such that I can attempt to "reason them away" with such thoughts like "well of course I'm tired I work all day!" and "well I can still do stuff its not like I'm totally bedridden or anything I can drag myself through ok". Still though like you say this can just lead to a continuous putting-off until it really does get too late and the body is damaged.

mushroom Proficient

Do it NOW, Nen - you've fudged around long enough :) And when you're nutrient testing don't forget Vitamin D.

beebs Enthusiast

I never saw the connection, because I didn't have typical symptoms. I had things like nose and mouth ulcers all the time, constant middle ear infections and constant chest infections, severe GERD etc

Nen Explorer

Made the call to the docs today to find out the cost of testing, and waiting for them to get back to me! :)

nvsmom Community Regular

Good on ya!

cyberprof Enthusiast

Are there percentages for the accuracy of the blood test? What I mean is is the percentage of false negatives high or is it low enough that the blood test can be a somewhat reliable barometer? Of course there are those who the blood test was negative, but the biopsy showed trouble. At the very least the blood test would be a start.

ETA: One other thing, I do have brief periods of feeling alright, like for a few days I'll realize my head isn't hardly hurting and I feel good, but it always comes right back again with one or a combination of any of these symptoms: (head pain, sinus problems, sore throat/glands, intestine issues, tired weak feeling, sore muscle/joints, tingling novicane feeling in various places, off balance spaced out feeling). These brief periods of feeling ok, can that still happen with celiac undiagnosed?

If the blood test is postiive, it's unlikely to be wrong - the test has very few false positives. However, if your blood test is negative the reverse is not true. There are often false negatives.

Yes, celiac can cause periods of bad followed by ok or even good. It is funny that way -not sure if anyone knows why.

Hope they give you the test without any drama.

Nen Explorer

Eh well a little more road-blocks put in the way. I guess our doc no longer draws blood in his office anymore at all so we would have to get ahold of a lab company and figure it out for the cost.

Nen Explorer

Looks like it would be a direct testing through LabCorp, and the panel tests for Deamidated gliadin IgA; tissue transglutaminase IgA; serum IgA quantitation. Does this sound good? I never know what all that means. Looks like it costs about $140 to get.

Giambi Newbie

There are home test available also. They are relitively cheap and as accurate as a lab test if done properly. The one i'm waiting on claims 93% accuracy. I'm going that route instead of thru a doctor. If I get a negative result I'm gonna leave it at that. If I get a positive result I will let my PCP know.

nvsmom Community Regular

There are home test available also. They are relitively cheap and as accurate as a lab test if done properly. The one i'm waiting on claims 93% accuracy. I'm going that route instead of thru a doctor. If I get a negative result I'm gonna leave it at that. If I get a positive result I will let my PCP know.

I think the 93% accuracy refers to the fact that it is 93% specific to celiac... The other positive 7% have something else. There is still a 30% chance of a false negative like the lab tests; there's just not much of a chance of a false positive.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,857
    • Most Online (within 30 mins)
      7,748

    LowellFrancis
    Newest Member
    LowellFrancis
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.4k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Rogol72
      Some interesting articles regarding the use of Zinc Carnosine to help heal gastric ulcers, gastritis and intestinal permeability. I would consult a medical professional about it's use. https://www.nature.com/articles/ncpgasthep0778 https://www.rupahealth.com/post/clinical-applications-of-zinc-carnosine---evidence-review https://pmc.ncbi.nlm.nih.gov/articles/PMC7146259/ https://www.fallbrookmedicalcenter.com/zinc-l-carnosine-benefits-dosage-and-safety/
    • Jillian83
      He is. Which makes everything even more difficult. I’m not a believer in “staying for the kids” but I have nowhere to go and it’s not just me, it’s me plus my babies. We live in a beautiful place, lots of land in the country and me and the kids love the place we’ve called home for their entire lives. But Im seeing that he’ll never change, that my kids deserve a happy healthy Momma, and that staying in this as is will be the early death of me. Then I look at the scars covering my entire body…this disease and the chronic stress I’ve been enduring for years that tell me I’m no longer beautiful and no one will ever look at me with interest again. I try self care, try to give myself grace so I can just start loving myself enough to gain strength but the slightest sparkle in my eye and skip in my step attracts his wrath and it all comes crashing ten fold. Life is just absolutely railing me from every single direction leaving me wanting to wave that white flag bc I don’t feel like there’s much hope no matter what happens. 
    • trents
    • Jillian83
      Hi, I was recently diagnosed with Celiac and dermatitis herpetiformis after years of suffering without answers. I lost my mind. I lost my job. I lost so much time. I lost Me. Conventional doctors are opulent come near me and the one who did sat across the room, misdiagnosed me, pumped me full of steroids which collapsed my entire hip for 6 months. So without answers I began my holistic journey. Fast forward a couple of years and still struggling with a mysterious whole body itchy, crawling “skin hell”, perfect teeth now deteriorating, thick hair now thinning rapidly and no more than a day or 2 at most relief….An acquaintance opened up a functional medicine practice. Cash only, I found a way. Within a month tests clearly showing my off the charts gluten allergy/sensitivity as well as the depletion of vital nutrients due to leaky gut and intestinal damage. dermatitis herpetiformis was more than likely what I was experiencing with my skin. I was happy. I thought this is easy, eat healthy Whole Foods, follow the diet restrictions and I finally get to heal and feel confident and like myself again very soon! 😔 Supplements are very pricey but I got them and began my healing. Which leads to the other major issue: not working, stay at home Mom of young kids, entirely financially dependent on my man of 7 plus years. He’s never been supportive of anything I’ve ever done or been thru. He controls everything. I’m not given much money ever at a time and when he does leave money it’s only enough to possibly get gas. His excuse is that I’ll spend it on other things. So my “allowance” is inconsistent and has conditions. He withholds money from me as punishment for anything he wants. Since being diagnosed, he’s gained a new control tactic to use as punishment. He now is in control of when I get to eat. He asked for proof of my diagnosis and diet bc he said I made it up just to be able to eat expensive organic foods. Then after I sent him my file from my doctor he then said she wasn’t a real doctor. 😡. I go days upon days starving, sometimes breaking down and eating things I shouldn’t bc I’m so sick then I pay horribly while he gets annoyed and angry bc I’m not keeping up with all the duties I’m supposed to be doing. His abuse turns full on when I’m down and it’s in these desperate times when I need his support and care the most that I’m punished with silence, being starved, ignored, belittled. He will create more of a mess just bc I’m unable to get up and clean so that when I am better, I’m so overwhelmed with chores to catch up that the stress causes me to go right back into a flare from hell and the cycle repeats. I’m punished for being sick. I’m belittled for starving and asking for healthy clean water. I’m purposely left out of his life. He won’t even tell me he’s going to the grocery or to get dinner bc he doesn’t want me to ask him for anything. I have no one. I have nothing. Im not better. My supplements ran out and I desperately need Vitamin D3 and a methylated B complex at the very minimal just to function….he stares at me blankly…no, a slight smirk, no words. He’s happiest when im miserable and I am miserable.  this is so long and im condensing as much as I can but this situation is so complicated and disgusting. And it’s currently my life. The “IT” girl, the healthy, beautiful, perfect skin, perfect teeth, thick and curly locks for days, creative and talented IT girl….now I won’t even leave this house bc Im ashamed of what this has dont to my body, my skin. Im disgusted. The stress is keeping me from healing and I think he knows that and that’s why he continues to keep me in that state. He doesn’t want me confident or successful. He doesn’t want me healed and healthy bc then how would he put the blame of all his problems on me? This journey has been hell and I’ve been in Hell before. I’ve been killed by an ex, I’ve been raped, robbed, held hostage, abused beyond nightmares but the cruelty I’ve experienced from him bc of this disease is the coldest I’ve ever experienced. I’ve wanted to give up. Starving and in tears, desperate…I found a local food pantry in our small town so I reached out just saying I had Celiac and was on hard times. This woman is blessing me daily with prepared gluten free meals, donations, educational info, people who know this disease and how they manage life and the blessings just keep coming. But it’s overwhelming and I feel like I don’t deserve it at all. He just glared and I know he’s going to sabotage it somehow. I don’t even know what to do anymore. I’m so broken and just want peace and healing. 
    • cristiana
      @Colleen H   I am just curious,  when you were tested for coeliac disease, did the doctors find out if you had any deficiencies? Sometimes muscle pain can be caused by certain deficiencies, for example, magnesium, vitamin D, calcium, and potassium.   Might be worth looking into having some more tests.  Pins and needles can be neuropathy, again caused by deficiencies, such as iron and B12,  which can be reversed if these deficiencies are addressed. In the UK where I live we are usually only tested for iron, B12 and vitamin D deficiencies at diagnosis.   I was very iron anemic and supplementation made a big difference.  B12 was low normal, but in other countries the UK's low normal would be considered a deficiency.  My vitamin D was low normal, and I've been supplementing ever since (when I remember to take it!) My pins and needles definitely started to improve when my known deficiencies were addressed.  My nutritionist also gave me a broad spectrum supplement which really helped, because I suspect I wasn't just deficient in what I mention above but in many other vitamins and minerals.  But a word of warning, don't take iron unless blood tests reveal you actually need it, and if you are taking it your levels must be regularly monitored because too much can make you ill.  (And if you are currently taking iron, that might actually be making your stomach sore - it did mine, so my GP changed my iron supplementation to a gentler form, ferrous gluconate). Lastly, have you been trying to take anything to lessen the pain in your gut?  I get a sore stomach periodically, usually when I've had too much rich food, or when I have had to take an aspirin or certain antibiotics, or after glutening.  When this happens, I take for just a few days a small daily dose of OTC omeprazole.  I also follow a reflux or gastritis diet. There are lots online but the common denominators to these diets is you need to cut out caffeine, alcohol, rich, spicy, acidic food etc and eat small regularly spaced meals.   When I get a sore stomach, I also find it helpful to drink lots of water.  I also find hot water with a few slices of ginger very soothing to sip, or camomile tea.  A wedge pillow at night is good for reflux. Also,  best not to eat a meal 2-3 hours before going to bed. If the stomach pain is getting worse, though, it would be wise to see the doctor again. I hope some of this helps. Cristiana    
×
×
  • 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.