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

Questions From A Newbie


Debra L

Recommended Posts

Debra L Newbie

I am very new to this board. I have never had a formal diagnosis, but my Korean thyroid doc told me I had a wheat intolerance. He did stool and salvia tests, and I cut gluten out of my diet. I started feeling so much better. I found out 2 weeks later that the tests had gotten stuck at customs and I have to repeat them. I had read that inorder to get accurate results I would need to be actively eatting gluten. I went back to my regular diet, and I feel sicker than I ever remember being before. I have Hashimoto's and Wilson's Temperature syndrome, he said that I had some kind of adrenal syndrome also. It feels like now I am sicker than before! Is this common? and can Hashimoto's be related to Celiac's? I saw that for the first time here, but I don't know much about it.....

any help is appreciated

thanks,

Deb

Daegu, SK


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



Celiac.com Sponsor (A8-M):



Eriella Explorer

Welcome to the board--

The best way to explain why gluten is affecting you so much more now is to think about alcohol. If you go out drinking every night for a year, you will get used to it, even though it is bad for your body and your body will be showing symptoms of being sick. When you stop drinking, your liver heals and your body goes through detox. Then, if you start drinking again, you will have lost your tolerance, so you will feel it more, and your liver will scream at you because you are making it sick again.

The same thing is happening with your small intestine. You were used to eating wheat, even though it made you sick. You stopped and started healing. Now you are interjecting this poison back into your body, and it doesn't like it and is letting you know. So yes, it is normal. So go off gluten as soon as you can, and you will start feeling better.

As far as the correlation with the other diseases-- if you have one autoimmune, you are likely to pick other ones up.

mftnchn Explorer

Sounds like your doctor has not done a typical celiac panel which would be blood tests. Interesting that your stool and saliva tests were being sent overseas.

I'm your neighbor, in Liaoning province of China. I figured I couldn't get accurate testing here so have just gone with a dietary approach to diagnosis.

You didn't say what your symptoms of gluten intolerance are. Can you get an intestinal biopsy done there?

Debra L Newbie
Sounds like your doctor has not done a typical celiac panel which would be blood tests. Interesting that your stool and saliva tests were being sent overseas.

I'm your neighbor, in Liaoning province of China. I figured I couldn't get accurate testing here so have just gone with a dietary approach to diagnosis.

You didn't say what your symptoms of gluten intolerance are. Can you get an intestinal biopsy done there?

I started by finding a doctor for Wilson's Temperature syndrome. I have all the hypothyroid symptoms with usually normal tsh (I am a mil spouse, so the docs usually just do TSH). This doctor is a Korean doctor that I am paying for out of my pocket (not covered by insurance). I thought that if I could get my temp up, I could start to not feel sick any more. I suffer from weight gain, bloating, off and on D and const. I usually have ZERO energy. I can sleep 11-12 hours at night, then take a 1-2 hour nap in the afternoon. I often suffer from a complete inability to remember things. Sometimes I forget my own name, but I thought that was because I don't speak Korean, but I try to do my best. Most of the time I felt all over sick, like I was being poisoned. I started feeling happier, better, more alive when I was off the gluten. {My Traditional Oriental Medicine doctor had told me that I should avoid wheat, but it just sounded like it was because I am over weight. She is treating me with acupuncture for my asthma. It is the best thing! No more inhaled drugs! It has stopped the every other month antibiotic cycle.} The specialist said that I was intolerant, so I figured that was more conclusive and it struck a cord. So I went to the internet and started checking it out. I don't think that I would want to get a biopsy here. I spent a week in the local hospital last year for my asthma and pneumonia, it was a very uncomfortable experience. I am leaving here in about 4 months, so I figured if I need a more conclusive diagnosis, I could get it when I go back to the US. I thought that one of the stool tests was for wheat intolerance, or possibly celiacs. My doctor speaks English, but prefers to speak to me through another person who translates. Korean culture and language is full of "understood" or implied understandings. And doctors here are still Kings. So it is difficult to get all of my questions answered.

sorry for being so long.

thanks for the reply, it actually makes perfect sense now, but I was thinking it might mean that I wasn't really having a gluten problem. I guess I am happy to know that it is 'normal' :D

Deb

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

    • 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    
    • Me,Sue
      I was diagnosed with coeliac disease a couple of years ago [ish]. I love my food and a variety of food, so it's been hard, as it is with everyone. I try and ensure everything I eat doesn't contain gluten, but occasionally I think something must have got through that has gluten in. Mainly I know because I have to dash to the loo, but recently I have noticed that I feel nauseous after possibly being glutened. I think the thing that I have got better at is knowing what to do when I feel wiped out after a gluten 'episode'. I drink loads of water, and have just started drinking peppermint tea. I also have rehydration powders to drink. I don't feel like eating much, but eventually feel like I need to eat. Gluten free flapjacks, or gluten free cereal, or a small gluten free kids meal are my go to. I am retired, so luckily I can rest, sometimes even going to bed when nothing else works. So I feel that I am getting better at knowing how to try and get back on track. I am also trying to stick to a simpler menu and eat mostly at home so that I can be more confident about what I am eating. THANKS TO THOSE WHO REPLIED ABOUT THE NAUSEA .
×
×
  • 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.