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

Gluten Intolerance/celiac disease? Or Something Else (long)


tiredtwinmommy

Recommended Posts

tiredtwinmommy Newbie

I finally got brave enough to post here, I know that becoming gluten free is a HUGE step. But I have wondered for a long time what was up with me. My name is Beth. I am 39, and mama to 3 1/2 year old twins. I want to be the best Mom I can be, but it is hard when I am sick a lot of the time. Let me start this way:

I think back when I was younger- I remember in 7th and 8th grade I would have HORRIBLE stomach pain right after lunch. I would wedge a book lengthwise between my tummy and the desk, the pressure on my tummy made me feel better. Then as a slightly older teen (19 or so) I remember being tired ALL the time, as well as depressed, although I really had no reason to be so. The tiredness and depression has been off and on for years now. Then I started having weight issues along with everything else, and my periods became irregular. As I got older, and before having kids, I started to occasionally wake up at night nauseous, sometimes throwing up for no particular reason. Then after having the kids (after LOTS of infertility treatments, another s/e of celiac disease), I got my rosacea outbreaks, my weight gains are worse, I get hungry all the time, I get terrible gas (frequency and smell), my stools are usually pretty loose and frequent now, I developed apnea (which I am STILL tired all the time, even with the CPAP), I am more prone to irritability/outright anger, and more depressed now. I also constantly seem to have sinus infections, and they are harder to get rid of. To me, all these things really point to at least gluten intolerance, maybe very slight when younger and just got worse as I got older/after childbirth.

I have had numerous and complete thyroid panels, all show normal. I had a false positive for lupus before I had the kids, but a more detailed blood test showed that to be a false positive. With my period cycles becoming longer and longer, I have had blood workups to check for early menopause- all showed normal... matter of fact, when we were diagnosed w/infertility, it was "unexplained" (oh, also I had had quite a few early miscarriages). My children were born prematurely, b/c of both my high blood pressure and the fact my daughter was not gaining any weight in the womb. My sleep apnea, was considered odd by my dr, b/c I was at my pre-pg weight when I was diagnosed (have gained 20 more pounds since then), and never snored or had appearance of apnea before that. My first indication of rosacea occured while going through infertlity treatments... when I would get upset my face would start getting large red blotches (these went away), and then one night I had a beer after not having one in a very long time and broke out in welts on my cheeks and nose- although I have not had that reaction to beer ever since, after the birth of my kids I started getting perm rosy cheeks that no medicine would cure.

So, what do you guys think? I really am thinking gluten problems. But I am a big chicken. Blood tests I can handle. Colonoscopies/intesting biopsies/endoscopies terrify me, particularly being such an easy gagger.

Thanks in advance for your help!

Beth


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



Celiac.com Sponsor (A8-M):



CarlaB Enthusiast

Beth, go get the blood test before you go gluten-free! Many consider a blood test and positive dietary response to be enough proof for diagnosis (not docs, but celiacs :)).

It could be celiac disease.

Even if the blood test is negative, I'd still give the diet a trial.

Bacterial dysbiosis is another GI issue with similar symptoms to celiac disease, so you might also want to research it a bit.

tiredtwinmommy Newbie
Beth, go get the blood test before you go gluten-free! Many consider a blood test and positive dietary response to be enough proof for diagnosis (not docs, but celiacs :)).

It could be celiac disease.

Even if the blood test is negative, I'd still give the diet a trial.

Bacterial dysbiosis is another GI issue with similar symptoms to celiac disease, so you might also want to research it a bit.

Thank you. I called my dr and asked for the blood tests, and she told me I would have to go see a GI dr :( for that. So guess that is my next step. I will also research bacterial dysbiosis as well. Thanks for your quick response!

Beth

mftnchn Explorer

I agree with Carla.

Also I think you have to consider what kind of diagnosis you need for yourself and why. Some want a gold standard diagnosis (positive biopsy) just for themselves as they know they won't stay on the diet without it. Some want it because of family and friends support--and those folk need "proof." Some want confirmation from medical people.

Some are simply content with the answer to "do I feel better when I don't eat gluten?" and don't need any further testing.

I think you should at least get the full blood panel (5 tests). If negative and you can't bring yourself to do the biopsy, you could consider Enterolab. You won't get a celiac diagnosis based on Enterolab, but perhaps some guidance about whether you react to gluten.

Greeneyes4950 Apprentice

Hi, i just want to tell you that i can definately relate. I'm 20, and have for years been suffering from stomach problems. The fatigue- my first year of college it was so bad that i was going to bed at 5:30 pm, sleeping for 12 hrs, and falling sleep in class. I literally couldn't function. By that point i had been suffering from secondary amenorrhea since i was 12. My doctor ran thyroid panels, checked my liver and kidney function, ovarian cysts and tested me for lyme disease. -- it all came back negative.

Things seemed to get better, i went on an ubbber healthy diet, and got more rest, and then the stomach problems began. So much that i would sitting in a ball at work on the floor sometimes. And oh yeah...the gas. it was never ending.

Then came last march, when outside my physiology lab, i blackouted, and fell on my face. yeah. ouch. ended up in the hosipital, where they couldn't find out what had happened.

In my post-hospital check up with my doctor, she suggested i may have celiac. --but decided not to test me, since i have a healthy weight. decided i had symptoms of "IBS" instead, and told me to simply "stay away from trigger foods" (but failed to mention what they could be) and eat more fiber, though my diet before was not seeming fiber deficient. -- but despite doing both, or trying to at least, it didn't help

So i went on a fairly restricted diet, that excluded gluten/casein/soy/egg/yeast/corn.

And my stomach problems nearly disappeared.

I decided to go through enterolab and get tested for celiac. My tests should be back within another week or two. I may be celiac, i may be not. but changing my diet has really helped my stomach problems and other health issues.

I know how feel, and it's almost weird to read about someone who shares many of the symptoms i do, especially about the periods. I would advise you see your doctor.

jerseyangel Proficient
Thank you. I called my dr and asked for the blood tests, and she told me I would have to go see a GI dr :( for that. So guess that is my next step. I will also research bacterial dysbiosis as well. Thanks for your quick response!

Beth

Beth,

Your doctor may not have known which blood tests to order. My mom's doctor had no idea. In any event, this is the Celiac Panel--ask that they do the whole thing:

Anti-Gliadin (AGA) IgA

Anti-Gliadin (AGA) IgG

Anti-Endomysial (EMA) IgA

Anti-Tissue Transglutaminase (tTG) IgA

Total Serum IgA

Matilda Enthusiast

...


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



Celiac.com Sponsor (A8-M):



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.