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

Does This Sound Like Celiac?


tchntm43

Recommended Posts

tchntm43 Newbie

I am 35. For most of my life, I have struggled with a low body-weight for my height. It seemed like I could not gain fat or muscle. I remember eating an entire large pizza in high school despite that I weighed only 105 lbs (I am male and 5'5"). This had no effect on my weight. My regular doctor always told my mom I just had a high metabolism. This continued until I was around 25. I started gaining a little more weight, and got up to 125. Then around 30 I went up to 140-ish. The gained weight is mostly fat around my abdomen. I still have just as much difficulty gaining muscle tissue as before.

The past few months, I have been feeling very exhausted. In addition, my body is producing a lot of very bad gas. I have realized that this seems to coincide with a time when I've been eating a lot of pasta and bread. I've been getting a heavy gluten dose with almost every lunch and dinner. Prior I had been eating a lot of rice for months, both with lunch and dinner, and had very little gluten in my diet. The only reason I made the change is I was bored with my diet and wanted to do something different for a while. Although from time to time I would still eat a sandwich for lunch or order out for dinner.

I had a similar incident about 7 or 8 years ago where I was exhausted for an extended period of time. I cannot remember if I had the gas with it, or what my diet consisted of at the time. Back then I had suspected lyme disease as a the culprit, and the symptoms actually went away before I got tested for that, so I went on as though nothing had happened. And I think I may have had another incident about 5 years ago, but much reduced in duration and how exhausted I felt. I thought that might have been mono, but that came back negative and also went away on its own. Again, I have no idea about diet and any changes to it.

I should mention that around the start of this current episode of exhaustion, I came down with shingles. I went to the doctor to confirm that and it went away in about 2 weeks.


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



Celiac.com Sponsor (A8-M):



guest134 Apprentice

How is your height compared to family members? Is your entire family on the shorter end of the scale or just you? I must say if fatigue is your main culprit with eating heavy pastas and such I would think of a blood sugar issue (not necessarily diabetes) before celiacs.

To me, these are your gluten alert symptoms:

Your height

weight

Excess gas

Those are very vague issues that can occur in many diseases as well as just normal people who go through bouts of stomach issues. If I go on a high protein diet I will pass a lot more gas and very smelly gas at that.

Do you have any other stomach issues? You could always test to be sure anyway.

GottaSki Mentor

Welcome!

While I agree your symptoms could be caused something other than Celiac Disease or Non-Celiac Gluten Intolerance -- I think it is very important to have a full celiac blood panel while you are still consuming gluten. Should these tests all be negative, it would be wise to remove ALL gluten for a period of three months (six is better) as elimination is the only test for NCGI which has many similar and quite serious symptoms of Celiac Disease.

Nutritional deficiencies is a strong indicator of Celiac Disease - B12, D and Iron are most common - these are the bare minimum that should be tested. My celiac doc tested all Bs, D, K, Iron, Ferritin, Copper and Zinc at diagnosis along with check ups.

Weight issues and periodic illness over many years is common with Celiac Disease. I had many "flu-type" illnesses that became more frequent over several decades until fatigue was permanent.

You do not need to have severe gastro symptoms with Celiac Disease. My GI issues were minor compared with my autoimmune type symptoms. I did not have severe bloating until my last 3 years prior to diagnosis. Here is the list of symptoms associated:

Open Original Shared Link

Make a list of your symptoms - past and present along with a list of questions and tests you would like to have run. Have this in your hand during your doctor appointment - I find my doctor appointments are far more productive when prepared.

Let us know if you have more questions.

Hang in there :)

guest134 Apprentice
Here is the list of symptoms associated:

Open Original Shared Link

It's funny, I have seen many people reference this list of symptoms but have never read it over. Upon quick review it seems like an alarmist list, like come on they are adding things like crohn's and ulcerative colitis? Not only that, they have pretty much every disease in the book listed from autoimmune to cancers. Obviously celiacs can cause other symptoms other than digestive but there were clearly things added to that list just to be able to label it "300 symptoms of celiacs".

I don't care what disease centre it is, if they were at all professional or even correct they would add foot notes referencing each symptom in clinical setting, I don't see ANYTHING of the sort ANYWHERE to crohns being cause by celiacs and quite frankly if I had the time would probably be able to prove they have no background to at least 50 percent of the symptoms they named. They are going off technicalities, maybe if celiacs was so bad in you that it caused several other autoimmune diseases you would have those symptoms, but that would be a symptom of the new disease caused by celiacs and not celiacs itself. I.E- If celiacs is not affecting your thyroid than I (along with many qualified doctors) simply don't believe it can cause obesity (and have yet to see anything that can prove otherwise).

From my extensive OCD research I have learnt that there is way too much false info being passed around on celiac and gluten sensitivity and too many people are taking what they hear from the next person at face value without validating it themselves, spreading the false info like wild fire (that is not an attack on anyone on this forum, I am speaking in general).

Yes celiacs is underdiagnosed but many of these sites make it sound like 90 percent of the population has the disease, if you were to go off those 300 symptoms you can certainly diagnose the world.

Sorry to derail the thread, let us know if you have any other questions.

GottaSki Mentor

I strive to always say "symptoms associated with Celiac Disease" and "testing should be done to before removing gluten". To the best of my knowledge I have never said a person has Celiac Disease until they report back with an official diagnosis.

For those of us that did go misdiagnosed, undiagnosed or dismissed by a multitude of doctors - until you have walked in our shoes, please don't discourage people from being tested BEFORE they either dismiss the possibility of gluten enteropathy or trial the elimination of gluten.

IMO you are doing them a disservice by dismissing their concerns because they lack "classic" symptoms.

This is certainly not the only testing that should be done in cases of digestive, autoimmune or non-specific symptoms, but certainly should be in the mix.

Celiac Mindwarp Community Regular

I took the 300 symptoms list to be 'associated with' rather than 'causal of' celiac.

Personally I have found this list and similar ones helpful to stitch together for myself all my apparently unrelated symptoms. If I hadn't seen recurrent miscarriage on a similar list I wouldn't have tied my other symptoms together. My GI seems happy with my research.

This is just my personal recent experience, I am not intending to generalize.

I am definitely with GottaSki on getting tested and fully exploring other possibilities. I couldn't do a gluten challenge, so wont get a full diagnosis. My GI is now working on ruling out other things and genetic testing.

IrishHeart Veteran

It's funny, I have seen many people reference this list of symptoms but have never read it over. Upon quick review it seems like an alarmist list, like come on they are adding things like crohn's and ulcerative colitis? Not only that, they have pretty much every disease in the book listed from autoimmune to cancers. Obviously celiacs can cause other symptoms other than digestive but there were clearly things added to that list just to be able to label it "300 symptoms of celiacs".

I don't care what disease centre it is, if they were at all professional or even correct they would add foot notes referencing each symptom in clinical setting, I don't see ANYTHING of the sort ANYWHERE to crohns being cause by celiacs and quite frankly if I had the time would probably be able to prove they have no background to at least 50 percent of the symptoms they named. They are going off technicalities, maybe if celiacs was so bad in you that it caused several other autoimmune diseases you would have those symptoms, but that would be a symptom of the new disease caused by celiacs and not celiacs itself. I.E- If celiacs is not affecting your thyroid than I (along with many qualified doctors) simply don't believe it can cause obesity (and have yet to see anything that can prove otherwise).

From my extensive OCD research I have learnt that there is way too much false info being passed around on celiac and gluten sensitivity and too many people are taking what they hear from the next person at face value without validating it themselves, spreading the false info like wild fire (that is not an attack on anyone on this forum, I am speaking in general).

Yes celiacs is underdiagnosed but many of these sites make it sound like 90 percent of the population has the disease, if you were to go off those 300 symptoms you can certainly diagnose the world.

.

My very celiac-savvy GI doctor refers to this symptom/conditions list when evaluating and meeting with new patients.

I know, because I printed it off and gave it to him ---and he was happy to have the handout.

I had about 65 of those symptoms myself. Yes, that's right. And that's how I knew I HAD celiac.

And to clarify, the list is adapted from Recognizing Celiac Disease by Cleo J. Libonati and her book has pages and pages of valid sources and medical references.

The first thing my doc checked me for after DX was Crohn's, inflammatory bowel diseases, ulcerative colitis and intestinal lymphoma.

If you do not know that lymphoma is often caused by long undiagnosed celiac, then you have not done enough reading.

It may not seem "possible" to some people, but celiac (no s, just celiac) is a head-to-toe disease and is often associated with dozens of AI diseases.

Why would a link to other AI diseases be so hard to believe?

They are all fueled by inflammation---- and there is no bigger inflammatory agent than gluten in celiac.

Not all people will have stomach or bowel issues, but instead, they exhibit a host of extra-intestinal symptoms (neurological, reproductive, rheumatological, etc.) that only a celiac-savvy doctor will recognize.

This is why the Celiac Center posted the list in the first place--as a guide.


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



Celiac.com Sponsor (A8-M):



Darn210 Enthusiast

The intro to the list: (the bolding is mine)

"Celiac disease is associated with approximately 300 symptoms, which are listed in alphabetical order below. These symptoms are not specific to celiac disease, however, and many may be uncommon. This list is intendend to illustrate the variety of subtle and seemingly unrelated symptoms associated with celiac disease and the resulting diagnostic challenge. The list is not intended to be used as the sole basis for diagnosis."

We were all surprised when my daughter was diagnosed, including the pedGI. He screened her for celiac disease because that had become an office policy for kids that presented with "generic" GI symptoms. The GI told me that prior to that, about three kids a year would come through the office with skinny limbs, distended belly and explosive diarrhea and hey, what do you know, this child has celiac disease. This is what he had been taught to recognize as celiac disease. After they started their new screening process, they were diagnosing about a child a week and he continued to be surprised by which kids tested positive . . . they didn't "look" like celiac kids.

That list helps people think outside of the box.

kareng Grand Master

It's funny, I have seen many people reference this list of symptoms but have never read it over. Upon quick review it seems like an alarmist list, like come on they are adding things like crohn's and ulcerative colitis? Not only that, they have pretty much every disease in the book listed from autoimmune to cancers. Obviously celiacs can cause other symptoms other than digestive but there were clearly things added to that list just to be able to label it "300 symptoms of celiacs".

I don't care what disease centre it is, if they were at all professional or even correct they would add foot notes referencing each symptom in clinical setting, I don't see ANYTHING of the sort ANYWHERE to crohns being cause by celiacs and quite frankly if I had the time would probably be able to prove they have no background to at least 50 percent of the symptoms they named. They are going off technicalities, maybe if celiacs was so bad in you that it caused several other autoimmune diseases you would have those symptoms, but that would be a symptom of the new disease caused by celiacs and not celiacs itself. I.E- If celiacs is not affecting your thyroid than I (along with many qualified doctors) simply don't believe it can cause obesity (and have yet to see anything that can prove otherwise).

From my extensive OCD research I have learnt that there is way too much false info being passed around on celiac and gluten sensitivity and too many people are taking what they hear from the next person at face value without validating it themselves, spreading the false info like wild fire (that is not an attack on anyone on this forum, I am speaking in general).

Yes celiacs is underdiagnosed but many of these sites make it sound like 90 percent of the population has the disease, if you were to go off those 300 symptoms you can certainly diagnose the world.

Sorry to derail the thread, let us know if you have any other questions.

The lists are made by medical experts to be easy to read by "normal" non-medical people . Copious footnotes, references, etc would make it unreadable to most. If you would like references for every thing on there, maybe you could find a list in medical journals or email the writer of the list?

guest134 Apprentice

I am not dismissing this persons symptoms, I told him to get tested but based on his results it could be other things and to not get so caught up on one disease like I have seen many people do, several different tests are required.

I never said it is not linked to other autoimmune diseases, I said that unless it is causing another one half of those symptoms are irrelevant to new people being diagnosed. By this I mean, if you have celiac but you have tingling in the hands, cold sensitivity, and trouble gaining weight, to test the thyroid and not just throw it into the list of "300 symptoms".

I am also aware that it can slightly increase your chances of lymphoma if left undiagnosed for decades, just like many other things in life.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,948
    • Most Online (within 30 mins)
      7,748

    Stephanie94
    Newest Member
    Stephanie94
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Jacki Espo
      This happened to me as well. What’s weirder is that within a couple hours of taking paxlovid it subsided. I thought maybe I got glutened but after reading your post not so sure. 
    • Mari
      Hi Tiffany. Thank you for writing your dituation and  circumstancesin such detail and so well writte, too. I particularly noticed what you wrote about brain for and feeling like your brain is swelling and I know from my own experiences that's how it feel and your brain really does swell and you get migraines.    Way back when I was in my 20s I read a book by 2 MD allergist and they described their patient who came in complaining that her brain, inside her cranium, was swelling  and it happened when she smelled a certain chemical she used in her home. She kept coming back and insisting her brain actually swelled in her head. The Drs couldn't explain this problem so they, with her permission, performed an operation where they made a small opening through her cranium, exposed her to the chemical then watched as she brain did swell into the opening. The DRs were amazed but then were able to advise her to avoid chemicals that made her brain swell. I remember that because I occasionally had brain fog then but it was not a serious problem. I also realized that I was becoming more sensitive to chemicals I used in my work in medical laboratories. By my mid forties the brain fog and chemicals forced me to leave my  profession and move to a rural area with little pollution. I did not have migraines. I was told a little later that I had a more porous blood brain barrier than other people. Chemicals in the air would go up into my sinused and leak through the blood brain barrier into my brain. We have 2 arteries  in our neck that carry blood with the nutrients and oxygen into the brain. To remove the fluids and used blood from the brain there are only capillaries and no large veins to carry it away so all those fluids ooze out much more slowly than they came in and since the small capillaries can't take care of extra fluid it results in swelling in the face, especially around the eyes. My blood flow into my brain is different from most other people as I have an arterial ischema, adefectiveartery on one side.   I have to go forward about 20 or more years when I learned that I had glaucoma, an eye problem that causes blindness and more years until I learned I had celiac disease.  The eye Dr described my glaucoma as a very slow loss of vision that I wouldn't  notice until had noticeable loss of sight.  I could have my eye pressure checked regularly or it would be best to have the cataracts removed from both eyes. I kept putting off the surgery then just overnight lost most of the vision in my left eye. I thought at the I had been exposed to some chemical and found out a little later the person who livedbehind me was using some chemicals to build kayaks in a shed behind my house. I did not realize the signifance  of this until I started having appointments with a Dr. in a new building. New buildings give me brain fog, loss of balance and other problems I know about this time I experienced visual disturbances very similar to those experienced by people with migraines. I looked further online and read that people with glaucoma can suffer rapid loss of sight if they have silent migraines (no headache). The remedy for migraines is to identify and avoid the triggers. I already know most of my triggers - aromatic chemicals, some cleaning materials, gasoline and exhaust and mold toxins. I am very careful about using cleaning agents using mostly borax and baking powder. Anything that has any fragrance or smell I avoid. There is one brand of dishwashing detergent that I can use and several brands of  scouring powder. I hope you find some of this helpful and useful. I have not seen any evidence that Celiac Disease is involved with migraines or glaucoma. Please come back if you have questions or if what I wrote doesn't make senseto you. We sometimes haveto learn by experience and finding out why we have some problems. Take care.       The report did not mention migraines. 
    • Mari
      Hi Jmartes71 That is so much like my story! You probably know where Laytonville is and that's where I was living just before my 60th birthday when the new Dr. suggested I could have Celiacs. I didn't go on a gluten challange diet before having the Celiac panel blood test drawn. The results came back as equivical as one antibody level was very high but another, tissue transaminasewas normal. Itdid show I was  allergic to cows milk and I think hot peppers. I immediately went gluten free but did not go in for an endoscopy. I found an online lab online that would do the test to show if I had a main celiac gene (enterolab.com). The report came back that I had inherited a main celiac gene, DQ8, from one parent and a D!6 from the other parent. That combination is knows to sym[tons of celiac worse than just inheriting one main celiac gene. With my version of celiac disease I was mostly constipated but after going gluten-free I would have diarrhea the few times I was glutened either by cross contamination or eating some food containing gluten. I have stayed gluten-free for almost 20 years now and knew within a few days that it was right for me although my recovery has been slow.   When I go to see a  medical provide and tell them I have celiacs they don't believe me. The same when I tell them that I carry a main celiac gene, the DQ8. It is only when I tell them that I get diarrhea after eating gluten that they realize that I might have celiac disease. Then they will order th Vitamin B12 and D3 that I need to monitor as my B12 levels can go down very fast if I'm not taking enough of it. Medical providers haven't been much help in my recovery. They are not well trained in this problem. I really hope this helps ypu. Take care.      
    • knitty kitty
    • DebJ14
×
×
  • 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.