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

Celiac Or Something Else?


V1981

Recommended Posts

V1981 Newbie

Hi everyone,

I am new to this forum and I am hoping I can get some help. I think I may have celiac, but it could very well be something else... Have any of you experienced the following symptoms -

Alternating constipation/Diarrhea

Gas and bloating

chronic rash in groin area

swollen lymph nodes in groin area and sometimes behind ears and on back of neck or lower jaw line

PCOS/Endometriosis symptoms

Weight gain

dry irritated eyes

Nausea

Chlorine taste in mouth and smell chlorine around you.

Dizzy to the point that the room is literally spinning.

I have been to the doctor and gotten many blood tests and most of them have come back "normal". I did however flunk (this is the term my doctor used) the Glucose Tolerance test and when I did a salivary hormone test my Progesterone, DHEA and Cortisol levels were below normal. I have been taking Iodoral for my thyroid (which is underactive) and started on some natural supplements to treat the PCOS symptoms. But, so far I only feel better part of the time.

Anyways, sorry to go on and on. I am just looking for some help so any feedback is appreciated.

Thanks!

V


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



Celiac.com Sponsor (A8-M):



bartfull Rising Star

"Flunking" the glucose tolerance test means diabetes. Did your doctor talk to you about that?

The rest of your symptoms sure sound like Celiac to me. Even the "diabetes" can be part of Celiac symptoms. Ask him to test you for it. I'm not sure which tests to ask for (there are several) because I am self-diagnosed based on family history, my symptoms, and the fact that the gluten-free diet cleared up those symptoms. But someone will be along shortly to tell you all about testing.

So welcome to the forum. Stick around and read a bunch. Ask as many questions as you can. There are some real experts here who are so helpful. In the meantime, here's a (((HUG))) and high hopes that you will be feeling better soon.

squirmingitch Veteran

I agree with bartful in that your symptoms sound like celiac. And get that flunking the glucose test straightened out with your doctor & make him/her tell you exactly what that means & what you are to do about it. And if the doc isn't forthcoming enough then get a new doc!

You should get tested for celiac. Make sure they do the FULL celiac panel! Double check what they order & make sure all these are on it.

Anti-Gliadin (AGA) IgA

Anti-Gliadin (AGA) IgG

Anti-Endomysial (EMA) IgA

Anti-Tissue Transglutaminase (tTG) IgA

Deamidated Gliadin Peptide (DGP) IgA and IgG

Total Serum IgA

The DGP test was added recently to the full panel.

Also can be termed this way:

Endomysial Antibody IgA

Tissue Transglutaminase IgA

GLIADIN IgG

GLIADIN IgA

Total Serum IgA

Deamidated Gliadin Peptide (DGP) IgA and IgG

And if you are going to be tested for celiac then no matter what the doc says DO NOT stop eating gluten until all celiac testing is finished including an endoscopy. Do not eat gluten light. There are enough false neg. on the tests --- you don't want to add to that. It's possible the rash is Dermatitis Herpetiformis (celiac rash). There is a biopsy for that too & if it turns up positive then that IS a diagnosis of celiac disease. There is a 37% false neg. return on hd biopsies though & you need to have a derm who is well versed & experienced in recognizing & taking biopsies of dh. And you MUST be eating gluten for the dh biopsy.

Welcome aboard. Ask questions & read as much as you can.

V1981 Newbie

"Flunking" the glucose tolerance test means diabetes. Did your doctor talk to you about that?

The rest of your symptoms sure sound like Celiac to me. Even the "diabetes" can be part of Celiac symptoms. Ask him to test you for it. I'm not sure which tests to ask for (there are several) because I am self-diagnosed based on family history, my symptoms, and the fact that the gluten-free diet cleared up those symptoms. But someone will be along shortly to tell you all about testing.

So welcome to the forum. Stick around and read a bunch. Ask as many questions as you can. There are some real experts here who are so helpful. In the meantime, here's a (((HUG))) and high hopes that you will be feeling better soon.

Thank you so much for replying. Yes, my doctor said that even though I "flunked" the GT he didn't think I have diabetes. More like Insulin Resistance I guess. I am definitely leaning towards Celiac though for the real cause of all my symptoms. It all started when I was a toddler and began eating solid food. No one new what celiac disease was back in the 1980's, so my mother had no idea that I shouldn't have been eating gluten.

V1981 Newbie

Thank you! I am going to have the tests done ASAP! :)

squirmingitch Veteran

Get a copy of the test results & the ref. ranges & post them here when you do if there is any doubt or the doc gives you grief. There are ppl here very well versed in interpreting the tests.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,954
    • Most Online (within 30 mins)
      7,748

    apage
    Newest Member
    apage
    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.