Jump to content
This site uses cookies. Continued use is acceptance of our Terms of Use and Privacy Policy. More Info... ×
  • 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

Help Me?


Ew...Gluten.

Recommended Posts

Ew...Gluten. Newbie

I've been gluten free for a little under a year. To spare gory details, I have depressive symptoms and "the foggy head." I am obsessive and follow the gluten free diet to the best of my ability, and still no improvements? The first few months we're better, but it went down hill from there. I believe I possibly have small slip ups, but I don't know where/when these occur. Any help would be greatly appreciated. I feel hopeless. Could depression/fog be caused by something else?


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



Celiac.com Sponsor (A8-M):



Welda Johnson Newbie

Hi,

I'm 64 and have had Celiac symptoms since age 8 (mine manifested as asthma, and, later, depression, anxiety, spastic colon, ulcer, etc.). I conducted food elimination tests on myself, since scratch skin tests and 3 years of allergy shots didn't help. I stopped all grains and felt better. Then all milk & dairy, then egg whites and yeast, along with casein and whey. Modified food starch also bothers me. My life is so much better now. I'm usually upbeat and positive, and am able to say that I am now truly "happy," after many years spent suffering after every meal that contained those foods to which I proved to be intolerant.

Now we are learning that family members have Celiac as well, and I am sometimes able to be of help in their quest for good health. I hope that you find success on this, YOUR journey to good health. Welda

missy'smom Collaborator

Gluten causes depression for me but I learned that depression can be triggered by other things(non-food) and was at least once when I had been completely and strictly gluten-free for a long time. The brain fog, in my experience, and I know other have different experiences, is only with gluten, but I do have more difficulty thinking when my blood sugar gets low. There are many things that effect our brain/mind/emotional functioning and energy levels. Sometimes if we have low energy for a long time we don't realize it and get depressed or low because we don't have the energy to accomplish what we want or need to but we don't always realize it because we're so used to feeling low in energy. It would be a good idea to get a CBC panel done if you haven't had one in a while.

Jenny (AZ via TX) Enthusiast

Ew..Gluten,

Depression and brain fog can be caused by other things, but for many of us, gluten is the culprit. Have you had bloodwork done lately? You could also be deficient in B12 and D3.

Check all of your supplements and meds to make sure they are gluten free.

I also switched my skincare, shampoo etc to gluten free products. Supposedly, you cannot absorb gluten through the skin. But, if you use a lotion that has gluten in it and you still have some on your hands when you eat, you can ingest it that way.

I didn't change all of that at first, but after reading more about it, I didn't want the risk.

Also, did you change your pans out (if not stainless steel), your plastic and wooden spoons, cutting boards, etc. Also, if you have baking powder, baking soda, sugar that you used prior to going gluten-free, you may have cross contaminated them by using measuring spoons that had gluten on them.

If you have a support group, you may want to ask for someone to evaluate what you are doing.

Do you have a shared kitchen?

You probably know most of this, but thought I'd put it out there to see if there is something you missed.

I hope you feel better soon!!!

dilettantesteph Collaborator

I think that you are probably getting gluten without realizing it. To give an example, I'll tell you about what happened yesterday with my son. He got sick but the only new thing that he had tried was Chebe bread made in a gluten free facility. We suspected two other things that he has been eating all along without problems. One of them, Amy's pizza I searched and found that other people on this forum had reacted to it. Their website says that they do tests to make sure that their foods are below 20 ppm as suggested by the FDA guidelines. My doctor says that some celiacs react to as little as 0.5 mg of gluten. At 20 ppm that is a 25 g piece, which is a 13th of one of those little Amy's pizzas. I tested it with a home test with a sensitivity of 10 ppm and it was positive. Now we think that is what we need to eliminate from his diet. Let's just hope he gets better and can attend school again soon.

Some celiacs are sensitive to very small amounts of gluten. If you are that sensitive you may need to eliminate all food processed in facilities that process wheat. That isn't always on the label. It is voluntary whether a company choses to label their foods that way or not. You may also have to eliminate vinegar and alcohol made from gluten grains. Also watch for wines, some of them have trace gluten from barrels or yeast, or the filtration process.

After the first while the body seems to get more sensitive to trace amounts of gluten. Depression sucks. I get it really bad when I get glutened.

I hope you get well.

whitball Explorer

I do acknowledge that part of my depression and anxiety are from being a celiac. But I have realized that I cannot continue to live my life with the depression and anxiety always at my doorstep. All of that said, I have had alot happen in my life, not all positive, so I have decided that antidepressants are what I need for now. I have also sought counseling. These are also options if the gluten free diet is not taking care of your depression, anxiety, etc. Don't let these feelings run your life. Not trying to tell you what to do, but just sharing my experiences. Hope this helps.

mef Newbie

If possible, you might want to have another panel done to check for antibodies. Have you checked for any other intolerances? Also, what types of gluten-free foods are you eating? When I eat too much of the gluten-free substitutes (ie the pastas, the breads etc) and not enough fruits/veggies/proteins, I find myself tired and drawn out.

I hope you can find some help here!


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



Celiac.com Sponsor (A8-M):



tom Contributor
Could depression/fog be caused by something else?

Yes.

Dairy & soy did it to me.

Have you tried eating free of those?

For me it took 2 entire weeks free of soy before I knew I was on to something.

I'd previously gone w/out for 4 or 5 days, per common recommendations, and didn't see a diff so went back to eating it.

Caused me to lose yet another yr or 2. :(

happygirl Collaborator

If you were diagnosed via bloodwork and/or biopsy for Celiac Disease, it may be worth it to have your Celiac panel re-run to assess the status of your healing.

GFinDC Veteran

I agree about the elimination diet idea. If you don't find anything in your diet that contains gluten, you may need to do an elimination. Maybe try eliminating some foods and see if you start feeling better after a week. I found that wine and dairy are problems for me, in addition to gluten. I think it is either yeast or sulfites in the wine that cause problems for me. Wiki says the diary casein protein molecule is similar to the gluten protein. I guess it might cause a cross reaction. Some people have problems with corn or taters etc too. You might have similar intolerances or different ones. I have been taking calcium and vit D each day but my doc says I am still low on vit D. Seems to be typical for celiacs to be low on vitamins, expecially D and B. So it might help to take a little extra of each beyond the minimum daily requirements for normal peeps. :)

  • 2 weeks later...
Ew...Gluten. Newbie

thank you to all- helped me out :D

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      127,973
    • Most Online (within 30 mins)
      7,748

    Barb5256
    Newest Member
    Barb5256
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121k
    • Total Posts
      70.5k

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Scott Adams
      It's possible he's in the early stages of celiac disease, and it has been caught before villi damage. The blood test results so far do indicate possible celiac disease, as well as his strong family history of celiac disease. If his symptoms get better on a gluten-free diet this would be another strong indication. Personally I think it's definitely better to proceed on the safe side and go gluten-free, rather than to risk severe villi damage and all that comes with it.
    • Dora77
      For some context: I have type 1 diabetes (T1D) (since 11 years) and celiac disease(since 4 years) For about a year now, I’ve been experiencing permanent floating and undigested stools. I’ve had a pancreas elastase test done. The first result was extremely low at 44, but a second test came back at 236. My doctor said that since one result is normal, it rules out pancreatic insufficiency because, according to them, elastase levels would always stay low if that were the issue. However, could the 236 have been a false result? My doctor also thinks I don’t have pancreatic insufficiency because I’m able to gain weight. I also get hgh injections as my bone age is younger than my real age, this also contributes to weight gain, so I dont know if weight gain can rule out malabsorption. But maybe if I had real malabsorption I wouldnt gain any weight even with hgh? For celiac, I’m on a gluten-free diet, but there might b small cross-contamination from things like pepper labeled as “may contain gluten.” or sausages which dont have gluten ingredient but say may contain. My doctor said that small amounts like this wouldn’t harm me and even mentioned that an occasional small exposure to gluten may not do much damage (which seems questionable since I thought even tiny amounts could be harmful). She also said that when Im older (Im m17) I could try eating small amounts of gluten and do antibody blood tests to see if I can tolerate small amounts or not. For reference, I’m asymptomatic when it comes to celiac, so I have no idea if I’ve been “glutened” or not. My first concerning celiac blood test was semi high IgA, then 3 months later we did a check up and my IgA was high so it was confirmed celiac. Since than I’ve had celiac antibody tests done yearly to see how my diet is going, and they’ve been negative, but I’ve heard those aren’t always reliable. I’ve never had a follow-up endoscopy to confirm healing. I also always kept eating „may contain gluten“ food. (I live in Germany so I dont know if „may contain gluten“ is as risky as in the usa but I suppose both are as risky) These stool issues started around the same time I was doing excessive heavy lifting at the gym. Could stress or lifting have triggered this, or is that less likely since the symptoms persist even after I stopped lifting? Occasionally, I’ll feel very mild stomach discomfort, but it’s rare and not severe. My doctor (also a dietist) said floating, undigested stools could still be “normal,” but that doesn’t seem realistic to me. Could this be impacting my vitamin or protein absorption? I also did a fructose intolerance breath test and had a high baseline of 20 ppm, but it never increased—only decreased over time. I fasted for 12 hours and didn’t eat fructose beforehand, but my stomach didn’t feel completely empty during the test. Could this mean the test was inaccurate? For lactose intolerance, I did the breath test but only fasted 10 hours and had eaten lactose prior because I wasn’t aware of the proper diet restrictions. My results were: 14, 12, 15, 25, 35, 40, 40 ppm—which would be considered positive. But given that I didn’t fast long enough or follow the right diet, could this result be unreliable? Has anyone else dealt with similar symptoms? What ended up being the cause for you? And sorry for the long text!
    • TerryinCO
      The Docs' and NP haven't committed to Celiac determination yet but say go gluten-free diet because...  And I have with improved physical results - feeling better; overall functions better, and more energy.  Still 10 pounds down in weight but I still have BMI of ~23.  It's been just over a month now gluten-free diet.  I'm fortunate I get along with diary/milk well and most other foods. I wanted ask about this site's sponsor, gliadin X.  If this is legit, seems like a good product to keep on hand. Though it says it's only a safety for incidental gluten contact - not a substitue for gluten-free diet. What's your input on this? This may be sensitive subject since they're a sponsor. I've used resources here and other sites for information, gluten-free food/product lists. So thank you for all that support. That's it for now - Stay warm...  -2F this morning in Colorado!
    • cristiana
      I did suffer with gastric symptoms before diagnosis, but got all sorts of weird and wacky symptoms after going gluten free.   Things got much better once my antibodies fell to normal levels, but it took years (please don't panic, many people's go to normal levels relatively quickly when following a gluten-free diet). Causes of the symptoms you mention that I also experienced were iron supplements, a temporary dairy intolerance (this is common in coeliacs and should pass when your gut heals properly), and eating oats, as mentioned above.  Other symptoms I got were musculoskeletal pain after diagnosis, but again, once my coeliac blood tests were normal, I had no more pain. I did notice patterns emerging in foods that I reacted to and learned to steer clear of them, then gradually reintroduced them when my gut healed, such as soya, pure oats and dairy products.    You might like to keep a food diary. Cristiana
    • Jy11
      Well the conflicting results continue as the biopsy has come back negative. 😵‍💫 Waiting to discuss further but I really don’t know what to think now? Eight biopsy’s were taken from duodenum which surely should be sufficient if it was coeliac? 
×
×
  • Create New...