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

Another Newbie


ppeterin

Recommended Posts

ppeterin Newbie

Hello,

I stumbled onto this site after furiously searching for an explanation to my sudden and not-so-sudden symptoms.

A little history,

I have had issues with anxiety and panic since I was a teenager. At the time I used an anxiety packet to get through and it seemed to help. Several years later I ended up on prozac to help with anxiety and depression. Starting around age 22-23 I started to have symptoms lactose intolerance and I cut it completely out of the diet. A year or so after cutting out dairy I started to develop IBS. Around the same time I developed asthma. Like a good boy I followed all the advice on how to manage IBS. That advice included lots of bulky and high fiber grains. Those have been my staple for years. I'll admit that I have also developed some bad dietary habits like eating far too much sugar and using far too much immodium to manage my IBS.

Fast forward 7 years. I am 30 now and recently I took myself off of my latest anti-depressant. For about a month after coming off I felt relatively health except that my IBS sypmtoms were worsening. I again started looking around online and stumbled across a couple of anti-candida diet websites. I figured that if cutting some foods out of my diet would help with my overall symptoms (even if one-tenth of what was promised was true) I would do it. I stuck to the diet for three days and got pretty sick and weak. However, my mood noticeably improved and my bowl symptoms were gone. I just felt really weak and that was what caused me to turn to bread for some sustenance once again. I would have tried rice but I was under the impression that white rice was worse in the diet than whole wheat bread. So I ate bread. A few days later I added some ghee to my bread because I was told it was lactose free.

I was fine for a few days after reintroducing a little bread with each meal. Three days after I couldn't fall asleep for any reason at all. WIDE awake for several hours until some Tylenol PM saved me. I haven't had insomnia in years. The very next day I start developing anxiety. Not the regular run of the mill anxiety but HOLY COW! this is insane I can't find relief anxiety. Then today. Horrible and painful diarrhea (tan and smelly - stetorrhea I guess it is called-I have had it before-for years in fact) and anxiety I haven't felt in years. Now I am sitting here almost unable to work at all. I can barely eat although I have finally figured I should be sneaking rice down the chute instead of bread.

That was the only time in my life that I can remember going without gluten for ONE full day let alone THREE. The conclusion I am moving towards is that it was the cutting of gluten, followed by reintroduction of gluten that has caused this sudden onset of suck. I also completely cut out refined sugars and anything that can easily be converted to sugar. I also continued on without eating any dairy products. I never drink anything with caffeine. When I reintroduced whole wheat bread I also reintroduced a little refined sugar from the honey and white-flour component of the bread (Whole- wheat my butt!). When I ate the ghee I reintroduced a little dairy (supposedly harmless :blink: ). So the question for me is which of the three things are causing my problems. Or are all three causing my problems. The dairy and the sugar are the most likely culprits unless you consider that my problems with dairy and sugar may actually be due to celiac. Did I just reintroduce three things I either can't digest

I am terrified. My wife and I just closed on a home and now I can barely function. I know that celiac can't be diagnosed as simply like lactose intolerance. I am just very frustrated and scared. I'm even crying and I NEVER cry.

My course of action is simply to cut out gluten from this moment forward and to see if I can return to those few days when I felt OK. I have an appointment with a PA in two days since I can't get in to see my primary until September. I'll ask for the testing though I know that not eating gluten can throw the tests off.

Thanks for letting me get that off my chest.

My only question is how long after stopping the eating of gluten will the tests still register the anti-bodies? Is two days without gluten too long?


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



Celiac.com Sponsor (A8-M):



Gutbomb Rookie

Are you sure you aren't telling my story? I don't have any answers for you since I am going through the testing phase myself but hang in there. Someone will come a long with some answers and just so you know I called out of work sick today. You aren't alone!

Amanda

gfpaperdoll Rookie

it is your decision but I would quit eating gluten immediately. If you are interested in any testing I would test thru Enterolab.com I like them & tested my family there. You can be gluten free for up to a year or two & not effect the outcome of the tests. They also do the gene tests...

with your strong neurological depression, anxiety, etc you probably have at least one DQ1 gene.

I have an 83 year old friend that had been sick with classic celiac symptoms for three years (she is also Irish) & about day two gluten-free her depression, panic attacks, & anxiety were gone. People were talking to her & not believeing the huge change in her.

Most of us with DQ1 do not have depression when we are gluten-free. well I am gluten-free, DF etc. most meds will not help depression caused by gluten.

welcome to the group & I hope you are better soon. Just quit eating wheat, rye, barley & oats. Giving up dairy & soy is also strongly advised...

good luck

GFinDC Veteran

Hi ppeterin,

This article on the forum might help answer your questions about testing.

https://www.celiac.com/articles/57/1/Interp...ults/Page1.html

I suggest you ask your doctor to do the blood test first, and a gene test. You can start reading up on G.F. eating and diet in the meanwhile.

ppeterin Newbie

Thank you for all the replies.

I spent the day in the ER because I just couldn't eat or drink. Far too nauseas. I got an IV and some anti-nausea medication. Feelings slightly better. The doc refused to run any celiac anti-body tests because I failed to eat anything with gluten for two days last week. I think he just didn't want to touch it. The good news is that visiting the ER got me on the fast track to see an GI doc. I will be getting a colonoscopy this Thursday. It is my understanding that biopsies for celiac come from going down the throat and sampling the jejunem. So I don't think I'll be able to get the proper biopsy off the bat. However, I will ask him to run the gene and antibody tests.

Either way, I am going to cut gluten and soy (and ghee) out of my diet and see what happens.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      130,022
    • Most Online (within 30 mins)
      7,748

    Casswithceliac
    Newest Member
    Casswithceliac
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.3k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Diana Swales
      After years of living with Celiac Disease, learning through every bump and breakthrough, and guiding others through the gluten-free maze — I've officially qualified as a **Nutrition Coach** with Precision Nutrition. Now I’m ready to take this journey deeper… but I need your help. To complete my final certification hours, I’m offering **a limited number of FREE spots** (yes, completely free!) to work with me over the next few weeks. I’m looking for **5 people** who: Are newly diagnosed with Celiac Disease or gluten-intolerant Feel overwhelmed, confused, or frustrated with food Want support from someone who truly understands Are ready to build confidence and calm in their daily eating We’ll work together on what matters to *you*: Your food choices Your mindset Your kitchen habits Your ability to speak up for your needs This isn’t just about avoiding gluten — it’s about reclaiming ease, joy, and nourishment. If you're interested, comment below or DM me the word **"Ready"** and I’ll send you the info to get started. Let’s make food feel safe again. With care, **Diana**
    • Dora77
      Hi everyone, I have celiac disease and I’m asymptomatic, which makes things more stressful because I don’t know when I’ve been glutened. That’s why I try to be really careful with cross-contamination. For almost a year, I’ve been having yellow/orange floating stools consistently. I’m not sure if it’s related to gluten exposure or something else going on. I’ve been trying to identify any possible mistakes in my routine. Today, I made myself some gluten-free bread with cheese. Normally, I’m very careful: I use one hand to handle the cheese packaging (which could be contaminated, since it’s from the supermarket and was probably sitting on a checkout belt that had flour residue), and the other hand to touch my gluten-free bread and plate. But today I accidentally touched the bread with the same hand I used to grab the cheese pack from the fridge. The fridge handle might also have traces of gluten since I live in a shared household where gluten is used. I’m worried this mistake could have contaminated my bread. There were no visible crumbs or flour, but I know even trace amounts can be a problem. Has anyone had similar experiences or symptoms from this level of contact? Could this kind of exposure be enough to trigger symptoms or cause intestinal damage? Thanks for reading.
    • Mswena
      So eight days in a row of gluten on top of gluten on top of gluten, I just had to resort to the EpiPen. I wish I could post a picture because you wouldn’t believe how enormous my gut is! It makes my head look like a pinhead.Ahhhgggsahhhhh!!!! I have discovered that I have to read the ingredients when I use a product up that I’ve been able to use without getting a reaction, because they can change the ingredients and bam my toothpaste now has gluten!!! my doctor told me gluten free means it has 20 ppm which someone with a severe a celiac as I’ve got that thing there kills me. I try to find certified gluten-free in everything. I can’t eat any oats unless it’s Bob’s red mill certified gluten-free. Good luck everybody this autoimmune disease is wicked wicked
    • Mswena
      I have been using a little bit of Lubriderm when I wash my hands because it’s the lotion offered at a place I frequent once a week. Assuming it was gluten-free I bought a bottle. I couldn’t figure out why I was getting gluten EVERY night. I use a little of the lotion in the morning on my neck, with no reaction, but at night, I use it on my arms and legs and face and get gluten gut pretty bad. After eight nights of having to have diphenhydramine injections for severe gluten, I googled “is Lubriderm gluten-free” and it led me to this forum. I am going to go back to olive oil as I have been gut sick sooooooo bad with a huge gut and pain eight days in a row now. Sick of feeling sick.
    • ShariW
      These look great!  I follow several people who frequently post gluten-free recipes online (plus they sell their cookbooks). "Gluten Free on a Shoestring" and "Erin's Meaningful Eats>"
×
×
  • Create New...