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

Magister Mundi

Recommended Posts

Magister Mundi Rookie

Hello all,

This is a long one, so please be patient or skip to the bottom for the TL;DR version.

So, a little background before I get into my weird post-gluten-free symptoms. I'm 23, male, and a student at the University of Oregon. This last summer I was given a presumptive diagnosis of celiac disease based on blood work (120/30 ELISA units on an anti-tTg IgA blood test). Because I wasn't going to be able to get in to see a specialist for a biopsy for six months due to insurance issues, I went gluten-free at the recommendation of my primary physician.

My symptoms did start to recede, ever so slowly... but of course, by the time I was starting to notice a real difference, I got a consultation with a GI specialist, who told me to resume a normal, non-gluten-free diet for two months so as to not throw off the biopsy results. I started eating gluten again for those two months, got an endoscopy/colonoscopy/small biopsy, and - surprise surprise with 4x the "normal" amount of ELISA units - was positively diagnosed with celiac disease.

I'm now gluten-free again. It's been two weeks, and I'm just now starting to get over the worst of the gluten withdrawals. With the exception of an incident of very mild cross-contamination at the end of last week, I've been doing alright in my recovery process... with a few weird exceptions.

First, my BMs. Surprisingly, while I was back on my gluten-y diet in the leadup to the biopsy, I was pretty regular, and everything was as it was supposed to be. No floating, no malodor, no excess mucous, no partially digested food, etc. However, in the past two weeks since going back onto the gluten-free diet, all of the traditional symptoms of celiac in that department have cropped up. I've become irregular in my BMs, the consistency is off, it's definitely malodorous, digestion isn't working properly, and there's far too much mucous.

Huh? Isn't the opposite supposed to be happening? Interestingly, the first time I went gluten-free I also had an abundance of mucous, but none of the other symptoms.

Second, allergic reactions. One of the recurring symptoms I had pre-diagnosis was constant itchy, runny, red eyes, even when it wasn't allergy season. In fact, this is so consistent that when I was gluten-free the first time, I used this reaction to tell when I had been glutened. So when I got that cross-contamination last week, my eyes got all itchy, as usual. But then, yesterday... they got itchy again. And I'm 100% certain I didn't get glutened yesterday, since I was at work all day in a food-free environment, and the only things that went into my mouth were very carefully vetted and screened by me beforehand (and were all things that couldn't have been exposed to gluten).

Again... huh?

TL;DR version: Going gluten-free again appears to have actively made my intestinal issues and allergic reactions worse.


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



Celiac.com Sponsor (A8-M):



GFinDC Veteran

HI Magister Mundi,

Welcome to the forum! :)

Going gluten-free seems to have an adjustment period for our guts, as well as our taste buds. Reversing damage to our gut and bodies can take some time, months or more even. It depends a lot on how sick a person was to start with and how much damage they have. But being back on the gluten-free diet means you have started down the path to healing, so that's good. :)

You could try taking some pro-biotics and digestive enzymes with your meals. Eating different foods can throw your gut bacteria off and that can cause symptoms. It also might be helpful to cut back on sugar and starchy foods for a while, until your gut bacteria stablize and your villi heal some.

Just for reference, I had hayfever symptoms that eased off over about 6 months after going gluten-free. Now they are very minor for me. So, your allergy responses may stabilize some as time goes on also.

Congrats on getting diagnosed!

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,545
    • Most Online (within 30 mins)
      7,748

    Jem68
    Newest Member
    Jem68
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.4k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):




  • Who's Online (See full list)


  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Beverage
      I had a very rough month after diagnosis. No exaggeration, lost so much inflammatory weight, I looked like a bag of bones, underneath i had been literally starving to death. I did start feeling noticeably better after a month of very strict control of my kitchen and home. What are you eating for breakfast and lunch? I ignored my doc and ate oats, yes they were gluten free, but some brands are at the higher end of gluten free. Lots of celics can eat Bob's Red Mill gluten-free oats, but not me. I can now eat them, but they have to be grown and processed according to the "purity protocol" methods. I mail order them, Montana Gluten-Free brand. A food and symptoms and activities log can be helpful in tracking down issues. You might be totally aware, but I have to mention about the risk of airborne gluten. As the doc that diagnosed me warned . . Remember eyes, ears, nose, and mouth all lead to your stomach and intestines.  Are you getting any cross contamination? Airborne gluten? Any pets eating gluten (they eat it, lick themselves, you pet them...)? Any house remodeling? We live in an older home, always fixing something. I've gotten glutened from the dust from cutting into plaster walls, possibly also plywood (glues). The suggestions by many here on vitamin supplements also really helped me. I had some lingering allergies and asthma, which are now 99% gone. I was taking Albuterol inhaler every hour just to breathe, but thiamine in form of benfotiamine kicked that down to 1-2 times a day within a few days of starting it. Also, since cutting out inflammatory seed oils (canola, sunflower, grapeseed, etc) and cooking with real olive oil, avocado oil, ghee, and coconut oil, I have noticed even greater improvement overall and haven't used the inhaler in months! It takes time to weed out everything in your life that contains gluten, and it takes awhile to heal and rebuild your health. At first it's mentally exhausting, overwhelming, even obsessive, but it gets better and second nature.
    • Jsingh
      Hi,  I care for my seven year old daughter with Celiac. After watching her for months, I have figured out that she has problem with two kinds of fats- animal fat and cooking oils. It basically makes her intestine sore enough that she feels spasms when she is upset. It only happens on days when she has eaten more fat than her usual every day diet. (Her usual diet has chia seeds, flaxseeds, and avocado/ pumpkin seeds for fat and an occasional chicken breast.) I stopped using cooking oils last year, and when I reintroduced eggs and dairy, both of which I had held off for a few months thinking it was an issue of the protein like some Celiac patients habe mentioned to be the case, she has reacted in the same fashion as she does with excess fats. So now I wonder if her reaction to dairy and eggs is not really because of protein but fat.   I don't really have a question, just wondering if anyone finds this familiar and if it gets better with time.  Thank you. 
    • Chanda Richard
      Hello, My name is Chanda and you are not the only one that gose through the same things. I have found that what's easiest for me is finding a few meals each week that last. I have such severe reactions to gluten that it shuts my entire body down. I struggle everyday with i can't eat enough it feels like, when I eat more I lose more weight. Make sure that you look at medication, vitamins and shampoo and conditioner also. They have different things that are less expensive at Walmart. 
    • petitojou
      Thank you so much! I saw some tips around the forum to make a food diary and now that I know that the community also struggles with corn, egg and soy, the puzzle pieces came together! Just yesterday I tried eating eggs and yes, he’s guilty and charged. Those there are my 3 combo nausea troublemakers. I’m going to adjust my diet ☺️ Also thank you for the information about MCAS! I’m from South America and little it’s talked about it in here. It’s honestly such a game changer now for treatment and recovery. I know I’m free from SIBO and Candida since I’ve been tested for it, but I’m still going to make a endoscopy to test for H. Pylori and Eosinophilic esophagitis (EoE). Thank you again!! Have a blessed weekend 🤍
    • knitty kitty
      Yes, I, too, have osteoporosis from years of malabsorption, too.  Thiamine and magnesium are what keep the calcium in place in the bones.  If one is low in magnesium, boron, selenium, zinc, copper, and other trace minerals, ones bone heath can suffer.  We need more than just calcium and Vitamin D for strong bones.  Riboflavin B 2, Folate B 9 and Pyridoxine B 6 also contribute to bone formation and strength.   Have you had your thyroid checked?  The thyroid is important to bone health as well.  The thyroid uses lots of thiamine, so a poorly functioning thyroid will affect bone heath.  
×
×
  • 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.