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

A Year In And Still Confused - Please Help


nomorepies

Recommended Posts

nomorepies Newbie

Hi everyone,

 

I have come here to post out of sheer frustration with the lack of improvement in my condition, and I have rarely been able to find anyone with a story like mine (though I perhaps have been looking too hard).

 

A bit of backstory:

 

  • Male, 183cm (6 foot) 70kg (155lbs) 24 years old
  • Glandular fever age 22. Severe fatigue followed, never fully dissipated
  • Age 23 - severe fatigue, depression. Over 10+ trips to the doctor before being referred to a specialist. I had some irregular bowel movements - mostly uncomfortable while passing stools, they were often very thin and unsatisfying (if that makes sense) to get out of my system. But probably only one instance of diarrhea, no instances of constipation. 
  • Only trigger was that a blood test indicated I had low ferritin stores (iron) and facial dermatitis
  • Diagnosed with Celiac via anti tTG blood test. Specialist informed me of 90%+ certainty of diagnoses, especially considering the other symptoms and low iron in a young male
  • Age 24 - symptoms of fatigue had not been releived. Went to a gastroenterologist.
  • Colonoscopy revealed certain Celiac diagnosis. Complete villous atrophy - i.e. as bad as it can get.
  • I had been gluten free for the large part of 9 months by this point and expected some improvement

 

It has been another couple of months since that doctors visit now. I still feel terrible on a daily basis. I used to be a sharp, intelligent person and I feel as though I have had years of my life stolen from me by this condition. I am just coming to you guys to get some further information or to see if anyone has experienced anything similar.

 

I have been gluten free, to the best of my ability, for 12 months now. I did consciously lapse for a 2 week period when I was in Japan travelling, simply because I just thought it was too hard to figure out what did and what did not have gluten in it, so I just decided to take a holiday as it were. This had pretty disastrous results, again uncomfortable bowel movements but just thinner than usual and more unsatisfying, and also facial dermatitis and fatigue worsened. Colonoscopy was probably 3 months after this trip.

The only thing I can think of that would affect me would be eating out and having things like corn tacos prepared on the same surface as flour ones, getting toast that has been in the same toaster as non-gluten-free toast, etc. I have only one toaster at home because I figured that 1-2 bread crumbs wouldn't make a huge difference - though I might be wrong.

The thing I am finding extremely hard to do is determine when I have had gluten. I don't know how I am going wrong here because my predominant symptom is fatigue, and I don't have any immediate discomfort. Don't get me wrong, my bowel movements are very rarely 'normal', but they seem to be just 'kinda bad' every day, and on the days in japan I did have beer and ramen etc, they were 'pretty bad'. I wasn't like immediately sick.

I just don't know what else to cut out. Am I doing something wrong? Do I need to buy my own toaster, eat in for all meals for a couple of months and hunker down? Or do I need to go on a low FODMAPS diet and give that a try in case I just have IBD as well? I have lost 3 years of my youth to this brain fog and fatigue, and I am at the point of losing career momentum because I cannot function at full capacity.

I hope that someone will be able to help as I am just overwhelmed at the moment. 

 

Thank you for reading this - if you want further info I am happy to provide. 


 


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



Celiac.com Sponsor (A8-M):



kareng Grand Master

It doesn't sound like you have really been gluten free.  I think maybe you should give a strict gluten free diet a chance for a few months.  That means no shared toasters or jams or PB or other condiment jars.  Stop eating out for a few months.  Maybe read the Neebie thread to see what else you may have missed.

 

https://www.celiac.com/forums/topic/91878-newbie-info-101/

frieze Community Regular

yup, it would appear you haven't been gluten free.  no eating out, no shared common food containers etc.  yes a few bread crumbs, esp. on top of other exposure, can be enough to be  a problem.  good luck.

MycasMommy Enthusiast

I concur, even when you thought you were being gluten free, it seems you probably were not. One of the best things you can do is follow the directions to the letter of getting gluten out of your kitchen (from pans to cutting boards to toasters)  I know there are some great "how to" links out there for that. 2nd read EVERY label. not just that but learn all the different forms and other names of wheat/barley/rye products so you can identify them.  For the longest time I did not realize why I was getting so ill from SOY SAUCE!!!  3rd... sad as it is.. do not eat out. DO NOT DO IT.  When you get these things under control, you SHOULD begin to feel better. But you cannot mess up, you cannot take a cavation, you cannot say "oh just for today" and it will take up to a year or even more to get better, Especially since your damage is so severe. This is a hard learning curve, but once you finally master it, it actually becomes easy and second hand nature. so it will be hard at first and you will think "how can I do this the rest of my life?"  but I promise it will get so much easy with a bit of practice. Just breathe, and start again.  You can do this and you will be so happy you did.

nvsmom Community Regular

I agree. It could be those crumbs that are keeping you feeling poorly.

 

A year ago, I accidentally bought my kids some frozen french fries that had some wheat flour on them (in the spices I assume).  I was clueless and ate a few (2-4) every few days when we had them.  I slowly started to feel not right, not horrible like I would if I drank a beer or ate bread, but not well.  I grew tired, got headaches, had minor stomach aches and such. 

 

I mention this story to show how less than a crumb can impact a celiac's health.  I was eating wheat on 3 fries once a week and it impacted me.  Crumbs from the toaster, shared butter or jam, or in the utensil drawaer may be making you sick.  Recheck stuff like soy sauce; shampoos, soaps and toothpaste (if it can get in your mouth); barbque sauces and even the barbque grill could have gluten stuck to it.  Being extremely strict will pay off when you start feeling better.

 

You also might want to have labs run.  Redo the celiac tests to make sure your numbers are coming down.  Check you nutrient levels. Celiacs often are low in B12, A, D, K, Fe, Mg, Ca, ferritin,, Cu, and zinc.  Make sure you aren't anemic - a very common celiac symptom, and one that is slow to change.  You may also want to check your thyroid; hypothyroidism can caus many celiac disease like symptoms.  Check your TSH (should be near a 1), free T4 and free T3 (should be in the 50-75% range of the lab's normal reference range), and TPO Ab.

 

Keeping a food and symptom journal can help you find other food sensitivities or missed gluten.  Just remember that symptoms can appear within minutes to a couple of days later.

 

Good luck.  I hope you feel better soon.

RMJ Mentor

You could ask to have your anti tTG blood test repeated. If still positive, it is likely you are still eating enough gluten to cause your symptoms (and I agree with the others, based on your description of what you eat it sounds like you are getting gluten contamination). If negative, you might need to look for another cause.

I have not eaten foods with gluten-containing ingredients for over 2 years and my blood tests are better but still aren't all normal. I don't have GI symptoms so It is hard to know exactly where the gluten contamination is coming from in my shared kitchen. I must be reacting to basically "invisible" amounts.

notme Experienced

many celiacs have a delayed reaction to gluten exposure, so the fact that your symptoms didn't appear until later is common.  i don't have a full-on reaction until 24-48 hours after i've had gluten introduced to my body.  don't forget:  this is a systemic disease, as in that it will cause a full body reaction and mess up everything with inflammation.  i don't know how long your symptoms last (i bet you don't either, because you haven't been doing this properly) but it takes 14 days to clear my system up to where i am back to 'normal' and feeling better.  read the newbie thread.  there is alot more to this diet than eating off the gluten free menu.  it's hard, but it will get easier.  and you will feel so much better!!  stop fooling with it and own it.  you can and you must :)  


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



Celiac.com Sponsor (A8-M):



sunny2012 Rookie

I agree that you are not 100% gluten free. Tiny bits can make us sick.

 

I was getting sick from walking in to purchase coffee in a famous doughnut chain. Then I realized breathing in the micronized flour floating in the air of an environment where so much flour is mixed might be causing it. Now a fellow worker goes in to collect the coffee.

ezgoindude Explorer

Another dude in the house, sup mang!

 

Not like I'd wanna curse you or anything, but being a guy with a gut problem my friends think I'm a wuss, IF THEY ONLY KNEW, ha.

 

Anyways, I know it's not the answer you're gonna wanna hear, but maybe your answer is all of the above?

 

I'm not confirmed with celiac but inflammation and food intolerance is present, but i'll tell ya, I borrowed my buddies blender to make my smoothies once and three days later I was stuck in the toliet all night.  My friends dietary supplements are loaded with dairy and gluten, both to my stomach is a big no.

 

In fact I'm currently in an extreme elimination diet of my own,  I'm barely holding steady in terms of health and thats AFTER cutting out dairy,soy,gluten, all grains (rice,corn,etc) and all legumes.  My current battle may be from too much fat intake.  I've been a university lab rat for almost 2 years now, and they've barely scratched the surface on how to direct my recovery process.

 

The only thing I could say for right now is to not make any rash decisions from your doctors in terms of getting you on over the counter perscriptions.  Like everyone else is saying, its gonna be a huge pain in the @$$ but I would try REALLY hard in watching what you eat and where it comes from, etc.  oh yeah and low fodmap has helped me a little, especially making sure food is cooked vs. raw seems to make a noticeable difference.

nomorepies Newbie

Thank you all - so good to get so many responses. I will definitely get stricter and it's good to know other people have delayed reactions etc. I will post back once I've had another month or two and hopefully things are better.

 

Thanks so much, means a lot

athomp34 Newbie

I agree with the others that the biggest reason you aren't feeling better is because it sounds like you are not really eating gluten-free. I was shocked at how sensitive I am. It's definitely an adjustment but it does become second nature eventually. 

I also wanted to add that taking a mulit-vitamin made a difference for me in terms of fatigue (I've been gluten-free/DF for 2 years now but still had fatigue until about 6 months ago when I started the vitamins). Finding a good gluten-free one can be tricky but is well worth the effort in my personal experience. With all the damage and malabsorption that celiac causes it makes sense that our bodies need a little extra help-especially if you are newly diagnosed.

Bobbie Jo Rookie

I'm just sorry for all of your pain. I have a gluten-free son to feed and I worry about him being on his own in a few years. It's not easy!

He fills up with lots of gluten free oats with milk every day!!! I know- not THE best, but he gets so hungry and wants something quick.

Praying for you. You can get through this.

Bobbie Jo Rookie

BTW, for your pie cravings, crumble up a bag of any gluten free cookies real good. Mix them up with a couple tablespoons of melted butter and put it in the bottom of a pie plate. Save a little of it for a topping. Put in your favorite filling if you don't mind the canned or boxed kind, then add the remaining crumbles... Maybe add whipped cream on top.

w8in4dave Community Regular

I have 0 energy , The Dr. took blood to look for D levels, Iron levels and Folic acid levels. My folic Acid was low. I have to say after taking Folic acid for a few days I felt so much better. Not as good as I could feel but , better than I felt before. You know they have sleeves you can get for your bread in the toaster. I would seriously tighten up your diet.  You know deep down thats probably the answer to your problems. 

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,917
    • Most Online (within 30 mins)
      7,748

    tiffanygosci
    Newest Member
    tiffanygosci
    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

    • tiffanygosci
      Hi! I had my first episode of AFib last May when I was 30 (I have had some heart stuff my whole life but nothing this extreme). I was not diagnosed with celiac until the beginning of this month in October of 2025. I was in the early stages of celiac, so I'm not sure if they were related (maybe!) All of my heart tests came back normal except for my electrolytes (potassium and magnesium) that were low when the AFib occurred. I also became pregnant with our third and last baby a couple weeks after I came back from that hospital stay. I had no heart complications after that whole thing. And I still haven't over a year later. It was definitely scary and I hope it doesn't happen again. I drink an electrolyte drink mix about every day, and I'm sure being on a gluten-free diet will help my body even more! I will pray for you in this. Taking care of our bodies is so challenging but Jesus is with us every step of the way. He cares and He sees you!
    • knitty kitty
      I followed the Autoimmune Protocol Diet which is really strict for a while, but later other foods can be added back into your diet.  Following the AIP diet strictly allows you digestive system to heal and the inflammation to calm down.  Sort of like feeding a sick baby easy to digest food instead of spicy pizza.   It's important to get the inflammation down because chronic inflammation leads to other health problems.  Histamine is released as part of the autoimmune response to gluten.  High histamine levels make you feel bad and can cause breathing problems (worsening asthma), cardiovascular problems (tachycardia), and other autoimmune diseases (Hashimoto's thyroiditis, diabetes) and even mental health problems. Following the low histamine version of the AIP diet allows the body to clear the histamine from our bodies.  Some foods are high in histamine.  Avoiding these makes it easier for our bodies to clear the histamine released after a gluten exposure.   Vitamin D helps regulate the immune system and calm it down.  Vitamin D is frequently low in Celiacs.  The B Complex vitamins and Vitamin C are needed to clear histamine.   Supplementing with essential vitamins and minerals boosts your intestines' ability to absorb them while healing.   Keep in mind that gluten-free facsimile foods, like gluten-free bread, are not enriched with added vitamins like their gluten containing counterparts are.   They are empty calories, no nutritional value, which use up your B vitamins in order to turn the calories into fuel for the body to function.   Talk to your doctor or nutritionist about supplementing while healing.  Take a good B Complex and extra Thiamine in the form Benfotiamine (shown to promote gut health).  Most B Complex vitamins contain thiamine mononitrate which the body cannot utilize.  Meats and liver are good sources of B vitamins.   Dr. Sarah Ballantyne wrote the book, the Paleo Approach.  She's a Celiac herself.  Her book explains a lot.   I'm so glad you're feeling better and finding your balance!
    • klmgarland
      So I should not eat my gluten free bread?  I will try the vitamins.  Thank you all so very much for your ideas and understanding.  I'm feeling better today and have gathered back my composure!
    • knitty kitty
      Some people prefer eating gluten before bed, then sleeping through the worst symptoms at night.  You might want to try that and see if that makes any difference.   Several slices of toast for breakfast sounds okay.  Just try to work up to the Ten grams of gluten.  Cookies might only have a half of a gram of gluten.  The weight of the whole cookie is not the same as the amount of gluten in it.  So do try to eat bread things with big bubbles, like cinnamon rolls.   Yeah, I'm familiar with the "death warmed over" feeling.  I hope you get the genetic test results quickly.  I despise how we have to make ourselves sick to get a diagnosis.  Hang in there, sweetie, the tribe is supporting you.  
    • Clear2me
      Thank you, a little expensive but glad to have this source. 
×
×
  • 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.