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

Optimistic Pessimism


pbsml

Recommended Posts

pbsml Newbie

gluten-free since the 3rd of July now... and still trying to debate whether or not I am feeling better. I understand that it has only been 2.5 weeks, but what I find odd is that within 2 days, my stomach was feeling considerably better, and then, after 5 days, it has gone back to where it was.

My tingling fingers and sweaty feet are nearly back to normal (or at least noticeably better, to the point of me being able to play guitar again :rolleyes: ), but there are just some symptoms that won't go away for good and keep surprising me at random times on random days.

This leads me to my questions for you all, if you can please help. Starting off, chest pains (sternum, ribs, and what seemed like heart problems) were my biggest issues, concerns. After getting that ruled out, and finding this unbearable intolerance to gluten, I felt more relaxed about how sick I was becoming, daily. At least I knew what it was, right?

Well, that being said, I've been uber-conscious about what I eat, and DON'T eat moreover. Weirdly, I seem to be falling back into the same state I was in pre-diagnosis.

I keep scaring the crap out of myself by feeling bad, resorting to thoughts that it could in fact be something worse and I'm starting to lose confidence that I have indeed found the answer.

Has anyone been here before? Felt better right away, and then started getting back into the original slump of it all? Could I be on the right track? Checking meds, all foods, liquid or solid....

My eyes simply won't stop burning, my chest unrelentingly won't stop giving me sharp pains, and sadly (mostly for my girlfriend), my stomach won't stop waking me up very early AM every day for the reason we all know...

I don't wish that anyone here can relate to what I keep feeling, however; I am sure that someone can and am hoping that I can be persuaded back into the optimistic climb I felt myself in a couple of weeks back.

Last, but certainly not least... if I were to get 'all glutened up' by accident, how long does it take from one meal with it for your body to recover again? Is it not as soon as your body has rid itself of the food?

Thanks for reading, and hopefully telling me that I'm not losing my mind!

sean


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



Celiac.com Sponsor (A8-M):



conniebky Collaborator

If you look around on this board you'll see the exact same post from me and a few others. My first few days of gluten-free were wonderful. I ate no gluten, and started to feel bad again, so I said, "ok, everyone's fulla beans and it's not gluten".....I've been going back and forth like this for, well, I;m not gonna tell you for how long.

I too, used to get this strange bad pain in my chest, almost like I'd pulled a muscle. I've had my heart checked out, and now it only happens when I eat gluten. And my eyes burn on fire still.

Anyone on this board will tell you what you are going through is VERY normal. When I went gluten free, I couldn't sleep or anything, just stay on the road you're on.

Keep on with the gluten-free. Also, I found out later, that your body gets pissed and wants its gluten, and that causes symptoms and problems, too. Hang tough, and I mean hang REALLY tough, cuz it is NOT easy or easily understood. Just hang tough.

T.H. Community Regular

We will all be definitely telling you that you haven't lost your mind! :)

1) You could be getting more sensitive to gluten. A lot of celiacs seem to get more sensitive to gluten once they go off of it, so small sources of gluten that wouldn't bother you at first may begin to give you a reaction the longer you go 'gluten free.' Also, are you checking for gluten ingredients, or looking for foods that list themselves as gluten free? Many foods that don't contain gluten ingredients can still have gluten. Like, say, if they are run on a machine that sometimes processes gluten foods, residue can be left behind and contaminate all your non-gluten food. For some people, this doesn't seem to bother them much, but many of us have problems with it. You generally have to call the company or sometimes google other celiac's posts to find out what's safe.

Ways you could be getting low levels of gluten:

1. Any of your gluten-free products, as to be gluten-free they need to be less than 20 ppm of gluten, but not zero ppm. Some of us celiacs can be sensitive enough to react to less than this. You may need to ask if any of the meds, foods, etc... you are eating are gluten free AND do they have anything that is derived from wheat, barley, or rye. I'm sensitive enough I have to avoid anything that is derived from wheat, because I still react to many of them, even if they test as gluten free. Also, if you are very sensitive? Anything wood or plastic, or teflon if it's been scratched, or cast iron if it's still seasoned, can have gluten that is being released back into your food.

2. Non-food items. Many construction products have gluten, like dry wall, so if you inhale the dust, you can get glutened as you'll swallow some of that. Tea bags sometimes get sealed with starch (can be gluten). Liptstick, makeup, or chapstick, even if it's from someone you kiss, can give ya gluten. Same with lotions or anything on the skin, if it gets in your mouth. Cat litter dust that you might inhale, shampoo if any gets in your mouth when you rinse your hair, toothpaste or mouthwash, and so on. Anything that gets in your mouth or even on your lips, essentially.

Another possibility is that you might have other food allergies. Many of us have other food issues that our celiac disease masked, and I know for myself, they don't show up as hives or itching, but somewhat similar to symptoms like getting glutened. Mine showed up about day 2 after going gluten free. I mention this partly because one of my symptoms from other food issues has been heart pain. It turned out to be this condition: Open Original Shared Link

This is something that doesn't involve the heart, although the symptoms all seem to be the heart itself. It's actually caused by inflammation of where the ribs connect to the sternum, and it goes away once the inflammation does - takes a few weeks to totally heal up. I was admitted to the ER with a possible heart attack because of the symptoms, and they couldn't figure out what it was until I lucked out and found a doc who knew of this condition and was familiar with celiac disease. I have since met many other sufferers of allergies who developed this when their systems got inflamed after eating something their body reacted to. I imagine both gluten and allergens could inflame things, however.

Oh, as for recovery time? Afraid it's longer than it takes to get rid of the food from your body. Your body gets damaged, so it needs to heal. It can take a few days at the least, or up to 2 weeks, depending on your body and how much gluten there was. Also, you will be immuno-compromised until your body calms down, which I believe takes a few days at least, as well.

It's hard at first to figure it all out, but it'll start to make sense eventually. :-)

sa1937 Community Regular

gluten-free since the 3rd of July now... and still trying to debate whether or not I am feeling better. I understand that it has only been 2.5 weeks, but what I find odd is that within 2 days, my stomach was feeling considerably better, and then, after 5 days, it has gone back to where it was.

Has anyone been here before? Felt better right away, and then started getting back into the original slump of it all? Could I be on the right track? Checking meds, all foods, liquid or solid....

Thanks for reading, and hopefully telling me that I'm not losing my mind!

sean

Sean, if you're losing your mind, so am I. ph34r.gif I felt amazingly well within 3 days of going gluten free and then after a few more days, my symptoms started again. I've now been gluten free for slightly over 4 months. For me that means daily D. I've checked everything, including meds, replaced a bunch of kitchen stuff (including buying a new toaster), cleaned out my pantry, etc. and I can't put a figure on what my problem is. It's very frustrating.

I have a Dr. appt. this afternoon and will find out the results of some blood tests and a RAST test checking for basic food intolerances. No clue what will become of that but feel I'll probably have more questions than answers, which will probably lead to more testing. At least it's a starting point. This disease is a total pain in the a$$!

pbsml Newbie

Thank you all for writing...

I'm curious as to whether or not I might be suffering from asthma at the same time as going through this new gluten-free lifestyle. I left for a week vacation on the 4th of July and that is certainly when I was feeling the best. In a way, that makes me wonder if there might be something in my own place that makes my symptoms worse. I have no doubt that being gluten-free is better for me. As I said before, i did notice improvements quite quickly, and right when I was getting back, everything seemed to get a little worse again. Slowly, but surely, I find myself near my original state before I went gluten-free.

Given how long this can take certain individuals to heal makes me want to stay gluten-free forever, but just like everyone else, I only want to feel better.

I have made an allergy/asthma testing appointment for tomorrow, so I'll have to see what comes from that.

I might just need to be more diligent when cleaning my house. I've read elsewhere that where you live can affect your symptoms differently too... whether that be due to humidity, average temperature, and even general food available in your area. I assume this would most affect asthma symptoms, or allergy induced asthma anyway, but it's worth me looking into at least. After all, I live in Southern Florida, and at this time of year, it's more humid than most places in the country. I'm originally from Canada, and have lived up north the in the US too and before moving this far south (5 years ago), I never experienced any of these signs.

Sa1937... I'm curious to know what you find out yourself from your testing. I myself have had a lactose intolerance for the past 10 years, and oddly enough, that progressed into a full-blown dairy allergy over the years. I don't know if that's just because my body got used to living dairy-free and then didn't know what to do when i ingested lactose free dairy products, but it certainly was a start to inhibiting my food intake. I always though that was a pain until a few weeks ago when going gluten-free. That's a tough combo when going out to restaurants. Here, in West Palm Beach, I'm finding that if I go to a restaurant, most servers look at me like I have two heads when I question whether or not a dish has dairy or gluten in it. You're spot on. It's a gigantic pain in the a$$.

Thank goodness for this site. I was thinking last night that it would be cool if there were local groups for people with our restrictions to just get together and party on. How accommodating would that be??? I'm 30 years old now and plan on living til 100, so I just hope I'm not too late finding all of this out to get there.

Preach on my fellow gluten-free preachers!

conniebky Collaborator

What is a RAST test? Is this different than the skin scratch tests?

sa1937 Community Regular

What is a RAST test? Is this different than the skin scratch tests?

Connie, It's a blood test rather than a scratch test. No clue whether it's any good or not.

Anyone else on this forum have any input on this type of testing??? I know there was a thread about food allergy testing but, alas, my other computer crashed about a week ago and is now in for replacement of the hard drive...


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



Celiac.com Sponsor (A8-M):



pbsml Newbie

good ol' wikipedia...

Open Original Shared Link

conniebky Collaborator

good ol' wikipedia...

Open Original Shared Link

thank you all. I read the link. I'm going to sign up!

rdunbar Explorer

just be patient and stick with it. I've had a little tingling in my right arm and shoulder the last few days, and this is after @ 4 months gluten-free; still it's not nearly as bad as it used to be, I was'nt able to ride my bike before.

I figure i must have gotten some cross-contamination or something.

I have Dermititas Herpetiformis on my scalp, and it's been getting better, but I understand that it can take up to TWO YEARS to go away if you can manage to be gluten free; at least you're not in that boat! and it's like torture, too!

going gluten free is not like waving a magic wand, but you are getting results, and you will continue to get results if you keep on it,

There are antibodies in your system, and they will slowly go away, and your body will stop producing them in the absense of gluten/(casien), and you will heal up, just be patient!

julandjo Explorer

This leads me to my questions for you all, if you can please help. Starting off, chest pains (sternum, ribs, and what seemed like heart problems) were my biggest issues, concerns. After getting that ruled out, and finding this unbearable intolerance to gluten, I felt more relaxed about how sick I was becoming, daily. At least I knew what it was, right?

Well, that being said, I've been uber-conscious about what I eat, and DON'T eat moreover. Weirdly, I seem to be falling back into the same state I was in pre-diagnosis.

I keep scaring the crap out of myself by feeling bad, resorting to thoughts that it could in fact be something worse and I'm starting to lose confidence that I have indeed found the answer.

Has anyone been here before? Felt better right away, and then started getting back into the original slump of it all? Could I be on the right track? Checking meds, all foods, liquid or solid....

My eyes simply won't stop burning, my chest unrelentingly won't stop giving me sharp pains, and sadly (mostly for my girlfriend), my stomach won't stop waking me up very early AM every day for the reason we all know...

Boy am I glad to have read this! I've been having SO much chest pain, and have visited the ER, my regular doctor, and most recently a cardiologist. I'm 31, and I was absolutely convinced I have a narrowed artery or other cardiac issues. The pain is often a dull pain radiating across my left chest and shoulder, down my left arm. At times it's very sharp and feels like a pin is being pushed into my heart. I very easily get myself all worked up over this pain, which only makes things worse. I was cleared by the cardiologist last week, which has put me at ease.

I've also been having strange shooting pains in my head and had a whole week of numbness and tingling in my right hand and foot. My doctor was suspicious of MS, so I had an MRI of my head last week too. Thankfully, it's all clear!

So yeah. I feel you. I've been scaring the crap out of myself on almost a daily basis. My body is doing things that make no sense and that mimic some really serious, scary things, ya know? Every doctor I've seen, even my GI, pooh-poohs my suggestion that this could be celiac-related. But I was at a celiac support group meeting last night and they gave me a handout about magnesium deficiency. Have you read much on this? Holy man do us celiacs need to know this stuff! Look into it and see if it doesn't match up with a lot of what you're experiencing. I called my GI doctor and said I want to be tested for this... we'll see what happens. Apparently it's much more involved than a simple blood test.

Anyway, just wanted to tell you you're not at all alone, and offer the magnesium info!

sa1937 Community Regular

Sa1937... I'm curious to know what you find out yourself from your testing. I myself have had a lactose intolerance for the past 10 years, and oddly enough, that progressed into a full-blown dairy allergy over the years. I don't know if that's just because my body got used to living dairy-free and then didn't know what to do when i ingested lactose free dairy products, but it certainly was a start to inhibiting my food intake. I always though that was a pain until a few weeks ago when going gluten-free. That's a tough combo when going out to restaurants. Here, in West Palm Beach, I'm finding that if I go to a restaurant, most servers look at me like I have two heads when I question whether or not a dish has dairy or gluten in it. You're spot on. It's a gigantic pain in the a$$.

Well, that was a complete waste of Medicare dollars! The RAST test I had was for the basic foods (milk, wheat, eggs, shellfish, peanuts, etc.) and everything came back negative. Obviously it was not the right test, if there is such a thing, as it was for IgE allergies. I already know I have celiac as I was diagnosed with a positive celiac blood panel followed on April 9 by an EGD/intestinal biopsy (also positive).

I do need to add Vitamin D3 and my Dr. suggested a probiotic, which I bought yesterday afternoon at my local health food store. It's a once-a-day capsule that contains 14 different bacteria and needs to be kept in the fridge. I'm hoping it works! In the meantime I plan to eliminate any prepared foods entirely and shop the outer rim of the grocery store. If that doesn't work, it'll be time to go on an elimination diet to see where that might lead. I'm hoping I don't have to go that route but I don't think I should be having daily D over 4 months into a gluten free diet. That really is my only problem except for a short time after going gluten free and then wham! It came back again as it does for so many of us.

Let us know how you make out on any testing you might have...

rdunbar Explorer

look up fibromyalgia; tingling, pain in tissue, muscles, often effects the body asymetrically, that is on one side or the other.

curiously enough, when I googled it, many sites claimed that there is no known cause. LOL. gluten isn't a known cause??? when will the medical profession ever get it?

and yes, calcium/magnesium, D3(5000iu), and sublingual B12, probiotics, and fish oil for omegas are crucial!

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      129,980
    • Most Online (within 30 mins)
      7,748

    mary lou grolimond olson
    Newest Member
    mary lou grolimond olson
    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

    • Scott Adams
      It sounds like your gastroenterologist is becoming increasingly confident that celiac disease is the likely diagnosis based on both your older and newer lab results. Her suggestion to call each Monday for possible cancellations is actually a great strategy—especially given how long the wait is until your August 29th appointment. It’s also a good sign that she’s advocating for you to be seen sooner, which shows she’s taking your case seriously. The fact that some labs might not have been drawn yet due to overlap with your functional health doctor’s upcoming testing adds a layer of confusion, but that’s unfortunately common when multiple providers are involved. Hopefully, the GI’s remaining labs will still get processed, or she can reorder them if needed. As for the colonoscopy prep, it’s totally understandable that you're dreading it—many people rank it among the least pleasant medical experiences. You’re definitely not alone in preferring the pill prep option over the liquid kind, especially if you don’t drink Gatorade and had a rough experience with Miralax in the past. Hopefully, your doctor will approve the pill form, especially since you’ve tolerated other options poorly before. Fortunately, the upper endoscopy doesn’t require any bowel prep—just fasting, usually starting the night before—so that part should be easier to handle. It’s great that you’re already trying to boost your gluten intake, but yes, tracking gluten content can be surprisingly tricky. You’re right that the general rule for wheat-based products is to multiply the protein content by about 0.75 to estimate the gluten content. That means foods like oyster crackers, while convenient, may not pack enough gluten to help reach the recommended daily goal of around 10 grams before biopsy. It’s helpful that you caught that early, and switching to more gluten-dense foods like regular wheat bread, pasta, or wheat cereals might make it easier to hit your target. It’s not easy eating more gluten when you’re trying to manage symptoms or just not used to it, but doing so can make a big difference in ensuring your biopsies are accurate. You’re on the right track—hopefully with a little luck, you’ll get a cancellation and be seen sooner.
    • cristiana
      Thanks for sharing that film, @trents.  I am not sure how I missed that film as I see it is a few years old, but it is very good.  I think you should be fine if you take your own packed lunch and eat it from your own lunchbox etc.  Might be worth doing a lunchtime recce to see how cramped the room is before making a decision - for all you know, there may be other people  there who don't eat gluten?
    • cameo674
      The GI doc messaged me this afternoon that she believes that the new blood work added to the old is definitely  looking like a celiac diagnosis is in my future.  She wants to me to call into scheduling each Monday to see if I can get my August 29th appointment moved up due to cancellations.  I have never had a doctor recommend that.  She also said there were additional labs that she requested still out that have not come back yet; so, they may have been missed drawing those since the functional health doctor has a whole slew of labs that I am suppose to be waiting until August 27th to do. I am still waiting to hear on whether or not she will allow me to do pill prep versus the typical gatorade prep that I did 8 years ago for that colonoscopy.  I do not drink gatorade to begin with and that miralax prep kept me in the bathroom up until we drove to the procedure.  My younger brother said the pill form was fairly easy when the liquid form is hard to swallow. Colonoscopy prep is definitely close to number one on the list of things I never want to experience again if I could avoid it.  Number one is a different medication that caused severe cramping that had me in tears until it wore off.  Never having had an endoscopy, I have no idea of what that prep is like, but it cannot be worse right? I started munching on oyster crackers last night.  It is shocking how filling they are.  I just read that I need to pay attention to the protein content of the wheat bread product or I will miss the gluten goal of 10 g per day prior to testing.  The post said that I should look at the protein and multiple that number by .75 if it is a wheat flour product to see how much gluten is in it.  No more oyster crackers for me.  I would have to eat 10 oz bag everyday to meet my goal.  not going to happen.
    • Alibu
      Well, I've made if from the pre-diagnosis forum to here!  I've been diagnosed with "latent" or "potential" celiac and my doctor has suggested me to go gluten-free before my appointment with him in October (first available, LOL).  My ttg-iga was 152, my EMA was positive, I have the gene, but my biopsy was negative (and he took 12 samples), so it makes sense to go gluten free to see if I improve. I know the basics - I can find lists of things to avoid, I know about hidden dangers, etc. all of that.  Where I'm struggling is just STARTING.  I need to go shopping and stock up on some staples.  My goal is to not try to find gluten-free alternatives, but to focus on naturally gluten-free foods like proteins, veggies, fruits, and carbs like potatoes and rice.  However, the rest of the household will not be gluten-free, which is fine, I don't want them to for various reasons.  But I have SO much food in my house in the pantry and fridge and cabinets, and it feels like I need to get rid of a lot in order for me to start fresh, but at the same time, I can't get rid of everything. I guess it's just feeling overwhelming and I've never given up gluten before so this is going to be a huge shift for me and I feel like I need SPACE, but I can't quite have that. Any advice on just getting started and organizing myself would be great!  
    • Scott Adams
      It’s great that you were finally able to see a gastroenterologist—and even luckier to get in the same day as your referral! It sounds like your GI is taking a very thorough approach, which is reassuring given your complex symptoms and history. The confusion around your different tissue transglutaminase (tTG) antibody results is understandable. The variation between your December and June labs may be due to multiple factors, including differences in the lab performing the test (Quest vs. Mayo Clinic), the specific assay used, and the amount of gluten you had been consuming before each test. Antibody levels can drop significantly when gluten is reduced or eliminated from the diet, even partially, which might explain why your recent tTG IgA was now negative and your tTG IgG was borderline high. That’s likely why your GI mentioned it was “usually the reverse”—typically, tTG IgA is more commonly elevated in confirmed celiac, not IgG alone, especially when IgA levels are sufficient, as yours are. Your gene testing confirms that you carry HLA types (DQ2.2 most likely) that are permissive for celiac disease, meaning you can develop it, but not everyone with these genes will. These genes don’t explain why your symptoms are milder or different from others with celiac—many people have so-called "silent" or atypical presentations like yours, with issues like long-term heartburn, loose stools, nutrient intolerances, or just gradually adapting to symptoms over time. It’s not uncommon to assume these symptoms are just aging, medication side effects, or lifestyle-related until someone finally connects the dots. It’s a good thing your daughter advocated for you to be tested—many cases are missed for years because they don’t follow the “textbook” presentation. As for the immunoglobulin tests, your doctor likely ordered those to ensure your immune system is functioning normally, particularly your IgA level, since a deficiency can cause false-negative celiac blood tests. Since your IgA level is normal, your tTG IgA test should be reliable (assuming adequate gluten intake), but again, if you weren't eating enough gluten, that could explain the lower antibody levels now. The comprehensive metabolic panel and negative stool parasite results are additional pieces ruling out other causes of your symptoms, like infections or organ dysfunction. The upcoming endoscopy and colonoscopy should provide more definitive answers, especially with biopsies looking for celiac disease, eosinophilic esophagitis, and microscopic colitis. It’s completely valid to feel unsure about what you’re experiencing, especially when your symptoms have been lifelong or gradually worsening without being severe. You’re not alone—many adults with celiac or gluten-related disorders report subtle or chronic symptoms they’ve normalized. You’re doing the right thing by staying on gluten now through your procedure date in August. Try not to stress about reaching the full 6-slice equivalent each day, but do increase your gluten intake as much as tolerable (e.g., a couple of pieces of bread, pasta, crackers, etc.) to give the biopsy the best chance of detecting any damage. Good luck with your upcoming procedures—you’re closer than ever to answers and a clearer direction forward.
×
×
  • Create New...