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

Somebody Stop Me...


RideAllWays

Recommended Posts

RideAllWays Enthusiast

I really want to eat a gluten product. I have been doubting my diagnosis for a while..and I can never tell if when I am sick it is because of gluten or not. I keep a food diary and eat pretty basic foods, and I can never track a reaction back to anything that should bother me. I live in a gluten free house. I rarely eat out, and only at one place that has a gluten free menu and is very careful about CC.

So I've been contemplating for the last couple months eating a McChicken (I don't know why, i never used to eat McDs before but now I just crave one so bad)

I just want to see what happens..if there is no reaction then I don't know what I would do...I don't think I could go through a gluten challenge and do another endoscopy...And I want to feel a REAL glutening so that I know what my symptoms actually are..do you think it is worth it?


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



Celiac.com Sponsor (A8-M):



missy'smom Collaborator

Maybe testing for food allergies and intolerances would give you some direction if you haven't already done it. It was very helpful for me. I had done a little previously but it didn't help so I found someone new who I could be on the same page with and got re-tested and wow, it was eye opening. I had SUCH a noticable change when I eliminated ALL the things that I tested positive to.

Find another way to direct your emotions and frustration-head out the door and take a walk every time you feel like caving. I have kept a bottle of mineral water on the counter and had a drink everytime I feel anxiety, or wanting to reach for something else that I shouldn't-keeps me well hydrated! And that puts my body in better balance then I really do feel better.

Putting poison in our bodies really doesn't solve anything. You know that, we all do. I do too. I know it's hard. Some of us have to work SO hard to maintain such delicate balances in our bodies. I have diabetes and have been coping with various emotions lately by overconsuming carbs and alcohol which both do nasty things to me. Sometimes we need to make the effort to be extra good to ourselves-some non-food treat, something we really enjoy, extra effort with self care tasks-things we've been neglecting, litterally counting our blessings-writing them down or posting them somewhere. It's OK to have a good cry or vent your frustration too.

MagpieWrites Rookie

.do you think it is worth it?

For what it's worth? No. Not really.

But here's why.

At about the 4 month mark - I was sick. Really really sick. (Dying actually. Brown recluse spider bites gone septic, septicemia, SHINGLES, my third set of wisdom teeth had come in... and had been causing a blood infection no one had caught for months. Not a good scene, I think we can all accept that?) And following the gluten-free diet with all that - I just felt miserable ALL the time, so why not just say to heck with it and eat something I WANTED.

Much against my husband desire... I had him take me to Long John Silvers (yeah. I know. Of all the ways to blow off the diet - go to the restaurant that no one over 19 should attempt to eat sober, no one over 25 should eat without a hangover. To this day I can't figure out why I didn't get a slice of good pizza, or some lasagna. Nooooo, I had to go for Uber-crap.) where I ordered 3 chicken planks.

It IS possible to feel even sicker than all the above issues might cause. I ate one and a HALF of the suckers.

Nearly didn't make it to the bathroom (a fun concept in our new Jeep) and spent the next WEEK wishing, rather loudly, to die. With gluten, there is no back button. There is no "Hurry the crappy feeling away" pill. You just get to sit in your own misery for the duration... knowing you did it to yourself. Not fun. On any level. But hey... made me stop thinking about the shingles and the teeth for a day or so. Equally damnable, but different, I suppose.

Maybe you wouldn't have such a bad reaction. Or maybe it would be worse. No way to know... and the dice roll isn't worth it. Let my stupidity be enough of a reason?

And what if the result ISN'T something bad - if you have the diagnosis that you need to go gluten-free... this is a dangerous and slippery slope. How bad is bad enough? You don't actually have to FEEL your villa being destroyed, you know. If you don't wish for death with this time, be honest with yourself - is it going to make it harder to stick to being gluten-free? Is the "Well, just dinner out once in a while won't hurt" or "Ehhh.. one slice of pizza can't be too bad" going to start belling in the back of your brain? Stomach cancer in 10 years isn't worth it. Even just a vague sense of unwellness isn't worth it. I know it's hard... but really. You're gluten free and managing it. Don't toss yourself off the train for this.

(If you really really need fried chicken? marinate some pieces of cut up boneless skinless chicken breast in Italian salad dressing and then mix up equal parts cornstarch and sweet rice flour, along with some garlic powder and seasoning salt. Dip the marinated pieces into the flour mix - for REAL crunchy decadence, double dip. Go back into the italian salad dressing and again into the flour. - Fry until cooked through and crunchy. NOT healthy by any stretch of the imagination - but tastes almost just like KFC's popcorn chicken bites. When I can't resist the siren song of fast food... I make a batch of these.)

Hope this helps.

K8ling Enthusiast

mmm I am making that next. I use chickpea flour and red pepper and italian seasoning and it makes an amazing crunchy batter (we had it last night). My husband is going to wonder whats with all the chicken!

And Magpie is RIGHT there is no back button. There is no rewind or undo...and oh my goodness am I sure you would regret it anyway because come on...it's mcdonalds. Gross.

eva-girl Newbie

ride all ways -

don't take this the wrong way, and i only say it because i think you need to hear it: asking others whether you should eat a mc chicken or asking them to "stop you" from eating something is really infantile. you need to take responsibility for your health, nobody else. you will either choose to eat gluten or you will choose not to - only you can make that decision for yourself, because you are the one who has to live with the consequences. i hope whatever you decide works for you.

RideAllWays Enthusiast

Thanks guys.

I just wanted to know if anybody else out there doubted their diagnosis. Obviously if I had had a for sure "your villi are damaged" diagnosis I wouldn't be considering it. An allergy doctor "diagnosed" me, so I was gluten free for 6 months before my endoscopy. I was more wondering should I try it and see, because if I am going through all this for a disease I don't even have it would be very frustrating.

I'm really good at the diet and have never cheated once in the year I have been at it. It's more the fact that I am SO careful and I still feel like poop half the time that I'm doubting it. So yes, I do crave foods as I'm sure many of you do, and I have thought of trying it to see if I indeed react or not, knowing very well that I might be in Hell for a few days. So maybe I need a kick in the butt, I'm not just saying this for attention or whatever else people might say, I came here for support because I thought maybe some people would be in the same boat. I don't eat dairy or soy, limited corn, and very few processed foods. It is expensive and a hassle, so if I don't need to be doing all this I don't want to.

I'm sick of feeling like crap and not knowing why, sorry for the whining. I appreciate you reading my posts.

ciavyn Contributor

RideAllWays -- you are human. You are allowed to feel weakness. :) May I suggest a different view...

You are eating so much healthier than you would otherwise. I know it stinks, but it is how we probably should be eating 90% of the time. So if that means goofing around with some alternative flour sometimes and having some junk food, I say go for it! But I do understand your frustration. I have a list of foods I will eat if I ever do a gluten challenge...just you wait and see...but I don't look forward to the after effects, because I know how awful I feel when I get it accidentally.

We all feel that way -- I don't think you are lazy or anything else. Hang in there...


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



Celiac.com Sponsor (A8-M):



eva-girl Newbie

ride all ways -

if you are doubting your diagnosis and want to reintroduce a small amount of gluten to see what happens, by all means do so - that is part of the diet manipulation we all need to go through as part of our diagnosis. but from the tone and subject heading of your first post it sounds as if you are just craving the food, which is a different story. just make sure you are glutening yourself for the right reason and not because you crave mc donalds. believe me, i could gluten myself with a box of krispy kreme doughnuts every day in the name of "testing" but i don't. because i know what will happen, and it's not pretty. by the way, do you keep a food journal? i did for the first year and it was so helpful.

WheatChef Apprentice

Three heavy doses of gluten poisoning have removed almost all of the cravings I used to get. Aversion therapy isn't the worst thing in the world.

Skylark Collaborator

I think everybody tests their tolerance to gluten. You'll laugh because my last real test where I ate bread was at Jack-in-the Box. Talk about not worth it! Some of us fare worse than others when we are inclined to test.

To have a shot at a "your villi are damaged" diagnosis, you would have to eat gluten for a couple months to do enough damage that the biopsy has a reasonable chance of sampling a damaged spot. Even then, there is no guarantee of the biopsy missing damage. :unsure: You can talk to a doctor about doing this.

ravenwoodglass Mentor

Three heavy doses of gluten poisoning have removed almost all of the cravings I used to get. Aversion therapy isn't the worst thing in the world.

I second that heartily! Kind of like Pavlov's dog in reverse. :D

Lgood22573 Rookie

I agree. I think many of us go through this. I did it myself a couple of months ago. I ate two sunchips, just to "see" what would happen. I WILL NEVER do that again. My reaction was so severe, I was sick and in agony all night long. If you decide to do it, just know that you could have that type of reaction.

RideAllWays Enthusiast

Well, I'm glad to hear I'm not alone in this thought process, but I'm sorry lots of you have done it and felt horrible. I've decided to wait. I will continue to eat very basic foods, get enough sleep, exercise, etc..and if I'm still feeling terrible I may try to introduce it. I guess I am just worried something else may be going on.

jackay Enthusiast

Possibly you have other food intolerances and or candida. After giving up gluten and being careful about cross contamination, the only improvement I had was that my anxiety went away. After three months, I went on elimination diet and started taking Candex to rid me of the candida.

I started out just eating chicken, turnips, olive oil and sea salt. Almost overnight, I saw improvement. I was finally able to get some consistant sleep. I have since added oregano oil for killing the candida. It has been about two months and I am not eating 40 different foods and adding something new every few days.

I never thought I could do the elimination diet but then I never thought I could give up gluten. Once I started feeling better, it got easy.

RideAllWays Enthusiast

I just want to make it clear, because I was not in a fantastic mood or state of mine when I was writing my original post...

This is NOT just over a craving. My thought process is a little deeper than that. I love to cook, and I've learned how to make everything I want gluten free. That is not a problem.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,546
    • Most Online (within 30 mins)
      7,748

    KimberlyAnne76
    Newest Member
    KimberlyAnne76
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.4k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Scott Adams
      Your post demonstrates the profound frustration and isolation that so many in the Celiac community feel, and I want to thank you for channeling that experience into advocacy. The medical gaslighting you endured for decades is an unacceptable and, sadly, a common story, and the fact that you now have to "school" your own GI specialist speaks volumes about the critical lack of consistent and updated education. Your idea to make Celiac Disease a reportable condition to public health authorities is a compelling and strategic one. This single action would force the system to formally acknowledge the prevalence and seriousness of the disease, creating a concrete dataset that could drive better research funding, shape medical school curricula, and validate the patient experience in a way that individual stories alone often cannot. It is an uphill battle, but contacting representatives, as you have done with Adam Gray, is exactly how change begins. By framing it as a public health necessity—a matter of patient safety and protection from misdiagnosis and neglect—you are building a powerful case. Your voice and your perseverance, forged through thirty years of struggle, are exactly what this community needs to ensure that no one else has to fight so hard just to be believed and properly cared for.
    • Scott Adams
      I had no idea there is a "Louisville" in Colorado!😉 I thought it was a typo because I always think of the Kentucky city--but good luck!
    • Scott Adams
      Navigating medication safety with Celiac disease can be incredibly stressful, especially when dealing with asthma and severe allergies on top of it. While I don't have personal experience with the HealthA2Z brand of cetirizine, your caution is absolutely warranted. The inactive ingredients in pills, known as excipients, are often where gluten can be hidden, and since the FDA does not require gluten-free labeling for prescription or over-the-counter drugs, the manufacturer's word is essential. The fact that you cannot get a clear answer from Allegiant Health is a significant red flag; a company that is confident its product is gluten-free will typically have a customer service protocol to answer that exact question. In situations like this, the safest course of action is to consider this product "guilty until proven innocent" and avoid it. A better alternative would be to ask your pharmacist or doctor to help you identify a major national brand of cetirizine (like Zyrtec) whose manufacturer has a verified, publicly stated gluten-free policy for that specific medication. It's not worth the risk to your health when reliable, verifiable options are almost certainly available to you. You can search this site for USA prescriptions medications, but will need to know the manufacturer/maker if there is more than one, especially if you use a generic version of the medication: To see the ingredients you will need to click on the correct version of the medication and maker in the results, then scroll down to "Ingredients and Appearance" and click it, and then look at "Inactive Ingredients," as any gluten ingredients would likely appear there, rather than in the Active Ingredients area. https://dailymed.nlm.nih.gov/dailymed/   
    • Scott Adams
      What you're describing is indeed familiar to many in the Celiac community, especially in the early stages of healing. When the intestinal villi are damaged from Celiac disease, they struggle to properly digest and absorb fats, a condition known as bile acid malabsorption. This can cause exactly the kind of cramping and spasms you're seeing, as undigested fats can irritate the sensitive gut lining. It is highly plausible that her reactions to dairy and eggs are linked to their higher fat content rather than the proteins, especially since she tolerates lean chicken breast. The great news is that for many, this does improve with time. As her gut continues to heal on a strict gluten-free diet, her ability to produce the necessary enzymes and bile to break down fats should gradually return, allowing her to slowly tolerate a wider variety of foods. It's a slow process of healing, but your careful approach of focusing on low-fat, nutrient-dense foods like seeds and avocado is providing her system the best possible environment to recover. Many people with celiac disease, especially those who are in the 0-2 year range of their recovery, have additional food intolerance issues which could be temporary. To figure this out you may need to keep a food diary and do an elimination diet over a few months. Some common food intolerance issues are dairy/casein, eggs, corn, oats, and soy. The good news is that after your gut heals (for most people who are 100% gluten-free this will take several months to two years) you may be able to slowly add some these items back into your diet after the damaged villi heal. This article may be helpful: Thank you for sharing your story—it's a valuable insight for other parents navigating similar challenges.
    • 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.
×
×
  • 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.