Jump to content
  • 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):

I can't deal mentally with the idea of not eating gluten, so I keep bingin.


Oxx

Recommended Posts

Oxx Newbie

Last November I was diagnosed with Celiac disease. Ever since I haven't been able to remain gluten-free for more than two weeks. I always make excuses and tell myself that I will start "tomorrow." Before being diagnosed, I thought I was gluten intolerant for over a year. I never visited a doctor or anything, I just had a horrible skin rash every time I ate gluten plus stomach pains and other symptoms so I made assumptions. The thing is,  when I thought I was gluten intolerant I had no trouble being gluten-free because I thought it was only a temporary or superficial thing. Like it was ok to get sick every once in a while if the consequence was only a skin rash and symptoms for some hours or a day. I ate almost fully gluten-free for the past year, except for special occasions when I made the decision to indulge. As many of you all know, it is mentally very difficult to accept that you have to restrict yourself from foods you love forever. I am Mexican and food is a central part of our life and family traditions, making it even more difficult. To make matters worse, my family owns a bakery that is next to my house so the kitchen is constantly filled with gluten treats, cakes, cookies, everything. But when I thought I was gluten intolerant, I had absolutely no trouble restricting myself from all the foods that were around my house. I also developed other food sensitivities recently: corn, legumes, most nuts, soy, etc. I also feel discomfort when eating gluten-free processed foods, perhaps because I haven't complied with the gluten-free diet for a long time. 

I most definitely understand how destructive gluten can be for a celiac. I know that by eating gluten I am damaging my body and health. It is not physically difficult to abstain from gluten, I am having trouble adjusting mentally and socially. I have read all the scary posts about what can happen if I don't follow a gluten-free diet, so I am not posting this so I can be motivated by scare tactics. I am posting this because I am honestly desperate. I feel physically terrible after eating gluten, but it is not enough to make me stop. In my mind, I justify myself by thinking that  I should eat X food one last time before actually starting my diet.  It is mindblowing to me that even if I know what can happen to my body, I just keep binging on gluten. I believe that a huge reason for this is that I feel misunderstood. I have never met another celiac in my life, so I don't really have anyone that actually understands how difficult it can be to change your lifestyle permanently. The advice I constantly get from my friends is "just stop because it makes you sick," which is not very helpful. 

 I really think that I need to talk with actual people that are also going through this or that have successfully transitioned to a gluten-free lifestyle postdiagnosis. I figured this forum was a good place to start, but I am new here and don't really know the "social etiquette" around here. I would love to connect with other celiacs and hear about how you managed to go gluten-free. What resources where helpful? Do you have any helpful tips?

 

Thanks for reading! 


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



Celiac.com Sponsor (A8-M):



Ennis-TX Grand Master

Half my family is also hispanic.....worse part is I did not get diagnosed til my immune system got other issues....including a extreme allergy to corn...yeah I wish I had changed earlier....I will forever never be able to have my grandmothers tamales, and many other dishes...>.< I did find a way to make enchiladas with almond flour tortillas but the price makes me not do it. I turned to the positive aspect of it. I was a good cook, I love food, and so I started converting and remaking everything in gluten free/corn free ways. I even started a small gluten free bakery. Heck I also got another AI disease due to celiac called Ulcerative Colitis that will not let me consume starches or sugars...(yeah there went beans) Again I adjusted my life and found a new cooking niche for diabetics and ketogenic dieters.....huge hit actually doing grain free baking. I have since perfected making grain free rolls, bread,s cakes, etc.

I got to admit the worse part is my parents could not do the transition....I kept on getting made sick by my family cooking with gluten foods in the house...I had to move out to my own dedicated gluten/corn free house...I have other allergies and intolerance issues but gluten and corn are hyper sensitive and honestly can not even risk touching foods with these.

If you want to reach out this is a great place, I started my own blog here with monthly highlights to let me vent, I started a recipe blog, I spend much of my time looking and helping people here. I have even composed comprehensive list on gluten free foods. This is a bit of family away from family, we have many different specialist in our group as well who can help you navigate this diet and provide emotional support....PS  I am a bit broke, between Asperger Syndrome, brain damage, and the whole celiac thing...I am a bit like Sheldon from big bang theory with a bit of a food complex. Welcome.

Jmg Mentor

Hi and welcome :)

4 hours ago, Oxx said:

I figured this forum was a good place to start, but I am new here and don't really know the "social etiquette" around here.

This is a good place to start, not the only one, but a good one. There's plenty of helpful people who are a lot further down the road than you or me for that matter and lots of help and support available.  There's also a great resource of previous threads which you can search through for answers on all kinds of weird things which gluten can do. I get that this may be your first forum and you'd be more comfortable with an instagram group or similar, but there's advantages to this kind of online contact which may make it a worthwhile alternative. Although you'll doubtless find plenty of people on other social platforms if you try. 

I think your post is one of the most interesting I've seen here. I find the psychological and emotional side of this condition much harder to deal with than the practical side. It's genuinely tough going at times, or at least for some of us. I'm also at the opposite end to you in that I have no trouble forgoing gluten for life, but I lack the diagnosis you've just been given, I'm 'only' gluten sensitive in other words, but the effects are enough for me to not want any part of it. 

I'm going to throw a couple of things out there that may or may not resonate with you.

First, have you thought about your brain's relationship with gluten? It's a very interesting thing, it has an 'opiod' effect which gluten sensitive/celiac people seem to experience particularly strongly:

Open Original Shared Link

The point being that you may be experiencing this, that your compulsion to eat gluten may be, at least in part, related to it's impact on the opiod receptors in your brain. I know this is something I believe I experienced. It's remarkable how many of the people here who were being made ill by gluten foods had a particularly strong attraction to them. 

Second, does gluten impact your capacity to focus / make good choices? It does for me, it gives me a brain fog, it screws with my mood, makes me slightly bipolar even, and the weird thing is that there's an almost addictive side to that mental state, damaging as it is.  If this is anything like you, then the good news is that if you can kick the gluten for sufficient time, you can start to get the sort of detachment and focus that makes it far easier to handle the diet choices.

Third, have you considered that you may have other issues going on? I found that dairy for instance was also messing with me and that my mental state was far better without it. 

Fourth and last, have you considered getting some counselling to help you process this? You've had a diagnosis that has big implications on your life and there's a grieving process to go through that none of your none celiac friends and relatives will really understand. Talking online can help, but it may be you could find someone near you also to try and talk through some of the emotions you'll be feeling.

Hope at least some of the above of help. :)

Best wishes,

Matt

Archived

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

  • Celiac.com Sponsor (A19):
  • Member Statistics

    • Total Members
      134,108
    • Most Online (within 30 mins)
      10,442

    MiaPiwo
    Newest Member
    MiaPiwo
    Joined
  • Celiac.com Sponsor (A20):
  • Celiac.com Sponsor (A22):
  • Forum Statistics

    • Total Topics
      121.7k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Who's Online (See full list)

  • Upcoming Events

  • Posts

    • Wheatwacked
      Chronic fatigue in the producer was the inspiration for the episode but I feel it touches on anyone that suffers and is dismissed as psycosomatic. The patient expressed my feelings elequently.  In episode 2 the doctor explains the problem well. I stopped all commercial milk protein like skim milk added to processed foods and in a few days there was a definate improvement in my  gut, bowel movements, discomfort etc. Still drinking several glasses of Pasture Fed grass fed milk with no negative effects.   Specifically, for myself Clonidine is the only medication that lowers my BP and the doctor did not renew it, insisting that I continue Losartan.  I think that she thinks I am abusing Clonidine and the reason the Losartan doesn't work is because I am non-compliant.  Absolutely not. Surprisingly after a few days withdrawal from the Clonidine my fasting blood sugar has gotten under control.  Fasting blood sugar near normal instead of over 160.  Last few days its been below 100.  I still need Glimiperide.  Without the clonidine my pulse rate is around 100 bpm, with it around 60.   Prescription of angiotensin receptor blockers in celiac disease is associated with persistent symptoms and surrogate markers of malabsorption.  https://pmc.ncbi.nlm.nih.gov/articles/PMC12323722/ Angiotensin receptor blocker-associated enteropathy (ARB-e) is an increasingly recognised clinical entity with symptoms and histological findings identical to coeliac disease (celiac disease). There is evidence to suggest immune-mediated mucosal injury in ARB-e with a high prevalence of DQ2/DQ8; however, as IgA anti-tissue transglutaminase (anti-TTG) is usually negative   https://onlinelibrary.wiley.com/doi/full/10.1002/ueg2.12117 NEW research [Nov 2024] presented at the American College of Gastroenterology (ACG) Annual Scientific Meeting suggests that angiotensin receptor blockers (ARBs), a class of drugs commonly used to manage hypertension, may be associated with poorer outcomes in patients with coeliac disease. Findings indicated that patients taking ARBs had a higher likelihood of experiencing persistent symptoms and markers of poor small bowel healing, such as anaemia and iron deficiency.  https://www.emjreviews.com/en-us/amj/gastroenterology/news/angiotensin-receptor-blockers-may-worsen-coeliac-disease-outcomes/
    • mermaidluver22
      @BarcinoHi! I am so sorry abt your son but also relieved to know I am not alone! My ttg iga is still mildly elevated but going down. Last time we checked I had some small erosions in my ileum but recently got an MRE that showed no inflammation. Calpro 70. We are still in limbo but we are taking a conservative approach as well. Please keep me updated about his situation and outcomes! I always love to hear others opinions/experiences especially ibd specialists. 
    • Scott Adams
      Celiac.com has published a book on our site by Jean Duane PhD called Gluten-Centric Culture, which covers many of the social aspects of having celiac disease: This chapter in particular covers issues around eating with family and others - Gluten-Centric Culture: Chapter 5 - Grabbing A Bite Together:    
    • BelleDeJour
      Oh, thank you all so so much! I have found my people.   ❤️ I am so sorry that we have all suffered with this torturous itching and resulting sore skin. Sue, I can relate to what you wrote about the dark thoughts, I have had them, too. It's very tough and painful.  I have now had a 2 day straight run of only minor itching. I woke up this morning and did not want to get out of bed because it is the first time in months that I have felt comfortable and actually been able to appreciate the lovely feeling of the duvet on my skin, rather than just waking in pain and thinking about where I need to put cream on before I dress for work. If I can continue like this, then I think I could manage without medication but every time I say this, I then have a flare up. I plan to be very careful about what I eat over the weekend and it won't be easy as we are out with friends for dinner on Saturday (the pub do have very good gluten-free options, I checked of course!).  I really, REALLY appreciate your words so much and am so glad to have found this forum. I am going to read the articles kindly posted now, thank you Scott.
    • Scott Adams
      I don’t know how common this is with celiac disease specifically, but significant inflammation, weight changes, aging, genetics, and skin elasticity can all play a role. It may be worth talking with both your doctor and a board-certified dermatologist or plastic surgeon to see what options are realistic, from skin-tightening treatments to surgical approaches, while also making sure there isn’t ongoing inflammation, thyroid imbalance, or nutritional deficiency contributing. You deserve support for both the physical and emotional side of this.
×
×
  • Create New...