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

Does This Happen To Others, Or Am I Weirdo?


VydorScope

Recommended Posts

VydorScope Proficient

Latly when I see heavey gluten foods on tv or in store, my stomache hurst! LOL I know Im just wierdo, but any others just as wierd? :huh::mellow:


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



Celiac.com Sponsor (A8-M):



skoki-mom Explorer

LOL, no, I have the opposite problem! I start drooling and my stomach literally growls!

sillyyak Enthusiast

I feel sick when I see gluten filled foods and I cannot believe I ate so horribly! I went to a staff Xmas party the other night and everyone there was pigging out on cake. I did not miss it at all. I just told myself "They are all going to get really fat with clogged arteries". That made me feel better.

What is curious is how my friends feel "guilty" eating around me. They feel "bad" that I cannot eat what they are eating. I am enjoying them feeling "bad". It makes it easier for me to stick to the gluten-free diet and probably less psychologically painful.

Nantzie Collaborator

I'm still needing to eat gluten for the biopsy, and I swear I have to force myself to do it. Every time I look in the cupboard, which is still full of what I used to enjoy eating, I get nauseous. I can just feel the nausea and other after-effects of it just by looking at it. So I'm there with ya.

I won't be surprised if my biopsy turns out negative anyway just because I seriously doubt I've been able to eat the "three slices of bread" equivalent of gluten.

It's amazing to me that once I figured out what the effects of gluten were on my digestion, body pain and moods, it all just looks gross.

Nancy

RiceGuy Collaborator
I'm still needing to eat gluten for the biopsy, and I swear I have to force myself to do it. Every time I look in the cupboard, which is still full of what I used to enjoy eating, I get nauseous. I can just feel the nausea and other after-effects of it just by looking at it. So I'm there with ya.

I won't be surprised if my biopsy turns out negative anyway just because I seriously doubt I've been able to eat the "three slices of bread" equivalent of gluten.

It's amazing to me that once I figured out what the effects of gluten were on my digestion, body pain and moods, it all just looks gross.

Nancy

I'm curious to know why you are putting yourself through the pain to get the biopsy. I mean, it sounds like even if it comes out negative you'd be staying away from gluten anyway, right? Is it just to get an "official diagnosis"? Plus, with the unreliability, a negative wouldn't mean much. I guess I can understand the desire to have some sort of confirmation, but to me the improvement in health since being gluten-free is all I need. I'll take that result over anything a lab tells me. It's one bodily response vs another, but one certainly seems more obvious.

A lot of people express the same need to know, so I'm just trying to understand the point of view, and the logic being applied. Can you shed some light on this for us?

nettiebeads Apprentice
I feel sick when I see gluten filled foods and I cannot believe I ate so horribly! I went to a staff Xmas party the other night and everyone there was pigging out on cake. I did not miss it at all. I just told myself "They are all going to get really fat with clogged arteries". That made me feel better.

What is curious is how my friends feel "guilty" eating around me. They feel "bad" that I cannot eat what they are eating. I am enjoying them feeling "bad". It makes it easier for me to stick to the gluten-free diet and probably less psychologically painful.

Good ole' negative association. Of course, for us it isn't hard. I look at that over-processed food and see wheat (BAD for me) hydrogenated oil, trans fats, sugar, more sugar and fat. Yum!. NOT! After having to be so careful about what I eat and preparing all of my meals, I'm much more aware of what is in the commercial stuff. I'll stick with this gluten-free lifestyle, thank you very much.

VydorScope Proficient
I'm curious to know why you are putting yourself through the pain to get the biopsy. I mean, it sounds like even if it comes out negative you'd be staying away from gluten anyway, right? Is it just to get an "official diagnosis"? Plus, with the unreliability, a negative wouldn't mean much. I guess I can understand the desire to have some sort of confirmation, but to me the improvement in health since being gluten-free is all I need. I'll take that result over anything a lab tells me. It's one bodily response vs another, but one certainly seems more obvious.

A lot of people express the same need to know, so I'm just trying to understand the point of view, and the logic being applied. Can you shed some light on this for us?

I can. :D

There are 2 reasons I see for this..

1) To eliminate the "what if its something else" nagging concern. Which COULD be real, and serius, or all in ones head. No way to know.

2) To get proper insurance coverage. For example without an "offical" dx of celiac disease, my ins company will not pay for the vitman screenings, the bone screenings, etc that should be done to anyone that has celiac disease discovered late in life.

There may be other reasons, but thats what drove me for so long.


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



Celiac.com Sponsor (A8-M):



key Contributor

I had borderline blood tests and i just tell people I have it(I was gluten-free for 5 weeks before the tests). If they think there is any question of whether you have it, then some people I swear think you made it up! WHy on this earth would anyone make this up. Anyway, I wouldn't go through eating the wheat for the biopsy to know. I felt too sick before. I can see though why someone would want an official diagnoses. It did take me about 3-4 good gluttening episodes after going gluten free to realize for sure I had a problem with it. Each time worse then the one before. SO if you had the positive result you wouldn't question whether you had it and gluten yourself and you wouldn't have to defend the fact that you have it. THis being said, my husband that is with me all the time can see a difference in me, supports me 100%. Number one he knows I smell better!! HA! I act better too. My GI feels that I have celiac disease, but that I wasn't eating wheat and that is why the tests were borderline. He even said that if a person didn't have a problem that their EMA(?) would be like zero and mine was 2points below abnormal and my IGg was way above normal. ANyway, I don't need to prove anything to anyone. Whatever makes me feel better is what I am going to do. My son that is 21 months also has celiac disease, so he needs some support!

As far as this question goes, I don't miss feeling sick and I ate healthy before really, but I miss whole wheat bread for sandwiches and some other things, but as far as greasy fast food, never ate it before and don't miss it.

Good luck with testing and hope you survive until the test.

Monica

Nantzie Collaborator

Well Riceguy, that's a LOADED question. A big part of the reason is that my dad died of stomach cancer a year ago, and I really do want to make sure there's nothing going on in there that is more serious. My mom also died of breast cancer when she was 46. So my genetic makeup is like a minefield.

Another thing is that most of my family has gone off the freaking deep end and has been really cruel and unsupportive and have even ridiculed me about all of this. Rather than be reasonable and be thrilled that I'm taking my health seriously and doing everything I can to be healthy, they've done the exact opposite. Even one of my closest friends, who has known my family for forever, has said that if she wasn't seeing their behavior with her own eyes, she wouldn't have believed it. They are starting to come around, but then I'll hear something about them bad-mouthing me again. So, whatever. The psychology behind it is probably that they are really freaked out about my dad dying and are just not dealing with it well. So instead of being able to grieve my father in the year after his death, I've had to spend the year tip-toeing around their freaking feelings. Anyway...

But the biggest reason is kind of morbid, but it's also true. If I die, I want FAMILY HISTORY OF CELIAC to be in big, bold letters on my kids' medical charts, so that if or when they start having problems, the doctor knows to look for it. Because if I leave it up to my family, I can guarantee you that they'd tell my kids that I was a hypochondriac who was on some weird diet. I don't want my kids to suffer until they're 35 and hope they figure it out for themselves.

And I don't want to put up with the eye rolling every time I have to eat with them.

Nancy

ianm Apprentice

I miss that junk like a great big gaping hole in the head. I don't crave it all. Watching people eat junk food is just too disgusting anymore. If people only knew, or cared about what it was doing to their bodies. The weirdos are the ones who eat gluten.

Idahogirl Apprentice

I really wish I felt that way! The reason that the junk food and fast food is so popular is because it tastes SO GOOD! I don't know if all of the negative association in the world could change that for me! If only I craved rice and veggies. My brain knows that those foods are supposed to be "better for you", but my body says something different. I've never been a health food junkie, and could never picture myself as one. Rather than eating stuff that's better for me (boring and gross), I end up eating way too much of what I can have that tastes good (Cocoa Pebbles, Fritos, tacos, etc.). I miss variety!

Lisa

ianm Apprentice

That junk USED TO taste good but now it just tastes gross. Now that my body is free from that poison I have learned to appreciate real food which tastes much better anyway.

SammieMtz Rookie

Hi all, my names Sammie- Im new on the board.. I was diagnosed about 6months ago and i thought it was dumb so I havent been followin a diet and now My condition is terrible. I get soo sick and i bloat. Im tired of it and im going to try to become gluten free..... any suggestions would be great... anyways on to the question.... right now at my stage i want the foods.lol but i try 2 make myself think badly of them so i dunno i guess im like Idahogirl- i love junk food.lol n its hard 2 switch but i have 2 make myself better. my doctor says im developing osteoporosis and im only 16..... if anyone can help id b grateful...thanx

CeliaCruz Rookie
I really wish I felt that way! The reason that the junk food and fast food is so popular is because it tastes SO GOOD! I don't know if all of the negative association in the world could change that for me! If only I craved rice and veggies. My brain knows that those foods are supposed to be "better for you", but my body says something different.

Word! For me, I KNOW that these foods are bad for me. Really really bad. Poinonous. 200x more chances of gastrointestinal cancer. Scar tissue in my intestines etc. But then I walk past a Cinnabons or a Subway Sandwich shop and that aroma calls to me like the Sirens to Odysseus. It's like being really really sexually attracted to someone who has a nasty venereal disease. I'm like, "I know it's not worth it...but it feels so RIGHT!!!!"

jojoe72 Rookie

What a great topic. Just reading this today made me feel really good knowing there are other people feeling the same way I do. It really puts things into perspective by thinking of gluten foods as poisin. What seems to be helping me with the cravings is l-glutamine. The other thing that helps when the cravings get really unbearable is having a cigarette. I know it may be the worst of the 2 evils but at least when I have a smoke I don't get messed up for the next week.

nikki-uk Enthusiast
That junk USED TO taste good but now it just tastes gross. Now that my body is free from that poison I have learned to appreciate real food which tastes much better anyway.

Spot on!

Actually it's my husband who is the coeliac dx about 14 months ago.

Around 6 months ago I joined him in going gluten-free to support him.

Never thought I'd notice any difference-but wow,a lifelong condition of eczema cleared up in a week!

We all eat so much more better now-and it's only my husband's condition that's made me look into diet & nutrition.

I shudder at some of the rubbish we used to eat.

My kids very very rarely eat McDonalds or KFC.

Back to basics,whole fresh(and if possible) organic.

This coeliac journey has been a real eyeopener.

I do miss the convenience and ease of eating on the go-but get me to eat a hamburger-no way!

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,856
    • Most Online (within 30 mins)
      7,748

    Sonya Haskin
    Newest Member
    Sonya Haskin
    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

    • Jillian83
      He is. Which makes everything even more difficult. I’m not a believer in “staying for the kids” but I have nowhere to go and it’s not just me, it’s me plus my babies. We live in a beautiful place, lots of land in the country and me and the kids love the place we’ve called home for their entire lives. But Im seeing that he’ll never change, that my kids deserve a happy healthy Momma, and that staying in this as is will be the early death of me. Then I look at the scars covering my entire body…this disease and the chronic stress I’ve been enduring for years that tell me I’m no longer beautiful and no one will ever look at me with interest again. I try self care, try to give myself grace so I can just start loving myself enough to gain strength but the slightest sparkle in my eye and skip in my step attracts his wrath and it all comes crashing ten fold. Life is just absolutely railing me from every single direction leaving me wanting to wave that white flag bc I don’t feel like there’s much hope no matter what happens. 
    • trents
    • Jillian83
      Hi, I was recently diagnosed with Celiac and dermatitis herpetiformis after years of suffering without answers. I lost my mind. I lost my job. I lost so much time. I lost Me. Conventional doctors are opulent come near me and the one who did sat across the room, misdiagnosed me, pumped me full of steroids which collapsed my entire hip for 6 months. So without answers I began my holistic journey. Fast forward a couple of years and still struggling with a mysterious whole body itchy, crawling “skin hell”, perfect teeth now deteriorating, thick hair now thinning rapidly and no more than a day or 2 at most relief….An acquaintance opened up a functional medicine practice. Cash only, I found a way. Within a month tests clearly showing my off the charts gluten allergy/sensitivity as well as the depletion of vital nutrients due to leaky gut and intestinal damage. dermatitis herpetiformis was more than likely what I was experiencing with my skin. I was happy. I thought this is easy, eat healthy Whole Foods, follow the diet restrictions and I finally get to heal and feel confident and like myself again very soon! 😔 Supplements are very pricey but I got them and began my healing. Which leads to the other major issue: not working, stay at home Mom of young kids, entirely financially dependent on my man of 7 plus years. He’s never been supportive of anything I’ve ever done or been thru. He controls everything. I’m not given much money ever at a time and when he does leave money it’s only enough to possibly get gas. His excuse is that I’ll spend it on other things. So my “allowance” is inconsistent and has conditions. He withholds money from me as punishment for anything he wants. Since being diagnosed, he’s gained a new control tactic to use as punishment. He now is in control of when I get to eat. He asked for proof of my diagnosis and diet bc he said I made it up just to be able to eat expensive organic foods. Then after I sent him my file from my doctor he then said she wasn’t a real doctor. 😡. I go days upon days starving, sometimes breaking down and eating things I shouldn’t bc I’m so sick then I pay horribly while he gets annoyed and angry bc I’m not keeping up with all the duties I’m supposed to be doing. His abuse turns full on when I’m down and it’s in these desperate times when I need his support and care the most that I’m punished with silence, being starved, ignored, belittled. He will create more of a mess just bc I’m unable to get up and clean so that when I am better, I’m so overwhelmed with chores to catch up that the stress causes me to go right back into a flare from hell and the cycle repeats. I’m punished for being sick. I’m belittled for starving and asking for healthy clean water. I’m purposely left out of his life. He won’t even tell me he’s going to the grocery or to get dinner bc he doesn’t want me to ask him for anything. I have no one. I have nothing. Im not better. My supplements ran out and I desperately need Vitamin D3 and a methylated B complex at the very minimal just to function….he stares at me blankly…no, a slight smirk, no words. He’s happiest when im miserable and I am miserable.  this is so long and im condensing as much as I can but this situation is so complicated and disgusting. And it’s currently my life. The “IT” girl, the healthy, beautiful, perfect skin, perfect teeth, thick and curly locks for days, creative and talented IT girl….now I won’t even leave this house bc Im ashamed of what this has dont to my body, my skin. Im disgusted. The stress is keeping me from healing and I think he knows that and that’s why he continues to keep me in that state. He doesn’t want me confident or successful. He doesn’t want me healed and healthy bc then how would he put the blame of all his problems on me? This journey has been hell and I’ve been in Hell before. I’ve been killed by an ex, I’ve been raped, robbed, held hostage, abused beyond nightmares but the cruelty I’ve experienced from him bc of this disease is the coldest I’ve ever experienced. I’ve wanted to give up. Starving and in tears, desperate…I found a local food pantry in our small town so I reached out just saying I had Celiac and was on hard times. This woman is blessing me daily with prepared gluten free meals, donations, educational info, people who know this disease and how they manage life and the blessings just keep coming. But it’s overwhelming and I feel like I don’t deserve it at all. He just glared and I know he’s going to sabotage it somehow. I don’t even know what to do anymore. I’m so broken and just want peace and healing. 
    • cristiana
      @Colleen H   I am just curious,  when you were tested for coeliac disease, did the doctors find out if you had any deficiencies? Sometimes muscle pain can be caused by certain deficiencies, for example, magnesium, vitamin D, calcium, and potassium.   Might be worth looking into having some more tests.  Pins and needles can be neuropathy, again caused by deficiencies, such as iron and B12,  which can be reversed if these deficiencies are addressed. In the UK where I live we are usually only tested for iron, B12 and vitamin D deficiencies at diagnosis.   I was very iron anemic and supplementation made a big difference.  B12 was low normal, but in other countries the UK's low normal would be considered a deficiency.  My vitamin D was low normal, and I've been supplementing ever since (when I remember to take it!) My pins and needles definitely started to improve when my known deficiencies were addressed.  My nutritionist also gave me a broad spectrum supplement which really helped, because I suspect I wasn't just deficient in what I mention above but in many other vitamins and minerals.  But a word of warning, don't take iron unless blood tests reveal you actually need it, and if you are taking it your levels must be regularly monitored because too much can make you ill.  (And if you are currently taking iron, that might actually be making your stomach sore - it did mine, so my GP changed my iron supplementation to a gentler form, ferrous gluconate). Lastly, have you been trying to take anything to lessen the pain in your gut?  I get a sore stomach periodically, usually when I've had too much rich food, or when I have had to take an aspirin or certain antibiotics, or after glutening.  When this happens, I take for just a few days a small daily dose of OTC omeprazole.  I also follow a reflux or gastritis diet. There are lots online but the common denominators to these diets is you need to cut out caffeine, alcohol, rich, spicy, acidic food etc and eat small regularly spaced meals.   When I get a sore stomach, I also find it helpful to drink lots of water.  I also find hot water with a few slices of ginger very soothing to sip, or camomile tea.  A wedge pillow at night is good for reflux. Also,  best not to eat a meal 2-3 hours before going to bed. If the stomach pain is getting worse, though, it would be wise to see the doctor again. I hope some of this helps. Cristiana    
    • Me,Sue
      I was diagnosed with coeliac disease a couple of years ago [ish]. I love my food and a variety of food, so it's been hard, as it is with everyone. I try and ensure everything I eat doesn't contain gluten, but occasionally I think something must have got through that has gluten in. Mainly I know because I have to dash to the loo, but recently I have noticed that I feel nauseous after possibly being glutened. I think the thing that I have got better at is knowing what to do when I feel wiped out after a gluten 'episode'. I drink loads of water, and have just started drinking peppermint tea. I also have rehydration powders to drink. I don't feel like eating much, but eventually feel like I need to eat. Gluten free flapjacks, or gluten free cereal, or a small gluten free kids meal are my go to. I am retired, so luckily I can rest, sometimes even going to bed when nothing else works. So I feel that I am getting better at knowing how to try and get back on track. I am also trying to stick to a simpler menu and eat mostly at home so that I can be more confident about what I am eating. THANKS TO THOSE WHO REPLIED ABOUT THE NAUSEA .
×
×
  • 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.