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Coping with Celiac Disease
Share stories, techniques, and information to help others deal with the disease and the gluten-free diet.
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Recent Activity
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- nanny marley replied to nanny marley's topic in Related Issues & Disorders13Manitol and mri
Oh yes I can understand the tiredness after going threw all that, must be exhausting especially on the mind I have high aniexty so I can understand that , I wish there more easier ways for people to get help , I had a MRI on my spine some years ago without anything it was really quick and no prep , I understand the need for them to see better with the bowel... -
- chrisinpa commented on Scott Adams's article in Autumn 2025 Issue7The Addictive Nature of Gluten and How to Quit Eating It (+Video)
I guess I must ask...are some people actually addicted to gluten or not? From what I have concluded it's not the gluten that I miss since gluten free substitutes are fine with me. It's what I put on the bread..(.jelly) etc.....or what is on the pizza that makes the difference. It seems to me the problem is what gluten was doing to me. Hopefully that...- 1
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- Colleen H replied to Colleen H's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease3Celiac attack confusion and anxiety
The previous post did not come through right. I wonder if tingling burning feet are part of it.. I'm not sure if it's the med reaction that people with gluten intolerance get or the food we ate It's frustrating because a person who did not want to admit to himself I had this condition wanted me to eat this chicken sandwich and now I'm stuck with... -
- Colleen H replied to Colleen H's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease3
Celiac attack confusion and anxiety
Hello I was glutened by a person that knew it. I'm having
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By nanny marley · Posted
Oh yes I can understand the tiredness after going threw all that, must be exhausting especially on the mind I have high aniexty so I can understand that , I wish there more easier ways for people to get help , I had a MRI on my spine some years ago without anything it was really quick and no prep , I understand the need for them to see better with the bowel ,but you think they would use something a little less traumatic for ibd sufferers on the bowels by now ,I hope your feeling better today 🙏 -
The previous post did not come through right. I wonder if tingling burning feet are part of it.. I'm not sure if it's the med reaction that people with gluten intolerance get or the food we ate It's frustrating because a person who did not want to admit to himself I had this condition wanted me to eat this chicken sandwich and now I'm stuck with a variety of symptoms plus now I'm hungry on top of it.. I'm new to this so I forget that "one bite" of the wrong thing can hurt us.😔. Do we stop eating if someone exposed us to gluten ?? My stomach is rumbling but my joints hurt ... It's weird because I can feel the anxiety coming on. I get joint problems , I don't know if anyone ever got hot flashes?? I suppose if it affects people head to toes you can get that too. It's weird...hard to decipher what is what. Also how long do I have to deal with this attack?? Makes me feel like not getting up out of bed. I get too many symptoms which horrible. Thank you for your response..
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Hello I was glutened by a person that knew it. I'm having
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By wellthatsfun · Posted
as my last post stated, i was diagnosed via endoscopy on the 14th of june. i have been eating amazing home cooked meals, luckily, mainly cooked by my boyfriend who is extremely careful about contamination (and is an incredible cook at that). however, i find myself in a mental rut still. being 18, this is the time in my life where i should be exploring things, going out, having fun. yet every corner i turn i'm tortured by the amazing smell of something i can't have anymore. the wonderful sight of such yummy foods. it's near torture. if my boyfriend and his friend who lives with us buy something i can't have, they'll usually eat it outside of the house or the car or wherever we are - which is greatly appreciated - but even seeing a burger or chips or a sausage roll in their hands guts me almost beyond repair. i just wanna have it again too. i miss it. i feel left out and it makes me very sad all the time. it's not their fault. they are allowed to eat whatever they want to, whatever their intestines will allow. it just stings, bad. and i feel so ungrateful given i basically have a private chef who is doubly the love of my life. but it's just so hard. i know i'll adapt. i haven't given up hope.i just wanted to vent. thank you for reading -
Thank you. I must have misinterpreted a study or something. Thank you for the clarification. Much appreciated. Almost three years into my celiac diagnosis and I'm still learning new things.
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