In the spirit of this morning’s article on possible connections between gluten and schizophrenia, I got curious:
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Do you think you have gluten intolerance?
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Have you been treated for gluten intolerance?
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Do you have Celiac Disease?
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Are you on a gluten-free diet or do you try very hard to be?
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Do you think gluten affects your MI symptoms?
Here’s a warning for anyone considering abstaining from gluten: rice is usually the grain that takes wheat’s place and rice is only safe in small quantities - it’s not something to use for cereal, bread and crackers in the same day - it’s got too much arsenic. There’s a lot on the web about it including safer quantities for consumption.
It was nice of you to be such a good sport about it, nevertheless 
My doctor says that I do not have celiac disease, but I feel bloated always after eat, and I used to eat a lot of bread and rice too.
In a short term, I can say that my best moments were when I wasn’t eating food with gluten, maybe I was also for the medicacion in that period, but I do not know.
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Cutting out gluten made a huge difference for me positive symptom wise. Also, the dose of my APs would go up gradually for years. After cutting gluten I haven’t had to raise the dose for a while now. I think it doesn’t hurt to try going gluten free for a while. Theres gluten free pasta and bread, though it is generally more expensive and might not taste exactly the same.
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This video briefly reports finding linking gluten sensitivity to schizophrenia.
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People have been asking me how I get by without APs. I think this may be it. I’ve been gluten free since shortly after I was diagnosed, I believe. I get mouth sores, bloat and irritability as well as digestive upset including heartburn when I ingest gluten.
Thanks for the video; it’s very simple and informative.
Hmmmm… I don’t know. I just find it interesting. I was talking to my husband this morning saying that I don’t understand why I haven’t needed as much medication as most schizophrenics take and something came up this morning about gluten and I had a light bulb moment: I don’t ingest gluten! I haven’t for a long time, so I am curious if that is the reason. I don’t have celiac, either but a multi-symptom intolerance.
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I read a few time ago, that a high percentage of neurotransmitters, are created in bowels, so, we do not used to give importance, but a good alimentation without intolerances ( like gluten) and taking probiotics could make a difference, It’s difficult to keep but I will begin to try next week.
I’m glad of you are doing well with few medications!! 
THANK YOU!
I forget stuff. I remember knowing that about neurotransmitters in the gut but I forgot. My husband and I ran out of digestive enzymes a while ago. We’ve still got fairly new probiotics in the fridge but we ought to take them…
Yes, please do try next week. It might really help.
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