Has anyone tried changing their diet to help with the symptoms associated with pernicious Anaemia?
I personally have stopped eating wheat and other grains like oatmeal . I get a constant dull pain on my lower back and did have sore feet . However, Since I went on a wheat free and oat free diet , my pains have stopped on my feet and eased on my back .
Be nice to hear some success stories and diet knowledge if anyone would like to share or maybe you can’t be bothered 😂
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Rhesus23
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Regarding diet , for Pernicious Anaemia patients , we have to bear in mind that they have low or no stomach acid .So a diet should take this into consideration . There are diets for P.A. patients with Achlorhydria and Hypochlorhydria. Might be good to consult a nutritionist .
In the first instance , food must be chewed thoroughly , enabling the enzymes in the saliva to start work on breaking down the food . Taking an acidic drink with a protein meal is also helpful for the digestion and breakdown of food .
Yes when I was first diagnosed that was two years ago. I cut out certain foods I do running and I noticed symptoms started a few years ago I was getting sharp stabbing pains in my feet , when I ran .
I bought new trainers etc that never helped
And also lower back pain and inflammation .
I read up on line and got different experts opinions .
I cut out wheat and oats ,grains and my foot pain went, when I stopped the wheat. when I exercised the oatmeal gave me cramps so cut that out .
Certain foods cause inflammation and when you have an autoimmune disease
I’m not sure what came first, my stomach issues or low b12. But they found I was very low in b12 this time last year. I had also had trouble with my bowels for a while, but just as lock down started it got really bad. Had a blood test for celiac which came back fine, but was told to get back in touch with docs when they are open again. I decided to cut out wheat and I am fine now. Occasionally have a flare up, like the time I drank lemon barley, not thinking about what was in it. I am hoping when I get myself sorted with self injections, after about a year, I might be able to introduce normal food slowly
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