My son has history with h pylori, which he was treated for, but the symptoms haven't gone away completely.
Last week I was talking about my own b12 deficiency and he informed me he has the same symptoms. I know he has been more tried than normal, but I put it due to the h pylori, after effects. As that is what his specialist alluded to. Luckily, his specialist also referred him on to see another specialist (due there in July).
When my mother heard about this, she collected some money and said get him seen privately. His b12 wasn't checked but his gastric parietal cell antibody was positive. His allergy test was also high, which they now want test further for.
Does having gastric parietal cell antibodies, always mean pernicious aneamia?
I been told to pick up a blood test form for Monday, from the gp yesterday. They need to do their own test, I been told. I don't really want injections for my 10 year old. But if he needs it, he needs it.
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Sorry I wrote a long reply last time, I guess it didn't post. I'm fairly new at pa diagnosis. I got tested and was told I was pa last month. It was in March I first got diagnosed with megaloblastic anaemia due to b12 deficiency. Then followed up with pa diagnosis.
My son gp sent him for a long list of things to check. The blood test was just done today. Took a while to get blood test appointment.
If he needs medication I would of course give it to him. I was just feeling sad when I wrote the first post.
Thank you for the reply. If he dose need it, I hope oral would work for him. Getting him to do the blood test was hard enough. Need to wait 7 working days for results now.
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