My Active B12 was just about into the sufficient range. My H Pylorii was negative, as was anti IFAB and coeliac. Homocysteine was fine too.
My neurologist’s physical exam was normal ( though the sharp stimulus was a little less sharp on the feet. )
I have been taking sublingual B12 and the tingling feet and fingers have improved, but not gone.
I’m confused about taking folate so I’ve been taking a supermarket B complex plus Marmite.
I’m still on omeprazole.
My GP referred for a gastroscopy but then the FIT stool test came back full of blood so I have been referred for a colonoscopy too. My GP does not think it’s cancer but I have been referred urgently.
My overall health is so poor ( eg sedation could have a bad effect ) that I have asked if I can have a CT scan instead and I will see the consultant about this at the weekend.
My grandad had a duodenal ulcer and his stomach used to swell up, which I’ve had too.
Any thoughts about this ? Are these overt gastrointestinal symptoms usual in PA ? What about the bleeding in the intestines ? If I end up having a scope, can they take a sample and check for autoimmune gastritis ?
I always expect the NHS to do half a job - ie check for cancer but never mind about the finer points of what type of gastritis etc.
Thanks !