Has anybody had side effects or adverse reactions to taking methylfolate? And if so, what kinds of effects?
I’m been experiencing a number of symptoms, for the past few months, many of which are similar to PA b12d symptoms. I’ve been increasing my injections but the symptoms remain and seem to be getting worse.
I’m await blood results to rule out anything else related to my symptoms.
But it occurred that me that I’ve been taking methylfolate daily since just before these symptoms all started creeping in - and now I look at my notes when I was first diagnosed with PA and started self injecting I tried taking Methylfolate daily and after a good week 1 by week 3 I was feeling dreadful - so reduced to take once a week just to keep it ticking along.
Interested to hear of others experiences.
I have deliberately not shared my symptoms/side effects here yet to hopefully not sway anybody's answers.