Hi all. I have been diagnosed with PA for over 5 years. I had 3 monthly jabs for 3 years and 2 monthlies since. I have been self- injecting every other day for 2 months but my jabs are making no difference to my Neuro symptoms, especially spasms in all the muscles in my legs. I recently looked at my folate history and my levels have varied hugely, being as low as 2.9 and as high as above top of the range but coming down again pretty quickly. My neurologist has ordered an electroneuromyagraph which I am having on May 11th. Just wondered if anyone else in this community has had one. The info on Google is very technical and non-patient friendly and I would just appreciate some anecdotal support as I try to work out what's happening.