After numerous GP appointments and a couple of MRI's I diagnosed my own AN on Google in 2015. As it had grown into giant category (>4cm) surgery was the only option.
To reassure some of you, surgery couldn't have gone better, leaving a tiny fragment behind because it is close to my brain stem. I quickly got used to my 'wobbles', loss of my left ear and can treat my eye (98% closure) so mostly good.
I had radiology last year (22) because the fragment had started to regrow. I hadn't noticed until the end of the year that I have some aphasia (just confirmed) but what I'm more interested in is whether people experience language issues - looking back now I can see symptons appeared over many years but its not until I had radiology, and saw some of these return, that I was alerted to it.
Apparently Expressive Dysphasia is more common with Strokes. I've read a lot of research associated with 'left' side lesions, has anyone else experienced language issues? And what kind of help/support have you received.