I am new to this site, although a regular on the Lupus UK & Vasculitis UK forums, due to other health issues. The doctors, & friends who have had this op, say I should feel more energetic for it. I've not experienced this, although my Lupus/vasculitis is very active at the moment, so this doesn't help. I do get restless, but my energy is soon expended.
It would be great to hear how other people have got on, & connect with those of you who have/are going through the same thing.