Posted 5/11/2016 11:56 PM (GMT 0)
I'm new to this forum but just wanted to say, it's really reassuring to hear that other folks with Lyme are dealing with these symptoms. For me the "neuro" aspects of the disease have been the most difficult to cope with. In my case they have included years of intense anxiety that did not respond to psychotropic medications (now overlaid with depression as well -- fun!), and blinding headaches that have impaired my ability to think straight. I was in talk therapy for years before the Lyme diagnosis and used to tell my shrink that my anxiety just felt so *physical*, like a physical state, almost devoid of psychological content -- not that the mind and body are so easily dissociated, but I mean at that point I had pretty much left no stone un-turned, I'd deconstructed all the old narratives, I just couldn't shake the bad feelings...and now it turns out the cause of those feelings probably *has* been largely pathophysiological.
Every day I feel like I'm wading through sludge as I try to stay on top of my most basic responsibilities. Everything is overwhelming, even the littlest tasks. I must confess to relating somewhat to Girlie's "I don't know who I am anymore" comment. It's like, I used to be interesting! And competent! And occasionally funny! And now I just feel so evacuated as a person.
It's really good to know that others have been through this and have found their way back -- if not all the way, then most of the way. I'll take it!