Hope is a good thing! I am ~six months into PCS. I am finally starting to feel a little better, my brain seems to be working better (still not normal, but better), I have a bit more energy, headaches are less frequent and severe. I am starting to believe that I actually might feel moderately functional again someday. I've tried to rest as much as I can (I'm a stay at home mom with 3 kids who I home school), take recommended supplements and avoid situations and places that make me feel worse (I still don't do well at all in crowded, loud situations or when I have to stand around and talk to people). I'm still having problems with dizziness, nausea, ear and eye stuff but I am feeling enough better to feel so HOPEFUL that I wanted to post this.