Ski,

It seems like you have a solid base of support and resources helping you.

A lot of this makes sense to me and I feel I have started making better decisions to make my days easier. The hardest part is making these changes and choices with NO help from anyone but this website (Neurotalk) and other information on the internet! Because I can tell my symptoms and overall condition seem to be different than others on this website...I actually feel my PCS isn't as bad as it could be.

My family doctor told me to start going on light bike rides and doing puzzles! I know I shouldn't do either of those things yet.

And now I wait to see a neurologist...which won't be for at least a month.

I've been reading that many NHL players are diagnosed with PCS and most return to play within a year...this pleases me.