Crap it cut me off..meant to add: I'll bet you're looking forward to Sat eh? kinda but not... if you want someone to go with you I'd be happy to.
You deserve a big bear hug! HI!! Haven't been on here in awhile thought I'd invest some time into it.
Just a quick note to say hi! Welcome to the Lupus forum. We're here to help.
Thanks for thinking of me. I totally agree about the medical system. I mean if it isn't the specialist's job to try to piece the puzzle together then whose job is it because that's the person we need to see. My family is so upset they want to pay to send me to the US for proper testing but I don't know if its worth it. I mean if they can't find anything and have no idea what it could be it seems pointless to spend more money to get the same results. I think I'm mostly mad at myself for getting hopeful that there might be an answer and help for me. Thanks for the encouragment. It really is the only thing that helps me not feel totally crazy right now. Anna
My dx as of today is 'acephalic complicated migraine with stroke-like symptoms'....no clue where it will lead me! I am hopeful it is right, but still think there is more going on. I wish you luck in your journey!!!!!