Yeah, what you said Cherie. Mine's a follow up 'look' into the inevitable. Either something they can't see, or "oh look, another lesion!". Hence it's on the back burner.
Frank, sadly I can't even get the prescription filled lol. It's just been sitting here in my wallet. I can't afford $500+.
I called the MS Society on Friday, and my pain doc's office and left a message (they were not in on Friday).
I'm to go back on May 22 to see the pain doc again, and it's supposed to be a follow up to see how the Sativex is helping me... that'll be kind of tricky if I can't even get the medication due to cost huh?