Tomorrow afternoon I have appointment with my MS doctor. It is my initial-three-months-of- drug-therapy check-up.
Translation: we've had you on a drug that we know can have serious consequences to your body, but somehow, we also believe that it has benefits to patients with Relapsing/Remitting Multiple Sclerosis, but we don't know why it works...and we want to make sure that everything is okay.
Oh yeah, and we're seeing you five months after you started it. I really shouldn't care about that part of it. I mean, their testing my blood frequently enough!
I really don't know what to expect tomorrow. It's the first time that I have seen a doctor regarding my condition, that I don't have a lot of questions. I hope that I get an opportunity to mention my fatigue...and that's about it. They will surely see the red marks on all of the injection sites, but I don't know what they will think of them. I have one on my stomach that has been there since May 30!
I promise to keep you posted!