I haven’t had a vacation in soooo long. I’m rundown, I’m cranky, and I’m SO OVER IT at work. Seriously, people. My last nerve. You are on it. Okay, so work’s not that bad (I dig it most of the time), but I am really, really looking forward to getting the funk out of town.
And I get to! This week! At this place!:
A couple of friends will be staying in Northern California for about 10 days and they invited me down to piggyback on their vacation for a long weekend. So, as of Thursday, I’ll be sipping wines in Napa and tripping over the rocks on a Sonoma County beach. Cannot wait. I hope to return refreshed.
My new life with MS means travel brings up a sticky issue–what to do about my Avonex shot. I take it on Fridays, so whenever I go somewhere, which is usually over a weekend, I try to do it a day or two ahead of schedule so I don’t have to travel with the drug. I’m glad Avonex is flexible enough that I can adjust the dose schedule a day or two ahead or behind, but taking it early this week means that I’ll be traveling with side effects.
I know, boo hoo. I get to go on a vacation, so this is really such a small thing. But I have to be at the airport at like 4am! That’s already going to hurt enough already (I am neither a morning nor an unholy-hour-of-the-night person) without the post-shot aches and pains. Must remember to pack lots of Advil for the plane….
I know I won’t be able to avoid traveling with my MS treatment forever, though. How do you-all handle travel and the drugs? Do you have any tips for packing them (mine has to stay cold until at least 7 hours before I take it)? Handling airport security? How do you travel with drugs like Copaxone or Rebif that have to be taken multiple times a week?
