Adventures in the offing, and Courageous Conversations

This last week has been crazy. You see, SC and I are heading off to the first of our big three conventions. During the Spring and Summer, I work as a part time vendor selling plushies (stuffed animals) at anime and science-fiction conventions. However, once a year I get to switch my seller hat for a buyers one. We start our year at Toy Fair!

Toy Fair New York is a trade show for just about everyone involved in the toy industry. Buyers, sellers, inventors , and investors, they will all be there.

For four days, SC and I will browse through a mindboggling array of booths looking for both plushies for the Boss and for new blog material for me. There are roughly 1060 vendors there, I’ve managed to winnow it down to a list of 200. Still, that’s a lot of people to see and talk to!

Let me introduce you to Jæger. He’s my ESP(emotional support plush). He’ll be popping up on both my Twitter and Instagram while I’m at Toy Fair.

That’s the fun part of this weekend, the not fun parts? We’re taking a train to NYC from Virginia. I love traveling, but hate the fact that my illness doesn’t agree with sitting for long periods of time. Also, NYC in winter is usually not my cup of tea. I hate being cold! The worst thing though, is that this year I’ll be renting a wheelchair.

I use a cane about 90% of the time, except on good days in my own home or at the homes of friends I know really well. I really only use the motor carts at the supermarket as an absolute last resort.

I don’t want to need to use a wheelchair, but after spending 9 hours on a train, arriving at 2 in the morning, and walking around Times Square to get to one of our favorite 24 hour diners (Tick Tock Diner), I’ll be completely wrecked. We did it last year with me on a cane and I ended up exhausted. I can’t do my job exhausted, much less out of spoons.

It sucks, and I had to deal with several anxiety attacks over the idea of transitioning to a wheelchair, even if temporarily. I fight constantly to keep as much of my independence as I can, and detest feeling like a burden.

SC, bless him, does his best to help me. He was the one to fight for me going to a cane instead of leaning on him for balance. I hated that back then, but he was right, once I got used to my cane it gave me back the pep and vigor I’d thought lost for good. Hopefully, using a wheelchair for a day or two will save the spoons I need to do my best at Toy Fair.

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