Monthly Archives: July 2010

Newly Nerfed has a birthday

One year ago today, I launched this blog. I’d just been through six months of wondering “What the hell do I do now?” I was paralyzed, demoralized, and utterly frustrated by having had to give in to my disability and quit working. It didn’t help that the job I quit was the best I ever had, but it also didn’t matter. A really big, heavy door had just slammed shut on a really big part of my life, and I was forced to examine my new situation and my new identity.

While beginning to work this out, I dove headlong into the waters I’d only been treading up till then for lack of time and energy. Skeptical blogs and podcasts began to fill my day, and my Twitter stream became more and more populated by other skeptics. I revamped my Facebook page so that I could keep up with the discussions happening there. At first, my appetite was modest, but the more I consumed, the more ravenous I became. (Skepticism as subtraction soup.) I put myself through a serious skeptical bootcamp that was nothing but fascinating, educational, and exciting.

I love to learn, and although I couldn’t work, I could still do that. The skeptical community offered a place for me to do grad-school amounts of reading and synthesizing information, not to mention daily interacting with intimidatingly smart people who wanted to use critical thinking to make the world a better place. It was inspirational, revelatory, and ultimately showed me an alternative to my feelings of helplessness and, worse, uselessness.

I didn’t intend Newly Nerfed to be a skeptical blog. I thought it would focus more on the things I do still write about a lot, disability and chronic illness and nerdy stuff like games and movies. But it proved to be impossible to leave the powerful new focus in my life out of this blog. I connected so strongly to skepticism that I wanted to write about it, even as a neophyte. And the rest can be read in my posts.

When I started this blog, people were talking about TAM 7. Fascinating, I thought, but I couldn’t see myself at that kind of conference. Surely it was for the professors and physicians and scientists I’d been reading, and not for someone like me. And then a year later I was discussing the effects of James Randi’s public and vehement support of science-based medicine during his cancer treatments…with James Randi.

I can’t even begin to express how much TAM 8 meant to me. I had every kind of experience you hear about: meeting “old” friends for the first time, meeting new friends for the first time, having practical discussions, having meta discussions, learning things that are directly applicable to my interests, having my mind blown open by new ideas, meeting heroes and having actual discourse with them, and laying the groundwork for future projects. I came away from TAM wonderfully energized with plans and schemes for the coming year (and with gratitude for the luminaries who kindly allowed me to ambush them with an idea, and for their support of that idea).

A year ago I didn’t know what to do. I held on to my passion for learning, for making a difference, and for writing, none of which got hit by the nerf bat. And then I found myself in a community of people who shared those passions, and I’ve started to find my way. I am so grateful for this year and the incredible people I’ve met and worked with (and will work with in the future). I thank all of you so much, skeptics and believers, friends and strangers, for helping, teaching, and of course entertaining me so damn much this year. I especially want to thank “Surly” Amy Davis Roth and Desiree Schell for their early encouragement of an avid but nervous noob, and Daniel Loxton for being a role model of skeptical communication to which I continue to aspire.

Most importantly, I thank my husband Paul. Not a single step on this wonderful journey would have been possible without his love, care, and support. Throughout everything from health woes to skeptical successes, he has been unswervingly by my side, which I assure you is not always an easy place to be. None of what I’ve experienced, learned, or accomplished this year means anything without the joy I take in having my best friend and twu wuv to share it with. He challenges me to be better, and accepts me when I fail. And I mean, he’s a skeptical atheist gamer geek who can kick serious ass in meatspace — did I win the lottery or what?

Here’s to sticking around for year two. I appreciate it.

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Weekend sendoff: Stars

Sometimes it seems like the coolest stuff is happening in Atlanta. Just before Dragon*Con in September, which has a Skeptrack of which I’d be stinkin’ jealous if I hadn’t had so much fun at TAM, the Atlanta Skeptics are holding Star Party 2010. From their site:

Please join the Atlanta Skeptics on Thursday, September 2, 2010 for stargazing, food, drinks and conversations with astronomers. We are once again hosting a star party to celebrate the beauty of the universe around us while raising money for a great cause.

Astronomers Pamela Gay and Fraser Cain will be hosting the event, leading guests in exploration of the skies, and discussing what we see. Musician, podcaster and science-lover George Hrab will also be providing entertainment.

This event is in honor of Jeff Medkeff, the Blue Collar Scientist, astronomer, skeptic and friend to many of us. Jeff succumbed to liver cancer in 2008. All proceeds will go toward the Leukemia & Lymphoma Society in Jeff’s name.

If you’d rather listen to the above in the form of a promo by Geo, and who wouldn’t, click here.

And speaking of stars and skepticism, you all know about the Jenny McCarthy Body Count by now, right? Did you know that the guy who runs it, Derek Bartholomaus, is about the nicest guy you’d ever want to meet? (Unless you’re Jenny McCarthy, I guess.) Besides being smart, sweet, and unassuming, he also chipped in a donation to the CFIDS Association of America during my little fundraiser, and earned himself my gratitude in the form of a sonnet.

One day a man was watching on TV
A vapid gal whose name denoted “fluff”
Now acting like she had a Ph.D.
And lo, our hero cried, “Enough’s enough!”

He started a campaign of science facts
To counter someone best known for her porn
And now the face of all that’s anti-vax –
The Body Count of Jenny thus was born.

Now J-Mac’s influence is clearly seen
The sick and dead for lack of common sense
Because this man is anything but mean
But could not bear this awful consequence.

So please, accept vaccines with calm and grace,
Or Derek B. may stab you in the face.

I send you off with a lovely song by the Amateur Scientist in honor of Jenny and her campaign. See you next week, when I’ll be celebrating Newly Nerfed’s first anniversary!

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Game a while in another man’s chair

When I was a kid, I was very curious about disabilities. I don’t know why; I didn’t have any friends or family members who were disabled, or at least not in the ways I could recognize. Yet in elementary school I avidly read biographies of Helen Keller, her teacher Annie Sullivan, and Louis Braille. By the time I was nine I had taught myself the sign language and Braille alphabets, and directed a video about Keller, in which I played the lead role (and left my glasses on in several scenes).

I never actually wished to be disabled, but I wanted to know what it was like for the people I’d read about. And reading wasn’t enough. I spent some days at my house blindfolded, navigating by touch and tripping over the cats. I spent a day at school not allowing myself to say a word. And I tried to “deafen” myself with earplugs and other improvised methods, only to be frustrated that I could still hear sounds.

Now I’ve had years of experience in college disability offices, been a sign language interpreter and teacher for deaf students, and know many people in “real life” and/or online with a range of disabilities. (I put that in quotes because who can tell the difference anymore?) And of course, I’m somewhat newly nerfed.

Speaking of the nerf bat, I’m writing a game review for AbleGamers, a website and foundation dedicated to improving accessibility in videogames, which I’ve recently joined as a staff writer. This means a new and challenging way to look at both games and disability. The questions I have to ask of a game force me not just to imagine what it might be like to be color blind, for example, but to really examine the functional implications of that. Is there any game information that is solely presented in colors without any other explanation? What about captions — are they available for both in-game and cutscenes, and what size and font are they, and how long do they stay on the screen? What if you only have the use of one hand? Are there gameplay or difficulty options for people with cognitive impairments?

It’s not just a checklist or a matter of scrutinizing the game’s options. When I’m considering all these questions and others, I play the game imagining, to the extent that I can, that I really need those captions, or can’t distinguish between green and red, or can’t use both mouse and keyboard. It’s like those experiments I used to do as a kid, testing an imagined lack of function against a world that’s mostly built to make use of that function. And something happened after I did my first game session analyzing its friendliness to color blind players: I found myself noticing some billboards or websites with problematic color schemes.

It’s good to look at the world this way from time to time. As more than one wise person has said to me, we’re all disabled in one way or another, or were, or will be, even if only temporarily. Maybe the next time you’re playing a game, turn down the volume all the way and see how it changes your experience. It doesn’t come close to the experience of being a deaf person, of course, any more than my day in a wheelchair at Blizzcon comes close to the experience of using a chair every day of one’s life.

But as I found out when I was young, even a short or small visceral experience can deepen your empathy, or help you consider the world for a moment in a new way. And besides, odds are relatively good that if you read this blog, you’re going to be playing a videogame soon anyway. (Anyone want to take a little survey on that? Leave a note in the comments or contact me.) And you can check on AbleGamers via Twitter or Facebook — one exciting development is an impending segment on CNN. And if I may end this post with a little fundraising, they will send you this limited edition poster by Justin Russo, the guy who did that other awesome videogame art, for a donation of $55 or more. It’s got a message that no gamer could disagree with.

This post contains only my own opinions and does not necessarily reflect those of AbleGamers. Full disclosure: I have been requested to plug this poster. Fuller disclosure: I didn’t actually know this before I wrote the post. Also: Many deaf people do not consider themselves to be disabled. In this post I’m using a very broad definition of “disability,” which does include deafness, for simplicity’s sake. And thanks to Patrick and Desiree for their kind assistance.

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