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Opening and closing theme: The Princess Who Saved Herself by Jonathan Coulton. Used with permission.
Generously transcribed by Crimson Square. Volunteer to transcribe a podcast.[Intro Music]
Chris: You’re listening to the Mythcreants podcast. I’m Chris and with me is…
Oren: … Oren…
Chris: … and special returning guest Fay.
Chris: So, this time we’re going to talk about harmful tropes in regards to disability, and Fay is a disability consultant for Mythcreants. So ze is going to help us break it down.
Fay: Absolutely, there’s so many! So many tropes… so little time. [Laughter]
Oren: Yeah, we’re not really going to discuss this time. We’re just going to list them for half an hour because we probably still don’t have enough time. [Laughter]
Chris: What place ,that might be a nice place to start since it can be a little overwhelming, is things that are Speculative Fiction related, in regards to how magic combines with harmful tropes sometimes, usually it’s magic – is not harmful in itself but it can be used to enable some really harmful tropes in stories.
And one of the things that I’ve definitely seen is a lot of using magic to basically erase representation for disabled people and a lot of times it is combined with stories that put a lot of emphasis on how tragic it is to be disabled. Which you know, it’s hard. It’s weird that people even object – you know, when I when I talk about this Trope because I feel like it should be intuitive that it would be hurtful if you watched a movie that talked about how tragic it would be to be you. [Laughter]
Right, and all the characters are motivated by not wanting to be like you and – but for some reason when it comes to disability people just won’t get that this is not an okay thing to be doing.
Fay – I know this is a complex issue because disabilities come in a huge range. Right, and I think you have said that some, you can consider limitations and some you can consider neutral. Do you want to elaborate on that side of things?
Fay: Yeah. So one of the things that a lot of people don’t understand about disability, is that there’s different ways to experience disability. And the main way disability is usually represented is that it’s a limitation, that it’s a limitation on someone’s life.
So, for an example, I have a chronic back condition and that is something that I do experience kind of like a limitation on my life. So, like, you know, I go to the grocery store and I have a lot of bags and I put smaller numbers of things in the bags and so it’s limiting how much I lift.
It’s changing my behaviors and how I live my life, but there’s another way to experience disability, which is also a common experience of disability, which is that it’s a neutral difference? And so – there’s a lot of different communities that particularly embrace this experience of disability, like the Deaf Community for example, and also there’s a lot of folks in the Autistic Community, who also have particularly been proponents of developing discourse around this.
And this is basically the idea of it’s a difference but it’s not better or worse than being able-bodied or neurotypical which is basically someone who doesn’t have a divergent brain or a brain that is different than what society expects, and so –
For myself, this is actually how I experience my own brain. So, I have anxiety but it’s actually part of a larger way that my brain works, which is that my brain is extremely good at noticing details and processing information and thinking through a lot of different possibilities.
There’s a lot of strengths I get out of that. There’s a lot of great skills, I use it all the time when I’m writing. I’m trying to keep track of different things at once. It’s a great skill set, but – it also leads to my anxiety in that if I’m thinking about something that’s a bit frightening and my brain is thinking through, like, a hundred bad outcomes, it can produce a lot of anxiety.
And so, the same part of my brain that gives me these great skills also produces anxiety that can be very hard to live with sometimes, and so this is where – it’s that sort of neutral difference. And, because I get a great strength and some challenges, and they both go together and –
I wouldn’t just change myself to have a quote “normal brain”, because that would be changing who I am. Would I like to have additional tools to help me manage the challenges that anxiety presents me?
Yeah, but that doesn’t mean that if I could change it, I would and that’s something that a lot of folks don’t understand that, there’s a lot of disabled people who would not – change.
They’re happy the way they are and that doesn’t mean that I wouldn’t take a magical cure for my back? Although you should not do that in stories because they don’t exist in the real world. So, when you do it in a story, the character – and you magically cure a disabled character or give them some sort of thing that means that the storyteller can treat them as if they are able-bodied and basically just ignores their disability almost all the time except for, like, one episode or whatever, that’s not actually representation of the experience of being disabled?
Oren: Yeah, and I would encourage all of our abled listeners to remember that you don’t really want to think about this in context of “Is this something that you would cure?” or – I mean, cure is even the wrong word – “Is this something that you would change if you had it?” Like – it’s not really about whether you personally would make that choice, right?
Because this is something that comes up a lot when we talk about why you shouldn’t just have a cleric come in and cast “Remove Disability” on somebody – and people just don’t understand. They’re, like, “But don’t you want that taken away? Like I know I would want that changed if I have that disability?” And it’s like, okay.
Well, first of all, you don’t know, you don’t have it but – assuming you are correct, right, let us assume that you acquired that disability somehow, so maybe it is a disability one can acquire, and that you still felt the same way. That’s not really what’s at stake here? Right, it’s not really about your personal preference. It’s really more about letting people see themselves and versions of themselves that are healthy, right, and not just covered in toxic tropes.
Fay: Right. And I think in terms of one of the tropes is the magical cure, and one of the other things that goes with the Magical Cure Trope is often that the character is obsessed with a cure.
And – I think one of the big things that’s lacking in disability representation is just – disabled people having meaningful, full lives, that don’t hundred percent revolve around their disability. Like, they have other stuff going on. They have families, and careers or passions and those aren’t a hundred percent wrapped around their disability. Even if someone’s a disability activist, like, you know, I’m a disability activist and a lot of my art and writing involves disability, but it also involves creating cool magic systems and creating awesome fictional worlds, and – it’s not just focused in on my disability.
So I think that’s the sort of aspect of – not reducing characters to their disability and not treating disability as if it’s somehow worse than anything else that could happen to a character, and this is the other thing is – like, oh you’re in a war zone where people you care about are dying every day, but your main concern is this potential possible future disability you personally might have.
Realistically, I hope you care more about your friends who are maybe going to die – like…
Oren: Right, because they were exiled to the Forbidden Forest from last episode. [Laughter]
Fay: You know, so it’s portraying disability as if it’s worse than other things is part of the issue, portraying it as if it’s such a big deal that it’s the entire focus of someone’s life. And that’s where the magical cure is, like, people pursue the cure and they obsess about it, and it’s, like, that’s a problem also in as much as just that obsession and that portrayal of disability, as if it’s this life-ending thing, like worse than death and it’s – not. I mean some disabilities are really hard to live with and some are, you know –
Some disabilities, the main problem that people experience is the ableism in society. Those are the main barriers. So it’s not that a person uses a wheelchair to get around that’s the issue. The issue is the lack of ramps. And buses that aren’t, like, always in good repair so they can always accommodate a wide range of wheelchairs, and, you know, all of these other super narrow doorways.
All of these things. That’s what’s making things hard. Not necessarily the fact that someone’s using a wheelchair to get around.
Oren: Right, and so, again, because this is something that’s often difficult for able-bodied people to understand, is that when you have a disability that infrastructure is just not set up to support you, right?
It is set up assuming that you have a different body type and there’s sort of a feeling among a lot of abled people, that, like “Oh, well, then obviously the solution is to remove the disability and then that person can fit with the infrastructure”, right? But to try to give a metaphor that I think might help some able-bodied people understand why that is a bad idea:
Let’s imagine that you have a society in which we have the capability to surgically graft wings onto your back. Let’s just imagine that’s a thing that could happen. And whether or not you – you might not want to have surgery to have wings grafted onto your back, but if enough people did it and suddenly the infrastructure was there but was assuming that everyone could fly, because a lot of people had wings grafted onto their back, that wouldn’t be a problem with you, who chose not to have the surgery because you didn’t want that, right?
That would be a problem with the infrastructure and it should be fixed there. The solution is not to force you to have this surgery, right? So, I don’t know, maybe that example will help a few people understand.
Chris: And I think with the other thing about magical cures is again to remember, anytime you have a character with a marginalized trait in your story that character is representation and people really, you know, that has emotional power for marginalized people, and so teasing that you might give them representation and then taking it away is just kind of a cruel thing to do and whether you’re just taking a character and holding the threat of “maybe this character might become disabled” over their head, or you’ve got a disabled person who is magically cured. It’s just, it’s not a nice thing to do to your audience.
Fay: Right… and one of the big things is – there’s not a lot of Happily Ever Afters for disabled characters and so stealing that Happily Ever After and turning it into “Oh, they’re cured.” Now there’s one less Happily Ever after. We have a disabled character with a bright future and – we get to have that as something.
Queer folks also have this with queer characters. There’s, there’s not enough queer characters with bright futures. It’s – or trans characters with bright futures. It’s – having the story end with someone having that bright future is really meaningful, and ending by taking away the trait you identify with robs people of having that bright, satisfying future.
Oren: One area that I know a lot of storytellers run into trouble. I am not at all sure what the right way to handle this is, is when it comes to either technology or magical powers used as assistive devices effectively? Because I know that it can be very easy to effectively erase the disability that way, but – I’m not really sure where the line is.
There may not be a firm line. It may be different, but like, you know, just – most people I’ve talked to on this issue agree that the Netflix Daredevil is effectively erasing his disability, but that the character of Toph from Avatar The Last Airbender isn’t. And – assuming you agree with that which you might not and if you don’t, that’s fine. But if you agree with that, I’m just curious if you can maybe talk a little bit about why that – why those two characters are different.
Fay: Right? And we’ll we have this kind of extremes on both ends of a situation where a character has magic or abilities or tech that – it’s so exactly replacing or make, often it’s thought of as making up for, which is a not a great model, but it’s that idea of making up for and it’s doing that so completely that the character is treated as able-bodied by the writers and they don’t run into any challenges or any aspects of disability that affect their daily lives.
Whereas the other extreme is the character that is in a situation where they’re not fully participating in whatever the adventure or the main aspect of the story is. And when a character is in a situation where their disability is preventing them from fully participating?
That’s a situation where we’ve gone too far. They don’t have the accommodations they need, they don’t – You know in the real world, we don’t – we’re not supposed to just shrug our shoulders and be like, oh, well, that’s the way it is. Because that’s not right and that’s not okay. The correct response is to be like – okay, you are not able to fully participate. What can we do to get you to fully participate?
And, so then – that comes into your accommodations devices and all of that stuff. Now, finding the balance is tricky because you want to find that space where the disability is part of the character’s life and it does affect them, but it’s not overwhelming their ability to participate because if that’s happening, they’re lacking in accommodations, and the main tool that I have for figuring out how to do this is really think about what your actual devices and accommodations are – because a lot of folks just be like, are just like, “oh it’s just like – the thing.”
So like in Star Wars – Luke has a prosthetic hand and outside of one moment where he gets a bullet hit at it and it’s “Oh, it’s metal. So he’s okay.”, there is no indication that the hand is any different from having a flesh-and-blood hand, and the writers just treat him as the same. But if you think about the reality of that, what would it actually mean to have that – like, how is that actually – does it need to be charged?
Does he ever have a situation where it’s low on batteries and it loses its coordination? Does it hurt? Does he have to take it off when he sleeps? If someone surprises him while he’s sleeping does he have – like, have to just “you know, oh, I don’t have time to put my prosthetic on”? You’re like, thinking about what it actually means.
What are the costs? What are the side effects? What are the limitations? Does it ever break down? What if the bullet had damaged it and – he doesn’t experience physical pain. You know, but it had actually damage its circuitry? So there’s just – so much there. If you think about what disability? Real experiences of disability are like, okay, you have a medication but it’s got side effects.
You could do a different medication with different side effects, but they all have side effects. And you think about wheelchairs and you have manual wheelchairs, and you have powered wheelchairs, and some folks – like, there’s one or the other that’s going to work significantly better for them. But some folks are in a fortunate position where they have both and they’ll have a choice of “Which one am I going to use today?”
And there’s actually different things to decide like a lot of power chairs are larger. They’re not necessarily going to fit through a super narrow doorway. Not all buses can necessarily accommodate them. They’re going to have a certain length of battery life. But a manual chair is going to have a bigger physical toll on someone, although it’s going to be smaller.
So the real experiences of disability involve these – trade-offs. And so one of the big things is to actually think through what the actual trade-offs are, and then that becomes part of your story.
Chris: So it sounds, like it’s fine that, for instance, we have, you know, magic or tech being used as an assistive device, but that it needs to – doesn’t necessarily have to be a real world assistive device with exactly the same details, but that it should be – so for instance, we have Geordi, right? Maybe Geordi’s, you know, assistive device just acts too much like he has sight, regular sight, you know, standard sight, all the time. You know, there are a few places where the visor does matter but it’s – not very common?
Fay: Yeah, I think with Geordi he’s one of those borderline characters, where some folks really like his representation, although they recognize there are certain areas of problems and other folks who are just like, “I don’t even consider him a disabled character” because of the way the visor is treated in the story and –
Some of the things that were effective are times when he has side effects from his visor – like pain? It does weird things to – I think there was one time where he got like an infection in his receptors?
Oren: There are a few times like that.
Fay: And it would be interesting if they explored more about his different vision that didn’t just make it only seem like a superpower? It also would have been really great if they didn’t have him spend a lot of time obsessing about having quote “normal vision”. That was – just get rid of it, please. All of those – if you just get rid of that, that would be so much better.
Oren: One of the things that I always felt was a huge missed opportunity with Geordi is that supposedly, he sees everything differently. They even occasionally, like, show us the camera filter that goes over what he sees, but he seems to have the exact same aesthetic sense as a sighted person?
Oren: And it’s like – why is that? Why is – Why aren’t his quarters super weird looking to a sighted person?
Fay: Everything’s beige, but he sees all these different colors that no one else sees.
Oren: Right, or like and there’s like – he has lights that emit light in frequencies regular humans can’t see and it’s like – what is that for?
It’s like, trust me. It’s really pretty. I like to watch it when I fall asleep, or something like that. Right? Just, just feels like a missed opportunity there.
Fay: Yeah. To go back to the examples that you previously mentioned, like, with Daredevil. If you – I believe he has sonars into it?
Oren: He has a lot of different things.
Fay: Well, to use sonar as an example. One of the things you could do with that – it’s not going to go through windows and it’s not going to go long distances. There’s just – if you actually think about what sonar is, it’s – it is different, you know, seeing in different wavelengths or in the case with sonar, which is a different way of perceiving your bouncing sound waves.
It’s not the same if you actually explore, like, the uniqueness of it. Of, like, oh, well other folks – that’s a painting but, because it’s a – say it’s a print of a painting. It’s a print of a painting, it’s pretty flat. I mean, he really going to be able to perceive, like, the subtle differences in a print? But then like maybe a sign – fine. And so if you actually explore what the actual thing is – and actually think about it, then you can get a thing where it’s actually going to capture something.
One of the things about Daredevil and Toph gets into kind of a related Trope which is –
Don’t give characters superpowers just to quote “make up” for their disabilities. This is a big thing where it’s – again, it’s centralizing disability as if it’s a uniquely disastrous thing in someone’s life, you know, a lot of things are in people’s lives. It’s not – more disastrous than other things. It’s a normal part of many people’s lives.
In fact, one in four adults in the US has a disability. It’s a normal part of life. For some people, it is a lot more – You have a bigger presence in some people’s lives than others, but it’s –
But the trick is to not treat it as if it’s somehow more life-changing than other life-changing things. If you have a situation where a character becomes disabled in a story, that it’s not more life-changing than losing someone you love or something like that.
And the whole idea of giving someone a power just to “make up for a disability”, again in quotes. I’m doing air quotes none of you can see. It sends this message that disability is more significant somehow.
Give them a power that makes sense for who the character is. So like Toph being an earthbender, that’s – her personality is all about Earth.
There’s a lot of earthiness in her personality – it really fits for her, and then she uses it for creating a type of perception that works for her. But, there’s areas where that doesn’t work. When she’s walking on Sand, – the sand doesn’t carry vibrations in the same way that a solid ground does. Toph does not – can’t use her vibration sense to perceive what’s going on in the sky.
All she’s got is being able to hear what’s going on. So, because it’s not this “perfectly designed to make up for” thing, it’s a thing where it’s like “This is the power that made sense for her.” How is she going to use it to meet her accessibility needs? Great. Okay, what are those areas where it’s not going to cover that? How does she deal with that?
So, basically, that is kind of one of those ways of doing that, is just to have the power that’s not the perfect whatever for the disability.
Another related pattern to this is the idea that any time a character gets a physical disability, they have to have a mental superpower.
So it’s not inherently wrong for Professor X to have mental powers. He’s so privileged, he doesn’t run into most of the everyday obstacles folks with wheelchairs run into?
Oren: Right, because he’s really rich.
Fay: Yeah, which does take away something from the disability representation, but – it’s not inherently wrong.
It’s just when the pattern is “Every time characters get a physical disability they’re only given mental powers”, as if the, you know, as if the fact of having some sort of physical disability means that someone could no longer be athletic or accomplish physical things? And that’s an issue. Obviously, disabilities will vary and certain physical disabilities –
It will make more sense to have folks with mental powers, but also keep in mind mental powers do not have to be, like, psychic and telekinetic, you can have folks that have social based powers, right? Like, that’s the other thing, is – we’re not we’re not seeing folks as – there’s not a perception of a wide range of options?
You know, you give someone a teleportation power, right? You don’t necessarily need to be super physically active to use a teleportation power, you know? And – but it’s like all physical powers. No, they must be mental powers only. You know, you can’t give someone Super Charisma – and it’s like, there’s plenty of charismatic disabled folks, give someone Super Charisma, like, give them that social power. Don’t limit it.
But also don’t be afraid to give a character who’s got a physical disability a physical power, give them super strength, right? I want to see those awesome wheelchair flips! Or, or whatever their thing is, maybe they have a chronic illness, and so afterwards they have to deal with the consequences of that – but for a brief period of time they have their super strength. There’s also kind of that pattern.
Oren: I also just want to take a minute to acknowledge that you can have characters who use real life assistive devices or assistive techniques in a spec fic story, right? Like, if you have your character with a disability and it’s a disability that you think they need some kind of assistive technique or device for, it doesn’t necessarily have to be a magic or super tech one. It, you know, like, my favorite example and the show has some other problems, but in Dragon Prince, we have General Amaya, I think is her name?
And she is deaf, and she just has a translator, and she has sign language and reads lips. There’s no magic involved there, she doesn’t have any kind of magic powers.
Fay: And they did the consulting they needed to do, although I get the impression they didn’t pay their consultants? Which, they have the budget, they really should be paying folks.
Oren: That’s really bad. I didn’t know that.
Fay: Well, they just talk all the time about going to the Deaf Community and talking to lots and lots of folks, which is great. But, I’m just, like, I’m really worried if you’re talking to lots and lots of folks and getting – I just, the way you talk about going to the community, I really feel like it doesn’t sound like you’re paying someone.
Oren: Yeah, it seems like, it seems like you should be hiring a consultant rather than going to Deaf Twitter and being like “Deaf Twitter, answer those questions.”
Fay: I think the one person they paid is their translator, which is cool and all – But they really should, like, I feel like they’re using like, the translator plus Deaf Community and it’s like – I could be wrong.
I hope I’m wrong. I really do, but with something a budget like that, you really, like, don’t just hire your translator. Also hire some actual Deaf folks from the Deaf Community, specifically, like activists and folks who are really, like, aware of the nuances of depiction and pay them money.
Oh, I did want to come back to Professor X, as Professor X is a good example of several different tropes.
One is the fact that disability representation tends to be dominated by privileged folks? People who are otherwise privileged, like – white men, straight white men, occasionally the straight white woman and there’s a real lack of intersectional representation. That’s one thing.
Also – and Geordi is an example of this too – of the fact that folks with disabilities aren’t usually seen as sexual or romantic partners?
I think Professor X does have one romance at one point in one continuum, but he’s generally not someone who gets involved in dating or anything. Not from the stuff I’ve seen.
Oren: Not in any version of the X-Men I’m familiar with. There is a lot of X-Men material out there, so I’m not going to like, swear there’s not, but I think that’s certainly not the image of him that comes to mind for most people.
Fay: Right. As an asexual person myself who is also disabled, it really gets into this weird space where we’re treating all – or media is treating all disabled folks as if they’re asexual and aromantic, but not – but they’re not explicitly asexual and aromantic, they’re just being treated as if they have no interest or no sex drives or anything. And that’s a major thing as well?
And I think the other thing I wanted to bring up is a couple examples. Better representation, which is in specifically looking at – Oh, sorry.
I wanted to go back really fast – with Geordi, actually an intersectional character – his disastrous dating life? I did want to also mention. Also due to the fact that he’s a black man, and there’s a lot of trouble representing black men with, in romances in media, as well. I wanted to be sure to mention that.
So, for him – he has kind of like the intersectional nature of it, I think, made it particularly hard for them, too, for some reason, to get past their internalized assumptions to actually write a good romance for – probably the most dateable character on the ship, honestly.
Oren: Yeah, this is LeVar Burton we’re talking about here.
Fay: I mean, as far as dateability, he’s a lot more sensitive than a lot of the other guys, he’s like super smart, and really caring, and really listens to folks. Like, the way he interacts with Data? He really listens to people, and accept them for who they are?
I mean, he seems extremely dateable. I’m just saying. [Laughter]
Chris: Honestly, it reminds me a little bit of the treatment of Ensign Kim on the Voyager. We’re obviously – Ensign Kim is also a person of color, and they have this ongoing thing about this – about the guy being unlucky in romance? And, it’s particularly weird, because setting up a character who’s unlucky in romance is basically starting an open plot thread, where the viewers are going to want to see that resolved.
They’re going to want to see them happily with a partner by the end of the show, and this doesn’t happen for either of those characters.
Fay: Robbed again.
Oren: It’s okay. Harry Kim gets a romance in the same episode he gets promoted, ba-dum-tss.
Fay: No… [Sigh] [Oren chuckles]
Chris: So, yeah, so yeah, that’s a – it’s a little frustrating. It’s especially weird if you’re going to again, have all, make that big a deal out of that – and that means that yeah, we get, we know that they’re not, you know, aromantic, right? Because they’re interested in dating. But we’re not going to actually let them happily – Again, again, it goes back to that happy ending thing that you were talking about, Fay – why didn’t they get one, in that instance?
Fay: So, the main thing I wanted to close with is some, a few examples of good representation? And one of the things I wanted to mention was that disability, like, there’s a way that disability can be represented when it’s someone who is disabled who is central in creating the representation.
So, two examples of this are Special and a YouTube video series called My Gimpy Life, where if you look at both of those – now, there’s some problematic elements from My Gimpy Life in terms of race, and how it portrays mental illness, but what’s really amazing about it is – having the way that it portrays the daily frustrations of being in a wheelchair in a society that is not accommodating and accessible for folks who use wheelchairs for mobility, and –
And, also have some good jokes that are just, like, frustrating funny things that happened? So, there’s a difference between humor that is using disability as a joke where it’s like, “Oh this prosthetic is ridiculous looking.” and that’s just awful?
But there’s also humor that – especially when folks who are disabled are writing it, about disabled experiences, that is – instead of other-izing, it’s – it brings people in, it increases empathy. And, so, I wanted to kind of pull those out, because I feel like it’s particularly rare to have – representations of physical disability, created by folks who are physically disabled, and are showing their lived experiences.
There’s a lot more good stuff that’s representation of what you call mental illness or neurodivergence? So, a lot of times you have to go into kind of, some of the more independent media, but we have a good explosion of that going on right now, and there’s a lot of audio fiction that has awesome representation of neurodivergent folks?
So, I mentioned the Bright Sessions in a previous episode, but that has an amazing interplay between characters having different kinds of mental illnesses, and divergent minds interplaying with their superpowers? The Far Meridian is about a woman with agoraphobia. A queer woman who’s also a person of color. [Squee]
It’s – the amount of intersectionality in some of these is just amazing. And, and she’s in a magical lighthouse in this kind of – it’s kind of a surreal realism sort of thing? And it’s traveling around to different locations. So, she has agoraphobia, and she’s struggling with it, but – the lighthouse is taking her to these different places that she’s then experiencing? Just to name a bunch of other ones without describing them, other audio dramas – Caravan, Love and Luck, Centered, all have main characters with various kinds of mental illnesses?
And – if you want to go for writing – “Disabled People Destroy Science Fiction” is an anthology you might want to check out.
Oren: That one’s good. I’m into it.
Alright, thank you for that excellent list. I think we’re going to have to – we’re like 10 minutes over our time now, [Fay, high-pitched: oh no!] so we are going to have to cut, call this to a close.
Fay: Oh my goodness.
Oren: But thank you for joining us, Fay, we much appreciate you.
Fay: Oh, thank you so much for having me. Obviously, I have a lot to say on the subject.
Oren: We may have to have you back to, for, like, part two of this episode at some point.
Fay: I know, there’s so many tropes we didn’t get to!
Oren: Those of you at home, if anything we said peaked your interest, you can leave a comment on the website at mythcreants.com.
But before we go, I just want to thank a few of our patrons – first is Kathy Ferguson, who is a Professor of Political Theory in Star Trek. Next is Ayman Jaber. You can find his stuff on thefantasywarrior.com. And finally we have Danita Rambo and she lives at therambogeeks.com.
We will talk to you next week.[Outro Theme]