Aug 312015
 

August brought us a lot of personal narratives, powerful, funny, sad, and thoughtful.

Topics include respectful personal care, dating, not-so-accessible sex toys, a moving day-in-the-life of a support worker for disabled folks who’ve experienced sexual violence, and so much more.

Disability Rights

A Bill of Rights as an Autonomous Disabled Person

No One Wants to Be Normal: So Why Are We Awkward Around Those Who Are Different?

On Not Being “Pretty”

Disability Housing: Living, Supporting, and Loving Intentionally

Gender, Sexual Expression, and disability

Gender Differences in Asperger’s: Being a Trans Guy and a Female-Socialized Aspie

Lawsuit: EHarmony Discriminates Against the Blind

Boys in Chairs and Their Toys: My First Experience With a Sex Toy

‘Deliciously Disabled’: Toronto’s Sex Ball for People With Disabilities

Sexual Healing

Dateable Self-Esteem: Danielle Sheypuk, Ms. Wheelchair NY, Discusses The Evolution Of Sex In The City

Secrets to Sexual Self-Discovery: Going deeper Is Key – Wheelchair Accessible Living

Sexual Abuse and Disability

Sexual abuse of people with learning disabilities is too often overlooked

Arts program helps women with disabilities navigate sex, relationships

Aug 282015
 

Then my behaviour therapist called, I asked him how to get a girl friend, he said he’d draw up a plan with a step by step process.

Did you know that there are 176 steps that you need to climb in order to get out of loneliness.

That’s a lot. Loneliness can feel like a deep pit can’t it?

One Step Out Of Loneliness, Dave Hingsburger

Watch this animated film from Dave Hingsburger It’s safe for work unless your workplace objects to words like sex and penis.

Read the transcript here. or watch below.

Aug 142015
 

This week’s film gives us a fresh way to look at sex.

A sexual “jam” is for everyone. It’s a way of looking at sex and sexuality that makes room for different bodies and minds, as well as different desires, needs, and preferences.

Karen B.K. Chan proposes that we look at having sex as like going to a musical jam, or improvisation session. If you’ve never been to a music jam, they’re events where musicians, who may or may not know each other, get together to play music. A jam is usually focussed around a specific kind of music (Celtic or jazz, for example) but people there will usually have all diferent musical backgrounds and levels of experience.

B.K. Says: “The point of jamming is to find out what happens and enjoy the process of getting there.”

That’s also the main recipe for having enjoyable sex.

I personally think this video is brilliant

Even better, there are English and French subtitles to make this important work accessible to even more people.

Enjoy, and here are a few favourite quotes to get you started:

  • “When we jam sexually, we’re not on opposite sides. Instead we’re collaborators.”
  • “Musical jamming can only happen when everyone involved is into it; it can’t be forced – and it’s the same with sex.”
  • “Pleasure is a renewable resource. Just like in music, pleasure is not better when it’s rare.”
  • “Our partner’s yes {to sex} isn’t just a technicality.”
  • “Imagine sex as a lifetime of jam sessions – some good, some not so good, all process, all plesurable, all collaborative.”

Aug 122015
 

Honesty, self-awareness, a wicked sense of humour, an unflinching sense of the ridiculous. You generally need all of these to be able to talk as candidly about your sex life as Kaleigh Trace has done in Hot, Wet, and Shaking: How I Learned to Talk About Sex.

These essays are about a lot more than talking about sex, though. They’re about love, and laughter, and what Kaleigh’s Grandma thought about the explicit language on her blog, and how to prepare for an interview at a sex toy shop (hint: you don’t need to be a sexual superstar), and first sexual experiences…

And through all of these stories, there’s pure, playful honesty about being disabled in a world that doesn’t easily accept people who are visibly diferent.

Hot, Wet, and Shaking is full of delicious details that made me feel like I was right there with the author. I feel like I could be right there with her when she’s talking about that time she pulled a sex ed prop out of her purse – in the middle of the grocery store (A Bag Full of Dicks). Reading Looking For Blood,I feel right along with her the fear and frustration of needing reproductive healthcare in a world that wants to make that hard to get, and wants you to keep it a secret. I nod knowingly as she describes her first crush on a woman: “My attraction was so painfully visceral that for a short time I was truly convinced not that I was gay, but that I had the stomach flu.”

Other stories share some of Kaleigh’s sexual misadventures (And The Warmth Spread Over Us), her awesome-sounding bike and it’s wobbly rider (How I Learned to Stop Worrying and Love My Tricycle), a delicious (in my humble opinion) piece of erotica written in a fit of frustration that there are almost no sexy stories about disabled people.

The Lady and the Butch is a contender for one of my favourite stories. It’s so delightful, I wish it were true – 100% all the way true. Really, an older lady coming in to buy her first vibrator ever, because her “queer lesbian” granddaughter told her to? It doesn’t get much more novel, and amusing, and ultimately touching than that.

But Kaleigh, while she wants to share with us the awesome experiences she’s had and self-discoveries she’s made since starting to work for Venus Envy takes her customers’ privacy seriously, so all store-related stories are fiction based on real-life people and events.

Where this book really shines is in the stories in which Kaleigh is being unfailingly vulnerable with us – not just because she’s usually talking about sex – though that’s great too – but because she shares parts of herself that make her uniquely her, and she sheds light on sexual stories and scripts we don’t usually get to hear but which are a part of a lot of people’s lives.

Fresh-Faced and Orgasm Free is some of the best writing in this book. It’s so much more than a “how I learned to masturbate” story. Kaleigh shares what it’s like to grow up with physical disabilities, to grow up interacting with her body in mostly medical ways. She describes lerning how to drain her urine through a catheter, how she became familiar with her genitals as a place she needed to manage.

As an adult she realizes: Touching myself was so common that it was hard to imagine it as a sexual experience. It was functional,
not hot. Necessary, not fun.”

Trying to learn about masturbation through the sex guides she sells at work, she realizes that none of them really speak to her experience. They all assumed that bodies work in certain ways…that all people can use their fingers to circle their clits, that everyone’s nerve endings fire in pretty much the same ways. “It occurred to me that perhaps I had yet to learn my way of coming because all the step-by-step methods I was reading, all the porn I had watched, and all the sex I had had thus far had not considered my disability.”

There’s so much more I’d like to tell you about this book, about the lyrical ways Kaleigh describes her body, about her observations of and fears around fitting into queer culture, about just how complex and unexpected the piece of erotica was.

But I’m not allowed to copy the book out here, so I’ll just encourage you to get it for yourself.

Thanks so much to Invisible Publishing for giving me an electronic copy of this terrific book.

Click here to hear the author reading from her work.

Aug 032015
 

Can we all agree that asking random people on the street (or in the mall, or anywhere, really) about their sex life is just plain creepy?

People with disabilities are asked, much more often than you’d think, how, or if, we have sex. No, really, this happens all the time. If it’s not about sex directly, it’s something to do with relationship status. Maybe it’s random questions about whether you’re married, or about your dating life. Maybe it’s your server at the fancy restaurant assuming the person you’re sharing a romantic candlelight dinner with is “just” a friend, or worse yet, your brother or payed caregiver.

***

Honey, if they’re with me then they’re not looking for normal — and I don’t mean because I’m crippled. Because sex with me can mean any fetish, any request you’ve always been afraid to make, any position you can think of. Because sex with me can be watching porn together, reading erotica together, or preferably making our own of both…

– Kelsey Warren, My Body

This poem is Kelsey’s answer to the question about her sexual relationship she couldn’t laugh off.

It’s powerful, edgy, and provocative.

As with anything both taboo and sexy, Internet news sources picked this up right away, with headlines like What It’s Like to Have Sex with a person With a Disability.

Kelsey’s sexuality is clearly broad and flexible, and she has the gift of a lovely voice and the art of creating words that grip us and won’t let go.

I know I’ll be going back to this video for inspiration -the sexy kind, not the inspiration porn kind.

But this doesn’t speak to all disabled people’s sexualities – and I doubt Kelsey means it to, since she named her poem My Body – even as it’s the perfect challenge to the idea that disability makes someone not-sexy and incapable of or uninterested in sex, or to the idea that “normal sex” – (whatever that is) – is impossible for disabled folks.

The lives of people with disabilities are so often boiled down to being about our disabilities alone, – usually because nondisabled folks can’t imagine how life with a disability would work – that the idea of grocery shopping, or getting dressed, or having sex with one’s partner become exciting or alien concepts nondisabled people want to learn about the way they’d learn about astronomy or the mating habits of giraffes.

There’s also the assumption that all of these life activities are controlled first and foremost by the disability – that disability changes everything. Newsflash: It doesn’t. We’re just as likely to swoon over cute puppy pictures (or stories for those of us who can’t see the pictures), have ridiculous laugh-fests with friends, or get frustrated over the rising costs of milk. The ways we get dressed – whether it’s how we know what colours we’re wearing or how we put on our underwear or tie our shoes – are just the ways we dress, not anything better, or worse, than dressing the “normal” way – because that way of dressing is normal for us.

***

“I want to learn more about accommodating people with disabilities if I’m going to have sex with them.”

This was one of the answers I got to a question on Twitter asking what people most wanted to learn about sex and disability.

Since it was sex we were talking about, I asked if this wasn’t actually more about pleasure than about accommodation. When I think about accommodation, at least when it’s related to disability, I think of Braille signs on elevator buttons, equal opportunity employment, or buses that announce stops and have wheelchair lifts – not sexual intimacy or X-rated play time.

It turned out this person was concerned about hurting a potential disabled partner if he didn’t understand how their disabled body worked.

Fair enough – but… We don’t know how anyone’s body works until they tell us, until we’ve spent enough time with it to learn what every little sound or wiggle means. It ultimately doesn’t matter what someone’s body does or doesn’t do; no “Sex and Disability 101” Or “Sexual Exploration for Everyone” workshop is going to be able to tell you how to have sex with them.

The fun, and fear, of sexy time with a new partner is the same regardless of ability. The challenges come up when we’re faced with things we’ve never encountered, and sometimes have never heard of.

Knowing something about different disabilities can take some of the mystery of disability out of the equation, and that’s a good thing. The more familiar words and realities like cerebral palsy, hemiplegia, degenerative retinal diseases, PTSD, etc, are, the less unfamiliar they’ll be to people, and the quicker they can get on with their everyday business, including getting it on with a new lover. It’s also a relief to disabled folks when people understand the basics of what we’re telling them, even if it’s as simple as knowing basic human anatomy.

Sure, there are general disability-related differences in romance and sex we can pretty much always assume to be true: A blind man can’t glance across the room and entice an alluring stranger with eye contact. A woman who uses a wheelchair to get around may, depending on the nature of her disability, need help in and out of the chair, with changing positions, with going to the bathroom after sex. A deaf person will likely want to leave the lights on so they can read a lover’s lips, watch body language, or do whatever they need to do to communicate while getting it on.

Understanding disability by studying WebMD and Wikipedia won’t help anyone learn a lovers’ body.

We want answers, and formulas, for sex, and for understanding disabilities, and there just aren’t formulas for understanding either, or both together.

No one’s limbs work the same way, no one’s brain chemicals do the same things, no one person likes exactly the same sexual activities in the same way.

Becoming an encyclopedia of disability and intimacy will only take anyone so far in growing a relationship with a disabled or nondisabled partner or playmate.

I don’t necessarily suggest conducting an interview with someone you want to have sex with – unless question-and-answer sessions light your erotic fire, and theirs – but discussing questions like the ones below can be a good place to start if you’re just not sure what to do with this playmate you find so hot:

  • What feels good to you?>
  • How do we have sex so I don’t hurt you?
  • I want (insert your deepest fantasy, or just what your body craves that day). What do you want?

***

I think the connection we need to keep making between disabled people and sexuality is our right to want sex, to think about sex, to be sexy and express our sexuality – or not to do any of those if we choose not to. For some people that includes the right to have sex, but for others it’s more about the right – and the responsibility – to live in a world that’s so often about sex appeal, and where so many interactions are expected to have sexual overtones.

…unless you’re disabled, in which case you’re assumed to be childlike, uninterested in sex and lacking a sexuality, even unaware of sex; in other words, nonsexual.

We used to describe these attitudes towards disabled people’s sexualities as seeing people with disabilities as “asexual.”

Asexuality is, however, an actual identity or orientation. It’s not generally seen as an absence of sexuality, but as a way some individuals relate to their own sexualities or with the idea of sexuality in general.

Disabled people can, and do, identify as asexual, without that having anything to do with their disability.

I think highlighting the variability of disabled people’s sexualities is important, and sometimes overlooked.

We emphasize so much that disabled people are sexual beings, that we forget that we’re allowed to be lousy lovers, or to have sexual relationships that don’t work, or to have lovers who just don’t enjoy our sexiness without that making them narrow-minded, ableist jerks. We forget that having sexual rights also means we have the right to be lousy in bed, that we have the right not to shock others with our sexualities, that we have the right to be celibate by choice.

So many disabled people don’t get choices, though. They don’t get privacy, or say in who provides their personal care, or who knows about their personal business. The idea that disabled folks who need physical assistance with daily personal-care needs (dressing, bathing, caring for their home, etc.) could also get assistance (without judgment) with the parts of their sexual and intimate lives they physically can’t negotiate themselves is deeply complicated.

There are no easy answers – so much of what I’ve brought up here would, and has, fill books – and there are no quick fixes for making mass changes to attitudes about disability, or sex, or disabled people expressing our sexualities. We’re talking about changing generations of attitudes about two experiences people hold so much fear around in general.

Maybe one place to start, for everyone, is to expand what we think of as sex in the first place.