Good Omens: a gentle reminder

ibelieveinthelittletreetopper:

neil-gaiman:

Your headcanon is your headcanon. The characters in your mind are what they are, and nobody is trying to take them away from you. Think of the Good Omens TV series as a stage play: for six full hours, actors are going to be portraying the roles of Crowley and Aziraphale, Shadwell and Madame Tracy, Newt and Anathema, Adam, Pepper, Wensleydale and Brian and the rest. Will they look like the people in your head? The ones you’ve been drawing and writing about and imagining for (in some cases) almost 30 years?

Probably not. Which is fine.

The people in your head and your drawings are still there, and still real and still true. I’ve seen drawings of hundreds of different Aziraphales over the years, all with different faces and body-shapes, different hair and skin, and would never have thought to tell anyone who drew or loved them that that wasn’t what Aziraphale looked like. (And a couple of years after we wrote it, I was amused to realise that the Aziraphale in my head looked nothing like the  Aziraphale in Terry’s head.) I’ve loved every instance of Good Omens Cosplay I’ve seen, and in no case did I ever think anyone was doing it wrong: they were all Aziraphales and Crowleys, and it was always a delight.

Good Omens has been unillustrated for 27 years, which means that each of you gets to make up your own look for the characters, your own backstories, your own ideas about how they will behave.

The TV version is being made with love and with faithfulness to the story. It’s got material and characters in it that Terry and I had discussed over the years, (some of it from what we would have done it there had been a sequel). Writing it has taken up the greater part of my last three years. You might like it – I really hope you will – but you don’t have to. You can start watching it, decide that you prefer the thing in your head, and stop watching it. (I never saw the last Lord of the Rings movie, because I liked the thing in my head too much.)

Remember we are making this with love.

And that your own personal headCrowleys and headAziraphales and headFourHorsemen and headThem and headHastur and headLigur and headSisterMary and all the rest are yours, and safe, and nobody is ever going to take them away from you.

I love Neil Gaiman so much.

How can we help people with disabilities? For example, autistic people who see the world differently.*

* This question was posted on another social media site. What follows is my answer.

1) Treat us as people, not as less. An adult or an older child being talked to in a baby voice is not on, regardless of how their disability presents. Talk to us at age appropriate level. If we’re interested in something, get excited about it with us, rather than telling us we’re boring. Sharing our interest is our way of trying to communicate. We love a thing. We’re opening up ourselves to you. It might not be how you’re used to doing a conversation, but it is meaningful communication, and it means we want to share that excitement with you. That’s a big deal. Recognise it.

2) Our diagnosis is none of your business, unless we feel comfortable talking to you about it. It’s really none of your business if we were diagnosed as a kid, an adult, self-diagnosed, or questioning. It’s none of your business if our autism has changed its presentation as we’ve aged. It’s really none of your business if you think you know what autism looks like, and we don’t match up with your preconceptions. And please, if we’re verbal, dressed appropriately, out in public and unattended, it’s not a compliment to tell us how well we’re doing. We’re just as autistic when we’re ‘passing’ as when we really aren’t. Passing for normal is not an achievement, it’s a monumental effort that most of us feel long term health effects from if we have to do it daily. Allowing natural autistic behaviours is something a lot of us have to relearn in adulthood to manage our anxiety. An adult flapping, pacing, tapping, or playing with a stim toy isn’t being babyish or playing at autism, they’re trying to take care of themselves. Don’t stare or tut or tell us we’re embarrassing you. (Telling us our Tangle is awesome and you want one is totally okay, though.)

3) Our sex life is none of your business, unless we’re in a sexual relationship with you. Just because we’re autistic doesn’t mean we can’t consent. That said, if there’s someone being weird and intimate with us when we’re a minor and they’re in a position of authority, make sure we’re okay. Compliance based therapies heavily used with autistic children (like ABA) make autistic children very vulnerable to sexual abuse, because they teach children to do things that are uncomfortable, painful or unnatural to them to please adults for rewards.

4) Make a conscious choice to be okay with difference, be it physical, intellectual, neurological, whatever. This might be harder than it sounds. Disability can come with mobility needs, sensory needs, dietary needs and routine based needs. It might require communication devices or sign language, or a picture-based communication system, even if to you, the person ‘seems’ verbal. It’s rare for an autistic person to have no difficulties with verbal communication, and if you’ve only ever seen them happy or relaxed, you might not know they need to use their phone to communicate when they’re upset or overwhelmed. Also, non verbal autistics might have a couple of words, scripted speech, or echolalic phrases they can use when conditions are right, even though they primarily use AAC or sign. Verbal ability isn’t a fixed thing. It fluctuates. Be patient if we’re struggling. It’s more frustrating for us than for you.

5) Everyone’s disability is unique. No two autistic people are the same. Likes, dislikes, sensitivities, strengths, difficulties. An autistic person might be sensory seeking, non verbal, highly intelligent, low anxiety, highly organised. They might be highly verbal, high anxiety, low executive function, mild intellectual disability, dyslexic, supertaster. They could have any combination of interests and personality traits, and come combined with a whole array of other disabilities. Don’t think because you know one autistic person, you know every autistic person. We’re individuals.

6) Listen to us, not to Autism Speaks or ‘autism moms’. Our experience is unique to us. It cannot be fully understood by a neurotypical bystander, regardless of how close that relationship is. Read books by autistic people (there are a lot). Donate to the Autistic Self Advocacy Network or Autistic Women & Nonbinary Network. Don’t light it up blue, put puzzle pieces on your car, or spread anti-vax rhetoric (which is fake science and basically hinges on the fact that a lot of people would rather have dead kids than autistic ones). Watch documentaries produced by autistic people about their experiences. Check out neurowonderful’s Youtube series Ask An Autistic.

7) Don’t assume we’re straight. Don’t assume we’re cisgender. Don’t assume we don’t understand the complexities of our multifaceted identities. Gender and sexuality variance is present in autistic people, just as it is in neurotypical people. In fact, there’s actually evidence there is a higher proportion of transgender, nonbinary and genderqueer people in the autistic community than in the genpop. Our experience of sexuality and gender is also viewed through our lens of autistic experience, and there are terms created specifically by autistic people to encapsulate this (like gendervague).

8) Don’t assume we can’t have relationships, friendships, and families outside of our parents and siblings. Don’t assume we can’t be awesome parents. Don’t assume we can’t make informed choices about our bodies and procreation. Autistic people have been here as long as people have been here. I’m from a multigenerational family myself, with both male and female autistic people, stretching back at least five generations, anecdotally (further than that, highly probably, but we don’t have the information).

9) Don’t think we’d be better off dead. This is why adults and children are murdered by parents and caregivers every year without legal repercussions. Our lives have value. The next time you see a news article where a parent cries about killing their child, don’t rationalise that ‘it must be so hard’ to be taking care of us. That’s essentially saying we’re responsible for our own murder, and that it was justifiable homicide. MURDER IS MURDER. If you want to campaign for better respite and support in your area, GREAT, but don’t give parents who murder their children a free pass. Parenting is hard, but people have a choice, and we must stop allowing people who make the choice to kill to get away with murder. Whenever it happens, someone else, somewhere, thinks murder is an appropriate solution to the problem of a disabled person needing care in their life, and another irreplaceable, unique person dies.

10) We have the right to exist in public spaces. Yes, that autistic person having a meltdown might be disrupting your shopping and hurting your ears. I can guarantee their life is harder than yours right then. Have some compassion (not pity) and give them some space. We have the right to be in restaurants, in theatres, in libraries and in schools. If you think a person with a disability being in those spaces is going to have a negative effect on your children, maybe you should think about your parenting, rather than about segregation.

thegirlthatdoesntexist:

image

It’s World Mental Health Day! (October 10th.) So I thought it might be useful to compile mental health resources for the Jewish community into one post. If you know of any that aren’t listed, please feel free to add them.

RELIEF – connects/refers Jewish people to therapists and other
mental health resources (focuses mainly on the frum community)

Elijah’s Journey – suicide prevention for the Jewish community (Facebook page)


The Aleph Institute
– provides spiritual support for Jews in
institutional environments such as prison, health facilities, and
rehab


No Shame On U
– aims to de-stigmatize mental illness by providing
comprehensive education


OHEL
– comprehensive services for those facing mental health issues, with professionals fluent in English, Yiddish, and Hebrew

Yad Rachel – for mothers facing postpartum depression, also helps educate family and health providers

Shema Koli – support for victims of abuse

Frum Support Forums – for mental and physical health

(NY) The Jewish Board – provides services for a number of things, including crisis support, supportive housing, and mental health services.

Torah and the Twelve Steps – spiritual-based rehab for those recovering from substance abuse

(UK) Jewish Helpline – 

0800 652 9249

(Mexico) Jewish Crisis Line – 

1118

(The two following aren’t specifically mental health resources, but I still felt they were important to add.)

A list of Jewish LGBT+ organizations

Keshet – Jewish LGBT+ educational resources

Many cities also have Jewish Family Services, which will often be able to refer you to a therapist or other local resources.

fangirlinginleatherboots:

symmetras-microwave:

fangirlinginleatherboots:

some things that horror movie culture has taught you are scary…. are just ableist

….clarify?

okay sure. psychosis? scarier to have than to know someone who has it. DID? im more a threat to myself than people around me. wheelchairs and psych meds? are tools that help people live more functional and flexible lives and are not judgments of the persons character and for sure are not scary things. and for real, intellectually disabled people are not threats, but movies love to make them villains because they act different and understand the world differently. and people with notable physical differences? people who’s bodies look different? people with scars, growths, amputations, etc? are literally just people. and seeing themselves painted like monsters on the big screen is absolutely sickening and damaging to how society will see them.

its not only bad writing but its extremely harmful to people who actually live with conditions that are misrepresented in media. when i found out i had DID, my mom freaked out because her only point of reference was Sybil. when i was younger and first went on psych meds, i thought it meant i was set on a track to be a bad person, because in so many movies and video games you find out the bad guy has medication in his bed side table for some sort of psych disorder. the worst thing a hallucination has ever made me do was wake my mom up at 3 AM to check my bathroom to see if the bugs i saw everywhere were real and the worst thing an “episode” of any sort has made me do is hurt myself. my ptsd doesnt make me kill people, my alters dont kidnap people, my autism doesnt make me so morally unaware that ill murder for senselessly, my ocd doesnt make me hurt people etc etc etc

literally the only “horror” is the ableism. and the only way you can write good horror about disability and mental illness is if the focus is on how society and the medical field treat us rather than focusing on how we are apparently so scary, threatening, and bad.

Everything You Know About Obesity Is Wrong

runcibility:

mschaos:

bogleech:

chrisco90-blog:

bogleech:

“Diets do not work. Not just paleo or Atkins or Weight Watchers or Goop, but all diets.
Since 1959, research has shown that 95 to 98 percent of attempts to
lose weight fail and that two-thirds of dieters gain back more than they
lost. The reasons are biological and irreversible.

Fatsplaining at its finest. I don’t give a fuck when someone chooses to not be healthy, but don’t sit there and make bullshit excuses and blame anything other than yourself and your lack of self control. Take responsibility and own up to it, you’re not fooling anyone.

I’m sorry other people’s shapes make you so angry that you pretend science is wrong

Obviously this person must think climate change is wrong and vaccines cause autism

Author posted some great follow up tweets: https://twitter.com/RottenInDenmark/status/1043141336239497217

Everything You Know About Obesity Is Wrong

ruffboijuliaburnsides:

i-aint-even-bovvered:

peptobismuth:

ibeautymarie:

mwanga-eunice-martell:

im-the-batmann:

malamatter:

ireallyseeupsidedown:

Is that…, josh peck…

If I don’t see this somewhere on my tl every Friday, I’m gonna be very upset

oh… she can sing

Why didn’t she release this version originally??

because she was 13 and had no control over it and now shes in her 20s lol

So when she was child, she was taken advantage of by her stage parents and a record label that seems very predatory (I believe it’s called lunchbox records or something) that promised said stage parents they would make her child into a star.

Remember that guy who did the rap part who was way older and seemed really out of place? Yeah, he’s the owner of that record label. He is also in ALL of the music videos they produce, and the singers are all young girls.

Rebecca was humiliated and bullied after the release of “Friday” and while we were all making fun of it in our private lives, she had to be homeschooled for the rest of her education.

Was the video terrible? Yes, but I feel bad for making fun of a girl who was really just a victim. I really hope that she has a good life and perhaps even a good career.

She has a youtube channel where she vlogs and sings and apparently has an EP out called RE/BL that was released last year!

And also?  She has the original video of Friday on her channel.  It shows up in the playlists on her homepage, so it’s not hidden deep in the archives, either.  Homegirl’s laid claim to it and it’s hers again, even if it was… not the greatest song or video.  And I’m honestly very happy for her.