Category

Self Advocacy

Film Review: Music (2021)

By Self Advocacy

This blog usually covers topics related to autism or topics related to neurodivergence. As such, my knowledge of the creative arts aren’t exactly necessary for this type of work. However, I am more than willing to make an exception or two should the need arise that requires perspective from a neurodivergent creative; this atrocity masquerading as cinematographic art is one such exception. I am of course writing about pop singer Sia’s debut ‘film’ Music.

Do not get me wrong. Portraying both non-verbal autism and having the autistic character be female (when most representations are male) are worthy concepts for a movie. However, this extremely patronizing and clichéd assault on cinematography was not the way to do it.

If you somehow do not take my word or the words of the several autistic YouTubers who commented on it, Rotten Tomatoes has given the film a 10% rating with an audience score of 15%. To put that into perspective, the film Cats got a 19% critic score and Batman and Robin got an 11% score on the same website. Getting a lower score than two of the worst films critiqued on that website is a horrid achievement in and of itself, but that is, thankfully, its only achievement.

This is not yet even getting into the controversies when it comes to the film’s creation, casting, editing, and Sia’s response to criticisms.

To begin, the film’s trailer was panned from the start over the reveal that Sia’s “muse”, neurotypical Maddie Ziegler, would be playing the nonverbal Music. Naturally, autists everywhere were outraged. One, Sia’s decision took away a casting opportunity from an actress who’s actually autistic. Two, Ziegler was uncomfortable in playing this role to the point that the poor girl had sobbing breakdowns on set over fear that people would hate her for this movie. Three, Ziegler having no say in this adds even further fuel to the abusive and manipulative implications of her relationship with Sia. And four, despite Sia saying that she unsuccessfully tried the role with one nonverbal actress and that she cast Ziegler “out of compassion”, reports and interviews from a few years prior state Sia developed the project with Ziegler in mind and merely lied about the nonverbal actress to save face. Not helping was the fact that the Australian idol had supposedly been researching autism for three years prior to production, yet the results of her ‘passion project’ show that either Sia is extremely ignorant and surrounded by enablers or that Sia cannot do her homework to save her life. Or in this case, her career.

The criticisms escalated once scenes were shown of the characters using prone restraints on Music to calm her during a meltdown. The one introducing the use of said restraints even refers to it as “crushing” Music with “love”. Being forcibly immobilized is incredibly traumatic to an autistic person both on a mental and physical level. The act is also incredibly dangerous as it can suffocate and kill the person being restrained; autistic children have died in the past because of this technique. I myself have witnessed firsthand prone restraints being used on distraught young teenagers. It does not calm them down or deescalate the situation. The criticisms reached a point that Sia stated that the scenes showing the use of restraints would be removed upon release and there would be a disclaimer advising against their use. The US release is unedited.

The final nail in Music’s pre-release coffin was an escalation of Sia’s responses to these criticisms. The most telling of these were her Twitter responses to the several autistic actors who rightly called her out on the fact that Sia put no effort into including anyone who was actually autistic in the planning of the film or made an effort to find an autistic actor. Sia’s responses range from “Maybe you’re just a bad actor” to profanity usage claiming that they have no idea what they are saying because they have not seen the movie.

Yet the ‘film’ was somehow nominated for 2 Golden Globes despite being so ill-received! This blogger speculates that the powerful devices called money and notoriety were at play here. Being the directorial debut of an incredibly popular pop star as well as said pop star’s financial influence were most likely the reasons why the movie was considered in the first place, sad to say.

Music’s premise is one that continues to reinforce harmful stereotypies about people with disabilities. The kind of movies that prop up the disabled as if they are some kind of inspirational paragon for going through life with their handicaps (“Oh, they’re so brave!”). Usually these paragons who can do no wrong are handed off to sullen family members who will slowly become happier over the movie as their disabled burdens touch everyone around them with their magical pixie dust brand of oblivious pluck (“I thought I was raising Music, but it was really Music raising me!”). The fact that these types of movies and other mediums are made primarily for Oscar bait and nothing else is downright insulting for people like myself who are usually the ones being depicted in them. The insincerity and artificiality in this one is sickening.

Music herself is portrayed as blissfully unaware of everything around her. We almost never find out anything about Music aside from her special interest – dogs – and the sequences that, supposedly, only take place in her head. However, the latter is rendered moot by her sister and the neighbor getting sequences of their own later. We never really learn anything else about her. Aside from her autistic traits, we don’t know what she likes, what she dislikes, or even how she feels about the new situation she’s in. Or any, for that matter. The movie claims that Music understands the situation she’s in and can comprehend what goes on around her, but every single scene has Music staring off into space with her mouth open in a dopey wide grin, doing something incredibly childish even by child standards, ‘attempting’ to speak like the Hulk (“Make you eggs!”), and flailing around so much that it looks like she is having a series of epileptic seizures. Sadly, this is likely how Sia sees autistic people in general – not as actual people with hard lives in a world that doesn’t understand them, but as props. Things to pity and nothing more. We only exist for normal people to feel better about themselves.

That’s not to say that the title character is the only problem with this movie, oh no. This movie is rotten to the core with its bad writing and clichés. As I mentioned earlier there continues to be a continuation of harmful stereotypes in this film and a disturbing parallel between Simple Jack (a parody film-within-a-film made 10 years ago on this very topic) and oh stars, does it show. The premise of the film is as predictable as it is insulting: the grandmother and sole caretaker of our title character dies and custody is given to the real main character of the film – unemployed recovering drug addict/dealer and half-sister Kazu, who is less than thrilled with her new burden. Over the course of the movie, Kazu tries, unsuccessfully, to pass off Music to anyone willing to put up with her, including dropping her off at an adoption agency. Eventually, she learns to ‘accept’ Music as Music changes the lives of everyone around her. Blech.

In addition, there is a boy, Felix, whose side plotline interrupts the film several times and never ties into the main story. Felix is also autistic and lives in an abusive family. It ends with his father killing him during a domestic dispute. That’s it. We never know what happened to his parents. His father never receives any sort of karmic justice. The side plot just ends on that grim note. It’s sickening.

As I’ve seen a couple others more familiar with her songs note, Sia’s view of the world is extremely idealized. Unfortunately, this transferred over to the film in the worst possible way. By idealizing Music’s experiences, Sia failed to capture the fact that being autistic is a struggle. Sia is of the mindset that, as long as Kazu accepts Music in her life, everything will be okay. Which is not true. The marginalized struggle because people will NOT accept them. Music would NOT be loved by everyone around her. Everyone would NOT treat Music with respect and, thus, make her life ‘better’. In the real world, Music would be given strange looks on her daily walks. She’d be bullied for acting out, even by her own family.  Music would have the cops called on her and possibly face charges for her meltdowns.

Sia, who need I remind you wrote, directed, and produced this ‘film’, claims it is a love letter to autistic people and the caregivers of the disabled overall, but I can see right through her. Sia does not really care about those affected at all, only what our struggles can do for her career. A reviewer mentioned something about her which I agree with. I don’t think Sia wants people who are different to actually succeed. Sia wants to accept us in our failures and not our successes. She only sees us for what we are and not what we can be. We are merely tools for other people to feel better about themselves. We are things to be used for Oscar bait.

They say the road to hell is paved with good intentions, but not Sia’s. Hers is merely a glorified vanity project that dares to pretend it is something more. To call Sia’s ‘movie’ tone deaf barely covers just how awful it is to all parties involved. In short, Sia’s vain off-key debut is best left on mute. Forever.

Identity First VS People First

By Self Advocacy, Uncategorized

Disclaimer: examples of ableist language are used

Language is a very powerful tool in society. It shapes how we think about and understand our world and the people in it. As society continues to evolve, so does how we communicate, especially when it comes to how we view our fellow man—to be more specific, the disenfranchised, those viewed as lesser. For example, calling someone “an autistic” is different than saying someone “is autistic” or “has autism” which is also different from “is a person with autism” or “is afflicted with autism” or “suffering with autism”.

It seems obvious no one would ever think to refer to a person saying “she is cancerous”; they’d say “she has cancer”. Originally this stood out to me because calling someone cancerous seems to clearly be equating/identifying a person with cancer in a negative way. This term is known as person-first language. Person-first language (aka people-first language, or PFL), while an attempt to move toward humanizing people, has its own issues and is certainly not a one-size-fits-all solution. In person-first language, I am “a person with autism”. This is not, however, how I refer to myself. Despite my opinions on the term, I can understand why the person-first movement started and why it is used by medical professionals, including my colleagues. I also believe that, as self-advocates, it is important that we acknowledge this term’s significance in our movement’s history.

Before its present use today, person-first language originally started in the AIDS crisis. In 1983, a group of activists stood up at a Colorado health conference and drafted a declaration known today as the Denver Principles, which included the following statement:

We condemn attempts to label us as “victims,” a term which implies defeat, and we are only occasionally “patients,” a term which implies passivity, helplessness, and dependence upon the care of others. We are “People With AIDS.”

And so, person-first language was born in a bid to refuse to be labelled a “victim” during a harrowing medical crisis. It was insightful, brave, and RIGHT. Even better, doctors at the time took notice as more and more research papers referred to “people” instead of “victims” or “patients”. For what was shown in studies at the time, person-first language was helping change perceptions about AIDS for the better.

Early in the disability rights movement it was common for a person’s disability or medical condition to supersede a person’s identity in a very objectifying way. Older historical terms included words such as “cripple”, “invalid”, and “cretin” were all very much used in noun form to supersede any ideas of personhood. We weren’t seen as people. We were seen as imperfect. Broken. Wrong. It was “that kid with cerebral palsy, Ben”, not Ben, who has cerebral palsy. We had no personhood. We were just societal burdens with a pulse.

When you’re referred to by terms like “moron”, “retard”, “idiot”, “imbecile”, and “stupid”, it only makes sense that you’d want to be seen as a person. To see the person first and then the disability. Granted, those terms were all once specific psychological/medical terms and retain a lot of that stigma even today, even though they are often used as generic insults now. In an effort to de-objectify us and to emphasize our humanity – which unfortunately could and can still be quite prejudiced and discriminatory – person-first language was magnified as the politically correct and preferred way to address not just people with AIDS, but people with disabilities as well.

In addition, there was a shift in language in the 1990s when the federal Education for all Handicapped Children Act was renamed the Individuals with Disabilities Education Act. The federal mandated change in terminology reflected a broader deliberation for identifying language. While this change still held stigma, it was a small step in the right direction for that time. However, because of this language change, and the broader cultural shift it represented, medical professionals in the 1990s were quite skittish at using identity-first language. For them, calling someone an autistic person didn’t sound quite right.

But that jargon is not a blanket term for all disabilities. The autistic, blind, and deaf communities haven’t been as affected at the same scale as the communities with intellectual disabilities. While we are still looked at with disdain, in recent times, we haven’t been locked away en masse. My community, the autistic community, seems to be the most passionate about this and with good reason. Despite society’s progress since the 1980s, the population is still by and large reviled, abhorred, and discriminated against by society as a whole, be it consciously or unconsciously. Even pro-autism organizations and events can fall into this, causing us to be seen as an epidemic of tragedies.

A new movement within the disability community is gaining traction by the day. The growing prominence of disabled people proudly accepting their disability as one with their identity and changing the game. Those in the movement, including myself, are saying that our disability shouldn’t be an afterthought. Moreover, our disability is not a bad word. There are many hashtags such as #SayTheWord on Twitter filled with tweets of disabled people who chose identity-first language.

However, at the end of the day, it is a choice. And the community it impacts is not a monolith. Disability touches every demographic imaginable. No two individuals will be impacted in the same way. Their different perspectives and life experiences dictate how they self-identify and their place or lack thereof in the community. It would be hypocritical for one disabled person to dictate another’s identity seeing as that is what the rest of the world is doing to us.

The main rules of thumb I can give for those unsure is as follows. If you are speaking with or about a disabled individual and are unsure of that individual’s preferences, ask them. Much like the autism spectrum itself, each of us is unique and have our own likes and dislikes. One of us may not mind being referred to in PFL, but another may not think so.

Words are important, and how we use them affects others and can also shape our personal and societal outlooks. Using language responsibly is something we should all strive, and it’s impossible to do so without listening, especially to the people you’re talking about and who your words most effect. So, thank you for listening.