The Curiously Oppressive Power of Positive Thinking

thebodyisnotanapology:

The Oppressive Power of Positive Thinking
by Rachel Cohen-Rottenberg, Content Intern

Occasionally, I read articles and see memes that suggest that loving ourselves and our bodies involves believing in the power of “positive thinking” – a belief that dictates that if we just believe in ourselves enough and put out positive energy into the universe, good things will happen. Following is an example of this type of meme:

image

Source: Facebook

[The graphic shows a watercolor-style picture of a woman with her eyes closed and her hair swept up. The text reads: “Believe in what you want so much that it has no choice but to materialize.”]

I have to admit a certain attraction to these kinds of graphics. After all, the way in which we carry ourselves in the world sometimes can have an impact on how people respond to us. For example, most people in our culture will respond more positively to a person exuding confidence than a person who is mired in self-hatred. So there is something to be said for increasing the possibility of positive responses by putting confident, self-loving energy into the world.

But for me, these memes go too far, for a number of reasons.

First, there is a vast difference between increasing the possibility of good things happening and actually guaranteeing a positive outcome. Loving yourself enough to exude confidence is one thing; believing that you can make your dreams come true through an act of attitudinal will is something else entirely. The former is an attempt at playing the odds; the latter is an example of a belief in being able to control what is essentially beyond us. A belief in one’s dreams is an essential ingredient of being able to realize them. However, no dream is guaranteed to materialize, no matter how badly one wants it to.

Moreover, for disabled people – as for any group of marginalized people – these kinds of messages can become oppressive, because they feed into the idea that if only we tried hard enough, or had a good enough attitude, we could single-handedly make our lives better. For disabled people, this way of thinking can take the pernicious form of being blamed for the state of our own bodies, as though we somehow caused our disabilities with poor psychological habits and could somehow cure them with the proper way of thinking. It leads away from self-love into self-blame.

Disability studies scholar Susan Wendell calls this kind of thinking evidence of “the myth of control” – the belief that one has the power to completely control the life of the body (Wendell 1996, 94). Likewise, writer Susan Sontag notes that the mid-20th century saw the flourishing of the belief that a person’s emotional and psychological states were responsible for illness; people had cancer, the story went, because they were “inhibited” and “repressed” (Sontag 2001, 39), and prone to “emotional withdrawal… lack of self-confidence and confidence in the future”(Sontag 2001, 55). The result is that people encounter blame for becoming ill, on the premise that they have the wrong state of mind, rather than receiving support and love while going through a difficult time. This type of blame is just below the surface of the following “positive thinking” graphic:

image

Source: Facebook

[The graphic shows a beach at sunset, with colorful stones in the foreground and blue water going out toward a yellow sun and an orange and blue sky on the horizon. The text reads: “The Universe is not punishing you or blessing you. The Universe is responding to the vibrational attitude that you are emitting. – abraham hicks.”]

Despite the disclaimer that one is not being punished or blessed, the graphic makes each person entirely responsible for his or her fate. Put out positive energy, and the universe will respond in one way; put out negative energy, and the universe will respond in another. So if something bad happens, it’s your own doing. This graphic in particular, and the whole notion of “creating your own reality” in general, ignores the many levels of structural oppression that keep people from realizing their dreams, no matter how much good energy they stream in to the world, and ends up blaming people for their own victimization.
People with disabilities routinely run into barriers that make realizing the life they want impossible. These barriers are not of our making and cannot be overcome by means of a positive attitude. A person in a wheelchair who is homebound because he lives on the fifth floor of a building without an elevator cannot, though the power of positive thinking, get to the first floor and onto the subway to a job. A young woman routinely denied employment because of a facial disfigurement cannot, through a powerful rush of spiritual energy, stop people from limiting her opportunities. The 85% of people with autism who are unemployed cannot, by adjusting their attitudes and hoping for better, make remunerative employment appear.
I know that some will answer these assertions by pointing out that individual disabled people have, in fact, overcome structural barriers. The implication is that if one disabled person can do it, then all disabled people should be able to do it. But that sort of thinking ignores the fact that exceptions to the rule are, in fact, exceptions because larger structural inequities make overcoming these barriers uncommon. The notion that, by force of will, we can always overcome structural barriers reinforces the pervasive American notion that individuals bear all of the responsibility for the outcome of their lives, and that society as a whole bears no responsibility at all. But disabled people, for all of their effort, still live with dizzying levels of unemployment, poverty, hate crime, and discrimination. No amount of positive thinking will keep someone from refusing you a job or committing a hate crime against you if they’re bound and determined to do it.

Ultimately, the driving force behind the “power of positive thinking” meme is the word “power.” If you’re powerful enough, you can make anything happen. But what about those whose bodies are not powerful? What about those who are vulnerable? What about those who are tired, isolated, and struggling? What about those who are ill? What about those who lack proper support? How do they make their dreams manifest?

My answer is this: Given that all bodies are vulnerable and go through fluctuating states of ability, disability, energy, fatigue, wellness, and illness, we cannot rely simply on our own individual power. Rather, we must collectively help make one another’s dreams manifest. We must remove the barriers and the inequities that keep people from realizing their dreams.

It’s not enough for each of us to do it for ourselves. It’s up to all of us to do it for one another.

References

Sontag, Susan. Illness as Metaphor and AIDS and Its Metaphors. New York, NY: Picador, 2001.

Wendell, Susan. The Rejected Body: Feminist Philosophical Reflections on Disability. New York, NY: Routledge, 1996.







fogblogger:

OH another thing I love is when you open up to someone about your disability and they tell you you shouldn’t let it take over your life and that you need to be more positive

It isn’t a matter of positivity if I’m giving you facts

Dicko

YOU KNOW WHAT I HATE? IS HOW /EVERY TIME/ YOU SEE SOMEONE WITH A DISABILITY ON A TALK SHOW they’re always praised about how ‘positive’ and ‘uplifting’ they are (and how ‘inspirational’ but we already know how that shit goes) and asked ‘how do they stay so positive ALL THE TIME; it’s ~such a beautiful thing~’ and i call BULLSHIT on it because, look, no one is positive all the time and it’s destructive to not allow yourself to feel your full range of emotions, especially in a situation that can have a lot of pain and grief and frustration and anger attached to it, so — basically, if anyone’s response to you being honest and open about your disability is that you ‘need to be more positive’; they can get the hell out of your life right then and there. 

fogblogger:

alemonlemoned replied to your post: alemonlemoned replied to your post: The worst…

well and like. exactly. it affects pretty much EVERYTHING in your life including and up to how you just interact with the world and THINK & its IMPORTANT, you cant erase it (+other ppl arent supposed to love you IN SPITE OF your disability jfc)

YES and I mean yo I can’t do anything without it affecting my disability everything revolves around that and it’s awful when people just completely erase or diminish what you’re going through especially when they think they’re being nice. And then it’s worse because seriously so many of us have spent SO MUCH TIME trying to convince people that we aren’t lying and that all this really is happening to us. Yeah for real like no it isn’t a flaw it’s a part of my body suck it up and don’t act like you’re five because love doesn’t work like that

I HAVE BEEN SLACKING ON MY SALT INTAKE BECAUSE I AM RIDICULOUSLY NAUSEOUS ALL THE TIME WOO, POTSies, GIVE ME HIGH SALT FOOD SUGGESTIONS? i’m vegetarian and can only have dairy infrequently/in small quantities b/c of allergies. HELP?

Played 22 times

alemonlemoned:

Tracy Chapman // Broken
You can close your eyes
And see a picture perfect life
Inside of your mind
Dreaming only of the days ahead
Wanted and wished for more than now
Or the days behind
You waste your time

The picture makes a promise
The flesh lets it be broken

You can never think
You can’t even stop yourself
Before the words have been spoken
And you’ve already said
You would give everything
And something for nothing
Everybody thinks you’re joking

The picture makes a promise
The flesh lets it be broken

For spoonies

seeker-wings:

I am going to be forced to work and study full-time with severely debilitating FMS. I want to prove to this person the severity of this illness. Reblog this only if you’re a chronically ill person who is unable to maintain a full-time job/school without it worsening your symptoms to the point of disfunction. Please help.

i had to completely drop out of high school at sixteen/couldn’t even manage homeschooling/online schooling (let alone even attempt to work a job!) because of the severity of my illnesses (which include fibro) since they are so debilitating in both my physical ability and my ability to concentrate/think straight. i fainted at the top of a flight of stairs at school (and was caught by a friend) before i dropped out because my body couldn’t handle the physical strain of trying to go to school. whoever thinks you can work and study full-time knows NOTHING about this illness and how severely it affects your ability to function. 

environmentalillnessnetwork:

“If disabled people were truly heard, an explosion of knowledge of the human body and psyche would take place.” - Susan Wendell

environmentalillnessnetwork:

“If disabled people were truly heard, an explosion of knowledge of the human body and psyche would take place.” - Susan Wendell

I’m so tired of people casually throwing the word ‘fatigue’ about.

rainbowspottedguineapigs:

Fatigue is not when you’re tired at the end of an 8 hour work day. That’s being tired.
Fatigue is not lacking energy at 6pm because you didn’t sleep well the night before. That’s being tired.
Fatigue is not looking forward to bed time because you’re tired after going to the supermarket, visiting your family, going to the gym and cleaning your house. That’s being tired. That’s your body’s rational feelings after doing a lot of activity, you’re tired.

Fatigue is when - after being awake for two hours and in those two hours you have only gone to the bathroom, forced yourself to ignore the nausea and eaten a small snack, and brushed your teeth - you feel like someone is sitting on your chest because breathing takes up more energy than you ever realised.
Fatigue is when you feel like your brain is shutting down and your eyes are going to fall out and your legs just will not move after forcing yourself to stay awake to finish that stupid essay.
Fatigue is the moment when you collapse on your kitchen floor when you’re trying to make dinner, when your energy levels reach the minus figures and for a moment you’re unsure if you’ll ever be able to get yourself standing again.
Fatigue is the restlessness, the frustration, the broken social life, the depression, the feelings that you are just sodding useless that comes with it all.

But I guess you can’t understand that until you’ve experienced it. Fatigue is a gut wrenching word and it changes your life forever.

TIPS FOR DEALING WITH PEOPLE IN PAIN

chronicallyvegan:

drhikaru:

Oh my, this was posted in one of my endometriosis support groups and I have to share:

TIPS FOR DEALING WITH PEOPLE IN PAIN— Thank you Tanya IH Mathis

1. People with chronic pain seem unreliable (we can’t count on ourselves). When feeling better we promise things (and mean it); when in serious pain, we may not even show up.

2. An action or situation may result in pain several hours later, or even the next day. Delayed pain is confusing to people who have never experienced it.

3. Pain can inhibit listening and other communication skills. It’s like having someone shouting at you, or trying to talk with a fire alarm going off in the room. The effect of pain on the mind can seem like attention deficit disorder. So you may have to repeat a request, or write things down for a person with chronic pain. Don’t take it personally, or think that they are stupid.

4. The senses can overload while in pain. For example, noises that wouldn’t normally bother you, seem too much.

5. Patience may seem short. We can’t wait in a long line; can’t wait for a long drawn out conversation.

6. Don’t always ask “how are you” unless you are genuinely prepared to listen it just points attention inward. A better question may be one that my psychologist asks “How’s the pain level today” You can assume I am in pain so “how are you” may be almost inappropriate or superficial.

7. Pain can sometimes trigger psychological disabilities (usually very temporary). When in pain, a small task, like hanging out the laundry, can seem like a huge wall, too high to climb over. An hour later the same job may be quite OK. It is sane to be depressed occasionally when you hurt.

8. Pain can come on fairly quickly and unexpectedly. Pain sometimes abates after a short rest. Chronic pain people appear to arrive and fade unpredictably to others.

9. Knowing where a refuge is, such as a couch, a bed, or comfortable chair, is as important as knowing where a bathroom is. A visit is much more enjoyable if the chronic pain person knows there is a refuge if needed. A person with chronic pain may not want to go anywhere that has no refuge (e.g.no place to sit or lie down).

10. Small acts of kindness can seem like huge acts of mercy to a person in pain. Your offer of a pillow or a cup of tea can be a really big thing to a person who is feeling temporarily helpless in the face of encroaching pain.

11. Not all pain is easy to locate or describe. Sometimes there is a body-wide feeling of discomfort, with hard to describe pains in the entire back, or in both legs, but not in one particular spot you can point to. Our vocabulary for pain is very limited, compared to the body’s ability to feel varieties of discomfort.

12. We may not have a good “reason” for the pain. Medical science is still limited in its understanding of pain. Many people have pain that is not yet classified by doctors as an officially recognized “disease”. That does not reduce the pain, – it only reduces our ability to give it a label, and to have you believe us.

Bolded the parts that are particularly relevant to my life.

tentaclecupcakes:

just a friendly reminder

  • invisible disabilities are still disabilities
  • so don’t judge if you see someone ~*that looks able-bodied*~ taking the elevator/escalator