Dispelling myths about disability

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The following blog was published in the Huffington Post and I think it is worthy of some comment and discussion. Please feel free to leave your opinions.

Headlined Basic Myths about Disability I Can’t Believe We Still Have to Debunk, the original blog was written by Sarah Blahovec, pictured left, described as an advocate for individuals with disabilities. Her words are in medium type, mine are in bold.

To be honest, I was really hoping that what I’m about to write was common knowledge by now. I really wish that society in general understood disability better, but in light of a number of concerning articles recently, from a USA Today article about people “faking” disability during travel, to a New York Times Magazine article about parents stunting the growth of disabled children through estrogen treatments, it seems necessary to counter the basic inaccurate beliefs people have about disability and those who live with it. Below are a few of the most popular myths.

Myth: If you’re in a wheelchair, you can’t walk

This week, a USA Today article called out “fakers” who allegedly make up a disability to get special privileges when traveling. In this article, examples include people who are able to stand in a buffet line or in the airport, but are later seen in wheelchairs during priority boarding. The author seemed incredulous that somebody who used a wheelchair could also stand, and accused those who are able to stand of faking a disability.

This is true, I can walk about 15 metres with assistance and stand for maybe two minutes but otherwise I do need to use a wheelchair.

Truth: You do not have to be paralysed to need a wheelchair

There are millions of individuals with invisible disabilities in the United States. These disabilities are not immediately apparent, but the pain and other symptoms that come along with them can be extremely debilitating. Take, for example, Multiple Sclerosis. MS is a disease in which the immune system attacks the myelin that covers nerves, damaging the central nervous system. Symptoms include fatigue and mobility issues, and vary from day-to-day and severity. About 400,000 people in the United States and 2.5 million people worldwide have MS. Keep in mind that this is just one invisible disability that can cause someone to need a wheelchair without being paralysed. There are many other disabilities and diagnoses that can cause chronic pain, fatigue, mobility problems, and other symptoms that necessitate a wheelchair.

It is true that paralysis is not required, nor should it be expected of someone using a reserved parking bay.

Myth: Only people with mobility disabilities have an accessible parking placard

On a similar note, we’ve all seen articles in which someone has left a rude note on the windshield of someone who “doesn’t look disabled” but has parked in an accessible parking spot. The people who leave these notes probably think they are being good Samaritans, protecting those who are “truly in need” from those who borrow grandma’s placard. However, they are neglecting, and possibly targeting, those with invisible disabilities.

It is certainly aggravating to see someone park in a space reserved for someone with a disability, only to see him or her walk away swiftly and unaided. Time to check for a disability card!

Truth: There are many conditions beyond visible mobility impairments that necessitate a parking placard

Heart conditions. Postural Orthostatic Tachycardia Syndrome. Lung disease. An amputation that may not immediately be visible. Fibromyalgia. People with invisible disabilities may not “look disabled” to you, but they are. They received the proper documentation from their doctor, and they went through the process to receive a placard. Chances are that when you’re calling out someone who “doesn’t look disabled” for parking in an accessible space, you are actually targeting somebody who has one of these or many other conditions that qualify them for a placard. You might even cause stress and worry that worsen their symptoms. So, instead of passive aggressively leaving a note on a windshield, leave the policing to police, and understand that the person who just parked in that space and walked out of their car may have challenges that you cannot see.

Yes, there are invisible illnesses and disabilities that are not always obvious and we shouldn’t always judge by first impressions. But some parking cards DO get abused by family members, so it never hurts to ask someone if he or she has a disability.

Myth: “Disabled” is a negative word. It’s always better to say “person with a disability”

There are a number of resources on people-first language (PFL). The mantra “see the person, not the disability,” has become extremely common when talking about disability language. Many people insist that this is the “proper way to talk about disability”—even going as far as correcting the language preferences of the disabled. I have been corrected about saying “disabled” instead of “person with a disability,” and I know many others who have received the same criticism.

Here, I need to state my opinion clearly. I wholeheartedly agree with everyone who says ‘I am a person with a disability’. I am me, describe me as a journalist or as a blogger. By all means say that I am a journalist/blogger who has multiple sclerosis or who has a disability. But never, ever, describe me as disabled.

Truth: Many disabled people prefer identify-first language (IFL)

Within the disability community, there is a popular school of thought called the social model of disability. The social model of disability does not see the group of people known as “disabled” as disabled by their individual impairments (the “medical” part of their disability), but by the fact that society does not consider their differences normal, and therefore does not accommodate them. In this train of thought, someone in a wheelchair is not disabled by not walking. In fact, using a wheelchair is just as natural to them as walking is to those who walk. They are disabled by the fact that a building does not have accessible ramps. The deaf are not disabled by their inability to hear, but by the fact that there is not an interpreter, or there is no closed captioning on a video.

Because of this, many disabled people see themselves as disabled by society. They see their disability as part of their identity, as a fundamental part of their experiences as a person. They do not separate the disability from themselves. It is not something that they carry around; in fact, many see PFL as an erasure of the obstacles they face, just like those who call themselves “colorblind” to race fail to recognize the pervasive societal obstacles to racial minorities.

Anybody has a right to determine their language preferences. Some like PFL, and some like IFL. Their personal preferences should be respected. To correct those who use IFL because they do not separate themselves from disability ignores the fact that they have a very legitimate reason to identify themselves in this way.

If that is how some people prefer to identify themselves, then that is their right. But those of us who prefer ‘people first’ have our rights too.

Myth: Disabled people are so inspirational. Look how they manage to live with such a burden!

Society largely views the disabled in one of two ways: as objects of inspiration, or as objects of pity. In both cases, the disabled are objects of the (non-disabled) person’s viewpoint. This is reflected in feel-good news stories: the football captain invites the disabled girl to prom. The restaurant employee is seen helping a man in a wheelchair eat. It is also reflected in popular memes: one you might be familiar with is the young amputee running on running blades, with the caption “the only disability in life is a bad attitude!”

In the disability community, this is known as Inspiration Porn, a term coined by late disability activist Stella Young in her iconic Ted Talk. The disabled are used as objects of a story to make non-disabled people feel better about their lives or humanity. Most of these stories also fail to interview the disabled person, but will interview other actors, such as the good Samaritan or the disabled person’s family. When the disabled say that they don’t like these stories, they are often told that they are bitter or ungrateful. After all, someone is being nice to you. Why don’t you accept it?

This is a good point. Years ago, I was involved as an adult leader in the Scout movement in the UK. There were numerous awards and commendations given for outstanding feats such as saving a life. All well and good, but I could never agree with the notion of presenting an award to a young scout for ‘bravely’ coping with an illness or disability. I saw this as an example of ‘Inspirational Porn’.

Truth: Disabled people are just people, and want to be treated as such

Inspiration porn is infantilising and condescending. It is a type of reporting that operates under the assumption that the disabled have lives that are inherently less enjoyable or valuable than non-disabled lives. When they get out of bed in the morning, live a normal life, and do everyday things, they are just so inspiring! This narrative promotes the idea that the disabled are in need of help or encouragement in doing basic tasks, and that people who help them with these tasks, even if they are not asked for their help, are heroes for helping them. However, when it comes to real things that the disabled want to do, such as hold a job or participate in a sport, they are immediately seen as a liability. After all, if it is such an achievement for them to get out of bed every day, how could they possibly perform at the same level of a non-disabled person?

It is true that we should all be kind to each other, and the football captain who invited the disabled girl to prom was doing a nice, innocent thing for a friend. That isn’t wrong, as long as it involves actions that are truly wanted by both parties (as opposed to unsolicited and unwanted help or attention). Kindness isn’t wrong. What’s wrong is that acts of kindness towards the disabled have become a genre of media that reduces disabled people to objects of pity or inspiration in stories that focus on the “heroic” actions of the non-disabled. We don’t want that. We want to be recognized as regular people. We want others to understand that our disabilities do not make our lives less valuable or less enjoyable; in fact, many of us take pride in our disabilities. In the words of Stella Young, we are not your inspiration. We are normal people, and we deserve to be treated as such.

I am not at all sure about the phrase ‘many of us take pride in our disabilities’. Certainly, I have no pride in having MS but choose to deal with it positively – by ‘living with it’ and not ‘suffering from it’.

Don’t be shy, please let me know your thoughts on all this.

 

Manufactured ‘evidence’ is not real evidence

maddie

Whatever happened to Madeleine McCann on the night of her disappearance from the family’s holiday apartment in Portugal in 2007 has been a hotly-debated mystery ever since.

Was she taken from the apartment in a pre-planned abduction, did she wander outside and be snatched by an opportunist, did she die inside the apartment, were her parents involved or are they innocent? These are probably the most popular theories but that is exactly what they are, theories; as of now, no-one seems to know the truth. And, if they do, they are not telling.

In courts all over the world, witnesses are required to swear or affirm, to make an oath to tell the truth; exact wording may vary but it will be something along the lines of “… that the evidence I give will be the truth, the whole truth and nothing but the truth”.

That is the key to what is legally defined as ‘evidence’. It needs to be the truth as far as the witness knows it, with nothing left out and nothing added in the way of opinions, supposition or hearsay – that is something heard from another person.

The only opinions allowed are from expert witnesses duly qualified in their roles.

There are, of course, room for various theories being checked out during the police investigation of a case, different leads are followed and many lead nowhere. That is only right as detectives should have open minds and no leads should be ignored. Similarly, people are often sought after being seen close to the scene of a crime – only to be eliminated from further enquiries.

When a case gets to court, however, those theories have gone. The court wants to hear the facts, the truth and nothing else.

Ok, there is often conflicting evidence given by prosecution and defence witnesses but, usually, it become obvious to jurors what is the truth.

In the case of Madeleine debate, however, there have been a number of instances of creation of supposed evidence to create backing for one theory or another – most often in support of a theory implicating her parents in her disappearance.

Now, I don’t know the truth; nor am I pushing forward any theory. Whether or not Kate and Gerry were involved is not my concern right now. I am just saying that it is extremely misleading for anyone’s words or pictures to be used out of context. It distorts the truth.

Such ‘evidence’ is actually influenced by opinion; it is not factual. As such, it would be inadmissible to a court and is unhelpful to everyone who is keen to find the truth.

As for my opinions, and I must stress that they are just that – opinions, do I believe that Madeleine will ever be found alive? Sadly, no. Do I think that we will find out what really happened? Again, no. Was she abducted or did she die in the apartment? I have no idea, the evidence so far is inconclusive. Were her parents involved? Once again, I have no idea but there is no evidence that they were, so ’innocent until proven guilty’.