What It’s Worth to Feel Self Worth

By Dawn M. Sanders

Just as we stand on the threshold of the labyrinth of life, our position and place in society is mostly cemented – albeit with a little help from external factors, such as breaking glass ceilings or barrier gates.

I have written extensively on this stuff, such as the Right to Self-Fulfillment or the importance of agency and emancipation, so won’t repeat myself, yet it simply can’t be said enough…

I recently participated in a debating workshop where the issue was how class influences climate change and how it affects the working-class the most and a guy made the point how ‘dis-abled people are still treated as the under-class.

He’s right, but I made my habitual point when he, like so many, placed the label before people. later emphasising ‘people’ with disabilities are in fact entrepreneurs, homeowners and parents so are people first – as more than one person in the room spoke of how ‘dis-abled people are on benefits by default, so come from fixed incomes and are inherently downtrodden.

Woman cringing

I read this story the other day with interest and took to Facebook – pointing out the condescending nature of the headline, “Disabled Man is Left Heartbroken…” Okay, so a lot of people prefer or don’t mind the social model of identity language, but it’s the way the media pushes for the all-encompassing label before the person or pity – adding to an unlevel playing field.

Yet, within the article Bryan is given his agency with his name and desire to become something from the age of 2 and despite his obvious experience of discrimination by a local authority, he didn’t just want to sit around and do nothing.

On a personal note, a week ago today, I guess I hit a kind of plateau – my last year of my 5th decade, where next year will see my descend.

At the risk of my own middle-aged musings, the above story just kind of wrote the answer to my latest agonising and pondering on what the actual hell am I going to do with the rest of my time here?

While raising my son who has complex additional needs, getting him into a specialist school/college; then watching helplessly while he lost the formative years of his adulthood in decline, stagnation and isolation. I engaged with not one, but two degrees at university and several in-between qualifications. Okay, so I spent years with my head stuck in academia to gain my own since of agency and confidence in a fast-moving world, but my very first experiences of looking for work with a 6-month work visa on an American exchange programme here in the UK, were not good and fraught with the slightest reason to discriminate when I had gone from one job to a better job three-fold in the US – my country of origin.

A couple of failed businesses, a lot of political activism in staying the course as a lifelong tryer, I could well empathise with Bryan.

So, when I read his story and how his mother has advocated for him and complained of how he has been treated, I just thought, so if he gets that kind of treatment as a young man, who’s going to want me, out of the job market for decades, aging and oh, let’s not forget with a severe visual impairment?

As I have to stand and fight, fight, fight because, the hearings have continued after ten agonising years defending my family’s human rights and autonomy in court. Grovelling with the trail of pain it has caused my tiny family – the sadness, losing myself to my son’s needs, worries and of course my own need to literally do something for myself, the community and my political conscious – I have had to do this Eeny-meeny-miny-mo thing of:

Maybe do some volunteering but, would I be valued? Maybe try to relaunch Barriers to Bridges, the online platform I founded which formerly provided some of the most marginalised in society, a voice, but it needs to be sustained and monetised.

Get more involved politically, locally – well, I’ve tried and the cliquey nature of Exeter and the southwest often looks like no entry signs with a superficial or fickle veneer – different from the north where it’s more working-class and warmer, despite the cooler temperatures…

I know, I know it all sounds like a lot of excuses and self-built barriers, but I need to be pragmatic with lived experience and wariness of all the new challenges within journalism itself – AI, the danger in being left-wing or just outspoken, but I’ve started with writing this, got the bright red fire back in my hair and nearly under my ass. Yet, with a never-ending battle comes exhaustion, black clouds and the deafening isolation and depression – whether I’m sitting in a crowded pub or within the sanctuary of my home, not to mention the sheer lack of motivation and lost confidence.

Like Bryan in the above story, I’m all too aware of the need for self-worth, my son’s need for self-worth and the burning desire to contribute to the world – use my skills, intelligence and lived experiences.

From the sounds of how Bryan describes his feeling of self-doubt after such a calloused rejection – I bet he wouldn’t mind being described as Bryan the binman – A Young man with his determination intact. Not “dis-abled man Rejected Twice after working for free.” Okay, it rightfully highlights the injustice is routinely faced by people with disabilities who often have to work harder to prove themselves and for that it has to be commended.

Nobody can put a price on self-worth and the confidence or since of wellbeing it brings us.

STOP DISSING AND START EMPOWERING

By Dawn M. Sanders

Last week witnessed the unleashing of, not only a budget and economic pledges or predictions we all feared, it was laced with the all-too-familiar ideologies embraced by the Tories.

Dawn Sanders at home
Dawn Sanders at home

We have a complex housing bill not yet understood by many, the rush to make every school (primary or secondary) an academy and most noteworthy, the further cuts to welfare benefits – adding to the despair of austerity.

So, focusing on the ‘dis-ability cuts as they are inevitably coined, I’m taking this opportunity to turn it all on its head by trumpeting my passions for equality, empowerment and true dignity…

Take note: I won’t be placing that all-prevailing, crippling label the main stay in this country insist on preceding before us as ‘people first’!

I have argued this point of contention time and again – mostly with ‘people’ with additional needs themselves and, I’m sticking to my guns!

My visual impairment is of course an integral part of my identity, but certainly not the first among equals in being a woman, mother or journalist…

A ‘dis-abled computer mouse is one that doesn’t work, ditto for toilets, cars etc.

Is it overly PC nit-picking? I think not…

As a journalist and writer, words, the connotations behind them and what they represent are hugely meaningful – especially when you’re on the receiving end of those negative connotations, such as lesser than, subordinate, weak – I could go on, but you get the gist.

The point is, just because I and others are visually impaired (or otherwise) doesn’t mean I can’t raise my son single-handedly as I’ve done; I still cook clean and maintain my home; I still have relationships with people in the human way most would expect and, I even enjoy some of life’s more clandestine pleasures…

This all isn’t to say for a second, that I and others don’t get blatant discrimination, especially in looking for work, social environments or on an equal playing field in the game of meeting a possible partner – in fact, being visually impaired, hearing impaired, wheelchair user, with learning/cognitive  difficulties, is often an extremely isolating place to be.

However, the argument of the so-called “social model” which dictates all of these social/practical constraints should dub us as ‘dis-abled to the tune of how society sees myself and others is simply backwards.

It all hinges on, what one cannot do, rather than, what one can do…

Enough said, so when people go out in force – protesting their benefits are being taken away against a backdrop of: “Is This Any Way to Treat ‘dis-abled People” as the banner read, I’m insulted at being considered inherently vulnerable or fragile.

These people who, insist on milking an entrenched victim culture, one I have to fight against every day to “prove myself” a capable parent, employable or dare I say it, a sexual being, are ‘not doing me any favours’!

I’m forever infuriated at being lumped in a category of the “sick and ‘dis-abled” as people with long term illnesses have their own specific circumstances and anyone with severe/complex needs, is an individual – there’s never a one-size-fits-all…

Ultimately, do we not have the right ‘not to be impoverished’?

Why aren’t the likes of Dis-abled People Against the Cuts crying out for more equality in the workplace, employment or closing the loopholes within the so-called anti-discrimination act.

Yes, this government and its ideologies have handed us a double-edged cross to bear: on one hand, because we are rarely taken for our hard earned merits and qualifications when job hunting. For example,  when employers take one look at me I get: “’Uh, how would you manage the stairs, finding the toilets – all delivered with an uncomfortable demeanour…

On the other hand, we’re told we’re scroungers if we’re not working in an environment which doesn’t give us half a chance and, supposedly the government is trying to get us into work?

So, what are they, the ideologists, doing to close the gap of discrimination for those of us who want to use our skills?

Nothing!

The DPAC (‘Dis-abled People Against the Cuts) movement is a short-sighted reactionary group – not offering solutions to the poverty trap most people with additional needs find themselves in – clinging onto the benefits system like a life raft.

In milking the victim culture, they don’t place us on an equal footing when the perfectionist bandits – standing outside nightclubs refusing to let us in under the guise of, health & safety or, we just couldn’t cope with a rough & ready mosh crowd.

By insisting to maintain the lowered status within society’s pecking order, those protesting against benefit cuts really should be protesting on why we are sentenced to a life absent of the same opportunities, most people simply take for granted.

Yes, the benefits we rely on help with added expenses: such as increased taxi fares, holistic therapies managing specific conditions or mobility equipment; (all of which should be secured) but being on state benefits is not an independent or dignified path and one which leaves us wide open to the shenanigans of the state.

Granted, there are those who cannot work due to their conditions, be it mental or physical, yet that should never be the thrust of what is perceived to be living “dignified lives?”

No, in my book of cross-cultural experience, dignity hinges on what I ‘can do’ and making it possible!

I want an empowering campaign which says: yes, I have limitations and additional employment/educational/support needs, but can still contribute to society in a meaningful way.

I want a campaign which says, I have to work harder, so deserve EQUAL PAY, OPPORTUNITIES promoting me as a social/sexual being. Not a campaign/culture of downtrodden, institutionalised oppression…

GET IT?

http://www.theguardian.com/society/2016/mar/23/disability-campaigners-occupy-parliament-over-benefit-cuts