Huffington Frenzy

Recently I’ve had a few comment pieces published on the Huffington Post website.

Most recent is one about an experience going for an MRI scan at a private health clinic through my GP. Called “Is The A Taste Of Tomorrow’s NHS? it describes my nightmarish trip to be scanned in all it’s glory.

Before that I wrote about some people’s obsession with the idea that faith can cure disabled and sick people in “Faith? Please Cure Us Of This Myth“. It might seem that there is truth in the idea but I ask is that right or even helpful?

To start the whole frenzy off I had my ode to love, luck and my wonderful wife Diane “Oh, Lucky Man” published. So glad they accepted it as it was our 8th wedding anniversary that week. Di loved it, I hope you do too.

On top of that I had my travel article on our recent trip to Barcelona published on Disability Now Online, “La Merce: a weekend in Barcelona” and if you want to read back issues of PosAbility magazine with my column in you can do it online now.

All this of this writing was drafted using a pen and paper. Old fashioned I know but I am currently studying a Creative Writing course at the OU and they advise students to do it this way. It really helps too. You can get those ideas out without fighting with a keyboard or other bits of tech. I really am a Luddite Mik eh?

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Pride… and Prejudice.

In my last blog I wanted to further explore some of the press I had done around my choices not to go ahead with trying to walk. I was shocked, and a little saddened by some of the replies and comments I received in reply to that blog.

The idea that disabled people can live lives that able bodied people might envy seemed to upset some disabled people. Yet surely the disability movement has spent years trying to get across the fact that disabled people deserve the same chances and rights as everyone else, and if given them disabled people would be able to experience life just the same as the able bodied. So why shouldn’t some able bodied people be envious of some disabled people? Disability is not a reason why anyone’s life will be less in some way.

Now of course many disabilities come with medical conditions. I have a spinal injury, and so am classed as Paraplegic, but the injury caused some nerves to be trapped in scar tissue. This leads to periods of chronic pain, and the pain killers I have had to take has led to problems with my digestive tract. These do disable me, but they are really ongoing medical conditions. Using a wheelchair will never make my life less that it would have been if I could walk. I think it is essential to make sure we understand the difference. I never wake up thinking “I wish I could walk” but I do wish “This pain would stop”. Yes, the pain is tied to the disability, but it is not the disability.

I hope that everyone agrees that disability as described by the social model is the way it should be viewed by society. So I am not disabled by my inability to walk, or by my pain or anything else but by the barriers put in my way by the larger society. It’s not being in a wheelchair that makes me disabled, but the steps into a building. That goes for all of us disabled people. In fact it goes for everyone. Everyone gets old, or sick. In a world that was shaped by the social model of disability and so was fully inclusive, many of the issues that they will face would not exist. It wouldn’t matter if they had trouble walking, or seeing or hearing, or needed a seat or whatever. The solutions would be built into every part of our daily life and the world we all lived in. Any medical issues would be just that. Separate and something to be treated.

At a time when the disabled, the elderly, and the poor are going to be a the sharp end of budget cuts, and when many people in society really believe that assisted suicide and mercy killing is a valid way to go, we disabled people must see that we need to be vocal. We need to shout how we are capable, and can experience anything we want to, if we are given the chance. We have to be proud of how we have got as far as we have, both as individuals and as a group. In 100 years we have fought to go from being shoved into institutions and pitied or feared, to living in the community and having a voice and shaping our own futures. We have made amazing strides forward and must keep on fighting to make sure we do not stumble and loose ground.

My story is a strange one, I admit. Not many disabled people have to make the choice I have recently, but as science advances more and more will. That decision will be up to the individual but I wanted to explain that being cured is not the answer to integrating disabled people. To integrate a minority, the answer is not to correct or eradicate the minority. If we go down that dark road then why not make gay people straight and black people white? Or just wipe them all out? Sounds familiar to me. Who tried that already?

No matter how much a disability, and it’s medical problems, effect your life, or how much you may sometimes feel that it gets too much, every disabled person on this planet has the ability to live the kind of life that would make able bodied people envious. We can find love, feel fulfilled and be happy. I know how few able bodied people manage to achieve that. Yes it can be a real struggle, but it is for everyone on this planet. It’s the extra barriers that are put in our way and the ignorance of what we can achieve that are the enemy, not our disabilities.

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