How a society treats its disabled is the true measure of a civilization.
My dad is disabled. I've only become more open about this in the last few years.
For a long while I just didn't see anything was different. Then one of the first people I talked to about it made horrible comments so it became something I didn't mention.
Dads disability was a hidden one for many years. I suppose in a way it still is. He has never had a real, solid diagnosis and we're coming up to twelve years. Can you imagine that? Being in pain day in, day out for 12 years. I live with him and some days I can't even believe he can stand it. We've had doctors tell him that it's this, it's that and most insultingly "it's all in his head" and my mother panders to him and makes it worse. Now they play with his medication, sign it off and he's on his way. The doctors he's seen have reached the consensus that they can't figure it out so from now on the best they will do is try to help with the pain.
Pain pills is the biggest argument inducing headache of the household. It's not unusual to be summoned just to be asked "have I taken my pills today?" "err yes." "shit." He's on so much medication that there are times when I think that if you shook him he'd rattle but it's the pill changes that are the worst.
The mixture kills his appetite stone dead which after all this time we're quite used to. However guests are not. Going out to eat is just a nightmare. He'll either order and barely touch it, eat like he's been starved or not order at all. The first time we went out with a friend he decided not to order and go for a wander instead, this obviously confused our guest so she asked if he was eating. My response of "No, he can have a bourbon biscuit or two later" didn't help matters. His diet does consist of bourbons, sausage rolls, oat and raisin cookies and beans. I've met toddlers that eat more.
Going out is a stress anyway. The last bonding experience we had was seeing batman at the cinema. We have to do reccie's for comfort before handing over money otherwise we'd be leaving half way through. Many mainstream cinemas have stairs and uncomfortable seats so finding a local cinema with sofas was a godsend. He still ended up stood up at the side inevitably being mistaken for an employee.
I'm still proud of him. I don't know anyone else who endures that kind of pain on a daily basis. This is why the governments overhaul of the benefits system upsets me quite so much. Unless you are disabled or live with someone who is, you don't know the power of "The Brown Envelope" which contains the dreaded ATOS form or an invite to one of their follow up interviews. As I mentioned Dad is never getting better, well baring a miracle or divine intervention, however they don't see it that way. He's been called for the interview/examination twice already this year. It's not a quick, clean and easy process. You get the initial letter, have to fill in quite a probing form, send it off and wait. There is a lot of waiting. In this time, people who don't know you from a stranger in the street are deciding your fate, deciding whether to give you your lifeline, the money keeping you afloat, the money that buys you necessities or in our case, the money that pays for the hundreds of pills he needs to get through the week.
Finally, a little story. I was once hailed a cab and got in, I mentioned I couldn't find the seat belt and the driver couldn't leave until I had it on. "No, the cabbie said, I wouldn't want that incase we have an accident and you end up like one of those cripples. I think they should all be shot. I mean, what good are they doing for the world." He seemed surprised when I unbuckled my belt, told him that my father was disabled and that he most definitely deserved to be alive because me and my family loved and wanted him there and got out. This moment is seared into my memory. A lot needs to be done to change god-awful opinions like his and I think that the paralympics has started to see a shift in attitude. I just hope that it continues.
