BBC BLOGS - The Ouch! Blog It's a disability thing

House of Commons overturns Lords amendments to welfare bill

Linda Debrah | 13:18 UK time, Friday, 3 February 2012


It has been a week of political ups and downs in benefits and social care.

Coalition plans to cut payments to families with disabled children were rejected by the House of Lords in a seventh defeat on Tuesday.

Neil Coyle, Director of Policy at Disability Alliance said:

"The government's decision to continue on a path which will deny help to thousands of disabled people and leave many more families in poverty is a bitter blow. It is hugely disappointing for the many disabled people and their families who have raised concerns with MPs and charities in an apparently vain attempt to ensure their voices were heard".

On Wednesday, the Bill with amendments from the House of Lords was overturned in the House of Commons. In the next stage, we will see the Bill back in The Lords possibly for an old-fashioned upper and lower chamber game of ping pong. Convention tends to dictate that the upper chamber will eventually concede to the will of the lower elected chamber. Charities have been out in force condemning the government for its actions.

Ministers argue the money saved will be spent on providing additional support to the most disabled adults.

In other news

All disabled people deserve the care Rick Santorum's daughter gets - SE Smith, The Guardian

Syndrome without a name: Living without a diagnosis - BBC News

EasyJet profits, while disabled passengers lose - The Guardian

Disability app designed by London terrorism survivor - BBC News

Why do some people never get depressed? - BBC News

Disability charity bus stolen in Manchester - BBC News

New study sheds light on why autism diagnosis can be so difficult - Huffington Post

">'Hollyoaks' bosses to cast deaf teenager - Digital Spy

Cinema opens up for Morocco's blind - BBC News

Autism: Brainwaves 'show risk from age of six months' - BBC News

Alastair Campbell: MPs should talk about mental health - BBC News

Measures 'reduced suicide rate' - BBC News

London 2012: Disabled artists tackle Olympic challenge in medieval town - BBC News

My Down's Decade (Disability Dads series)

Guest Guest | 12:02 UK time, Friday, 3 February 2012

Stan Palmer has Down's Syndrome. As his tenth birthday draws closer, his dad Steve blogs about the first decade in 'Down's world', for the first of our series on dads and disability.

Ten years ago, my sometime blokey self was looking forward to a date later in 2002 when I imagined both of my perfect children, my three year-old and my yet-to-be-born son, would be sleeping through the night and everything would be going smoothly. But, now I know what I know, I'm grateful for Stan, arriving - with an extra chromosome - like a juggernaut through my hopes.

I would probably have hit middle age with an air of unattractive parental smugness had it not been for him. It's amazing what a massive change of perspective can bring.

Flash forward. On New Year's Eve 2011, a totally different me, with ten years Down's dad experience under my belt, I found myself in a pub disco with Stan, dancing to the camp classic 'It's raining men' by The Weather Girls. And I was blissfully happy.

So, how did I get from 'pipe and slippers' to becoming an active and positive 'disco dad'?

It's 2002. I'm holding my son and I've just been told he has Down's Syndrome. I place him in his cot, and I'm a bit shocked ... I'm not sure I can deal with it.

I've always been haunted by this memory - at the moment he most needed me, just after he came into the world, I appeared to be rejecting him.

When I think about how we reacted on the day he was born, I feel silly. After being told, I spent the first few hours in a denial phase, looking to see if the fold in his hand went straight across - apparently a sure-fire confirmation of the syndrome - when in fact I just needed to look at his face.

A day later, the silliness stopped. I had my 'get it' moment in Homebase. I don't know why I'd nipped out to the DIY superstore with all that was going on around me, but I did. And I fell in love with Stan whilst there.

I was at the till when I suddenly realised that I had two sons now, not one, and that Stan needed me. I got my act together just in time. Right there, amid the tools and hardware, Project Down's Dad had begun. I was on The Mission. 'The Mission' was to achieve the best life possible for my son and to teach people along the way.

If the ghost of birthday future had appeared and listed what Stan and we, his family, would accomplish in the following ten years, I wouldn't have believed it.

• When Stan was four, our experiences were turned into Petal's story on EastEnders, when a child character with Down's was born to Honey, one of the main characters on eastEnders at the time.

• He's been the star of two Christmas pantos.

• He's conquered electronic devices with ease.

• He's been horse riding.

• He's received many awards at his school.

• And more besides.

A mate of mine reminded me today that when he heard Stan had been born with Down's, he was concerned, but that he knew that I was the man for the job. You know, Down's Dad. And once I'd had the DIY store / road to Damascus moment, I suppose I just got down to it. The Project. The Mission.

In the last ten years, I've written blogs, appeared on radio shows and generally been a Down's activist much like Eva Longoria from Desperate Housewives, but without the looks. But it's equally important to have a normal family life, and to be seen to be having one.

If we all go out to eat, Stan isn't the centre of attention. He tries to be but he is included equally, one part of our family. The extended family all love Stan; they've all watched him grow up to be a cheeky, exasperating, lovely boy and they contribute to his life.

We also have support from a local group. It's great that we can all get together and share ideas, and, at times, our worries.

Looking back at this decade, there is one thing I'm particularly proud of, that's bonding with other Down's dads.

A group of us now regularly go out for a curry and it's just a really good time to have a chat, about non-Down's stuff, and about Down's stuff.

Those dad conversations have been perhaps the most intense and satisfying discussions I've had about the issue.

I've written on my personal blog about why it's important for men to have their own time to discuss issues. We lads can be a bit backward in coming forward, and it's important for us to be fully involved with schools, hospitals, doctors and all the appointments our kids tend to have. And the really good news is that, this year, Stan has a male teacher too.

The other good news is that the Mums are so impressed, they're now doing their own curry night.

At Stan's tenth birthday party, many of his classmates will be there. We use to worry that he'd never have any friends but, these days, they're queuing up. And why not? We're so proud of both of our children.

And yes, in this blog I've left out some of the difficult times because, today, we celebrate ten years of a life less ordinary. He's survived two heart operations - a common complication in Down's - he's established himself in a school where he's part of the furniture, and he's single-handedly educated a whole swathe of people about Down's just by being himself.

At the disco on New Year's Eve, the other members of our party abandoned the dance floor and it was just me, Stan and The Weather Girls. And I had one of those dad-son moments that I dared not to dream about ten years ago.

I'm going to have to break off now. I've just got into trouble for not taking Stan his drink. Instead of being the great Down's Dad on The Mission and getting mucked in, I've been caught writing a blog entry about it.

Stan says hello.

The Disability Dads series continues next Friday.

Are you a dad to a disabled child? Do you have a support network like Steve or do you go it alone? Tell us in the comments below.

Talk Show 82: Ruby Wax finds her people

Emma Emma | 12:21 UK time, Thursday, 2 February 2012

Ruby Wax with Rob, Liz and Emma

Comedian Ruby Wax pops by to talk about her new social networking site for people with mental health problems. Kevin Mulhern pulls apart the latest on welfare reform and Meet Jody Cundy, top GB Paralympic cyclist. Liz Carr and Rob Crossan present.

Listen to or download the show by following this link

Read a transcript

• Liz and Rob discuss living life in your head when physical activity is not an option. Does it do your head in? They get sporty with Tony Garrett and speak to the fastest Paralympic cyclist in the world, Jody Cundy who talks about his decision to switch from swimming to cycling in 2005 and what he and sprinter Oscar Pistorius have in common.

• Comedian and TV personality Ruby Wax joins Liz and Rob in the studio. Ruby remembers the moment she came out as having a mental health problem. She talks about Losing it, the successful two-woman stage show which followed and introduces blackdogtribe.com, her new social networking site for people who experience mental illness.

• Ruby stays with us to play the Vegetable Vegetable or Vegetable game, where we guess the disability of the person on the line. Lets just say Ruby takes to the game like a duck to water. But does she get it right? Listen and find out.

• Blind TV producer and disability commentator Kevin Mulhern reviews the month in disability news. Nothing if not opinionated, he expresses views on the welfare reform bill, budget airlines and press reaction to so-called miracle cures.

• Meet Kalyn Heffernan, MC and producer with the US hip-hop group Wheelchair Sports Camp. She explains where the band name came from and introduces her track, Smells Like Funk.

Pod Talk

You may imagine that our meetings are full of pastries and delicious coffees from the BBC budget, sadly this isn't the case. But this month, I did take some sweets along to our recording for the first time . They went down a treat with presenters, producers, guests and facilitators alike. It did however result in some lines having to be repeated due to excess crunching, sweet bag rattling and sugar induced hyperactivity.

We did record some enlightening and intriguing extra bits, so look out for a valentine's themed Podcast Extra later in the month.

In the meantime, cosy up warm and enjoy Ouch! Talk Show 82.

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