Following on from my long and detailed analysis of the coalition government’s potential position with regard to Disability Living Allowance (DLA), I urge you to read @BendyGirl’s post on what DLA means to her.
It’s an exceptional post, and highlights just one case of thousands relating the difference DLA makes in everyday lives.
Here’s an excerpt, though I urge you to read the rest:
So, as someone who can’t even sneeze without dislocating a rib I don’t receive any support from the local authority, the justification being that I can manage. And, to an extent I can. But I only manage because I receive DLA. The care component of DLA allows me to purchase support, and the mobility component to fund transport costs in whatever way I see fit. I use my DLA for things as diverse as paying someone to provide care, through to the additional heating I need to keep warm, pretty much year round, ready prepared food, physiotherapy or grocery shopping on the internet. At the moment I’m using my DLA to fund the cost of a mobility scooter and the costs of the adaptations needed to allow me to have that mobility scooter at home. Without DLA I would immediately lose my ability to cope by paying for these extras and have no choice but to throw myself on the mercies of the local authority. As would every other disabled person, and as most of us fall into the ‘considered to be coping’ category that would be an awfully high proportion of disabled people suddenly having to be admitted to hospitals until the local authorities could figure out some way of either providing the support they require or passing off the responsibility to the NHS.