A quarter of people with Parkinson’s have lost money in the switch from the disability living allowance to personal independence payments
Imagine living with a condition that is only going to get worse but being told you are going to lose the support you rely on. That’s the reality facing thousands of people as a result of the move from the disability living allowance (DLA) to personal independence payments (Pip), and it’s having a disastrous impact on people with long-term conditions such as Parkinson’s.
I started as a welfare rights adviser in 1986 and, while the situation wasn’t ideal back then, it was far better than now.
Continue reading...from Voluntary Sector Network | The Guardian http://ift.tt/2iH03QO
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