Personal
independence payment (PIP) was introduced in England, Scotland and
Wales in 2013, replacing disability living allowance (DLA). The
benefit is supposed to cover some of the additional costs of having a
long-term health condition, and is available to people in or out of
work. It is worth up
to £87.65 a week
to
meet daily living needs, plus up to £61.20 a week for the mobility
element, depending on assessment.
But
since PIP was introduced, 65% of claims from people with epilepsy who
did not have DLA were rejected, while 54% of those in receipt of DLA
were turned down for PIP, the second-highest refusal rate of all
health conditions and double the national average. Of those who
challenged the decision 78% won on appeal.
According
to Epilepsy Scotland, which obtained the figures, the benefit
assessment system is flawed because it fails to take account of
fluctuating conditions like epilepsy. Claims assessors focus too
heavily on the type and number of seizures a person has, while
ignoring other symptoms like memory impairment, confusion, anxiety
and depression.
Frances
Brown, Epilepsy Scotland’s welfare rights officer, says: “About
70% of my work is PIP-related. Since 2017 we have had to double our
workforce to cope with demand and have recovered £1m in unpaid
benefits, including PIP.” Being denied
PIP brings financial hardship but also damages mental health. “We’ve
had numerous people tell us that they don’t want to be here any
more – that they have had enough,” says Brown. “It’s that
feeling of not being believed – of not being listened to.”
Epilepsy charities in England and Wales are also reporting soaring demand for help. Daniel Jennings, senior policy and campaigns officer at Epilepsy Action, says the number of people contacting their helpline about PIP rocketed by 123% between 2016 and 2017. “Many people use that benefit to travel to work on public transport, as a lot of people with epilepsy can’t drive. If people lose that money, they lose the one thing that might give them their one bit of independence,” he says.
An early-day motion, signed by 34 MPs, expresses “serious concern” at the number of people with epilepsy being denied PIP, and “alarm” at rejection rates.
https://www.theguardian.com/society/2019/jun/12/disability-benefits-claimants-epilepsy-denied-payments-cost-living
Epilepsy charities in England and Wales are also reporting soaring demand for help. Daniel Jennings, senior policy and campaigns officer at Epilepsy Action, says the number of people contacting their helpline about PIP rocketed by 123% between 2016 and 2017. “Many people use that benefit to travel to work on public transport, as a lot of people with epilepsy can’t drive. If people lose that money, they lose the one thing that might give them their one bit of independence,” he says.
An early-day motion, signed by 34 MPs, expresses “serious concern” at the number of people with epilepsy being denied PIP, and “alarm” at rejection rates.
https://www.theguardian.com/society/2019/jun/12/disability-benefits-claimants-epilepsy-denied-payments-cost-living
No comments:
Post a Comment