Harefield Gazette

Dying while waiting for urgent financial support

CAMPAIGNER­S SAY HAVING TO PROVE UNIVERSAL CREDIT CLAIMANTS HAVE SIX MONTHS TO LIVE IS ‘INHUMANE’

- By JACOB PHILLIPS Local Democracy Reporter @myldn

THOUSANDS of terminally ill patients in London have been forced to sign up for Universal Credit when they have less than six months to live.

In the past three years, 7,485 people in London have applied for urgent support after being diagnosed with a terminal illness, including cancer.

Patients can get emergency access to benefits payments and at a higher rate if their doctor says they have six months or less to live.

But around 100 people in the UK died before they got their end-of-life payments.

In Croydon, 102 people applied for end of life benefits in the last year while 95 people applied for the emergency payment in Ealing – a Freedom of Informatio­n request from the BBC Shared Data Unit reveals.

A high number of people applied for the end of life payment in Greenwich (82), Bromley (85), Hillingdon (69) and Hounslow (69).

The number of people applying for the payment was much lower in Central London.

There were 29 people who applied for the end of life payment in Hammersmit­h and Fulham last year while 13 people applied in Kensington and Chelsea.

Around 23,000 people a year apply to the Department for Work and Pensions for support after being diagnosed with a terminal illness.

End-of-life campaigner­s are now worried that Londoners are being left stressed waiting for payments in their time of need.

Many terminally ill patients have also been left without payments as they are unable to prove, or do not know if they have six months to live

Madeleine Moon, former Labour MP for Bridgend, has campaigned to remove the six-month time limit and replace it with a clinical judgement made by a doctor or nurse.

Mrs Moon, who lost her husband Steve to motor neurone disease, said: “The cruelty, if not the inhumanity, of the current system is shocking.

“We are asking people to say ‘I’m dying’ and the last thing they want to say when they are dying is that.”

Motor Neurone Disease Associatio­n charity chief Susie Rabin added: “Frankly, the Special Rules for Terminal Illness process doesn’t work for some people.

“It’s a real challenge for people with Motor Neurone Disease (MND).

“MND is very unpredicta­ble which makes it very, very hard for a clinician to give a prognosis and that makes it very hard for people with MND to access benefits through the special rules route. “One third of people die within one year of diagnosis but it’s very difficult for an experience­d neurologis­t to say how long a patient has left.” Reforms have been promised by Westminste­r, which will extend the six months end-of-life rule to 12 months. But critics say the timetable for reforms is unclear, and that the proposed changes – although an improvemen­t – do not go far enough. They have called on the Government to scrap the requiremen­t for people on terminal illness benefits to be reassessed every three years, and to accep t the prognoses of medical practition­ers. A DWP spokesman said: “Terminal illness is devastatin­g, and our priority is dealing with people’s claims quickly and compassion­ately. “Those nearing the end of their lives can get fast-track access to the benefits system, with the majority

The cruelty, if not the inhumanity, of the current system is shocking Madeleine Moon

receiving the highest possible award and paid within three days of making a claim. We will be extending the current six-month end of life rule to 12 months so more people can get the vital support they need.”

 ?? ?? Madeleine Moon
Madeleine Moon

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