East Midlands: Parkinson’s patients face ‘scandalous’ standards of care in hospitals
Over six in ten people with Parkinson’s who experienced medication problems in hospital saw a significant impact on their health
Seven in ten people with Parkinson’s experienced increased anxiety when in hospital due to medication concerns
From smuggling in stashes of vital medication to daily battles over drugs – hospital can be one of the scariest places to be for people with Parkinson’s
From being forced to smuggle in medication to being subjected to shocking levels of drug deprivation by hospital staff, data commissioned to time with the launch of Parkinson’s Awareness Week paints a deeply disturbing picture of life in hospital for those with the degenerative condition – with four in ten (44 per cent) people with Parkinson’s denied regular access to the medication they need to keep their Parkinson’s under control.
Medication is a lifeline for people with Parkinson’s, with some people taking in excess of ten tablets a day as part of a strict regime just to be able to move or communicate with those around them. Over six in ten (63 per cent) of those who did not have regular access to medication in hospital felt there was a significant impact on their health.
Far from being isolated incidents, seven in ten (73 per cent) people with Parkinson’s reported experiencing increased levels of anxiety whilst in hospital because of the difficulties around getting their medication.
Understanding of hospital staff about the condition remains woefully inadequate; with just under a third (27 per cent) of people with Parkinson’s reporting that hospital staff had a poor understanding of the importance of giving medication for the condition on time – which can lead to catastrophic consequences.
Steve Ford, Chief Executive at Parkinson’s UK, explains: “Our research confirms that hospital – where people with Parkinson’s should feel safest – can actually be the most dangerous place for them to be.
“Being admitted in hospital can be difficult enough, but when that is coupled with the fear and uncertainty of being deprived of your drugs – it can become unbearable.
“Time and again people tell us that they leave hospital with their Parkinson’s in a far worse state than when they went in. Nurses tell us they receive an hour, at most, of specialised Parkinson’s training and this fundamental lack of education has resulted in people with the condition being so terrified by their previous experiences in hospital that they use their wash bags to smuggle in their medication.”
Worryingly, the research also revealed that four in ten (43 per cent) of people with Parkinson’s who were unable to take their own medication found hospital staff were unhelpful in making sure medication was given on time, resulting in over seven in ten (74 per cent) people feeling more anxious at the prospect of having to go into hospital again in the future.
Steve Ford continued: “One of the ways for the NHS to tackle this growing problem is to allow people with Parkinson’s to take their medication themselves – in fact around 70 per cent of hospitals and health boards across the UK have a system in place that would allow people with Parkinson’s to do just that, yet it is clear that these processes simply aren’t being implemented.
“Taking medication on time can often feel like the last bit of control that people with Parkinson’s have over their condition. Contrary to popular belief Parkinson’s doesn’t just makes a person’s hands or arms shake, there are a myriad of other severe symptoms that leave people feeling powerless over their own bodies and, ultimately, their lives.
“For people with Parkinson’s to continue to fight such titanic battles just to get their medication in hospital is plainly wrong. We hope that our campaign will equip all hospital staff with the right knowledge to deliver the improvements in care people with Parkinson’s so desperately need.”
Throughout Parkinson’s Awareness Week (7-13 April), Parkinson’s UK are urging hospitals across the UK to work with them to help put people with Parkinson’s back in control of their condition, by arming themselves with basic information about the importance of timely medication and taking advantage of the free education and resources open to them.