#Neurorestart calls on NHS to recommence neurology services as quickly and safely as possible in wake of COVID-19
The Neurological Alliance are running a campaign that calls on NHS England and NHS Improvement to support the recommencement of neurology services as quickly and as safely as possible.
The campaign uses a survey which shows the insights of thousands of people with neurological conditions who have shared their experiences of the COVID-19 pandemic. The evidence is clear, routine treatment and care and support have been severely disrupted, having a huge impact on people with neurological conditions, their friends and family, as well, of course, the hundreds of health and care professionals who have sought to maintain some support during these unprecedented times.
The report details the experiences of more than 1,672 people with neurological conditions who took part in the survey between 9 –20 June 2020. The report found that:
- 72% of respondents reported having had their NHS appointments delayed – 4 in 10 people didn’t know when until.
- Almost 4 in 10 people (39%) due to see a neurologist were not given a future date for their delayed appointment, leaving them in complete limbo.
- 19% of respondents felt lonely, 1 in 10 felt hopeless.
We are supporting #Neurorestart because we want those affected by Huntington’s disease to receive the best care and support from the NHS in the wake of COVID-19. We are advocating that all treatments, doctors’ appointments, counselling sessions and testing regimes be reinstated and revert back to normality so that those affected by Huntington’s can live life to their fullest, receiving the care they deserve.
Cath Stanley, Chief Executive said:
"Huntington's is a complex illness that requires specialist care and constant monitoring. The restarting of neurological and genetic services is key to people affected by Huntington's getting the care they need"
Please share this article and use #Neurorestart to raise awareness around this campaign. You can follow the Neurological Alliance on Twitter for updates and to show your support.
If you are affected by Huntington’s disease and need support or advice, please contact us on 0151 331 5444 or email info@hda.org.uk.
COVID-19 has had a dramatic effect on our way of life. This has significantly impacted our fundraising efforts, threatening our ability to help those affected by Huntington’s disease. If you would like to donate to help us support those affected by Huntington's during this time, please click here. #HDAppealCV19
The Neurological Alliance are running a campaign that calls on NHS England and NHS Improvement to support the recommencement of neurology services as quickly and as safely as possible.
The campaign uses a survey which shows the insights of thousands of people with neurological conditions who have shared their experiences of the COVID-19 pandemic. The evidence is clear, routine treatment and care and support have been severely disrupted, having a huge impact on people with neurological conditions, their friends and family, as well, of course, the hundreds of health and care professionals who have sought to maintain some support during these unprecedented times.
The report details the experiences of more than 1,672 people with neurological conditions who took part in the survey between 9 –20 June 2020. The report found that:
- 72% of respondents reported having had their NHS appointments delayed – 4 in 10 people didn’t know when until.
- Almost 4 in 10 people (39%) due to see a neurologist were not given a future date for their delayed appointment, leaving them in complete limbo.
- 19% of respondents felt lonely, 1 in 10 felt hopeless.
We are supporting #Neurorestart because we want those affected by Huntington’s disease to receive the best care and support from the NHS in the wake of COVID-19. We are advocating that all treatments, doctors’ appointments, counselling sessions and testing regimes be reinstated and revert back to normality so that those affected by Huntington’s can live life to their fullest, receiving the care they deserve.
Cath Stanley, Chief Executive said:
"Huntington's is a complex illness that requires specialist care and constant monitoring. The restarting of neurological and genetic services is key to people affected by Huntington's getting the care they need"
Please share this article and use #Neurorestart to raise awareness around this campaign. You can follow the Neurological Alliance on Twitter for updates and to show your support.
If you are affected by Huntington’s disease and need support or advice, please contact us on 0151 331 5444 or email info@hda.org.uk.
COVID-19 has had a dramatic effect on our way of life. This has significantly impacted our fundraising efforts, threatening our ability to help those affected by Huntington’s disease. If you would like to donate to help us support those affected by Huntington's during this time, please click here. #HDAppealCV19