May 082021
 
DPAC Logo with text underneath "Disabled People Against Cuts" and then web address dpac.uk.net

The People’s Covid Inquiry has been called by campaign organisation Keep Our NHS Public.

The Inquiry has been hearing testimony from many witnesses and takes place with support from a wide variety of individuals and organisations including Disabled People Against Cuts.

The Inquiry Panel, is chaired by Michael Mansfield QC.

Find out more including how you can have a say see: Home | PeoplesCovidInquiry
The next session Profiteering from the people’s health? will be held on Wednesday 19 May from 7pm with witnesses including:

David McCoy – Professor of Global Health Medicine, Institute of Population Health Sciences, QMUL; Centre for Health and the Public Interest

Dr David Wrigley – GP in Carnforth, North Lancs, Deputy Chair BMA, co-author ‘NHS for Sale’ and ‘NHS SOS

Caroline Molloy – Editor at openDemocracy and ourNHS/openDemocracy

Dr Michelle Dawson | NHS Consultant Anaesthetist, trustee Healthcare Workers’ Foundation charity (previously ‘Heroes’)

As well as a special guest appearance by Michael Rosen – author, poet, broadcaster and former UK Children’s Laureate

You can register for this session here: Profiteering from the People’s Health? | PeoplesCovidInquiry

 

Disabled People Against Cuts contributed to Session 4 of the Inquiry which explored the impact of the population – Families, social care, disabled people

Jan 052021
 
DPAC Logo with text underneath "Disabled People Against Cuts" and then web address dpac.uk.net
Copied from: Reviewing the use of do not resuscitate decisions during COVID-19 | Care Quality Commission (cqc.org.uk)

In October, the Department of Health and Social Care (DHSC) asked CQC to review how do not resuscitate orders were used during the COVID-19 pandemic, building on concerns that we reported earlier in the year.

Person-centred, advance care planning enables people to have conversations and make informed decisions about their future care and what matters most to them. Do Not Attempt Cardiopulmonary Resuscitation (DNACPR) orders can be part of this planning and to allow people to make their wishes clearly known ahead of time.

Since the announcement we have been working with people who have experience of this issue to help shape our approach. The valuable insight shared by stakeholders, people who use services, and providers, means we can focus our attention on the things that matter to people.

What will the review look at?

By talking to a wide group of people with experience in this area, we have been able to hear examples of good practice and where decisions or processes do not appear to have been person-centred.

The review will take a national view of how these decisions were made in and across different types of services – including hospitals, GPs and care homes – using all the information available to us. By doing this it will inform national learning and support good practice development as the nation continues to respond to the pandemic.

It will include examples of best practice in this complex area, as well as times when procedures may not have always been followed so that any mistakes are learnt from.

How will the review be carried out?

We are currently analysing what we know so far from initial conversations with people who have been affected by this issue and other stakeholders, concerns raised with us, and the existing literature and guidance on this sensitive topic. Interim findings from this work will be reported later this year.

The interim findings will also provide a base for fieldwork that we will carry out in seven local Clinical Commissioning Groups across the country. This will focus (but not exclusively) on the experience of older people and people with a learning disability or autism. Doing this will allow us to explore how primary, secondary, social care and system partners have worked together in an area – including the impact of commissioning arrangements.

As well as taking into account the information shared with us, these CCGs have been selected to cover a cross-section of areas and a mix of demographics so that the lessons we learn will be of value to people in health and social care across the country, wherever they are working.

To look at a range of ways of working and experiences, the seven areas we will be looking at are:

  • NHS Birmingham and Solihull CCG
  • NHS Bristol and North Somerset CCG
  • NHS Cambridge and Peterborough CCG
  • NHS Morecambe Bay
  • NHS Sheffield
  • NHS South East London CCG with a focus on Greenwich
  • NHS Surrey Heartlands CCG with a focus on East Surrey

We expect to start fieldwork later in November and publish a final report in early 2021. We anticipate this will include recommendations on how people can be properly supported in this area and support good practice that protects people’s human rights.

How you can help

This work is being developed and carried out at pace during November, December and January. We are keen to hear from people who would like to share their experiences.

If you would like to tell us about your experience, or that of a loved one, we would be grateful if you could get in touch. Please let us know using our Give Feedback on Care service, or by contacting our National Customer Service Centre.

Survey on do not resucitate orders during the coronavirus pandemic

We’re using this survey to hear the experiences of people who have had a DNACPR or had one reviewed since the start of the pandemic in March. Share your experience of DNACPR.

Apr 102020
 
DPAC Logo with text underneath "Disabled People Against Cuts" and then web address dpac.uk.net

DPAC is aware that some disabled people are not receiving essential support and resources from their local Council that they need during the pandemic.

Disabled people with certain impairments and health conditions are among those most at risk from Covid 19. At the same time, the government and medical professionals have made clear that they will not even be admitted to hospital let alone prioritised for treatment. The situation many disabled people living in the community have been left in has then put them at much greater risk, without access to food deliveries or protective equipment for the personal assistants coming in and out of their homes to provide indispensable support with fundamentally important daily tasks such as eating, drinking, using the toilet and staying clean.

Some local authorities are operating good practices such as contacting everyone in their area with disability related support needs and co-ordinating deliveries of food and other supplies.

Sadly, others are not.

Inclusion London has produced a useful template letter for individuals who have not been provided with the PPE (Personal Protective Equipment) that they need for their personal assistants.
The letter can be downloaded here: https://www.inclusionlondon.org.uk/wp-content/uploads/2020/04/template-letter-re-LA-failure-to-supply-PPE.doc

Scope has information on their website about how disabled people can access food and other essentials during the pandemic, including how to register as a “vulnerable” person with the government in order to access priority deliveries from supermarkets. Go to: https://www.scope.org.uk/advice-and-support/food-and-essentials-during-coronavirus/

The link to register with the government as “vulnerable” can be found here: https://www.gov.uk/coronavirus-extremely-vulnerable

Disabled People’s Organisations have raised concerns about the creation of a government register of “vulnerable people” including data protection implications. There are 14 Million disabled people in the UK, qualifying for reasonable adjustments of one sort or another, but this register will only assist an anticipated 10% of disabled people. Read what Chris Fry of Fry Law has to say about the register here: http://www.frylaw.co.uk/archives/articles/dont-share-the-vulnerable-people-register/

Fry Law have developed a template letter to enable disabled customers to challenge supermarkets about lack of access to online delivery services. You can download the letter here: www.dpac.uk.net/2020/04/18010

DPAC understands that provision that is in place on paper (or on websites) too often fails to translate to provision on the ground to the people that need it. We also understand that not everyone will have the energy to both battle for your survival and share your experiences, but where possible within your individual circumstances we would like to hear about any difficulties you have faced or are facing in accessing the resources and support so that we can campaign for improvements – either using the comments below or by emailing mail@dpac.uk.net.