NHS Change Challenge Innovations

The NHS Change Challenge site continues to publish the most impactful initiatives submitted. Wave two included a number of digital initiatives and wave three will be related to rheumatology services. Each idea has a short slide deck explaining the change and how it was done, the impact and issues to consider for embedding it.

The information is brief and practical, enabling you to easily use the initiatives that are helpful to you. If you want to comment you can also join the discussion.…

Read more of this article

Survey on the effects of COVID-19 and lockdown

Around half of those with arthritis report increased pain during the pandemic
With over half finding it more difficult to access healthcare

During the COVID-19 pandemic, 42% of people living with arthritis reported that their pain has increased [1] according to a survey by UK Charity Arthritis Action looking at the effects of COVID-19 and lockdown on the daily lives of people with arthritis. Considering there are over 10 million people living with some form of arthritis in the UK [i] this would equate to over 4 million people experiencing increased arthritis pain during the ongoing pandemic.…

Read more of this article

New Report on workforce challenges

The role of osteopaths as AHPs in the NHS

An independent panel of leading healthcare professionals, chaired by Professor Adrian Newland CBE, has authored a report including its findings on the role of osteopaths as Allied Health Professionals within the NHS, and their potential to provide much needed additional capacity to the delivery of NHS MSK services to improve patient care.

The report was launched at a virtual event with NHS commissioners, at which Sue Brown, CEO of ARMA, joined as part of the panel.…

Read more of this article

NRAS Work survey

In July and August 2020, NRAS ran a survey asking about the impact of the Covid-19 lockdown on the working lives of people living with rheumatoid arthritis or another form of inflammatory arthritis.

The survey received 348 responses and a short report will be published next month. The overall picture is a concerning one: people reported that their career opportunities, in-work support and the understanding they experienced from colleagues and employers dropped slightly during lockdown. Asked about their expectations for the future, many expected this trend to get worse.…

Read more of this article

Pain in the …Big toe

by Anthony Maher. BSc Hons, MSc, FCPodS, Clinical Lead Consultant Podiatric Surgeon, Nottinghamshire Healthcare NHS Foundation Trust.

A lot of the time we pay little attention to our feet, that is until something goes wrong. Most of us, luckily, will only occasionally experience foot pain sometime in our life, but for some that pain can be significant, causing pain when walking, limiting choice of footwear and even reducing activity or increasing the risk of falls.

The big toe joint or 1st metatarso-phalangeal joint is one of the most common areas of the foot to become painful (Gilheany, Landorf, & Robinson, 2008; Maher & Kilmartin, 2011).…

Read more of this article

The Doctor Will Zoom You Now

The Doctor Will Zoom You Now was a rapid, qualitative research study designed to understand the patient experience of remote and virtual consultations. The report makes recommendations for both patients and healthcare professionals for getting the most out of a remote healthcare experience.

Remote consultations and the use of technology offer some great opportunities to make significant improvements to general practice, hospital outpatient and community appointments, but making the most of this opportunity means understanding the patient experience. The project was led in partnership with Traverse, National Voices and Healthwatch England.…

Read more of this article

Women and young people hit hardest by lockdown

Study suggests women and young people have been hardest hit psychologically by coronavirus lockdown

A new study, published in The Lancet Psychiatry, has looked at the potential impact of the coronavirus pandemic on population mental health.

  • It found that there was an overall increase in mental distress in people aged 16 years and older in the UK.
  • This did not affect all groups equally, with some subgroups showing marked increases. Factors most strongly linked with mental health deterioration were those associated with pre-existing health inequalities, such as gender and age.


Read more of this article

What are the experiences of ethnic minorities with pain management?

invitation posterAn invitation to participate in research: We want to know your experiences of living with pain in London

Recent findings have shown that chronic pain affects up to 50% of the UK population [1]. Of this, Black adults have been found to have higher levels of “high-impact” pain in comparison to their White counterparts [2]. This disparity in the incidence of pain is also reflected in the contributory factors to pain. Researchers [1] have found many factors that are associated with the development of chronic pain including comorbidity, mental health and employment status – factors that are more prevalent in ethnic minorities [3] [4].…

Read more of this article

Important new axial SpA & COVID-19 APPG Clinical Survey

NASS would like to bring your attention to an important new clinical survey on the impact that COVID-19 is having on axial SpA (AS) services and care.

The survey has been developed to help inform the work of a new inquiry that is being carried out by the All-Party Parliamentary Group (APPG) on Axial Spondyloarthritis. Findings from the survey will support the APPG, the National Axial Spondyloarthritis Society (NASS) and other stakeholders in the area to identify key recommendations that can be put forward to help safeguard the provision of axial SpA (AS) care and ensure that patients are able to receive the best care possible in the months ahead.…

Read more of this article

What questions would you like to see answered by psoriatic arthritis research?

The British Psoriatic Arthritis Consortium is working with the James Lind Alliance to run a priority setting partnership (PSP). The aim is to create a national top-10 list of research priorities for psoriatic arthritis. They want ideas and thoughts from people with different experiences and backgrounds: those with psoriatic arthritis, their families, carers and clinicians.

The survey has now been open for two months and 228 surveys have been completed. You can read information on who has completed the survey so far in the survey’s update document.…

Read more of this article