Meeting Centres – the international perspective

At the start of February over 20 people got together online from different countries to get an update on what’s going on with Meeting Centres across the world. The session builds on the regular fortnightly meetings that we’ve been facilitating in the UK and those taking place in Scotland, where we find it useful to keep track of who’s doing what. It provided an informal chance to catch up with each other and share experiences, challenges and ideas.

Dr Shirley Evans led the session, but we were pleased to welcome Professor Rose-Marie Dröes who developed the Meeting Centre model and was the driving force behind Meeting Centres in the Netherlands.

There was a strong UK contingent from England, Scotland and Wales, but also representatives from the Netherlands, Singapore, Italy, Poland, and Australia. As it was the first meeting there was a fairly open agenda, with ideas being shared about what it would be good to cover in future sessions. The main part of the session revolved around getting a short update from each country.

image showing attendees on a Zoom call
The international group

Scotland – Meeting Centres Scotland, an independent third sector organisation, has just been established and is now up and running. Meeting Centres feature strongly in new Scottish Dementia Strategy, and the Meeting Centre network has a good relationship with the Scottish Government. A lived experience panel was a core part of the strategy development. An implementation plan is coming soon (mid-February) and again Meeting Centres will be part of that. There are nearly 20 Meeting Centres across Scotland with a good amount of interest at both a local and national level.

Singapore – After two Meeting Centres were set up as an initial pilot there are now seven Meeting Centres with another coming soon. They are getting interest from other areas to look at setting up Meeting Centres in Dementia Friendly Communities, of which there are 17 in Singapore. Dementia Singapore has moved to helping other partners to help set up new Meeting Centres instead of running them themselves as they did with the pilot. They are using a ground-up approach, identifying the needs in the local community, so people can see the purpose of getting new Meeting Centres up and running. There was government funding for the two pilot Meeting Centres, but the other Meeting Centres are funded by individual partners as part of their existing work.

Poland – The two Meeting Centres set up as part of the initial MeetingDem project are still running. There have been challenges trying to get further Meeting Centres set up, but it is hopeful that a change in government may improve the situation and get a Polish Dementia Strategy in place. Work has been going on engaging different professionals and students at Meeting Centres to help offer a variety of activities. There has been interest from other parts of Poland but it is currently unclear what progress has been made. Hosting the Alzheimer’s Disease International conference in Krakow in April this year may help to stimulate more activity.

Australia – Two Meeting Centres had been running and working really well, but the impact of Covid and other internal issues meant that neither is currently running. They are taking a step back to plan a new approach to get things going again, hopefully in collaboration with other organisations such as Dementia Australia. Potential funding is being identified that could help to start new Meeting Centres, and the future is looking quite positive as the Meeting Centre concept has already been proved through the previous piloting work. They have found it useful to learn from other countries to know how to overcome some of the barriers that they have encountered previously.

Italy – The initial Meeting Centre from the MeetingDem project is still running, and Meeting Centres are promoted as a social intervention as part of the regional strategy in Bologna. They are planning to open a new Meeting Centre in a different part of the city later this year after being delayed by the pandemic. Elsewhere, Meeting Centres are seen more as a medical rather than social intervention. The network of Meeting Points may be a useful route to developing further Meeting Centres and is worth investigating. Work is also in progress to set up more Meeting Centres in different parts of Italy which may have their own challenges, such as being close to the border with other countries.

Wales – Five Meeting Centres have been set up in Powys with four currently in operation covering four very different towns and communities across the county. Grant funding is becoming harder to secure as Meeting Centres are no longer a ‘new project’. The Meeting Centre provider has been trying for many years to access Welsh Government funding and was only able to do so recently, due to being on the brink of closure, but not at the levels they were aiming to secure. The Welsh Government has been addressing funding issues in The Senedd and putting pressure on the local Regional Partnership Board to fund the Powys Meeting Centres. The Meeting Centre provider is leading on the Community Engagement element of the Active Listening Campaign in Powys which is feeding into the All Wales Dementia Care Pathway of Standards. Work is also underway to set up a Meeting Centre in the Neath Port Talbot area of Wales.

England – Meeting Centres have taken off after the initial two pilots started as part of the MeetingDem project, both of which are still running. There has been lots of interest from across the country, and at a regional level, such as Council funding to open nine new Meeting Centres in Worcestershire. Many Meeting Centres tend to be in small market towns although there are some in more urban areas and cities. Work is still underway to get Meeting Centres up and running in London, but there is some interest currently so that is looking promising. It was recognised that a lot of organisations struggle with funding and getting Meeting Centres running for more than one day a week, as it can be difficult to be self-sustaining and funding tends to be short-term and focused on new ideas. It was also commented that Meeting Centres need to engage with other community groups so people have something to move onto when a Meeting Centre is no longer appropriate or able to support their needs.

It was questioned whether it could be easier to access arts funding rather than social care funding, as Meeting Centres are social clubs and can often have a strong arts focus. This is an area for some Meeting Centres to explore in the future.

It was great to hear from people around the world and appreciate the spread of Meeting Centres as it can be easy to get caught up in your own area and not realise how you’re part of something amazing on a much bigger scale. We’re hoping to have another session in the summer where we’ll aim to hear from a couple of Meeting Centres in more detail. Thanks to everyone to contributing to this first international session, I think we can say that it was a success!

For those who were unable to attend the session or who would like to find out more, a recording can be found here.

Connect with Meeting Centres on twitter @MeetingCentres

Connect with ADS on twitter @DementiaStudies and on Facebook @adsuow  We’re also on Instagram, Threads and LinkedIn so have a look and find us there too.

Season’s Greetings from ADS

As it’s nearly Christmas we’ve decided not to have a formal blog this week. Instead we just wanted to say thank you to everyone for your support and interest, and we look forward to starting again in the New Year. We’ll try to keep our blogs varied and interesting, and keep you up to date with what we’re doing on our various projects. We’ve already got a few lined up so watch this space!

Just to give you a bit of an insight, our top three most popular posts have been:

Continue reading “Season’s Greetings from ADS”

From Amsterdam to Worcester, a dive into research on people with dementia and their family carers in the UK – part 3

Hi again, for the last time. My time as a research fellow at the Association for Dementia Studies (ADS) is over and I would like to reflect on some of my experiences. To see what my goals were and my reflections when I was about halfway through, read my first and second blog posts.

First of all, what I noticed was that the ADS is a really active research group. A lot is going on, in research and various events. For example, during my time here I went to a Dementia Friendly workshop, where I learned more about environments and their influence on people living with dementia; I attended the HDRC Annual Knowledge and Learning Exchange Event where I heard about a lot of interesting developments in the world of technology in relation to dementia care and I was a part of the family care symposium where the 10th year anniversary of ADS was celebrated. And these do not even include the various projects, workshops and external events that took place while I was here. I learned a lot from my new colleagues here at ADS and I am forever grateful to them for making this fellowship a great success.

Continue reading “From Amsterdam to Worcester, a dive into research on people with dementia and their family carers in the UK – part 3”

Worcester and beyond – ADS in an international context

In one of our previous blog posts we said that although the Association for Dementia Studies is based in Worcester, we do a lot of work in different countries. We thought we’d give a bit more information about what we’ve done over the past 10 years outside of the UK, using our ‘international infographic’ as a starting point.

Infographic about our international work

Continue reading “Worcester and beyond – ADS in an international context”

From Amsterdam to Worcester, a dive into research on people with dementia and their family carers in the UK – part 2

Hi again. In my previous blog I described who I am and why I am currently working for three months with the Association for Dementia Studies at the University of Worcester. I have been here for almost two months already and I would like to share with you some things that I noticed.

But first, I would like to start by mentioning how everybody has made me feel very welcome. Not only my colleagues at the University, but also all the people I met during my visits to care homes, at workshops and courses. That has been a good basis for making me feel comfortable in asking questions and learning about research on and support for people with dementia and their family carers in the UK.

Continue reading “From Amsterdam to Worcester, a dive into research on people with dementia and their family carers in the UK – part 2”

The Citizenship and Dementia International Research Network – 2018 meeting in Berlin

Chris Russell, one of the ADS PhD students, recently travelled to Berlin to participate in the Citizenship and Dementia International Research Network Meeting of 2018. Here he reflects on his trip and provides his personal thoughts on the future.

Citizenship is a complex and diverse phenomenon. At heart it is about how society operates, in particular how individuals within society contribute to its function, and draw rights and protections as a result. It has always appealed to me because citizenship necessitates questioning unfairness and oppression, whilst at the same time exploring how opportunity can be promoted. People with dementia are facing constant injustices, and it is thus unsurprising and essential that notions of citizenship are applied in this context. Understanding has been refined and developed over the last few years with social citizenship emerging as particularly relevant, because it relates to the active participation by people with dementia in their own lives and wider community. Social citizenship is a lens through which I am viewing my PhD study, which explores how people with dementia engage in physical activity and sports post diagnosis, and how this influences their sense of them self.

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Arts and dementia in Japan: Report from a research visit

Offered the chance to speak at an arts and dementia symposium in Tokyo, ADS PhD student, Karen Gray, jumped at the chance to combine this with further research visits and conversations.

Japan: A super ageing society

Japan is a ‘super ageing society’, in which a currently reported 4.6 million people live with dementia. This figure is expected to nearly double over the next 10 years. While Japan has much to teach the world about being a society living with dementia (it provided the model for the UK’s Dementia Friends movement, for example), the arts and dementia field there is still very young.

Continue reading “Arts and dementia in Japan: Report from a research visit”