Engage Aotearoa

Category Archives: Service-user Movement

British Psychological Society releases position statement on psychologists with lived experience

The British Psychological Society’s Division of Clinical Psychology released a position statement on clinical psychologists with lived experience of mental health difficulties on the 19th of August.

The document opens by stating, “The Division of Clinical Psychology publicly recognises and supports the unique and valued contribution that lived experience of mental health difficulties brings to individuals working within clinical psychology.”

It goes on to recognise how many therapists with lived experience there are among the profession, the diversity of these experiences, the complexity involved in making decisions to disclose these experiences, the impact of stigma, and the value these experiences bring to the work and the field as a whole.

They close by writing, “Overall, this statement wishes to make clear that lived experience of mental health difficulties does not have to be a barrier to training or practising as a clinical psychologist. On the contrary, people with lived experience are an asset to the profession and make a significant contribution to it”.

As a therapist with lived experience myself, it is a wonderful thing to see these points written down by such a well respected group. I look forward to the day that the professional bodies here in New Zealand take similar steps. I am incredibly grateful to the good folks at In2Gr8 Mental Health for the hand they had in making this a reality.

Read the full position statement here www.bps.org.uk/news-and-policy/statement-clinical-psychologists-lived-experience-mental-health-difficulties


Support group for people with experience of bipolar disorder

The Bipolar Support Group at DRIVE is run by and for people with lived experience of bipolar disorder in the Counties Manukau area. The group meets on the first Friday of every month at DRIVE Consumer Direction in Manukau to share challenges, offer support, and gather strength and hope. New members are welcome. At this stage this group will run until April 2021. More information can be found on the official Facebook Event Page here:https://tinyurl.com/y9rhd46k

For more information ring DRIVE on 09 263 6508 and leave a message.
Text 021 921 738 or email counties.bipolar@gmail.com

Out of hiatus and open for private practice!

Engage Aotearoa is finally ready to come out of hibernation and you’ll notice a few changes have taken place over the past few months.

The big news is that after five years working full time as a psychologist within our DHB services, I have now freed myself up to add one day of private practice to the Engage Aotearoa web-resources. I have teamed up with the good folks at Changing Minds for a space to see people and am looking forward to working from a service-user led setting once again. You can find out more about my private psychology services here.

I’ve simplified things a fair bit and Engage Aotearoa has returned to its original form as a self-funded, non-profit initiative, now with a small private practice on the side to help sustain it. Over the last few years, Daniel has taught me everything I need to know to keep the website updated by myself and more than a decade after setting out on the Engage Aotearoa journey it’s an exciting step to be able move forward on my own two feet.

I am in progress with reviewing and updating all of the resources on the website. You will notice that the links to some resources have been disabled while I do this. A number of the info packs have already been reviewed and you can read them online here. The Butterfly Diaries Volume 1 has now been made available as a PDF e-book you can download and share around at will. And the Community Resources Directory has been moved onto its own series of webpages so you no longer have to download a long pdf document to read it – you can still download it to share around in the real world if you’d like though. Updating the directory after a five year hiatus is a pretty big task and a lot has changed in that time. If there is something you would like to suggest I add, do get in touch.

Please note, that I have updated my contact details.

Viva la revolution!

Miriam

Dr Miriam Larsen-Barr
DClinPsych, MNZCCPTLE



Online Wellbeing Sessions from Changing Minds

During lock-down Auckland’s service-user network, Changing Minds, started sharing free peer-led support sessions online and this project has grown wings to make it easier for people to connect and take care of themselves during this extra stressful time.

Visit www.wellbeingsessions.nz to select from a menu of options from mindful journaling, fitness sessions, poetry readings, a drop-in support group, a supporting families group and more.

More results from The Experiences of Antipsychotic Medication Study

Read online at Science Direct
or request a copy of the full-text on Research Gate

New Research: Support makes a difference in antipsychotic medication withdrawal

An important part of my doctoral research and some further analysis has just been published in Social Psychiatry and Psychiatric Epidemiology. You can follow this link to view a copy of the full text online, but will need a subscription to download a pdf copy to keep:  https://rdcu.be/MpKs

Here’s a screenshot of the abstract for quick reference…

Abstract Attempting to Stop Antipsychotic Medication Success Supports and Efforts to Cope

The Latest from the British Psychological Society

In case you missed it, on the 1st of February the Division of Clinical Psychology at the British Psychological Society published a new report that presents a different way of looking at mental-health problems,  The Power Threat Meaning Framework.

The announcement explains, “A group of senior psychologists (Lucy Johnstone, Mary Boyle, John Cromby, David Harper, Peter Kinderman, David Pilgrim and John Read) and high profile service user campaigners (Jacqui Dillon and Eleanor Longden) spent five years developing the Power Threat Meaning Framework as an alternative to more traditional models based on psychiatric diagnosis. They were supported by researcher Kate Allsopp, by a consultancy group of service users/carers, and by many people who supplied examples of good practice that is not based on diagnosis.”

You can read the full Power Threat Meaning Framework or a shorter overview.

Find the original announcement here.

People’s Review of the Mental Health System

Share your story and help create a better mental-health system.

The people at Action Station have teamed up with Kyle MacDonald to create a People’s Review of the Mental-Health System. They want to gather together as many personal stories as possible, to convince our politicians of the need for improvements.

Their question to you is simple: what has your experience of the public mental health system been?

The public invitation goes on to say “Everyone has a story about mental health in New Zealand. Whether you work as a mental health professional, have experienced the mental health system directly yourself or someone in your family has, your story matters. We don’t need more statistics, the numbers already add up to make it clear that we have a crisis and need urgent action, and still nothing has been done. But personal stories can do what numbers cannot – they can move Ministers to action. Stories create empathy, and empathy creates change.

Find out more here.

Engage Consideration: Dutch initiative challenges mainstream thinking about psychosis

This post highlights a relatively new Dutch initiative that works to promote a helpful way of thinking about experiences of psychosis. The team at Engage Aotearoa recently stumbled across it on Facebook and thought it was full of information others might like to consider – either in their own recovery or in their efforts to support others seeking recovery.

Jim van Os and others have created a website, manifesto and set of audio-visual ‘explanimations’ to help people understand psychotic experiences in a way that allows for meaning-making and hope for recovery.

Much of the website is in Dutch, but an English-language version of the core resources on the “Schizophrenia Doesn’t Exist” website is available. It’s a provocative title, but the project creators do not mean to say that extreme experiences like hallucinations and delusions do not exist.

If you are not much for reading, you can watch Jim van Os’s TED Talk and get it all in a 15-minute nutshell or explore the 2-minute ‘explanimations‘ about psychosis and recovery on the website.

Visit the Schizophrenia Doesn’t Exist English-language webpage to find everything in one place. 

The Manifesto outlines “14 Principles for Good Care of Psychosis”. The first 7 principles address current thinking that frames psychosis as a brain disorder called schizophrenia and set out evidence for an alternative – Psychosis Spectrum Syndrome or PSS. The final 7 principles set out a vision for recovery-based practice, these state…

“8: To recover from PSS, a person must be offered hope and perspective from the very first moment. Recovery is a psychological process. It is a process of learning to adapt and develop a new perspective. With support from people with lived experience of psychosis and, where necessary, from doctors and therapists who support the process of recovery.

9: Every person with PSS should have access to a person with lived experience of psychosis from the earliest phase of treatment. A person with lived experience is in a unique position to offer perspective and hope (‘I was able to recover as well’).

10: The primary goal of treatment is return to the person’s environment, education and/or work. Education and work are prerequisites for recovery: even if residual symptoms remain, people can start picking up where they left off. The practice to wait for full recovery is counterproductive.

11: Anyone who enters the mental health system with PSS should be encouraged to talk about their psychosis. The content of the psychosis should be seen as meaningful, and may represent the key to underlying issues.

12: Psycho-education should not introduce an unproven biomedical model of brain disease as a central theme.

13: Anyone who suffers from psychosis should have access to psychotherapy by an experienced therapist.

14: Antipsychotics may be necessary to reduce psychosis but do not correct an underlying biological abnormality. Antipsychotics are no cure. Much more attention is required for individual dose optimisation to reach the lowest possible dose and to avoid irrational polypharmacy.

Schizophrenia does not exist, which is a good thing.
Because much can be done about PSS.”

~ Quoted from, Manifesto: 14 Principles for Good Care of Psychosis. Schizophrenia Does Not Exist website, 12 July 2015.

 

 

Sign up for the Mental Health Foundation’s E-Bulletin

The Mental Health Foundation of New Zealand’s latest weekly E-Bulletin was delivered to inboxes on the 24th of June. Delivered weekly, the E-Bulletin provides links to resources for researchers, academics, mental health workforce, people interested in new research, information and developments in the field of mental health and wellbeing.

Follow this link to subscribe to the E-Bulletin.