Відео

Hmm 😖😅 the segue or non sequitur from the enthusiasm about the conference at the end of the curry analogy chapter to feeling uncomfortable: the mirroring, warmth and acknowledgement dropped off a cliff 😜. This happens in clinical interviews too and can be really unsettling and uncomfortable. I understand when you're duck-pedalling to remember all the questions or talking points and in a time limit there's a mismatch - but ideally acknowledge what's said and then acknowledge and apologize for the awkward segue and the duckpedalling, both in clinical and media interviews: it's really something that gets on my goat. We're supposed to be authentic, responsive and mirroring to be deemed healthy, but professionals aren't!? 😜😅 I know I'm thinking like a fixed solution thing there. But again there's a symmetry with how therapy goes. Disappointment, harm-causing and 'sitting with uncertainty' (my mind going same place as André, but it is broader 😅) these are all therapeutic concerns for/at patients but maybe it needs to be a 360° thing. Embedded into it. People have been talking about the mental health of NHS practicioners across the board and "physician health thyself" for a long time. But that is framed or thought of in a more combative, adversarial, defensive way. Or can become so!? And there is a tension between therapeutic use of the self and safe boundaries, especially in that context. But awareness of overstep, boundaries of that kind are part of normal community interactions, without being formalised, militarized borders. That and the thing about relational Vs rational is stuff that has come up in a variety of settings, outpatient psychotherapy, iapt/wellbeing definitely stuff that has come up. But less so with a neurodiversity specialist. Definitely too easy there and with the overcoming books to get into the long grass over rationally and emotionally fair statement or assertion, what verbosity and stilted speech are in comparison to technical language too - and where the blind spots or inconsistencies and rationally taking the model apart to check it - in a "he said, she said ' way of countermanding. Maybe tit for tat instead of tic toc (treatment interfering cognitions vs treatment interfering cognitions column techniques). In that, treatment always has to be right and it's a kind of battle over which side has the last word. But perhaps especially getting into it and piqued by it all as a latterly diagnosed AuDHDer. Uncertainty, disappointment , dissatisfaction, regret and risk-awareness - sitting with it, being open and organic resolution: maybe more kishotenketsu plot structure than outline structure or traditional western plot structure. I think kishotenketsu might be less confrontational, less relevant overarching point and relevant evidence delivered directly, bish bash bosh. Both have their good points but there's definitely something smoother about accepting twists and imperfect resolution and starting from the kind of substrate or overall picture. Same as divergent thinking that can produce many answers in a design process Vs convergent thinking that seeks to narrow it down quickly. And intersectional awareness of course takes big pictures of dynamics but infinitely varied stories of people at the intersections. The various stories and agendas that have their own wholeness despite combined rhymes and reasons and discord

Go Dan! Great interview! My colleague is doing a phd with a longitudinal study looking at MH nurses attitudes and how they change during the end of training and in the first few years after. Fascinating but so sad

Thank you SO much, so inspiring and affirming to hear!!

Sagahimara re carer burnout, also many survivor stories, racial disparities, other intersectional effects and some of the COVID situations like coerced DNRs as well as expansions of assisted suicide also loom large as broader fears in the area you're talking about. But detailed conversations are indeed probably the answer. Therapy for therapeutic services like the scientific study of science: and also that's a false dichotomy. Like "patient" and "staff" can be, people sometimes afraid to address their own mental health in mental health services in general!? And not always holistic and solidly on point enough. Just a messy wall of potential referrals.

Edit: I'm grateful for help I have got. We have got as a family. Some of the services stuff I mentioned is well in the past. People have been working very hard on our behalf, throughout. And many people do seem tireless. I fear I don't do enough or the right things. And things are just difficult generally right now. ---- There's aspects of this conversation that apply much more broadly. Especially with the funding crisis in the UK. But it is very variable how much stigma is applied. The details as well. Also defensive professional criteria that in practice puts some of the most vulnerable struggling people in a hole in-between services. So people sympathise but they just can't give you the points or accept you on the books, and we're shuffled back and forth exhaustingly. And in theory of course a diagnosis is supposed to be a Hippocratic collaboration tool towards the overall best outcomes for everyone but especially the patient. And a "label" can be any kind of noun that socially is given weight and power and the problem is more bad attitudes and how the words tie into it; labels in that sense including more explicit slurs and colloquial terms of exclusion and destructive distancing. Whilst on the other hand outside of metaphorical idiom, a label is actually a very functional and purposeful set of information but like with chutney you don't actually know what it tastes like or everything about it until you do interact. This is the perspective of a late diagnosed AuDHDer who was nearly diagnosed with borderline due to self harm and literally threw myself down the stairs once to escape relational emotional agonies. And also speaking from experience with a lot of different services - social care and health for myself, as a parent carer and as a partner. And online supporter of a lot of people over a long time, with a mix of ND and PD diagnosis especially autism and borderline, other parents of kids with higher care needs and mh struggle. I am not a perfect collator of experience. Not perfect "client". Neither really exists. But I did find with C&F social care that statutory rubric can also influence how more seasoned and burnt out practicioners think and certain key words become indicators cum triggers in situations where that doesn't actually make sense or wasn't the correct or most helpful interpretation but as a "client" a compassionate politeness paired with self advocacy and explaining the system/interaction as you see it to the different parties can go a long way, I found. But then you worry you talked your way out of things and have a dark triad kind of personality disorder. Meh. Btw. I have written several songs and poems on these topics and will likely continue to do so. What's in a Noun!? is probably one of the most relevant, and Paint Away. Obviously experience differs and I certainly haven't had the diagnosis, the inpatient experience nor the worst of stigma when distressed, though it was quite a ride after my first ADHD assessment said no, probably OCD and a personality disorder (and then two psychiatrists said no to both and then 15yrs later got more thorough assessment in an overhauled service that has now fallen apart again, especially for aftercare. And I hate filling out surveys and consultations, and PQ9s too. But I'm waffling bad now. Have a fun conference.

Thank you for sharing! I’m in a Master of Social Work graduate program in the U.S. and I can see similar patterns happening here across care settings when working with clients who have been diagnosed with BPD or other serious and persistent mental health challenges. I’ve worked in hospice and palliative care, both in hospital and in the community, and see this kind of “compassion fatigue” come up often. I feel my personal values and professional ethics require me to be vigilant to recognize and address burnout and compassion fatigue in myself and colleagues. I would love to read Dan’s thesis!

Clear and concise points in a short discussion. Very informative and I learnt a lot in my understanding for when working with, and supporting, people with this 'diagnosis'. Thank you

First time hearing about Sentia. I hope the marketing department are properly funded.

Participatory Action Research (PAR) can bring together essential elements of lived experience and scientific research methods avoiding the dangers when these are used exclusively.

Will doing a valiant job summarising the questions/comments we were unable to hear

Interesting topics especially the loneliness thing ,it was a time in my life I felt that and among lot of things I did to get out from that circle is listening to some lovely songs like " all about your heart" by mindy gledhill Cheers Dr

Thank you for this insightful video! Any change there is a way of connecting with current students pursuing this programme? Thanks:)

May I know what is TAU mentioned in 25:00?

It will be better if you put the topic of the video first in the title, and then the name of the speaker. In my opinion the best way is Topic, Name of Speaker, Conference, Date (or Year). This way we can see immediately the topic at a glance and I think it would attract more viewers or help viewers choose what video to click on.

ABSOLUTELY AGEISM! Thank you for continuing your work.

Is there any way for an interested layman to get a look at your data? I've suffered severe depression for years, can't get any meaningful treatment from the NHS, just SSRIs and SNRIs which do nothing but give me awful side effects.

Thank you Pim Cuijpers!

It would be very helpful to understand those behaviours which may be attributable to safeguarding e.g the the level of safeguard and frequency of safeguards (for each individual) which may go some way to explain some of the behaviours described.

Great stuff, a link to the slides would be helpful please

Another informative lecture, a reference list would be very helpful please

There's a book I like called 30 Days Without Social Media by Harper Daniels. Helps me take a break from my phone and apps and practice mindfulness. It's so important to learn to be calm and let distractions go.

I love his work and very happy to be able to listen to him on UA-cam 👏🏻

Dr.Romaina Iqbal our PI ❤️

Happy Birthday x

Are we able to listen to his full talk somewhere? :)

💃 Promo*SM

Hello, came here from Luke from mind recommending. Where can I buy this issue? ❤thanks amazing

I’m also a EBE, this podcast should be interesting!

Oliver Dale is a pompous jerk. Therapy with him was being judged by a 'doctor'who fits an NPD diagnosis themselves.

A survivor here....thank you for sharing. This was educational on many levels

Would you be interested in publishing something for one of the main ME charities in the UK? I'm sure sufferers would enjoy hearing about your research and findings. I'm a big fan of the ME Association but Action for ME and the 25% group are also great. Thank you for paying some attention to us sufferers.

Life has proven to far gone and the strongest are the ones who survive with nothing but evidence of the facts proven with homelessnes and all large hospitals shut down long ago and would have helped to give this destruction a boost.

ALGORITHMICS DOES IT LIKE TRUTH? Your right on the fact truth of what your trying to teach . life is to far off in natural selections and big bangs causing more head aches and the Book of powerfull Promise that never gave any power over the smallest base vegie plant never mind a Human . many have a feeling of human distinction as negative as this may sound . How much control does a Human have . Hopefully Good aliens if any at all will come and rescue us hopless Humans befor the Wild creeping unknown intruders out smarts us. i will not say there is no superior power but sure seems cruel to believe.

Off a bit as the mental health provider with so called skill, or education in the drugs that dilutes the person in to a substance at least pays the worker some thing . this is not going to help a patient or person in any long term but very short term and eventually agony and soon Death. Side effects from theses little sugar pills injections could kill a horse. to many become 2-4 months of a high period calling that a merical then side effects causing there Death like creeping johnsons desices or recoverying with no help but suicide or in a home some place they have no clue about. this U.K. AUSTRALIA and U.S. life coming to its senses of a near Hell with out the help from so called Natural selection or some dried up book that Commands humans out of pushing pure pressuring Fear. God is sopposed to be the great love maker but has proven to have the power of the most usless simplest plant based vegetable. Truth is a lie and simply to lie is telling the truth yet no one can prove iether causing nothing but frustrations. Science stuck in a natural selection of head migrating big Bangs hurt also.

Interesting!:)

Virtual Psychiatry, excellent.

PS UA-cam search "Psychiatric drugs are more dangerous than you think" by Peter Breggin. Him and a lot of videos are now floating around now that ACTUALLY LONG TERM USE OF ANY PSYCHIATRIC MEDICATION MAKE YOUR BRAIN WORSER AS THE YEARS GO BY! MATT

I do want to say something about long term usage of any type of psychiatric drugs. People like Peter Breggin and Joanna Moncrieff have now realised that these types of drugs can do ALOT TO DAMAGE TO THE FRONTAL CORTEX OF THE BRAIN LONG TERM, if not regulated over a period of time. I do want to say something everybody needs to be aware of with taking these medications. If anyone is taking Zyprexa, Benzoidiazipines. What works for some people may not work for others. My other family member is still taking Zyprexa today, and has been using Zyprexa for at least 20 plus years and I have seen a REAL EVIL, DEMONIC SIDE, to this drug. I don't believe also my other family member has been diagnosed properly with SCHIZOPHRENIA. Our country here has privacy laws in the country here in NZ. I can understand DOCTOR TO PATIENT CONFIDENTIALITY, yes I will accept. But to get a drug and say to others "oh you just need to shut up and suffer the consequences" knowing full well, that the medication itself can made things worse, well I can call this mental and psychological abuse, for not communicating to others in the family about what medications have worked or not worked, what needs reducing, what needs coming off, the lack of communication withing the family. I have made a COMPLAINT TO MY LOCAL PHARMACY ABOUT A WRONG DIAGNOSIS IN OUR HOUSE AND I BELIEVE THERE HAS BEEN FORM OF MEDICAL NEGLIGENCE TOO IN OUR FAMILY. I ALSO HAVE BEEN TRYING TO FIND SOME LOCAL NZ LAWYERS TO TALK ABOUT WHY THERE HAS BEEN A MISDIAGNOSIS ON OUR HOUSE AND WHY MY OTHER FAMILY MEMBER'S DEMEANOR HAS GOTTEN WORSE AS THE YEARS HAVE GONE BY! Matt

Thank you for publishing this openly. My work related to commissioning for M H Social Care. I think the term complex emotional needs could be really helpful in shaping services.It's a big ask but is there a reference that stands out introducing Complex Emotional Needs as a meaningful and helpful term?

i specifically came here from the exposure therapy video and i would like to say; that your channel is very helpful! and i hope that you wouldn't get tired posting more informative videos :))

Master Apollo

Fantastic insights , thank you for this.

Hi by any chance you have a LinkedIn ?

Your video is very beautiful. I like it a lot. I have been trying to talk to you for a long time. I am waiting for your response. Please give me a chance to talk to you.💗👌

p͓̽r͓̽o͓̽m͓̽o͓̽s͓̽m͓̽ 💘

I really appreciate this video. Love the message on resilience, and what he said about the ripple effect 🙏

Perhaps providing some coping strategies would help.

Nesrin senturk 😀 😀 😀 😀

*Excessive snowflake artifical politeness by the host was very off-putting.*