“Graphista, the point was not that they want to remain anxious or depressed but that the pay off for it is greater than getting better”
I understood the point perfectly well thanks and I find that comment quite patronising and condescending.
Just because I’m mentally ill doesn’t mean I’m stupid.
Nor does my disagreeing with the point made mean I didn’t understand either.
“I completely agree with all you say about the state of mental health provision in this country. Many CBT providers in the NHS have just done a twelve month course, and there is so much more to therapy than just techniques and homework.” With how poorly I now know it was implemented I would actually be AMAZED if the people I was stuck with for this had even done that much training! In one case I actually know (found out later) they’d ONLY done a 12 week course - but actually only 12 DAYS because it was a one day a week course! I kid you not - someone who’d only had 12 DAYS of “training” on the technique was considered sufficiently trained to do such a therapy with frequently very ill and distressed patients. That’s not only negligent I consider that harmful!
I’ve considered private therapy, the difficulty is partially cost (though a relative has kindly said they’d cover if necessary) but also at the moment as I’m housebound I can’t access it (none here do house calls not even private practitioners), and I have no idea (and I’ve TRIED to get info and advice on this) how to ensure I was using a good quality practitioner.
Without wishing to sound flippant I wish there was a review site available for such services. A sort of tripadvisor type thing?
I am bringing my experience to bear on the situation under discussion but disagree I’m projecting.
So often “refusal to engage” is cited as a fault on the behalf of the person needing help - but they’re ill! It’s not as simple as just forcing them to participate in treatment that they are wary of.
Instead the people supporting them should find ways to reassure them, listen to their concerns and find solutions to those concerns.
Eg “I don’t want to take that med because I’m worried about side effects/dependency/I’ve heard they zonk you out” - a different med or lower dose can be suggested, discuss concerns re side effects possible preventive actions etc
“I don’t like talking to strangers” - common issue with therapy - discuss this with them, reassure them about confidentiality, that they don’t have to see that person again if they don’t “click”, that they don’t have to talk about the “issue” straight away they can get to know the therapist first etc
“Talking about the issue makes me feel worse” - discuss that they don’t have to at least not straight away, that they can talk about the things that DO help instead, or the effects. Reassure them that they can stop at any time etc
I think a BIG reason why a lot of people “refuse to engage” is because they don’t KNOW what therapy is really like (film & tv don’t help with exaggerated/unrealistic examples for dramatic/comedic effect)
Another is that especially with the cuts at the moment we’re (the mentally ill) are being listened to even less.
Yes this is my personal experience but it’s one I’ve heard is happening to a lot of people:
Being told you’ve no choice of therapist
Being told no choice of meds or being pushed into accepting meds that don’t work/Make you worse because they refuse to give you (often the more expensive) meds you hope/even know do work.
The “hard sell” of whatever meds are “popular” with hcps at various times is appalling! I well remember at the start of my journey being prescribed prozac which was being feted as a “miracle” med and being completely disbelieved when it did NOTHING For me. I was accused outright of lying, not taking it “properly” when I Absolutely was!
Sometimes too yes people will take eg antidepressants for maybe a week or 2 and feel it’s not working for them when it can take 6-8 weeks to begin taking effect. Still hcps are not always making this clear to patients and also the importance of taking at the same time every day etc.