When I say "severe pain" I mean: my knees buckled, and I screamed, and I fell, and I sobbed with the agony of it. His 'pain' means 'kind of sore.' He's incapable of understanding my meaning. We don't speak the same language. He's useless to me. I'm changing doctors.
Yes, and words many times are based upon one's experiences. When one's experience goes beyond the capacity of another's experiences for that word, unless that person can get one's head around the fact that perhaps these things CAN and DO happen, and explore from there, then trying to get to answers, express what one is attempting to express becomes a moot point.
I'm curious where you get the 'obviously' from -
Because this Stockholm Syndrome thing has come up more than once with me. The posting yesterday brought it up yet again. I get it, some people can't let sleeping dogs lie. I have opinions on Stockholm Syndrome that don't mesh with Anons. I am not certain how that got tangled up AGAIN, in a thread that had nothing to do with Stockholm Syndrome.
Why is a proper Mental Health Language repertoire important to you and to this board in general?
Due to an issue with the DSM IV, I was denied proper treatment, over and over and over again. Catatonia did not exist, they said, without Schizophrenia. I was violently abused by health care workers, I was denied proper medication, I was called names I don't want to repeat. And what happened in the DSMV? They recognized (ooops) that Catatonia CAN exist without Schizophrenia. 8 years of hell because nobody would read between the lines of the DSM ICD and compare that withwhat my ACTUAL experience was.
That taught me something. Just because the DSM says so (or says it isn't so), doesn't mean it is so. So I fought literally, for my life to get people to 'get' that something horrible was happening to me and it wasn't good enough that they tell me because it wasn't in a book that it couldn't exist.
Telling people to rip you to pieces if it suits them, kind of sets a rough tone for the thread.
I actually put that in there because there have been repeated issues with this fighting about words for me from certain members. I needed to see how deep it goes. And that I did. Anthony, it is actually NOT my fault that Anon chose the words they did to express their contempt for me. I appreciate the lesson in how to take responsibility for another's attitude though. I did that for a ton of years, and I am not going to do it anymore. Anon chose the words they did. That is on them. Not me.
Looking to start a flame war, not so much.
The war actually started months ago with that Stockholm Syndrome thread. I have no interest in having a post that is months old coming back to haunt me over and over again. Enough.
It's important to me that disorders be understood with the fullness of what is available to us.
I agree with this. Unless current psychology is not reflecting the reality of situations. I was diagnosed 10 years ago with DDNOS. That was fine. Not otherwise specified is a good way of saying that something could include lots of things. Manuals are great as a guide, but we are people, and each of us unique. I can't help but feel that being validated by a manual just isn't enough. Especially a manual that keeps getting revised.
If it wasn't for the works of Pete Walker, whom I have known about for a decade, who first put out there theories and validating information for my catatonia.... I don't know what I would have done. Because I was being invalidated and humiliated over and over again by front line doctors. So I believe that as much as the DSM is very helpful in so many ways, up and coming research is helpful to toss around as well. Looking at things that make sense against the sufferer's experience makes sense.
And even if one believes that they are flat out wrong - I think it's more productive to understand a different point of view in the context of those codified diagnostics.
Would you mind explaining this to me? I am not quite sure I understand. If you don't mind, can you package that around my experience with the Catatonia and the lack of a Schizophrenia diagnosis.
And, others will contribute by totally disagreeing with me (or whomever).
And does that disagreement need to become the gift that keeps giving? Or should it be more like I disagree and let's drop it?
Part of the stated intention of MyPTSD is to promote education of PTSD and the issues around it.
And let's face it, education, reworking a comfortable frame of reference, can be uncomfortable. But it is the reality of our mental health system. We learn stuff. We are supposed to be learning stuff. Telling people that their experiences, that don't fit neatly into their mental health world view does not make it wrong. Nor is it a reason to attack one's character. But so be it.
Well, I do, if it doesn't make sense to me.
Yes, you are right. I do too. And I also agree with them if something rings true. Or I research it, or ask on the board about it. And it is a process to see if it 'fits'. Which is why asking questions (even if on the wrong track) can be helpful.
that we value diversity of opinion.
That we VALUE diversity of opinion. And experiences.