Does anyone have ideas and/or experience in communicating with physical therapists or similar folks about trauma-related issues, especially when dissociation sorts of issues might be slowing down one's ability to relax and make "normal" progress?
I have been working with a great person and find it very helpful in both continuing to function at times but also can feel a lot more of my back and neck muscles... However I am worried that either she, the insurance company, or whoever might stop the treatments because it's so slow.
I have a habit of reading things from peoples' facial expressions and making catastrophic conclusions though, then have to catch myself... but I feel confused after lots of doing that, what is the reality...? Yes, I know, I'm supposed to ask the person, but what if the person isn't a regular T and maybe isn't supposed to cross into the "psychology" stuff per legal issues?
I've been in the PT work for about 2 years; I had really awful posture, muscle knots that just recur... I have also been getting massages which has helped a lot in feeling safe with feeling the muscles.
The DSM-V addition to PTSD for dissociative stuff is so new that I suspect many medical people here in the U.S. still haven't heard of it, unlike parts of Europe... In spite of the dissociative stuff being really common for those of us with long-term childhood trauma a lot of us just hid it or I guess our therapists thought we were "treatment resistant" or whatever.
I'm thinking of printing out some of those studies showing the differences in brain changes between "regular" PTSD and the dissociative PTSD subtype(s) for the PT.
If you're working with people who are professionally supposed to be working with physical -- not psychological -- issues, where is the boundary given that our brains are physical and have been affected/damaged/whatever?
Wouldn't they feel ok working with someone who'd had a brain injury from a baseball bat? If ours was from repeated threats with the same bat but we have neurological/structural brain changes from the experience, not the bat, somehow it's different...?
Some background on my issues...
My sense is that some of the muscle problems causing my joint problems is from tension from childhood stuff that I'm just very slowly starting to deal with in regular therapy. I am not really aware of how tense I am a lot of the time though I think I'm making progress. I exercise regularly which has helped my body not fall apart totally. :-)
I only got a therapists who really "gets" dissociative parts (like DDNOS probably) last year in spite of 25 years in therapy... the others helped with lots of stuff, I function well in a lot of ways, but I think the dissociation kept lots of other stuff from being treatable. I consciously thought I was really trying to heal all that time. It's like some traumatized "parts" would just vanish in therapy sessions but I never thought of them as parts, I would just feel differently different times but various fears/stress/(derealization?) just kept coming back -- so I'm really glad for the new "structural dissociation" model, very helpful mentally. I have been sort of partly in "derealization" chronically most of my life I think, it's just normal, the "really being here" feeling was the weird feeling for me. As I understand it from some new studies, that might mean my brain functions abnormally but there's no test for most of us.
So, how to describe/communicate this mess to a professional who has neurological/physical training but who maybe our culture's separation of physical from psychological has affected... sorry for the bad sentence structure.
I have been working with a great person and find it very helpful in both continuing to function at times but also can feel a lot more of my back and neck muscles... However I am worried that either she, the insurance company, or whoever might stop the treatments because it's so slow.
I have a habit of reading things from peoples' facial expressions and making catastrophic conclusions though, then have to catch myself... but I feel confused after lots of doing that, what is the reality...? Yes, I know, I'm supposed to ask the person, but what if the person isn't a regular T and maybe isn't supposed to cross into the "psychology" stuff per legal issues?
I've been in the PT work for about 2 years; I had really awful posture, muscle knots that just recur... I have also been getting massages which has helped a lot in feeling safe with feeling the muscles.
The DSM-V addition to PTSD for dissociative stuff is so new that I suspect many medical people here in the U.S. still haven't heard of it, unlike parts of Europe... In spite of the dissociative stuff being really common for those of us with long-term childhood trauma a lot of us just hid it or I guess our therapists thought we were "treatment resistant" or whatever.
I'm thinking of printing out some of those studies showing the differences in brain changes between "regular" PTSD and the dissociative PTSD subtype(s) for the PT.
If you're working with people who are professionally supposed to be working with physical -- not psychological -- issues, where is the boundary given that our brains are physical and have been affected/damaged/whatever?
Wouldn't they feel ok working with someone who'd had a brain injury from a baseball bat? If ours was from repeated threats with the same bat but we have neurological/structural brain changes from the experience, not the bat, somehow it's different...?
Some background on my issues...
My sense is that some of the muscle problems causing my joint problems is from tension from childhood stuff that I'm just very slowly starting to deal with in regular therapy. I am not really aware of how tense I am a lot of the time though I think I'm making progress. I exercise regularly which has helped my body not fall apart totally. :-)
I only got a therapists who really "gets" dissociative parts (like DDNOS probably) last year in spite of 25 years in therapy... the others helped with lots of stuff, I function well in a lot of ways, but I think the dissociation kept lots of other stuff from being treatable. I consciously thought I was really trying to heal all that time. It's like some traumatized "parts" would just vanish in therapy sessions but I never thought of them as parts, I would just feel differently different times but various fears/stress/(derealization?) just kept coming back -- so I'm really glad for the new "structural dissociation" model, very helpful mentally. I have been sort of partly in "derealization" chronically most of my life I think, it's just normal, the "really being here" feeling was the weird feeling for me. As I understand it from some new studies, that might mean my brain functions abnormally but there's no test for most of us.
So, how to describe/communicate this mess to a professional who has neurological/physical training but who maybe our culture's separation of physical from psychological has affected... sorry for the bad sentence structure.