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Recently, I’ve been thinking a lot about misunderstandings and how people very confidently believe things that are trivial to demonstrate as Not True, either as a result of trusting someone who told them something incorrect or because they heard something unfamiliar, imagined what that might have meant, and assumed they were correct. So in the one case, the person was specifically told something that was incorrect. The other case, they were told something, but misunderstood it and as a result now believe they were told something wrong (that they weren’t — they didn’t understand).

That was confusing, and boy, it’s even more confusing when it happens.

Today’s Say What Now involved a request to start a refund process with Amazon. The item in question was cheap enough (around $20) that I probably would have donated the item rather than return (tray for a walker that did not work out for the person who needed a tray for their walker). However, if they want to drive it over to return it, I will do the two minutes of work on the web to make that happen. Which I did. I had a choice of Kohls for free or two different UPS for $6.99 options. I went with the Kohls AFTER checking to make sure there were Kohls options close to where the item was currently located. There’s one 6ish miles away, 20 minute drive, and there’s a person involved who has a vehicle. Kohls it is.

She had specifically requested a Staples, which confused me, because I can only do what options Amazon presents. I told her nope on Staples, but Kohls instead.

“ We apparently don't have a Kohl's...”

Say what now.

I went back, this time to google maps instead of the Kohls store locator, confirmed the presence and the Yep Still In Business status of the two closest Kohls and sent that information along, and asked where they were that there wasn’t a Kohls. This took a while to get an answer, but basically, the person’s elderly mother told them that there wasn’t a Kohls nearby or perhaps that it was inconveniently located.

!!!

The mad disrespect these people routinely point in my direction. I mean, they don’t _mean_ it. But every single time I suggest something and they shoot it down _because of something false or confused_, it is fundamentally a choice on their part to believe a bad source or something garbled (as in the, shooting down Harmony because of a bad review of Homeland, but turning around and going with Homeland anyway), versus whatever I said. I’m extremely accustomed to being told No You Can’t Because on the house project, and at this point, I just view it all as, tell me exactly why I can’t, and I’ll use that to find how I actually can so much faster with that information.

But having it happen in this other context is raising a lot of questions in my mind. I want to be clear _I am not taking this personally_. I _am_ being disrespected, unless you really want to be finicky in which case you could say I am merely being disregarded, and I will look at you and go, my point exactly. I am choosing to view this as an opportunity to better understand why people would do this.

I think the easiest way to understand this choice to disregard or disrespect or treat as less trustworthy a suggestion, idea, or information from me, versus the sources that _are_ being attended to, is to look at motivation. The motivation in all of the above cases is crystal clear: an anxious adult daughter, attending to her aging mother, is hearing conflicting statements about reality from her mother than from her cousin’s wife. I mean. Obviously you believe the aging mother, right? Anything else would be Being a Bad Daughter, right?

And obviously, it would NOT be being a bad daughter to disregard the easily checkable and factually incorrect stuff coming out of Dear Mother. If you argued with mom, THAT might be Being a Bad Daughter. Mom’s in a care home and doesn’t need any additional stress. But why make Mom get every last little detail correct? So the issue I am having here is not the obvious one: is Mom more believable or is Walkitout more believable. No, the issue here is, Why Does Daughter Think She Has to Believe the Stuff Mom is Saying?

And I think the answer there also is motivated. I think if at any point Daughter starts critically thinking about the stuff Mom has been saying for Daughter’s entire life, Daughter would have a radically different set of thoughts, feelings, beliefs about herself, her mom, and their relationship. And she doesn’t necessarily want to commit to that.

Who really does, anyway?

I mean, obviously _I_ do. I’m Team Reality, and I have the terminated relationships to prove it. So why is it when we talk about “critical thinking” we don’t talk about the impact on relationships of engaging in critical thinking? I asked the therapist yesterday how do you teach people to have discernment and to make good choices. And she was talking about trust. And boy, she’s just not wrong at all. The people you choose to trust create the structure of what you can and cannot think and know and believe about reality.

As a little addendum, I was told:

“Ok. Already have several things to go to Staples for Amazon returns.
And I have to FedEx something else.
So I'll add Kohls to the list and hopefully get time to do all those before I go to placenameremoved.

(Though when setting up Amazon returns you can pick a specific Staples, but can actually take it to any Staples.)”

This actually has nothing at all to do with Mom. This is straightforwardly the person telling me how to do the return process at Amazon, which, LOL. I had _already told her_ that I didn’t have a Staples option; I had to repeat it for it to get through at all. I mentioned that in my part of the world, the good choice is a UPS store which is free, and she finally seemed to absorb the idea that maybe the choices are different in different places. *shrug*

Anyone who read this far and is wondering why I’m doing this at all, this was a conscious choice on my part and it’s not driven by pity. I chose to provide a certain type of support (problem solving and at times monetary support) in her journey to manage anxiety and motivation issues that I see very broadly in my husband’s family. Because I have kids with half that DNA, it seemed like it might be useful to get a real insider perspective on what it’s like to live with these issues (since they very much are not issues I have personally!), and to get some perspective on what helps and what doesn’t in a person who also has that DNA. I got roped into this Mom Fell etc. situation, and chose not to step away because there’s a pretty clear need and I hate watching people do things in the obviously wrong way. It’s not actually taking up much of my time or money and the germophobia guarantees I won’t be asked to provide any hands on support. And boy, am I learning a ton from this process. Way more than I would have expected. I learned about respite, I learned pricing (in that particular area), I’ve learned about a bunch of equipment and therapy for rehabbing from this kind of incident, I’ve learned about transportation and all kinds of other stuff. But mostly, I’m learning a ton about how distortions in relationships can really limit the ability of people to understand reality and to make better choices in reality.
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I went to my new PCP today and everyone was so nice! No problem parking. Pleasant waiting room; nice people waiting. The nurse who roomed me asked if I could be weighed today! Woot! I said, sure, and what number it would say (I was .4 pounds less than what I said it would be). She offered to chart what I said my weight was at home. Love this place!

They made sure I had been seated and calm for 10 minutes before taking blood pressure and made sure my arm was supported. I got the low end of what I measure at home! It’s been a couple decades since that was true — I’d started to doubt my cuff, honestly.

I got the referral I wanted. A student came in to poke at my face and answer questions about it. I got another week of Bactrim, sigh. Oh well. NP thinks the dermatologist may just yank the whole thing out tomorrow. That’d be awesome, altho I personally doubt that will happen. I think they’ll want the infection calmed down a bit more, but you never know. NP says that if I didn’t already have the dermatologist appointment tomorrow, she would have tried to clean it out some.

We did go to the therapist (all three of us). R. picked up A. while I was getting my antibiotics from CVS (another $1.20), and then I joined them. We had a nice conversation. It started off on something R. and A. had been talking about in the car, but I diverted to the conversations A. and I had been having about a student at school who is trying to get a borderline diagnosis (*let me just point out the incredible self-insight that adolescent must have to ask for that as a teen*). We had a nice discussion all around, that ultimately started poking at A.’s really high degree of commitment to making sure the people around her are happy. somehow, being in public school apparently resulted in some weird flavor of Stockholm Syndrome in my daughter. Probably very common, actually, now that I think about it.

In any event, it made me optimistic, because not talking about stuff isn’t usually helpful, and sometimes once you start talking, things improve very quickly. Fingers crossed.

In a weird development, when JB at the builder went over to Mercier to try to find a better option for the curved wall in the pool room, Mercier found some Forbo commercial wetroom product that they can order from Australia (!), and a Roppe baseboard to go with. I had actually seen the Forbo product online, but never brought it up, because I figured N (the architect) would have a really negative reaction to the word “vinyl” (we’re calling the siding “polymer”, apparently, whatever). When JB was talking about it during the OAC meeting on Tuesday, she said, I bet you already know about this. I was like, I bet I don’t. She showed the web page and I was like, actually, you were right I did know about this. LOL. Fingers crossed this all works out; it would be a fantastic solution and really help with acoustics in the pool room.
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R. is attempting to get the home internet working again. Apparently something in the basement is connected to a GFI breaker that keeps flipping and he’s trying to track that all down. In the meantime, cellular. Really, a reminder about the utility of automated failover systems. Not that I needed it.

We let water sit in the citric acid cleaned water bottles overnight, and they were still tasty this morning, so I think we have a strategy going forward! A few observations. First, the bottle with the straw needed a lot of treatment on the straw specifically. Second, these are both _new_ bottles, one metal (from WDW) and one plastic (from Fusion). The objection was to “new” related smell/taste. In generally, we only put water in our water bottles, and once they’ve been in use for a while, ordinary water rinse or occasional soap and water (and even less often brush with soap and water) is fine to maintain them at acceptable levels of smell/taste. I _assume_ that what A. is complaining about (and which I can only sometimes detect myself) is chemicals association with manufacturing, and once we’ve had something in use for a while the microbiome is stable enough to not generate anything gross. It helps that we have some whole-house filtration, so we never have to deal with scale or anything like that, and we only fill from double-filtered (cold water in the kitchen, cold water in the master bath and the fridge all have their own filter) sources (except when out and about, but usually there is will be from a water bottle filler or a bubbler which _usually_ have filtration as well).

The therapist described A.’s meltdown on Wednesday (when I was not there) as being anxiety related, and it took until _today_, as I was re-downloading The Worry Trick and buying the audible book of it so A. could also read it easily, that I went, wait a second. That is NOT right! This is NOT The Worry Trick problem. That’s, “But What If” self-jump-scare, and A. does that only extremely occasionally and it is stupidly easy to resolve. She has some long-standing, life-limiting fears associated with heights/elevators, crossing streets alone that do not have a guard or a light control, that are reality based and that I expect we will eventually resolve the same way her water issues were resolved (talk it to death, basically, and increase her skills so that she believes that she has the skills needed to adequately manage the risk), which is to say, NOT stupidly easy, but this is not the looping jump scare stuff of The Worry Trick.

A.’s meltdowns are driven by a combination of sensory overload plus frustration, so I’ve been tackling this by trying to get her into environments that are less sensorily challenging, and which will provide understandable explanations to her (which has been a major source of frustration). I’m also really excited that Fusion offers the potential to have martial arts and/or dance as PE, one on one, and the instructor totally gets the proprioception issue and seems excited to help her with that. A. recently sent me a quote from something (probably wikipedia) she was reading about proprioception and autism, and then summarized it as follows:

“ Wait, let me get this straight, neurotypicals can walk around without hurting themselves accidentally without thinking about it _at all_? Were you aware of this?”

Obviously, I was aware of this, and obviously, I would love to get this fixed for her _before_ she turns 30, unlike how it worked for me.

Anyway. Functionally, a frustration driven autism rage cycle is going to look suspiciously like a panic attack or severe anxiety in some respects — ya got woofed and it took a while for all those chemicals to clear back out of your system and it’s somewhat psychologically traumatizing.

It occurs to me that getting woofed might be an unfamiliar concept. So I googled that for you!

https://www.martialtalk.com/threads/adrenaline-stress-training.29836/

Also, think about that for a while. When I retired and did martial arts for a few years, a component of what I did (minus the suit) was practicing skills in the context of the instructor _intentionally_ woofing me. All, obviously, pre-discussed, consent was observed yada yada yada. I paid for this, and this absolutely was not how we _started_. The reason for incorporating this was _because_, as noted in the thread, “It's amazing how many highly skilled martial artists cannot adequately defend themselves under stress.”

I talk all the time about how martial arts stopped me running into things, and how amazing that lasting change in my body is one of the best things that has ever happened to me. I only occasionally talk about this training, altho I am reminded often that _other people_ respond to that adrenaline dump wildly differently than I do. I probably should talk about this more.
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A. got up on her own for piano. The piano is loud, obviously, but even so, I usually have to go get her up. Not today! She got up in the middle of R.’s lesson, came down, ate, put her plate over by the dishwasher. I am stunned. She was up until midnight. I had warned the instructor that she might or might not be participating today and why. He was extremely understanding.

I decided to take a look at what the People Online have to say about parents, schools, students and therapy. Yes, I know, probably should have done this before!

Some discussion is teachers looking for guidance on whether it is overstepping to suggest to parents that therapy for the kiddo might help. They were discouraged in general, often on the grounds that this would result in therapy being the financial responsibility of the district. Let me just say, the amounts of money I shelled out for various therapies suggested by that flaming asshole OT that CASE inflicted on T. I have a policy, where if I am in conflict with someone intransigent, I will do everything (okay, nothing that is contra important values, obviously) they suggest will “fix” the problem. If things improve, yay! They were right! I had a good outcome! If things do not improve, or, as is more typical, got worse, I now look like the reasonable one (I tried the things I was told would help If I Just, and we’ve already exhausted their initial list of But If You Just). Over the years, this policy has become tattered and threadbare. It now stinks really bad. I’m probably never going to do this again. And also, I’m going to start attending to the timeline much more closely.

To be clear: it’s not that I will never listen to anyone again. I _do_ listen to people! They are often super helpful! My life is not All Conflict! Altho, a disproportionate amount of my blog is, in part because I need to have something to refresh my intentionally suppressed negative memories, and in part because Drama Makes for Engaging Content (<— that is mostly, but only mostly, a joke).

Some of the discussion online is about having specific behavior or attitude goals for the therapist and the kid to work on, and then leaving them to it and not being overly intrusive. There are also remarks about Don’t Expect to Be in Every Session with Therapist and Kiddo. All of _this_ is hilarious, not in a way that makes them _look_ bad (I mean, it kinda does, but that’s not WHY it’s funny; that’s just sad). It’s hilarious because I got the therapist for T. because he insisted that’s what he wanted. I didn’t have a goal. I just ask how things went and express generic hopes that it was helpful and/or enjoyable, and that if he ever wants to talk to me about it more, he absolutely can, but there is literally no pressure. The second therapist happened because I was getting a lot of pressure from the school psychologist to get A. a therapist and, “A. says she doesn’t understand why she needs or should have one” didn’t seem to be compelling as an answer to anyone (I was fine with it). When the pressure did not let up, I engaged in malicious compliance and got a Team A. therapist and consistently ignored all efforts to have any communication between the therapist and the school. A. wouldn’t go to the therapist without me, and the therapist does family therapy and was fine with this, so that’s what we do (oh, look, I have a therapist too! Whee!). I had no “goal” for therapy, and this also seems to be fine (I picked a relational therapist and I’m paying her directly). The rapid swap from the use of the word “punch” and the phrase “handbook violation” in an email from the vice principal (since retracted as noted in earlier post) to pressure to sign the form allowing communication is why I’m doing this research.

I’ll be back; I have to do before noon duolingo.

A.’s piano lesson really went great and she’s in a good mood. I said, hey, we’re going to learn a new Adult Skill: cleaning a toilet. She was not enthused, but I said, this is the Watch One stage. She helped clean the sink and the counter and we roped T. into helping declutter the counter. This was awesome!

T.’s off to see a play at the jr hi. We’ve scheduled a test drive for the first of a list of candidate vehicles to buy him for graduation. He identified the dealership and that they had the right car available. After the play, he’ll go over with his dad but in separate cars, and they’ll do the test drive and then T. is off to work, conveniently in the same town as the dealership. Progress on multiple fronts!

Meanwhile, A. is reaching out to a friendly-acquaintance, potential friend at school to schedule some online gaming. Mental Health Day is the gift that keeps on giving, along with a plan that gives us hope.

Back to the therapy communication research!

We have teachers wondering if they can recommend therapy and everyone piling onto them saying no, don’t put your district on the hook financially (*sigh*). We have advice to parents to set goals for the kid’s therapy. (*double sigh*) At least that’s being used to manage parental expectations / set boundaries. What else do we have?

We have an assumption that there isn’t a 504 or IEP already involved, and assumptions that the kid doesn’t already have a diagnosis. LOL. My kids have both had diagnoses since they were wee. They’ve been receiving services since pre-K (T.) and early intervention (A.). We’ve had to escalate to get appropriate services for T. AND we’ve requested return to district for T., when an appropriate in district program was created. Ironically, the district did not tell us that program was created, _even tho the teacher designing the program designed it with T. as the target audience_. I mean, what. (How do we know that? The teacher told us that’s what she did. I know it can be difficult to believe if you’ve recently had an interaction with me that R. would describe as I Disapprove of Reality So I Will Remake It the Way I Want It to Be, but I actually do care about relationships and I have some weirdly good ones with people.)

Anyway. None of this helps me? The school knows the sensory issues. _The school sent me email about evolving symptoms that are almost certainly seizure activity ramping up._ They did that when A. was in pre-K, too; they’d send email about her staring off into space and not responding and I was like, whatever, until they said, her face went white, and after I got over the initial, uh, she’s pretty pale, my brain caught up and said, wait, no, that’s a petit mal. We haven’t been able to get the sensory issues adequately mitigated in this school environment. Partly, that’s a Them Problem. A pass to switch classes early or late would help with the passing time crowding overwhelm; an escort would also help, and could help with the Too Much Stuff to Manage problem that means she doesn’t want to bring her over-the-ear headphones because it’s Just One More Big Thing to Manage. Until A. found the migraine glasses, we were seeing a _lot_ of seizure activity; the glasses absolutely fixed that.

If there’s a lesson here, it’s that I probably should have involved a neurologist last year. But we’ve never managed to get any action out of the neurologist we had, because we never actually caught anything on EEG (didn’t do a take home, just a sleep deprived, and honestly, that was the problem). We’ve done well enough managing triggers that I lulled myself and everyone else into a sense that the problem was gone, much like there are people around me who lose track of the food allergies and picky eater issues, because I’ve gotten so good at navigating restaurants. Fundamentally, we don’t really _want_ any of us to be on long-term medication (we resent having to take antihistamines, honestly). We are definitely part of that problem.

OTOH, I’ve _never_ thought it made sense to medicate so you can do something that makes you non-functional without the medication. Avoid the trigger! I’ve been on cruises and took a quarter tab of dramamine every 4-5 hours to do so. Yes, I am a hypocrite. Yes, I had to wake up in the middle of the night to take one. _And it was a cruise._ It wasn’t going to school for years. I basically got on a boat with my extended family and the boat entertained everyone else and I lay around in a haze for several days. The dramamine helps with allergies, and I could still have one drink, so it was actually a fantastic experience. The only downside was my sister kept wanting me to go do shit with them, and my entire plan had been to NOT do anything.

The specific reason I’ve been reluctant to get a behaviorist oriented therapist and/or have the therapist communicate with the school is because I believed that the goal for the school is to fit A. into their environment and have her perform at a high and increasing level. We all know that the school is a bad fit for what A. needs in life to thrive. I’ve expressed concern that this is not an appropriate placement (I did that at the junior high, too, but that was only 2 years, and those were the coming-out-of-the-pandemic years and everything was weird anyway. Plus, junior high.), and I did that when T. was transitioning from pre-K to K (and K was an unrelenting disaster that the district pulled the plug on before I had all my experts fully onboard with the plan).

On FF last night, E. really objected to me using the word “bad” to describe this environment triggering increasing seizure symptom situation. E. likes nuance, which is normally fine and also wildly insensitive in this particular context. I’m not sure precisely what she was getting at, _and I don’t care_. The second sense of “bad” in Oxford languages online (what you get when you google “define bad”) is “not such as to be hoped for or desired; unpleasant or unwelcome”. I just don’t understand how this word could possibly be other than the right word for this situation. E. tried a bunch of ways to express her values, and I suspect the core idea involved concerns about ableism. I think it’s obvious that if you are being pressured into doing something you don’t want to do, that is harming you, and that is causing you to have a lot of unpleasant seizure type symptoms, that’s “bad”. It’s not “bad” that you happen to be the kind of person who has this type of reaction to an environment that is unsuitable for you. E. is probably thinking about this in the context of people in E.’s life who are struggling to find appropriate niches, and whose appropriate niches become less and less supportive as the people in them age and eventually pass away. E. may also be thinking about how for some people, embracing the dissonance, the “not fitting in” is part of them “thriving”. I would _much rather_ be the boring person in the middle, than the person who everyone looks at and goes, this is definitely the one that doesn’t quite belong. I don’t want for me, or anyone else, especially my daughter, to always be the one that doesn’t fit in, no matter how hard they try to find their people. At some point, there is a surfeit of being special, an excess so great that even the numbing properties of great wealth and awesome vacations and amazing friends are not enough to overcome. There are not enough carbs in the world. At some point, ya gotta pull the plug and say, if I don’t fit in anywhere, let’s make a place where I do.

R. and I have been framing “homebound” incorrectly. We look at all the outside-the-home things that people don’t get to experience. But they _do_ get to fit in, within their home. I don’t want to be limited to my home (yet), nor do I want that for my daughter. I now want, badly enough, clearly enough, that I’m not going to tolerate any more, the places where I cannot fit, the places where my daughter cannot. I’m afraid I’m going to have to, once more, Replace Reality with a Better Way of Doing Things.

We are going to make our environment Fit For Us.
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http://www.valueoptions.com/april06_newsletter/friendly_feuds.htm

This is from spring of 2006, from a behavioral health concern of some sort. I know nothing about them; I landed there in the course of thinking about and googling about handling conflict in a social context. This is _not_ about conflict in a work context, or a family context, or some sort of activity context.

The example given is: friend didn’t show up for a birthday luncheon. Birthday friend was hurt and no-show was put off by the standoffishness.

Obviously, from an etiquette perspective, the Correct action is for the No Show to decide whether or not this is a friendship she wants to actually have. I mean, if No Show is doing a slow face / ghosting Birthday friend, then carry on! But if No Show wants to keep this friendship, an apology, and delivery of the birthday tribute, should help mend fences. But no, that’s not where this goes! It is amazing! I can only conclude that this is basically a slide for people doing DBT.

“ Sometimes, it may seem easier to walk away from a friendship than address a serious conflict.” And: “ They can help you get ahead.” (Other, more typical reasons to have a friend are also listed — I’m only quoting the nutty parts.)

“Effective communication involves two parts: presenting information and active listening.”

!!!

I can’t even type I’m laughing so hard. “Presenting information.” I mean, sure, you _can_ frame expressing emotions, concern, care, affection, etc. as “Presenting Information” but _why_ _would_ _you_ _do_ _that_? In a behavioral health context.

Anyway. There’s a lot more there, and on some level, was probably helpful to some people, some times. In terms of helping with the issue I am currently mulling over, NOT helpful! I’m currently trying to figure out just how much effort I should be putting into conflict within certain social contexts. I have identified my pattern of how I deal with conflict within certain social contexts, and concluded I am putting _way_ too much time and energy into these contexts. I know _why_ I did this (only option when I was a child in a cult, who could not live a life aligned with the cult’s value system without complete self-annihilation) and I was _really really good at it_, so good, that I got all kinds of positive reinforcement from just about everyone about how amazing I was because of how good I was at it. However, just because people say nice things, doesn’t mean you are doing the right thing. Just because you are good at something, does not mean it is worth your time and energy. I’m now trying to reassess how much time and energy to put into this, and really struggling with that.
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There are two more episodes coming; I will try to listen, review and link back to this one and forward to that review if I remember. In the meantime . . .

Nocera used to write at NYT; he now writes at Bloomberg. He has been fairly public about developing depression / bipolar disorder as an adult:

https://www.bloomberg.com/opinion/articles/2018-06-11/let-s-talk-about-kate-spade-anthony-bourdain-me-and-depression

This puts him in a really interesting and if not unique then rare position: he has quite a lot of visibility, he is open about mental health challenges, he has both resisted and pursued treatment AND he does not seem to have a bunch of truly horrifying stories about awful things he did to other people before attaining more stability. Either he really did develop bipolar disorder in mid-life, or whatever was going on earlier was at a low enough level that it did not lead to the kind of Hey Let Us Put That On TMZ type event that discredits people.

I am extremely pleased that he is using this if not unique then rare position to take on a particularly challenging problem: what about when you seek help, and that actually makes it worse?

The podcast is a romp of a story, if at times feeling like a psychological horror story. Nocera is humane enough in his presentation, and he has a gentle and compassionate sense of humor that keeps the focus on, what were people thinking as this process (being taken advantage of by a deeply problematic psychiatrist) ticked along over the course of years, or, in the case of some, decades. For me, “that’s crazy” is not the end of analysis, but rather the beginning. I want to know the mechanics of the crazy, and Nocera really does a dive into this one.

That said, I wish, a little bit, that Nocera had a little bit more perspective on the larger pictures. Obviously, what the therapist did was cartoonishly awful. At a minimum, overcharging for bad advice, with job lots of boundary violations thrown in (at least so far, no obvious sexual misconduct). Nocera spends a lot of time talking with “Judith”, about her issues with an abusive mother (a holocaust survivor) that led her to the psychiatrist, and who says she was strongly encouraged by the psychiatrist to cut ties with her mother, and not to be swayed to visit her as her mother was dying, or to attend her mother’s funeral or to sit shiva.

Abusive family relationships within tight knit communities which take sides when there is a definitive split are really, really awful. Without endorsing the advice given by the psychiatrist, it could be observed that “Judith” got a really great deal here: she got to avoid her mother, go to great parties, feel important and minimize contact with a community that was not working for her. Then, later on, when she wanted back in, she could blame it all on the psychiatrist. I smell splitting. I feel like Nocera should have caught a whiff of it, too, because the main story of the first few episodes reek of splitting.

Anyway. Great story, and if you are ever complaining about therapists who do not tell you anything about their own lives, but just basically encourage you to talk about what you are feeling and experiencing, or who only want to focus on supporting you in making concrete plans to do more of what is working and figuring out ways to incrementally approach the miracle of Being Better, take a step back and go, hey, at least this therapist is not like that therapist. Also, wow, what psychiatrists do has really changed since the 1980s.

ETA: First episode is how Nocera fell into this rabbit hole. Second episode is how the psychiatrist interfered in a sibling relationship. Third episode is how the psychiatrist weaseled his way into President of his client’s company and an employee at that company describing how good the psychiatrist is at lying with no tells at all. Fourth episode is the psychiatrist fostering relationships between patients, and the parties at the house. I started with 4, then listened to 1, 2 and am currently halfway through 3.
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Subtitled: Staying well with Manic Depression/Bipolar Disorder

This is a collection of responses to a questionnaire by people diagnosed with manic depression/bipolar disorder. The group is from Australia, so the details about the health care system (and the spelling of some words) will be unfamiliar to a United States audience. Because it takes a "wellness" perspective, the responses are about how do people with this diagnosis live their lives and avoid further episodes of their illness (either by reducing the frequency, intensity or both). Almost, but not all, of the respondents are on medication (mostly some form of lithium, altho there is a range of prescriptions used to manage this illness, including some people who only take lithium or anti-psychotics part of the time, or take anti-depressants part of the time because that works best for them, and other strategies as well). All of the respondents are accepting of their diagnosis, altho some of them downplay the seriousness of it.

Many of the people in the book had one or more hospitalizations before they received the correct diagnosis that led to an appropriate treatment strategy that then helped them avoid further hospitalizations. The most common misdiagnoses were for schizophrenia, altho there were some for unipolar depression and other things. The people who had wrong diagnoses were very relieved to finally receive a diagnosis that led to successful treatment.

Some of the people in the book changed careers. Some retired and receive a disability pension. Some were diagnosed quite young and have held a few jobs but not established a career. Some had partners and/or children. Others did not.

It is striking how many of the people describe the great care they take to maintain daily routines and a rhythm to their lives: consistent times getting up and going to bed, activities like exercise, meditation, yoga, etc. to help them maintain perspective and stable mood, relationships they maintain with people who can tell them when they start to "speed up". Overwhelmingly, they have reduced or eliminated their consumption of alcohol and other recreational drugs, and many of them carefully limit caffeine as well. They are cautious about travel across time zones, and they very carefully manage their response to springtime.

This is a wonderful book in that it goes beyond the take-your-medication-or-else approach, while strongly supporting effective medication strategies. It's a rare and useful combination. While some reviewers on Amazon seem to think this book only includes people whose lives were not that disrupted by this illness, a careful reader can clearly see otherwise. Any reader -- whether they have bipolar, know someone who has bipolar, or has an interest in better understanding neurodiversity -- can learn a lot about the importance of self-insight, and developing compensating habits in life to become aware of and effectively deal with stresses before they overwhelm one.
walkitout: (Default)
Subtitled: A Revolutionary Six-Stage Program for Overcoming Bad Habits and Moving Your Life Positively Forward

It's not clear exactly when the last substantive revision of this kindle edition occurred. No OCR problems, typos, grammar issues, wtf were apparent in the course of a single read-through. Because the original book dated from the 1990s, the contents are somewhat, er, dated. For example, we have made much more progress towards what they call "social liberation" with respect to smoking, and to a lesser degree with respect to drinking. For example, most indoor and some outdoor public places in the US and many other developed nations are now, by law, smoke-free. Far more people have quit smoking since this book was written, and the phenomenon they describe (of smoking becoming increasingly covert, hidden even from family members) has progressed even further, albeit electronic cigarettes have produced a new wrinkle. Because I've been paying a lot of attention to alcohol portion sizes, the text has a single-alcoholic-serving as 12 oz beer, shot (1.5 oz) serving of spirits (both the same as now) or a 4 oz glass of wine.

Before anyone goes, OMG, do you drink/smoke/have a whatever problem, the answer is, of course I have a whatever problem. Almost everyone has a whatever problem. And this is a systematic way of thinking about whatever problems and what people do about them without involving professional assistance and when that works and, when it doesn't, why. Their theory, the TransTheoretical Model of Change (TTM) is a very 90s, pre-CBT approach to Helping People Help Themselves. Starting from then-current research that indicated that virtually all theoretical approaches in the helping professions (he calls them psychoanalytical theories, and quotes Freud without apology, altho fortunately not often) were roughly equally efficacious. Not too long after the TTM model was devised as a way to map approach to "stage" in the progression of change, the helping professions in general explored and adopted a bunch of Brief/Quick/client-centered approaches to helping -- they are now more or less lumped together as cognitive-behavioral therapies.

In any event, a bunch of people and organizations have adopted TTM as a way to better match therapeutic tools (whether that is consciousness raising or putting together a plan of what to do instead of whatever, or rallying one’s social network to provide support or any number of other things) to where in the change process the complainant/client/patient/addict/etc. is. In general, matching the appropriate tool to the person is a Good Thing; one of the major complaints about TTM is that 6 months out, a lot of people need a fairly significant Readjustment (whether that’s a relapse, or a secondary problem that was why the person had the bad habit in the first place, or one of their coping strategies has gotten out of hand, etc.). TTM is pretty much just like everything else in that respect, offering little more than platitudes about Hey, Lather, Rinse, Repeat.

Many brief, quick, CBT type therapies, however, address the readiness for action problem very differently. If someone is sitting in front of a professional, they are ready for _some_ kind of action; these therapies are much more rigorous about having the client define the goal state. Prochaska et al are here to tell you what your goal state should be, and thus they generate a lot more classic therapeutic resistance. They are _smarter_ about responding to that resistance, but they still generate resistance.

Prochaska et al also stumbled across some perceptual things (like how bad punishment is, how good praise is, ratios of positive to negative statements to be perceived as balancing out as positive, the importance of making a goal more attractive vs. the current state of being less attractive, and having some numbers on that) that are pretty widely recognized by NLP types. In good news, this group of authors is considerably less cult-y than some NLP outfits. In bad news, their therapeutic tricks are a lot sloppier and thus take longer and don’t necessarily “stick” as well.

But if you are looking for a theory of habit change, this is a good one. While the primary focus is on smoking, drinking problems, anger management, exercise/diet/weight control and other health interventions and so forth, you could kind of use it for almost anything. One of the most consistently wonderful things about this book is its honesty about the crankiness of people who are in the process of major self-change, and how a lot of bad habits are the result of people trying to suppress negative emotions or avoid enforcing boundaries, and other things that cause social conflict. They emphasize the importance of developing assertiveness, and recognize that some relationships may need to end (temporarily or permanently) if they are getting in the way of necessary changes.

They do devote a chapter to exploring how to tell when it is time to involve a professional in the change process.

However, I’m going to look around and see if there is anything better out there.
walkitout: (Default)
Subtitled: Using Play to Enhance Emotional And Behavioral Development for Children With Autism Spectrum Disorder

_Replays_ has a straightforward central idea: take some ideas from play therapy (hamming it up, using dolls/puppets/figurines as proxies all in the service of helping a child figure out how to deal with a difficult situation) and some ideas from desensitization and sort of merged them into a framework for helping kids who have a lot of communication and social development issues (and possibly other issues as well). The central problem in using play therapy ideas with kids on the spectrum is that in general, their pretend play is limited to nonexistent, which would seem to make this a nonstarter. Within some constraints, however, Levine and Chedd claim that it works, and I am inclined to believe them. A lot of _Replays_ is devoted to describing how to use this framework in a variety of cases; theory and limits and how it interacts with other therapies such as RDI, ABA, SCERTS (hey, first time I heard of it, too), Floortime/DIR, etc. consumes the rest of this slim book (which I bought on the kindle! Yay!).

Levine is a smart, intuitive therapist with a great sense of humor who is open to a lot of strategies and approaches. This comes through in the text. It was a quick read, and while most of what I've done with it is more the quick form than the extended form, it has been useful. If nothing else, Levine and Chedd are a great reminder that a huge chunk of helping anyone at all is making sure they feel like they've been heard, and their feelings are taken seriously.

While A. and I were waiting for the train in StoryLand (we'd just missed the previous one, so it was a longish wait), we went into the candy and toy shop next to the stop and picked out a plastic train whistle (very cool -- it does a 3 note chord) and a Gund monkey. Monkey turned out to be quite helpful for the rest of the trip, doing all kinds of things with the kids, including a fair amount of misbehavior. It got to the point where A. wouldn't get in the stroller to leave unless we brought monkey with us. I'm too aspie to think to do this very, very normal kind of play, but _Replays_ reminded me of all the times I've seen other parents and caregivers do it, and explained enough of the "rules" to give me some repertoire. Lots of fun!

This is the first book about autism spectrum stuff that I truly enjoyed reading.

May 2026

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