When we talk about hypokalaemia (e.g., from a channelopathy) as a cause of #SensoryOverload, many people think that a lab test will reliably reveal whether you lack potassium. So: no, lab tests are often unreliable for this. ncbi.nlm.nih.gov/pmc/articles/P…
To add to the confusion, hyperkalaemic sensory overstimulation (sensory overload from too much potassium) can externally look similar to hypokalaemic sensory overstimulation (sensory overload from too little potassium).
As the paper states, "Potassium is predominantly intracellular; hence small shifts can cause large changes in the measured value. [...] clinicians must have a high-index of suspicion [...] when the laboratory values are not concordant with the clinical picture."
But there is a problem when clinicians do not even know what the clinical picture of hypokalaemic sensory overstimulation looks like. This is the primary reason why most autistic people who suffer from this treatable medical condition never get medical treatment for it.
And to make matters worse, the lack of suitable formal diagnostic treatment guidelines for hypo- and hyperkalaemic sensory overload in autistic people seems to have some kind of logical error behind it, something like this:
There's not a lot of research on potassium-related sensory overload in autistic people specifically (even though genes associated with hypokalaemic periodic paralysis, which also involves sensory overload) are also associated with autism...
...and therefore only people with diagnosed ion channel diseases are likely to get guidance or treatment. And do you know how few people get diagnosed with those ion channel diseases? Those diseases are considered rare.
Never mind that hypokalaemic sensory overstimulation can also happen to non-autistic people who don't have ion channel diseases, if they are simply undernourished.
We are not going to see an improvement in treatment for many debilitating medical conditions which affect autistic people as long as behaviourists are doing autism awareness training for healthcare practitioners.
Do you know which other people typically experience severe sensory overload? People with #MECFS and PASC (#LongCovid).
And do you know what else? These people ALSO often experience electrolyte dysregulation and potassium loss.
If the role of magnesium in treating hypokalaemia was commonly understood in the healthcare industry, you wouldn't have this professor bothering to do an entire online lecture about it to healthcare professionals.
I've met hospital doctors who can't tell you what a clinical presentation of magnesium deficiency looks like, by the way. Not kidding.
Do you know how often I come across autistic people who say they're OK with being autistic, they just wish they didn't have to face discrimination and sensory overload.
What are the chances of either of those being addressed as a priority in a healthcare setting while clinical professionals are getting training on the red flags and deficits of autism from people who make their money from ABA?
Man, this is an interesting exchange. Many people are disadvantaged in this kind of situation: most of us don't have the full set of weapons and skills—body language, posture, tone, eye contact, reading the other guy's responses, quick thinking. This guy has… a lot.
The argument wasn't won entirely on logic and words. The squeaky guy was discombobulated and allowed himself to be overpowered. The use of the chair was masterful. This whole scene could be analysed by students in a drama class.
Squeaky was like, “OK, I am not getting a chance to come in with a considered response, so let me just allow this person to go off on a tirade and end up looking stupid”—except his tactic backfired, as the big guy ended up spouting a whole lot of good points—
What these people are advocating is child abuse. I know the way they put it doesn't sound bad, but this is about a very controlled, clinically callous form of manipulation. I'll drop some more links below so you can understand the context.
[THREAD]
Why is it so hard for people in the field of ABA to improve the field, even with the support of autistic activists? One of the reasons is this:
Powerful people in the industry will try to destroy you for listening to autistic people, for trying to do a job compassionately, and for calling out the abuse.
I'm going to ask Jennilee Sunshine, a BCBA, whether I might tell her story here verbatim. It's already public on Facebook.
Vladimir Putin's standard modus operandi is to make agreements and then demonstrate his power by breaking them with impunity.
Any suggestion that Ukraine should negotiate a settlement with Russia is borne either out of ignorance of this long track record, or out of ill logic, naïvete and stupidity (like, "I know, but I'm sure it won't happen again") or straight-up support for Russia.
Ukraine must WIN this war. Its allies are wasting time, money and lives, and strategic opportunities by holding back the support that's needed for victory. Ukraine has more than proven itself to be deserving.
[THREAD] Request to
#BCBA
#BehaviorTwitter #BehaviorAnalyst #BehaviorAnalysis
Content warning: ABA, child abuse
The following account was posted in an ABA survivor group. I have permission to share it to ask what this person can do to stop the abuse.
1/x
"I have step kids that are currently in the custody of their maternal grandparents. Dcf is involved and put the youngest in ABA (I have no say in her care as of now, and neither do her parents)."
2/x
"When I was over at their house most recently, I heard her crying and went to go see what was going on, her ABA therapists pulled me aside and told me we were now ignoring her when she cries until she calms herself down and uses a happy voice."
3/x