WEBVTT

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Before we begin this episode about reading, I

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want to say there's lots of neurobiology, measurement

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instruments, and brain waves, sometimes called

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oscillations or frequencies. However, I will

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hopefully provide easy -to -understand analogies.

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We will go through the entire reading process

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from the moment, light, hysterectomy, to formulating

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speech. We will also compare so -called normal

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readers, the autistic phenotype, and dyslexia,

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and at times the odd contrast of the autistic

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phenotype and dyslexia. Today's episode is all

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about reading. We will discuss the reading process,

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the neurobiology of course, a breakdown of visualizing

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the text and transforming that into understanding.

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comprehension, how to formulate that into speech.

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You will find out if you don't already know we

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use speech even when silently reading to ourselves.

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100 % of autistics have a problem, some sort

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of problem with speech and language. We will

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also explore the spelling issues, why and how.

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Some people, especially autistics, can get caught

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up on reading fluency. We will discuss dyslexia

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and several brain regions. Reading is a sophisticated

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cognitive process that transforms written text

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into meaning through a left -lateralized brain

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network. Considering the autistic phenotypes

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fast, sensory processing Let's start before the

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brain even makes sense of the words. Which is

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in the little neculi in the occipital temporal

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lobe which is a combination of the occipital

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and temporal lobes called visual word form area

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VWFA We'll talk a lot about that later. Let's

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start with the retina. When you look at a word

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like dog on a page light hits your eyes. You

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probably know about the rods and cones and then

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the retinal ganglion cells that track back through

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your thalamus. The thalamus is going to be a

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first stop here, the lateral geniculate thalamus.

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We talked about this with the oxytocin, the magnocellular

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and parvocellular types of cell types used for

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vision. Now also remember the lateral geniculate

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is right there by the midbrain. It essentially

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reaches out and high fives things like the superior

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colliculus and so forth from the midbrain discussions.

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So from the lateral geniculate, the optic nerve

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to the primary visual cortex, which is V1 in

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the back of your brain. V1 is active 50 to 100

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milliseconds. This is like a sketch artist just

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kind of mapping out the drawing and this is spotting

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the lines and curves of the D or the O for the

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dog example. EEG catches this spike and fMRI

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shows the V1 lit up. MEG confirms it's the first

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stop with precise timing. Next secondary visual

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areas which is V2, V3, and V4 take over from

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100 to 150 milliseconds. They're like puzzle

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-builders. They are just piecing together these

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lines into letters and shapes, ensuring, for

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instance, that D isn't a B. EEG shows early signals

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before the N170, and ItMeG maps connections to

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V1. And fMRI pinpoints these areas. V4 starts

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saying, by the time we get to the last visual

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process here of the visual cortex, V4 says, this

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is text. This isn't something insignificant.

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This is all happening before the visual word

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form area recognizes this as dog. Hard stop here,

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a cool side note. kind of independent from this

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conversation about autism, dyslexia, and reading.

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And this is how blind people kind of repurpose.

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They have neuroplasticity in this V1 through

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V4 areas for reading tactile in the braille.

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And they also repurpose these V1 to V4 areas

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for auditory sensations. So there's kind of a

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heightened area here. Words like amazing and

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fascinating don't even describe how wow this

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is. Now here's how it works. Typically congenitally

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blind individuals or those that luster eyesight

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early in life will better repurpose these areas

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and these V1 to V4 areas are recruited for that

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sensory processing with the BREL. Neuroplasticity

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in the human living organism is wild. So let's

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talk about two different things here that's been

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mentioned several times across the podcast. One

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is the heightened so -called heightened sensory

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processing and the mechanism by which this happens

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is neurooscillations or brain waves. We talked

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about those both in several episodes but let's

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expand on those. Often I've mentioned the waves

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and not really having direct order, but let's

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clarify this. The lowest oscillation is delta,

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0 .5 to 4 hertz. Theta, 4 to 8 hertz. Alpha,

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8 to 12 hertz. Beta, 13 to 30 hertz. And then

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there's gamma, anything over 30. However, Gamma

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has two different kind of stages, low gamma,

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which is 30 to 80 Hertz and high gamma over 80

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Hertz. The best way to think about this, I think,

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is if you have one trial learning, let's say

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you're in a traumatic experience or near tragic,

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maybe you're driving in the road and somebody

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runs a stoplight and it almost hits you or it

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does hit you. At that moment, your body is sent

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into these high gamma waves. This means your

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body is going to remember this incident much

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easier. This is the biggest thing with trauma.

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People that experience a traumatic experience,

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their body, just all of these brain waves are

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sent into high gamma. This is the... so -called

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origin of one trial learning. It only takes you

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one time to really learn from that experience.

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Another example is if you touch a stove or touch

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something hot, you typically remember not to

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touch that again. However, independent of this

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one trial learning, everything operating on our

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insides are running on these oscillations. They

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are constantly on oscillations. This is a big

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indicator of our so -called internal states as

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well. Calm or excited, stressed or relaxed, whatever

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the case may be here. Just insert whatever. So

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let's talk about the sensory processing between

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non -autistics versus the autistic phenotype,

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especially with reading. So the different brain

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waves or frequencies, neural oscillations and

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so forth. In non -autistics, V1 through V4 is

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operating at alpha waves and beta waves. Alpha

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helps you focus, like ignoring distractions while

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reading dog. Beta links the V1 to V4, ensuring

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those letter shapes come together smoothly. EEG

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picks up alpha suppression when you're engaged,

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while MEG shows beta connections between visual

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areas. Gamma waves over 30 Hz are there too,

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but they're less dominant, helping fine -tune

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details, like making sure the O in dog isn't

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a C. Unlike in autism where gamma waves go into

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overdrive, non -autistic brains keep a balance

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mixed, ensuring efficient processing without

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getting stuck on every detail. FMRI supports

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this by showing steady activation in V1 through

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V4, not the hyperactivity in autism. In the autistic

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phenotype, it's mostly or completely entirely

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all gamma waves. This is the so -called heightened.

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So let's start making sense of what the eyes,

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the retinas are sending back to the rest of the

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brain, starting in the occipital lobe. The visual

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word form area in the occipital temporal cortex

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recognizes letters and words as visual patterns,

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acting like a pattern detector to identify familiar

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shapes and sequences, such as distinguishing

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dog from bog, the temporal parietal cortex, including

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the superior temporal gyrus. And the angular

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gyrus maps these visual forms to sound, enabling

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mental or vocal pronunciation, like sounding

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out dog as dog. The inferior frontal gyrus, which

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does include Broca, we're not limiting this area

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to just Broca. However, it does include two more

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little nuclei involved in this process, involved

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with integrating word meanings akin to a storytelling

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piece to gather a narrative to understand that

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dog refers to a pet these regions are linked

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by the arcuate fasciculus a white matter track

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facilitating communication for phonological and

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semantic processing that ensures seamless coordination

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if you remember the speech and language episode

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We spent a lot of time on the arcuate fasciculus.

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It's a white matter track connecting Varanaki

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and Broca. Remember, these are two distal areas.

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Functional magnetic resonance imaging measures

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blood flow to pinpoint active regions, showing

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robust visual word form area activation for word

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recognition. coming at 150 to 200 milliseconds.

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And this is using an N170 for EEGs or M170 for

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MEGs. These are the same instruments we talked

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about in part two of the sensory processing episode.

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Same stuff. EEGs capture electric brain activity

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with millisecond precision. and this detects

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rapid neural responses like N170 for visual processing

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and 400 so roughly 400 milliseconds for the meaning.

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MEGs measure magnetic fields and this offers

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precise timing and moderate spatial resolution

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so within two to five millimeters to map connectivity

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between the visual word form area and the superior

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temporal gyrus. The temporal parietal lobe handled

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phonological processing roughly 200 to 300 milliseconds

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and the IFG, the inferior frontal gyrus, supports

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the semantic integration happening roughly at

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300 to 500 milliseconds. The dual stream model,

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the so -called dual stream model here, includes

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a ventral stream. This includes the VWFA and

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the semantics for familiar words, like instantly

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recognizing dog, and a dorsal strain, that temporal

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parietal for phonology, for decoding new, and

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pseudo words. Hard stop. The pseudo word, for

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example, zob. We will discuss this a little bit.

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But you should know that pseudo words are very

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common in achievement type tests given to mostly

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kids. These are things like the Wyatt Ford, the

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Weschler Individual Achievement Test or the KTEA,

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the Kauffman Test of Educational Achievement.

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These are very common types of tests used in

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psychological assessments or school assessments,

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school placement type of activities here. Diffusion

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tensor imaging, DTI, also talked about in the

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part two of the sensory processing episode, reveals

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higher fractional anisotropy in the arcuate fasciculus,

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indicating a strong connectivity here, which

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predicts reading fluency. So in other words,

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the higher this connection here, the better the

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reading fluency. So it might be a good time here

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to kind of describe this fractional anastrosophy.

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Here on after I'm going to call this FA. It's

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just easier. This is, I'm going to give some

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easy to understand examples here. This is measuring

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water. The DTI diffusion tensor imaging is measuring

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water. Diffusion is just nerd speak for movement.

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So how water is moving throughout the brain is

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what this is doing. with these different connections,

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even distal connections, we talked about myelin.

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Myelin being like a, the difference in myelin,

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well myelination, like driving on an interstate

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versus a gravel road. FA, it's measuring this

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number. One is optimal, like massive amounts

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of water flow. Zero is no good. There's some

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disruption going on. So like the gravel road.

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So the higher, the better. And if you think about

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the myelin being straws, straws having a good

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water flow, but if there are kinks in the straws

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or the straws are narrow versus wide straws,

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there's going to be a disruption of water flow.

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If you think about garden hose, if you have kinks

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in the garden hose, the water coming out at the

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end is massively implicated. The pressure and

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water flow here is very weak. It's very frustrating

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if you're using a garden hose and that's delaying.

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It's delaying this distal connection in the brain.

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So those receiving regions post -synaptic connections

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and so forth are delayed and we've talked about

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this in the sensory processing where the earlier

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stops are heightened but the distal connections

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are kind of slowed or impaired. And this is going

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to come into play later when we talk about autistics

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reading and that heightened visual processing

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and dyslexics having a weakened FA with these

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distal connections. It's going to all make sense

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I hope. Silent reading involves something called

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subvocalization or silently speaking. Readers

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here internally articulate words. engaging in

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phonological areas with less of the IFG activating

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than oral reading, which recruits the pre and

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post -central gyri for motor coordination and

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speech production. Now we are silently speaking

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to ourselves when we are reading because we are

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speaking up to the cortex and other strong areas

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of the brain. we are teaching ourselves what

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is being read. This is a huge part with learning.

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The overall goal of this network here is to efficiently

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decode the text and convert it into sound and

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derive meaning, enabling fluent reading measured

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as words per minute. So either way, reading to

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the cell or out loud, you are essentially Speaking.

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So let's break down the reading process. Step

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one is we are decoding something called orthographic

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processing. And this involves the VWFA, that

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visual word form area, to identify letters and

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words as those visual patterns, like recognizing

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book on a page as familiar shape occurring within

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150 to 200 milliseconds. FMRI shows that this

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VWFA activation and EEG captures the rapid electrical

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spike and the MEG localizes it to the occipital

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temporal cortex. Remember from the Sensory Processing

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Part 2 episode, EEGs are much better at kind

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of local distinguishing, local findings and so

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forth and EEGs are much easier to use. less dangerous

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even. However, MEGs are better for distal connections,

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kind of spotlighting the whole brain to see what

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is all active. The VWFA's goal is to quickly

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and accurately process visual word forms, preparing

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the brain for sound and meaning. This is step

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one. So what does processing visual word forms

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mean? This involves the brain's ability to recognize

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and interpret written words as visual patterns,

00:19:24.799 --> 00:19:28.299
a key step in reading. This process primarily

00:19:28.299 --> 00:19:32.980
engages the VWFA for the initial recognition,

00:19:33.579 --> 00:19:36.519
identifying letters and words. This is going

00:19:36.519 --> 00:19:40.839
to be orchestrated by this rapid visual processing

00:19:40.839 --> 00:19:43.759
that relies on the brain's ability to match that

00:19:43.759 --> 00:19:49.519
visual input. stored to the orthographic representations.

00:19:50.700 --> 00:19:53.660
Does the brain recognize this sequence of letters,

00:19:53.980 --> 00:19:56.480
this sequence of letters that make up this word?

00:19:57.119 --> 00:20:00.839
Does the brain recognize this? The role in reading

00:20:00.839 --> 00:20:03.579
here is huge. This step prepares the brain for

00:20:03.579 --> 00:20:08.099
subsequent phonological mapping and the semantic

00:20:08.099 --> 00:20:12.720
integration. This is like step one. If your dominoes

00:20:12.720 --> 00:20:16.420
are off and the first domino is off, The second,

00:20:16.519 --> 00:20:18.759
third, fourth, everything downstream is going

00:20:18.759 --> 00:20:24.059
to be delayed. And this is facilitated by the

00:20:24.059 --> 00:20:28.000
arcuate fasciculus. Once again, so the arcuate

00:20:28.000 --> 00:20:31.900
fasciculus is involved in reading and speaking.

00:20:33.220 --> 00:20:37.940
In fluent readers, this VWFA enables automatic

00:20:37.940 --> 00:20:41.700
word form processing. It automates it. This is

00:20:41.700 --> 00:20:43.500
what the central nervous system is trying to

00:20:43.500 --> 00:20:47.950
do with everything. And this contributes to efficient

00:20:47.950 --> 00:20:52.529
decoding. So some disruptions in this, for instance

00:20:52.529 --> 00:20:57.990
in dyslexia, the VWFA is underactive and this

00:20:57.990 --> 00:21:02.269
leads to delayed N170 and impaired word recognition.

00:21:03.490 --> 00:21:08.450
However, the data for autism shows hyperactivity

00:21:08.450 --> 00:21:13.369
of the VWFA and that bilateral activation reflect

00:21:13.369 --> 00:21:18.579
a visual spatial bias, and enhances the decoding

00:21:18.579 --> 00:21:23.920
speed, but not always comprehension due to the

00:21:23.920 --> 00:21:27.059
frontotemporal under -connectivity. We've talked

00:21:27.059 --> 00:21:30.619
about this a lot with autism, those heightened

00:21:30.619 --> 00:21:34.720
connections early in processes, but then downstream,

00:21:35.599 --> 00:21:38.400
it gets delayed, it gets disrupted, those more

00:21:38.400 --> 00:21:42.460
distal connections. And you should not be surprised

00:21:42.460 --> 00:21:46.519
here with this hyperactivity of the visual word

00:21:46.519 --> 00:21:50.660
form area because of the visual processing, those

00:21:50.660 --> 00:21:56.200
high rates of speed with visual processing. Another

00:21:56.200 --> 00:22:01.599
area from the Reza Shadmir episode, the cerebellar.

00:22:01.960 --> 00:22:04.380
This is a very underrated area and we'll talk

00:22:04.380 --> 00:22:08.299
a lot about the cerebellum today. Purkinje cells

00:22:08.299 --> 00:22:11.599
in the cerebellum refine the timing and coordination

00:22:11.599 --> 00:22:15.240
of the eye movements. These are often called

00:22:15.240 --> 00:22:19.920
saccades. In needing to scan word forms, this

00:22:19.920 --> 00:22:22.579
is what it's trying to accomplish here. With

00:22:22.579 --> 00:22:27.160
climbing fiber afferents, correcting errors in

00:22:27.160 --> 00:22:31.119
real time, and parallel fibers integrating visual

00:22:31.119 --> 00:22:35.680
cues. In dysfunction, as seen in the autistic

00:22:35.680 --> 00:22:40.859
phenotype, with progeny cells, 25 to 50 percent

00:22:40.859 --> 00:22:45.059
cell loss in the autistic phenotype. for Purkinje

00:22:45.059 --> 00:22:50.299
cells, and in dyslexia, there's a disruption

00:22:50.299 --> 00:22:54.480
of this precise affecting fluent word form processing.

00:22:55.940 --> 00:22:59.339
So this process is foundational to reading, linking

00:22:59.339 --> 00:23:03.839
the visual input to the sound and meaning through

00:23:03.839 --> 00:23:08.539
a coordinated neural network. This is not about

00:23:08.539 --> 00:23:12.240
turning the word into visual thinking. It is

00:23:12.240 --> 00:23:15.039
about seeing the pattern of the letters for reading

00:23:15.039 --> 00:23:21.460
the word. So spelling difficulties. This is an

00:23:21.460 --> 00:23:25.799
area of interest here for us. Particularly if

00:23:25.799 --> 00:23:28.779
you remember from the Kanner kids and Asperger

00:23:28.779 --> 00:23:33.640
kids, as well as those with dyslexia and or the

00:23:33.640 --> 00:23:37.380
autistic phenotype as a whole, are best explained

00:23:37.380 --> 00:23:40.890
by challenges in the orthographic processing

00:23:40.890 --> 00:23:44.869
phase here with additional contributions from

00:23:44.869 --> 00:23:49.930
related stage and neural networks. The primary

00:23:49.930 --> 00:23:53.390
point in spelling is the orthographic processing

00:23:53.390 --> 00:23:57.250
and this is occurring. This phase that involves

00:23:57.250 --> 00:24:01.089
the visual word form area for the decoding process.

00:24:01.430 --> 00:24:04.190
Now if you think about it, think about that hyperactivity

00:24:04.190 --> 00:24:08.019
and autism. With autism, you know about that

00:24:08.019 --> 00:24:11.519
black and white thinking as well. This hyperactive

00:24:11.519 --> 00:24:17.259
VWFA with that bilateral activation, this leads

00:24:17.259 --> 00:24:22.079
to a hyper -focus on spelling, but a poor integration

00:24:22.079 --> 00:24:27.799
with phonology or semantics due to that frontotemporal

00:24:27.799 --> 00:24:32.000
under -connectivity. Again, more of the Purgenje

00:24:32.000 --> 00:24:36.079
cells are involved here, and... an area that

00:24:36.079 --> 00:24:38.940
we've recently discussed over the last winter

00:24:38.940 --> 00:24:43.160
in several episodes the dorsal striatum the dorsal

00:24:43.160 --> 00:24:46.740
striatum is our input area of the basal ganglia

00:24:46.740 --> 00:24:50.119
i know a lot of a lot of regions here a lot of

00:24:50.119 --> 00:24:53.299
different brain regions here but they're all

00:24:53.299 --> 00:24:56.559
very important and fascinating the dorsal striatum

00:24:56.559 --> 00:25:00.480
is the input areas of the basal ganglia in other

00:25:00.480 --> 00:25:05.029
words this is what's going to coordinate or conduct

00:25:05.029 --> 00:25:08.450
the downstream movements remember the basal ganglia

00:25:08.450 --> 00:25:12.630
is go and no -go area and two big things here

00:25:12.630 --> 00:25:15.650
with the dorsal striatum is it's heavily involved

00:25:15.650 --> 00:25:22.130
in learning and goal -directed activity and habitual

00:25:22.130 --> 00:25:26.609
responses remember autism and those habitual

00:25:26.609 --> 00:25:30.890
responses or the lack of adaptive responses we

00:25:30.890 --> 00:25:35.640
can get caught up on things very easily. A second

00:25:35.640 --> 00:25:37.819
consideration for spelling difficulties here

00:25:37.819 --> 00:25:42.400
is following the orthographic recognition, which

00:25:42.400 --> 00:25:46.019
is the phonological processing. This is involved

00:25:46.019 --> 00:25:49.859
with that temporal parietal cortex, the superior

00:25:49.859 --> 00:25:52.920
temporal gyrus and the angular gyrus, those two

00:25:52.920 --> 00:25:56.700
specific areas. This maps spellings to sounds.

00:25:58.640 --> 00:26:02.460
disruption of the cerebellar timing via the purgenji

00:26:02.460 --> 00:26:06.720
cells affect broca area for articulation and

00:26:06.720 --> 00:26:09.759
this can hinder spelling by sound and this leads

00:26:09.759 --> 00:26:14.839
to phonetic misspellings for example here phone

00:26:14.839 --> 00:26:21.160
f -o -n -e for phone it's very confusing the

00:26:21.160 --> 00:26:23.660
Kenner kids were so funny with this if you read

00:26:23.660 --> 00:26:27.559
the Leo Kenner 1943 paper Another region of interest

00:26:27.559 --> 00:26:30.940
is the arcuate fasciculus. This track reduces

00:26:30.940 --> 00:26:34.500
with that F -A in dyslexia, remember that water

00:26:34.500 --> 00:26:38.259
flow, and with the autistic phenotype, the connection

00:26:38.259 --> 00:26:41.880
between phonological output, the Broca's area,

00:26:42.319 --> 00:26:46.299
and comprehension, Ferenke's area. This disrupting

00:26:46.299 --> 00:26:49.220
the feedback loop. All of these things are basically

00:26:49.220 --> 00:26:52.440
running in a loop updating each other. And this

00:26:52.440 --> 00:26:55.410
is needed to verify spelling correctness. In

00:26:55.410 --> 00:26:58.450
the Autistic Phenotype, under -connectivity further

00:26:58.450 --> 00:27:02.470
complicates integrating spelling rules. There's

00:27:02.470 --> 00:27:06.329
a downstream area here for the semantic integration

00:27:06.329 --> 00:27:09.130
we haven't discussed yet, but with spelling,

00:27:09.589 --> 00:27:12.950
it's important to mention this now. That inferior

00:27:12.950 --> 00:27:16.390
frontal gyrus, remember including the broca area,

00:27:16.650 --> 00:27:20.430
links spellings to meaning. But this is delayed

00:27:20.430 --> 00:27:24.220
using N400 in the Autistic Phenotype. so roughly

00:27:24.220 --> 00:27:27.900
400 milliseconds this is supposed to come online

00:27:27.900 --> 00:27:31.339
but that is due to the frontotemporal deficit

00:27:31.339 --> 00:27:35.019
that under connectivity in dyslexia there's an

00:27:35.019 --> 00:27:37.980
over activation and this can lead to semantic

00:27:37.980 --> 00:27:41.859
based spelling errors the examples here are something

00:27:41.859 --> 00:27:48.880
like there t -h -e -i -r for there t -h -e -r

00:27:48.880 --> 00:27:53.960
-e when meaning is more important than Orthography.

00:27:55.220 --> 00:27:59.539
Okay, so meaning is more important in this situation

00:27:59.539 --> 00:28:03.660
than the orthography part. Spelling difficulties

00:28:03.660 --> 00:28:06.920
indicate kind of a bottleneck in the orthographic

00:28:06.920 --> 00:28:11.079
encoding, often exacerbated by the cerebellar

00:28:11.079 --> 00:28:15.380
cortical loop disruptions. I remember in the

00:28:15.380 --> 00:28:18.799
third grade, anecdotal time I guess, I remember

00:28:18.799 --> 00:28:24.900
spelling movie. M -O -V -E. And I got it wrong,

00:28:24.980 --> 00:28:29.759
of course. M -O -V -I -E. And I just remember

00:28:29.759 --> 00:28:33.039
sitting there thinking, looking at movie. M -O

00:28:33.039 --> 00:28:36.680
-V -E is like, no, that's right. I was just completely

00:28:36.680 --> 00:28:39.960
lost. It doesn't make any sense. If you find

00:28:39.960 --> 00:28:42.359
yourself easily confusing and getting stuck on

00:28:42.359 --> 00:28:47.200
words like accept and expert while reading, or

00:28:47.200 --> 00:28:53.220
words like expectation, extinction or extermination

00:28:53.220 --> 00:28:56.400
like I do all of those words kind of look the

00:28:56.400 --> 00:29:00.539
same I still get caught up on this even at 45

00:29:00.539 --> 00:29:03.920
years old this is likely happening at the orthographic

00:29:03.920 --> 00:29:07.779
processing phase with potential considerations

00:29:07.779 --> 00:29:11.859
contributions from subsequent stages we have

00:29:11.859 --> 00:29:14.559
all of these words spelled the same but have

00:29:14.559 --> 00:29:19.319
multiple meanings or Said the same with different

00:29:19.319 --> 00:29:24.079
spellings. Many different if -then rules in language.

00:29:25.579 --> 00:29:30.200
I just cannot unsee Genesis 11, 1 -9 now. Especially

00:29:30.200 --> 00:29:34.420
verse 9. And that's in large part thanks to Veritas.

00:29:35.279 --> 00:29:39.240
At 44 Veritas on X. He really captured that for

00:29:39.240 --> 00:29:43.359
me. The Tower of Babel. And it's just Babel.

00:29:43.619 --> 00:29:47.049
Humans love Babel. A primary point here with

00:29:47.049 --> 00:29:53.309
that example like except and expert. White confusion

00:29:53.309 --> 00:29:56.230
occurs here with the similar letter patterns.

00:29:57.049 --> 00:30:05.869
Except EXCEPT and expert EXPERT share initial

00:30:05.869 --> 00:30:10.130
letters EX. This can lead to visually similarity

00:30:10.130 --> 00:30:14.690
confusion if the FWVA struggles to distinguish.

00:30:14.920 --> 00:30:20.359
subtle differences and both words have a downstream

00:30:20.359 --> 00:30:28.099
E P and T very confusing for people like me.

00:30:28.599 --> 00:30:31.960
This could indicate under activation or the inefficiency

00:30:31.960 --> 00:30:37.440
in that visual word form area as seen in dyslexia

00:30:37.440 --> 00:30:41.079
where they have a delayed N170 which reflects

00:30:41.079 --> 00:30:46.309
impaired word form recognition. And getting stuck

00:30:46.309 --> 00:30:49.670
is difficult with processing beyond these words.

00:30:50.069 --> 00:30:52.430
Often whenever I'm reading and I come across

00:30:52.430 --> 00:30:55.849
a word like this, I just get stuck. This is likely

00:30:55.849 --> 00:30:59.089
a bottleneck in the decoding, possibly due to

00:30:59.089 --> 00:31:02.109
erratic eye movements or those saccades, influenced

00:31:02.109 --> 00:31:05.269
by cerebellar Pugigi cells, that dysfunction,

00:31:05.750 --> 00:31:09.450
and also remember the superior colliculus, which

00:31:09.450 --> 00:31:12.349
projects up to the frontal eye fields of the

00:31:12.349 --> 00:31:16.289
sensory motor area. top middle of your brain

00:31:16.289 --> 00:31:20.069
cortex area. This is heavily involved in kind

00:31:20.069 --> 00:31:23.289
of modulating eye movements. Sometimes those

00:31:23.289 --> 00:31:26.190
letters in the letter sequencing that form a

00:31:26.190 --> 00:31:30.329
word are very challenging. It's all due to that

00:31:30.329 --> 00:31:34.309
rapid visual processing and in combination with

00:31:34.309 --> 00:31:40.029
the lack of progeny cells. If the FWVA fails

00:31:40.029 --> 00:31:43.869
to quickly disambiguate these orthographic forms,

00:31:44.109 --> 00:31:47.269
it will delay this process especially if the

00:31:47.269 --> 00:31:49.609
dorsal striatum involved with that procedural

00:31:49.609 --> 00:31:53.930
learning and the habitual word recognition because

00:31:53.930 --> 00:31:56.509
remember the brain is predicting so it's anticipating

00:31:56.509 --> 00:32:01.750
what this word might be versus what it is so

00:32:01.750 --> 00:32:04.549
that wraps up the decoding or the orthographic

00:32:04.549 --> 00:32:09.349
processing which is a very large and very complex

00:32:09.349 --> 00:32:12.930
first step so the next step the second step in

00:32:12.930 --> 00:32:15.940
reading is phonological processing. We've touched

00:32:15.940 --> 00:32:18.220
on it a little bit with explaining the different

00:32:18.220 --> 00:32:21.660
kind of phenomenas associated with reading, but

00:32:21.660 --> 00:32:24.440
this is going to what phonological processing

00:32:24.440 --> 00:32:28.180
is really trying to accomplish. And this is including

00:32:28.180 --> 00:32:31.559
that temporal parietal cortex and the superior

00:32:31.559 --> 00:32:35.539
temporal gyrus and the angular gyrus. So this

00:32:35.539 --> 00:32:38.039
is mapping visual words to their sounds, like

00:32:38.039 --> 00:32:42.019
mentally pronouncing book as book. This is like

00:32:42.019 --> 00:32:44.700
a translator converting text to speech in your

00:32:44.700 --> 00:32:48.140
head. This is occurring at roughly 200 to 300

00:32:48.140 --> 00:32:53.220
milliseconds in EEGs and MEGs. And the fMRI highlights

00:32:53.220 --> 00:32:59.099
STG and AG activation. The magnetic form measurement,

00:32:59.380 --> 00:33:03.420
the MEG, shows arcuate fasciculus mediated connectivity

00:33:03.420 --> 00:33:09.500
to the FWVA. And the EEG tracks the timing. The

00:33:09.500 --> 00:33:13.019
goal here is to link visual input to phonological

00:33:13.019 --> 00:33:17.940
output, enabling pronunciation and aiding with

00:33:17.940 --> 00:33:23.160
the comprehension. So here comes the sound. In

00:33:23.160 --> 00:33:26.059
phonological processing, the focus shifts to

00:33:26.059 --> 00:33:29.759
mapping the recognized word forms. Remember with

00:33:29.759 --> 00:33:33.119
the predicting and reading, visualizing the words,

00:33:33.839 --> 00:33:36.839
the letter sequencing, to their corresponding

00:33:36.839 --> 00:33:40.519
sounds and initiating the groundwork for speech.

00:33:40.720 --> 00:33:43.500
We're building up a foundation here to speak.

00:33:44.599 --> 00:33:47.160
This process primarily involves the temporal

00:33:47.160 --> 00:33:51.779
parietal cortex. And we can speak this or we

00:33:51.779 --> 00:33:57.119
can silently speak this up to our cortex. Remember

00:33:57.119 --> 00:34:01.559
the Reza Shadmir episode. For speech, this sets

00:34:01.559 --> 00:34:04.619
the stage for articulary planning in Broca's

00:34:04.619 --> 00:34:08.760
area. which coordinates tongue and speech movements.

00:34:10.039 --> 00:34:13.280
This is why I mentioned Dr. Shadmere again because

00:34:13.280 --> 00:34:17.719
the Purgenji cells are involved in slowing the

00:34:17.719 --> 00:34:20.679
tongue down. And this was shown in his recent

00:34:20.679 --> 00:34:27.159
paper. The Purgenji cells refine timing and accuracy

00:34:27.159 --> 00:34:31.039
while sounds and speech begin to form here. Actual

00:34:31.039 --> 00:34:33.780
vocalization, the speech requires further motor

00:34:33.780 --> 00:34:38.199
execution. during reading aloud. But before that

00:34:38.199 --> 00:34:42.039
we must have the semantic integration. The inferior

00:34:42.039 --> 00:34:46.059
frontal gyrus. Remember Broca. A lot of people

00:34:46.059 --> 00:34:48.980
know about Broca. This connects words to their

00:34:48.980 --> 00:34:52.179
meanings. Like understanding book as a reading

00:34:52.179 --> 00:34:56.920
object. This is akin to the library finding the

00:34:56.920 --> 00:35:00.199
right story. And this is occurring at 300 to

00:35:00.199 --> 00:35:07.489
500 milliseconds. on EEGs or MEGs. fMRI reveals

00:35:07.489 --> 00:35:11.090
this activation of the inferior frontal gyrus

00:35:11.090 --> 00:35:15.630
and the EEG tracks meaning processing while the

00:35:15.630 --> 00:35:19.889
MEG maps frontotemporal connections. The goal

00:35:19.889 --> 00:35:23.550
here is to build coherent understanding especially

00:35:23.550 --> 00:35:30.190
for the complex or abstract text. So silently

00:35:30.429 --> 00:35:33.829
speaking, that so -called sub -vocalization.

00:35:34.750 --> 00:35:38.889
In silent reading, readers internally articulate

00:35:38.889 --> 00:35:42.610
words like silent, saying, book, while doing

00:35:42.610 --> 00:35:46.489
the reading. This engages the superior temporal

00:35:46.489 --> 00:35:51.769
gyrus and the angular gyrus. While the fMRI shows

00:35:51.769 --> 00:35:56.429
the temporal parietal activation, MEG confirms

00:35:56.429 --> 00:36:00.349
that articulate fasciculus connectivity. The

00:36:00.349 --> 00:36:03.949
goal here is to reinforce phonological processing,

00:36:04.590 --> 00:36:07.409
aiding comprehension by linking visual words

00:36:07.409 --> 00:36:12.289
to their auditory forms without overt speech.

00:36:13.110 --> 00:36:16.489
And a big thing here is we are teaching ourselves.

00:36:16.670 --> 00:36:19.429
We are speaking up and teaching ourselves like

00:36:19.429 --> 00:36:23.010
professing. And this is a big form of learning,

00:36:23.369 --> 00:36:26.869
reading out loud. This extends silently reading

00:36:26.869 --> 00:36:30.619
to vocalization of the speech. requiring motor

00:36:30.619 --> 00:36:35.179
areas to articulate words and manage porosity,

00:36:35.800 --> 00:36:39.860
like reading a book aloud with proper tone. FMRI

00:36:39.860 --> 00:36:43.500
shows increased motor and inferior frontal gyrus

00:36:43.500 --> 00:36:48.260
activation. EEG captures motor related signals

00:36:48.260 --> 00:36:53.360
and the MEG tracks articulation timing. The goal

00:36:53.360 --> 00:36:57.630
here is to produce accurate and fluid speech

00:36:57.630 --> 00:37:00.969
while maintaining comprehension. So let's put

00:37:00.969 --> 00:37:03.989
some oscillations on this part of the process

00:37:03.989 --> 00:37:11.809
here. In the VWFA, autistic phenotypes spot words

00:37:11.809 --> 00:37:15.409
much faster. This is shown with that EEG MEG

00:37:15.409 --> 00:37:19.309
and that hyperactivation in fMRI. The delta here

00:37:19.309 --> 00:37:23.610
is autistics process this in gamma waves while

00:37:24.090 --> 00:37:27.010
Alpha and beta waves are used for non -autistic

00:37:27.010 --> 00:37:30.610
brains. Making visual processing extra detailed,

00:37:31.010 --> 00:37:35.030
sometimes we have called it heightened. But the

00:37:35.030 --> 00:37:38.489
connection to the inferior frontal gyrus, the

00:37:38.489 --> 00:37:43.570
storyteller, that Broca region, is weak. MEG

00:37:43.570 --> 00:37:48.409
shows low alpha and beta coherence, and EEG catches

00:37:48.409 --> 00:37:54.769
a delayed N400, meaning comprehension lags. Especially

00:37:54.769 --> 00:37:58.170
for abstract stories. This should be all making

00:37:58.170 --> 00:38:01.949
sense to you how autistics have difficulty with

00:38:01.949 --> 00:38:04.750
that downstream sensory processing and making

00:38:04.750 --> 00:38:08.050
sense of things and needing to catch up. We might

00:38:08.050 --> 00:38:11.250
have a hard time keeping up in social situations

00:38:11.250 --> 00:38:14.010
and remember the speech and language episode

00:38:14.010 --> 00:38:16.869
with the two different types of of echolalia.

00:38:17.610 --> 00:38:20.809
The two different sources kind of of echolalia.

00:38:21.150 --> 00:38:25.369
One is keeping up. So you must repeat it. This

00:38:25.369 --> 00:38:27.909
should be all making sense to you, but I don't

00:38:27.909 --> 00:38:31.269
think people understand this. Especially with

00:38:31.269 --> 00:38:34.210
assessing the Autistic Phenotype. This is heavily

00:38:34.210 --> 00:38:37.829
missed, and I'm telling you that. I know that.

00:38:38.250 --> 00:38:41.309
And it should be no surprise here that Articulociculus,

00:38:41.550 --> 00:38:44.949
that brain highway, remember with the FA measuring

00:38:44.949 --> 00:38:49.389
water, has reduced strength. It is a gravel road.

00:38:49.449 --> 00:38:54.340
It is a kinked water hose. From point A to point

00:38:54.340 --> 00:38:59.039
B destination example. Let's just use this analogy

00:38:59.039 --> 00:39:02.099
that we've mapped out here. There's a destination

00:39:02.099 --> 00:39:05.400
point A to point B and there's five stops for

00:39:05.400 --> 00:39:08.400
the autistic phenotype. Maybe the first two stops

00:39:08.400 --> 00:39:12.239
come fast versus the non -autistic, but the next

00:39:12.239 --> 00:39:16.739
three are delayed while the non -autistic gets

00:39:16.739 --> 00:39:21.079
there much smoother. I have something exciting.

00:39:21.260 --> 00:39:24.219
I want to introduce a product unlike any other

00:39:24.219 --> 00:39:28.920
product available. A highlight is the product

00:39:28.920 --> 00:39:32.639
from Daylight Computer Company created their

00:39:32.639 --> 00:39:36.699
product based on these factors. The Daylight

00:39:36.699 --> 00:39:42.280
Computer is completely blue light free. It has

00:39:42.280 --> 00:39:46.719
no flicker. Short wavelength flicker is extremely

00:39:46.719 --> 00:39:50.400
harmful for our eyes and downstream biology.

00:39:50.860 --> 00:39:54.360
light flicker is constantly turning our central

00:39:54.360 --> 00:39:59.340
nervous system on and off. Essentially, it is

00:39:59.340 --> 00:40:02.579
like going to a light switch and repeatedly turning

00:40:02.579 --> 00:40:07.940
it on and off. The problem is blue light and

00:40:07.940 --> 00:40:13.139
LED light does this and it is so rapid you cannot

00:40:13.139 --> 00:40:17.960
even perceive this in real time. The daylight

00:40:17.960 --> 00:40:22.679
computer is the lowest stimulation and foremost

00:40:22.679 --> 00:40:27.659
for sensory sensitive users. It is no question

00:40:27.659 --> 00:40:31.880
that the alternative product especially when

00:40:31.880 --> 00:40:36.659
used at night do not address or consider this

00:40:36.659 --> 00:40:41.900
in their product. It is so toxic to human biology.

00:40:42.380 --> 00:40:46.840
Big tech corporations have patents on how their

00:40:46.840 --> 00:40:49.840
short wavelength implicate the human nervous

00:40:49.840 --> 00:40:55.579
system. And a bonus, despite daylight computer

00:40:55.579 --> 00:40:59.980
not having backlight, it is very functional for

00:40:59.980 --> 00:41:05.000
outdoor use. And of course, increased sunlight

00:41:05.000 --> 00:41:10.380
is always preferred. I am happy to offer a discount

00:41:10.380 --> 00:41:14.300
for the daylight computer. You can use the code

00:41:14.300 --> 00:41:20.119
autism for a $50 off discount. Again, use the

00:41:20.119 --> 00:41:25.800
code Autism and the discount code for $50 off.

00:41:26.340 --> 00:41:29.619
See the link in the show notes to Daylight Computer

00:41:29.619 --> 00:41:32.519
Company or just give it a quick search in your

00:41:32.519 --> 00:41:37.679
internet browser. Use the code Autism for $50

00:41:37.679 --> 00:41:44.239
off. I would like to mention Chroma, lights designed

00:41:44.239 --> 00:41:49.650
for humans. Chroma, a Seattle -based innovator

00:41:49.650 --> 00:41:54.550
founded by ex -NASA and Air Force engineer Michael

00:41:54.550 --> 00:41:59.090
Shapiro is on a mission to enhance physical and

00:41:59.090 --> 00:42:04.250
mental health with purpose -built devices, unlocking

00:42:04.250 --> 00:42:08.889
peak human health, cognitive function, and performance.

00:42:10.090 --> 00:42:12.969
Shapiro launched Chroma to restore the natural

00:42:12.969 --> 00:42:18.269
light lost to screens in indoor living and delivers

00:42:18.489 --> 00:42:22.369
faster recovery, sharper minds and better sleep.

00:42:23.349 --> 00:42:27.289
Their products hit hard. The Iron Forge speeds

00:42:27.289 --> 00:42:31.269
muscle repair with red and near -infrared light,

00:42:31.650 --> 00:42:36.090
while the Skylight mimics sunlight to boost sleep

00:42:36.090 --> 00:42:41.630
and energy. A standout, the Forge Lamp, is a

00:42:41.630 --> 00:42:47.550
portable gem that fires 660 nanometer and 850

00:42:47.659 --> 00:42:52.440
nanometer light to energize mitochondria and

00:42:52.440 --> 00:42:56.820
heal tissues on the go. Remember the four red

00:42:56.820 --> 00:43:00.380
light chromophores on cytochrome C oxidase frequently

00:43:00.380 --> 00:43:05.679
talked about in the podcast. This is why their

00:43:05.679 --> 00:43:09.099
products are built with military grade durability

00:43:09.099 --> 00:43:15.800
to have lasting impact. Chroma's tech fuses precision

00:43:15.800 --> 00:43:22.349
and power. gallium titride power supplies smaller

00:43:22.349 --> 00:43:26.949
cooler and stronger than silicon provide flicker

00:43:26.949 --> 00:43:31.070
free light that's easy on the eyes high -powered

00:43:31.070 --> 00:43:36.289
LEDs target key wavelengths for skin tissue and

00:43:36.289 --> 00:43:39.929
cellular health with smart heat management for

00:43:39.929 --> 00:43:44.090
the lasting impact every design decision chroma

00:43:44.090 --> 00:43:48.260
make serves a purpose to create devices that

00:43:48.260 --> 00:43:52.860
are precise, durable, and effective for improving

00:43:52.860 --> 00:43:57.760
human life. Remember, humans use different wavelengths

00:43:57.760 --> 00:44:03.179
of light for different functions of life. Remember

00:44:03.179 --> 00:44:10.320
when I ask, what do you think light is? Chroma

00:44:10.320 --> 00:44:15.219
designs with our biology in mind from sleep aids.

00:44:15.440 --> 00:44:20.139
and wound healing to mitochondrial energy, full

00:44:20.139 --> 00:44:22.920
body lights and blue light blocking glasses.

00:44:23.960 --> 00:44:28.380
They are US made and chroma ships globally and

00:44:28.380 --> 00:44:36.820
accepts FSA and HSA payments. Use autism at checkout

00:44:36.820 --> 00:44:43.579
for a 10 % off discount. That's autism at checkout.

00:44:43.880 --> 00:44:47.960
for a 10 % off discount. If you are listening

00:44:47.960 --> 00:44:50.900
to the podcast, listening to the episode, please

00:44:50.900 --> 00:44:54.380
feel free to leave a review or rating. In podcasting,

00:44:54.579 --> 00:44:57.059
reviews, ratings, and downloads are huge, and

00:44:57.059 --> 00:44:59.500
I very much appreciate your feedback. You can

00:44:59.500 --> 00:45:05.619
contact me on X at RPS 47586. We can discuss

00:45:05.619 --> 00:45:08.260
anything and everything about autism. I very

00:45:08.260 --> 00:45:11.159
much appreciate your comments and your interactions

00:45:11.159 --> 00:45:14.679
on X. You can check out the YouTube page for

00:45:14.679 --> 00:45:18.079
all the videos, full -length videos, shorts,

00:45:18.219 --> 00:45:23.820
and clips. You can email me info .fromthespectrum

00:45:23.820 --> 00:45:28.980
.gmail .com. Thank you for listening to From

00:45:28.980 --> 00:45:30.739
the Spectrum Podcast.
