The More You Know…

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I’ve started substitute teaching. You probably remember crusty, old geezers teaching your class when one of your teachers was gone. These fossils were fond of telling students that they don’t know what hard work is, that they had to recite the pledge of allegiance in Greek and had to learn math with an abacus.

 

Whatever the case, there was always the assumption that, like teaching vampires who only came out during the school day, subs didn’t have an everyday normal life; when the school day was over they’d retreat to the school basement to read the textbooks for enjoyment before using them as a bed to sleep on until they were called to action again.

 

My point is that, with a single day substitute, there isn’t really a chance to get to know the sub.

 

I typically sub at the school where I once taught and assisted librarily, so I know most of the teachers and they know of my condition. Given enough notice, I’ll offer to give a presentation to the kiddos about me. This way the teacher doesn’t have to prepare as much and the students get first-hand knowledge of why I am the way I am. I’ve posted a version of this presentation before (LINK), but it was a raggedy old PowerPoint.

 

AND THEN…last summer – I went to a writer’s conference to pitch my memoir. I wanted to stand out, so I put together a presentation. I had just given the students a crash course in PowerPoint presentations and Prezi, so I thought I’d give that a try. I didn’t get a book deal >:(, but my presentation was pretty sweet. Find it HERE

 

AND THEN…a new school year started and the sub jobs came pouring in. So far, I’ve presented to about 250 seventh graders, most of the eighth graders saw it last year.

 

AND THEN…my younger sister, a Latin teacher (She teaches Latin, she’s not a teacher who is Latin, no one is or really has been since the Roman empire), asked me to come talk to one of her classes. I thought that this nexus of presentation opportunities called for a revamped presentation.

 

AND THEN…I combined the raggedy PowerPoint with the fresh, shiny Prezi to create a PreziPoint (PowerPrezi?). The svelte can be viewed in all its smoothly transitioning glory HERE. Or, for your convenience, I’ve reproduced the presentation here in slideshow form.

 

AND THEN…actually, ‘AND THEN…’ doesn’t work here, but I’m nothing if not consistent, the frames with a 🌟 in the lower right corner were adapted from the original PowerPoint. This means that the ones without a star make up the original Prezi.

 

AND THEN… If you don’t notice, apart from the book excerpts, it rhymes! Isn’t that delicious?

 

AND THEN…FIN

 

AND THEN…@JarrettLWilson

 

A Picture is Worth a Thousand…Pictures…

All Done

All Done…or 93 pictures if you’re the GIF above. By that count, if a picture is truly worth 1,000 words, that GIF is a tidy package of 93,000 words. Add to that the words you’re reading, and you have the world’s longest blog post. Honestly, I almost could’ve written 93,000 words in the time it took to make this GIF.

While I explain what it is, I’ll explain how it was made. I have the MRI images for most of my scans, in total I found/used eight sets of scans. Then, I made some pictures with my webcam of my profile and the top of my freakishly large head. If my math is correct, that makes 8+1 = 9 sets of images. Each set has roughly 10 pictures – including multiples of the original and duplicates of the fading shots. The sequence of the scans is chronological (For instance, a scan from 2010 would come after a scan from 2009, a scan done in May of some year will come before a scan…scanned in September of that same year…And so on).

The images are labeled with the reason for and date of the scan. I’d only point out the first scan from May, 2009 showing a big blob of white stuff just below the very center of my brain profile and slightly off center looking at the top. It’s almost as if someone tried to white it out. Really, it’s blood, the doctor injects you with the air from inside a blacklight, then your blood glows white.

The magnetic manipulation of the various cells and particles that form a mass called “Jarrett” (Magnetic), and the clicking and knocking noises (Resonance) labored to produce the this Image a few days after the hemorrhage.

The magnets and sounds continued their unlikely coupling through my skull on August 15, 2016, one day before my appointment with my neurosurgeon (I verbally sparred with both the doctor’s office and the insurance company for a month and had to reschedule twice, but that’s a different story altogether).

On the last MRI image, notice all the white out has been removed. When looking down from the top of my head, the “cavern” that the cavernous malformation called home is still a dark hole. I can only speculate that this is why I forget stuff almost as quickly as it pops into my head, it gets sucked into this vortex of blackest black, of darkest dark, of ebon opacity, of obsidian obscurity, etc.

Anyway, this GIF sums up seven years of the physiological side of brain injury recovery. I’ll stop writing now as this post has now reached a staggering 93,443 words.

This is all to say that my latest scans show no activity, and my recovery continues.

FIN (93,460 words if counting the number)

@JarrettLWilson (93,468)

Jarrett vs. Health Insurance

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output_0fhCWAGreetings, the internet!

I apologize for my overlong absence from posting here. This here story I’m about to unfold gives some insight into why I’ve neglected this beacon of organized nonsense. Before I get into the reading portion of today’s entry, we’re gonna do some math –

#1. Affordable Care Act + dude with extensive medical needs = grumpy insurance company.

#2. Grumpy insurance company + dude with extensive medical needs = sub-par coverage and service

#3. Dude with extensive medical needs is due for an annual MRI + sub-par coverage and service = dude pays for MRI

#4. Dude keeps records of all the times he tried to contact the insurance company + dude pays the bill anyway = legal action against insurance company.

#5. Legal action against insurance company^2 = 11…

#6. The square root of 11 is 3.31662479 – on a phone, these numbers could spell “DEMOBIPY” or “FENMAGRY”…which kinda rhymes with “gravy”, a delicious substance that clogs arteries, thus leading to more claims for the insurance companies, making them more grumpy.

I digress…

…Listen, part of my ongoing upkeep is a once yearly visit with my neurosurgeon. That annual visit is preceded by an MRI. When I was employed and insured through a PPO, I didn’t need a referral. Having an HMO (stands for Has Many Obstacles) through the Affordable Care Act, I need to get a referral to blow my nose. As if that bureaucratic labyrinth wasn’t enough, math problem #2 takes form in the…uh, form of unreturned messages and “health assistant” buck passing…hmmm, if you are a health assistant that had been passed a buck, you shall henceforth be called a “health passistant”.

Gosh, I’m all over the place, let me summarize – I need an MRI by mid August. I started the referral/prior authorization process for this about a month ago (after already having it approved, then losing coverage, but that’s a horse of a different color). All I’ve gotten in response is “I’ll reach out to your doctor’s office to see where they are in the referral process”. Three things about this –

1. The way they talk about trying to get in touch with my doctor’s office, you’d think they were trying to contact Santa Claus on Christmas eve.

2. The doctor himself told me that the paperwork was sent on June 2nd.

3. Every time I’ve called, I’ve spoken with a real person in the department I intended.

Here’s what I’m getting at – MRIs are expensive. I had one last year before paying my deductible ~ $1800. Call me paranoid, but I believe that when an insurance company is looking at paying that amount of money, there phones stop working, emails get sent to spam more often and the fax machine works maybe half the time. After all, HMO stands for Healthy Monetary Outlook. So I would have you bare witness, interwebs – I’ve done and continue to do my part to ensure that the MRI will be covered.

One more thing – I’m not slamming Obamacare here. I’m grateful that I have insurance, limited though it may be. And if there’s one thing I’ve learned, you are your best advocate. Even the best insurance companies can’t get inside your head, even if they do pay for an MRI of your brain, and decide what’s best for you.

Also, I thought of one more meaning of HMO. For this one you need to use a salty New Yorker accent – HMO = Healthy?!? Meh, Oh well.
FIN

@JarrettLWilson

Presenting – My…Presentation

I used to work at a middle school.

I’ve was employed there in some fashion for a number of years.

My first two years I taught 8th grade US history and coached boys’ athletics. The next year I taught 8th grade English and coached girls’ athletics.

At the end of that school year some blood vessels in my brain leaked like so much kiddie pool left to rot in the sun.

I taught 8th grade English for half of the next two school years. I came back the next school year as the assistant librarian and have filled that role for four years.

Assuming my math is correct (2+1+.5+.5+4), I’ve been working there for 21,554 years – this raises a few questions.

Firstly, I’m only 32 years old. Secondly, the school has only been there for 40ish years. Let’s round that figure down to eight school years.

I did so enjoy working with students. Thing is, I’m was’t like any of the other teachers/professionals in the school.

When I returned to teaching after the hemorrhage, I created a PowerPoint presentation about my condition to show to my class to prepare them for my uniqueness.

Recently, I had the opportunity to speak to the new seventh graders. I modified the presentation to fit my condition today. I thought I’d share it with you, the internet –

1

This is the title slide – note that it has the title written (in English, no less!) on it.

2

This slide is for a handout. The students were given the same graphic, but with blanks. In essence, they started with an empty brain and ended with a full one (symbolic, no?)

3

In the same fashion as the previous slide, the students filled in the blanks on the same graphic.

4

This slide is a pictorial representation (pictoriational?) of the functions of each lobe. For instance, the temporal lobe (orange) controls the instinct to swat things away from your ear (actually, that represents hearing), and the frontal lobe controls the confusion that comes from staring at gibberish on a sign post (actually, that represents planning).

5

Now we get to my contribution – you see, the seventh grade reading classes at the school where I work are covering non-fiction. They are reading Gifted Hands by Dr. Ben Carson – the brain surgeon that removed half of a girl’s brain. One of the teachers is a friend of mine and asked me to present my experience as a primer. The image in the slide is my brain (isn’t it beautiful?). The white dot in the middle is my cavernoma isn’t it (or rather, wasn’t it) ugly?

6

Not much to say about this slide that isn’t in the slide. I’ll just add that the symptoms listed are enough to get you a 20 minute helicopter ride.

7

Much like the image in the “My Brain Issues” slide – the head pictured is my head. My head is perfectly round and my brain has many different colors. I know what you’re thinking, “But Jarrett, there weren’t no color in the other image and your head ain’t perfectly round.”

I’ve a twofold reply to this comment. First of all, I was joking – that’s not my head. Secondly, you need to work on your grammar. Moving on, this one has info about the surgery. That fact weighed heavily in my decision to title the slide “The Surgery 9/2009.”

8

A few summers ago I went on a tour of a Nair factory – this happened to be the day that Gillette planned to sabotage the Nair factory. They set explosives…I’m tired of this explanation. It started off with promise, but now I hate it!

Truthfully, a few summers ago I wanted to see the scar, so I shaved my head.

9

This slide is linked to a file with moving pictures and sound! This “video” is about *drumroll* neuro-plasticity! A fancy term denoting the brain’s ability to form new connections.

10

This is a visual representation of how your brain thinks. For instance, you see a donut with your occipital lobe. That info shoots to your frontal lobe and activates your happy gland. Your happy gland shoots a message to your parietal lobe “GO GET THAT F’N DONUT!” Someone gets it before you can, so your temporal lobe tells you to break out your megaphone and shout obscenities at this person and threaten to call the police. This guy grabs a nearby napkin dispenser and wangs you in the Temple…

11

…That blow to the Temple gives you a TBI. Your brain rewires itself and finds an alternate route to your happy gland.

12

I included this slide to give the students an explanation as to why I sometimes shake when I speak and why I walk with a limp and hike up my left arm like so much Bob Dole. It also helps explain the little girl in the moving picture mentioned earlier. It also gave me a chance to…

Treating Hypertonicity with Pic

…mention the painful treatments. One thing I’ve learned from working in a middle school is that, as much as the kids want to be treated as adults, they still love to hear about people getting poked with needles and meeting a real life cyborg.

13

I like to pepper in some humor here and there to make sure the kids are awake. When this slide appears, it’s accompanied by a very loud, obnoxious laugh.

15

I don’t really do any of these anymore, but I mention it because I did it for so long, and it drives home the point that I’ve had a long road.

16

In my mind, all of these will someday be replaced with “Painfully normal”. For purposes of this presentation, it gives the students an idea of what to expect when they see me.

17

It can be difficult to work around young people with my disabilities. Instead of hiding or pretending that I’m no different, I encourage the students to come talk to me if they have a question. I want to think that I’m an ambassador for the disabled. Hopefully, these students will apply what I’ve tried to teach them to others with disabilities.

I included the last bullet because I’ve had some students speak very loudly and very slowly to me. You see, they have to tell me their student ID number to check out a book. In previous years, a student or two would speak to me as if I was unable to type and listen at the same time.

18

I’m a pretty smart dude and I can be pretty creative, but I didn’t discover any of this and I didn’t make this sh*t up.

If there’s one thing I learned in college, it’s that Keystone Light is super cheap and tastes like weedkiller. If there’s a second thing I learned in college, it’s that plagiarism is bad (I remember a syllabus that said there’s a special place in hell for those that plagiarize).

We try to instill that fear into the students, so I model the proper citing of sources.

FIN

@JarrettLWilson

Presenting – My…Presentation

I work at a middle school.

I’ve been employed there in some fashion for a number of years.

My first two years I taught 8th grade US history and coached boys’ athletics. The next year I taught 8th grade English and coached girls’ athletics.

At the end of that school year some blood vessels in my brain leaked like so much kiddie pool left to rot in the sun.

I taught 8th grade English for half of the next two school years. I came back the next school year as the assistant librarian and have filled that role for going on three years now.

Assuming my math is correct (2+1+.5+.5+3), I’ve been working there for 21,553 years – this raises a few questions.

Firstly, I’m only 32 years old. Secondly, the school has only been there for 40ish years. Let’s round that figure down to eight school years.

I do so enjoy working there and continuing to work with students. Thing is, I’m not like any of the other teachers/professionals in the school.

When I returned to teaching after the hemorrhage, I created a PowerPoint presentation about my condition to show to my class to prepare them for my uniqueness.

Recently, I had the opportunity to speak to the new seventh graders. I modified the presentation to fit my condition today. I thought I’d share it with you, the internet –

1

This is the title slide – note that it has the title written (in English, no less!) on it.

2

This slide is for a handout. The students were given the same graphic, but with blanks. In essence, they started with an empty brain and ended with a full one (symbolic, no?)

3

In the same fashion as the previous slide, the students filled in the blanks on the same graphic.

4

This slide is a pictorial representation (pictoriational?) of the functions of each lobe. For instance, the temporal lobe (orange) controls the instinct to swat things away from your ear (actually, that represents hearing), and the frontal lobe controls the confusion that comes from staring at gibberish on a sign post (actually, that represents planning).

5

Now we get to my contribution – you see, the seventh grade reading classes at the school where I work are covering non-fiction. They are reading Gifted Hands by Dr. Ben Carson – the brain surgeon that removed half of a girl’s brain. One of the teachers is a friend of mine and asked me to present my experience as a primer. The image in the slide is my brain (isn’t it beautiful?). The white dot in the middle is my cavernoma isn’t it (or rather, wasn’t it) ugly?

6

Not much to say about this slide that isn’t in the slide. I’ll just add that the symptoms listed are enough to get you a 20 minute helicopter ride.

7

Much like the image in the “My Brain Issues” slide – the head pictured is my head. My head is perfectly round and my brain has many different colors. I know what you’re thinking, “But Jarrett, there weren’t no color in the other image and your head ain’t perfectly round.”

I’ve a twofold reply to this comment. First of all, I was joking – that’s not my head. Secondly, you need to work on your grammar. Moving on, this one has info about the surgery. That fact weighed heavily in my decision to title the slide “The Surgery 9/2009.”

8

A few summers ago I went on a tour of a Nair factory – this happened to be the day that Gillette planned to sabotage the Nair factory. They set explosives…I’m tired of this explanation. It started off with promise, but now I hate it!

Truthfully, a few summers ago I wanted to see the scar, so I shaved my head.

9

This slide is linked to a file with moving pictures and sound! This “video” is about *drumroll* neuro-plasticity! A fancy term denoting the brain’s ability to form new connections.

10

This is a visual representation of how your brain thinks. For instance, you see a donut with your occipital lobe. That info shoots to your frontal lobe and activates your happy gland. Your happy gland shoots a message to your parietal lobe “GO GET THAT F’N DONUT!” Someone gets it before you can, so your temporal lobe tells you to break out your megaphone and shout obscenities at this person and threaten to call the police. This guy dressed a nearby napkin dispenser and wangs you in the Temple…

11

…That blow to the Temple gives you a TBI. Your brain rewires itself and finds an alternate route to your happy gland.

12

I included this slide to give the students an explanation as to why I sometimes shake when I speak and why I walk with a limp and hike up my left arm like so much Bob Dole. It also helps explain the little girl in the moving picture mentioned earlier. It also gave me a chance to…

14

…mention the painful treatments. One thing I’ve learned from working in a middle school is that, as much as the kids want to be treated as adults, they still love to hear about people getting poked with needles and meeting a real life cyborg.

13

I like to pepper in some humor here and there to make sure the kids are awake. When this slide appears, it’s accompanied by a very loud, obnoxious laugh.

15

I don’t really do any of these anymore, but I mention it because I did it for so long, and it drives home the point that I’ve had a long road.

16

In my mind, all of these will someday be replaced with “Painfully normal”. For purposes of this presentation, it gives the students an idea of what to expect when they see me.

17

It can be difficult to work around young people with my disabilities. Instead of hiding or pretending that I’m no different, I encourage the students to come talk to me if they have a question. I want to think that I’m an ambassador for the disabled. Hopefully, these students will apply what I’ve tried to teach them to others with disabilities.

I included the last bullet because I’ve had some students speak very loudly and very slowly to me. You see, they have to tell me their student ID number to check out a book. In previous years, a student or two would speak to me as if I was unable to type and listen at the same time.

18

I’m a pretty smart dude and I can be pretty creative, but I didn’t discover any of this and I didn’t make this sh*t up.

If there’s one thing I learned in college, it’s that Keystone Light is super cheap and tastes like weedkiller. If there’s a second thing I learned in college, it’s that plagiarism is bad (I remember a syllabus that said there’s a special place in hell for those that plagiarize).

We try to instill that fear into the students, so I model the proper citing of sources.

FIN

@JarrettLWilson

Did You Really Think That Was It?

…Moving on, recall from my last entry about the second part of my first entry, which had six entries on the first of July, being the seventh month of the year 2009…uhh…backfire – in my cute attempt to confuse I confused myself…I ran into a doorway at the Target and went back to a hospital (not because of the doorway).

During my stay at the rehab hospital, I’d make frequent trips to Dallas to see my neurosurgeon, Dr. Jonathan White, when I say his name or picture him in my head I hear the angels singing; this man is a god as far as I’m concerned. Here are the particulars –

The Doctor Visit
On June 30th, Jessica, My parents and I met with Dr. White, a neurosurgeon, at UT Southwestern. I also got an MRI. The doctor (and the scans) suggested I wait a while longer as there is still too much blood in my head. BUT, surgery is possible given the current location. I will go back in two months and do the same thing and hopefully the blood will have absorbed (enough to operate anyway). The surgery itself is risky and will likely send me back to rehab (if not worse). The tradeoff is a lifetime without fear of this recurring with some permanent damage or the possibility of recurrence and the fear that that possibility brings. I am opting for the former (surgery).

Dr. White looked at the pictures born out of the loud noises shot through my skull and reckoned we wait until the bleed site becomes not so bloody. I was a bit upset about this, I was ready to have that thing out of my noodle. If I may borrow the tone from the JG Wentworth (this blog sponsored by lump sums for structured settlement payments) commercials – IT’S MY CAVERNOMA AND I WANT IT OUT! I do worry about it growing back, but I’m glad I don’t have to worry that it’s gonna erupt again. I sometimes think how it might be if I hadn’t had the surgery, then I think about not walking and paralysis and that thought quickly goes away. For those of you contemplating surgery, many will say “it’s a very personal decision.” To me, that part is implied, my advice is this – if your doctor is confident he/she can cut it out with a minimum of residual damage and you trust in this doctor after having done your research on him/her – cut that sucker out of there; don’t wait for it to bleed again. What’s next?

Location, Location, Location
 My cavernoma is located in the Pons region, located on the brainstem which controls (from what I understand) –

– Autonomic function (breathing, heart rate…stuff that just happens automatically *gulp*)
– Sleep (This I know)
– Messages between the cerebrum and cerebellum
– Hearing
– Fine motor skill (This I know)

There are more, but these seem to be the most prominent. Again, this info. is from my limited understanding.

I’ve written about the Pons more thoroughly HERE. For the most part, the functions listed above are accurate. I’m starting to suspect that most of the issues I’ve experienced and continue to deal with have more to do with the bridge function of the Pons rather than the functions it controls. Here’s a better explanation: let’s say the the Pons is a silly doorman at your apartment named…Pons (I couldn’t think of anything else), the apartment building is the cerebellum, the area outside the door is the cerebral cortex, and you are a message. Pons is a pretty eccentric dude, he wears sunglasses all day, and once tried to give a swirlie (swirly?) to a solicitor. You’re not concerned with his personality, you just want him to open the door. One day, he decides he doesn’t want to open the door anymore. Now you have trouble getting from the building (cerebellum) to the outside (cerebral cortex). What’s more, Pons has no direct control over your balance, but he can put a trip wire across the doorway, much like…

TBI is…Tempest Blows Indoors. I tweeted this one earlier in the week, but I’d like to give it more explanation. Here is the original explanation – For no reason, I’ll flail my arms about to regain my balance after thinking about tacos or something. You see, I often have to think about walking the way most people would think about math. That is, I have to think pretty hard about the terrain, wind, fatigue, etc. As I’ve mentioned before, there are shiny things everywhere. If/when I get distracted I can lose my balance pretty easily. Luckily, I still have a pretty good reflex to keep me upright. This comes out to – Jarrett is walking down an aisle at the store, Jarrett spots a fancy, yet useless gadget in the “As Seen On TV” display, Jarrett loses his balance, it looks like Jarrett is swimming through the air as he tries to regain equilibrium.

FIN
@JarrettLWilson

More Time Travel and Jean Claude Van-Damme

I’m not sure why, but in my early entries I’d post multiple times in one day. This vexes me verily (vexily?). Granted, there was a lot going on at the time, but could I not gather my thoughts enough to include everything in one entry? I picture myself going back in time to find out why. I get there and say, “Dude! Why do you post multiple times in one day?”
I look at myself, puzzled, and reply, “Dude! You had the opportunity to travel back in time and you choose this time and place?”

Feeling like a dimwit, but wanting to redeem myself, I ask, “When/where would you have gone?”
We get into a long discussion about orangutans and breakfast cereals, etc. Eventually, I insist that I answer my question. Just as I’m about to speak someone walks in with a box of donuts; we both reach for the maple cake donut, Our fingers touch, we both turn into big blobs of flesh, coagulate into a puddle that shrinks until it disappears (watch Timecop, it’s based on a true story of a corrupt, time traveling senator and how Jean Claude Van-Damme is a weiner. I can’t find the scene itself, but here’s a TRAILER). Anyway, I never find out why I posted several entries in one day and I blot out my own existence.

Moving on, recall from my last entry about the second part of my first entry, which had six entries on the first of July, being the seventh month of the year 2009…uhh…backfire – in my cute attempt to confuse I confused myself…I ran into a doorway at the Target and went back to a hospital (not because of the doorway).

During my stay at the rehab hospital, I’d make frequent trips to Dallas to see my neurosurgeon, Dr. Jonathan White, when I say his name or picture him in my head I hear the angels singing; this man is a god as far as I’m concerned. Here are the particulars –

The Doctor Visit

On June 30th, Jessica, My parents and I met with Dr. White, a neurosurgeon, at UT Southwestern. I also got an MRI. The doctor (and the scans) suggested I wait a while longer as there is still too much blood in my head. BUT, surgery is possible given the current location. I will go back in two months and do the same thing and hopefully the blood will have absorbed (enough to operate anyway). The surgery itself is risky and will likely send me back to rehab (if not worse). The tradeoff is a lifetime without fear of this recurring with some permanent damage or the possibility of recurrence and the fear that that possibility brings. I am opting for the former (surgery)

Dr. White looked at the pictures born out of the loud noises shot through my skull and reckoned we wait until the bleed site becomes not so bloody. I was a bit upset about this, I was ready to have that thing out of my noodle. If I may borrow the tone from the JG Wentworth commercials – IT’S MY CAVERNOMA AND I WANT IT OUT! I do worry about it growing back, but I’m glad I don’t have to worry that it’s gonna erupt again. I sometimes think how it might be if I hadn’t had the surgery, then I think about not walking and paralysis and that thought quickly goes away. For those of you contemplating surgery, many will say “it’s a very personal decision.” To me, that part is implied, my advice is this – if your doctor is confident he/she can cut it out with a minimum of residual damage and you trust in this doctor after having done your research on him/her – cut that sucker out of there; don’t wait for it to bleed again. What’s next?

 

Location, Location, Location

My cavernoma is located in the Pons region, located on the brainstem which controls (from what I understand) –

 

– Autonomic function (breathing, heart rate…stuff that just happens automatically *gulp*)

– Sleep (This I know)

– Messages between the cerebrum and cerebellum

– Hearing

– Fine motor skill (This I know)

 

There are more, but these seem to be the most prominent. Again, this info. is from my limited understanding.

I’ve written about the Pons more completely HERE. For the most part, the functions listed above are accurate. I’m starting to suspect that most of the issues I’ve experienced and continue to deal with have more to do with the bridge function of the Pons rather than the functions it controls. Here’s a better explanation: let’s say the the Pons is a silly doorman at your apartment named…Pons (I couldn’t think of anything else), the apartment building is the cerebellum, the area outside the door is the cerebral cortex, and you are a message. Pons is a pretty eccentric dude, he wears sunglasses all day, and once tried to give a swirlie (swirly?) to a solicitor. You’re not concerned with his personality, you just want him to open the door. One day, he decides he doesn’t want to open the door anymore. Now you have trouble getting from the building (cerebellum) and the outside (cerebral cortex).

TBI is…Tempest Blows Indoors. I tweeted this one earlier in the week, but I’d like to give it more explanation. Here is the original explanation – For no reason, I’ll flail my arms about to regain my balance after thinking about tacos or something. You see, I often have to think about walking the way most people would think about math. That is, I have to think pretty hard about the terrain, wind, fatigue, etc. As I’ve mentioned before, there are shiny things everywhere. If/when I get distracted I can lose my balance pretty easily. Luckily, I still have a pretty good reflex to keep me upright. This comes out to – Jarrett is walking down an aisle at the store, Jarrett spots a fancy, yet useless gadget in the “As Seen On TV” display, Jarrett loses his balance, it looks like Jarrett is swimming through the air as he tries to regain equilibrium.

The (Near) End of Phase Three

My time at Pate and away from home is coming to a close. This Friday, I will go outpatient. As far as I know, I will be picked up and brought to Pate every weekday at first and gradually taper off.

I walk with a cane or independently now. Without a cane, I would look like a mummy if I stuck my arms out…but it’s walking. I do mostly physical therapy as cognitively I haven’t lost much if anything. Physical therapy consists of whatever my therapist cooks up (lately its been lunges), leg biking, treadmilling and what I can best describe as yoga (contorting my legs and midsection into various uncomfortable positions).

Otherwise, I make preparations for the coming school year or test my reaction time on the computer on a program called VMR to earn driving privileges back (this way I don’t run into the little yellow block).

I have another MRI and appointment with Dr. White on August 18th.Hopefully, I’ll be ready for surgery at that point and can get it scheduled ASAP. After that, more rehab (yippee!)