Pretty basic. He has run his old ones through the ringer; full of stress
fractures and scratches to the point where he basically can't wear them
anymore.
2.) Get 'The' Nose Job:
The actual procedure is called
Radiofrequency Turbinate Ablation. A brilliant local ENT will be doing the procedure, which a minimally
invasive office thing.
The goal is to help my asthma and overall breathing, as well improve
use/function of my CPAP machine. Dr. S. was like "That ride one is pretty big.
It's normal to see a bit of a size difference between the two sides, but it's
rare you see a difference this big."
ME THINKING ABOUT ALL THE "RARE/DIFFERENT INTERESTING" THINGS ON/IN MY BODY:
3.) Pay Off Some Medical Bills:
I feel like this is self-explanatory.
4.) Be More Productive on my Social Medias:
This is more of the same, it's kind of an every year thing, like clockwork.
Specifically -
❖ I have tried some beauty products and not made a video or even a mini StAB review.
❖ I have watched plenty of movies and either never bothered to review, or started a review and never got around to finishing it.
❖ I have tried some new foods but have not made a singleLet's Eat! video demonstrating them.
❖ I also would like to have some more coherence to my State of the Body vids. I definitely get to disorganized rambling A LOT and in editing my last video, I was like "Can you say any word other than "Um?" I also feel like I look away from the camera too much. The only reason that video made it through was because I didn't feel like making it again.
So I guess that's going to call for me to maybe make a bullet-point topic cheat sheet so I stay somewhat focused. I would also like to post a little more frequently on this subject. Maybe more frequent, but shorter videos. I have a list of topics I'd like to address that aren't just straight updates. Would anyone be interested? (Let's be honest, I'll probably do it regardless.)
Also, QUESTION:
I have considered doing Film Friday reviews by video, but I'm not sure if you would like that. Some of the reason I have considered this is because some of the reviews I abandoned would have come across better in verbal format. The one video Film Friday I did do years ago was just terrible on multiple levels.
I am also going to post this question probably in an actual video. I'd definitely appreciate any feedback.
5.) Speak (Be) Kinder to Myself:
I have a habit of being pretty terrible to myself, especially when I'm struggling, which seems to be all the time now.
I can have a self-deprecating sense of humor. But one day at work, my inner monologue was running it's venomous mouth; I stopped and realized - if I were to witness anyone treating another person the way I talk to myself, I would be horrified. Because in literally any other situation, my own self-talk would be abuse. Not like "That's not nice."
Literal fucking abuse.
Well, those are the big 5. I have more - some smaller, some more complex, some that are dreams and some that are definitely tangible. I find I sometimes want to do a seasonal or other holiday/event relates goals list, so I decided here to focus on The Big 5.
Also, note I avoided the word "resolution." To me, resolution has a connotation that leans toward perfection and completion. That absolutely does not work for me. Goals, I feel, is more indicative of progress, continuing in working toward something, and when you achieve that, you continue as well as build on it.
Okay. First I was introduced to the EMG technician, Ross.
He did the most basic introduction and took my vitals, then it was time for
the neurology fellow, who is my primary on the case, to see me. I will call
her Dr. Fellow, because she is in her Fellowship year. And guys...she LISTENED TO ME.
She actually carefully read over my timeline of symptoms/events etc., and
asked insightful questions about it.
She did a full neuro exam from reflexes to finger-touch-nose to a whole bunch
of shit. Reflexes, sensation, flicking my fingers and flexing various body
parts. Much of which I kinda failed. My reflexes were pretty hyper, which I
knew. Evidently I had many problems with temperature, sharp, vibration,
awareness of location in space, all the things. (It could've been so much
worse.)
We spent like, 2 hours on this.
Then it was time for the EMG.
Ross returns. He is a skilled and friendly lab tech. He does the first part of
the study, which is the nerve conduction/velocity/whatever part.
They use the thing that to me, looks like the love child between a
self-defense taser and a barbershop razor.
This is where it gets interesting. He kept having trouble for some reason.
After a few minutes, a guy, we'll call him Zach, came in. I quickly learned he
was a neurology resident who happened to want to see an EMG in progress
because he didn't have much experience with them. He kept asking "Is that
normal?" and Ross was like "Um....no." Then Zach kept asking more questions
and the two of them kept attempting different things. After a while, Dr.
Fellow comes back in and she joins the "WTH?" club. Zach leaves for a minute
and then returns. Then, a minute later, another neurology resident appears in the room, announcing, "Hey, I heard there was a really
interesting EMG going on in here."
Me:
I wasn't upset by this, I am a firm believer in education and if I can offer
something new and interesting to people who are intrigued rather than
dismissive, then great. But it was unnerving. I mean, there are times when you
kind of DON'T want to be interesting. (Although, given how I'd been treated by
many of the doctors up here, I was also relieved top find that no, this was
definitely NOT in my head.)
So everyone is asking questions/offering suggestions like "press harder",
"check the electrodes", and my favorite, "turn up the voltage."
Ross decides he needs an expert and leaves to get the head technician. Let's
call her Debbie. Debbie comes in and is very friendly with me but also is very
no-nonsense with the two residents. Debbie is helping Ross figure out the
problem, telling him to press down on the electrodes while she turns up the
voltage and pushes the button.
At this point it's been a while so - let's call her Dr. Small - the overseeing Clinical
Professor - appears.
It felt like that scene from Spies Like Us.
And they all kept commenting on how interesting it all was. Ross was
quite thrilled to have such an exciting and unique case to mix up his day and
the residents were delighted to see something so weird and new. After a bit,
Dr. Small allows the first portion of the test to be concluded and sends the
two residents on their way so she can perform the second part of the test,
which is where they stick the needle in the muscle and compare totally relaxed
readings against flexed readings.
For that test, things went swimmingly. (Not comfortably, but quickly.) Dr.
Small has a sense of humor, because when I ask how things are going, she's
like "Quite normal. In fact...unnervingly
normal."
Me: PUN APPRECIATED.
Things are a bit more interesting when they do my lower half, but not as crazy
as they were when attempting the first part on my upper half.
They called Shawn back into the room and Dr. Small started manipulating my
left leg, which is the one with the heavy limp. She asked me:
"Do you have significant lower back pain?"
Me: "Yes." (Mentally: Duh. What gave it away?")
So. The reason they had so much fun with the first part of the EMG was because
they couldn't get a measurable response from my nerves, no matter what they
did. Which was why they kept doing different things, checking the machine and
turning up the voltage. Because they would shock my nerves and although the
arm would physically respond with a minor jolt, and I could kinda feel it, the
nerves themselves would not show a response to the stimuli. So. That's fun.
(Note: poor Ross kept telling me how great I did and how easy I was making his
job and he kept apologizing if he was hurting me. And I was like "My dude, the
electric zaps my body sends through my own system are so much worse than what
you're doing right now. No worries.")
Dr. Small and I had this conversation:
DS: So, you've never had a limp before this started?
ME: No.
DS: And any time you've ever had back pain before, it's resolved in a couple
days?
ME: Yup.
DS: (Incredulous): So you developed sudden, persistent back pain severe enough to send you to
Urgent Care and a limp at the same time and they didn't do any tests?
ME: Nope.
DS: And this limp hasn't gone away since it developed and neither has the
pain?
ME: Correct.
DS: And they developed at the same time?
ME: (Nodding)
DS: (Annoyed) And no one thought to put to 2 & 2 together and do more
testing?
ME: Nope.
DS: Rolls her eyes.
ME: Agreed.
Which is why I am now scheduled for a 3D spinal MRI on the 13th of
September. (It's being done up here, but on the order, it was very explicit
about what she wanted and expected from the imaging.)
So they (at the time) suspected I had Charcot-Marie Tooth Disease, and
one of the rarest forms of the disease, to boot. (Blood tests would later
conclude that no, in that regard I am normal and do not have CMT.)
We also discussed the fact that yes, there are multiple things happening in my
particular problem soup.
There is 100% an extremely pinched nerve in my lumbar spine, but until they
get the results from the second MRI, they won't know the reason why. Is it
from spinal stenosis? The herniated L5S1? Something else? Don't know yet. But
they compared it to someone grinding their heel down on a hose to stop the
water flow. Nice.
There is also evidence of damage in my cervical spine, but they don't know the
cause yet because stupid people up here didn't send any actual images to U of
M, just the radiologist's report. And if there is one thing I have learned,
it's to not trust what radiologists report. (From my own experiences, not from
other doctors indicating I shouldn't. I can do a post about this later on. For now, please
enjoy this short clip by Dr. Glaucomflecken.)
And my neurologist seems to feel the same way. Like, great, you gave your report. Now I want to see the images for myself, dillhole.
It is currently suspected that the cause is another severely pinched nerve.
It could also be a few other things. So they also need to see the brain/cervical
spine MRI images before anything can be done.
There is also evidence of upper motor neuron degeneration.
And that is a whole other can of worms. Because how much of it is UMN degeneration and how much is spinal damage? Are the symptoms of one masking symptoms of the other, or exacerbating them? Who knows?
Current Status:
Scheduled for 3D MRI on: September 13.
Next U of M appointment: October 12.
I am on an anticonvulsant which has helped calm the over-excitement of nerves. With it, my electric zaps have reduced significantly (I still get bad ones in my hands), my skin doesn't feel like it's on fire all the time, and of course, the seizures I've been suffering have also significantly reduced. (Still have occasional convulsions, but not nearly as many and not nearly as bad.)
Leaving U of M, driving home, I told Shawn how, for the first time since I can remember, I have felt a sense of hope, of optimism. I genuinely don't know what's-the-what, but I have suspicions. However, assuming my limp is a hardware issue and not a software one - that would be amazing. The possibility that I could walk normally again. Honestly, it was something I had let go of and that hope is back. I might be able to walk normal again. And depending on what's going on in my cervical spine - well, I might be able to one day regain control of my hands. I may again someday be able to put a necklace on without help. These things are in the future and will require a lot of treatment - but the likelihood is there. I could walk normally again someday! And that is something to look forward to.
Dr. Glaucomflecken <<<do yourself a favor and check this guy out. He's on youtube & tiktok
Ok, so I tried to share a widget and a button and all the things but
apparently Firefox is like fuck that noise so maybe I need to switch to
Chrome? At any rate, I got around it by doing a copy/paste/add a link thing,
which is why this appears so wonky.
Hi! Thanks for taking the time to read this. My name is Becky, and my body
& mind seem to be degenerating before my very eyes. It started as numbness
and weakness in my hands, making it difficult to type. It progressed to the
point where I cannot put earrings in for lack of sensation & dexterity.
Sometimes things just randomly fall out of my hands. I have developed a
severe, unrelenting limp that put me in the hospital and led to a toe
amputation and multiple foot operations.
I've been struggling with so many things I cannot list them here, but suffice
to say, these days, it is a constant struggle to control my body. Medications
help, but they are expensive, even with insurance.
I am being treated by experts in the field of Degenerative Neurological
disorders at University of Michigan Hospital.
Thus far, we don't know the underlying cause. We do know it is a progressive
issue that has to be watched over time to measure strength, nerve response,
degeneration, and a whole host of technical medical things to get to the
bottom of it. We do know there is trauma to both my lumbar and cervical spine,
which we hope to treat with a multi-prong assault in order to improve my
quality of life.
But multiple specialists, legions of tests, long drives and numerous
medications are expensive; and have left my husband and me in heavy debt with
more on the horizon.
My husband and I both work full time; he is in maintenance and I am a pharmacy
technician. We have applied for assistance across the board, but do not
qualify. To be perfectly honest, we even examined the option of my leaving
work so I could heal and we might qualify for some kind of support from
somewhere. Ultimately, my husband makes just a little too much for us to be
eligible, even if I'm not working. And truth be told, I love my job, and I am
the insurance carrier in our house. Without my insurance, we wouldn't be
getting ANY treatment and I would just rapidly degenerate without
intervention.
If you can donate, we would both deeply appreciate it. The money would go to
paying our multitude of medical costs, which may soon include spinal surgery,
depending on the tests. (Fingers crossed it doesn't come to that.) Medical
intervention by the experts at U of M is the only reason I am still able to
work to pay for things like rent, food, etc. In fact, without my medication, I
can barely function, let alone work.
We are trying hard to keep pushing forward and looking to the future with
hopeful hearts, but we desperately need help.
Every tiny bit matters. Whether you are able to help or not, we ask you to share
this fundraiser so others might see it. Thank you.
The trip to U of M went really well. But I have to do an entire post about it (which will likely be long), in order to properly discuss everything. That is in the works. But the main thing is we have started working toward SOMETHING. People (cough: doctors) LISTENED. I normally am pretty patient and understanding with the medical profession. I am very aware of how overworked, understaffed, and abused they are (both physically & mentally). But in the past few years, I have become intimately acquainted with the side that makes people say "If I was having a stroke, I'd rather die than have that doctor treat me." (-Me)
I Confess:
When my PCP sort of implied - READ: ["I'm not saying it is, but have you considered this could be ConversionDisorder?"] <<< direct quote>>>
I
sort of lost my shit. I had been teetering on the edge for quite a
while but this ending up being the last cherry on the sundae. Which is
how I ended up the behavioral health specialist's office, sobbing on her
couch for an hour, which is what ended up with contacting my
psychiatrist, which led to the psychiatric leave. I return August 1, and
I am looking forward to it.