This is what it feels like waiting for COVID-19 to kill me.
This is what it feels like waiting for COVID-19 to kill me.
I am terribly depressed.
Life circumstances, work being really slow, being diagnosed with new issues that require care and attention and, worst of all, my weight has hit an all-time high… all have combined to submerge me into the waters of depression.
I am distraught mostly about my weight. I had an RNY Gastric Bypass, for fuck’s sake. Granted it was 19 years ago, but still. You know it’s bad when the Pulmonologist, who has just diagnosed asthma and sleep apnea, then prescribed several inhalers and a CPAP machine, asks, “Can you do the gastric bypass again?”
I see the psychiatrist on the 12th and it cannot come soon enough. He changed the meds slightly last time, but I have fallen deeper and I am in that place of just not caring if I get out of bed, if I work, if I write. I just don’t care.
And I hate that I don’t care because I know it is depression and not me.
While my Hemoglobin A1c is a not bad 6.4, it is up from 5.8 a few months ago. The Lantus was upped again, to 85u daily, but about 4 hours after I injected it into my fat belly this morning, my Blood Glucose went down to a 38, the lowest I have ever seen it. I thought I was going to have to call 911, and probably should have, but I kept slamming juice pouches until it hit 60 and I began feeling… feeling… again. I ate a PBJ with very little J and my BGs have been better this afternoon… around 100.
And yes, I do know insulin causes weight gain.
It’s just overwhelming sometimes.
I love Audible so much I could cry. I listen to books for several hours a day and am plowing through piles of them.
Newer books I love:
The Originals: How Non-Conformists Move the World by Adam Grant.
By far the best “self-help” book I have ever read. My entire mental process has shifted and when I write, am writing without the self-judgement I was giving myself. Many, many other incredibly valuable pieces of information are in the book, from parenthood to dying. It’s just beautiful.
Daisy Jones and the Six by Taylor Jenkins Reid
Besides the intricate personalities between band members and their intertwined stories, I listened to this thinking what an amazing writer Reid is. She has multiple characters and speaks as them in first person and each character sounds exactly as they should and so so different from the others in the book. Listening, you get different people speaking the parts whereas reading, you “hear” them in your head. I believe this would be one time when Audible is far preferable to reading it.
Yes, I’m reading children’s books I missed growing up. My grandkids have read them, now it’s my turn.
I’ve seen several incarnations of The Secret Garden in movies (and a new one comes out April 10, 2020), but the book was so different than any of them and so filled with magic and the love of the earth, I was mesmerized with every syllable. Pure poetry.
Black Beauty is the horse’s autobiography, told by Black Beauty himself. Clever, wondrous idea! How did Ms. Sewell ever conceive of this is beyond me. And that this was the only book she every wrote! She began writing it when she was 51 and finished when she was 57, dying 5 months after its publication. I’ve not been into horses like a lot of my friends, but I can see why after reading this… a fantastic book.
Writing about the books helped. I don’t feel so desperate and alone with them.
I’ll go read now.
Due to a glitch in my insurance and the Latuda company’s lack of medication, I went about a week without it. Might have been more. I have been back on it for 4 days now, but have fallen into depression. I wasn’t sure at first, but after sleeping 20 hours a day 3 days in a row, I think that qualifies as depression.
And the crying.
I hate the crying.
The welling up of tears for (seemingly) no reason. The way they fall unabated, no amount of logic stopping them. They just turn on and off at their own whim.
What am I sad about? Nothing. There is no precipitating factor here, merely biochemical.
I want out of it.
This was the Prompt:
This is what I wrote in 30 minutes (unedited):
Deep inside my colorless cocoon, I have a vague sense of other lives nearby.
I slither through their reality; where is my own? Surrounding myself with the darkness of my depression.
My mirror’d existence bursts into color, fireworks exploding with energy that drains my body, but never my mind.
Having Bipolar Disorder 1 is, quite literally, opposing colors of my brain. I see auras anyway, but during a manic episode, the colors scream off my body, tsunamis of energy crashing into my brain again and again. Voices screech… or whisper… I, never knowing which will be next… raging about how I look, feel, need to act, need to fly, need to find this or that, things that are elusive even after hours of mentally and physically searching.
Exhaustion never comes.
When the electricity finally dissipates after months of zapping me, I collapse into that dark world once again, struggling to keep breathing and not smother myself with the thought that this will go on forever.
Reaching outward, always outward, needing several hands to keep me alive, I am fed my medication, waking only to swallow, then sleeping yet another 23 hours.
Writing is my emotional gauge. By how many words I write in a day, I’m able to see where I stand psychologically.
Not writing for days, weeks, months… I am in that dark place and need help. Too often, because I am alone, I do not recognize the need for many weeks and, by then, am buried by the pain.
However, when I write 20,000 words in a day… several blog posts for me, blog posts and essays for work… long emails to friends and family… run-on sentences with divergent topics… it is they who sense my need for help and their well-rehearsed phone calls are made to see who can get me to the doctor the fastest.
Walking the tightrope, umbrella in hand, I teeter, side to side, always searching for that inaccessible balance.
Yeah, the Mania has returned.
Once again, I am a live wire that hums like a fluorescent bulb, sleeping 2 hours a day, am a writing banshee and logged into work for many hours at a time.
It seemed to take forever to get control over the hallucinations and be able to sleep, and when I did, I slid into Depression mid-December. The fight to find balance between soaring highs and plunging lows has eluded me. Just when I think I am finding stasis, I slip by it and move to the next level of distress.
And here we are, mid-January 2017, and I am, once again, having hallucinations, staying awake for far, far too long.
Will I never find balance?
I’ve had increasing hallucinations for at least 2 weeks now. They aren’t terrifying yet, but they are on their way there.
Today I was visited by a bat!
Fucking thing was flying around the room then dove right for my head. I ducked and covered myself, but, of course, it wasn’t real, so if someone had been watching, it would have given them a hearty laugh. Other visual non-existent treats have been my clothes on the back of the door lifting off and swaying back and forth a couple of times and nondescript somethings sitting on the dressers or on my bed.
(I feel like a crazy woman sharing these things. How can I talk about what is going on so casually? I think it is just getting to be so normal, I am more shrugging than freaking out about it.)
The auditory hallucinations have returned, my hearing all sorts of crazy noises from windstorms to doorbell chimes. And the incessant whispers, always just out of earshot and too low for me to understand, but they are not happy noises. “Ominous” is the word I would use to describe them.
Oh, the goddamn tactile sensations. Again, feeling like I have bugs crawling on me. Not lots so far, but just enough to make me slap myself periodically.
Not smelling anything (yet) – olfactory hallucinations – but those are probably what’s up next on the Manic menu.
And so I write. Here, in my work blog, in Facebook. The words tumble out of my fingers even when I am meditating trying to sleep. I cannot keep them still as they search for a keyboard upon which to create.
This is the part of the Mania that keeps me from telling my doctor or taking more Risperdal because the deliciously creative period would be fleeting and, right now, the negativity of hallucinations is balanced by the verbosity of my words.
So shhhhh. Keep my secret quiet for now.
And watch the words spill from my psyche.
I feel like cutting my tongue out. I swear someone is using a course-grit sandpaper, rubbing it over and over and over, while I sleep.
What’s sucky, too, is the Tardive Dyskinesia is doing overtime even while I am awake. Unless I am purposefully monitoring my tongue and jaw action, my tongue is scraping across my molars or my front teeth. Continuously.
Thank the Universe no one is noticing.
I am lost over what to do about the TD. I would need to cut down or quit the Wellbutrin and I feel so, so much better on it. The prospect of stopping it terrifies me. (And the TD might not go away after stopping the medication anyway!) I see the Psych in a week and will talk to him about it, but the decision is 100% mine about what to do: stay on it OR go off of it and try yet another medication that might cause TD even worse, and possibly permanent symptoms, than this.
Fuck, I hate dilemmas.
So, I still have hallucinations, minor visual ones, not scary. But for a couple of weeks now, I have been having visions… premonitions are what they feel like.
I meditate and have vivid images cross my mind. They are different than the fleeting, wandering thoughts that float around inside my head during meditation. These are more solid than vapor-y… and so, so, so real. They come with emotions, sometimes intense. So far, all good, but I am a tad nervous about seeing scary things; trying not to focus on them, though.
They do not only come when I meditate, but they seem to come easier at that time. Sometimes I am in that half-asleep place, going to sleep or waking, and they appear, too.
I saw a dear single friend of mine sitting in a library and a woman came to sit by him. She was dressed modestly, something that is important to my friend and struck him immediately. I saw them meeting, marrying and having a family together. All within moments. It was so real I almost reached out to touch them.
I’ve seen my grand-babies, growing through their lives… specific activities that I’ll leave a mystery for now.
I’ve sat in a meadow touching a rainbow.
Google-ing visions with bipolar disorder, one gets “schizophrenia.” Eek! Really? I see the Psychiatrist in a couple of weeks and will ask him what might be going on.
Until then, I’ll take what I see, write the visions down and not worry too much about this new phenomenon in my mental illness.
I’m pretty upset as I write this. I’ve known I spent money during the Mania… enough that I am in quite a hole I cannot seem to climb out of… but I did not know how much.
I could have gone and looked at my bank statement when I realized the money was gone so I knew where it went, but I was sticking my head in the sand, ashamed of what I had done… too embarrassed to even disclose it to myself.
But I found a pile of Blu-Ray DVDs 3 days ago; all 6 seasons of Northern Exposure and Season 1 of St. Elsewhere. I’m enjoying Northern Exposure (am on Season 5 now), it being one of my fave shows of all time, but I cannot help wishing I had the $400 back instead.
Today, I decided to be brave… and humble… and go look at the accounting of my spending during the Mania. It isn’t pretty. I didn’t have lots of new things in my small space, so was baffled what I could have spent the money on.
Apparently, I was benevolent.
Not needing to share the organizations I picked… I’ll just say I chose ones who were either in Syria or were attending to Syrian Refugees. 3 different ones.
1 of them twice.
Trying to put the pieces together, I looked here in the blog and, as the Mania was ascending, I had written about my utter horror and distress about the Middle East. Clearly, it affected me deeply considering the amount of money I donated very soon after writing those posts. There is no way I could say, “I wish I had the money back,” but I still wince seeing how much I sent out.
I’ve been trying to figure out a way to not have that happen again. As far as I know, I didn’t tell a soul I had done it. If I had, maybe someone could have questioned me? I have zero recollection of spending anything during that time. I don’t have anyone to watch over my finances (which Zack used to do). I don’t have credit cards, but spent everything I had plus more I had in the bank, so can’t even cut up cards to try and save myself from me.
I’m lost. Maybe someone will have some good ideas for not having that happen again?
Holy crap! I am finally awake more than 2 hours a day. I worked right about 500 minutes last pay period (I usually average over 1000)… and yesterday alone, I got almost 300 minutes!
So upping the Wellbutrin to 400mg a day and the Risperdal down to 1mg a night seems to be the ticket. At least for now. How many times do I have to do this readjustment? Over and over again. Very frustrating.
However, I took no nap yesterday, so that was good. I laid down this morning, but not sleeping, just dozing.
I am cranky. (Oh, well. I have good reasons.)
I do hope I keep feeling better.
I am immobilized by depression now.
I cannot work. I can barely write. I am sleeping 100 hours a day.
Over and over and over I go, like on a loop, sitting in the Psych’s office, trying to form words that explain how I feel:
And words I do not share because they will toss me in the hospital if they fall out of my mouth. We’ll just let them sit in there and rot.
Another change in meds. Lowering the Risperdal, upping the Wellbutrin. Will it make one iota of a difference? Can’t I have some speed, please? “We don’t want you having those horrible hallucinations again, do we?” (Yes, please. If I can stay awake.)
Change cannot come soon enough.
Apparently I am really sensitive to medications, especially Psych meds. Over the last 2 years, I have tried 6 meds (not all Psych) that I eventually had to quit because of (what I would consider) intolerable Tardive Dyskinesia. I know that many others have it worse, have to take the meds that cause TD and that, for many, it never goes away. I have been lucky that mine generally went away.
Except the last time.
The first time I experienced the TD, it took a couple three weeks to figure it out. My tongue kept burning… then I would wake up with blood in my mouth. I couldn’t figure it out. My teeth? They all felt fine.
So I meditated on it, talked to myself about paying better attention, slowing down the movements so I could figure it out.
I began paying attention as I fell asleep, honing in on my mouth.
A couple of nights after this new mindfulness thing, I relaxed and let my mouth do its thing. And boy did it ever.
Scraping is the best way to describe it. My tongue, clearly having a life of its own, pushed through my teeth, first pressed upward, then pulled back, my top teeth sliding against my raw tongue. Over and over and over again. Apparently, all. night. long.
Oddly, it didn’t do it as much when I was awake. I realized it did some, but not a lot. It was at night that my teeth assaulted my tongue. And holy fuck did it hurt.
I Googled “tongue scraping” and TD came up. Medications were the culprit. Sometimes ones a person had taken for many years.
I’d recently started some medication or another (cannot remember and for whatever crazy reason, I didn’t note it or write it anywhere), so went off and within a week, the TD had disappeared. The doctor tried another one to replace the first. Same thing, but this time I figured it out a lot sooner. Went off, it went away, and tried a third medication. This time it was fine.
Fast forward to this recent Manic Episode when I had to go on Risperdal for the hallucinations, then when I fell a tad too low, increasing the Wellbutrin… a med I have been on for several years. I hadn’t an issue with the Risperdal, but began noticing some light TD symptoms after upping the Wellbutrin. No blood this time, but the scraping had begun.
I lowered the dose of Wellbutrin for a couple of days with no changes, so upped it back to the 300 mg my doc agreed to (after I’d upped it myself). It didn’t get worse, but was still annoying.
I seem to be in the place where the TD isn’t going to go away, but it isn’t going to get any worse, either.
It is definitely worse when I am tired or sleeping. I wake up with a very sore tongue and can feel I have been rubbing it against the roof of my mouth. I am happy that I am not waking up with a bloody tongue or enormous sores from the vicious play of teeth and tongue while I am unconscious. I am also quite lucky I do not have the serious symptoms of TD that include protruding tongue or uncontrollable facial tics that are obvious to anyone looking.
Still, my TD is annoying. It gets in the way of my work at times, having to make adjustments to my speech because of my involuntary mouth and tongue actions. But so far, nothing has been irreparable.
So, I shall just keep being Mindful and do my best to stay on top off the Tardive Dyskinesia, maybe lessening it over time.
One can only hope.
It’s really sucky to just be living your life, tooling along as usual, talking with your friend… and then BAM! have your head smacked with a baseball bat and suddenly being an incoherent, crazy person contradicting yourself and being mean to the last person on earth you want to be mean to.
I can’t even find the words yet for how embarrassed and ashamed I am for hurting someone I really love.
I know. triggers are triggers and sometimes cannot be helped because seeing them down the road isn’t possible.
They still suck.
Last night I was talking to my friend. We were ranting a lot about that Hitlerian President-Elect, sharing our thoughts, our fears… our terror… then I needed to write.
So I went to work on Stunned, Shocked & Saddened and right as I got to the end, I began to feel crappy, then worse, my heart started racing, my stomach was in knots, I began sweating like a piglaletta and finally I told my friend, “I feel like shit! I need to go lay down.”
Once I was on laying on my bed feeling horrid, I began breathing deep to try and lessen the distress.
Then I thought, “Oh, I recognize this. This is an Anxiety Attack.”
I situated myself on the bed, laying down, feeling my body’s frantic fight to keep control over my mind, but I strong-armed the panic so I could do my Mindfulness exercises.
I felt the sheets under my arms and legs… listened to the air conditioner’s humming… smelled the scent of cinnamon from the witch’s broom I have in the corner.
When I could, I texted my friend that it was an Anxiety Attack so he wouldn’t worry. He then asked if I had meds for that.
Later, when I could explain better, I shared that I grew up in a Pill-for-Every-Ailment kind of family, so I have always seen meds as a free-for-all. My mom, sister and I have all been addicted to pills of one kind or another… my sister dying of an overdose of pain meds, mainly the 4 Fentanyl patches she had on when they found her. I am now about 2.5 years clean from Opiates (Percocet & Norco). I then shared that while acknowledging my forever-need for Psych meds, I do try to minimize other meds where I can.
Anti-Anxiety meds (Benzodiazepines) are one of those types of meds I would rather not be using. I tried them when I had the Agoraphobia and hated them; I was doped into a stupor. I was on a dozen other meds including the opiates, so probably to be expected, but still. So I made the choice to not use the Benzos, but Mindfulness and Mindfulness Meditation instead.
I was confused why the Panic Attack even hit in the first place, but my friend reminded me (lovingly and gently) that the (fucking) Election has brought out intense emotions and then I spent a lot of time writing the previous post. Then the Panic consumed me.
Now that I remember what they feel like, I am on alert (not HIGH alert, though) for when/if it comes a’callin’ again.
Of course, I hope I don’t have another, but if I do, I am ready…
I am horrified to learn I live in a country with so many bigots, xenophobes and hate-filled people that they would elect a crazy man to lead our country.
But, I refuse to give up.
I don’t know what or how yet… and the only thing I can physically or financially do is write… but I will write until my fingers bleed trying to share, in words that have not already been said a million times, the impact of this Hitlerian President on those around me. And on me, a mentally ill Latinx on Obamacare, a femme Lesbian, an extremely pro-choice feminist woman who is scare for her Muslim friend.
I am embarrassed to say…
When I went to the Psych a few days ago, he changed my Wellbutrin from 100 mg once a day to 100 mg twice a day. I asked if we could do 3 times a day. (You know, if 1 is good, 10 has to be better, right?) He said no to the 3 because it could send me back into Mania… and I wouldn’t want that would I?
I said what he wanted to hear, but began calculating how many Wellbutrin I had at home to be able to take 3 a day.
Just for a few days, you know. Just to get me over this sleeping 18+ hours a day thing.
Probably the bad part is it’s working. Not sending me to Mania that I can tell, but boy howdy, when I start to get that overwhelming sleepiness, I take a Wellbutrin and perk right back up for several hours.
I really am only taking 3 a day. I promise. (If I was going to confess this, I might as well go all the way, right?)
Not sure when (or if) I will lower it. Then I have to decide if I am going to tell the Psych when I see him again in 2 weeks.
The name of this art piece, as well as the art itself, says it all.
I don’t even know what to add at the moment.
I think I’ll go take the second 4-hour nap of the day.
It’s bittersweet even saying it.
I miss being awake almost all day (or a couple of days at a time). On Halloween, I slept 19 hours. As I have written, that isn’t the first time I have been asleep more than awake. It’s not only annoying me no end, but it is severely limiting my being able to work.
Even when I am awake, my brain is not functioning. I have no memory. Thoughts jump around until they are in a jumble in the center of the room. I am still struggling with the fucking homophones (week/weak, right/write, breech/breach, etc.) spilling out of my fingers as I type. Annoying!
Until this manic episode, I was able to tell a depression was coming because of the hallucinations I almost always have them turning ominous. I’d mentioned to my Psychiatrist several times about the hallucinations’ slow transitions from pleasant to less pleasant, but I felt fine! (emphatic “fine!”) Now I know it was because I was shimmying UP instead of sliding down. 1998 had been my last manic episode and even that was only my second, so seeing this one coming was virtually impossible.
I have been concerned about depression setting in for awhile and talked about it at therapy today. I remember when I told the Psych my concerns a couple of weeks ago, he said that anything after where I had been is going to feel like depression.
I am really good after 38+ years with diagnosed mental illness, at being able to see my depression setting in. Or I thought so, anyway.
Being able to write is a litmus test for me; if I can write, I’m not in a catatonic depression. I can still write, so that’s good. Even if it is a scrambled mess.
So the Manic Episode officially (by my designation) began on or around September 1st and I declare it officially over on October 31, 2016. 61 days of Mania… the first 19 days lifting off; the last 18 the beginning of the end. 24 days of really distressing, trying to keep myself out of the hospital, bullshit. Give or take a few herky-jerky days on each end thrown in for good measure.
I miss the mania in several ways, mostly the being awake so much and the incredible productivity. I do not miss spending money I did not have and that I have zero to show for what I spent and the gigantic hole I am now in financially. No, that I could do without.
I keep being reminded that the mania came at a price (not just financial). I really did think I was losing my mind in the midst of it all. I am so thankful I am aware of when I need help.
I am finally finishing this 5 days after beginning. I have slept so much I can hardly do anything, including work.
The sleeping is out of control.
I just got back from the Psych… next up.
I was going to see President Obama on Friday, October 28, 2016. Strategic obstacles left me out of the crowd (another post), but lots of feelings of anxiety crept up that I needed to write about.
I was extremely excited, but I was also terrified. I was scared there would being a bombing, an assassination, a mass shooting, a stampede… you name it, my mind could create a scenario for its occurring during in any public function and in any space where people congregate.
I had agoraphobia (the fear of the marketplace aka the fear of leaving the house), a form of an anxiety and panic disorder, for an 18-month period about 4-5 years ago. I only left home when I could go with my then-partner Zack; he was my talisman against freaking out. I was even able to go to Costco (the most open marketplace ever invented!) with Zack in attendance. Alone, I could not even get to the car in the driveway without a panic attack.
Only in the distant retrospect am I able to see the agoraphobia was in response to 1) being ostracized from my midwifery community and 2) Zack’s coming out transgender. The stress of the two kicked my anxiety level into overdrive.
My least favorite memory was when I laid on the floor of Target, after the registers, before the doors (in front of god and everybody) and EMS tried to talk me into getting up and sitting on the Starbuck’s couch. I was so immobilized it took many minutes for me to even hear the requests/commands to move already. It was after that I didn’t leave the house alone for over a year.
So, GAD isn’t a label I wear, but have worn for a short time in my psych history. It came right after the agoraphobia, before the depression, during my opiate addiction. The Panic Disorder came with the agoraphobia.
Despite being on Norco and Percocet, along with a (literal) handful of other psych meds taken 3x a day, I was prescribed Benzos -anti-anxiety pills. Benzodiazepines are highly addictive. I took a few of the pills over the next few days, but they put me in a stupor (not surprising at all considering what else I was on) and decided they were not for me. However, I knew I would turn to them when/if I ran out of my opiates, so had Zack lock them up from me. I do not recall ever wanting them again. Over the years, I have met so many benzo addicts I am so glad I never got into them.
I have written about Mindfulness Mediation before in relation to getting clean from opiates. It was also responsible for my climbing out of agoraphobia eventually. I went to a class at UCSD on Mindfulness-Based Stress Reduction (MBSR)… it taking extraordinary effort to get there each time… but the new skills helped tremendously and I was able to gradually let go of the anxiety and resume a life of going to the store without Zack again.
The state of the world makes me very nervous when my family and friends go out to festivals, restaurants, concerts, etc. I am able to stay safe for the most part, being disabled, but the fear of violence (which does not have a “phobia” name that I can find) nearly paralyzes me at times. I think twice, three, four times before heading out to even the store. I have to breathe, remind myself: It is on the news, that’s how rare it is.
But Pulse was a few miles from my home. And that made the news. Those 49 Doves gone in a matter of hours. It could happen again, right? And, to be honest, we all know it will happen again one day. Worse even.
So when things tangled into such a mess that I could not go see the President, I was able to exhale and sit in a small out-of-the-way restaurant with my mama instead.
I don’t know if I will ever be totally free of anxiety… it seems not… but I just keep breathing.
Monday, 10/24/16, 1:56am
I thought I should have a title for these Bipolar posts. I came up with Bipolar Diary. Original, I know. laughing
Today (10/23/16) has been a really difficult day. I went to bed at 5:00am, slept for 3 hours or so, then up for a few hours, then down again. And again. And again! I keep napping for 1-3 hours at a time. Where is this fatigue coming from? Am I depressed?
This happened a week or so ago, too. I don’t have the patience to go search and see how far back it was. I don’t have much patience for anything. If I hadn’t been in menopause for 8 (or whatever) years, I would think I was having PMS. I cannot keep a thought in my head, am so scattered. I am sure this post will be ghastly, but need to write anyway.
Most of the hallucinations have gone, but the visual ones are making me crazy.
How I was more tolerant of the slew of visual, auditory and tactile hallucinations than I am with just the visual is beyond me, but I think much of this sleep crap is because I am overwhelmed with the visions I keep seeing. Roaches, yes… some… but mostly like things are just moving. Sliding around. The covers shifting, the pillow edging over, the carpet rising.
It’s like I am on a tilt and everything is going to fall off the edge.
Frustrating is an understatement.
Also, I have very little attention span. I have tried to watch Grey’s Anatomy, a show my daughter recommended, but it is too much new information to retain so I end up watching Sex & the City or Friends again (on Amazon & Netflix), two shows I practically have memorized. (Monster’s Inc. is on as I am writing this; another movie I know by heart.)
It is difficult to work in this state. My mind flits from thought to thought and I keep talking over clients. I try so hard to pace my words, but they just tumble over each other.
And, as a few weeks ago, my fingers are fumbling with the keys on the keyboard… spelling homophones instead of the correct word (reed instead of read, meat instead of meet, etc.). Argh! I hate having to re-type the right word! (Write came out first. Fuck me running.)
When I saw the Psych last week, he was happy the auditory hallucinations were gone and said I was on the right track. Today I had the first tactile sensation after several days without any; brief, but still there.
I hate the see-sawing of emotions. One day feeling great and doing well, the next (today) being total shit and missing a day of work. Isn’t there supposed to be balance sometime?
I don’t even know where to go from here, so I’ll just end.
Tuesday, 10/18/16, 7:06pm
You know that sound they make? That incessant buzzing?
That’s what I feel like.
And in perpetual motion.
I don’t know who I think I am fooling when I sneakily “forget” to take the Risperdal. Up for 25 hours, trying to sleep periodically and feeling like I am electrically charged, getting back up again a few minutes later.
I’m somewhat productive, writing posts for work and here, organizing my Kindle music library, pulling things out of drawers and stuffing them into garbage bags, but I feel sad all at the same time. Not that wonderful, blissful feeling of the last few weeks. My therapist, just like my Psychiatrist, reminded me that it was not all that “blissful” and my mind is playing games with me.
TAKE THE FREAKIN’ RISPERDAL.
I hadn’t been to therapy in a couple three weeks because I was working with the doctor instead. It’s almost an hour to get there and the prospect of taking that trek twice in one day was too daunting. I did it today, but probably shouldn’t have.
I barely remember anything we talked about, knowing I wouldn’t even as my lips were moving. The whirring so loud in my head and coursing through my body.
What I remember is that I need to honor my Self and take my meds every day and on time.
It’s the goal for the next few days.