The Stress Monster Is Melting My Brain – Today Sucks… Wonder Why?

I have Bipolar Disorder and ADHD. You will see them both in today’s post. This post will not be edited by anyone. I suspect that the door in my brain is going to try to say things a beta reader would catch. If you would like to see the bullet main points, if there are any, read on. The full story will follow that.  

Why should YOU read further? 

Reason: I hope from all the bits of my heart that you might see something of me in you and know that you really aren’t alone. You’re not. Please, LOOK at me. 

Now, here I am…. this is my version of transparency.  

Today started pretty slowly, but good. And then I left my room. Sigh, sometimes the spaghetti hits the wall early in the day. Normally, I would say that the old spaghetti trick isn’t necessarily a bad thing. Spaghetti good: encourages and stimulates my ability to see more ideas and options. Spaghetti not so good: other stuff out of my control. 

I wouldn’t normally share the specifics of a particular day with you because, well, this isn’t that sort of place for that. However, today, I think that when I talk about stress I’d like to share with you some of my own stresses. I’m going to limit it to this morning and stop right now (1:47 p.m. PST). 

Stress is a constant ANXIETY feeder in my brain all the time. Constantly. It never stops. I never feel “at peace.” What has been happening today demonstrates exactly what happens when it passes over an imaginary thresh-hold beyond which I flounder and may crash and bury my head someplace where the world stops for a moment. 

I clicked on the Word icon and waited for it to launch. I was planning on writing to you. Then Office said it was updating Office. Then it said I was dumb and that it wouldn’t play and was taking its ball and locking me out. This was the last straw. It was the “break the camel’s back” sort of straw. (What does that mean anyway?) 

I became aware that my breathing was very shallow and quick. My throat tightened and my forehead and eyes scrunched up in emotional pain. I began to cry… So, I texted my support team which includes my kids Jessica and Kyle whom I share a home with. We have a group text for things like who is going to making dinner, where we are, grocery list items, giving voice (expressing) to great things and crappy things in our days. Oh, and loads of funny pictures of our pets. 

This is the text I sent them: 

Ok, keeping it brief:
– Word keeps trying to update, fails, then refuses to open
– one the boys in the big boy tank is visibly sick [Fancy Guppy]
– twitch won’t run, so no escape in minecraft
– my anxiety is way past healthy
– only 2 chill pills left
– I am going to blog/write but I guess it will be on paper or Google docs
– I’m soooo frustrated
– I still want to get some new guppies to not kill. To put where? With Banana boy.
– insert much foul mouth swearing
– and… Son of [Some content removed. Sorry.] crispy cracker with toilet exploding hot sauce
– So I can’t play, I can’t write…
on the flip side:
– We did get back from a walk just as the weather freaked out again
– I’m not dead
-I have you guys
– my hand feels better, mostly
[during a wind storm a few days ago I dropped a heavy sharp corner of a bookcase shelf on the scar of the thumb I just had the joint replaced last December 17th. I have RA and OA.]  

I followed that up later with:

I’m struggling

What brought me to this state, besides the obvious? I’ll bet you may have experienced this yourself. (Wait. How can I “bet you may have”? Anyway, on with the.. Uh… show.)

Bailey and I escape the house to walk around the block walking as fast as we can to beat the wind and rain. And… home dry!! That was fun.

I take multiple mood stabilizers. I have Bipolar Disorder Type 1 and run manic most of the time. I experience mixed states and enjoyably also cycle rapidly. Fun! Additionally, (sounds like a speech) I also have the stimulating ADHD. Yippie! We’ve elected not to treat the ADHD with medication. Who needs a stimulant to stimulate an already over-stimulated brain? Not me, thank you very much. 

FYI: I’ve recently, after years of refusing to do it, switched over to having a pharmacy send my medications to me in bubble packs. One of the major reasons I wouldn’t do it is because brain meds can be changed fairly frequently when we are trying to find the right combination that works for me and keeps me from driving everyone around me to the point where they want to duct tape me to a chair in my room and shut the door. 

Anxiety. Remember that? Unless a person has Bipolar Disorder they simply cannot understand what having it is like. They just can’t. I’ll try to sprinkle in a few things to help explain what’s so important about this stuff.

That’s the setup. 

I take:

1. Mood stabilizer in the morning (A)

2.The same mood stabilizer in the evening only double the dose (A)

3. I take another mood stabilizer in the morning (B)

4. I take the same mood stabilizer in the evening (B)

5. I take a “chill pill” (one in the “benzine” family) ( C) 

6. I take one before bed (D)

Fine. I do that. Only at the moment, I’m completely out of

1. A in the evening

2. B morning and evening

3. C (OMG)

4. D

These are ALL MOOD STABILIZERS! I don’t have any of them. 

Remember my mentioning my thumb. The next day I fell on that thumb and while it saved my face from planting itself in the garden at the Vet’s office. ALL my weight landed on that hand. I weigh over 50 lbs. I’m sure 50 lbs would have hurt a lot. I weigh over 100 lbs above that. My thumb/hand has been hurting, but only when I use it, touch it, or put pressure on it – think ice pack or heating pad. 

I called the bubble pack pharmacy again (did it yesterday as well) and practically begged the poor lady to tell me that my missing FOUR brain meds would be here yesterday. She couldn’t. 28 minutes later I came away with a USPS tracking number and the medications that should be in it. ALL of the medications [A, B, C, D] are in that box. 

Of course, I jumped on Jessica’s computer (now not trusting my own) and looked it up. [Insert creative bad words developed while growing up on a ranch. Use your imagination.] They appear to all be in the same package. The package took 24 hours to leave OH. (Uh…) 

See – things progress. I don’t pop on Facebook to visit friends. Rarely. It is now 4:08. While I sent myself that text message from my phone (SMS) to FB messenger, copied it, and pasted it here I saw an ad that indicated it might lower our energy costs. Stupidly, I clicked it. Ten minutes this sales guy calls me. Seriously. I had just been trying to find out if they were legit (I couldn’t) when this name pops up on my phone, “Blah Blah Solar Company.” Oh hell no. No, no, no, no. Nuh-uh. Having been in businesses I and my family have owned I can tell you that this ad clearly misrepresented themselves and what they were offering.  

I am known in my family as the one to go to if you need someone to kick-back. Meaning since I think I know more than they do I will explain to them what exactly I think about whatever-it-is and how it’s going to be. I shot of pic of the ad from the monitor and was getting ready to send it to my city utility company to see what they knew (and probably to show them something possibly fraudulent – no, I have no idea what I’m talking about. 

Remember how things are going today and that those precious lost medications for anxiety, that’s part of mood stabilization, are completely out of my system. Blotto. 

Blotto. I don’t know what that means, but I like to say it. [Use Google Mom!] Google says I was spelling it wrong, but it essentially means “extremely drunk. ‘we got blotto.’”)

When I use the word “blotto,” which I do, I mean something like “the shit hit the fan.” Yes, I think that works. Or maybe more gently, “Crap.” But sometimes I just say “blotto” just because I like the way it feels when I speak it. Weird. Right. 

Can you see anything? Yes, of course, you can. Bipolar mania. ADHD. 

How is my day? Blotto. But, it’s getting better. 

4:35 p.m. Kyle get’s home from work. He asks me how I’m doing. I say, “Fine.” (More abbreviated chit-chat. I hate it when I talk like that.) “I’m not making dinner. Can you two deal with it?” He says they will. I make licorice tea (decaf). Set a five minute because I always forget it. Put on headphones. Stop writing this for a few minutes while I get ready for music. The playlist I made to help me hold on has been “misplaced,” so I’m making a new one. Bluetooth. Headphones. Volume is very high. Kyle comes back in and gets my attention. He didn’t know I’d plugged my head in. My tea, it was done. Oh yeah. Yeah! Headphones die. Kyle sets them to charge. He loves me. “Mind if I play music, uh, loud?” Sure. :0)  

YouTube playing. Right now. Breath… out. Imagine with me just that. Breath… out as the music draws me in. Eyes close. Head embraces the sounds. Nods. Taylor Swift. Gretch Wilson. What??? 

5:00 p.m. “Redneck Woman.” I sigh and begin to relax. “Fight Song.” (“…. cause I still gotta lot of fight in me.”) 

Hours remain before bedtime and I’ve lost focus. I’ve written all this down (thankfully skipping all the interruptions like talking for 28 minutes to the new pharmacy and all that stuff) for just two reasons. 

Reason 1: In some crazy way I hope you focused a little on my day and not your own. Maybe this you were entertained? ;0)

Reason 2: I hope from all the bits of my heart that you might see something of me in you and know that you really aren’t alone. You’re not. Please, LOOK at me. 

5:15 p.m. Pink “Just Like Fire.” The music helps. First deep breath. Thank goodness. 

…… And now the med provider has called to try to rescue me!!! I’m talking to you while I listen to him type out “emergency” orders for my local pharmacy. So funny.  ADDENDUM: The pharmacy received the orders. Insurance denied. The pharmacy says  I can pay cash. No, I can’t. Called the med provider and left another message as he asked me to do if there was a problem. There is indeed a problem. Further TRANSPARENCY: Thankfully my kids kept bugging me to try cannabis (legal here) just like my MD has been trying to get me to do for over ten years. 

Alright. I think that covers the majority of my day. I hope I haven’t bored you or convinced you to head for the hills. This, this post, is me being “transparent.” I’ve wondered what a day in the life of a “stable and normal” person is like. I see them posting about how I can conquer my anxiety and depression and they know because they’ve done it too. I’m sure some have and are doing great. The problem is that I’m reading what they say from a bunch of clean whiteness with sharp letters that make up clean looking lines containing words. What? It looks, with the eyes, clean. Life isn’t clean. It is so messy. I’m messy. I’m guessing you can see that. I just always want to know something of their story. What were they like before they were able to write this logically layed article with bullet points? 

Robin, STOP. FULL and or HARD STOP. 

Okay, geeze. 

Always honest. Always trying to be better. Always here, even when I’m stuck inside my head. Please reach out or feel free to leave comments. How are you as we head into more stressful days. I don’t know about you, but this Thanksgiving especially is going to be more stressful than the normal stressful. We don’t want to give or get the covid. (That’s what we call it now. Just, “the covid.”) It gets complicated. 

I’ll be back. 

A question I was asked today: 

Do you have any desire to harm yourself?   [something like that]

No. No, I do not. 

(This is what transparency looks like from me.) 

Bipolar Carnage – The Aftermath

Since I posted on the third, my brain has imploded. You know how it is. Imagine being on the top bunk of a three-bed bunk bed, in a tree fort, playing on the ladder against the house, running up the giant stack of bales of hay, climbing on the dirt dad just had delivered for the front lawn, you know, fun stuff, and then falling off straight away and landing on your face, the top of your head and your feet all at the same moment. Then, when you get around to it, you open your eyes only to discover that someone is standing on your face while they’re attempting to ascertain if you’re alright because you’re so dirty that they can’t tell which way your face should go. That is what my brain has been doing with all its time.

Fun.

I won’t give you a messy laundry list of my troubles because I don’t think that’s necessary. I do believe it is essential to share a couple of really critical truths that we must all remember even when the you-know-what goes sideways when it hits the fan.

  1. Life rolls along for everyone like the surface of the ocean with ups and downs all the time. Sometimes, those peaks and valleys thrash about much higher and lower for some of us. That is OKAY. We don’t need to punish ourselves for that. We’re not bad people when we become angry or depressed or talk a lot. We are not mean, we are not evil, we are not trying to hurt anyone.
  2. We often are not able to (or equipt to) deal with our emotions and situations that cause them to intensify so when they grow and grow, they eventually reach critical mass and we implode. (Which was my case this time.) What have I learned? Stop punishing myself and blaming others for not rescuing me. It happens. Stuff happens. Reset. Get rest. Recreate. Hit go and begin again. Oh, and maybe cry and scream and barfing might help too. And throw something. But only break things that are yours and don’t cost anything. Seriously.
  3. I realized some time ago that at the top end of mania is anger and then rage. Deep below that dwells depression and anger and then the rage. Why always the rage? That’s how it is for me. I’ve asked several counselors and they seem to see that as well. Have you found that too? When you’re very depressed to you rage at the world because it has abandoned you? Has your world collapsed and left you to die? Tell me. Do you feel the rage too? It’s okay to feel the rage. Would you know it if you’re feeling it? Words. Do you know the words to express it?

I realize that’s only a couple things to think about, but this isn’t a book and a couple things to think about is plenty when your brain is Bipolar. Just considering the idea that I’ve been blaming myself for the way my illness makes me feel has been a bizarre thing to think about. I mean… what the heck am I supposed to do with that? If I were a public speaker, I’d wave at the screen behind me and say something wise like, “Now let’s unpack that…” Sure. I’ll have to think about it longer. That’s the best I can do. I’m still picking my face up.

Wait! I had two very specific moments that set me off into Never Never Land and I was trying to do the same thing both times. It was that CPAP thing. I don’t like things covering my face, blah, blah, so on and so forth…. I just couldn’t do it. I literally ripped it off my face and became hysterical. The first time (I practiced watching TV trying to get used to it) I managed a panicked 20 minutes. The second time I made my kids try it first (they didn’t mind it) and I lasted something like 0 minutes before I ripped it off with the same hysterical glee as the first time. Nope. Not gonna happen. “And I am unanimous in my decision.” (See Are You Being Served, A British comedy show that I think is sooooo funny. You can find it on Amazon Prime via BritBox)

I’m up because my kidneys are suffering a bit from the medication I take for my RA. I can’t take Advil or anything like that because it makes it worse. So, in my infinite wisdom, to get rid of the headache I was giving myself because I was getting myself all wound up, again, I took some Excedrine Migraine (has caffeine) because I really didn’t want to throw up. That’s what that particular sort of headache does to me. The headache goes away, but I’d like to bang my head until I’m asleep before that happens. I mean, we have five or so ice packs and I’ll have them all up and down my back, neck, and head and the headache will still be there. Then heat, gentle stretching, gentle exercise, moving around, walking, etc. Uhhhh. Anyway… (Thinking Carol Burnett at the end of her show… wow, brain, slllooooowww down!!!) (See Taylor Swift’s new song, “You Need To Calm Down.”) Holy cow Batman!!! Someone, take my laptop away!!!

Remember me? Manic … uh …. Mommy??? Lol That’s a Hard Stop. Hard NO. Full Stop. (Did I get any of those right?)

Good morning people. I’ll be sharing the playlist I made to help myself stay afloat during my “time” (honestly, what DO you call it?) with you tomorrow. I think I finally have it the way I want to share it. I’m picky you know. Sometimes. Here, I’m talking with you. Conversation. Not so pucky… picky. ;0) Anyway, I’ll put the link up here tomorrow. It’s already publish under my name on YouTube. (shhh… so is a bunch of junk playlists…) I bet you can’t figure out which one it is.

I promise, it will be here later today… I really should learn not to say things like that.

Bipolar – There’s Manic, Then, Then There’s Really Manic!

I started seeing a new counselor this last Friday. So far so good. Straight away, I told her I felt I was a handful because I am. Then I explained what my med provider had as my diagnoses and what my counselor had. The previous counselor only had Bipolar 1 listed. That’s it. The med provider had much more. The most significant of which, and what I want to mention today, are Bipolar 1 with a PhD in mania, mixed states, and rapid cycling, and ADHD. We’ll leave the rest out for now.

We started forming a treatment plan, and one of the things I wanted to do was figure out how to stop.

I just want to stop sometimes.

Last week I told people on my mental health team that I feel like my brain is on fire. I couldn’t explain it. It just feels like that. I’m on, I’m manic, I’m thinking, my brain is doing ALL THE TIME. It never ever stops.

My counselor reminded me that the typical pattern for Bipolar is most of the time, the person struggles with depression and the mania only comes around ever so often. It took me 37 minutes to lay out what I thought were the important things she needed to know to get started that she might ask questions about or whatever. I’m sure I missed a ton. But still, 37 minutes. That’s some fast talking, even for me.

In the past, I used to ask my doctors if it was possible to have my adrenilen stuck on all the time. They always said that it wasn’t. I think they were closer to being wrong than right. I am manic 96% of the time. I’m manic right now.

I also have some chronic pain in my sciatic nerve. When it’s hurting, which is every day, and my brain is toying with me, things go to pot pretty fast. Then I get mad. I might become enraged. Then depression pops in for a jig and the pain is magnified, and I can’t stand it. I kick and cry and rock back and forth. I ice and heat and wish I could take something for the pain. I do all my PT, am active and go for walks. Nothing works. It’s a nightmare.

And yet, I’m allowing another potential nightmare to happen on the 17th. I’ve already had my right knee replaced twice (long story). Now, my left thumb joint has to be replaced. JOY!!! Not. I’m scared. Joint replacement isn’t my favorite sport. Nope. Not. Scared. Maybe terrified..

Now, add to that acute mania, and what do you think my brain and my amped-up emotions are doing?

The reason I’m mentioning that I’m nearly all manic is that each one of us is totally unique. The ubiquitous norm is a cycle of depression with less mania. I don’t hold to that norm. I don’t know, maybe you don’t either. Maybe you only become manic once a year or once every two years. It doesn’t matter. What matters is that whether you experience your moods frequently or more slowly, you still need to be prepared for them. Be ready for the good and the bad.

Be ready for the depressed days, the good normal days, and… the manic days. There is so much to learn from each of them.

I get this dog.

Bipolar Disorder – A Manic Pause in Motion

I’ve often thought about how to explain more about how I think my brain works so that you might understand where I’m coming from… but heck, I’ve not nothing. Well, nothing simple or short anyway.

Most of the time, I hesitate for days and even weeks to post my thoughts to you for one main reason: I don’t think they’re perfect. I can’t believe I just wrote that. Perfectionism is NOT something I’ve ever been accused of. At least, not loudly enough for me to remember hearing.

Baby steps.

I’m having surgery on the 17th, and it might just slow my already lagging posting schedule down. My goal and my intentions aren’t to allow that to happen. This begins right now.

I’d like to share with you something that I have always found fantastically funny. As a matter of fact, I have gone through all 10 seasons on Amazon Prime and have now started watching them on YouTube so I can share them with people like you, people I want to help find lighter things, funny things, silly things to laugh about. Things that frankly don’t matter beyond what goes on once it goes into your head.

I do hope you’ll take a half an hour and give the series a try. There are far too many episodes for me to sit and watch them all and pick a favorite one to recommend. Most of them are ridiculous. Just last night, my 27-year-old daughter and 25-year-old son watched a random episode with me and we all laughed. They said that I didn’t need to have tricked them into watching it. All I needed to do was to tell them what it was. They would have stayed in the room and watched it anyway. Now that’s a gold star!

Give it a go and let me know what you think. If you love it and search for other episodes please don’t pick the ones with the show playing in the little box in the corner. If you have Amazon Prime, so much the better. You’ll need a subscription to Britbox at Amazon Prime, but I love many of the British shows available through Britbox. If not… hey, here it is, for free. One last thing, remember, this is a British television show from the 1970’s – a lot of things are different. Give it some room and go with the flow. I think it is hilarious! I hope you enjoy it too!

On with the episode. Season 8, Episode 3

Opioid Dependence and Mental Illness

Pile of pills

I’m not an addict. I’m not! I’m mentally ill. I have Bipolar Disorder. I also suffer from chronic pain in my lower back.

My primary care doctor (PC… PCD? Uhh… let’s go with MD) had been prescribing me oxycodone for the server and persistent (chronic) pain that I’ve had for years. After being active and doing something super strenuous like gardening for 15 minutes I think I’m dying. I’m exaggerating of course, but when I work as hard as Atlas does while holding up the world my eyes leak, I whimper and sit down. Sometimes I end up laying on the floor. The floor is such a very bad idea. If I straighten my legs my whimpering becomes desperate and I realize I’m crying. If I forget myself and straighten my legs I’m done. I can’t move. The pain paralyzes me.

I’m NOT an addict.

When I can think again, I try to find my phone. If I can’t find it right away I feel the panic rising and it triggers thoughts and emotions I thought I’d had under control.

This last time I thought I was managing my mania and depression (mixed state, rapid cycling) pretty well. I haven’t bought piles and piles of books on ducks or Oprah or how to be an astronaut. Honestly, I really haven’t. But please, don’t ask me what I’m thinking about. Also, I’ve been able to get out of bed AND wake-up in the morning and even go for walks. My depression skips through the dandelions with the mania comingling into a mixed state, which is always confusing.

I’m not an addict.

After many months of giving me a legal way to get my the Oxycodone I take for pain legally, and for free. The label on the bottle says I’m to take the little unassuming pills three times a day. They are 20 mg. Currently, I’ve convinced the assistant fellow at the pain clinic to reduce my Oxycodone to 20 mg twice a day.

I’m not an addict.

I’m mentally ill. I have Bipolar Disorder, ADHD, chronic pain, and other stuff.

I was referred to a pain chronic clinic… ah… chronic pain clinic, where my Oxycodone prescription was reissued. A five-minute verbal probe, that’s what it took for the doctor to determine whether or not I needed the narcotic. We didn’t talk about Bipolar Disorder or any potential interactions the Oxycodone might have with drugs that are meant to manage my wild emotions or tame my fantastic panic attacks. I’m not certain she has any record of my current medications. She asked questions, and I quickly tailored my answers to fit what I thought she was waiting to hear. She made a few notes on a paper as small as her palm. I wondered if she was actually making notes that she could refer to later. She thought for a few seconds and then wrote the prescription. I sighed in relief.

I’m not an addict.

A while later, like over a year or maybe two, I’m still taking the narcotic. The clinic has new owners and staff. They no longer asked me questions. Sometimes they required a urine test. Then, they stopped asking me anything at all. We spent my appointment chatting. I started asking if we could please try to figure out what was causing the pain and try to deal with it by correcting the problem. I wanted the pain to stop.

They didn’t listen. They wrote the prescription without hesitation.

I’m telling you, I’m not an addict.

My mental health drug dispenser began paying attention after I updated her about my drugs and included Oxycodone in the list. She stopped talking about whether or not my meds were working to stabilize my moods and started talking about “Black box” warnings.

She had my attention. I started to panic.

At the time I had over five medical people prescribing medications. They didn’t know what the other office prescribed me. They relied on me to tell them the truth. I didn’t have to tell anyone I was taking Oxycodone. That got me thinking.

I’m not an addict.

Later…

I’m still asking the medical folks to figure out the cause of my chronic lower back pain. I’m still not getting results. I’m getting way too much Oxycodone every bloody month.

Because I can, I’ve been researching my of collages of illnesses, disorders, and psychological malfunctions.

Ah ha! Black box warning. Do NOT take anti-anxiety medication (benzine’s) – death may result.

Oxycodone 20 mg

I recently saw Dr. T, my very superior knee surgeon. He saw the condition of my spine when he was looking at the x-rays of my hips. He was making certain that my persistent knee pain, post second replacement, wasn’t being caused by anything running amock in my hips. He was eliminating any possible cause of my knee pain before he even considering using surgery to further correct the inept effort Dr. B made the initial knee replacement. Dr. B successfully replaced my knee, but that’s where the project ended.

It sucked. My leg from the knee down, well, it kind of turned the wrong way.

Dr. T corrected the first replacement. He tried to minimize the damage his surgery could do while trying not to blow up my entire joint… okay, the joint that was already gone.

Dr. T showed me the x-rays he’d just had taken and explained where and why he left Dr. B’s “efforts,” while replacing the replacement. A month ago we tried a shot to relieve the pain and keep from having to have surgery again.

Nope. I’ve had no relief from the pain. In fact, my brain was overjoyed and thought that my knee was doing awesome. Holy cow! I should NOT have knelt down like that! Looks like surgery is probably what our next conversation will be about. I’ll need to be on pain medication again…. I intend to be off Oxycodine ASAP. I would really like to have some kind of painkiller to take after surgery – assuming I have it. Always be prepared! Sigh…

I’m not an addict.

After my constant complaining about my back pain that happens every time, I do regular human type activities involving the lower back. I’ve finally had x-rays of my back taken. Holy heck. Next stop is at a spine doctor.

The online personal information provided by my medical organization includes this: Opioid Dependence.

My chronic pain clinic instructs me to continue taking the Oxycodone. I haven’t been able to identify any specific relief from the pain in a long time. I have never felt any “fun” results from taking it. It has never made me feel sleepy.

I have found that taking Oxycodone at bedtime with the medication I take for Restless Legs Syndrome (RLS) helps me to get to sleep and not wake up in agony caused by the RLS.

Am I an addict?

“Taking opioids over a long period of time produces dependence, such that when people stop taking the drug, they have physical and psychological symptoms of withdrawal (such as muscle cramping, diarrhea, and anxiety). Dependence is not the same thing as addiction; although everyone who takes opioids for an extended period will become dependent, only a small percentage also experience the compulsive, continuing need for the drug that characterizes addiction.”*

I’m mentally ill. In my opinion taking any medication, especially one that alters my brain chemistry (opioids do this), should be thought about and discussed with other medical personnel who are also responsible for my continued living – and to live my best life.

Am I an addict?

No.

I have Opioid Dependence.

Dependence. I can live with that, but look, let’s get rid of that too. Okay?

{I have Bipolar Disorder. I’m a little manic now. I’m using it to write and post while I can. So, for now, I will post often because tomorrow, I may be depressed and unable to say what’s on my mind. I may not have anything on my mind.}

* https://ghr.nlm.nih.gov/condition/opioid-addiction