Bipolar Disorder |  When Stress Becomes Danger | 4 Hours Left

I’ve been meaning to sit down and talk to you about this but, you know how it is. Stress sidelines the DOING bit after the brain thinks of something to do. In my case (this time), I have an excruciating surgery tomorrow morning, and I’m not looking forward to it. I’m not looking forward to the pain. Being able to use my thumb without debilitating pain aim definitely look directly at it. You see, I had the same surgery done on my other thumb two years ago, and I know how horribly, terribly, and frightening that pain was.

Let me quickly bring you up to date. We’ve since discovered that I have the nasty illness commonly called Fibromyalgia. I refer to it as Fibro because that’s just too long. We think that the constant pressure of the cast sent the pain level of a routine harrowing hand surgery above the charts. And no, pain meds didn’t work.

Ah yes, what’s the surgery? I’m having something put between the bones in my thumb joint. I have Osteoarthritis; this disease eats away at the stuff that keeps your bones from grinding against each other and causing intense pain.

Since it is now 2:45 a.m. I’m going to move on quickly. Leading up to today, life has been chaotic, emotional, and expensive beyond our means to pay for.

Bailey, my Kelpie (She’s a cattle dog. Google Kelpie, they’re pretty great dogs.), has struggled with severe skin issues all spring and summer. Our regular vet is booked out for months. Covid hit, and all the vets disappeared. I’m completely serious. In this area, Puget Sound in Washington State, veterinarians have been scrambling to find staff. While we waited to get in, the problems worsened. This leads us to take her to a doggie dermatologist. This is all so expensive. This is also so stressful and is especially so because of my surgery being tomorrow today at 7:30 a.m. PST.

We have a radioactive cat. Maks has growths on his thyroid and had to have feline hyperthyroid radiation treatment. I think I got that right. Anyway, he’s on the mend and zooming around the house. He’s gaining weight, and I think he’ll do really well. While he’s healing, we have to put all the dirty litter in bags, and those bags have to go in buckets, and those buckets have to sit around for 80 before we can take them to the dump. Apparently, they don’t want radioactive waste in landfills.

All these things combined with life in general, Bipolar Disorder, ADHD, PTSD, RA, OA, and Fibromyalgia, and I’m a sitting duck for a generous helping of losing control. I’ve stopped saying that I’m super stressed out because these life events are painful emotionally and overwhelming financially. Marriages and partners break up because of money. Imagine me and my underemployed family (I’m on disability so I’m broke all the time.) We had to borrow money from my mother and charge the rest. She suggested that we put the animals down if we couldn’t afford to get them help. Seriously?

Anxiety, stress, anger… entering the danger zone. And now it’s 3:03 a.m. I think we should add fear to that little list.

I need to post this now. I’ve run out of time to catch you up. Stay tuned to see how this mentally ill woman deals with family members not too willing to stay with me for a while. I won’t be able to do so many things. This time it’s my very dominant hand. My left one thinks I’m dumb if I think it’s going to do right-hand stuff. Self-righteous little bugger. This is a team effort. That hand better get with the program.

I’m going to attempt to get on Twitter and tweet updates on how things are going since blogging are iffy for the time being. I’ve never used Twitter more than a tweet here and there, so this should be interesting. I hope you’ll follow along! Join in my mad life and all the fun and bonkers ways I manage, primarily, to live my Bipolar and highly complex life.  I need to learn to do voice-to-text. (I’m too tired to edit this, so I hope it makes sense.)

Follow me on Twitter @etiquetteofmad

See you on the other side.

What My Med Provider Means to Me

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I’ve complained about my med providers and their apparent inability to comprehend the word ANXIETY for over a year now. You could assume that I don’t like med providers… that I don’t trust them, that I think they’re stupid. Well, umm, yes, that’s basically how I’ve been feeling. I’ve been living a nightmare that has been driving me downward toward my old companions: anger and rage. It makes me feel like they’re getting out of prison and are moving into the house next to mine. I’ve been really scared that I was about to lose control of my emotions again, and eventually, my mind. It has happened before.

I last week I spoke with my counselor (Lee) before my visit with my med provider (Susan) this week. He thought the Ritalin obviously wasn’t working and that my ADHD was out of control. I allowed myself to interact with him the way I do at home with Jessica. My inability to control things like how fast, how much, and how many topics I covered while speaking certainly indicated that this was true.

<OMG! Alexa is playing music from the 1950’s for me. I LOVE THIS MUSIC!>

I was stunned. ADHD? If he was right, this could change everything about the way I approached my brain. I was told I had ADHD just a few years ago and had never taken the time to learn anything about it. Wow, that wasn’t like me at all. I love research! Following rabbit holes is my favorite pastime!

Anyway, I assumed Susan would look at my chart to see what notes Lee would have put in it before she saw me. Doing that would give her knowledge she should have used to help her understand where I was at and she would have seen what Lee was concerned about. It was an assumption I shouldn’t have made. Apparently, things don’t actually work that way.

Every time I see Susan 12 times a year. Yikes! So many times. One of the first things she asks me is if I feel like… if I FEEL like the Ritalin {1} is helping me focus? Focus? What does that mean? How can I tell it’s working? I can pay attention in class. Is that what she means? My attention is crap at home. I can’t ever do just one thing at a time. I have to leave the commercials in when I watch from the DVR (DISH) so that I can read or research stuff online that they just talked about. Is it working? I suppose so? I always replied that I guessed it did. I guess that was silly of me. I would say that because I had no idea what else to say. If I was a little boy, I could probably mean that I’d slow down and stop bouncing off the walls and maybe stay in my seat. But as an adult… I had no idea what that looked like. If I said the wrong thing, she might mess with my meds and right then, they were treating me okay. I wasn’t raging at anyone that day and I didn’t feel depressed.

After I mentioned what Lee and I had talked about and that he was very concerned she took a minute to read his notes. Suddenly she made a whole new treatment plan. I had been on Lithium when I was first diagnosed with Bipolar Disorder (BD). The first book I read on it was: “An Unquiet Mind: A Memoir of Moods and Madness” by Kay Redfield Jamison. I was deeply touched. I felt like I understood what she was talking about, like we were kindred spirits, linked through the ether by BD. Jamison was very sick when she was diagnosed.

Let me attempt to generally get right to the point for once. Jamison was placed on Lithium to treat her BD and it worked. So, that’s what I asked to be given. My personal doctor (MD), was the one who initially treated me. He said that Lithium has been around for many years and there is a lot of evidence that it works.

The Lithium worked.

Susan felt that since the Ritalin was obviously not helping me focus. I guess that made her rethink her strategy. She finally agreed that my brain was hopping along on two of four legs. She told me that does think I have ADHD she now believes that I’m far more manic, which was making me act like that bouncy ball they teach kids to sing songs with. Do you know what I mean? It might be too old for some of you. They wanted to teach kids songs so a character on a film or on TV would get you to sing along as it had a bouncing ball hop around on the lyrics so we could see the lyrics while we sang. It was great fun! than anything else. Sure I talk incessantly to Jessica, but my brain was exploding with ideas. It was time to help me continue to be creative, but to control my mania so that I could be productive.

The plan: no more Clonazepam, no more Ritalin. Start Lithium.
*The reason I went off Lithium was that my PC (Primary Care) had been highlighting the dangers of being on Lithium more than he was the benefits of it. It was because of these side effects, that I requested I be put on something else that didn’t have the same drawbacks. Lithium toxicity can occur even at a low dose. While on Lithium, the user has to be closely monitored so that the dose can be adjusted as needed. The symptoms of Lithium toxicity are numerous and I already have several of them for other random reasons. This website lists the long lists of side effects. In addition to these potential problems the user (remember this is me) has to carefully watch their intake of salt, caffeine, and alcohol. And get this… some of the other medications that may interfere with Lithium and increase the risk of toxicity are ibuprofen (Motrin, Advil) and naproxen (Aleve). Oh, and I can’t leave out this one: acetaminophen (Tylenol). So… yeah. I had a lot of scary reasons to ask to be taken off the drug that was helping me but was also kind of terrifying too. 

Susan believes that this change in medications should make my extreme moods in control much better.

Excuse me? As long as I’ve been seeing the professionals in this clinic, I’ve never had anyone decide to try Lithium again. All this time… lost. Years of feeling my little grey cells melting, running out of my ears. But then again, Lithium toxicity…

I want to be a writer when I grow up. I once heard that writers go through life with their head cocked a bit to the side. I showed Susan a piece of paper that was covered with writing on both sides. It was filled with websites, blogs, and email addresses that I’d created. She studied it for a while. I asked her if I was stupid and delusional to think that I could do all these things and believe that they were not just good ideas, they were great ideas. They were creative ideas. Is my mind actually existing in a consistent state of delusions of grandeur?

Delusions of grandeur. I’ve always been afraid that people would remember that part of the list of symptoms for BD and dismiss me as a kook. Am I brilliant? Or am I bonkers and deluded? I’ve always believed my ideas were great. Yeah. Delusions of grandeur?

She said no. It wasn’t that. Yes, my thoughts are crazy fast, but I am very creative and smart.

Me – creative and smart. OMG!

Of course, now I respect her. She believes in me. She agrees with me that I’m smart and creative. No one has really said that to me. No one has said, “Robin, you’re not delusional. You’re smart. You’re creative. You have good ideas… cleaver… innovative. Don’t worry about being crazy. We just need to slow you down so you can get things done.

Since then, I’ve discovered additional information that indicates that one aspect of BD is the tendency to be super goal oriented. Yep, that’s me. Why haven’t I’ve seen that before?

Watch out! Corner coming!

What are the good things about having BD? I’ll have to think on that for a while.

Go ahead, get mad when the medical professionals don’t seem to be listening. Pester them until they hear you. Then, you listen to them. Work together. Hope that things will finally start to workout. Now that Susan and I are communicating, now that she hears me, we have a new plan. Maybe my mind won’t keep leaving the scene without me.

Yes, it really has done that. We’ve called professional trackers to find it a few times now. It-is-very-embarrassing when your mind is so exposed, so naked.

New plan. New hope.

Bring it! I’m ready.

I’m more than ready –

{1 – Concerta and Ritalin are stimulant medications used to treat attention deficit hyperactivity disorder (ADHD). They’re both different brand-name versions of the same drug, called methylphenidate hydrochloride.  https://www.healthline.com/health/adhd/concerta-ritalin}

Bipolar – I Think You Should Take Fewer Pills

I’m going to notify my counselor that I must be rid of my med provider as soon as it can be arranged. I’ve told Arthur, my counselor, that I don’t feel that Jamie (med provider) is working in my best interest. My next appointment with her she started right off by confronting me about what I’d told Arthur. I confessed thit it was true.

It got me no where.

She says that I’m on too many pills and she doesn’t want to add anymore. Apparently, this is her rational for not giving me medication that might actually have helped me.

I’ve been practically begging for something for my anxiety that only get’ s increasingly more consuming with each passing day

This whole school year has been like a nightmare.

She doesn’t want to give me more pills? Bull!! It is not her choice to decide whether what other doctors prescribe me for illnesses she knows even less about than I do.

She has repeatedly used this as an excuse not to give me something that could prevented me from my brake down. I have high cholesterol, my thyroid is out of whack, I have chronic horrible lower back pain, I have FM, RA, OA, a facial tick (probably stress related), PTSD, and have recently been diagnosed with IBS-d. It’s a crap load of stuff, but they have all been dealt with by someone more intelligent than she is.

I’ve asked each and every visit for something to help with the burning anxiety. She refuses. She gives me fewer chill pills.

Does she think I like taking a handful of pills twice a day? Moron.

I’ve finally had a breakdown. I blame her. In December I confessed I’d been having thoughts of harming myself. I’d hidden that for years, but at that point it was too much, and I confessed it.

She did nothing.

If I can’t trust my med provider to guard my mental wellbeing, than who will? There aren’t many options here.

I’ve started to shake, Twitter, and twitch again. I’m graduating today. My anxiety that mixes like a charm with my mania and depression making my constant mixed state even more confusing and painful. It’s too much to handle anymore.

I’m firing her. She truly doesn’t have my best interests in mind. I don’t need one of my medical professionals contributing to my madness. That’s just sick.

Bipolar: It Is Very Difficult to Know

A lot of the time I hesitate to post because I don’t know what you, my reader, expects to read. I struggle with this every day. I could tell you about my day, but that’s so boring – dull! I could stick to only write about myself and what I’ve learned about Bipolar, but I really feel strongly that this kind of important thing deserves a website of its own so that people in pain or who are looking for answers can go to that site and find answers and acceptance right away. So, I’m developing a website to do just that.

I have Bipolar Disorder Type 1 with mixed states. I also entertain much of the rest of the alphabet. I could drone on and on and try to… well, I think you know where that was going.

Basically I’m a normal 55 year single mom of three who is interesting and has a good sense of humor. I have some compelling stuff following me around that makes me complicated, but who doesn’t? Surely everyone has experienced the strange things accompanying Bipolar, anxiety, depression, ADHD, PTSD, FM, OA, etc.

I have a Japanese Fighting fish like all your neighbors do and speaking of neighbors, also just like you, I politely file noise complaints regarding one nice household whenever my TV starts to loudly rattle. Seriously.

I’m so normal I could bore you silly. Although… did I mention my eldest daughter will be moving in with me in a few months? (Honestly, it’s for the best. I need the support and we can both use help with housing expenses.)

In fact things are sooo boring that I’m going to need to graduate from college with another bachelors degree and I’m going to have two sons and a daughter instead of what has been the standard at my house with two daughters and a son.

See? Boring.

I am first and foremost a woman who deals with an incurable illness and will continue to do so until I die. Well, and perhaps afterward too. I mean, who really knows?

If you don’t mind too much, I’m going to write about all of these things. I might even add in the bits where one of my family members believes that God has them on this earth for only one reason and that is to save his children and to draw them back to Him because they are lost.

Maybe I’ll recount some of my experiences growing upon a ranch as a teen who presented with Bipolar at a very young age and how well that went over with my undiagnosed Bipolar father. Maybe I’ll include fun times at the church I was attending that was into casting out demons. Yeah. Fun times.

Have I mentioned I went to Bible College searching for God? I wanted so desperately for Him to take away the pain I felt that was crushing me from within every day. No? Bipolar, prayer, and demonic possession… seems like there’s a story in there, somewhere.

What’s on your mind? Should I throw caution to the wind and open up a bit more? It all, and I do mean all, ties directly back into this sickness, this life long illness I struggle with. It is all infused with, you know it, Bipolar.

I don’t believe it is a disorder. I believe it’s a disease, an illness and should be treated with the respect it deserves… that we deserve.

Talk to me my Readers. Tell me what you think. Do you have questions? I can’t guarantee I’ll answer, but I’ll read all of them. 🤔

Be well.

Robin

Bipolar – TV

tvI want to believe that although I have Bipolar Disorder, depression, GAD, PTSD, ADHD and so on I can still be successful.

I want to live an active and full life. Much of the time I convince myself that I can’t do that. I look at my situation and I conclude that if I haven’t started living by this time in my life, that maybe I won’t ever have the life that I want. It’s tempting to fail myself and believe that.

One of the reasons that I sit static in my living room and don’t try to actively change my life is that I watch TV all the time. It is on all the time. I used to listen to music. Now it’s just the TV. As long as I have that continuous stream entering my brain I don’t use it for anything else. It’s so easy to be a spectator.

During school I finally admitted to myself that I was having a hard time doing my homework because it was on all the time. As much as I’d like to think that I can focus effectively on other things while the it is on, it isn’t true.

It’s hard to turn off the TV. It’s my companion. Right now, remarkably, it’s off. I’m listening to classical music on my phone. I’m trying very hard not to watch one of the many shows I have DVR’d. I’m practicing having it off so when school starts next week I’ll be more likely to switch it off while I’m doing homework. I’m sure that I’ll have an easier time doing the work if the TV isn’t invading my brain.

It also keeps me from dealing with myself. I can ignore the fact that I’m not dealing with my ongoing anxiety because I’m occupied with the TV.

I need to have quiet time so I can think. I don’t think well while the TV is on. Heck, I don’t think much at all when it’s on.

I’m finding that I’m having a hard time with this post. It feels disjointed and awkward. Maybe that’s because my companion is silent and I can really hear what I’m thinking. Maybe. I’ve been thinking about having the TV off for some time now. I’m impressed with myself that it is off. There is so much more interesting and important stuff for me to feed my brain with than TV. I’m not saying TV is bad. I’m just saying that when it is the only thing going on in my head it’s a problem.

A man (I can’t recall who) wrote that he used to go into a room every day with a pen and paper and shut himself inside and just think. He didn’t see people; he didn’t read anything. He just thought. I remember when I first read that I thought it was an amazing idea. I practiced it for a while, then, I went back to filling my brain with static.

I don’t make New Year’s resolutions. I know I wouldn’t be able to keep them so I don’t make them. However, right now seems like a good time to change my behavior. I’ve pinpointed a problem: I don’t think. I listen to the TV.

Napoleon Hill (1883-1970) wrote: “What the mind can conceive and believe, it can achieve.” I’ve always liked that quote. Thinking… that’s a problem. My medications help a lot. Counseling has helped too. My counselor has helped me identify problem thinking and correct it. (Napoleon Hill quotes)

What’s next? Well, my brain is full of what I put into it or what I allow to be put into it. I allow someone else to put their content in it the whole time the TV is on, which is most of the time I’m awake.

The solution seems easy doesn’t it? Turn the TV off. Easy.

Right now… the TV isn’t off.

I’ve learned a lot. Time to change. I should turn it off. I should–