Waking Up Depressed

The sun was up and shining on the wrong side of the house as usual. The sun only ever warmed the living room and kitchen side from sun up to sun down. I swung my legs off the bed began the inevitable. I got dressed and put on my shoes and socks. Bailey studied me lazily. I knew she wouldn’t get out of bed unless she knew I was going to take her outside to do her business.

I sighed, irritated that I’d woken up late. My inner perfectionist was already at work, and I was worse for it. I should have already taken Bailey out and fed her and everyone else. I mentally smacked myself for my indiscretions.

After doing the morning chores, I sat down, and I thought I was attempting to complete an online class that I hoped would move me towards earning an income.

An income. I haven’t had one of those since before I was married, not since 1988. 1988. That’s so long ago.

I feel like a failure again. Always a failure. I took a breath, trying to calm myself, and felt depression flow into my chest. It’s a crappy way to start the day.

Struggling, I remembered I’d fed all the animals, now it was time to take care of myself. I got my pill container and flipped open the lid for today. Dumping them in my hands my heart sunk lower. It looks like I’m an addict. My hands shook as I took my meds. At least today, I remembered them.

I eventually went outside to do some trimming in the garden. It wasn’t raining yet, and the sun was out. My beautiful Bailey was out with me. Oh my god we’re both so fat! I’ve been trying to help us both lose weight, but…well, we’re still working on it. Great. I feel like crap again.

My daughter came home a few hours later. My glum mood had moved on, and I encouraged (read: told) her to come out and work with me. I felt good and my head, my emotions, felt clear, maybe even happy.

The question I have to ask myself is this: What the hell did I do to change from feeling crazy-eyes depressed to happy and joyful? That’s exactly the right question. And can I do it again?

I believe that my poopoo mood changed and lifted me higher because I “acted” like I was happy. I played with the animals. I did some of the work for my online class. I took Bailey for a walk. (When I take her out I use an app that maps our trip and counts the miles and such. If I think we’ve done well, I take a screenshot and send it to my kids and my Mom.

Then I sat my hiney down and did my class. That really felt good.

Now that I’m recalling how bad I felt this morning, I’m beginning to feel like I’m grieving. I think I’m grieving for myself, for all the time I’ve lost standing in the clouds, not functioning like a normal person at all. Maybe I wasted my life. I’m supposed to have all these mental illnesses, but why can’t they cure them or at the very least enable me to act normal.

Normal. That’s a fat laugh.

Uhg! I’m tired. Figuring all this out and, exercising and learning to understand myself… yikes. Maybe I’ll go barf now. What’s tomorrow going to be like? Huh, maybe it will be the way I choose to make it. Chose to make it a good day and it will be a good day? On the other hand… maybe I’ll need to stay in bed. Need. What will I need?

Tomorrow, I think I’ll take more of an active role in my day and use the S.M.A.R.T.

5-Minutes

5minutes Are you listening? Can you hear me?

I need you to hear me.

I need you to know what I mean when I say, “I just can’t!”

You really need to understand this illness before we talk about, “I just can’t” It will make so much more sense then.

I’ve written about my troubles for years in my paper journals. I’ve always imagined that when I die, one of my family, my kids perhaps, would read them and finally understand me. They would finally understand that I’m not a bad person, a lazy person, or a freeloader.

I’m sick. I’ve always been a sick person.

With technology what it is today, it’s easy to find an informative book that explains what it is to have what I have. I’ve searched YouTube for videos that explain me and have found a few that try to do it and seem to do it well. We’re all different of course so what describes one person may not completely fit me. But if the person watching will just listen, listen and hear the pain and the wrongness of it all.

Wrongness. That’s what it is.

You’d think, maybe this is the child whose rage never seemed to end, a brat that pushed and pushed…. Wouldn’t you like an explanation?

I’d think someone who claims to love me would take a few minutes to watch a 5-minute video, just a five-minute video, to learn about me. Surely, someone, anyone of you must care enough to sit for five-minutes for me? Did you hang out in line for coffee or in line at the grocery store? Is that silly? Have you “liked” any funny pictures or memes today? Did you watch ANY TV? What were you doing on commercials? Why is this so hard for you?

Did you watch the news today or read your Facebook feed? Have you texted anyone or talked on the phone?

Would you think I didn’t love you if I didn’t return your calls or texts for two or three weeks? Would you call and check on me?

How much energy does it take to watch a video?

What are you afraid of?

I’d have thought I’ve shown you enough of what this illness is that you have nothing left to fear.

And yet, you don’t hesitate. You completely stop.

“I don’t have time.”

Will you have time to visit me in the hospital?

I’m not going to try to kill myself just to get your attention. But I can’t promise to do what’s best for me all the time.

Maybe I’ll have to mourn the death of you so that I can learn to live without you. Because you see, I already live like this. You are emotionally unavailable to me. Without “my people” surrounding me in a protective layer of love to cushion me when I fall….

Adults are just like children. We all have a fair expectation of being loved. When that expectation is not met we wither and begin to slip away.

Do you have five-minutes?

I need you to listen to me today.

Just follow the link.

Then maybe we could talk.

I’ve had a thought. I’ve unwillingly learned more about inappropriate relations whether they be physical, racial, or political just watching prime time TV than you’ve learned about me on purpose.

It isn’t rocket science. But it is science. I am sick. Unlike some illnesses like some cancers where the patient may go into remission or finally be overcome by it, my sickness has not given me a moment’s rest.

Sometimes I wish I had an illness you could see so that you would mourn me when I die. But for today, I live as though I’m normal. That’s how you see me. Normal. That’s how I look. This illness is rude beyond anything I’ve ever seen. It grabs hold and never lets you go. It bombards me from within, from where you cannot see. This illness, it stays in the “ON” position from before I was diagnosed until I die.

That’s right. I have it now. You cannot see it. I will die with it.

Would you watch the video?

Or would you rather I had cancer? Then you’d have something you could see.

I’m tired of being unseen for who I am.

Please, are you listening? Can you hear me?

I’m wondering if you’ve ever felt anything like this. This is all true in my life. What about you? If you have known that, I hear you. I will listen to you. I have way more than 5-minutes to give you.

* I had my counselor read this yesterday so that he could see what’s in my brain. I told him I was going to edit it, polish it up before I posted it so it would be clearer in some places. He suggested that I not do that. He felt that letting you see where my brain was at was a place of raw emotion. He urged me to keep the “rawness” in it. So, here it is. Right from my brain and served up to you on a virtual platter.

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}

Frankenstein – Bipolar & ADHD

Frankenstein-tumblr_ovgh5egVdd1wzx3t8o1_1280 I’m aware, that when given the chance, I will, without question, talk until the air has been sucked out of the general area and everyone has passed out. So normal.

Anxiety – After I graduated, and a few weeks had passed I could tell I was under stress from that. My anxiety has gone down. It did get better, for a while. I got to the point where I didn’t quite feel like my brain has been stuffed full of raging bees. Awesome!

ADHD – I was under the assumption that I was taking Ritalin to help me focus my attention so I could do well in my classes. I was always confused when my med provider asked me if I felt the Ritalin she was prescribing was helping me to focus better. I always said, and continue to say, “Um… I guess so.” I’m manic! What does she want me to say? I work very hard when I meet with her to sit, shut up, and answer her questions honestly. She terrifies me. What if I answer wrong and she changes my meds again? I’ll say something than think, “Crap! Why did I say that?” I always say that I guess it was working well. I suppose. Now I think that I was wrong.

More ADHD – I accepted the diagnosis of having ADHD because it was about not being able to focus on one thing at a time and I knew I couldn’t do that. But, being Bipolar was always the main objective of both my counseling sessions and appointment with the med woman.

Bipolar 1 – I assumed that my Bipolar was worse (or more dangerous to me) than ADHD could be. Wasn’t it?

You know how a doctor will sometimes leave a small tube that goes through an incision so that the area can drain and heal properly?

Yeah, I don’t know where I was going with that—

Switch – I have some ideas that I think are pretty good. I’ve done one or two or three big projects that have come out great. The other 45 ideas that are going around in my mind appeared to be stuck in orbit. I remember the video I watched on YouTube yesterday about ADHD and I was shocked. Frankenstein!

FRANKENSTEIN – I’ve come to think of Bipolar/ADHD as a Frankenstein type of symbiotic relationship. I can’t imagine why my diagnoses has always focused upon Bipolar Disorder. In counseling I talk faster and faster and cover an impressive variety of topics.

Pressured Speech (Bipolar) – Thought very little about ADHD or how to deal successfully with it. I’ve been taking medication for it for three years. In that time no one has talked to me taught me to handle it. Why not?

FRANKENSTEIN – Why hasn’t anyone explained how the two disorders interact, and how the medications for each may also affect each other. (“Do you think that the Ritalin is making your mania worse?”)

I have been primarily a mixed state, high functioning, Bipolar type 1 for years now. I always thought that my constant mental zooming about was just my amazingly stunning mania. (While I mostly talk about my being manic lately, let me just say that depression has played a big part in my mental health too.)

My daughter went with me to my last counseling appointment. We talked about my inability to stick with one thing and see it through to completion and how it was impacting her. Basically, I’m driving her bonkers. These are some of the things that I do: TALK CONSTANTLY NO MATTER WHAT WE ARE DOING, change topics as fast as I talk, pick up a pile of laundry in the living room to put it away, stopping to talk to our beta fish (Victor and Batman) and feed them a few dried wormy things and set down the laundry, forget that I had a mission with the laundry, see that the dog/cats water bowls are empty and fill them, read 1.75 pages in a book. What was I doing? Let the dog out to do her business. Hours later I discover the laundry next to the fish… you get the idea.

My new counselor, my daughter and I decided that I need to focus on being able to focus. Yes, my Bipolar mania hops it up like jet fuel in a race car, but with knowledge and tools to help me with my ADHD and settle on one thing, even for an hour, I might just begin to get a handle on my anxiety/stress and even mania.

Maybe. This is stressing me out. Bothering my daughter this bad is building an anxiety that is part of everyday life. Sigh…

Who knew that pressured speech and mania aren’t the same thing as ADHD? I really don’t understand what the hell is going on. I feel like my brain has been sewn together with blue and green colored twine and slip knots.

One final thing: It has taken me three days and four hours to type this. Just kidding. Two days. Honestly, I have no idea. I need a time-out.

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 – Stoned Siblings

I just got off the phone with my youngest child and I’m heartbroken.

He says he tells people all the time what a badass I am. He’s a psych major and he now understands a tiny bit of what it must have taken for me to raise three kids with my illness. He tells people how I raised them sick and even had a knee replacement, twice. It’s a good story to tell people to get them to buck-up. He tells them to get over themselves. Look what my mom did.

He was telling how great it has been lately for him when he spends time with his brother. They’ve been bonding, getting stoned, hanging out. (We’re in WA and it’s legal here.)

I was crushed.

I’m a mom. A parent. I’m weird… but I’m a parent. I’ve always pushed myself to be the best parent I could be. Suddenly, again, I feel like I failed. It doesn’t make any sense I suppose. It doesn’t really have to because I know how I feel and I FEEL like I failed them.

I know I’m being emotional. I am emotion. Always emotion.

I feel like I failed my babies. Why? Things have been going pretty well. They’ve been bonding when they’re high. Okay. Okay. I feel, like I failed them because they have to be high to bond. To relax around each other they’ve got to be stoned. So what. So what?

I was just having a great conversation with him on the phone. The longer we talked the more I realized that he was being the most relaxed talking with me that he’s been in a long time. Awesome! Right? Right.

I’m a good parent. I know I am. But –

Why do my kids have to be stoned to be loving?

It isn’t a big deal. It’s legal.

But why do they have to be stoned? Why stoned? Why?

I’m going to bed. I’m too tired to handle this. I can’t do effective damage control in my brain trying not to blame myself when I’m tired. I am blaming myself. I don’t feel like I did a good job raising them if they have to be stoned to be good people to each other, to me.

Again, I feel like I failed.

Should I get stoned too?

No…. not more drugs. Not stoned. Not me. I just can’t do that.

Bipolar – You’re Freaking Insane!

Today, I’m not insane. I trust that since you’re reading this that you aren’t either.

There are people though – I just- I just have to reconsider what insanity is. I FEEL it in my ever so raw emotions, the there are way more nuts 🥜 around us than we realize.

I think, that when someone loses touch with reality they’re psychotic. Good nuff? That’s not being insane.

My phone ☎️ just told me that insanity is the state of being seriously mentally ill. And Madness, is the state of being mentally ill, especially severely.

What was that?

Let’s break it down to today, and to one moment during this day. This might be a reach, but bear with me.

I believe, with my blessed bipolar and somewhat of an authority on mental illness brain, that there are a more ways one can be “insane” than by those ways we’ve been taught and told.

Example. Full disclosure-this Professor 🤓 in no way has my respect and I would love it if he hadn’t just made tenure.

Now, the example. I’ve never approved of his teaching methods. He lets the class of people who can’t write, critique each other’s stories. He sits there and says stuff that … blah blah blah. Okay. He read everyone’s first short story this term. Then he selected a book of short stories based on what he saw when he read those stories. So each student was assigned a collection to read, then do a presentation on, of the book he specially selected for us. He waited, until well after he read them to assign them. We were led to believe that our particular book was just for us and it would actually fill a void in our training,

Right. Nothing crazy, right?

I bought my book and have been trying to read it. . . . I don’t have any clue what is going on and frankly, I don’t care to know. It’s bonkers. I wrote him an email asking for guidance.

No reply. So today after we workshopped and he sat there reading email for the entire class, I asked him about my book. Does he know anything helpful about the book? Never heard of it. (Excuse me?) Do you know anything about the author? Nope. (Beg pardon?)

I have just spent three long, very difficult, mentally, and emotionally and stressfully and often painful years PAYING for this tenured Professor 👩‍🏫 to assign me something for my final senior project, something my dog could have done a better job picking.

Insanity? Robin, where’s the insanity? That’s just the way things are.

Yep. That’s right. I owe thousands upon thousands of dollars, to be unprepared to be employed.

That’s the way things just are. Forget about it. There isn’t anything you can do. You can’t change anything.

And that’s…… what’s insane.

Anyone expecting me to accept the illogical as what is normal I will tell tell them to their foolish face that they are insane – not me. Not you.

I believe, that expecting others to accept lies and the illogical as as truth are insane… damn bonkers.

I’m a lot of things and sometimes I’m not always kind or think before I speak, but I never tell people that things will never change, that they will never change, or that they will never change things.

This is possibly unfair of me, but I’m mad so I ask you to judge me kindly, I am calling this professor out. I believe he has behaved in an irrational and insane manner. I do not believes he has earned the job based on the three years I’ve had classes with him.

We can’t accept it when people tell us things like student loans are going to get us a job. We can’t accept it when professional teachers take our money then don’t train us.

Ok, so I’m mad. I’m even admittedly pissy. But I believe things can Change. I believe professors can really train us, teach us to be great at something.

I’m not insane today. Nor was I yesterday. Next week? Dunno. But by all the stars in the heavens above don’t ever, don’t never, tell me things can’t change. Or that I can’t change.

That’s insane. Just plain insane.

How do you feel about it? Is sanity something more than how our brain is behaving in a moment? Is it possibly claiming not to have a mental illness and yet purposely living one’s whole life in an illusion?

In any case, things can change, they always do. And we can change, and we always will.

Be well my friends

Robin

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 – Med Provider Day

I’m unstoppable.

I’ve been trying to sleep, but it eludes me like a chicken running for its life.

I’m going to see my med provider at 10 in the morning today. I hope she listens this time. If she doesn’t I’ll be requesting someone else and informing them of why I’m choosing to under go all the stress that comes with a decision like that. I’ve had enough.

I’m going to confront her with the facts. I’ve been keeping a list of my symptoms since I saw her 30 days ago. It has grown quite long. It looks even worse than before I was being medicated.

I’m unstoppable.

My pain management guy and I had to ween me off one of the long acting pain killers I’ve been taking for a couple of years because of supply issues. I went from 100 mg twice a day to 50 mg over night because there wasn’t anymore to be found anywhere. No one knew it was going to happen so there was no helping it. It didn’t feel so great. Then we kind of gradually weened me off the rest. Now my pain level is constantly higher. Also, the torn fascia in my foot still isn’t healed. It’s painful. I got special shoes for it today. But as the compassionate woman said while I walked around and around testing shoes, my foot was going to feel soar and tired. It still is. It wasn’t fun.

All this has added to my overall stress level, as you can imagine. Withdrawal is never a good time, nor is added pain.

I’m unstoppable.

I will be thankful if my counselor, Arthur, can make it to my appointment. He said he’d try. He feels it is important for her to understand my mental state from his side of the equation. He’s been with me two previous visits.

It hasn’t helped.

I’m still choosing to be unstoppable.

I may stumble, and I may fall over and over, but this damn illness is not going to continue to run my life. I’m very ill. I’m too exhausted not to fight anymore. I feel like my life has been a waste.

I’ve had enough.

I’m unstoppable.

Help me. Or, stay out of my way.

I refuse to stop!

I’m Bipolar 1-How Much Further Must I Go?

I’m dang angry. I’ve worked my agitated ass off for three years, stumbling under the nightmares of depression and raging as anxiety unleashed tries to undo all that I’ve endured. So close. One more quarter and I’ll graduate from UWT. One more quarter and I’ll have to get a job and support myself.

Listen to me dear Reader, if you have a medical professional who won’t listen to you or thinks your complaint is in your head (duh) or is in some way not treating you with the dignity and respect that your insurance dollars demand of them… stand up and say something! You do not always need to be nice. Trust me on this one.

I learned long ago to hide much of my mental crappiness that was going on in my skull. I was super high functioning. I had kids to raise. I can play the “I’m fine, I’m a great” parent game.

But you know what? Turns out that didn’t help the “me” of today. The “me” of today STILL needs something for anxiety. Go ahead moron. Yes, you Jamie, you have ignored my pleas for something to do for me what all the hundreds of hours of counseling have been unable to do… relieve my over the top anxiety.

I’ve asked this woman for something for anxiety since the first time I saw her. You know what she did? She started lowering my Clonazapam (spelling). Every time I’ve seen her, she reduces it. “It is just one less pill. You’ll be okay.” [bitch]

I went home with 10 pills for 30 days.

She increased my Ritalin dosage and made it extended length. I didn’t ask for that. What? You want me to calm down so we can finish our 20 minutes on time? Have you dosed me so that I’ll be a good woman and let you get done with me?

Well guess what? The shits hitting this fan.

Can any of you relate? Have you felt unheard and improperly treated? Guess what? You are NOT ALONE. Not by a screaming momma long shot.

I have IBSd. I had to talk to my counselor from home. Since I was in my own I felt FREE to explain again about my anxiety and graduation and jobs and money and acting out in class because I simply cannot contain the mountain of anxiety spilling … over into my phone call.

For an hour I yelled about Jamie to my poor counselor. I accused her of having her own agenda and it didn’t include my mental health. I’m done. She either treats my anxiety when I see her next week or –

Or I will hand deliver a letter I’ve been writing about our times together to the facility director. I’m done.

I’ve worked my hardest, trying to keep hold of myself while my wild mood swings tried to prevent me from my goal – getting a college degree at 55.

This, this Jamie, she can’t seem to hear, see, understand, empathize or give a rats ass whether I self-destruct because my anxiety has paralyzed me again. I sit on the sofa and I cry because I’m terrified I’ll fail. So I don’t start. Then the panick sets in as I realize I can’t write the paper.

In the name of the oath that we have been lead to believe that those in the medical profession must swear to, treat me for my illness.

I cannot imagine going through the graduation ceremony in the Tacoma Dome with my freaking anxiety not treated.

I cannot imagine the day after graduation when I need to be looking for a job, but because Jamie didn’t treat my well documented illness I am instead sitting in the back yard vegetable garden pretending to being weeding. The problem with this scenario is that I have arthritis, and if I have sat in the garden without anyone home to help me up… I’m not going to getup. It would mean that I’d given up. It would mean that I’d be punishing myself for continuing to be the Bipolar failure that I’ve always been. (How I feel.)

And Jamie? Still with me? You could have prevented me from losing all the ground I’d worked so damn hard all these years to reach. And why? For what? From here it just seems you’re stupid. Some medical “professionals” are stupid you know. I’ve even taken my counselor with me on two occasions to verify what I tell her.

I’m done.

I’m saying Hell No! That’s enough of this irresponsible crap. You expect those of us with mental health issues to behave? Then treat us right. Hear us when we call for help. If we bring backup pay special attention. I’m trying to get my son to go with me. He’s a psychology major.

To all of you struggling to work with your own Jamie’s, you stand fast. Do not let them push you around. They’re there to serve your medical needs. Document what you talk about and when. Keep a clear record so if you need a new med provider you can state your case and prove that they aren’t listening.

One reminder though. If you’re really messed up you may not be thinking straight. No worries. You just take a family member or someone who you can trust with you.

You’re not alone.

Oh, and if you happen to be a Jamie, what’s your damn excuse?