Category Archives: depressed

Bipolar – Verbal Dump

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I have Bipolar Disorder and ADHD. I was diagnosed with Bipolar Disorder over twenty years ago. At least, that’s about when my brain says it remembers it happening – I’m super reliable when it comes to the passing of time. Umm, no way! Don’t let me tell you otherwise. I was diagnosed as having ADHD only a few years ago.

The other day my mom told me she’d had a major breakthrough in her thinking about ADHD. Apparently, she’d talked to her realtor and she had told him that I have it. I know she shares stuff about my brain (problems) to people in the town/city we live in and with Rhett (the fellow I just mentioned who sells property) who lives in another one.

That’s two.

Back to the breakdown.

I know my mom loves me. She expresses it in a sort of micro-managing way, but she loves me nonetheless.

I’d hate to have had a child like me. How did she not accidentally roll over me in the family car? I would have had a daycare person come take me away. A nanny. Anyway, Rhett told her that he has ADHD too. {Deep sigh coming from my side of the conversation.}

You know how we can look up literally ANYTHING online? I really don’t think she understands that she can Google Bipolar Disorder and ADHD and not have to rely upon the information she can glean from a single person. There are many fantastic sites to visit that contains a lot of very good information on both BD and ADHD.

But, you know what, the idea that she can talk to someone about me, without asking me first, and telling him my very personal business is just bad.

My mom thinks of Rhett as another son. (I have a brother.) She knows more about him than she does about me. Sometimes I discover I have feelings of resentment and anger toward the nice guy. I don’t like feeling that way.

I guess accepting and understanding something about Bipolar Disorder have to continue to wait.

I believe, that if she understood a little about Bipolar Disorder and how I present, we would get along better. We might even want to spend more time together. Maybe she’d trust me more. Forgive me more. I admit, there is much I want to be forgiven for. I think she’s better at letting things go than I am so maybe she doesn’t need to be able to forgive me once she understands I don’t really control myself sometimes.

My experience with Bipolar Disorder is that about 80% of the time I’m manic. All the time I’ve been alive, I’ve been either straight up manic, or in a mixed state featuring the bits that tend to “intensify” my emotions. I’m confused, being depressed while manic.

My most blatantly obvious symptom… I never, ever stop talking. When the rare moment does happen, my friends ask me if I’m okay. I think that even Bailey notices. (Bailey is my support dog. She’s wonderful.)

Bailey is my emergency brake. When I’m frustrated, angry or yelling, she finds me and sits directly facing me, very close, toes to paws, and with her beautiful sad brown eyes and waits for the noise to stop. Honestly, she won’t budge even if I tell her I need to pee. No mercy from my faithful pup.

My chart at the mental health place I go to says that I say I think I’m smarter than they are. My current counselor asked me if I really believe that. Without a pause, I said, “YES.” I reminded him of how they let my stress / anger / mania / and anxiety cause all the suffering I experienced while I was going to school. over the last year, my symptoms intensified, and I broke.

Have you heard the axiom do no harm or through inaction to cause harm?

So, the reality is that they watched and did not intervene. They listened and didn’t reach out to catch me while I fell and fell farther and farther down. If you think about it like that, like what role they played in my unwilling self-destruction, then YES, I think they’re morons and I really am so much smarter than they are. My counselor asked me if I thought I was smarter than he was. I grinned and told him, “that remains to be seen.”

Delusional? Grandiose thoughts? Delusions of grandeur? Or brilliant or very smart? And who’s to judge which is which?

ADHD, Bipolar… Let’s figure it out. I promise I’ll own it.

You have just been exposed to an often irritating and yet integral bit of my brain in all its glory. It’s what I call, “a verbal dump.” My kids prefer saying I barf words. Wait, maybe it was that I vomit words. Well, in any case, it’s not great.

Please write to me or leave a comment. I love hearing from you.

Be well,

Robin / Un-niche-able Me

Bipolar – The Diagnosis

This week a situation came up in which I was able to ask each member of my family if any of them have ever tried to learn anything about Bipolar Disorder. Every one of them said, no. I have always been the source of the storms in my family group: parents, brother, and kids. I was always angry or striking out at them (verbally) while in a devastating tsunami of rage. I was unstoppable, and I was very ill. I was a bad child. I constantly fought with my father who had anger demons of his own.

I don’t actually know if learning about BD will enable them to understand me, and even to help me when I’m helpless.

There’s just one problem – Not a single soul on this blue world completely understands Bipolar Disorder. Not one. Even those doctors who are afflicted with the illness do not know precisely how it works or what it is. And the meds I take, almost all of the fine print says it is used for things like seizures and a variety of other things, but not for BD.

Meds for BD are prescribed because the medical community has discovered that in general, some medications seem to help control the symptoms.

Symptoms. This means that the meds are not fixing Bipolar Disorder itself. The meds are just meant to enable us to coexist with other humans.

The fact is that no one understands Bipolar Disorder, not the doctors, researchers, interested persons, or those of us who live with it. You can take a little quiz online that will tell you whether or not you have it (OMG – burn all these quizzes. What? They’re digital? I guess we’ll have to be creative and figure it out.

The reason I’m so irritated and upset about this is because my much younger cousin has been spending gobs more time with my mother than I am. She keeps telling my mom that she has all these mental illnesses. My mother responds with compassion and encouragement. She tries to help her. She spends time with her. A lot of time.

I pointed this out to my mother and she didn’t say anything. The problem is that it’s true. They really haven’t done ANYTHING to try to understand, to keep track of how I’m doing, to be compassionate to ME. It really hurts.

Have you ever experienced something like this?

There are thousands of websites, books, and experts available to people so that they CAN learn about BD, so that they CAN love me despite my extra quirks and behavior that makes them not want to be around me. (This has gotten better, but let’s face it, the BD brain isn’t exactly reliable or dependable.)

I wish, that they would watch a four-minute video or read a nice and short informational page on a website.

I wish.

My mom knows someone better than she knows me. She’s embraced her and is compassionate and supportive of her. She makes excuses for her. She never has done any of that for me. She says that when I was a kid they didn’t know anything about BD so she didn’t know what to do.

“But what about now? 

“Family, I’m 55. Have you ever tried to learn about my illnesses? Ever?”

“No. Well, they didn’t know anything about it back then.”

“Mom, what about now? Today? I still have it. You know I still suffer from it. Why don’t you just Google it or search for a book on Amazon about it?”

I try to ignore the emotional pain that this lack of real love causes me (that’s how it seems to me). The daughter that lives with me has had to learn a little about it because if she didn’t she would have gone crazy. I admit that I’m not the easiest person to live with.

I can only put myself out there hoping that they will demonstrate to me that they love me with the kind of love that refuses to let me go and will do anything it takes to help me. Am I being selfish? Maybe, but I believe that love, well, love does… I don’t know how to say it.

If you have a grasp on how to describe the kind of love I’m trying to explain, please post it in the comments section. I’d love to hear what you have to say about it.

For now, I’m going to go to sleep. Tomorrow is a new day and another day I can work to keep my mental difficulties (read: demons) at bay. I enjoy my work. Once I get going I can work for hours and become completely engrossed in it. But depression has been kicking my legs out from under me this whole week and I have to say that I’d like for it to take a hike now because I’m exhausted and frankly, would rather be manic.

So good night dear Reader. Sleep well.

Bipolar Mixing Ahead

I’m feeling manic and depressed and distressed and full of anxiety. I hate these feelings. I’m coasting along, knowing these are the better days and I should not waste them. The plan… I have a plan. I have part of a plan.

And my cat is kneading the edge of my blanket that’s sticking out from under my head. OMG! He purrs SO LOUD! – I digress…

I haven’t looked at Facebook for weeks. I want to connect with old friends, but I’m afraid. (This bit is what triggered me) A while back I finally found a friend I’d lost long ago. This friend is doing well. In fact, when I ask how things are going I’m always told that things are perfect. Couldn’t be better. Married the love of their life. I guess I’m happy that things are so perfect for this friend. But I’m not, and it has nothing to do with this stinking sudden mixed episode I’m currently enjoying.

I watched the whole speech given by the student about all the loss and pain that murder by gun has brought us recently. Emma González speech

Then I read about a friend’s dad that went scary nuts at the hospital, and about another friend (about 25 years old) whose grandfather just molested her. You know how family members are often in denial? Grandma denied it and she ended up in jail. I don’t have the details and I don’t care about them because details are not what I’m so freaked out about.

Another friend is excited to not have needed pain meds today and is looking forward to doing chores and growing her eyebrows back in. Then I saw an honestly beautiful painting a dear friend just finished of three burrows… I think it was the burrows that got me.

My mixed state is just like our worlds today. I say “worlds” because we each live in our own little spheres, our worlds. None of them are like another.

There is nothing I can do to influence any of these people’s lives right now. But I’ve been working on influencing mine. I’ve been expressing to you what I’m thinking and feeling right now.

I feel my emotions smoothing out, the peaks aren’t so drastic.

Have you ever tried to listen to music or waterfalls or rain and soft music at night to help you get sleepy? I have. I’ve tried dozens of sounds. I’ve found something that I didn’t even know existed while chasing rabbits on YouTube. It’s a train going down tracks, at a constant speed, with no whistles, no horns, just the steady and almost hypnotic sound of a traveling train.

Wow, thanks for walking with me through that. If the circumstances had been different, well, I’d rather not go there.

I’d like to get my perfect friend to more than tell me we all have our own journeys
we must live. That’s crap. If you have a friend you know is in pain, and you have training in that field and you don’t reach out…. shame….

Shame on me.

Things to do ASAP: call Karen, email Marcella, email School the email, get pic of Bailey, myself and my daughter Jessica with the Easter bunny, clean hardwood floors, throw ball for Bailey on obstacle course, use elliptical, write, do class time in online classes on mindfulness and short story writing… today. If I can get my butt out of bed when the alarm goes off and don’t watch TV I have a good chance of getting it all done. If not, some will roll over into Monday.

And yes, I do sometimes do exactly what I say not to do. I set my bar too bloody high. Yep. I do that… sometimes.

(Written last night at midnight)

The Aftermath of Latuda & Despair

solar flareThe Latuda that was destroying me is gone now, though it has left a lasting mark that lives on within me. It no longer provides mood stabilization for my overloaded brain. The good that it may have done is far outweighed by the damage that it has left behind. Often, I cannot speak for long before I lose the ability to be understood. My speech becomes silenced and my face jerks and spasms as though in pain. Large muscle groups jerk and move without my involvement. It all devastates me. I feel locked inside my body, my brain unable to freely communicate even with those who are closest to me.

I’ve recently come out of a period of not feeling anything but anxiety. My actions indicated that I was depressed, but I didn’t exactly feel depressed. Recently, that has changed.

Last week I crashed. I felt the old familiar feelings and thought things that hadn’t consumed me for some time. I looked at all my pills (I have many) and considered how easy it would be to stop. Just to stop.

But, I didn’t touch them. I called my children and I reached out for help. My girls both came to me and loved me… they helped put away those feelings of purposelessness and thoughts that I have no reason to live.

Why have I not taken all my pills? I have no purpose, no reason to burden those around me. You see, I want to have a purpose. I want my life to matter. While I currently feel I have nothing to offer the world… I think, if I don’t give in to the depression that loves me without reservation, that it might be possible to find that singular purpose that is meant for me.

I suffer from Bipolar Disorder Type 1 with rapid cycling and mixed states. Perhaps I am able to find this ever so small spark of desire to find my purpose because in my manic delusional state sometimes I have delusions of grandeur. Who knows, maybe my periodic delusions will give me my missing purpose. I hope so.

I need a reason to carry on. For now, the love of those who care for me is what I am holding on to. I have to wonder… how long it will be before even that is not enough.

At this moment, I don’t want to die, but I am encompassed by a cloak of useless despair.

I desire purpose. I want inspiration. I resisted the urge to give in and bring this fight to an end. Intellectually, I want my end to be celebrated with the acknowledgment of a fulfillment of purpose and leave an honorable legacy that says my life meant something, that I lived with purpose and left a remarkable mark on my world.

I don’t want to be an unnumbered footmark in the annals of the world, but I can’t seem to master what my brain chemistry is doing to me.

Now, it’s time to start my two-hour ritual of preparing to sleep. Maybe I’ll get lucky and I’ll have a temporary respite and I’ll sleep an emotion free night.

Bipolar – Learning to Live with Anxiety

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Bipolar anxiety is no joke. I already live with a wicked mix of depression and mania and when you add to that general anxiety, well, I feel like I might just be out of luck. I was. For several months the pressure in my brain was so bad that I could hardly talk. I couldn’t get myself to go to the new grocery store near the house I’d just moved into by myself. Week after week I convinced my kids to go to the store with me even though we didn’t live together.

It couldn’t last forever. I knew I’d have to go to the store alone one day soon. None of the counseling was helping. I was walking and playing with my dog. That wasn’t helping. I was eating and cut caffeine out of my diet. Nothing. I took all my meds as prescribed every single day and I stopped taking my Ritalin—just in case it made some small difference. I started trying to meditate and practice mindfulness to no avail.

If you feel like you’re holding on for dear life… you are. Don’t let go. It can get better.

I was at the point where I felt like I couldn’t do it anymore. I was overcome with despair.

I started taking Gabapentin and my symptoms got worse. My face developed Turrets like symptoms. They were violent and I was biting my tongue and cheeks. I couldn’t talk normally. I was scared. I know that ticks caused by medications can quickly become permanent.

I couldn’t get into see my doctor or my med provider. I was starting a new term in college and I was freaking out. I’m still trying to relearn how to learn. I went to community college some 30 years ago. It’s difficult.

I talked with the triage nurse on the phone since I couldn’t get in to talk to anyone. She told me to stop taking the Gabapentin immediately.

Then the med provider told me to take my chill pill twice a day if I needed to and to go back on the Ritalin at least once a day. Slowly, day by day, and doing all the other things I was already doing to help myself, I started to calm down. The Gabapentin scare really freaked me out. I thought I was losing my last hold on reality. I felt like an alien, unable to breathe the air around me.

I suffer from chronic back pain and I’m see a new pain management doctor now. While all this was going on she was treating me like she was going to take away my pain meds because she thought I was abusing them… which I wasn’t. They just counted the pills wrong. Not my fault. That added a massive amount of stress to me too.

Today I go to the grocery store—when I’m totally out of everything, but at least I go. I’m not freaking out about school, not yet anyway. And I’m finally sleeping a little better.

Then I was in a car accident on my way to a school event. Side swiped. My car is totaled. I like my car. It’s a good car. I know I won’t get enough money from the insurance company to get one as good as this one. Stress. Anxiety. Take a pill. Remember what it feels like to calm down. Never abuse my meds. Especially not my chill pill or my pain pills.

It’s time for me to do homework now. I stress and have anxiety over homework. I’ll take a chill pill and wait for it to work before I sit down to do some serious writing.

Anxiety is like a beast that has already pounced and has its claws plunged clean through you. Believe me when I say that the claws can be removed. It is slow and painful, but it can be done. So don’t give up. There’s hope for you too.