Tag Archives: Latuda

The Aftermath of Latuda & Despair

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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 resisting the urge to give in and bring this fight to an end. Intellectually, I want my end to be celebrated with the acknowledgement 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 – Latuda

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I usually check carefully over the side effects and warnings on my new medications. I’ve been taking Latuda long enough that I assumed that I’d do okay with it. But, I guess I didn’t do it because if I had, I’d have noticed right off that the source of my ticks and twitches was probably right in front of me.

From the Latuda.com website: Tardive dyskinesia (TD) is a serious and sometimes permanent side effect reported with LATUDA and similar medicines. Tell your doctor about any movements you cannot control in your face, tongue, or other body parts, as they may be signs of TD. TD may not go away, even if you stop taking LATUDA. TD may also start after you stop taking LATUDA.

I have Tardive Dyskinesia. It is sever and interrupts my communicating with others. It is especially a problem in my classes at the university. This morning I actually had to stop talking. I felt that I had to explain my difficulty because they were trying to listen to me and I couldn’t talk. It was maddening.

This condition may be permanent. I’m not taking it at all now. I stopped two days ago. I hope that as the drug passes out of my system the tic will subside. God I hope so. I’m trying to relax. I’ve noticed that when I get nervous it gets worse. Talk about motivation to learn to chill out.

Bipolar – Tick Crisis!

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tics7089581_sThe last month has been a horror. I’ve developed my facial tick again and nothing we’ve done has slowed its march to make it so bad that I can’t have a conversation. In my classes at University I’m usually very outgoing and participate in class a lot. With this disability, and yes, that’s how I think of it, I can’t talk and participate with the others. It just kills me to just sit there. Sometimes I choose something short to say and I raise my hand and try to say it. My courage is met with stuttering, ticking and humiliation.

On the 10th I went to the ER because it was so bad that I couldn’t be understood when I talked. My eldest thankfully happened to have time to take me in. It was good because she had to translate for me at times. The doctors took me off my last added medication and prescribed me to take Lorazepam. The problem with that is I can’t take the Lorazepam if I plan on functioning. I have classes five days a week and two of those days are in the morning and in the afternoon so I couldn’t just come home and take it. So, it didn’t work. The ER wanted me to see my MD within 3 days of my visit to the ER. I tried, but my MD said that the ER always said that and that it wasn’t necessary. I disagreed. I was still ticking at a 7 out of 10 in intensity. It was a nightmare.

I finally got in to see him. He was of no help. He rudely informed me that it was probably permanent and was caused, he felt, by my Latuda, which I’ve been successfully taking for some time now. He also told me he wasn’t going to prescribe me anything new because he didn’t want me to go to the ER again for it because it would get him black listed at the hospital. I don’t know if he meant that there was a real black list, but he acted as though there was.

I asked to see a neurologist. After some maneuvering he agreed and picked a random one out of the directory and sent the referral through. I don’t think he thought that a neurologist would be of any help. Then he prescribed one of the medications I’d already tried for the tick. The problem with that is I’ve lost track of which medication caused which reaction or positive outcome.

I got ahold of the neurologist on my own and they could tell I was in crisis and tried to get me in earlier than the July dates that were for new patients right now. The helpful lady called me back the next day and sadly told me that they refer ticks to the mental health people and would I like their number? I told her I had it already. She was nice.

I had an appointment with my counselor this morning. Unfortunately, I locked myself out of my house and out of my car. I texted my eldest daughter and begged for help. She left class early and came to my rescue. I did happen to have some homework with me so I spent my time waiting for her doing that.

When I got back inside I called my counselor and got through! I asked her if we could do the appointment on the phone. She was great and agreed. My tick was at about a 5 for most of the visit although sometimes it got worse. She listened to what I’ve just recounted to you of my last few days and weeks and said I need to talk to my med provider ASAP. She put me on hold and went looking for her. Amazingly she found her and she was free so we stopped our conversation short and I waited for Sara, my med provider, to call me momentarily.

The call from Sara came right away. I went over all the stuff again and through asking questions about what new prescriptions I’ve started taking in the last month. I started a medication for restless legs (which worked!) and Lyrica. She has me discontinuing the Lyrica (which is funny because we’ve been fighting with my insurance for months to get it approved) and the last med that my MD had me start taking for the tick. Then she did some research and found out that indeed Lyrica can cause the tick and so can Latuda, which I’ve been taking for some time. Now were stopping the Latuda. I’ve just gone from 120mg to 80mg tonight. Last time we tried to lower my Latuda was during the Christmas holiday and it didn’t go well. Instead of being well medicated and under control, I began to have violent emotions and lashing out at my loving family. It didn’t feel great. But here we are, trying it again. I’m going to have to watch myself.

So now were taking action. I feel better about it. I see Sara on the 11th I think. We’ll reevaluate my condition at that time. She’s not happy with the way this has been handled. The ER should have referred me to my med provider, not my MD.  My MD couldn’t give a shit. I’m looking for a new one. Around here it’s really hard to find new ones. New patient appointments have waiting lists going out months. It’s frustrating.

I’m a communicator. It’s what I do. I am fully involved in all my classes. I can’t do that right now. It drives me crazy. Sometimes I raise my hand thinking I’m going to say something brief. Unfortunately, it turns into a long ordeal as I stutter and tick my way through what I want to say. Sometimes the friend I sit with tries to finish talking for me. It’s embarrassing. I know there’s nothing to be embarrass about. It isn’t my fault I can’t control my mouth. Thankfully I can control the content of what I want to say.

I’ve been using my situation to really make sure that what I want to say will really be helpful or ask a really good question.

My kids have been good about it. They laugh at me when it gets really bad. I’m glad. I can’t take it too seriously (though god knows it is). They help me keep my chin up. And, thankfully, they translate for me. Seriously. Even when I’m just talking to them they have to finish my sentences for me (when I’m at a 7 or higher). I’m thankful for my kids, my mom and my brother for their patience in waiting for me to struggle through a conversation.

So, maybe the next few days will be better. I’m not going to class tomorrow. I’m going to work on calming down. I need the time to rebound and relax. I have a ton of homework to do so I’m going to give myself the time to do it. Lowering my stress can only help my situation.

If you find yourself in a similar situation remember that freaking out doesn’t help. Well, doesn’t help much. Sometimes you get like I did and can’t talk at all and they take you seriously. But, in general, it’s best to persevere and keep bugging people, doing research, calling anyone you can think of till you find the right person to talk to. Now, I hope it works.

Tonight, as with the last two nights, I’m up late with back problems. It’s like all the nerves in my lower back are firing at the same time. I can only describe it as sever lower back pain. I take Oxycodone for that. You’d think that would help my tick and the stress associated with it. Nope. Nada. Zilch.

Sighing…. This tick seems like such a waste of time. I was thinking of getting a summer job, but that will never happen with this tick.

I’ll let you know what happens next. I’m afraid of myself. I’m afraid my Bipolar is going to come raging back like it was in the past and torment me. Hopefully I can use the tools I’ve learned since my last crash to keep me from going into crisis but you know, if it’s going to come, it’s going to come. I can’t stop it. But I can combat it.

So here we go, on my first day with my Lyrica gone and my Latuda going down. I have to admit, I’m more than a little scared. What if I flip out? What happens if the tick becomes permanent? What if? What if? What if? What if I get better?

My back is feeling better now. I’ve sat on ice and now the heating pad. Time to try to go to sleep again. Good night my friends. May you be able to speak your mind wisely and with confidence.

Bipolar – Never Far Away

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I reached a stasis point, a time of going to neither depressed nor manic poles. I thought I was emotionally cramped or stunted. So, as I’ve said, my med provider and I decided to lower my Latuda to 80mg. It’s been about three weeks now and I can say without a doubt that I’m swinging again and in a bad way. I just called one of my daughters (I asked my family to watch me) and she said she’d noticed something had changed too and was wondering if that’s what was up.

Of course, I denied it. I realize now (30 minutes later) that I was protecting myself. I’ve worked for so hard for so long to be stable I didn’t want to admit that I’d have to up my medication again. I wanted to believe I could do this, be normal on my own.

I guess I feel like if I can’t be “normal” I won’t have really lived, I won’t really have given to my world or amounted to anything. I think those thoughts and feelings are always beneath the “calm” exterior of my well medicated self. It’s frustrating.

I’ve gone back to school so I can get a job. I’m 54 and I’m just going to school for a career now. It makes me so sad. See, the depression is coming like a vengeful lover, rough and dark.

If I’m already behaving “mean” towards my daughter and feeling depressed and like I’m about to have a fight I guess I’m not ready to be on a lower dose of my Latuda. So, it’s either go back up or change to something else. I’ll need to call the nurses line tomorrow and see if I can talk to my med provider as soon as I can. This isn’t the kind of thing that I should just wait until my next visit to handle.

Tomorrow I also see my counselor. We definitely have something to talk about.

Today I saw my pain management specialist. She ordered an MRI of my lower back. For some reason no one has ever had one done. I would have thought that having me on pain medications as long as I’ve been on them that someone would have had one done, but I can’t find it if they did.

Well, my new reality and I are going to read for a few minutes and then go to bed.

Be safe my friends.

Bipolar – Hidden Emotions

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After months of not really feeling anything accept sever anxiety, my emotions are waking up again. I’m hoping that all the months of counseling have prepared me for my feelings, my moods.

I took a poetry class this last quarter. I had a difficult time writing the poetry because my emotions were packed away in a closet inside my brain. I wrote very clinically, very much cerebral and didn’t feel inspired or moved at all.

I’m enrolled in the disability program at the college and one of the things I get is time and a half for exams. Of course there aren’t exams in poetry, but the first quarter that I had this professor with I’d gone in and went over my disability papers with her and explained about how this was my first year back to college and I that was having a hard time. I took a chance and told her about my having Bipolar. I haven’t really thought it was necessary to tell my other professors what my disability is, but I felt like I was connecting with this professor and I also felt like I would be able to come and her and talk if I needed to.

I talked to her about how my BP was affecting my writing and she suggested I read “Touched with Fire” by Kay Redfield Jamison to see how many artistic people have mental illness (especially Bipolar Disorder). Funny thing was, I have read it. I’ve spent so much time in it that the pages have come off the spine of the book and nearly every page has notes and things underlined in it. It is in such bad shape that I purchased another copy so I could read it again. This is one of those books I bought in paper back and not as an eBook. If I have a book I want to markup I always get it in print. It’s just easier for me to make notes and find things in.

The first thing I encountered in Jamison’s book was a through recounting of all the symptoms having to do with Bipolar Disorder. Having been only anxious and not having mood swings for a few months per se, I was shocked as I remembered all the emotions that are currently hiding behind my medications.

I’m glad that I read what the symptoms are again because of the fact that we’ve lowered my Latuda and I need to be on the watch for symptoms to return. I have to admit, I’m worried now. I forgot how bad it has been for me. I rate on the top of the Bipolar Disorder Type 1, but I’m also high functioning so I’ve been able to hide it from most people. At least I think I have. Who really knows what others think of us when we’re in the midst of an active outburst of violent emotions.

So here I go, with an intentionally lowered mood stabilizer, and me waiting to see if any of my old enemies come sauntering out of the closet. I must remember not to hold my breath.

Bipolar 1, ADHD, FM, PTSD, Anxiety, Chronic Pain, OA – Now What??

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If I’d started my blog off listing all my bits of my alphabet you might have clicked off and dismissed me as a hypochondriac. Personally, I might have too. However, the fun facts pile continuously up and I wonder if I might be much older than my drivers license says I am.

I’m 51 degrees old. Wait. 51 years old. Yes, that’s it. I think it’s time I leveled with you and give you my “medical” life. I am much more than my medical stuff. I’ve had my right knee replaced twice – in just two years. I know, that’s very young to even have it done once, but twice on the same knee… Skip that. Here’s a “brief” list. Each item is a medically real thing for me.

Bipolar 1
ADHD
FM
PTSD
Anxiety
Chronic Pain
Degenerative Disk Disorder
OA
2 Total Knee Replacements
Cataracts
Allergies – environmental, biological and food
Depression
Manic
Stress – Excessive
Obsess
Asthma
Dentures – Full

I’ve also had a ruptured appendix, broken ankle, blood clots, carpal tunnel syndrome, rage… I think you get the idea.

Over the last couple of months I’ve thought I’ve been falling asleep while driving. It freaks the freak out of me. No matter what I do I don’t seem able to prevent it. I even pull over and try to nap just so I can complete a 40 minute drive home. I’m not able to nap when I pull off the road. I try. No go. I can sleep in a parking lot when I’m too tired to drive, but it’s not working now. I sing, I scream, I pound my feet on the floor, I hit my steering wheel… Nothing helps.

It’s very scary. No, it terrifies me. Suddenly I’m about to rear end another car or find myself drifting to one side or the other. I’ve been asking my health care people what it could be. I eventually got around to my pain management specialist. I described it to her and asked if she thought it might be any of my many medications. Like my med provider, she didn’t think so. She wanted to know if I was born prematurely. Nope. Seizures? Nada.

Michelle, the pain specialist, asked if I could describe what happens as a “loss of time”. Maybe I’m not really falling asleep. Maybe I’m just losing time and tune back in just seconds later. Do I remember actually falling asleep or feeling sleepy. No. I’ve even tried coming home and trying to sleep. Not sleepy. No naps.

She sent me home charging me with looking into Absence Seizures. She knows I love to research stuff. I appreciate that she lets me learn and talk with her about my health care. I have read a bit about Absence Seizures. I think she might be right. Before I left she agreed she would get me in to see a neurologist she likes to use in a city about an hour from here. I’m going to have an EEG to see what’s going on.

New bipolar med on Wednesday… Friday a possible new diagnosis to add to my alphabet soup. Know what I keep thinking?

… Well shit.