I’m living with bipolar fallout, those symptoms that occur after extending yourself too much. I had two road trips in a week, followed by normal running around and then EMDR started in earnest. That was intense! I had fantastic trips. Then EMDR started all sorts of mental memories percolating and feelings being processed. Afterward I just needed a hug.
Now, a couple days later, I’m mentally and physically exhausted, with tons of anxiety despite meds. My thoughts are racing, clouding my ability to think and make decisions. My mood is still stable, thank goodness, but I’m living in fear it won’t be. I’m worried that the exhaustion and anxiety and racing thoughts will trigger a mood state. I usually pace myself for energy-exerting activities to avoid this kind of fallout that leads to fear and worry like I’m experiencing.
I’m just needing to veg out, I think, and practice breathing and grounding skills for the anxiety. But even doing that is tiring. I’m fried. Not even coffee is helping! Spending time alone away from family and the new puppy and then spending time with my girlfriend Is Helping. But I’m still recovering even after a few days away. I hoped that writing about it would help, yet I’m not sure this blog post even makes much sense.
I’ve got a lot on my mind – coming out, new committee work, suicidal thoughts and feelings, a new love interest maybe, a new tattoo and that it means I’m in control of my treatment and my body and who I tell what to, filling out end-of-life paperwork. All in all I’m overwhelmed with me, and a bit hypomanic from the mucinex, and together these things are causing me distress. And anxiety. Lots of anxiety. Just doing the paperwork reminded me that doing such things are a symptom of thinking death is near. And of course I’m having such intense and frequent thoughts of suicide, but in a more abstract way, not a concrete plan, thank goodness.
I just need a place I can be fully me, and be cared for, and share my piled-on thoughts with. Right now that place is church. I’m grateful for the people there that accept and care for me, as well as for the opportunity to do something (social justice team) that speaks to my heart’s burden to make the world a better place. It’s a process of becoming, isn’t it? Becoming a stable person with bipolar, becoming someone who loves in different ways, becoming a leader again. I’m generally someone who pays attention to process, and lets it unfold. But when it comes to me, I’m impatient!
That said, I’m hopeful about entering the process of EMDR to end the suicidal thoughts, and I know it could take a while. I’m hopeful about the person I’ll be and the opportunities I can take when I’m no longer regularly hospitalized and don’t have the terrible thoughts. So I suppose I am paying attention to process because I’m looking to the future and I Will allow it to unfold. And there Will Be a Future. I’m going to keep fighting.
So I’m still struggling with suicidal ideation. I found a recent medical journal article that described what I go through EXactly. “Intrusive Suicidal Imagery” that is unbidden and unwanted, yet can lead to suicidal behaviors just to try to stop the imagery that by being so intrusive leads to hopelessness and then desire to kill oneself. It’s an endless, eternal circle and cycle that I live with. Here’s the article: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5551152/ The first third describes what I go through Every.Stinking.Day. The rest is about possible treatment…
What??? There might be treatment for chronic suicidal thoughts? Yes, EMDR as described in the above article has been successfully used for PTSD and trauma for about 30 years. In the last 10 it has been used successfully with other mental disorders and now finally with bipolar and with chronic suicidal ideation. Something to think about, research more, and see if insurance will cover.
This idea of possible EMDR is one of the really helpful things my therapist told me about last visit. The other is that by even trying just a little bit, just one teensy step, I Am Not Failing. Part of me thinks I fail every time I DON’T go through with suicide – too chicken maybe, since the suffering is so ridiculously unpleasant that I ought to have ended it already, having already gone through every.treatment.possible. Part of me believes doing so many coping skills all the time is failure because surely one of them ought to have worked by now – same with medications and other treatments. I must be doing something wrong.
I complained to my therapist that my brain is trying to kill me. He thinks it is just afraid, and again, that I am not failing. I continue to try: to live, to combat the thoughts or at least try to detach from them. And that struggle has made me who I am. And he thinks that’s a pretty awesome person. Meanwhile, I’m still over here planning my death, but I AM still trying to live. Aren’t there better ways to make someone an awesome person? Asking for a friend…
I feel… Balanced. Emotional. In the middle of the two poles, yet still experiencing polar emotions, such as highs where my thoughts zoom and my feelings soar and influence decisions, as well as lows where I again contemplate suicide though never with intent. But I’m never high enough or low enough or there long enough for it to be a mood state.
I haven’t had anything to “talk” about here with my mood so stable. I even had nothing to talk about at my last therapist appointment. Cool changes are going on in my life – new nutritious eating, trying some additional exercise, a new organization membership. All good things, and nothing too particularly about bipolar to write about.
Except maybe this? I’ve talked with a couple people in academia about what I could expect as a PhD student and adjunct or tenured professor so I can decide if I can expect it of myself with this limited brain. I know that “limited brain” sounds like negative self-talk, but in this case it’s self-care because I am learning to accept my limitations and have realistic expectations of myself. A couple of the limitations I have now are that I don’t remember what I read very well (fiction is easier than non-fiction!), and that in conversations or when asked a question I have a hard time coming up with an answer or sorting my thoughts out to sound coherent or finding the right word. So I have a lot to think about to decide if I can do PhD work.
Let’s just enjoy my normal and hope it lasts a while!
I felt alone. It seemed everyone around me wanted me to continue with ECT. Yet it’s my decision. It’s my body. I live with the illness – and it’s consequences. I live with the treatments and the symptoms of anxiety they cause in me. Here is what I decided after several conversations with my therapist, my psychiatrist, the ECT team, and my mom. I even read medical journal articles.
I want my life back. I want the anxiety I’ve been living with to be back to reasonable levels that I know how to live with. My mood has been stable and my psychiatrist expects it to stay that way. I hope he is right! I’d like to learn how to live with a mood that experiences many emotions without dropping or accelerating into a mood state.
I decided NOT to do ECT anymore. I want to try medications again if my mood becomes depressed or manic again, or if I become suicidal. I have to get the port in my chest removed again since I no longer want to do ECT. (The port was used to access a vein so that nurses didn’t have to try multiple times per treatment to create an IV.) ECT has been helpful for getting my mood to baseline, and perhaps it would help in the future too. I’m just not sure, I don’t like the reaction I have to treatments (days of anxiety), and I’d rather work with pills. ECT had been a last resort when I started it last fall, and resumed it this spring and summer. I just don’t think it has to be my Go-To treatment method anymore.
I will be super vigilant about routine, schedule, taking meds, nutrition, exercise, coping skills, and sociability as I try to maintain a stable mood with these things that have Not proven to work before. But I will do what is personally in my power to care for my multiple mental illnesses. I will work with my psychiatrist for meds and therapist for coping and exploration as needed. I will reach out to others for support on a regular basis. So don’t be surprised if I contact YOU!
I’m taking my life back.
I am living with anxiety: I have coping skills. I have reminders from my therapist. I have a benzo I take 3x/day.
My anxiety was at a 10 on Thursday morning as I met with the doc for the second opinion on ECT, and then with the regular team I see before ECT to talk about the anesthesia trauma and the unbearable anxiety I’m living with. Man, I used every possible coping skill that morning, and I still blubbered all over the place as I talked about what I’m living with.
Ultimately that morning, no final decision was made about ECT. I Did Not Have a treatment that morning. I did not schedule a treatment. I only agreed to talk about the future of ECT and me at a later time when I was calmer an in my own home, not staring at the ECT trappings that reminded me of bad experiences. So Monday I will talk with a person who understands where I am coming from – knowing both the benefits I’ve experienced and the trauma and anxiety I cannot live with.
I was told that there is a med I can take that would drastically reduce my anxiety the day of ECT. And there is something (not sure what – find out Monday) that can be done to prevent anesthesia problems.
I am in the driver’s seat, and I am left with a horrible decision: Do I trust the ECT team with the things they can now do to earn my trust back for smooth ECT experiences, even though they were not offered when I had talked about my experience and great anxiety BEFORE? OR do I stop all ECT, and possibly never do it again, choosing instead to play medication roulette again should my mood waver again or I get suicidal again?
Decisions, decisions. I will get more info Monday.
I deal with anxiety on a daily basis, besides the bipolar disorder. I have generalized anxiety disorder including some form of OCD. I take meds for it, and I use a lot of grounding and mindfulness skills to work through the moments of unease and of panic.
The whole process and concept of ECT weirds me out and makes me anxious, starting several days before treatment. I have trouble managing the anxiety. And then I had the unfortunate experience of waking up after anesthesia was administered and before the procedure started to a feeling of not being able to breathe and not being able to move or talk to tell anyone because of the paralytic administered for the treatment. The experience lasted only a handful of seconds but scared the bejeezus out of me. And so now I Really Hate ECT and get super anxious leading up to treatment. Doggone it that it works for me!
This experience happened to me again last Thursday. I talked to my psychiatrist and to the ECT team about my anxiety-attack-level of panic, but it was my therapist the next day who Finally had something sympathetic and helpful to say! My anxiety is normal and doing what it is supposed to do – warn me of danger – he said. And all the coping skills I’ve learned and practiced for mood shifts and crises Will Work for this anxiety too. Now that my mood is stable, I have the opportunity to use these skills for naturally occurring emotions, and to deal with my anxiety disorder.
Hallelujah! Something to tell myself in the moment, as well as “tricks” to try when the anxiety prevents me from being in the moment, such as writing about the anxiety, both to get support from my support system, as well as to sort out what I’m feeling, and get some distance from what I’m feeling. And What Am I Feeling? Vibrating in the center of my solar plexus. Shallower breathing than I should be doing. Thoughts jumping from partially-formed thought to an awareness of panic that stops all thoughts. Fear. Paranoia. Failure.