Category: Hypomania

Blogs that include the topic hypomania

Allan’s Mania Season

People seem to be aware of depression occurring during the darker months in Canada but there is a different season that those of us who have bipolar disorder have to pay attention to and for different reasons. It’s springtime. I like to refer to the spring as, “mania season,” because this is the time of year when I, and many people I have met who have bipolar disorder, are more likely to experience hypomania which can build to full-blown manic episodes. This phenomena is officially called Spring Mania (Psychiatric Times) .   

I live in Calgary, Canada and during the winter we have approximately 8 hours of daylight per day. In the springtime, that changes to 15 hours a day. My bipolar disorder can react to the increased number of daylight hours in a dramatic fashion. Most of my hypomanic and manic episodes have occurred in the spring. For me, the consequences of this happening are extreme because I have the more severe type of the illness, Bipolar 1, which means I have full blown manic episodes that can include psychosis. This has happened 3 times in my life and all of them caused irreparable harm to relationships with colleagues, some friends and family members, job loss and a struggle with maintaining enough money to meet basic needs. Since the consequences are so severe, I am hyper vigilant in keeping an eye on my mood in the spring and if something starts to go wrong, I act immediately to ensure that I don’t become acutely ill.

I have learned that the first symptom I experience when my mood is becoming elevated is irritability. I notice that when I talk to people my words have a tiny bit more of a bite to them than usual. Nobody else notices the change but I can because it’s not like my usual demeanor and the way I communicate. I also notice that I have thoughts that describe my irritation with the world. Thoughts like: Why do people in Costco always get in my way? How come everyone is driving like idiots? Why is person x taking so long to complete x?  

The other symptom I notice is that it is very difficult to calm down and rest. It feels like my blood is almost vibrating at a different frequency than the rest of my body. Regardless of how tired I feel, if I lie down, take deep breaths or close my eyes, my body will not calm down. I feel like I must keep moving but that makes the feeling worse.

When this happens, I go into my bathroom, put a towel at the bottom of the door so that it is completely dark and wait and see if anything changes. If I start to feel better, it confirms for me that my mood is becoming elevated. I sit in the dark for as long as possible and that stops my symptoms from getting worse. After I feel more settled, I close all the blinds in my house and wear sunglasses. I don’t do anything stimulating. I don’t go on my phone, watch TV or go outside. I just sit in as dark a room as possible and try to stay bored. I cancel all of my commitments including work, socializing and sports activities. If my symptoms get worse, I will call my psychiatrist and she will decide if any adjustments need to be made to my medication. Generally, when I do this my symptoms only last a few days. I have not had a manic episode since 2010 and I believe this self-awareness and my medication has made this possible.

This strategy will not work for everyone. Bipolar disorder presents differently in every single person. Unfortunately, the only way to figure out a method for yourself is to reflect on what was going on before your last and previous episodes to see if you can identify any patterns that can give you a clue that you may be becoming unwell and then working with your psychiatrist to develop interventions that will work for you specifically. For me, this process took many years and I think it is important to have some space after an episode to grieve the losses you may have experienced, heal from the shame and physically recover from the depression that follows before you start thinking about how to identify when you may be experiencing an uptick in your mood.

For family and friends who have loved ones in their lives who have bipolar disorder there is very little you can do to help in this learning process other than be supportive and compassionate just like you would for any other physical illness. It is difficult for people who don’t have bipolar disorder to understand the subtleties of the start of mania. I have heard many stories of well-meaning family members expressing concern over someone who has bipolar disorder’s mood when often the person is simply having a normal valid emotional response to a certain circumstance. Peer support provided by people who have bipolar disorder are better able to have these conversations that people can learn from. Organizations such as the DBSA, The Depression and Bipolar Support Alliance have online peer support groups for people who have bipolar disorder.

I have heard many mental health professionals say that bipolar disorder is an illness that can be managed. I think that is unfair to us. I think we can thrive and have exceptional fulfilling lives with meaningful volunteer or paid work, and healthy relationships with colleagues, friends, family, and romantic partners. We may not be able to engage in specific activities and everyone who has bipolar disorder differs in their capacity for how much activity they can do in one day. I believe with the right medication and strategies based on self-awareness it is possible for all of us to have a positive life.

The “I Am Ok” Costume

In my experience, most people who have bipolar disorder put a lot of effort into acting like they are fine despite the fact they are really struggling. This problem is not unique to bipolar disorder, but since it is the illness I have, I will focus on it for this blog.  

Many of the symptoms of bipolar disconnect us from people. At times, the illness prevents us from physically experiencing enjoyment. When this happens conversations are extremely difficult. People generally like to talk about positive experiences they’ve had or are having. When depressive episodes rob you from physically experiencing joy then that changes how you interact with people.

For example, depressive episodes prevent you from finding anything entertaining. You could go to a movie with a friend and when they ask you if you liked it you cannot say, “Normally, I would love it George, but right now I am experiencing a depressive episode which messes with neurotransmitters in my body, and as a result I cannot experience enjoyment right now.” I suppose you could say that, but it would probably be hard to maintain friendships if you did this on a regular basis and it is unlikely that your friend would understand what you mean. It is simpler and better for us if we just put the ” I am Ok” costume on and say we liked the movie.

It’s not just depressive episodes that are problematic. Hypomanic symptoms also require a lot of energy to make one appear “Ok.” During one of these episodes, you might notice that people keep asking you to stop interrupting them because you are talking too much or your brain is screaming at you to buy a bunch of stuff you do not need. You cannot say, “Please ignore me for awhile I’m hypomanic. Can I buy your shoes? I love this song. Do you love this song? Let’s dance on the escalator.” Instead of saying or doing these types of things you have to grit your teeth, put the costume on, smile and try not to say anything.

All of this may not seem like a big deal but it’s exhausting. Bipolar disorder is a chronic illness, so our medication helps a lot, but we still have to deal with our symptoms to varying degrees on a regular basis. When we are not well enough to get the costume over our shoulders the consequences can be harsh. A parent may be at a graduation or wedding and be unable to experience the joy of the moment and can be accused of being uncaring or cold. Someone who is hypomanic can lose a lot of money, relationships, and employment.

For me, the only relief I got from wearing the heavy, “I am ok” costume was attending peer support groups at OBAD. The format is simple. You show up at a meeting and just exist without any judgement or expectation. My first meeting was such a relief. My depressive episode was so severe I could barely manage to keep my eyes open and get a word out of my mouth. It didn’t matter. Listening to other people who had bipolar disorder talk about their experience made me feel connected and not alone. I could just be ill, and everyone understood, and they were comfortable with it.

What can people who do not have bipolar disorder do to help us when they notice we are struggling to get the costume on? Unfortunately, there is not much anyone can do. My neurotransmitters do not speak English so pep talks, advice or punitive judgement will not pop me back into wellness. I just need people to be patient and compassionate with me and, in time, I will feel better.

Discussing Peer Support, Hypomania and Creativity with OBAD Executive Director Kaj Korvela

Photo by Tima Miroshnichenko from Pexels

This week my blog features a podcast interview with Kaj Korvela, Executive Director of OBAD, the Organization for Bipolar Affective Disorder. We discuss the value of peer support, hypomania and how creativity is experienced by people who have bipolar disorder.

Discussing Peer Support, Hypomania and Creativity with OBAD Executive Director Kaj Korvela

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