When It's Hard to Accept a Late Bipolar Disorder Diagnosis

I was diagnosed just a few months ago. I suppose I always had a hunch. Others in my family history have dealt with this disease. But I thought I only had major depressive disorder and generalized anxiety disorder (along with its friend social anxiety) and post-traumatic stress disorder and oh yeah, I’m a recovering alcoholic, too. (This long list just made me laugh a little out loud, I suppose it’s because I have an odd sense of humor…I think it’s called gallows humor.)

I’ve experienced symptoms of these other mental health issues since my teenage years. I was always been told I was dealing with major depressive disorder, and I always have, off and on. I’ve had three hospitalizations now, four if you count the outpatient partial hospitalization program I went through a few months ago. But maybe it wasn’t until I became more knowledgeable about the symptoms of these different disorders — or noticed the times I overspent money and/or times I felt super euphoric for no real reason or for the littlest reason, only to come crashing down. I’m not sure exactly when, but something in the back of my head thought it was possible. Something else in my head said, “No way! You don’t do the extreme things that are said to be symptoms of bipolar disorder.” Even my psychiatrist said I didn’t meet the criteria when I mentioned it to him a few years ago.

But this fall, when the most severe symptoms of depression worsened and I began my descent into the pit, my therapist at the outpatient program I mentioned previously confirmed my concerns. Then in November, the doctor at the hospital where I was an inpatient confirmed my concerns. And finally, my new psychiatrist after the hospitalization confirmed it as well. Bipolar type 2 was the general consensus.

Something in me didn’t believe it, though. Something in me didn’t want to have that diagnosis. Something told me I was going to face a whole new set of stigmas, and I did not want to deal with that. Something in me said, no way.

But I took the new medications. I hated the new medications. We switched around some of the medications. We’re still switching around some of the medications. And, believe it or not, I think I’ve turned a corner and I don’t feel like dying most of the time. (Praise God.) But something different is going on with me now.

I’m waking early in the morning before my alarm clock goes off. (This is really odd for me, as I am a sleeper!) I can’t fall back asleep these days. I now have new found hobbies and interests that are consuming most of my thoughts and time. As in, I can’t stop thinking about them and all the things I want to do and what I should do next and all of the ideas are flooding my brain at once. My mind is racing as if it’s trying to catch something and I’m running with it (and running really isn’t something I do). It’s not simply that I have a lot of thoughts, I have a lot of thoughts all at once and they are grand and filled with the greatest optimism. My days are full somehow. There are so many things to get done! But guess what? None of them are things that I really should get done. If it weren’t for my meds, I doubt I would go to sleep at night at all, at least not until very, very late. Additionally, I may or may not be spending money on things I shouldn’t be…and rather impulsively.

I added all these thing up in my head and I did a little research on “what hypomania feels like.” It turns out, I could so relate.

I had an appointment with my psychiatrist yesterday. They took my blood pressure. It was unusually high for me, not dangerously high, but high for me. I found this interesting considering how I’ve been feeling. I told my doctor about all of these symptoms I’ve been having and yep, she thought I was definitely experiencing hypomania. She believes I’m in what’s called a mixed state right now, because I still have depressive thoughts and moods, but am also experiencing the hypomanic highs. She’s made a few adjustments to my meds (again) and now I’m a little worried I’m going to feel sad all the time.

And truth be told, I’m also a little sad that it’s true. I really do live with bipolar disorder and I have been for a long time. I suppose there is a little bit of grieving that goes on with any new diagnosis, a grieving for the health we had or the health we thought we had, whether it be true or not.

The good news is I finally know what I’m dealing with and I honestly have no reason to attach any kind of stigma to myself. Living with bipolar disorder is no more shameful than living with arthritis. Unfortunately, if I’m really being honest, it’s going to take me a while to believe that in my heart, because for some reason I feel a little more faulty and a little more broken right now.

Follow this journey on Mommy Muddling.


When Living With a Mental Illness, Don't Forget to Live

There is more to you than what is wrong.

That doctor said you were anxiety’d, depressed, bipolar’d, schizophrenia’d or OCD’d? They like to tell you what’s wrong. I get it. There must be something wrong with someone who overthinks everything all the time.


Place a label on my thought structure. I will sit and take your medicine. But there are worlds that you have not thought of.  Therapies that I am on the cutting edge. I have a PhD in late night dance parties. I am summa cum laude of emotional rants about truth. I just wrote a dissertation on how hot and sweet love can drip off your tongue.

There is more to me than what it is wrong. It takes a person in a box to place a person in a box. There are so many boxes, it feels like I have just moved a thousand times. How many houses do I have to live in, to keep going forward in my life?

There is more to my life than echoed pasts of what you said in your manual. There is more to life than your diagnosis check list. I prefer step by step instructions to find joy. Step one, step out of your comfort, step two, jump and fly, step three, feel the wind on your face, thermals under your wings.

I take your medication to make sure it’s safe for me to walk through the world. But also try hugs and support and cradling my head as I lay down at night, listening to the world take me away. There is always a thought of death, loss, suicide, anxiety, pang, paranoia, always incessant, always oozing.

Step into my office and I will show you what it is to love. I will show you what it is to look at yourself and see that there is actually nothing wrong with you. There is nothing to fix, break, flip over, change, reboot, compress, tighten or even speed up. 

Try theirs, but also try mine. Try sitting with a newspaper and a hot cup of coffee on a Sunday morning, try running and screaming until your heart gives out, try drinking a cool glass of water, try diving into icy oceans, try staring at the sky and catching snowflakes, try letting a puppy lick your face, try turning on the light to see there actually aren’t any monsters under the bed, they are just in your head.

Instead of running from that achy haze, turn around and float yourself into its gravity. You are alive. Live it when you can. Ride waves of unconscious pain. Some doctors will tell you what you need to do to get by. I think about the thrive.

Follow this journey on Adventures of a Little Boy.

The Mighty is asking the following: Tell us a story about a time you encountered a commonly held misconception about your mental illness. How did you react, and what do you want to tell people who hold his misconception? If you’d like to participate, please send a blog post to [email protected] Please include a photo for the piece, a photo of yourself and 1-2 sentence bio. Check out our Submit a Story page for more about our submission guidelines.

I Thought I Was the Only One I Knew With Bipolar Disorder

When I was diagnosed with bipolar disorder type II after 20 years living with a depression diagnosis, it felt like a king-sized relief. At last there was an explanation of what was happening to me, my brain and with my behavior. 

Then, I realized — I didn’t know anyone else who lived with bipolar. So there I was all super-freaky, out there on my own like a dog in a yard. My diagnosis was no longer the supreme relief I originally thought it was.

My psychiatrist gave me a copy of Kay Redfield Jamison’s book “An Unquiet Mind: A Memoir of Moods and Madness. I am a prolific and fast reader. Add a topic I have a vested interest in and I become a voracious reader. I read the book overnight and then read it again. It was an amazing and insightful explanation of how bipolar type I affected Redfield Jamison. It spoke to my experiences over the past 20 years. Although Redfield Jamison’s experiences, her manias, were far more extreme than mine have been, they resonated. As did her depression. The book was so valuable because it was an open sharing, a full disclosure.

It became my inspiration. Not only to stand up and be counted. Not only to speak openly and comfortably about mind health matters on a weekly radio program, but to also share my story in short snippets as well as in my own book.

And as I started telling people about my 20-year experience with depression and my recent bipolar diagnosis, something interesting happened. Suddenly, every person I spoke to wanted to tell their story. It became OK to share their work, social, familial or personal experiences of mind health matters with me. I heard about my uncle who lived with bipolar, a primary school friend’s mom’s long-time challenges of living with bipolar. People who were diagnosed with or lived with someone living with schizophrenia, borderline personality disorder, OCD, generalized anxiety disorder and the all too common depression and bipolar disorders all came out of the woodwork.

The lesson for me: my mind health is journey. The experience of living with a bipolar type II diagnosis can shift from feeling broken, alone, worthless and pitiful to rising to periods of unstoppable invincibility and ecstasy before finding a balance, leaving me feeling strong, resilient and balanced. Accept the journey for how it shows up. Find your lesson. Live your life to the fullest.

Why? Because your mind health matters.

The Mighty is asking the following: Tell us a story about a time you encountered a commonly held misconception about your mental illness. How did you react, and what do you want to tell people who hold his misconception? If you’d like to participate, please send a blog post to [email protected] Please include a photo for the piece, a photo of yourself and 1-2 sentence bio. Check out our Submit a Story page for more about our submission guidelines.

When Mental Illness Stigma Is Self-Imposed

I have been stable for the past four years, but now my bipolar disorder has resurfaced. It could have been triggered by stress, meds or the weather change — or equal parts of all of these things — but the reality is that I’m unwell.

It was when I said this that my husband asked if I was hypomanic. Calmly, he described my behavior. I trust his judgement enough to know it must be true. Saturday highlighted this, as I was in a full hypomanic episode. Upon reflection, it had been building all week but I didn’t realize it. I had been having extreme anxiety all week and had been very agitated. I wasn’t sleeping and I was extremely volatile. By Saturday, this agitation and anxiety had turned into excessive, delirious energy and despite working out for two hours, taking anti-anxiety meds and trying to take a calming bath, it wouldn’t go away. My speech was rapid and bouncing from one thought to the next. I couldn’t sit still. I was moving like I was on speed. I had great ideas. (I saw a girl with half of her head shaved and thought that would be an awesome look for me, too. And while it might be an awesome look for me, it’s not a decision to be made while hypomanic.)

I’m equal parts frustrated, disappointed and defeated. It has been so long since my mood swings have been so volatile and explosive. It has been a long time since I felt manic. It has been a long time since I have felt so completely out of control.

Under the suggestion of my doctor and psychiatrist, I’ve taken a leave of absence from work. To be honest, this has been the hardest thing I’ve had to do in my life. I feel like I have admitted defeat to my illness. I feel like my leave of absence is showing the world my illness makes me weak and that I can’t hack it in the real world.

Rationally, I know this is totally unsubstantiated. I have a supportive partner, family and friends. I have previously disclosed my illness to my boss in preparation of writing this blog and she had demonstrated my illness didn’t taint her view of me. But there’s nothing I love more than feeling guilty, so I still beat myself up.

We often speak of stigma in terms of external judgement — how others perceive those with mental illness. But a form of stigma we don’t often talk about is the self-imposed stigma. Will I get fired for taking a leave of absence? Will I be given less interesting projects because they’re less stressful? Will they think I’m less capable because of my illness? Do my colleagues think I’m lazy and just don’t want to work? Are people whispering about the crazy girl who had a breakdown? I am so consumed by thoughts about what other people might be thinking about me, I neglect what’s most important — what I think and need. 

I try to situate my mental illness like someone who has cancer. If a colleague took a leave to get chemotherapy, would I judge them? Of course not. I would probably send them an email wishing them well or send flowers to their hospital room. But we don’t think of mental illness in this way because its symptoms are not visible. My moods are visible — I’m agitated, I’m teary, I don’t sleep — but the “proof” that the actual illness exists isn’t visible. It’s my word and a doctor’s signature on some paperwork.

Last week, these self-imposed judgments were spinning in my head increasing my agitation and anxiety. In an attempt to help, my husband and I set out on a walk of undetermined length. As we walked, I explained all of these thoughts to him.

“I’m regretting taking this leave of absence. Maybe I could take back the paperwork that had been submitted. I could go to work and have my medication readjusted — I could handle that. I didn’t really need this leave of absence at all. But on the other hand I’m so tired and angry — what if I blow up at work? I already snapped at one co-worker when I normally wouldn’t. I could lose my job. Also, I was sobbing at my desk on Tuesday. That’s not right. No, I do need this leave. It’s good for me. But on the other hand…”

After listening patiently to my rambling and often contradictory thoughts for the better part of an hour, he finally said something: 

“I know deep down you know this is the right decision. In the 10 years we have been together, this is the first time I’ve seen you choose yourself over other people. I’m proud of you.”

This stopped the self-stigma in its tracks. He reminded me this leave is only a minor setback. I haven’t surrendered to my illness, I’ve just retreated. No general would continue when the battle is surely lost. A general would regroup, tend to the wounded, gather reinforcements and re-strategize. And that’s all I’m doing. I may have lost this battle, but there’s still a war to win.

Follow this journey on Mad Girl’s Lament

There Is Hope After a Bipolar Disorder Diagnosis

I feel like there’s been a lot of attention lately on people with mental illness. There has especially been a focus on overcoming stigma in the world, to help people who are struggling feel safe talking about it. We all know the statistics. We know that because of stigma, people are less likely to seek treatment. We know serious mental illnesses can be lifelong. And we know that despite sensational media reports, people with mental illness are far more likely to be victims of crimes than perpetrators. These are sobering facts. Even with these sobering facts, I feel like there is still a disproportionate shortage of hope being spread about serious mental illness, and that’s why I’m writing today.

I have a serious mental illness. I’ve lived with it for most of my life. I’ve been diagnosed with bipolar disorder type I. I go through extreme mood swings, varying from periods of mania, where I’m euphoric and make really poor choices because I feel indestructible and on top of the world, to periods of severe depression, where I feel utterly worthless and think life is meaningless, and that my family would be better off without me. I manage to stave the worst of these highs and lows off with medication management and therapy.

What do I know about hope and mental illness? I was once a train wreck of a typical case. I was untreated, court committed, in and out of hospitals and well on my way to being another statistic. I hit rock bottom in my life about 10 years ago, right when I was first diagnosed, actually. It was about this time when I lost everything of value to me. I lost my car, I lost my apartment, I lost my job, my family shunned me and I lost custody of the one thing that meant the most to me, my daughter. I literally lost my will to live at this point. I earned myself a six-week stay at the local psych ward during this time, and I had a lot of time to reflect on just how much I’d ruined my life. I finally got out close to New Year’s, and as that year drew to a close, I knew without a doubt I was closing a chapter that had been the worst of my life, and I was never going to repeat it again.

I woke up to a new year, and I was a new woman. I was determined to get my life back together somehow. So I did. Very slowly. My family unwillingly had let me come home, and I had determined that the first thing I needed to do was find a job. I immediately stated putting out applications. Once I got my job, I got a phone. Then, a car. I also made sure my daughter was back in my life, too. After I got into the groove of working, I decided to go back to school. Now, I’m not saying this all happened smoothly, but it happened. I still continued to struggle with my bipolar episodes, but I had a lot of support from my friends and family to help me through them when they happened.

A few years after I had my epic breakdown, I met a really wonderful guy, who treated me amazingly, and we got married. He’s been a great support to me as I’ve had ups and downs with bipolar disorder moments. We have three kids together, in addition to my oldest. I may have bipolar disorder, but I’m doing something right by these kids. I send my kids off to school every morning, and not one of them will leave until they get a hug and kiss.

Now, here’s the important part — I still struggle. I’ve been hospitalized more times than I care to admit. I’m not perfect. I still have moments where I don’t know if carrying on is worth it. But I know I’m in a good place. I’m doing good things. I have a part-time job that I’ve had for over a year. I work at a place where I actually feel like I make a difference. I write articles I feel are helping people and have the potential to help a life. I’m constantly improving myself. I know myself, I watch myself constantly for fluctuations in my mood and I’m am on top of seeing my doctor if I sense a disturbance in the force. I regularly see my therapist, and I’m dealing with issues that have been holding me back all my life.

I may have bipolar disorder, but it doesn’t have me. I’m not defined by it. I have value and I see that. I may need medications for the rest of my life, but that doesn’t make me “less than.” Considering the weight gain it causes, it actually makes me “more than.” I jest, I jest. I like me. I’ve been told I’m an innately likable person. Being bipolar doesn’t take away from that. It doesn’t take away the fact that I’m a very authentic and real person, or that I love serving others or that I love writing and being creative.

There is hope after a mental illness diagnosis. I lost hope after I got my diagnosis, I think. I felt like I would just be a waste of space, and why try because I was just going to be a label no one would ever see past. I’m happy to say people all around me see past that label all the time. My boss sees past it. My coworkers see past it. My husband sees past it. My friends see past it. People who know me just see Tricia, not bipolar.

If you’re struggling to find yourself in the midst of an mental illness identity crisis, I promise you, you’re in there. There’s nothing wrong with needing help from a support person to find yourself, or perhaps needing help from medication to find your best self. Just keep reaffirming to yourself who you are, and keep hanging on.

'Functional' Is a 24/7 Job When You Live With Bipolar Disorder

In the dark of morning, I struggle the most. Every day, I wake up and try to convince my rapid cycling bipolar brain to function. There is a debate. Every day. I stand at my bed and argue silently as to whether or not I should crawl back into it. It is in this moment I struggle with being functional the most. This exact moment.

Realistically, I don’t actually get to claim the title “functional” until I am up for about two hours. Technically, I claim it as soon as I hit the shower.

For a moment, let’s back track to the night before. At 10 p.m., which should be my bedtime, my brain suddenly decides that it’s time to take over the world. Fractions of ideas, half concocted story lines, bits and pieces of thoughts and images project into my consciousness. They’re just semi-completed annoyances trying to self-actualize into my brain without actually being a whole self. Nothing is accomplished, as I allow them to stream through without attaching any value statements to them.

But they certainly keep the lights on while they party, while I lie in my bed, awake.

As anyone who takes psych meds may know, well, sometimes they can destroy us with side effects. It’s like stopping that party by literally burning the house down, party-goers inside. (On a side note, one med is trying to ruin my cholesterol, but that’s a different story.) In this instance, another med makes me drink ridiculous amounts of fluids to combat the vicious, unending thirst that accompanies the ridiculous and incessant urination. I wake up every two hours to take care of business. I am in the process of getting blood analyzed and all that jazz to determine if this is, indeed, the problem.

So, I go to bed every night with the synapse remix blasting in my head, preventing me from going to sleep, and the brutal side effects of the sacred medication cause me to continually wake up. Often less than five hours total, no more than two hours at a time. 

Yes, I am tired. In the dark of morning, I struggle to reason that going to work is the most logical conclusion at that particular point in time and space. But I am here to rise, period. Sucking it up one day at a time just seems like the right thing to do. It’s a fight, right? We don’t get paid, and we can’t win, if we just sit in the corner.

In the dark of morning, with little to no faculties available, I can’t give in. I just can’t. So I don’t.

The Mighty is asking the following: For someone who doesn’t understand what it’s like to have your mental illness, describe what it’s like to be in your head for a day. If you’d like to participate, please send a blog post to [email protected] Please include a photo for the piece, a photo of yourself and 1-2 sentence bio. Check out our Submit a Story page for more about our submission guidelines.

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