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Real Stories

Just a small bit of advice

*Content Warning: This piece contains a reference to suicide, which may be triggering to some.* 

Someone asked me recently what advice would I give to a person newly diagnosed with mental illness. That question has stuck with me since. It’s a tough one. Takes a lot of thought to answer.

I think about what I wished someone had told me when I first was diagnosed with bipolar disorder. But I’m not sure I cared at the time. No matter how good the advice, I’m sure I wouldn’t have listened. I was off in my own chaotic world. No matter how much external input I got, I wasn’t receptive. I was reaching out to my psychiatrist, but it was only because life had become intensely overbearing and I had no other options. But even then I wasn’t being open and transparent to my doctors, I wasn’t truly investing in getting help.

Then I think about the things I wished I did at that time, and the things I wished I hadn’t done. And I think about how I wasn’t being receptive to external advice and what I might have been open to. What was I capable of doing in those moments that could have made a difference?

In times of depression I sought out support more readily because deep down I didn’t want to have to resort to suicide to escape the weight. Before I was diagnosed with bipolar disorder, I only talked to my psychiatrist about the depression. But what would’ve happened if I talked about my moods in those therapy sessions that my depression wasn’t ruling my life?

What if I had voiced more of the feelings and emotions trapped inside my head? I really had no understanding for what I was going through and maybe my psychiatrist could have intervened more if I had said something. Maybe if I hadn’t disregarded the shifting moods, I would’ve gotten my bipolar diagnoses sooner. Maybe I wouldn’t have made some of the mistakes I made or maybe I would have received better help from my support.

I never mentioned the racing thoughts and the early episodes of mania. I never understood that the internal chaos I was experiencing was not normal until it exploded and impacted my external life. Because I didn’t express what was going on with in me, other than life feeling devastatingly dark, my mania built up and leaked out into the world. The anger, the discontent, the rush of moods overpowered me until everything and everyone around me were engulfed in my psychosis.

Maybe if I had said or even written about feeling endless amounts of energy and riding high above the clouds, someone would’ve recognized my instability. If I had just voiced that my mind was filled with so many racing thoughts that I had trouble processing basic tasks. If I had expressed the immense amount of anger that controlled everything I did. If I had told someone I felt like rebelling against everything good and stable in life and running away to the moon, maybe someone would have changed my diagnosis sooner. Maybe if I had talked more about my experiences in the times without depression, it would have prevented the life altering decisions I made during mania.

But maybe not. I can’t change the past. But these thoughts lead me to the answer to the question.

If you are newly diagnosed with mental illness, do your best to speak up and get help. When talking to your therapist or psychiatrist, tell them about all the things in your head and all the moods you experience even when it seems like overkill. Just because depression may be the underlying reason you’re reaching out, doesn’t mean there aren’t other things you need help with. Just because you don’t recognize the instability in your life, doesn’t mean someone else won’t. Talk about all of your struggles, maybe it will prevent future heart ache. Maybe voicing your experiences will get you the type of help you need sooner and more effectively.

Have hope. Speak up. Pursue help.

Comment
by Christi Anne Ng

People always say your illness doesn’t define who you are, but honestly I completely disagree. I am my disorder. I am bipolar disease. I wouldn’t be who I am today without it. And at several points in my life it controlled me, but I am happy to say today it does not have as much power over me. I don’t think defining myself by my disease is a bad thing. I think it gives power to how much I have overcome.

Hi, I’m Christi Anne and I’m bipolar. It’s a part of me. It’s my friend and it’s my foe. On my bad days, I am insane and psychotic. On my sad days, I am depressed and bed-ridden. On my good days, I am unstoppable.

Mental illness has never been unfamiliar to me. I started seeing a psychiatrist when I was 7. My mom always says I was her easiest child until I started going to school. So 7. I started going crazy at 7. ADHD was the first diagnoses. I remember certain days in 5th grade when I was bouncing off the walls and just would not shut up, my teacher would pull me aside and whisper, “Did you take your medicine today?”

Of course, I didn’t.

I’m 10 and I want to be bouncing off the walls.

Little did I know, these were the earliest days of mania. But I actually don’t remember much about my childhood. Another lovely side effect of my beautiful disease, memory inhibition. And what I do remember, I only think of negatively. I remember the anxiety so high that my heart would be beating out of my chest and my muscles would feel stiff. I remember depression so low that the floor of my bedroom was the only place I could be, wailing until my tears turned dry. I remember rage. Oh how I remember rage. I remember kicking a hole in that wall. I remember screaming at the top of my lungs. I remember my vision being blurred with red.
I wasn’t even diagnosed with bipolar disorder until I was 18. It took me moving to Chicago, spending a total of 2 days on my new college campus, then running away to get the diagnose. I don’t blame my doctors though. I’ve had very good doctors. I’m just a really complicated patient. Plus, I didn’t ever understand myself enough to express to the doctors what I needed help with. I didn’t think the anger and rage was unusual. I just thought the anxiety and mania was normal because I didn’t know otherwise. So in those therapy sessions, I only talked about the depression. I only discussed the intense sadness that overcame me and the times I felt like killing myself.

It wasn’t until my “brief college experience” did I open my eyes to the intense high followed by crashing so low. Even then, it wasn’t that clear to me. All I knew was my mind was racing and I felt totally and completely insane. I called up my parents begging for someone to save me and give me a break from my mind. I couldn’t handle being with my thoughts anymore. So they flew me out to their house and signed me up for psychiatry again. It was then when the doctor said, “It’s called mania. You’re a manic depressive.”

And oh I wish it was a quick fix then and there with the diagnosis. It would’ve prevented a whole lot of broken relationships and damaged souls. But again, I’m not that simple. It’s been 6 years and I’m still battling this disease. But now I can confidentially say I am surviving.

I take six different medications on a daily basis. Yes, six. And I wouldn’t hesitate to add more if needed. I dedicate my life to my medications. They have saved me from my mind. I have found a mental illness cocktail that works for me. And after 6 years and 6 medications, I finally feel hope. I see a bright and successful future down the path. And I am excited. And I am happy. Yes, happy.

If there is one thing I would want people to understand about me, it would be that every day I have to make the decision to get up and be stronger than my illness. That rolling out of bed and getting started with the day takes immense amount of energy. Because every day could have the potential for mania. Honestly, there is not a night that goes by that I don’t wish I could close my eyes and stop my mind forever. But the morning always comes and I always decide to wake up.


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