Sunday, April 26, 2020

Accepting My Bipolar Disorder Diagnosis

By National Institute of Mental Health (NIMH), National Institute of Health (NIH), U.S. Department of Health and Human Services. - https://www.nimh.nih.gov/health/publications/bipolar-disorder/index.shtml#pub1, Public Domain, https://commons.wikimedia.org/w/index.php?curid=80579612


 
Getting sick is a typical part of one’s life. But however minor it may be, nobody wants to experience such. We want to remain healthy and free of any medication. But what if you’ve been diagnosed with an illness that would stick with you for the rest of your life?

Pre-Hospitalization

Three years ago, I was living nonchalantly as a law student in my second year. It was tough but manageable. I was determined and set on a goal to finish that winding journey despite some poor grades, bad recitations, and failed subjects. There was still a chance, I kept consoling myself. Prayers and study time were there. I also bonded well with my family and friends. Everything seemed right.  However, things would go downhill one day.

My mind started to be hyperactive, making me too alert and awake that I cannot go to sleep. Back then I started to think that my brain overclocked like that of a CPU. My mood was elevated unexplainably. I just thought it’s attributed to me reading some articles on boosting your self-confidence. The tipping point of all of those was what I considered as “vision” back then of nuclear war after my sleepless nights. It made me cry so hard. Lastly, I became suspicious of the people around me.

Attempts on poisoning me, reading people’s minds, the house being bugged, FBI monitoring me, and so on were just some of the things I felt that seemed so real. It felt too realistic that when my Dad was telling me that we should go see a doctor because something’s wrong with me, I didn’t believe him. It reached that point where he had to ask four strangers to enter our home to forcibly bring me into a vehicle. I knew back then I was done—finished. “I am not doing anything wrong,” I told them. They would then reply I’d see a Doctor. I would, however, interpret it as a moniker for their evil boss.

Confinement

My arrival at what I considered as a safe house for kidnapped victims was rough. I panicked. But everyone seemed so calm so I asked what’s wrong with them. I didn’t know it was the other way around. I was the one in need of fixing. Those things I experienced eventually had a label—delusions and hallucinations. I had psychosis, a symptom of mental illness.

My stay lasted for two months. During that period, I took medications, both oral and injectable. My family was also allowed to visit me after my first month every weekend. We were emotional during our first meeting as I faced them with the realization of what had happened to me. As I was nearing my discharge, I was pumped up to resume what I missed.

Discharge

Returning home felt surreal. I was in disbelief about my behavior two months ago in the same house. Was it really me? Did it ever really happen? Those were the questions popping on my mind. But what I was certain was that it’s not the same anymore. I can’t feel the excitement I envisioned and expected. I lost interest in everything (called anhedonia) like playing games or watching movies. And my sleep still hadn’t returned to how it’s used to be. “Is this the new normal that I have to live with?”—I asked myself. So I researched how to fix my predicament. I learned these could be an after-effect of having psychotic episodes, symptoms of depression, negative (lack of or loss of) symptoms in mental illnesses like schizophrenia, or side effect of my antipsychotic med.

I ended up trying to seek help from a quack doctor, stopping my medications without Doc’s approval, seeking opinions from two other psychiatrists, and switching medication.

At present, I can say that things have improved over the past three years that I’ve been on meds and regular consultation with my original shrink. It’s just recently that he confirmed that I indeed have Bipolar Disorder I. He claims it’s like a ticking time bomb or an innate seed within me that went full blown after varied stressors got the best of me. That’s why it just manifested at age 24 (going 28 this year).

In a Facebook support group I was in, there was someone who said he has been on meds for a decade and continuing. Reading that comment upon my discharge felt alarming. Who would want to be on meds for life? Not me. But as days went by, I had accepted this new life that’s before me. 

Scripture

Among the many factors that helped me cope was this verse (2 Corinthians 12: 7-9):

...Therefore, in order to keep me from becoming conceited, I was given a thorn in my flesh, a messenger of Satan, to torment me. Three times I pleaded with the Lord to take it away from me.  But he said to me, “My grace is sufficient for you, for my power is made perfect in weakness.” ...

Here, St. Paul the Apostle was given a thorn in the flesh that was not removed despite his deepest desire. In exchange, it made him more humble and dependent on God’s grace. Meditating on this passage made me thankful for the blessing of humility.

Key Things

Other factors that helped me accept my diagnosis are the following:

1) Going through the denial phase
Despite this being a negative one, I think it’s important to highlight the role of this stage in each person’s recovery whatever illness it may be. This helped me transition toward the new normal and made me learn that holding on to what had been in the past is not always healthy. It made me value what’s in store for the fresh start I needed to have.

2) Discussing in support groups
I did this online through Facebook primarily. If you’re not yet feeling confident enough to disclose your real identity (like me back then), a second account could help. Do this until you’re confident enough to use your actual one. This outlet was really helpful as you get to know people with similar situations and even chat with them with their permission. Good support groups have established rules and moderators to ensure members they are in a safe place even if it’s virtual. Message me for those I recommend.

3) Try not to overreact to people’s misconceptions
When I was barely a month outside of the psychiatric ward I was in, I’d get triggered easily by people who’d belittle mental illnesses. It would make me put myself on an unnecessary mission to educate these ignorant people that it’s a real sickness. But this made me anxious and stressed. Now, I learned that I can still spread awareness in a chill and calm way. The key is to not take it personally. We are not our disorders.

4) Keep your condition a secret not due to shame but for your protection
Some might say it’s okay for them to be open in talking about their mental health issues with anyone. But based on my Doc’s advice and my experience, it’s better not to mention it unless in very important cases. An example would be if you have anxiety and panic attacks that would significantly affect your work. So take the time to choose the person or people you’ll share this secret with as this can be used against you (worst case scenario of course). When you get to pick the right ones, it’ll feel rewarding and comforting at the same time.

Conclusion

I hope you found my first entry worthy of your time. Though not yet 100% back to my original self, I’m getting the hang of it. Let’s endure and enjoy our precious life whatever circumstances we might be in or might face. Having bipolar disorder or any mental illness is not easy. But with faith, professional help, and a support system, we can keep going. You can send me a message at neoalva.info@gmail.com for questions or maybe casual conversations.

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