Things I Wish I Was Told When Diagnosed With Depression

Things I Wish I Was Told When Diagnosed With DepressionAll of my remembered life I have been depressed. Therefore, depression feels deeply entwined with my identity. Most of that time I felt ashamed of being depressed and, therefore, ashamed of who I was. This is the tragic nature of the stigma surrounding mental illness. Because of the stigma, I thought I was alone, and, that I should keep my symptoms to myself for the benefit of others.

I can only speak to my feelings and experiences of depression, but it feels important to normalize some of the realities of mental illness I faced. I think it would have served me greatly to understand these components of depression earlier in my diagnosis. I am not clinically an expert, but, I have spent 10 years living with and navigating this diagnosis. As such, I have compiled some of the things I wish someone had told me when I first became depressed.

  • It’s scary to lose a feeling of connection to your dreams.
  • There’s a dull, aching numbness that comes from looking at something beautiful and feeling indifferent.
  • Even when I experience excitement for the progress and successes of those around me, it’s really painful to watch the world go on when I feel like I can’t.
  • Sometimes my thoughts are wrong.
  • My feelings are never wrong, but, they may be a byproduct of distorted thinking.
  • Managing mental illness is never linear and it can feel really devastating when the valleys arrive.
  • Sometimes I will feel unbearably scared.
  • The genetic component to my disorder will make me more vulnerable to major depressive episodes due to external triggers.
  • My depression will wear different masks, exhibit different symptoms, and I will not always be able to detect its presence using the same criteria.
  • Managing mental illness is exhausting.
  • I am often my greatest obstacle.
  • Depression and trauma are often accompanied by somatic expressions of these experiences.
  • I will often be asked to choose life when I really don’t want to.
  • Psychiatric facilities in hospitals can be really scary.
  • People will feel frustrated by my symptoms at times, especially those that have chronic nature.
  • Some people won’t be able to sustain a relationship with me, romantic or otherwise, due to my illness.
  • I will have to live my life differently than I may want to.
  • I will often be met with doubt when it comes to the validity of my statements.
  • Sometimes I will simply have a day.
  • Not all depression is the same. Try not to feel discouraged when methods that are useful to others are not for you.
  • Waking up and surviving can be an incredible accomplishment.
  • People whose intentions are to help you may not be actually doing so. It’s okay to let those people go.
  • A medical or psychiatric doctor’s arrogance has the potential to be dangerous.
  • No one is going to “fix” me.
  • Try not to be too preoccupied by the fact that a major role I will play in life is that of a patient.
  • It’s really brave to communicate when I am having the urge to cope with maladaptive behaviors.
  • An absence of feeling, numbness, and indifference hurts in a different kind of way.
  • Treasure laughter.
  • My unexpressed feelings will not vanish. If I eliminate verbal expression, I will likely find myself communicating behaviorally.
  • Normality is a social construct. I must try not to feel discouraged that my path deviates from the norm.
  • My maladaptive coping mechanisms came to be as a protective measure. Try to have compassion for them.
  • I must try, even when my brain insists I shouldn’t, to have compassion for myself.

I hope that through sharing my experience, even one person can feel slightly more understood. Living with depression is inherently difficult, but, I believe the more we talk about it, the more we shed the stigma, the more bearable it becomes. I believe we can all learn to combat our depression, but, it’s a lot easier if we do it together.

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