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Updated: Jan 19

Me manic, me depressed, me healthy
Me manic, me depressed, me healthy

Many people don’t realize that bipolar affects not just my brain but my actual health. The photos above were all taken within a six month period, in my opinion I look like a different person in each of them. This summer my kids went through some very challenging things, even with my best effort it still impacted me deeply, I ended up manic. People also don’t realize that because of my mental illness I don’t always seek out the medical help I need, therefore I can go long periods of time with unaddressed health issues especially if I’m having episodes, which is what happened this summer. I had a physical collapse and ended up in emergency. I eventually found out I was dangerously anemic and my blood pressure was really high, it took me being barely able to walk to seek help. People think mental illness is just in our heads, but mental illness impacts ALL of my life. My brain is literally the lens in which I experience the world and when it’s not well many areas of my life are impacted, including my physical health, I think the photos above really show the reality of this.

I share this to share the reality of life with mental illness, for those that live with these challenges it’s an ongoing battle with our own brains for our health, it’s why being supportive is so important, sometimes when we are not well we neglect ourselves to a dangerous end.

 
 
 

I grew up with the bible, and some things I read growing up make sense to me now, like this scripture:


“It is better to go to a house of mourning than to go to a house of feasting, for death is the destiny of everyone; the living should take this to heart.”


As a young person this scripture seemed backwards, having a good time is…..well a good time.

But as an adult who has had many challenges and losses this bit of the bible makes sense now.


It’s easy to be around people in a perfectly staged setting, when they’ve got it all together, or during a happy season. It’s easy to be there during a good time, it’s much harder to sit with others as they grieve and weep and ugly cry. But those are the times people need presence most. Everyone loves to be there for a party, but often as humans we grieve alone. Grief is something we all have in common, but humans often feel awkward around heavy feelings.


Being present when someone is weeping is a privilege, it’s incredibly vulnerable to express pain in the presence of others, our first instinct often is to hide our pain. Crying in the presence of others takes some trust, offering trust and safety is exactly what those who grieve or are sad need. The awkward feelings happen when we feel the need to fix things. When I am sad or grieving I don’t want to be fixed, I want to know I’m not alone, I want another humans presence. The knowledge another person is there and has felt pain too.


Don’t we all want that….presence in the good times….and the bad times, I certainly want that, and I also want to aim to be that for others.

 
 
 

Updated: Jan 16



Growing up without the label of neurodivergent felt like every difference I had was made into a failure of character. Being unable to connect socially became “socially awkward”, it meant always feeling on the outside of life and being treated like a burden for wanting what everyone else seemed to access so easily, things like being included.

Expressing honest feelings became “being dramatic” or “overreacting”, Often times I was treated like my very real feelings were overreactions.

Being blunt and straight forward became “rude”

Asking for clarification became “nosey and annoying”

Needing more rest then others because of overstimulation became “laziness”

Having extreme mood shifts became “attention seeking”

Sensory issues become “fussy”, or “picky”

Almost every neurodivergent trait I had was made into a character failure by family or religious beliefs. I masked heavily for years.

After a breakdown I had to begin to take myself seriously, even if others didn’t.

I had to rally for myself with the support of my partner.

And it was hard. People will show up to cheer others on at a marathon, people tend to go pretty silent when others share about the difficulty of recovery from mental illness……

When I finally started getting help I was at a point I felt stripped of everything. I could barely leave my room….yet house. I was put on stronger anxiety meds and that went very badly…..I soon was back on the phone with my dr (I did phone appointments for nearly 3 years, because I could barely leave my house) and he began asking some questions, questions that led to my bipolar diagnosis, which then changed my treatment. I’m not that far into recovery, and recovery is what this experience has been. I went from barely leaving my room, to starting to go downstairs more to now beginning to cook more often and tidy without overwhelm. I now can go out a bit more without panic.

All this to say when I was finally diagnosed I was in a state, I had tried to hurt myself. It has taken years to come back to feeling more myself. Going undiagnosed was a living hell. There isn’t a word to describe the state I was in, the exhaustion of feeling everything at maximum intensity, to a painful intensity. I was experiencing mania then depression on rotation for years.

Living undiagnosed nearly killed me, and I remember telling people about what I was experiencing and it wasn’t really a blip in their radar of caring, yet it was one of the hardest things I’d ever been through. I felt as many neurodivergent people feel, alone, misunderstood and not taken seriously by people whose support I needed.

The people I relate with most are other neurodivergent people, they understand the experience of being continually misunderstood and continually having needs ignored. The same people who claim to be kind, understanding and empathetic don’t extend that attitude towards neurodivergent people. So neurodivergent people go through years of the pain of being undiagnosed, and eventually find out the cause of all the struggles only to be treated like our diagnosis hasn’t or doesn’t impact us, and often we are simply not believed or taken seriously.

I hope living undiagnosed into adulthood stops being a reality for people. I hope as information continues to become more common and made public people will seek help earlier. I also hope neurodivergent peoples experiences will be believed and the pressure to prove our diagnosis stops being a thing. I hope the rate of severe burnout that is too common for neurodivergent people goes away because the proper support becomes more accessible to those who need it. As always I hope for a better and more accessible world for myself and everyone.



 
 
 

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