I’ve noticed during this period of depression and psychosis that I’ve been a lot more outspoken about what I’ve been going through. Here are a couple of posts I’ve made as an example of the sort of thing I’m referring to:
So basically they were a bunch of self-pitying, self-loathing, feeling pretty bad about being alive posts. I’m completely against the whole idea of Christmas this year and the whole festive thing is making me feel ill too, especially when our planet is dying and everyone is just looking on, laughing and drinking as they watch it burn. Also one picture is when I decided to smear acrylic paint all over myself and take pictures. I’m not sure that was the greatest thing for my eyelashes but it summed up my mania from that moment perfectly.
I began pondering whether I am actually doing the right thing by posting how I feel. After all, if I had a broken leg and was finding it hard to get around or I had cancer and was struggling with the side effects of the medication no one would bat an eyelid. I certainly wouldn’t. I would be thinking let that strong badass woman fight her battles however she wants to. Unfortunately I consider myself to be neither strong or a badass and prefer not to think about myself at all if I can help it. Just recently though I have started to accept that I AM unwell. I may have times when I am a bit better, times where I think everything will be ok after all, but the reality for me is that this IS my reality. I am on the best drug regime that my Doctors have found and it works in as much as I am more stable, I’m able to recognise when I need to add in an extra antipsychotic or anti-anxiety medication and although I still go through the periods of madness for the most part they are be shorter and less intense (touch-wood). So if I’m unwell and there is no way that I will ever be ‘cured’ why can’t I talk about it? Having Bipolar Disorder is bloody awful, it has turned my life up and down and up again and left me in a state of limbo that took years to free myself from.
So when I post a picture of myself with my hair tangled into what can only be described as a bird’s nest or share an Instagram story in my PJ’s complaining about whatever physical or mental symptom I’m suffering with, (yep, lots of physical symptoms are part of Bipolar too) it isn’t me looking for sympathy or a reaction. It certainly isn’t me boasting about being at home all day and not being able to work (I would give anything to be well enough to earn a wage and contribute). It’s me posting my life, as it is for me. There may be photo’s of me all dressed up but again these just show a snap-shot of my life. A single second in a day of 86400. Sometimes I’ll get all dressed and be about to leave but then my anxiety kicks in so I end up stay at home, feeling defeated. Sometimes I can be crying and raving, seeing monsters and hearing voices and then an hour or so later I can gather myself together enough to maybe get a coffee of take the dog for a walk. Sometimes I wont leave the house or wash or brush me teeth for a week.
What I’m try to say is that this is my new normal. My new normal is abnormal and I never know what is going to tip it one way or the other although I am getting better at recognising triggers all the time.
I miss my old normal, even if my old normal was littered with episodes of mania which were the most exhilarating and destructive times in my life and the deepest suicidal depressions. At the time I fumbled along as best as I could, seeking advice from friends and being told ‘it is what it is’. What does that even mean? It is what it is? I didn’t know so I carried on stumbling along in the dark until I found the light in my life and my saviour and began to recognise that maybe it wasn’t just that I was a reckless, unemotional wild thing on a mission to self destruct but someone who actually had a medical condition which could be helped. I don’t know where I’d be if it weren’t for my soulmate, I certainly don’t think I’d be here anyway.
So that’s it for today. My meds make my brain slow and this has taken me an absolute age to type. Apologies also for typos and grammatical errors. I’m normally so fastidious but even sending a quick text is taxing at the moment so I doubt my proof-reading is up to much. If you know me in real life feel free to reach out to me. In fact PLEASE reach out to me. Long term illness, especially psychiatric illness, is a very lonely place to be and lets face it I haven’t got many friends after my last big manic blow out. So maybe just say Hi, I’m just trying to be a strong, badass Woman beneath all the tangled hair and dirty pyjamas and trying to find my way in this ‘new ‘normal’