Dear BPD - A Letter to The Devil On My Shoulder.
Dear BPD,
I hate you.
You sneak around in the background, lurking in the shadows. Then you rush out at me, screaming, and make so much noise I just can’t think. You wear so many different masks and disguises, I never know what to look for from one day to the next. You rattle my nerves and keep me anxious – never able to relax and enjoy the moment because I’m always trying to head you off at the pass.
I hate you because you hold me back. Constantly whispering doubt in my ear about everything – parenting, friendships, relationships, work, hobbies, me and my abilities. You make me feel like I have to justify everything to everybody – even the fact that I’m here at all.
You stop me doing the most basic things that everybody else can just take in their stride, and when I stand up to you and attempt a display of defiance, you just laugh and punch me in the gut. I hate you because I have had to spend so much time and energy learning your ways, how to walk through each day avoiding you – how to keep you quiet. There are so many things I would rather have spent that time doing.
I hate you because there is no middle ground. Either you have stolen all of my energy and I can do nothing, or you are barking at me, sending me into constant physical and mental motion until I am completely exhausted. You sit in the corner, quietly pushing buttons and plucking at nerves while nobody is looking, until I explode with unprocessed emotion and have to deal with all the consequences that follow.
I hate you because to everybody else you are an all-encompassing label. People can just attribute all my behaviour to you and dismiss it, when sometimes, I’m actually just being me. You are a chain around my ankle, weighing me down - giving me just enough room to move so I think I can soar, then yanking me back down into your pit.
I hate you because my children deserve better.
But here’s the thing about you, BPD: as much as you want to be pulling the strings like some evil puppet-master, I will always have choices. Sometimes, I forget. But then I remember. I have choices, and that is why I will always come out the other side.
I choose to accept your presence, since you are never going to leave, and I accept the reasons you arrived in the first place.
I choose to accept that I have no control over the reactions I get from others – people are people and I am responsible for my own conduct only.
I choose to accept that if I incorporate management strategies into my daily life, then over time, you will get smaller and more insignificant. I will then have to waste less time focussed on you. I accept that sometimes, on occasion, you may still get a bit too big for your boots, but now I accept that that’s OK, because I can put you straight back in your place.
Finally, I choose positivity.
I choose to believe that you are simply a tiny part of my life, as opposed to the powerful, labelling force I could easily let you be. While I accept that hatred and resentment are two perfectly valid emotions that may well up from time to time, I choose not to let them overwhelm me.
I choose to learn from my experience, and use it to improve my parenting, friendships, relationships, work, hobbies, me and my abilities.
I make these choices because my children deserve better.
Yours calmly,
Sarah Myles
Comments
Many thanks for your comment :)
Sarah Myles
That's really kind. Thank you :)
LOVE your attitude!
Thanks, Jade
Thank you.
Sarah Myles
Thank you for your comment.
I'm not referring to myself as BPD, but rather to BPD as being something separate to myself. Hence the title "A Letter To The Devil On My Shoulder".
Reasons for using any diagnostic label to refer to one's own mental illness could fill a blog post of its own - which I may cover next time I post.
Thanks for the idea.
Sarah Myles
I don't feel the themes in this post are particularly complex. The letter is simply a reflection of how I felt at the time (and at many other times), during a "bad" day.
In terms of this process of creative expression being helpful - yes it is. Some people paint it out, some rock it out. I write it out.
Thanks for reading,
Sarah Myles
Thank you - that's a brilliant outline of that dilemma.
First off, a gentle disclaimer - I'm not a health professional of any kind, so my thoughts and comments are only ever based on my own personal experience.
I will blog about this in-depth at another time, but I do think that the way in which an individual deals with and accepts (or not) their diagnosis and/or illness is a massively personal thing. There is no right or wrong way to approach it, which is why it is such a long and difficult process.
My psychologist once pointed out to me that what little self-esteem I had was entirely based on the thoughts and reactions of other people, which is something I have no control over. At the time, I couldn't see what else I would base it on! Much later, that proved to be a very important realisation for me - helping change my thought processes in all areas, including my attitude to my diagnosis.
Thanks for joining in the discussion,
Sarah Myles
Not as much as I used to be, but I still have to work at it every day, like everything else.
At this point, it's still a conscious thought process I go through each time to head it off at the pass, but I'm beginning to see and acknowledge the progress I've made and that keeps me motivated.
Thanks,
Sarah Myles
This is a truly fascinating question, and I've been mulling it over all day. It's taken me through a really interesting thought process.
My instinctive answer is yes, it is metaphorical - but looking a bit deeper it's not actually that clear-cut. The BPD itself is a part of me, yes, but the way I regard it (I now realise, as a result of your question) follows the pattern of coping mechanisms I have unconsciously employed since childhood - the externalisation of anxiety. I've always followed this pattern (the result of emotional dysregulation) and it is the cause of many of my other symptoms - most notably my OCD. I have investigated that pattern through my treatment, but never really noticed I was doing the same with my illness.
It sounds obvious, but that realisation is something of an epiphany for me! Thank you for the prompt (and more ideas for future posts...)!
Sarah Myles
My anxiety developed from very specific experiences at a very early age. Externalisation as an unconscious coping mechanism comes directly from that - with emotional dysregulation making me unable to process or tolerate extreme emotions, my mind automatically projects them onto something outside of myself which I am able to physically deal with. I don't think I would describe myself as having become self-absorbed - I generally have very little regard for myself in any way.
I enjoyed your interpretation of the letter being a prayer for Grace. Personally, I am not religious (though I have come to my own spiritual beliefs), and so the letter really does not mean that for me. What I am noticing, however, is that the letter seems to mean different things to different people, and that is a very comforting response.
Many thanks for your comments,
Sarah Myles
Hi Maggie,
Speakup (CIC), formerly known as East Kent User Forum? I'd be honoured. I'd love to see it too, if possible. If you could contact me through my Twitter account (@sjmyles), I can let you know where to send/email it.
Thanks for your interest,
Sarah Myles
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