So I was re-reading the first post I made, it kind of skimmed over my history with this illness. And I mean it was a VERY abridged version, there’s so much more depth that I didn’t even get in to, but I would be at this keyboard for a week going in to all the nuances. I did go in to depth on how an attack makes me feel, like I need to get away and get help from somebody, anybody, nobody. My ways of coping and working through an attack really vary as to what symptoms I’m feeling, as how my attacks manifest themselves have changed over the years as well. It was the head pressure at first, next was heart palpitations, next was a tightness in my chest that feels like a pallet of brick is weighing my chest down making it so hard to breathe. All of it manifests and sends my brain into fight or flight mode pretty quickly. It’s quite hard to trick myself into believing it isn’t real, that no, I’m not going to die. So I guess if I really do (God forbid) have a heart attack or a stroke one day I’ll be sitting there trying to convince myself that I’m just psyching myself out again!
I have a few different ways I’ve been coping with my attacks and the build-up symptoms, some work almost all the time, some only work seldom. I like to keep my mind busy when I can feel one coming on, first thing I do is watch a movie or go do something on the computer. Laying down and relaxing really doesn’t do much but accelerate things, gives my mind time and space to think and self-analyze, which is a BIG no no for me. I also like to hang out in the bathroom. I know, weird, right? It was the first place I ran to when I first started getting my attacks and ever since then there’s been some calmative effect associated with the restroom. I’ll usually look at myself in the mirror, study my skin (which almost always is in need of a good aesthecian), extract blackheads (ew, I know), just breathe and try to put my mind back in a better place. My boyfriend has recently introduced me to taking a walk when I get anxious, not too bad when it happens during the day but at 1am it’s hard to do. I’ve gone out to Walgreen’s (which is 24 hour by my house) and shopped during my late night attacks. It gets me walking and my mind thinking about something other than my attack, but it also leads to $50 tickets at the register (Ooh! I need more shampoo, let’s get THIS ONE with the NEW SHINY LABEL! Price?!?! Who cares?!? New makeup? Don’t mind if I doooo!).
I’ve been able to do without a daily therapy medicine for a lot of the time I’ve had this disorder. I do know when I’ve met my match though and need some “better living through science”, as my boss likes to put it. I’m beginning to think that soon, very soon, I’ll need to go back on daily therapy. I’m giving myself a little more time to see if it was just an unusually rough patch I went through or if my disorder is morphing yet again and until I can learn to cope with this new wave of changes I need a little help. I don’t like to ask for help but I’m not afraid to anymore.
Well, I think I’ve said enough for now. As I type my 2 little monsters are splashing in the bath, probably making a soggy mess of my bathroom. It all dries though, I’m not worried:)
~Amber