Okay that last bit I lifted from an old, haunting story Mija wrote about a girl who suffered this fate at the hand of her top. I reread the story the other day after thinking how much I was starting to feel like a ghost-girl, albeit one who has had even less choice in choosing my circumstances. It's not just that the illness makes me feel like shit all the time, but illness also includes a never ending list of bureaucratic issues - appointments to make, transportation to schedule, prescriptions to order and manage, Medicaid & Food Stamp re-certification with receipts and letters and bank statements to sort through, Home Care Worker to hire, Home Care Worker benefits cut due to the state budget shortage, state officials to lobby, medical clinic changes narcotic pain management policy, doctor decreases narcotic meds even though my pain has not decreased, doctor tries out other meds with varying effectiveness, surgery to have, surgery to recuperate from (successful on both accounts), Home Care Worker benefits restored (yay!), Home Care Worker to hire (but now without A.'s help), medical clinic refusing to relent on pain meds, more tinkering with meds (sleepy, nauseous), Home Care Worker hired (yay! oh please work out this time!), letters to be written to medical director and state pain commission, pain meds going down...down...pain going up...up.
For the last month and a half, the bureaucracy has been like climbing a vertical face.*
I'm probably starting to sound like Eeyore on Twitter anymore. With a brief break in the woe a week ago to celebrate -- sorta -- the recent finding that the connection to XMRV made last October has been confirmed -- sorta -- by finding retroviruses related to XMRV in another group of ME/CFS patients (aka the Alter/Lo paper). On the one hand, any hope right now that there might be real treatments for this illness besides lots of narcotics, expensive supplements, and extortionate experimental treatments is helpful. But knowing that it's still a few years away whereas this Saturday I begin tapering off the Vicodin I've been on for years now makes it all a bit...inadequate.
Kink and any energy to write about it jumped out the window after I posted that first of a two part post that I thought I would quickly follow with a second (I just knew that was going to happen if I posted the first part without have the second definitely done!). Lord Something-o-ruther didn't even let me post anything when the six year anniversary of this blog (August 10th) came and went (can you believe it's been six years already? can you believe it's only been six years given all that's happened?). A couple of weeks ago it did let me take my post-surgical pelvis/abdomen for a spin (like any dom, it only allows me to masturbate with its permission). I wanked and came with little pain - certainly none of that horrible, feels-like-I'm-ripping-something pain I had pre-laparoscopy. So, you know, very cool! But as the horrible, feels-like-someone-is-burning-me-from-the-inside-out pain that I live with every second of every moment of every hour of every day in my arms and legs was increasing because my doctor was required to reduce my narcotic medication, Lord Something-o-ruther had tied me up and locked me in the closet again.
Until this weekend. Natty came back. Mostly because my doctor was able to switch me back to my earlier narcotic dose -- but start tapering down again -- as well as try an increase in an anti-seizure medicine I also take for pain so that my pain has been back to being quite manageable for a couple of weeks. Sure, I also wanted to sleep more. But laying in bed in a drug-induced reverie was the first moment of freedom from Dom Lord Something-o-ruther I've had for awhile. I could actually think about something besides it. I could be little again. At first Michelle was having none of it. My grown up self was still climbing the vertical face -- which is clearly not an activity for kids.
Or is it?
I've been wanting to write about the dominance of my grown-up self (the real Lord Something-o-ruther?) versus my Natty self (along with the legion of other topics I've thought about while laying in bed -- alas, the dearth of posts is never because I don't have anything to say). And I don't know that I'll get into the full analysis I've been pondering over the last few months tonight. But as I've been vomiting out all my white-knuckled frustration of the last month and a half onto this Blogger compose interface, it wasn't until I wrote the above paragraph that I remembered how much I need Natty. Many years ago my therapist told me to treasure her. But lately I've wondered how to do that. Or even if I should do that. I mean, isn't she just this way I escape reality when I can't handle it? Isn't it healthier to just learn to live with life the way it is rather than hide away in some overactive part of my imagination? You know, embrace the present, yada yada yada (which is also what that therapist said)?
And then I remembered the last bit in that first post with which I began this here blog those six years ago about rediscovering Allie (proto-Natty) when I was first getting sick and disabled ten years ago.
I realized how much I needed her back. Her emotional energy. Her willfulness. Her playfulness. Her immature selfishness. I need her to feel the feelings my intellect has long ago explained away. To temper my endless caregiving with the demands of my own needs. To stamp her foot and say, “it’s time to play.”
I actually (with tongue somewhere in cheek) list as my occupation "personal care coordinator" as that really is what I do all day when I'm not sleeping or trying to eek out a social life online. And Personal Care Coordinator Michelle needs a break. She needs Natty to help her play. Especially as the coming weeks are going to be hard. Distraction is an important pain management tool and after next Saturday I'm going to need to use every non-narcotic tool even more than I already do (meditation, yoga, qigong, physical therapy, massage therapy, acupuncture, heat/cold, supplements, non-narcotic prescriptions, warm baths, guided imagery...). My doctor has me on a list to have my case reviewed by an Opiate Review Board, but I have no idea when that will be or if it will be successful. I feel hopeful that at some point we'll get me back to an adequate narcotic dose or find some other medication to help (not that we haven't already gone through just about every anti-seizure or anti-depressant that's also used for pain that my insurance will cover) for no other reason than I can't imagine being in that much pain for an extended period of time.
So Natty plays. A. gave me my first tele-spanking in months the day before last. It was just a handful of quick strokes and yeah, my shoulder was quite sore the next day (that's why a quarter of my freezer is devoted to ice packs!) but I'm hoping we'll be able to play some more over the phone this week. And, of course, A. and my illusory Nanny are already helping me manage my activity levels since overexertion exacerbates my pain and gives Lord Something-o-ruther an excuse to lock me away in a dungeon that's anything but a playground.
Hmm...Maybe that's another way Natty helps me with illness....Oh dear, speaking of managing my activity level, I've just got so carried away with my de-facto journaling here that I totally lost track of the time. Like, wandered away from the track and the field and have been following a butterfly so far into the woods that the roads no longer have those green street signs but wooden posts with numbers...
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*And just to make life even more fun than it already is, I found out last Friday my apartment building is being remodeled in November requiring us all to move out for a week. They are hiring third party movers to pack and move our stuff (which is good cuz I can't do shit!), but I'll have to unpack everything once they're done. All 1200 books, etc. that took months to unpack... ::sigh::
Note: September is Pain Awareness Month. If there is anything I've realized from this experience with the change in narcotic pain management policy at my clinic is that nobody with chronic pain in this country is safe from interference with their narcotic pain medication. I always thought that because I did everything right and I had a caring, competent doctor, I was fine. But not only is the War on Drugs locking away people who don't need to be and crippling us economically, but it's also keeping sick people from getting the treatment they need. Yes, pain builds character but chronic pain also atrophies the brain and may increase your risk of death from any cause by as much 49% - up to 68% if just looking at cardiovascular-associated mortality. (I keep meaning to do a post(s) on the science of pain and spanking...) The next time you see a story about prescription narcotic addiction, remember all the people who are are not getting their pain adequately treated (or treated at all) because of the overhyped fear of narcotic addiction. Yes, addiction happens (though to less than 1-2% of those using it for pain). Yes, narcotics will kill you if you don't use them right - as does my Coumadin.
::stepping off soapbox and off to bed::






