Of drugs and other things
Over the holiday weekend I realized that soon bloggers will start compiling lists of “What Happened This Year.” I started thinking about the year in general and boy has it been a rough one. I realize I am quite young to say this but it may have been one of the roughest years of my life. Also, gonna go ahead and say that I use writing for therapy. Sometimes just writing things out and hitting publish helps me to get some things out of my mind, which is a far better alternative to letting them rattle around in there on their own for days and days.
In January I started a 20 week Accutane treatment. I can’t recall if I ever mentioned it here; it was an extremely rough time. I thought almost everyone knew what that horrible poison is but apparently, some do not. It’s technically a drug called isotretinoin and is used as an aggressive acne treatment. This is what dermatologists put you on when all other methods have failed. Methods such as but not limited to hormonal birth control, various cleansers and creams, and months of antibiotic treatment. I was in such misery emotionally and physically (it was painful for areas of my skin to be touched by my clothes) and in danger of scarring my face that I signed up for the overwhelming list of possible side effects. If anything, the knowledge that certain side effects were simply possibilities, especially those that affect pregnancies (trust me, it’s terrible, they put pictures on every single 10 packet of pills; I had to take two pills a day so I saw the pictures a lot), scared the ever living daylights out of me even though I never experienced some of them. I have no doubt that I suffered more than a little depression as a result. It was a horrid, terrible experience that I hope to never put myself through again. At this time I do think it was worth it. I was becoming depressed anyway and my little self esteem was plummeting.
To say that I was excited for my treatment to end in June and my last dermatologist appointment in July is a huge understatement. My skin is miles better than it was and whatever does come up will be dealt with. It will take a lot to make me even think about considering another round of Accutane.
One of the many potential side effects of that vile stuff is headaches. While I was taking it I brushed off anything I had as being due to it, took some tylenol or whatever and that was it. I didn’t keep a close track of anything but I think in July they started to get worse. Still no problem, Excedrin Migraine and some sleep fixed everything.
Then. Then came August 26 and… something that left me in such pain and discomfort that I was barely able to sleep for two days and no pain relievers worked. That started a cascade of doctor’s visits, prescriptions, diagnostic tests, insurance hassles, and ~SIDE EFFECTS~ Pesky thing about drugs: they seem to break more things than they fix, sometimes. After determining that I have no tumors or some other cause of my headaches my neurologist decided to bump up the anti depressant I was put on in order to try to prevent the headaches. By the way, it bothered me to find out after I had my prescription filled that it was an anti depressant. Shouldn’t doctors be telling their patients what sorts of things they’re being given? Anyway. The increase? Big. Mistake. After experiencing crazy heart rates (120 while sitting!!) and bizarre vertigo they backed it down. After weeks of that, though, it didn’t seem to be doing any good. Solution? Switch to another drug! Start Topomax at 25mg and increase to 50mg after just a week. And by the way, side effects for this only include confusion, inability to concentrate, forgetting things, small stuff. Oh yes, while not an anti depressant it can increase depressive thoughts. Just a few days after I went to the higher dose my lips and eyes to twitching enough to drive a person insane. Back to 25mg it was.
That’s where I am now. Except I don’t think the lower dose is really doing enough to prevent the headaches. But what can I do? A higher dose will drive me crazy and I’m talking certifiably, not the “she’s different and that makes me uncomfortable so I’m going to call her crazy to make myself feel better” type crazy. I honestly feel like I have absolutely no way to tell what is or isn’t helping. I have a very sneaking suspicion that stress is playing a huge part in this giant cocktail of whatever it is that’s wrong with me. That Which Shall Not Be Named has caused more than its fair amount of stress this entire year. (I am most curious to know which sentence in this post wins “Understatement of the Year.”)
Life has been stressful. Add in the smorgasbord of drugs that I’ve been on this year it is absolutely no wonder that I feel like an emotional wreck right now. I really don’t understand it myself. There is not one single thing that I can pin down (I might be lying to myself right there but will leave it as is) but I am just super unhappy, especially here in the last few weeks or so. And you know what? I’m tired of living like this. I used to wonder why when researching different headache disorders so many different sites suggested support groups or counseling or therapy for pain management for the person with the disorder and the ones close to them. I get it now. When there is absolutely nothing that anyone can do life turns pretty bleak. You don’t want to always complain about feeling bad yet there are no times in which you feel better. Your friends and family want to help but when they know that they can’t even fetch you a tylenol to help it sucks. The doctors seem to be treating you like a science experiment, guessing how much of which drug to give you.
So. I am endeavoring to change what I can. I have no solid plans at the moment because there are a lot of things I don’t have answers for right now. And even if I did, That Which Shall Not Be Named is so called for a reason. What plans can be wisely and safely shared will be. Gosh, that makes it sounds like I’m planning a rebellion or something equally nefarious. I’M NOT. I SWEAR. I’m just altering my outlook and goals. (Does that sound better? Maybe?) More of which I will be saving for a later day. It is late and I let myself get distracting researching symptoms on Wikipedia. FYI, NOT a smart thing to do to yourself at 11:30PM. But for what it’s worth, I’m pretty sure I don’t have fibromyalgia. Mostly sure.