woah woah woah, so a few of the comments on this article say that the title is misleading. 40% of Americans do not make less than 1968 minimum wage ($1.60/hour - source), the purchasing power of the minimum wage in 1968 ($9.22/hour in 2012 dollars - source) or the 1968 minimum wage adjusted for inflation (which I can’t find a good source for but looks like it would be about $10.00/hour). what they’re saying is that 40% of Americans make less than minimum wage would be if minimum wage had kept pace with worker productivity increases since 1968.
which is also horrifying, but it gets even worse when you look at the quote this article uses to support that statement. which doesn’t actually say that 40% of Americans now make less money hourly than they would make if 1968 minimum wage had grown at the same rate as productivity did. it says:
“If the minimum wage had risen in step with productivity growth [since 1968], it would be over $16.50 an hour today. That is higher than the hourly wages earned by 40 percent of men and half of women.”
(Dean Baker, source)
40% of men and half (presumably about 50%) of women is not the same thing as 40% of Americans! particularly not when according to the 2010 US Census briefs (issued in 2011, pdf here) we had a 2010 population made up of 50.8% women.
so I am really, really curious as to how, in a society that has more female members than male, anyone could get “40% of Americans” from that quote.
idk, I tried to switch to only reading f/f fanfic for a while, and it was impossible. with m/m fic it’s like INTENSE and SEXY and IN DEPTH PLOTTY and f/f tends to be either tragic or very desexualized? which is not appealing to me.
yeah obviously i’ve been thinking about this at great length already lql and i’m wondering if there’s just a certain dynamic i enjoy that you never much read about when it comes to more female centric media. or if i’m just missing it because it’s not that popular!
one of the few f/f fic i’ve read was written by a guy and that was just instant ewww.
that said i did write some f/f once (b5, talia/ivanova) and it felt so intensely personal i just couldn’t finish it. idk.
yeah, I definitely think it has a lot to do with the way that f/f fic is written, in addition to the way that we interact with it. I completely relate to fic being way too personal - it’s like, you can talk about dudes boning for ages and it’s just fun, but when you talk about women, suddenly NOTHING IS SIMPLE EVER AGAIN.Read more
#2 is really nice
ty ty. it is so important to me that we show respect for ourselves, out of habit if not because we really believe in it, because jeez the world is messy enough when we do take all of the good things we are entitled to.
and I mean maybe I am big on symbolism and maybe I spent too much of my childhood in the Unitarian Universalist church for anyone’s good but it is it is important to remember that we have inherent worth & dignity. we all deserve to be treated, and treat ourselves, as things that are precious. I think that is a good starting assumption to make, even if it’s a hard one. we all deserve to be proper nouns.
I’m writing from a chronic fatigue syndrome (myalgic encephalomyelitis, post-viral fatigue syndrome, chronic fatigue immune dysfunction syndrome) perspective. CFS is associated with the following localized and/or widespread chronic pain symptoms: muscle pain and soreness; joint pain, soreness, and stiffness; nerve pain; headaches; migraines (also migraine without headache); abdominal pain (and irritable bowel syndrome); chest pain.
I am blessed with 24/7 access to a massage recliner, and even so, my bod hurts. all the time. searing pain, nauseating pain, nebulous pain, minimal but i n c e s s a n t pain.
analgesics are divided into categories of mechanism, strength, and whatever (and these days, narcotic is primarily a legal term, not a pharmacological class. when people refer to a painkiller as “narcotic” they usually mean “opioid” or “addictive”):
- non-steroid anti-inflammatory drugs (NSAIDs) are available over-the-counter and treat mild pain. common NSAIDs include aspirin, acetaminophen/paracetamol, ibuprofen, and naproxen. they’re not addictive, but taking too many at once or over an extended period of time is bad for you, so don’t do that. aspirin especially thins blood. ppl with liver problems, kidney problems, heart problems and blood disorders need to discuss NSAID/aspirin use with their docs to weigh the pros and cons. womp womp I got my wrist slapped for relying on acetaminophen.
these are not analgesics per se but they have that effect and therefore are used for chronic pain. they’re actually the first choice for chronic pain because opioids are do not fuck around with opioids.
- SNRI (e.g., Cymbalta) and tricyclic antidepressants
- antiepileptics e.g. Lyrica
- muscle relaxants sometimes
like I would like to discuss painkillers with one of my many doctors but I know that I am not going to like my options. I do not want to begin an SNRI like Cymbalta because I was on Effexor XR for three years and lost both my appetite and my libido. I have told my therapist and primary that I absolutely should not go back on it because of the likelihood that I would relapse into a restricting-type eating disorder. plus my sex drive. I like that thing. I do not want to go on an opioid or some of the antiepileptics because my father is is addicted to/abuses them and I worry that (1) I would become addicted +/or (2) my father would discover that I am on an opioid/select antiepileptics and steal them because he has stolen my medication (which I needed for a condition [that he knew about]) from me before (it was Ativan then).
ok that leaves some options between tricyclics and the rest of the antiepileptics. cool, good.
So partysoft pointed out that our situations are really similar in a lot of ways, and I’ve gone through just about all of these meds, so I figured I’d poke my head in. tw addiction, addictive medications, medical/chronic pain stuff
My current diagnosis is migraines and/or cluster headaches that more or less don’t go away. I’ve been trying to deal with them since September and I’ve finally gotten treatment that means that, if I’m lying down with ice on my head and no stressors/triggers, I have a few symptom-free hours a day. Most of my pain is in my head, but I also have numbness & tingling on my left side & extremities, and sharp pain all over parts of my body.
So uh I’ve been on anticonvulsants (tramadol, gabapentin/neurontin) and a TCA (nortriptylene) with mixed results that are really not generalizable but that I can talk about if anyone cares. I was also on blood pressure meds (nadolol) for migraines, which are not on your list but w/e.
If you haven’t tried muscle relaxants yet, I’ve found them really effective for times when the pain is so bad that you just need to be out, or when it’s bad enough that you’re tense as all fuck and the tenseness and the pain are cycling. The one caveat is that they make me feel unbelievably vulnerable. I can’t and don’t take valium because it turns me into a weepy mess, so I take tizanidine, which is a skeletal muscle relaxant. And it makes me sleepy and floppy. Like, tripping onto my bed because muscles are hard sort of floppy. I respond really weirdly to most medications, so my reaction isn’t necessarily generalizable, but they do by definition relax your body. So if feeling safe where you are is a problem for you (which it is for me), that might be something to consider. It helps me to have a cup of tea, someone I trust around, or w/e when I’m on them, because I get nervous about my ability to keep myself safe when I’m on them.
As for opiates… yeah. Almost everything about using them for chronic pain sucks. They’re my only option (besides the muscle relaxants, which I use probably 2x/month since I stopped living with partysoft for the aforementioned reason) for acute pain relief, because basically the only thing I can take. The good thing is that hydrocodone, which is what I have, works really well for me. One of the problems I have, which I’m positive you have experienced, is that when I’ve been hurting nonstop really badly for a really long time or I’m having certain types of migraine symptoms, my emotional regulation and critical thinking skills go DOWN DOWN DOWN. The doses I take aren’t usually enough to get rid of my pain, but they bring it down to manageable levels, and the drugs tend to smooth out my emotions so that I go from being a total mess and feeling like I’m going to shake myself apart to feeling like the world is O.K. and I can cope.
And then there’re the bad things. I also have a significant family history of addiction, as do a lot of people I’m close to, so it’s really hard for me to NEED a drug that is so highly addictive and makes me feel so good. (Or even just not bad. I don’t know if you’re like me, but 80% of the time I don’t remember what feeling physically “good” is like, because a “good day” means you feel shaky and weak and nauseous and have pain but not so bad that you can’t think or do things.) Every time I take my hydrocodone, I have to go through the checklist. So, subby, are you in pain? Is it REALLY BAD pain? Are you SURE? Is the PAIN bad enough that you should have hydrocodone, or is it just that you’re a pitiful crying BABY who can’t handle a little headache? Have you been a good enough person to deserve narcotics today? Is getting rid of this pain important enough to you that you are willing to become forever addicted to hydrocodone and/or never have it work again?
It is, honestly, really dysfunctional, and every time I do it I know it’s dysfunctional, but I’m usually in too much pain to really manage my dysfunctional thoughts by that point. Even worse are my feelings around having/not having it. Last night I went out to dinner and realized as soon as we got to the restaurant that I was in unbelievable pain and wouldn’t be able to eat or make conversation or do anything but make sad faces if I didn’t get pain relief medication. And I’d forgotten it. And my mom didn’t have hers, and there wasn’t any in the car. Then, on the way home, I realized that I had some in my jacket pocket from the last time I’d gone out, but hadn’t bothered to look. Our thought processes are less than optimal when we’re in unbearable pain, and having medication that we need to stop that pain that is also incredibly addictive is probably one of the most twisted situations we could be put in. Every time I’m crying because I hurt so badly and trying to decide if I want to make the pain go away this time, while risking all future times and there will be many, I sort of want to punch the universe in the face.
But, I was actually hoping to talk about ways to manage taking opiates for chronic pain and walking the line between torturing yourself and using them irresponsibly. This is just what I do to handle being a barely-adult who uses hydrocodone as a part of her day-to-day treatment plan.
Obviously ymmv, but having guidelines makes me feel better, and might be a good idea if you do go on them.
Also, I don’t know what kind of migraines you have, but there are supposed to be great anti-nausea meds in this world if that’s a problem for you. I’ve been seeing doctors about this since October and it hasn’t occurred to me to ask for them until the appointment I have in a few days, so I thought the reminder might be helpful.
What strikes me most about this article (as an EMT and as someone who’s been a patient way too many times) is that patient advocacy is often more important than any particular treatment or procedure. This woman needed someone within the system to stand up for her. And when we choose not to fight for our patients - because we disagree with their decisions, or we think they’re scumbags, or we’re just having a bad day - sometimes that choice kills them. I don’t think that’s something we can ever afford to forget.