AreaCode7O7
Senior member
- Mar 6, 2005
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Fast forward three years and Belgium winds up pissed that they have to go back to privatized health care because foreigners with extremely expensive conditions move in (re: Hawaii). Hyperbole? Absolutely. However, the basic principle is there; health care isn't free and if ultimately it costs more than we have, either individually or as a country, it's no longer available. The difference is whether it's no longer available to an individual or a country.
I'd prefer to have health care unavailable to me personally and still see it available to others than to see all of us equally screwed. That's saying quite a bit, since I have a degenerative disease that requires constant, and very expensive treatment. A more realistic example of my hyperbole above is the UK's treatment of one of my drugs.
I have rheumatoid arthritis. Sucks, no cure, constant treatment. One of the best treatments out there right now comes in the form of a biologic. These drugs are newer, TONS of R&D costs in getting this to market, and because they're so effective, that TONS is still cheap. Biologics takes the shape of Enbrel, Humira or Remicade. Often one won't work and the docs try another which does.
Yay, I can walk again and use my hands! If you've never been 18 and unable to walk, not knowing if you ever will again, you cannot possibly know the relief it is to suddenly live a normal life again. The price of these drugs can range up to $30k a year. Sure glad I have insurance; sucks that some people don't. I will do ANYTHING to maintain a job with that insurance; if that meant I cleaned subway toilets, I would do it.
On the flip side, we have the lovely old UK and their helpful health provision for their citizens. Which just happened to determine that this drug is too expensive to experiment with; you get to try one of the flavors and if it doesn't work, too bad, no more tries. Everyone for whom try #1 doesn't work gets to live with not being able to walk or use your hands. Sucks.
Lower the prices? Producing these drugs, even without the R&D costs factored in, is obscenely expensive. Beyond that they're still working on better drugs and (I'm not holding my breath) a cure. Eventually these will quit working, for me and for others. It's the sad fate of anybody with my disease; nothing works permanently.
So yeah, go to Belgium for your health care because the mean old United States won't pay for it. And then deal with it when Belgium decides it's too expensive to allow you to have the best possible treatment, because too many people take advantage of the system, because treatment is an art rather than a pure science, because the country has to provide mediocre treatment for all.
Being without health insurance terrifies me but I can take some responsibility for my life; if I don't have it, I'm not doing my part to take care of myself. No matter how disabled I get, as long as I have my mental faculties I will hold some type of job that keeps me insured. Being on government-controlled health care scares the living shit out of me because then, no matter what I do, I've turned over the keys to my health and life to someone other than me.
Yeah, they'll do their best, for me and for everyone... just like they're doing in Britain, where I wouldn't be able to walk or type right now.
[edit] Just for fun: UK discussion about trying to get Enbrel. This is old, 2004. The UK has since TIGHTENED restrictions on accessing this particular drug and anything else in that family, entirely because of the cost. It's not an opiate or painkiller, not addictive, no street value or potential for misuse.
http://www.psoriasis.org/forum.../index.php/t-9341.html
More recent article about UK restrictions: http://www.thisislondon.co.uk/...g+rationing/article.do
I'd prefer to have health care unavailable to me personally and still see it available to others than to see all of us equally screwed. That's saying quite a bit, since I have a degenerative disease that requires constant, and very expensive treatment. A more realistic example of my hyperbole above is the UK's treatment of one of my drugs.
I have rheumatoid arthritis. Sucks, no cure, constant treatment. One of the best treatments out there right now comes in the form of a biologic. These drugs are newer, TONS of R&D costs in getting this to market, and because they're so effective, that TONS is still cheap. Biologics takes the shape of Enbrel, Humira or Remicade. Often one won't work and the docs try another which does.
Yay, I can walk again and use my hands! If you've never been 18 and unable to walk, not knowing if you ever will again, you cannot possibly know the relief it is to suddenly live a normal life again. The price of these drugs can range up to $30k a year. Sure glad I have insurance; sucks that some people don't. I will do ANYTHING to maintain a job with that insurance; if that meant I cleaned subway toilets, I would do it.
On the flip side, we have the lovely old UK and their helpful health provision for their citizens. Which just happened to determine that this drug is too expensive to experiment with; you get to try one of the flavors and if it doesn't work, too bad, no more tries. Everyone for whom try #1 doesn't work gets to live with not being able to walk or use your hands. Sucks.
Lower the prices? Producing these drugs, even without the R&D costs factored in, is obscenely expensive. Beyond that they're still working on better drugs and (I'm not holding my breath) a cure. Eventually these will quit working, for me and for others. It's the sad fate of anybody with my disease; nothing works permanently.
So yeah, go to Belgium for your health care because the mean old United States won't pay for it. And then deal with it when Belgium decides it's too expensive to allow you to have the best possible treatment, because too many people take advantage of the system, because treatment is an art rather than a pure science, because the country has to provide mediocre treatment for all.
Being without health insurance terrifies me but I can take some responsibility for my life; if I don't have it, I'm not doing my part to take care of myself. No matter how disabled I get, as long as I have my mental faculties I will hold some type of job that keeps me insured. Being on government-controlled health care scares the living shit out of me because then, no matter what I do, I've turned over the keys to my health and life to someone other than me.
Yeah, they'll do their best, for me and for everyone... just like they're doing in Britain, where I wouldn't be able to walk or type right now.
[edit] Just for fun: UK discussion about trying to get Enbrel. This is old, 2004. The UK has since TIGHTENED restrictions on accessing this particular drug and anything else in that family, entirely because of the cost. It's not an opiate or painkiller, not addictive, no street value or potential for misuse.
http://www.psoriasis.org/forum.../index.php/t-9341.html
More recent article about UK restrictions: http://www.thisislondon.co.uk/...g+rationing/article.do