• Aceticon@lemmy.dbzer0.com
    link
    fedilink
    English
    arrow-up
    15
    ·
    edit-2
    3 hours ago

    Having lived in two countries with universal healthcare, that meme is absolutelly true and you’re the one bullshitting.

    The most “extreme” it can get in such systems is that they won’t pay for very expensive treatments (i.e. the kind of stuff that costs a million dollars per shot) if a person can keep going with cheaper ones even if they’re not as good.

    Even then, sometimes they will if it’s actually worth it (as in: for something that’s a cure, not for something that just keeps the patiet going and is only 10% better than the next best option whilst costing 1000x more).

    That’s “your quality of life won’t be as good if you have a chronic disease that makes your life miserable and the best treatment in the market is insanelly expensive because they’ll only pay for a not as expensive one”, not “death panels”.

    People in those countries absolutelly aren’t going bankrupt due to being denied life-saving treatment and having to pay for it from their own pocket.

    As for any complains you might have heard from people in countries with universal healthcare, them complaining about it is like people in Scandinavia complaining about public services: relative to what they have there are bad parts, which is something altogether different than it being bad relative to the World and when it comes the healthcare the US is 3rd World when it comes to results delivered relative to the amount spent in it.

    • FundMECFSResearch@lemmy.blahaj.zone
      link
      fedilink
      arrow-up
      8
      ·
      edit-2
      2 hours ago

      Sorry then.

      I guess me living my entire life in a system with universal healthcare, being denied treatments that could have prevented me going deaf and needing a feeding tube is all in my imagination.

      The treatments for these werent extreme. It was a fairly simple drug therapy that costs around 5’000 Euro per year and is sold in my country.

      It just isn’t on the list of drugs covered by public health insurance. As I’m surviving on 12k per year disability benefits, I could not afford the treatment.

      But just because it never impacted you you assume my experience doesn’t exist, because you have the privilege that the system never didn’t work for you, so you assume it works for everyone.