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Politics : Formerly About Advanced Micro Devices

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To: J_F_Shepard who wrote (797248)7/26/2014 6:40:43 PM
From: Brumar89  Read Replies (1) of 1579681
 
Kathy Shaidle on her lupus:
........

In socialized medicine, shortages aren’t bugs, they’re features. The system can only “work” if care is parceled out slowly and stingily, so that – frankly – enough sick people will conveniently die, thereby freeing up spots on the always-lengthy waiting list.

Picture a Ponzi scheme, but with patients instead of investors.

My cat can get an MRI faster than I can.

I was getting sicker and sicker, but had to wait months between appointments and bloodwork, so I could get yet another tweaked pharmaceutical regimen (that still didn’t help.)

I was only hospitalized when I was on death’s door, and finally received the high-dose prednisone treatment that turned me around.

Even then, my rheumatologist had to fight to get me a bed.


Having said all that:

Lupus never cost me a nickel out of pocket. My examinations, treatment and drugs were all covered by some government program or other.

Buying private health insurance or paying for your own treatment is – mostly — illegal in Canada, so I had no option . Canada’s wealthy and privileged do, of course, and exercise said options regularly.

So while on principle I objected to receiving “free” healthcare (and then going on government disability), my only other choice would have been to continue to endure searing, incapacitating pain and, I suppose, eventually die either by lupus or by my own hand.

I believe in a mixed private/public health care system.

I did before I got sick and believe it now.

..........
http://pjmedia.com/lifestyle/2014/07/26/3-things-getting-lupus-taught-me/?singlepage=true
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