Living on disability is not all some apparently crack it up to be. Trust me.

Now I realize we all don't have the same experience's, but in my experience, once you do get your disability, after fighting with government pencil pushers who don't have the first clue as to what a headache is, much less a disabling medical condition.
 
Every so many years these same pencil pushers will  "review" your disability as they are doing mine now.

And if the pencil pushers in your state are anything like the one's here, they will try to cut your disability off. (Because then the state can keep that money for other things Which I hope President Obama will put a stop too.)

One of the things I get my disability for is a genetically inherited diseas that is a close cousin of parkinsons diseas. I, um shake, my hands, arms, fingers, neck, and head shake, and tremble all the time, and sometimes, I'll have involuntary hand/arm "twitches" that will cause me to throw or drop something if I'm holding something. Yep I can't even draw a straight line with a pencil. There is no cure, and no treatment, and as I age it will only continue to get worse. But like clockwork every few years, especially when the state has budget shortfalls, suddenly I'm cured, and I can go back to work now as an O.R. Tehcnologist, to hear the pencil pushers tell it. Now seriously, who in the hell in their right mind, would think a patient would let me come anywhere near them with a needle or scalple? And what surgeon would in their right mind, with medical malpractice being what it is, would hire me?  :roll: 

 

"The Blood is the life!"