Benefits of a Dialysis Patient

“It can’t be the heat, I came from a tropical country,” I said.
“You’ve been here two years now, your body has adjusted to American climate,” the Elder said.
There in my car, I cried. I realized for the first time, it wasn’t the climate, it was the kidney disease. My new husband divorced me after I was diagnosed. I lost my job the month I started dialysis. I could no longer afford the red coupe. I was told by my doctor to quit wearing high heels. He said if I should suffer a fall I might get crippled.
So, where did the benefits come in? First I got unemployment benefit for one year and a half. With nothing to do, I started writing a book. When I traveled, I got a wheelchair and a man pushing to take me to my next gate, no more stress over missing my next flight, or lining up at airport Immigration counter, or catching my luggage at the revolving ramp.
When the unemployment benefit was exhausted, I got social security SSA and SSI. It’s a very small amount compared to what I was earning but I got my basic needs. I got disabled parking. I still have time in my hands to write some more, so that I finished two books. I got a blog going, then a YouTube channel. Those were not enriching, not exactly fifteen minutes of fame, but gratifying.
I found friends in Facebook groups of dialysis patients. I have patient friends I found at the dialysis center lobby while waiting for our treatment. There, early mornings on Tuesdays, Thursdays and Saturdays, all five of us ladies, one American, one Chinese and three Filipinas, sit in a half circle and discuss our concerns. The techs call us “The View, broadcasting live from the lobby of DaVita!”

See also:5th AnniversaryVitamins to a Dialysis Patient Response to John Oliver
Published on June 25, 2018 22:58
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