Dialysis or Transplant – Which is the lessor evil/better salvation?

Some good points about experience with dialysis and transplant.

eleisawifelife

I have been inspired to write about this difficult topic by Big D and Me’s blog post Dialysis or Transplant:  The Big Decision.  He shared his experience and really voiced our experience also.

In our early years of dialysis the nephrologist said that not everyone chooses a transplant.  They had someone on dialysis for 20-years.  We laughed.  Who in their right mind would choose to be hooked up to a machine if they had a chance at their ‘real’ life that’s free of dialysis, restricted diet, routine hospital appointments, liquid restrictions (no more than 2L a day!), pills with their side effects, vacation restrictions and costs, etc.  After a few more years we still remembered this conversation and turned bitter/conspiracy theorists.  The doctor probably wanted the funding for his dialysis career and wanted to keep people dialysis.  We were young….in our twenties, naive, ignorant, and bitter.

When Franklin got…

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About DevonTexas

I am a person with ESRD (End Stage Renal Disease) which means my kidneys don't work. Forty or so years ago that would have been a death sentence but today there is Dialysis which means I could be hooked up to a machine that would clean my blood as the kidneys should. Three days a week, I went to a dialysis center and had too very large needles stuck in my arm to remove and replace my blood as it passed through a process where it was cleaned and the fluid was removed, a process taking a little over four hours each time. In November 2017, I received a kidney transplant from a deceased donor. My life went into overdrive. With a "new" functioning kidney, I no longer had to go to a dialysis center and my days were not open to be lived rather than recovering from dialysis which meant dialyzing for three days and resting for 4 days a week. I work full-time and often 50 hours per week. It is something I never imagined. I highly recommend it! HeeHee I want to advance knowledge about dialysis and transplant so that others can learn from my experience and mistakes. We shouldn't have to reinvent the wheel, eh? There is so much to be learned and experienced about our predicament. There are vast resources available to support us and enrich our lives but many patients don't know about them. There are also many issues that we have to deal with whether we want to or not. So I blog about them in www.DevonTexas.com All comments are confidential until I approve them. If you don't want your comment public, let me know and I will respect that. So, feel free to leave a comment. I also blog in LegacyTales in WordPress if you are interested in the ramblings of a Old Man. Give a peek and let me know what you think. https://legacytales.wordpress.com/ Enjoy.
This entry was posted in dialysis, ESRD, fluid control, Home dialysis, Obamacare, Transplant, Uncategorized and tagged , , , , , , . Bookmark the permalink.

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