Dialysis and Questions

Update: 11/09/12: I will be back on line soon.  I am occupied with some personal issues and having difficulty seeing. In the meantime, please answer the poll.  Thanks. 

I get a lot of readers who get to this blog site by search engines and the questions they ask are really good.  Sometime the questions give me good ideas for things to write about.  But, I’d like to make sure the people searching for answers are finding them.

For example, in the past, people had these questions and were led to my blog by the search engines:

obama care removes life helping kidney dialysis medicine
obamacare dialysis over age 75
obamacare ethics panel for dialysis
if a dialysis patient doesnt have enough fluid removed what are the consequenses?
i am a dialysis patient that cramps on the machine. what can i do to help
dialysis diarrhea
esrd and obamacare
usage of computer tablet at dialysis centre
kidney armband

These are really important questions and concerns and I’d like to know if these and any other questions are being answered.  Please answer the survey to let know.  Even if your question, concern, issue, etc was not in the above list, I’d like to know if you’re getting what you seek by coming to this blog.  Thank you!


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.
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1 Response to Dialysis and Questions

  1. Sara says:

    Hi Devon–your blog is coming through in Spanish so please change that for my address so it doesn’t end up in Spam! I think I found your blog by chance; have in-laws in Texas, had a child in Texas and was curious I guess about the Texas part of your name! Can’t remember where I saw it, but probably in someone else’s blog that referred to ones that they read. Let’s hope besides tax reform and conversation we will see health care just get going and leave the talk behind.

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