Dialysis and News – May 2015

RSN Newsletter 1The Renal Support Network has published it’s newsletter.  I thought you might like to take a look at it and sign up/register to get it in your email.  They are very patient-centered and their founder is a transplant/dialysis patient with a passion for getting information to the dialysis community (like me).   To access their newsletter CLICK HERE. 

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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 can be hooked up to a machine that will clean my blood as the kidneys should. Three days a week, I go to a center and have too very large needles stuck in my arm to remove and replace my blood as it passes through a process where it's cleaned and the fluid is removed, a process taking a little over four hours each time. I want to advance knowledge about dialysis so that other patients 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. 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. Enjoy.
This entry was posted in dialysis, ESRD, kidney, New Patient, patient care, Transplant and tagged , , , , . Bookmark the permalink.

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