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Author Topic: Finding Time  (Read 1936 times)
murf
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« on: April 06, 2010, 05:37:29 PM »

I need some advice from experienced PD patients. I find that some of the activities that I used to do whilst on hemo, I can no longer do. If I want to go out for the day with my friends is impossible as I must be back within six hours for my next exchange. That means I can't go out traveling, go to the cricket for the day or say overnight with friends. At least on hemo, I had four days a week to do these things. Is there a way around this dilemma or is it the price we pay for better dialysis at home?
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Started Hemodialysis Anzac Day 2005
Patiently waiting for a transplant
Started PD New Year 2010
Taken off transpalnt list, Jan 211
george40
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« Reply #1 on: April 06, 2010, 06:27:00 PM »

Hi murf, Ive been on pd for about 1.5 years. I was doing 4 manual exchanges which made getting out and about easier. Recently they bumped me to five exchanges and I have been literally doing pd all day it seems. But, I do go for overnight trips often. I have a little travel kit I put together and purchased one of those mini portable IV poles. I think it is important to let your friends know the deal so that if you do go away for a trip they will know that you have to break away every six hours or so to do an exchange. Also push comes to shove, there have been times when I have gone 8 hours between exchanges and when I do this I keep my eye my fluid intake. So, the things you did on hemo you maybe can still do, you just have to do a little more planning.
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8/2000 - Diagnosed ESRD / Hemo begins with perm cath
1/2002 - Transplant No. 1
4/2006 - Transplant failed due to CMV virus/ Back to Hemo
11/2008 - Moved to PD Modality
9/2012 - Transplanted!
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