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Author Topic: I start my PD training tomorrow  (Read 3837 times)
MaryD
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« on: December 11, 2011, 03:14:31 AM »

Tomorrow is my first day of PD training. 

My stash of stuff arrived on Thursday.  There's nowhere near as much as I was expecting.  I cleared out the small bedroom to get it all fitted in and I think I could still swing several cats in there.   I'm missing the bits of hardware I was expecting but I didn't realise until Saturday by which time it was too late to do anything about it.  It'll all be sorted out tomorrow.

I expect I'll be sorted out tomorrow, too.

I'm surprised how I feel that my catheter has become part of me in the seven weeks since it was put in.  I hardly think of it now, apart from the few minutes it takes to care for it after a shower.

Tomorrow, I hope for nerves of steel and a steady hand - a clear head would be good, too.
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highway61
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« Reply #1 on: December 11, 2011, 04:57:49 AM »

Tomorrow is my first day of PD training. 

My stash of stuff arrived on Thursday.  There's nowhere near as much as I was expecting.  I cleared out the small bedroom to get it all fitted in and I think I could still swing several cats in there.   I'm missing the bits of hardware I was expecting but I didn't realise until Saturday by which time it was too late to do anything about it.  It'll all be sorted out tomorrow.

I expect I'll be sorted out tomorrow, too.

I'm surprised how I feel that my catheter has become part of me in the seven weeks since it was put in.  I hardly think of it now, apart from the few minutes it takes to care for it after a shower.

Tomorrow, I hope for nerves of steel and a steady hand - a clear head would be good, too.

Don't worry Mary. I went through the process last week. They go over everything step by step and explain everything clearly. I also asked a lot of questions here, which really helped.
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cassandra
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When all else fails run in circles, shout loudly

« Reply #2 on: December 11, 2011, 05:13:35 AM »

yeah don't worry, it will all go smashing I'm sure, and I hope you will feel a lot better after that. But good luck all the same and lots of love Cass
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I started out with nothing and I still have most of it left

1983 high proteinloss in urine, chemo, stroke,coma, dialysis
1984 double nephrectomy
1985 transplant from dad
1998 lost dads kidney, start PD
2003 peritineum burst, back to hemo
2012 start Nxstage home hemo
2020 start Gambro AK96

       still on waitinglist, still ok I think
JLM
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« Reply #3 on: December 11, 2011, 07:00:30 AM »

I have been doing CAPD since the last of April.  A month after I started with F, I left for WI for 3.5 months and had to go to a B clinic.  My biggest problem I see, is that I usually am a night owl.  One of the reason I am is because my husband has ALZ and when he goes to bed I can unwind from the stress of "dealing: with him.  Now I use the exchange time to "hide" from him, but I have to go back to the behavior he tossed at me.
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I'm just where God wants me to be, not one step ahead nor one step behind.
billybags
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« Reply #4 on: December 11, 2011, 09:16:57 AM »

MaryD, good luck to-morrow, you will be fine.
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Atooraya
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« Reply #5 on: December 11, 2011, 02:16:47 PM »

Best of luck. It's easy and I'm sure ull be fine.
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MaryD
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« Reply #6 on: December 11, 2011, 08:50:43 PM »

The mind is completely boggled, but I think I'm getting the hang of it.

I didn't even feel the two litres when it was in, but I worked up an awful backache after standing up for a while.

Tomorrow is another day!
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Joe
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« Reply #7 on: December 12, 2011, 06:16:02 AM »

Good luck today Mary, I'm sure you will do just fine.
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Live simply. Love generously. Care deeply. Speak kindly.
Leave the rest to God...
drgirlfriend
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« Reply #8 on: December 12, 2011, 08:11:47 AM »

Sounds like you'll get the hang of it in no time! Good luck!
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Boyfriend diagnosed with renal failure Feb. 2011. Cause unknown.
PD Catheter "installed" June 30, 2011.
Began CAPD August 11, 2011.
On transplant list 11/23/11.
Started Liberty Cycler 12/1/11.
MaryD
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« Reply #9 on: December 16, 2011, 03:48:37 PM »

Four days into dialysis and I'm flying!

It's much easier than I thought it was going to be.  I'm still going fairly slowly and checking each step.

I feel really good (which is not because of the PD), and I'm OK to eat practically anything - in moderation.  Blood tests next Tuesday.  I'll be interested to see if there is much of a change
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lmunchkin
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"There Is No Place Like Home!"

« Reply #10 on: December 16, 2011, 04:32:07 PM »

 :bandance; :yahoo; :clap; :cheer:
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11/2004 Hubby diag. ESRD, Diabeties, Vascular Disease & High BP
12/2004 to 6/2009 Home PD
6/2009 Peritonitis , PD Cath removed
7/2009 Hemo Dialysis In-Center
2/2010 BKA rt leg & lt foot (all toes) amputated
6/2010 to present.  NxStage at home
Joe
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« Reply #11 on: December 17, 2011, 07:20:28 AM »

That is one of the neat things about PD Mary, far fewer restrictions than if you were on Hemo. But all in moderation.
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Live simply. Love generously. Care deeply. Speak kindly.
Leave the rest to God...
kporter85db
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« Reply #12 on: December 19, 2011, 07:01:12 PM »

I have almost no diet restrictions with the exception of the low sodium and diabetic, which I would be on even if my kidneys worked. PD is great.
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May/2010 Sulfa based antibiotics killed my already weakened kidneys, almost
Feb/2011 PD catheter placed
July/2011 Started Peritoneal Dialysis
Nov/2013 Started NxStage 5 days/week

Ken
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