I Hate Dialysis Message Board
Welcome, Guest. Please login or register.
November 22, 2024, 12:02:04 PM

Login with username, password and session length
Search:     Advanced search
532606 Posts in 33561 Topics by 12678 Members
Latest Member: astrobridge
* Home Help Search Login Register
+  I Hate Dialysis Message Board
|-+  Dialysis Discussion
| |-+  Dialysis: Home Dialysis
| | |-+  Urinating at Night
0 Members and 1 Guest are viewing this topic. « previous next »
Pages: [1] Go Down Print
Author Topic: Urinating at Night  (Read 6237 times)
oleboy
Full Member
***
Offline Offline

Posts: 135


« on: April 01, 2008, 08:37:44 PM »

Here is a question for those of you doing CCPD, I still make water and usually go to the bathroom 2 to 3 time a night, once I start doing CCPD will the cycler help reduce these trips to the bathroom,or will I need to have wheels on my cart with an extension cord?
Logged

'hold fast your dreams for if dreams die life is a broken winged bird that connot fly.'
flip
Elite Member
*****
Offline Offline

Gender: Male
Posts: 1742


« Reply #1 on: April 01, 2008, 09:25:58 PM »

I don't know about CCPD but I imagine hemo is similar. Before I started dialysis, I had to get up and pee 5-6 times a night. Now I never do.
Logged

That which does not kill me only makes me stronger - Neitzsche
KICKSTART
Elite Member
*****
Offline Offline

Gender: Female
Posts: 2786


In da House.

« Reply #2 on: April 02, 2008, 03:07:55 AM »

Well i do CAPD so dont need to disconnect anything , but yes i still go 4 or 5 times during the night and it drives me mad!!!
Logged

OH NO!!! I have Furniture Disease as well ! My chest has dropped into my drawers !
KT0930
Elite Member
*****
Offline Offline

Gender: Female
Posts: 1831


« Reply #3 on: April 02, 2008, 03:19:12 PM »

Yep, when I was on the cycler, I was still getting up my usual 1-3 times per night. My tube was just barely long enough to make it to the bathroom without disconnecting, but an extension cord and cart might not be a bad idea. When I was on vacation and couldn't reach the bathroom, I also took a 5 gallon bucket with me...not pretty, but it got the job done.
Logged

"Dialysis ain't for sissies" ~My wonderful husband
~~~~~~~
I received a 6 out of 6 antigen match transplant on January 9, 2008. Third transplant, first time on The List.
MiSSis
Full Member
***
Offline Offline

Gender: Female
Posts: 222


« Reply #4 on: April 06, 2008, 06:21:14 PM »

I'm currently on PD and have been on it for a little over 4 years and I still pee, even during the nights sometimes.  I use a Fresenius cycler and supplies and I'm able to attach a 10 ft. extension to the regular tubing which allows me to reach the bathroom.  My husband and I do quite a bit of traveling and sometimes the bathroom has been further away and there've been occasions where I've attached 2 of the 10 ft. patient tubing extensions.  I think Fresenius offers a 20 ft. extension but since I don't normally need that much extra, I stick with the 10 ft. and use 2 of them when I need to.
Logged

"Keep your face to the sunshine and you will not see the shadows."  Helen Keller
KT0930
Elite Member
*****
Offline Offline

Gender: Female
Posts: 1831


« Reply #5 on: April 06, 2008, 07:58:04 PM »

After reading about them on here, I asked my PD nurse about the tubing extensions (I also was on Fresenius), and she told me they no longer offered them. WTF!!!
Logged

"Dialysis ain't for sissies" ~My wonderful husband
~~~~~~~
I received a 6 out of 6 antigen match transplant on January 9, 2008. Third transplant, first time on The List.
MiSSis
Full Member
***
Offline Offline

Gender: Female
Posts: 222


« Reply #6 on: April 06, 2008, 08:25:13 PM »

Wow, KT.  I'm thinking she must just not have wanted to make a simple phone call.  I'm still receiving the extensions, no problem.  I can't imagine having to use a bucket!
Logged

"Keep your face to the sunshine and you will not see the shadows."  Helen Keller
KT0930
Elite Member
*****
Offline Offline

Gender: Female
Posts: 1831


« Reply #7 on: April 07, 2008, 07:59:28 PM »

Thankfully I only went on one vacation where I had to use the bucket, though it's definately an experience I would NOT want to repeat!
Logged

"Dialysis ain't for sissies" ~My wonderful husband
~~~~~~~
I received a 6 out of 6 antigen match transplant on January 9, 2008. Third transplant, first time on The List.
jbeany
Member for Life
******
Offline Offline

Gender: Female
Posts: 7536


Cattitude

« Reply #8 on: April 07, 2008, 08:09:35 PM »

KT - the fresenius website is www.fmcna.com.  Follow the link on the home page to the product catalog.  The 20 foot extensions are listed in with the cycler accessories, somewhere around pg 43 of the 64 pg catalog.  Print it out and smack your nurse over the head with it.

 :Kit n Stik;
Logged

"Asbestos Gelos"  (As-bes-tos yay-lohs) Greek. Literally, "fireproof laughter".  A term used by Homer for invincible laughter in the face of death and mortality.

Adam_W
Elite Member
*****
Offline Offline

Gender: Male
Posts: 1139


Me with Baron von Fresenius

« Reply #9 on: June 07, 2008, 06:59:37 PM »

If I do CCPD, I'll be on the Baxter machine. Does anyone know if Baxter makes the long extensions as well?

Adam
Logged

-Diagnosed with ESRD (born with one kidney, hypertension killed it) Jan 21st, 2007
-Started dialysis four days later in hospital (Baxter 1550-I think, then Gambro Phoenix)
-Started in-centre dialysis Feb 6th 2007 (Fres. 2008H)
-Started home hemo June 5th 2007 (NxStage/Pureflow)
-PD catheter placed June 6th 2008 (Bye bye NxStage, at least for now)
-Started CAPD July 4th, 2008
-PD catheter removed Dec 2, 2008-PD just wouldn't work, so I'm back on NxStage
-Kidney function improved enough to go off dialysis, Feb. 2011!!!!!
-Back on dialysis (still NxStage) July 2011 :(
-In-centre self-care dialysis March 2012 (Fresenius 2008K)
-Not on transplant list yet.


"Don't live for dialysis, use dialysis to LIVE"
mikey07840
Elite Member
*****
Offline Offline

Gender: Male
Posts: 1225


Her royal highness Queen Ruth on her throne, RIP

« Reply #10 on: June 08, 2008, 03:59:12 AM »

Baxter makes patient extensions. My PD nurses prefer I don't use them: they explained that the extensions need to be primed and that means that there is more fluid that doesn't get drained really, just stays in the line. I have a urinal I keep in the bedroom at night while hooked up to the cycler in case I have to pee.

Hope that helps.

Mike
Logged

06/85 Diagnosed with type 1 Diabetes
10/04 Radical Nephrectomy (Kidney Cancer or renal cell carcinoma)
02/08 Started Hemodialysis
04/08 Started Peritoneal Dialysis (CAPD)
05/08 Started CCPD (my cycler: The little box of alarms)
07/09 AV Fistula and Permacath added, PD catheter removed. PD discontinued and Hemodialysis resumed
08/09 AV Fistula redone higher up on arm, first one did not work
07/11 Mass found on remaining kidney
08/11 Radical Nephrectomy, confirmed that mass was renal cell carcinoma
12/12 Whipple, mass on pancreas confirmed as renal cell carcinoma

• Don't Knock on Death's door; Ring the bell and run away. Death hates that.

• I'm not a complete Idiot -- some parts are missing.
Kini
Newbie
*
Offline Offline

Posts: 32


" Just keep Swimming "

« Reply #11 on: July 12, 2008, 07:24:42 AM »

My Daughter has been on PD for 5 yrs. she still make urine although not as much. I was told it's not unusual to stop totally. Guess everyone is different. I keep a potty chair in her room near her bed.
Logged

Mother of daughter on PD dialysis. Transplanted 1991, dialysis June 2003, transplanted 2004 this transplant never took, still on PD and waiting 5 yrs. and when the gift of life is once again never shall we be tied down, look out Hawaii we are coming back !! it's my daughter's dream.
petey
Newbie
*
Offline Offline

Gender: Female
Posts: 0


MEMBER BANNED

« Reply #12 on: July 12, 2008, 07:13:26 PM »

Disposable urinals (they have male and female) are another option.  Check with your local drug store or pharmacy.  Unfortunately, Marvin hasn't urinated in a little over four years.  He wishes he could, though (still has the urge -- and sometimes it's a very, very strong urge -- goes to the bathroom, but nothing!  Poor Marvin!)
Logged
peleroja
Elite Member
*****
Offline Offline

Gender: Female
Posts: 1585


I have 16 hats, all the same style!

« Reply #13 on: July 15, 2008, 11:21:31 AM »

I don't usually have to pee in the middle of the night, but I usually have to do "other" stuff first thing in the morning.  Kaiser was kind enough to provide me with a bed pan which has come in handy on occasion!  You do what you gotta do, right?!
Logged
twirl
Member for Life
******
Offline Offline

Gender: Female
Posts: 8960


« Reply #14 on: July 19, 2008, 07:09:03 AM »

my husband, the coach, had knee surgery
and had one of those portable pee containers
he got home with it and when he was better and could walk he wanted to keep it
he gets up a lot to pee pee at night
I said NO
I wish I could pee pee at night
oh the memories
Logged
Ken Shelmerdine
Elite Member
*****
Offline Offline

Gender: Male
Posts: 1646


Life's a bitch and then you go on dialysis!

« Reply #15 on: July 20, 2008, 11:29:40 AM »

I keep a 1 litre pee bottle at the side of the bed and empty it in the morning when I disconnect from the cycler. I could get a 12 foot extension tubing but I figure that walking to the bathroom would make me too awake to get back to sleep again.
Logged

Ken
Pages: [1] Go Up Print 
« previous next »
 

Powered by MySQL Powered by PHP SMF 2.0.17 | SMF © 2019, Simple Machines | Terms and Policies Valid XHTML 1.0! Valid CSS!