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Author Topic: Happy on CAPD, made to start APD  (Read 4362 times)
-Lady Noir-
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Where's your will to be weird?

« on: August 26, 2009, 01:07:51 PM »

Has anyone changed from CAPD, to APD?
My fiance has been on CAPD for only 2 months, and has been told he has to go on APD because he is what you may call a 'fast transporter'...
Thing is, the CAPD is going well, his blood results are all fine, he's still passing urine, he's not retaining any fluid or anything!
 :urcrazy;
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Expose yourself to your deepest fear. After that, fear has no power, and the fear of freedom shrinks and vanishes. You are free

..Nik..

Fiancee to Mike
Mikes 'history'....
Born September 12 1983
Seizure July 2003 [Unrelated to kidney]
Diagnosed with 'Polycystic Kidney Disease' July 2003 (Wrong diagnosis)
Diagnosed with  IgA Glomerulonephritis April 2004
On active transplant waiting list 2006
Hyperparathyroidism developed gradually
Parathyroidectomy May 2009 (Affected kidney function)
Hospitalized for hyperkalemia June 2009
Catheter inserted June 2009


Started CAPD June 2009
Stared APD September 2009

ABO Incompatible transplant 01 December 2010
Donor = Mikes father Greg
Red from Canada
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« Reply #1 on: August 26, 2009, 01:23:35 PM »

APD is absolutely the best.  Wait til he gets used to it and he will never go back.  All his days will be free and you only do it at night when you're sleeping.  I've done all 3, CAPD. APD and Hemo and believe me, APD is THE best!
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Restorer
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WWW
« Reply #2 on: August 26, 2009, 08:47:59 PM »

I was a fast transporter and happy on CAPD. But eventually I started losing more kidney function (it goes faster once you're on effective dialysis), and CAPD was no longer working for me. Since I was a fast transporter, I was reabsorbing a significant amount of fluid, and many of my exchanges were negative UF. When my kidney function was still up, it wasn't a problem because I was able to pee out what I absorbed. But after I lost more function, it was more of a problem.

Your fiance might find the same problem eventually. APD is much better for a fast transporter, not to mention the freedom during the day.
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- Matt - wasabiflux.org
- Dialysis Calculators

3/2007Kidney failure diagnosed5/2010In-center hemodialysis
8/2008Peritoneal catheter placed1/2012Upper arm fistula created
9/2008Peritoneal catheter replaced3/2012Started using fistula
9/2008Began CAPD4/2012Buttonholes created
3/2009Switched to CCPD w/ Newton IQ cycler            4/2012HD catheter removed
7/2009Switched to Liberty cycler            4/2018Transplanted at UCLA!
-Lady Noir-
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Where's your will to be weird?

« Reply #3 on: August 26, 2009, 11:01:04 PM »

Thanks guys! Sounds great!
Can i ask, how many hours a night are you on APD? We havn't been told this yet..
Logged

Expose yourself to your deepest fear. After that, fear has no power, and the fear of freedom shrinks and vanishes. You are free

..Nik..

Fiancee to Mike
Mikes 'history'....
Born September 12 1983
Seizure July 2003 [Unrelated to kidney]
Diagnosed with 'Polycystic Kidney Disease' July 2003 (Wrong diagnosis)
Diagnosed with  IgA Glomerulonephritis April 2004
On active transplant waiting list 2006
Hyperparathyroidism developed gradually
Parathyroidectomy May 2009 (Affected kidney function)
Hospitalized for hyperkalemia June 2009
Catheter inserted June 2009


Started CAPD June 2009
Stared APD September 2009

ABO Incompatible transplant 01 December 2010
Donor = Mikes father Greg
sico
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Posts: 310


wheres my bike gone?

« Reply #4 on: August 27, 2009, 05:24:09 AM »

The other good thing about APD is there is only 1 connection and disconnection per day, unlike CAPD where you do 4 or 5 of each.
Therefore less chance of infection.
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Brad      "Got myself a one way ticket, going the wrong way" - Bon Scott

6/11/08 diagnosed with ESRF, dialysis that day

HD and PD

8th of April 2010 Live kidney transplant from my father.
Jenabcd
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« Reply #5 on: August 27, 2009, 06:50:12 AM »

Hello!   I agree that using the machine at night is great, so MOST of the day is free, but everyone is different, and I do have to do one exchange during the day too.  (Still, not bad)
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LightLizard
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« Reply #6 on: August 27, 2009, 08:53:31 AM »

i've been doing the night cycler for about two years now and i think your boyfriend is going to be pleasantly surprised. once he adapts to the routine, that is.
 :thumbup;
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KICKSTART
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In da House.

« Reply #7 on: August 27, 2009, 11:04:05 AM »

It tends to vary how many exchanges you do through the night and how many hours you are on , but roughly on average its 4/5 exchanges and about 8 hrs. Some people go empty during the day, others dont. APD certainly gives you back some freedom though!
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OH NO!!! I have Furniture Disease as well ! My chest has dropped into my drawers !
Restorer
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« Reply #8 on: August 27, 2009, 12:39:40 PM »

My treatment each night lasts 9 1/2 to 10 1/2 hours. On my cycler, it varies depending on how long it takes me to drain each time.
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- Matt - wasabiflux.org
- Dialysis Calculators

3/2007Kidney failure diagnosed5/2010In-center hemodialysis
8/2008Peritoneal catheter placed1/2012Upper arm fistula created
9/2008Peritoneal catheter replaced3/2012Started using fistula
9/2008Began CAPD4/2012Buttonholes created
3/2009Switched to CCPD w/ Newton IQ cycler            4/2012HD catheter removed
7/2009Switched to Liberty cycler            4/2018Transplanted at UCLA!
Hanify
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Posts: 1814


Hadija, Athol, Me and Molly at Havelock North 09

« Reply #9 on: August 27, 2009, 03:35:04 PM »

Thanks guys! Sounds great!
Can i ask, how many hours a night are you on APD? We havn't been told this yet..

It'll probably be a 9 hour cycle.  Ask about having extraneal in during the day - that means he won't have to do an exchange. They might want him to try the machine for a bit before the go to that though.
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Diagnosed Nov 2007 with Multiple Myeloma.
By Jan 2008 was in end stage renal failure and on haemodialysis.
Changed to CAPD in April 2008.  Now on PD with a cycler.  Working very part time - teaching music.  Love it.  Husband is Paul (we're both 46), daughter Molly is 13.
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