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Author Topic: First full day on CAPD  (Read 4282 times)
Adam_W
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Me with Baron von Fresenius

« on: July 04, 2008, 09:22:38 PM »

Well, I did my full four exchanges today at home, and except for a little fine tuning that is needed by me, my doctor, and my nurses, it went really well. Even though it does have it's downsides (every type of treatment does), I can definitely say PD ROCKS! It was so nice to be able to dialyze and not have to worry about blood, needles, big machines, etc. It does feel weird walking around and doing things for four hours at a time with 2L of fluid sloshing around inside me, but it really doesn't feel as bad as I was expecting. A year ago I was so excited to have that NxStage machine in my bedroom, but now I'm saying "get that bloody thing out of here". The biggest problem I had today was removing fluid. Because I re-absorbed some fluid, and used a dextrose level that was too low on my last dwell, I ended up 1.1 kilos heavier than I was this morning. I'll get it worked out soon, though.

Adam
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-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"
Sluff
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« Reply #1 on: July 04, 2008, 09:32:08 PM »

Glad things went fairly well today.  :beer1;
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Joe Paul
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« Reply #2 on: July 04, 2008, 10:08:45 PM »

Good to hear you like PD.
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"The history of discovery is completed by those who don't follow rules"
Angels are with us, but don't take GOD for granted
Transplant Jan. 8, 2010
MIbarra
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Stopping to smell the bluebonnets

« Reply #3 on: July 04, 2008, 10:29:16 PM »

That's great that your first day went so well. I wish my dr. had been willing to talk to me about PD more but she just brushed that option aside. I think it was because she partly owned her own hemo dialysis unit. I'm looking forward to hearing about your experiences.
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Cadaver transplant April 29, 2007
okarol
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Photo is Jenna - after Disneyland - 1988

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« Reply #4 on: July 05, 2008, 12:12:59 AM »


I hope you are videotaping your new experiences!
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Admin for IHateDialysis 2008 - 2014, retired.
Jenna is our daughter, bad bladder damaged her kidneys.
Was on in-center hemodialysis 2003-2007.
7 yr transplant lost due to rejection.
She did PD Sept. 2013 - July 2017
Found a swap living donor using social media, friends, family.
New kidney in a paired donation swap July 26, 2017.
Her story ---> https://www.facebook.com/WantedKidneyDonor
Please watch her video: http://youtu.be/D9ZuVJ_s80Y
Living Donors Rock! http://www.livingdonorsonline.org -
News video: http://www.youtube.com/watch?v=J-7KvgQDWpU
David13
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« Reply #5 on: July 05, 2008, 04:52:16 AM »

Glad to hear that your PD experience is going well.  I had a feeling you would like it!   :2thumbsup;
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“The first human being who hurled an insult instead of a stone was the founder of civilization” - Sigmund Freud
kimcanada
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« Reply #6 on: July 05, 2008, 04:55:57 AM »

Hi Adam, I am in about my 6th week... I had fluid problems at first also...  I used all 2.5 bags and they put me on 5 treatments a day to get it under control.  Once you get to your goal weight the gains will be minimal... keep us posted :)
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monrein
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Might as well smile

« Reply #7 on: July 06, 2008, 03:54:13 PM »

 :bestwishes; Adam
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Pyelonephritis (began at 8 mos old)
Home haemo 1980-1985 (self-cannulated with 15 gauge sharps)
Cadaveric transplant 1985
New upper-arm fistula April 2008
Uldall-Cook catheter inserted May 2008
Haemo-dialysis, self care unit June 2008
(2 1/2 hours X 5 weekly)
Self-cannulated, 15 gauge blunts, buttonholes.
Living donor transplant (sister-in law Kathy) Feb. 2009
First failed kidney transplant removed Apr.  2009
Second trx doing great so far...all lab values in normal ranges
pelagia
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« Reply #8 on: July 06, 2008, 04:13:49 PM »

Now, aren't you going to have to change your photo?  So happy to hear that it went well.  Hope you don't get seasick from that sloshing  :)
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As for me, I'll borrow this thought: "Having never experienced kidney disease, I had no idea how crucial kidney function is to the rest of the body." - KD
mariannas
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« Reply #9 on: July 06, 2008, 11:32:36 PM »

YAY!  Glad to hear you're doing so well!  I love PD - it's so easy and no needles for a wimp like me!  You'll get used to that full feeling in no time.  Now, it's only with the first fill that I feel a bit uncomfortable.  Luckily that one isn't in very long and as soon as I drain and refill I feel totally normal (even though I feel like I look like a whale!).  One thing that *does* helps me feel less "full" is to fill a bit slowly and move around a bit (well as much as one can when tethered to the pole I suppose) - dance around a bit, lean from side to side - that seems to distribute the solution a little more evenly so I don't feel like I just ate an entire Thanksgiving turkey!
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KICKSTART
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In da House.

« Reply #10 on: July 07, 2008, 01:37:47 AM »

Glad you like pd ! You will find that you re-absorb some fluid from time to time , i do if i go over my exchange time. Thats the great thing about pd though , you can be a bit more flexable!
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OH NO!!! I have Furniture Disease as well ! My chest has dropped into my drawers !
peleroja
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I have 16 hats, all the same style!

« Reply #11 on: July 15, 2008, 09:57:24 AM »

I've always loved my PD.  I do it just about anywhere.  I travel a lot with a seniors travel group and do it in the back of the bus.  I've done it in my car and even (gasp) in an airport restroom (hey, any port in a storm, right?)  I agree with others about the flexibility.  Love it.  Glad it's finally working out for you!
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Adam_W
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Me with Baron von Fresenius

« Reply #12 on: July 15, 2008, 10:56:03 AM »

One of the things I like the most about PD is the flexibility of where you can do it, even without leaving home. When I'm doing my exchanges, once I'm hooked up, I can roll my IV pole anywhere in the house, and I'm not stuck in my bedroom. Next month I plan to go to the Indiana state fair, and I'm usually there all day. I plan to keep my bags in a cooler in the car, and I'll just return to the car every three hours and do my exchange in the parking lot. I have actually heard of people doing PD exchanges on airplanes. We should start a new thread: "What's the strangest/most unique place you've done a PD exchange?"

Adam
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-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"
Ken Shelmerdine
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Life's a bitch and then you go on dialysis!

« Reply #13 on: July 21, 2008, 08:15:28 AM »

I've always loved my PD.  I do it just about anywhere.  I travel a lot with a seniors travel group and do it in the back of the bus.  I've done it in my car and even (gasp) in an airport restroom (hey, any port in a storm, right?)  I agree with others about the flexibility.  Love it.  Glad it's finally working out for you!

How do you keep to the handwashing and cleanliness routine in such places? Surely you must be taking a risk doing an exchange in a washroom?
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Ken
peleroja
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I have 16 hats, all the same style!

« Reply #14 on: July 21, 2008, 10:13:00 AM »

Ken, I haven't washed my hands for dialysis in over 3 years.  I either use Purell or the handi wipes that my nephrologist gives me.  In over 5 years of PD I have never had peritonitis or any other problem.  As I once told a doctor, there is optimum and adequate.  I'm doing adequate and it works just fine for me.
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