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Author Topic: Haemodialysis Sessions  (Read 12586 times)
Chicken Little
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« Reply #25 on: May 07, 2007, 12:49:24 PM »

I'm 3 hours, 3 times a week.  I still pee though.
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charee
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« Reply #26 on: May 07, 2007, 02:49:09 PM »

I'm in my 4th week and are up to 5.5 hours 4 times aweek by the time i go home (i'm training for home hemo) i will  do 8 hours 4 times a week. Since i have started i have been able to stop caltrate and i only have a blood pressure meds every 2nd day and so far i am able to eat what i want.
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Home Hemo  18 months
Live donor transplant 28th October 2008
from my beautiful sister
Royal Prince Alfred Sydney Australia

Live donors rock
susie q
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« Reply #27 on: May 07, 2007, 04:34:16 PM »

Four.... lllooooooonnnngggg hours.   :(
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Ang
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« Reply #28 on: May 07, 2007, 06:27:58 PM »

3*4hours,seems  like  it  never  ends  somedays :banghead;
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live  life  to  the  full  and you won't  die  wondering
Adam_W
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Me with Baron von Fresenius

« Reply #29 on: May 07, 2007, 07:33:43 PM »

I have the "one size fits all" time of four hours, three times a week. When I start with NxStage, I will run 2 to 3 hours six days a week.

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"
tamara
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WOO HOO NEW KIDNEY PEEING !!!(Transplant 23/10/07)

« Reply #30 on: May 07, 2007, 07:37:25 PM »

Every Second Night during my sleep for 8 hours.
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ABO Incompatible Transplant from my loving Partner 23/10/07
after over four years on the D Machine 

                                                                                                                  
Dialysis Sucks and Transplants Don't.................So Far Anyway !!!!!
babi68
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« Reply #31 on: May 07, 2007, 10:47:21 PM »

I do 5 hours Mon, Wed, Fri, but am starting night dialysis soon and will be the same as Tamara. Liz :beer1;
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Amanda From OZ
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« Reply #32 on: May 08, 2007, 03:51:01 AM »

I make sure i do 25 hours within the 7 days.... !! between 6 - 8 hours a session.
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brenda
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« Reply #33 on: May 08, 2007, 09:10:47 PM »

I run 3.5 hours 3 x a week. When I go on nocturnal, I will be running a min of 6 hours a night, 6 night's a week.
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Life is what happens while your making other plans.
stauffenberg
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« Reply #34 on: May 11, 2007, 10:32:36 AM »

Since normal, in-center hemodialysis of 4 hours, three times a week only replaces 10% of normal renal function, it is best to go for as much dialysis time as you can tolerate, since much of the rapid aging and physical deterioration of renal patients is a function of their not being as fully dialyzed as they would have been with two natural kidneys.
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pierrat
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« Reply #35 on: May 13, 2007, 11:59:58 AM »

I'm on for 3 1/2 hours, I'm scheduled to go 3 times a week but I usually call in one session a week so on average I only go twice a week. I still have some decent kidney function remaining. My stats, even with 3 1/2 twice a week have been perfect for the last 4 months since ive been doing it. Meaning all my lab results are within normal parameters. I don't know how long this will last but hope I can continue like this for some time to come.

Oh and I've been on hemo for about a year now, with a fistula access.
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keefer51
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« Reply #36 on: May 13, 2007, 06:14:30 PM »

i am on for four hours three times a week. One time they put in The wrong time and i had to stay another hour. I didn't feel any different.
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i am a 51 year old male on dialysis for 3 years now. This is my second time. My brother donated a kidney to me about 13 years ago. I found this site on another site. I had to laugh when i saw what it was called. I hope to meet people from all over to talk about dialysis.
ILOVEFLUID
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« Reply #37 on: May 14, 2007, 04:56:03 AM »

Before i started home hemo, I was on 4 sessions a week...3 of them were 4.5 hrs and one of them was 3 hrs.  Made for a hell of a lot of time at the hospital.
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Each day at a time, one drink at a time (or two, or three...etc)
bolta72
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my best friend

« Reply #38 on: May 16, 2007, 05:49:31 AM »

closing in on 1 year on hemo, 3 1/2 hrs 3 days a week, getting use to it I guess, some days are better than others.
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gotta do what I gotta do.. 2 yrs in ctr hemo
mdorn
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« Reply #39 on: May 20, 2007, 06:21:31 PM »

I've been doing 3x3.5hrs for almost 3 years now. My clinic doesn't use the URR mearsurement, only KT/V, which mine is around 1.50 (minimum they want is 1.4) my dry weight is 87kilos. The only people that run for 4 hrs or more are very overweight people. I think I would go crazy running 5+ hours every time!! Also, my clinic doesn't have nocturnal dialysis.

Marv
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charee
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« Reply #40 on: May 20, 2007, 11:28:30 PM »

. The only people that run for 4 hrs or more are very overweight people.
Marv

At my centre I have been told even if someone is 70kg they still need at least 6 hours to clear ALL the toxins properly.
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Home Hemo  18 months
Live donor transplant 28th October 2008
from my beautiful sister
Royal Prince Alfred Sydney Australia

Live donors rock
kianhu
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« Reply #41 on: May 21, 2007, 11:40:42 PM »

A majority of our patients run 4 hours.  A few run more and a few run less. 
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Kimberly
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« Reply #42 on: July 17, 2007, 12:47:52 AM »

7 - 8 hours for me as I'm on noctural home hemo every other day.
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RichardMEL
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« Reply #43 on: July 19, 2007, 06:49:54 AM »

I run 5 hours and yeah it's a real pain when people come in AFTER me and waltz out before I'm done :( like there's one patient who does 3.5 hours and she complains it's so long!! HA!! I get the usual "it's better for you to do more and you should be glad you're healthy enough to cope with the longer session" - which I do understand but it doesn't help when I'm the last one there feeling very lonely!
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3/1993: Diagnosed with Kidney Failure (FSGS)
25/7/2006: Started hemo 3x/week 5 hour sessions :(
27/11/2010: Cadaveric kidney transplant from my wonderful donor!!! "Danny" currently settling in and working better every day!!! :)

BE POSITIVE * BE INFORMED * BE PROACTIVE * BE IN CONTROL * LIVE LIFE!
kitkatz
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« Reply #44 on: July 19, 2007, 02:04:49 PM »

I turn out the lights when I am in the center almost every time.  Wednesday I had a bleedy needle all treatment, and would't you know it.  The darn thing sprang up and bled just as i was up to go.  I was there until almost 8 last night. Late night for me.
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lifenotonthelist.com

Ivanova: "Old Egyptian blessing: May God stand between you and harm in all the empty places you must walk." Babylon 5

Remember your present situation is not your final destination.

Take it one day, one hour, one minute, one second at a time.

"If we don't find a way out of this soon, I'm gonna lose it. Lose it... It means go crazy, nuts, insane, bonzo, no longer in possession of ones faculties, three fries short of a Happy Meal, wacko!" Jack O'Neill - SG-1
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Goofynina and Epoman - Gone But Not Forgotten

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« Reply #45 on: July 27, 2007, 04:06:25 AM »

It has been a bit strange recently (but good strange!).  I am going in with about 4 kg to take off.  Before when I took of that much, I had cramps, headache, low BP, everything.   Now, I do get low blood pressure - I even went down to  77/40 on Wednesday, but I have had no cramps, and I come off feeling good.   On Wednesday, I ran down the steps to the car!  Is my body getting accustomed to dialysis?
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"To be found in Him, not having a righteousness of my own ...but that which is based on faith"



I LOVE  my IHD family! :grouphug;
goofynina
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He is the love of my life......

« Reply #46 on: July 27, 2007, 06:50:46 PM »

It has been a bit strange recently (but good strange!).  I am going in with about 4 kg to take off.  Before when I took of that much, I had cramps, headache, low BP, everything.   Now, I do get low blood pressure - I even went down to  77/40 on Wednesday, but I have had no cramps, and I come off feeling good.   On Wednesday, I ran down the steps to the car!  Is my body getting accustomed to dialysis?

Hi Aurora :)   It sounds like perhaps you have lost some dry weight and they are actually able to remove the fluid with no problems, they can probably take off a little more (but i wouldnt try it unless your ready for the cramping and the crashing)  :P  But that is what i am thinking, and as far as being able to run down the steps, that is AWESOME, i cant even run to the damn toilet :P :P :P  Keep up the great work my friend  :cuddle;
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....and i think to myself, what a wonderful world....

www.kidneyoogle.com
Adam_W
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Me with Baron von Fresenius

« Reply #47 on: July 27, 2007, 08:23:32 PM »

When I was in-centre, I ran the "standerd" 4X3 (four hours/three days/weed). Now I usually run 2 to 2 1/2 hours (depending on how much fluid I need to take off) six days a week.

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"
goofynina
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He is the love of my life......

« Reply #48 on: July 28, 2007, 04:10:51 PM »

When I was in-centre, I ran the "standerd" 4X3 (four hours/three days/weed). Now I usually run 2 to 2 1/2 hours (depending on how much fluid I need to take off) six days a week.

Adam

Adam, are your fluid restrictions the same with NxStage as it is on Hemo?  or do you feel like you can more fluids since you are dialyzing daily??  :popcorn;
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....and i think to myself, what a wonderful world....

www.kidneyoogle.com
Adam_W
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Me with Baron von Fresenius

« Reply #49 on: July 28, 2007, 04:32:17 PM »

I still have to go easy on the fluids, especially on my day off, but I don't have near the restrictions that I had before. Except for my day off, I can drink a fairly decent amount of fluids and still almost never have to take off more than a kilo.

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"
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