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Author Topic: Things not to do to me while I am at My dialysis center.  (Read 13830 times)
donnia
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me and my donor Joyce

« Reply #25 on: April 11, 2008, 05:12:45 PM »

I only have one, and it is directed at one tech.... I'll call him Wayne, cause thats his name...... >:(


DO NOT throw my glove in my lap when it is time for me to hold my sites, cause next time you do so I will throw it back and I'll add a few four letter words with it!     :sir ken;

The rest of my techs and nurses are the best.... love them all! :cuddle;
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Born with one kidney 1972
Ureter re-constructured 1975 (reflux had already damaged the kidney)
Diagnosed and treated for high blood pressure 2000
Diagnosed ESRF October 2006
Started dialysis September 2007
Last dialysis June 4, 2008
Transplant from my hero, Joyce, June 5, 2008
thegrammalady
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« Reply #26 on: April 12, 2008, 10:31:23 AM »

if i'm sleeping don't wake me, unless the building is on fire or i'm bleeding to death. only the doctor can because he comes specifically to see me, everyone else works in the building, they can wait till i'm awake.

labs are done on monday, results are in on wednesday. if they are all so fired important why should i have to wait two weeks to get the results. yes, i realize i'm not the only one who has lab work, but come on now the results print out is a computer program, really how long does it take to push a few buttons. i'm not 5, i don't need (or want) the kindergarten version. i can read and understand the same print out the doctor gets (for reallies)

and if i have a problem, don't send the social worker to talk me out of it (unless you want an irritated mad raging bull) just get the problem fixed (i'm really not a nice lady, it's all your imagination and i can prove it if you really want)
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s
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If you can smile when things go wrong, you have someone in mind to blame.

Lead me not into temptation, I can find it myself.

Life isn't about waiting for the storm to pass, it's about learning how to dance in the rain.

Some mistakes are too much fun to only make once.

Meddle Not In The Affairs Of Dragons
For You Are Crunchy And Taste Good With Ketchup
Chris
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« Reply #27 on: April 12, 2008, 12:53:40 PM »

if i'm sleeping don't wake me, unless the building is on fire or i'm bleeding to death. only the doctor can because he comes specifically to see me, everyone else works in the building, they can wait till i'm awake.

labs are done on monday, results are in on wednesday. if they are all so fired important why should i have to wait two weeks to get the results. yes, i realize i'm not the only one who has lab work, but come on now the results print out is a computer program, really how long does it take to push a few buttons. i'm not 5, i don't need (or want) the kindergarten version. i can read and understand the same print out the doctor gets (for reallies)

and if i have a problem, don't send the social worker to talk me out of it (unless you want an irritated mad raging bull) just get the problem fixed (i'm really not a nice lady, it's all your imagination and i can prove it if you really want)
This damn smiley face crap seems to be a universal dialysis clinic approach in the United States the more I read on here. I hated those darn stickers, they are useless. Why can't they get it thru their thick skulls!

I guess I would have to  :Kit n Stik; into them to give me actual lab results.
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Diabetes -  age 7

Neuropathy in legs age 10

Eye impairments and blindness in one eye began in 95, major one during visit to the Indy 500 race of that year
   -glaucoma and surgery for that
     -cataract surgery twice on same eye (2000 - 2002). another one growing in good eye
     - vitrectomy in good eye post tx November 2003, totally blind for 4 months due to complications with meds and infection

Diagnosed with ESRD June 29, 1999
1st Dialysis - July 4, 1999
Last Dialysis - December 2, 2000

Kidney and Pancreas Transplant - December 3, 2000

Cataract Surgery on good eye - June 24, 2009
Knee Surgery 2010
2011/2012 in process of getting a guide dog
Guide Dog Training begins July 2, 2012 in NY
Guide Dog by end of July 2012
Next eye surgery late 2012 or 2013 if I feel like it
Home with Guide dog - July 27, 2012
Knee Surgery #2 - Oct 15, 2012
Eye Surgery - Nov 2012
Lifes Adventures -  Priceless

No two day's are the same, are they?
thegrammalady
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« Reply #28 on: April 12, 2008, 09:35:22 PM »



I guess I would have to  :Kit n Stik; into them to give me actual lab results.

it's really not all that difficult, i simply ask the nurse for the print out on wensdays when i arrive. it's much more complete than the kindergarten version the dietitian trys to give me a week or more later. i just smile at her and say "i've seen them" and she keeps walking.
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s
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If you can smile when things go wrong, you have someone in mind to blame.

Lead me not into temptation, I can find it myself.

Life isn't about waiting for the storm to pass, it's about learning how to dance in the rain.

Some mistakes are too much fun to only make once.

Meddle Not In The Affairs Of Dragons
For You Are Crunchy And Taste Good With Ketchup
Chris
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« Reply #29 on: April 13, 2008, 06:33:16 PM »



I guess I would have to  :Kit n Stik; into them to give me actual lab results.

it's really not all that difficult, i simply ask the nurse for the print out on wensdays when i arrive. it's much more complete than the kindergarten version the dietitian trys to give me a week or more later. i just smile at her and say "i've seen them" and she keeps walking.
My center was not like that dimwit one and dimwit two (social worker and dietician) would never give me a print out of my results. I only got a weeks worth of true results post trasplant from the center because the transplant center requested them for comparison values. Those darn smiley face stickers irritate the heck out of me still when I think of the center.
Logged

Diabetes -  age 7

Neuropathy in legs age 10

Eye impairments and blindness in one eye began in 95, major one during visit to the Indy 500 race of that year
   -glaucoma and surgery for that
     -cataract surgery twice on same eye (2000 - 2002). another one growing in good eye
     - vitrectomy in good eye post tx November 2003, totally blind for 4 months due to complications with meds and infection

Diagnosed with ESRD June 29, 1999
1st Dialysis - July 4, 1999
Last Dialysis - December 2, 2000

Kidney and Pancreas Transplant - December 3, 2000

Cataract Surgery on good eye - June 24, 2009
Knee Surgery 2010
2011/2012 in process of getting a guide dog
Guide Dog Training begins July 2, 2012 in NY
Guide Dog by end of July 2012
Next eye surgery late 2012 or 2013 if I feel like it
Home with Guide dog - July 27, 2012
Knee Surgery #2 - Oct 15, 2012
Eye Surgery - Nov 2012
Lifes Adventures -  Priceless

No two day's are the same, are they?
RichardMEL
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« Reply #30 on: April 16, 2008, 12:39:13 AM »

What the...? smiley faces??? sheesh. I just ask for the printout or the numbers and they read it off the computer to me. No fuss no issue.

We get a dietician visit once a year (ugh what a chore.. tell me about your average meals in a day.. blah blah blah.. yeah miss I drink 3 litres of coke and eat chocolate cake all day what do YOU think. If my labs are off tell me I should eat more of X or less of Y.. don't make me repeat the same crap over and over... oh and by the way my labs ARE fine because *I* take an active interest in my body and the results on a monthly basis and if something's a bit up I'll adjust accordingly).. blah

Of course they did send this CUTE student dietician the other day... now she can come back anyday hubbay hubba ;)
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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!
kimcanada
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« Reply #31 on: April 16, 2008, 10:41:39 AM »

Richard made me think of this...

Why with a disease where diet is SO important , would I have only seen a dietitian once in a year and a half??  Would you not think that they would offer classes or even a handout of a healthy recipe once a year or something??? :rant;

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thegrammalady
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« Reply #32 on: April 16, 2008, 11:01:32 AM »

Richard made me think of this...

Why with a disease where diet is SO important , would I have only seen a dietitian once in a year and a half??  Would you not think that they would offer classes or even a handout of a healthy recipe once a year or something??? :rant;



we have a dietitian and a social worker on staff at my center. i don't always see them wandering around talking to people every session but if i need one of them all i have to do is ask.
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s
......................................................................................
If you can smile when things go wrong, you have someone in mind to blame.

Lead me not into temptation, I can find it myself.

Life isn't about waiting for the storm to pass, it's about learning how to dance in the rain.

Some mistakes are too much fun to only make once.

Meddle Not In The Affairs Of Dragons
For You Are Crunchy And Taste Good With Ketchup
kitkatz
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« Reply #33 on: April 16, 2008, 09:29:59 PM »

All i have to do is holler and I get the dietician or the social worker anytime.  I am lucky I sit right up front and they are walking back an dforth a lot.
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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
Adam_W
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Me with Baron von Fresenius

« Reply #34 on: April 16, 2008, 10:20:36 PM »

I see my dietitian and social worker once a month, but I can call them anytime I need them.

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"
kimcanada
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« Reply #35 on: April 17, 2008, 03:46:47 AM »

you guys are lucky, we do see thw social worker once a week , she will walk around and ask how things are going... dietitian... once , last May
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kellyt
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« Reply #36 on: April 17, 2008, 11:57:38 AM »

you guys are lucky, we do see thw social worker once a week , she will walk around and ask how things are going... dietitian... once , last May

That's crazy...
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1993 diagnosed with glomerulonephritis.
Oct 41, 2007 - Got fistula placed.
Feb 13, 2008 - Activated on "the list".
Nov 5, 2008 - Received living donor transplant from my sister-in-law, Etta.
Nov 5, 2011 - THREE YEARS POST TRANSPLANT!  :D
monrein
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Might as well smile

« Reply #37 on: April 17, 2008, 12:15:33 PM »

Kim, have you asked to see the dietician?  I did a student social work placement in a big Toronto hospital and the dietician was a huge part of the team.  Last week when I saw the new renal management team here, again the dietician was one of the folks I met.  Ask the social worker how come your dietician is so missing in action?  I personally like it when I see the SW and the dietician only when I want them but when I need them, I want them to be available.
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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
Neo
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Dont let dialysis stop you...

« Reply #38 on: April 21, 2008, 02:30:32 PM »

WoW I should totally post this on my door at my unit!! This is great we should print theses and give them out to the staff!!
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« Reply #39 on: April 22, 2008, 08:14:29 AM »

:bunny:
 missing my Lucky Bunny since last May RIP Lucky!


Reading these postings makes me sick! You are the damn customer and client.
This crap should Not be taking place.

Too many staff members have the attitude that WE are there for their benefit.

As for the gross, dirty, noisy patient next to you, the staff should say something to him or her.

The staff gets paid to show you every due consideration.

Managers need to insure that patients come first!

The nurse is supposed to be your #1 ADVOCATE not the advocate of the clinic or hospital.

........bdpoe/ Florida
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spacezombie
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Melissa: ESRD since 1992, transplant June 10, 2008

« Reply #40 on: April 22, 2008, 04:14:02 PM »

Oh man, this list was great. Most of the hospital staff has no idea what it is like to be a patient.

My list of things not to do to me while on PD:

* DON'T just start trying to yank out my PD tube to inspect it. ASK first. I don't want your grimy doctor hands on it spreading germs and it is rude to unbutton someone's pants without asking first.

* When my phosphorus is bad, understand that I get lectured about it 700 times. I know what foods are bad to eat. Also, don't lecture me about my bad phosphorus last month until you see the new labs from this month!!

* Do not treat me like a child. I know I look like I'm 12 but I'm actually 30.

* Do not treat me like a criminal when my labs are bad. I make every attempt to take care of myself but sometimes my body does not cooperate.

* Doctors: when you have bad news for someone, do not make the nurse deliver the news for you!

* Do not make important health decisions without consulting me first. Do not schedule surgery without telling me then leave a message about it on my answering machine!

* I'm on time to my appointments. Be on time to yours! Do not leave me waiting for 3 hours every month.

* Don't hug me, don't shake my hands unless you've washed yours first.

--

Things not to do to me on Hemo:

* When I tell you I have gained actual fatty weight, do not attempt to pull off this extra weight as water.

* Show me what you are doing. My treatment should not be a secret.

* If I freak out in fear before my hemo treatment, it is not because I am a baby: it is because I think the techs/nurses might kill me.

--

Things not to do to me in the Hospital:

* Don't give me a cup of pills without telling me what each one is, their side effects, and why I must take them.

* Read my chart! There is quite a bit of information on there. It'll keep you from lecturing me about blood sugar when I am not a diabetic!

* Quit giving me milk and yogurt!

* Do not put people with horrible contagious diseases next to me! No, I hadn't had the chickenpox yet, thanks!

--

I'm sure there is more. The hospital always pisses me off! At least right now I have an excellent PD nurse that always takes good care of me.  :waving;
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I have Alport's Syndrome. My kidneys failed when I was 14 and I was on PD for five years before receiving a kidney transplant from my mother. That kidney failed in 2004 and I've been back on PD ever since. I am undergoing treatment for my high antibodies at Cedars-Sinai medical center. I had a kidney transplant on June 10, 2008. My boyfriend was the donor.
JasonEb
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« Reply #41 on: April 23, 2008, 02:00:38 AM »

I think I've got a few...

Please don't lecture me about anything kidney/dialysis related.  You've been working here 2 years while I've been living it for nearly 10, as well as living with someone who's worked in the field for nearly the same amount of time.  I'm sure I could train new workers at this point.

Please, if you're a fat nurse/doctor or reek of cigarette smoke as you hover over me, don't lecture me about how I need to improve my lifestyle, or how I'm "killing myself" by skipping a treatment now and then.

Please change the policy about not being able to use the restroom during treatments.  When the techs, nurses, or doctors are willing to come out on the floor, put those flimsy, see-through screens around themselves and sit on a port-a-potty, then so will I.  Until then, take me off the machine for five lousy minutes so I can go use the restroom like a civilized person.

I understand that the bleach water that has the clamps in it has to go somewhere, and I'm resigned that that place is near my chair, but PLEASE do not toss the clamps into it so that I continuously get bleach splashed on me.

Please, when I eat my lunch each day during treatments, come up and ask me "Did you take your binders?".

Speaking of lunch, can we please take down (or at least move it out to the lobby or something) that awful poster that's right next to the scale that shows people toes and other body parts rotting off.  Every time I weigh in, I have to see that thing just before I eat!

If I want to be taken off early, do NOT try to talk me out of it, or try to compromise with me.  I TOLD you I want to be taken off, it wasn't an invitation for a debate.

If you're using that sling thing to put someone in a chair across from me, when he/she is in the chair, don't just push the sling so that it rolls across the aisle and runs into my chair.  The same holds true for garbage cans and wheelchairs.

If you're wheeling someone out, and have to stop in order to take care of something else, do NOT place them so close to me that I could kiss them if I wanted to.

And lastly, DO NOT SQUEEZE THE CHARMIN!!

No, wait...forget that last one.

~Jason E.
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spacezombie
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Melissa: ESRD since 1992, transplant June 10, 2008

« Reply #42 on: April 23, 2008, 02:17:46 AM »


Speaking of lunch, can we please take down (or at least move it out to the lobby or something) that awful poster that's right next to the scale that shows people toes and other body parts rotting off. 

Hahaha, I agree. There is a horrible poster in my dialysis unit of infected catheters. I really could do without seeing that.  :puke;
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I have Alport's Syndrome. My kidneys failed when I was 14 and I was on PD for five years before receiving a kidney transplant from my mother. That kidney failed in 2004 and I've been back on PD ever since. I am undergoing treatment for my high antibodies at Cedars-Sinai medical center. I had a kidney transplant on June 10, 2008. My boyfriend was the donor.
twirl
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« Reply #43 on: April 23, 2008, 03:24:31 AM »

:banghead; a policy not to get off to go to the bathroom    where did you get dialysis    in Hell >:D
at least if I beg enough, I am blessed to go to the bathroom
I'd get off early every treatment due to waste products on the floor, chair and my jeans if we had that policy
and I bitch about a 30 minute wait after asking to go to the potty
it must be a pitiful day in dialysis if you have direaha
we should start a new thread--- things to do while you are trying and sweating and praying not to have an "accident" :o
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Adam_W
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Me with Baron von Fresenius

« Reply #44 on: April 23, 2008, 09:39:52 AM »

Don't jump to conclusions and assume I'm going to hurt myself or others and make me end my treatment early because I'm upset. During one of my emotional breakdowns I had in-centre, They were assuming that, and they made me leave with and hour and a half left in my treatment. Just before that, the patient next to me requested to get off the machine early because he thought I was "dangerous". I later set things right with the patient and we continued to be friends, but the staff had me labeled as emotionally unstable the rest of the time I was there. I kept expecting for them to make me do dialysis in a straight jacket".  :Kit n Stik; "Assumption is the mother of all f***ups" (line from the movie "Under Siege 2"). 
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"
Chris
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« Reply #45 on: May 02, 2008, 06:47:21 PM »

"Assumption is the mother of all f***ups" (line from the movie "Under Siege 2"). 
That is a classic line/quote that is very useful.
Logged

Diabetes -  age 7

Neuropathy in legs age 10

Eye impairments and blindness in one eye began in 95, major one during visit to the Indy 500 race of that year
   -glaucoma and surgery for that
     -cataract surgery twice on same eye (2000 - 2002). another one growing in good eye
     - vitrectomy in good eye post tx November 2003, totally blind for 4 months due to complications with meds and infection

Diagnosed with ESRD June 29, 1999
1st Dialysis - July 4, 1999
Last Dialysis - December 2, 2000

Kidney and Pancreas Transplant - December 3, 2000

Cataract Surgery on good eye - June 24, 2009
Knee Surgery 2010
2011/2012 in process of getting a guide dog
Guide Dog Training begins July 2, 2012 in NY
Guide Dog by end of July 2012
Next eye surgery late 2012 or 2013 if I feel like it
Home with Guide dog - July 27, 2012
Knee Surgery #2 - Oct 15, 2012
Eye Surgery - Nov 2012
Lifes Adventures -  Priceless

No two day's are the same, are they?
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Step back. Im full of toxins.

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« Reply #46 on: May 02, 2008, 06:57:53 PM »

You guys are hilarious.

Mine is simple.

1. Yes, i do consider asking for Tylenol a medical emergency. Dont take your sweet time. I have a headache. :Kit n Stik;
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"All we are is dust in the wind," dude.
Bill and Ted's Excellent Adventure

http://ihaveesrd.blogspot.com/
Alports @ age 19 hemo in center 4 months
20 paternal kidney transplant 14 years
Present 1 1/2 yr PD
4 month in center
now 6 months @ home NxStage Daily
Soon Nocturnal!
spacezombie
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Melissa: ESRD since 1992, transplant June 10, 2008

« Reply #47 on: May 03, 2008, 03:57:12 PM »

You guys are hilarious.

Mine is simple.

1. Yes, i do consider asking for Tylenol a medical emergency. Dont take your sweet time. I have a headache. :Kit n Stik;

Hahaha, I agree. After my first transplant, I had a horrible cyclosporine induced headache and I could not get anyone to bring me something for it. I finally sat on the floor in the hallway until they helped me. I found that sitting on the floor in the hospital and crying gets you morphine very quickly.
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I have Alport's Syndrome. My kidneys failed when I was 14 and I was on PD for five years before receiving a kidney transplant from my mother. That kidney failed in 2004 and I've been back on PD ever since. I am undergoing treatment for my high antibodies at Cedars-Sinai medical center. I had a kidney transplant on June 10, 2008. My boyfriend was the donor.
alrightstill
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BAH!

« Reply #48 on: May 03, 2008, 08:11:25 PM »

Wow, I couldnt agree with all of you more!

I do the nXstage 6 days a week. 

Here's a little list of my things not to do to me while I'm dialyzing at home.  Now, mind you, the following may have only been done once (some more --) but once is enough! haha.

  - Please do not invite people over while I'm on the machine - even if they don't come in my dialysis room.  I'm nosey as all hell and hate to feel like I'm missing out on fun. 
  - Please do not cut thru the dialysis room to get to our balcony and leave the dogs in the room with me barking up a storm cuz they want to go outside with you. 
  - Pleaseeeee do not hand me the phone while I'm on the machine.  More than likely I'd rather not talk .. to anyone.
  - Please do not say "geesh its like a sauna in here" everytime you walk in the room.  Yes, I need my portable space heater with a remote.. even in the middle of summer!
  - Please understand that afterwards I may have a hot flash and then need my air conditioner on - I'm not indecisive.  Ok, I am.. but I'm also an unpredictable dialysis patient.  ;)
 
For the people living downstairs (my neighbors slash landlords):
   - Please dont point out and say something everytime I get a delivery.  Yes. He's here again with 22 boxes.  He's been coming every 2 weeks for 3 and a half years now.. do we still have to point it out each time?
    - Please let him pull up as close as he can to the front porch.  Those boxes are heavy and he then has to carry them up 18 stairs.  It wont hurt your halfdead grass to have a car parked on it for a half hour every 2 weeks.
    - When we're all sitting outside enjoying the sun with your children's friends over - please do not bring up my colonoscopy .. or yours .. or the fact that I don't pee.
    - Please do not ask me why I dont fall asleep every night (morning) til 7am.  I'm an insomniac.. and I can't help it.  You should know this by now.

Ohhh. one more for the neighbor.
   - Please do not walk your dog during the delivery, especially if he was just out an hour prior to the delivery.  We all know you're just trying to be nosey!
 And another - Please do not ask me to hurry up when I'm outside with my dogs because you want to bring your precious little dog out to do his business.  Our yard is huge and theres enough room for all of us to be out at the same time and not disrupt one another.    (Thats not dialysis related, but its been bothering me hahaha)
« Last Edit: May 03, 2008, 08:31:40 PM by alrightstill » Logged

1992 @ age 12 i was suddenly diagnosed with ESRD. 
1992 - 1995: Peritoneal Dialysis
1995: Cadaver Transplant
2001: Kidney rejects, back on PD
2002: too much scar tissue prevents PD from succeeding, go on hemo via permacath,
         transplanted kidney is removed.
Dec 2004 -- 2009t: on NXSTAGE (with the bags NOT pureflow) 6x a week via permacath
Dec 2009: Transplant from a pal
Oct 2016 - present:  Transplant fails, back on NxStage w/pureflow via femoral cath, patiently waiting for next kidney
tubes
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Posts: 598


Miss you so much Susie. Will always <3 you!

« Reply #49 on: May 03, 2008, 08:23:59 PM »

I have one....

At the end of treatment when I'm being taped up...PLEASE, don't wrap the tape all the way around my arm. I have to rip that crap off the next morning. NOT FUN! ! ! 

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"To be happy is the choice I wish to make in spite of the circumstances that are strewn in my path."

1996 - started incenter hemo
a few months later, started PD
2005 - started incenter hemo
AGAIN
  - on transplant list as of August 7, 2009.
2011/June - 15 years on "D"
Transplant - Tuesday October 18th 2011
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