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Author Topic: First Day of Dialysis  (Read 3544 times)
pklipe57
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« on: April 21, 2009, 07:58:32 AM »

Friday at my appointment with my nephrologist they told me it was time to start dialysis.  My function wass 12 and my creatine was over 4.  My PTH is 200.  I had an appointment with my surgeon on Monday to check my fistula.  It is 9 weeks old.  I went and saw the surgeon and he said I needed angioplasty on the upper part of my fistula and sent me off to the hospital.  From there I went to dialysis for the first time.  One needle went in just fine and worked, the other needle went in but didn't have the blood flow it needed.  So my first dialysis lasted less than FIVE minutes.  Now I am scheduled to have a catheter put in tomorrow morning and and then straight to dialysis.  Hopefully I will only have the catheter a few weeks. 

This wasn't exactly the best way to start.  Has anyone else had a similar experience that they could share? 

Pam...
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paris
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« Reply #1 on: April 21, 2009, 08:15:30 AM »

Pam, I will be thinking of you tomorrow.  Let us know how the second try goes.   :cuddle;
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It's not what you gather, but what you scatter that tells what kind of life you have lived.
Stoday
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« Reply #2 on: April 21, 2009, 08:23:23 AM »

That's tough. I hope I don't have your bad luck when I start in six months time.

How long will your fistula take to repair?

Couldn't your dialysis start be delayed until it had been repaired? Or wasn't that an option?
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Diagnosed stage 3 CKD May 2003
AV fistula placed June 2009
Started hemo July 2010
Heart Attacks June 2005; October 2010; July 2011
willieandwinnie
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« Reply #3 on: April 21, 2009, 08:48:20 AM »

 :cuddle; Oh Pam. I am so sorry. I hope they get your fistula working correctly. Let us know as we will be thinking of you.  :cuddle;
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"I know there's nothing to it, but I want to know what it is there's nothing to"
G-Ma
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« Reply #4 on: April 21, 2009, 09:22:20 AM »

 :grouphug;
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Lost vision due to retinopathy 12/2005, 30 Laser Surg 2006
ESRD diagnosed 12/2006
03/2007 Fantastic Eye Surgeon in ND got my sight back and implanted lenses in both eyes, great distance & low reading.
Gortex 4/07.  Started dialysis in ND 5/4/2007
Gortex clotted off Thanksgiving Week of 2007, was unclotted and promptly clotted off 1/2 hour later so Permacath Rt chest.
3/2008 move to NC to be close to children.
2 Step fistula, 05/08-elevated 06/08, using mid August.
Aug 5, 08, trained NxStage and Home on 9/3/2008.
Fistulagram 09/2008. In hospital 10/30/08, Bowel Obstruction.
Back to RAI-Latrobe In Center. No home hemo at this time.
GOD IS GOOD
hurlock1
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« Reply #5 on: April 21, 2009, 11:03:31 AM »

Well, I guess that I was blind going in. I had my fistula and cathetor put in at the same time. I had my cathetor put in and was using that until my fistula "matured" While I was asleep one night, I musta' put my elbow of arm on my cathetor, turned over, and woke up the next morning with the catheter laying in the bed. I couldn't figure out why I didn't bleed to death. The tried the fistula, it didn't work. So I had to go and get another catheter, this one sticking out of my neck. I was horrified. I couldn't go outside, couldn't see my grandkids. but finally some time later, I was able to use the fistula. Just a little helpful hint. It is OK to use Emla Cream. When you get to a 15 or 14 guage needle, They HURT going in. For me it's a pain in the back (only lower) remembering tp put the Emla Cream on an hour before dialysis, but it helps
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Savemeimdtba
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« Reply #6 on: April 21, 2009, 02:31:16 PM »

Well, I haven't had your exact experience.. but I did have the catheter and it's not SO bad.  It doesn't hurt or anything, it's just a pain to bathe and sleep.  But, you just have to keep thinking about it being gone soon and look forward to that.  I always find it's easier to deal with things if I think of something to look forward to.  The surgery itself won't hurt at all and you'll get some nice twilight meds to keep you calm and hopefully dialysis will help you feel better.. good luck!
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-Kristi-
12/2008 - Began Hemodialysis
03/2009 - Began P.D.

"You gotta swim, swim for your life, swim for the music that saves you when you're not so sure you'll survive"
angellady07
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« Reply #7 on: April 21, 2009, 06:49:30 PM »

Take care Pam. I hope the angioplasty on your fistula goes well. I was lucky I only had my cath a couple of months before they started using second graft. I agree bathing is a real issue. I wrapped myself like a mummy with saran wrap and plenty of tape. I enjoyed a brief break from the needles.
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pklipe57
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« Reply #8 on: April 23, 2009, 07:02:05 AM »

I had my catheter put in Wednesday morning and was taken straight to dialysis and was home by 12:30 in the afternoon.  They only did a 2 and a half hour run.  Friday I will have 3 and a half hour run.   Everything went smooth.  Maybe it's just me, but I feel better already - I know a lot of the anxiety is now gone.  Thanks to everyone for their encouraging words.

Pam...
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angellady07
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« Reply #9 on: April 23, 2009, 12:10:38 PM »

I'm glad you are feeling better. Take care.  :waving;
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Savemeimdtba
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« Reply #10 on: April 23, 2009, 12:40:36 PM »

Excellent that you are feeling better!  Maybe after Friday you will be feeling even more healthy since you are getting rid of some of those toxins that have been building up.  I don't know about you but I never knew how much my low performing kidneys were affecting me until I started PD - I just thought it was normal to feel the way I did. 
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-Kristi-
12/2008 - Began Hemodialysis
03/2009 - Began P.D.

"You gotta swim, swim for your life, swim for the music that saves you when you're not so sure you'll survive"
okarol
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« Reply #11 on: April 23, 2009, 01:22:52 PM »


Jenna's fistula took 6 months to mature, which I think is very unusual. But she used the chest catheter during that time with no problems. I took her to a little hair salon to have her hair washed, which made things easier. She really did enjoy those first showers after the catheter was removed!
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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 -
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pklipe57
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« Reply #12 on: May 04, 2009, 08:50:55 AM »

I have now finished two weeks of dialysis using my catheter and am beginning to tell a difference.  I had a followup with the surgeon to recheck my fistula and the blood flow is great - however the vein is too deep in my upper arm.  He wants to go in and remove fat tissue so the vein will be closer to the surface.  Can anyone who has had this share their experience?  Thanks for your time.

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dwcrawford
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Getting the heck out of town.

« Reply #13 on: May 05, 2009, 07:00:51 PM »

I fihished two weeks of d Friday.  Cath and fistala put in two weeks ago Monday.  Surgeon said he may have to do more work on the fistala because it might be too deep, similar  to your problem I think.  I check in next Monday.  In the mean time:

Did you all experience exhaustion at first.  On days when I feel human, all I want to do it sleep.  I'm either asleep or on my way to dialysis.  I'm also having blurred vision.  Is that typical.  Also, lack of appetite (probably attributable to the food we're supposed to eat).  I'm deathly afraid I'll pull the cath out or get it wet.  I want a long tub bath.
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Come to think of it, nothing is funny anymore.

Nothing that I post here is intended for fact but rather for exploration into my personal thought processes.  Any slight, use of words with multiple connotations or other percieved insults are totally unintended.  I reserve my insults for private.
pklipe57
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« Reply #14 on: May 06, 2009, 09:11:09 AM »

I was afraid of pulling the catheter out.  When they changed my dressing of Monday, they put something around the two tubes (whatever they are called) and the bottom of it sticks to my chest wall with a large sticky bandaid of some type.  It is much more secure and I don't feel like it is going to come out. 

I want to take a long hot shower and really wash my hair about 10 times.  Washing my hair in the sink isn't cutting it.  I did get a hand held shower head and I can have a shower or some sort.  It is better than nothing.

 
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monrein
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Might as well smile

« Reply #15 on: May 06, 2009, 10:16:32 AM »

Please be very very careful about the showering and hair washing.  An infection in a permacath could be life threatening and isn't worth the risk IMO.  Some people have bought these Korshields to keep the catheter dry and safe.  Not cheap but way better than risking infection.

http://www.korshield.com/
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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
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