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Author Topic: Nephrectomy tomorrow. (12 Jan)  (Read 11168 times)
Des
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« Reply #50 on: February 02, 2010, 03:09:13 AM »

Hi,

I will start by saying ,thanks to all of you for caring. :flower;

I NEVER EVER want to go through that again. It is official : I am a wooz!

I had the nephrectomy on the 12Jan, spent 6 days in ICU. (dreadfull place to be :puke;

Had an epidural which did not work so the nursing staff thought - she is crazy- so they just pushed and shuved (spelling sorry) me around. Then on day three they realised the epidural was not working. oops.. sorry. She can now get some pain meds. Once I remembered screaming for 10 min non stop after they just turned me on my side!

I did not eat or drink anything for 6 days - just sips of ice water. Then the doc thought - "lets make this interesting." He gave me stuff to "start" the bowels moving so had gastro for the next 7 days.

After 8 days in hospital (still feeling like death warmed up) I just wanted to get out of there. I went home for a few day just to go back to the hospital to get my fistula.

You will never guess where he put it??!!! On my right arm (I am righthanded) smack in the bend. Yep, I can't bend my right arm again... ever again. This is so stupid!! :stressed;
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Please note: I am no expert. Advise given is not medical advise but from my own experience or research. Or just a feeling...

South Africa
PKD
Jan 2010 Nephrectomy (left kidney)
Jan 2010 Fistula
Started April 2010 Hemo Dialysis(hate every second of it)
Nov 2012 Placed on disalibity (loving it)
Des
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« Reply #51 on: February 02, 2010, 03:15:17 AM »

Oh , I forgot to mention... currently I have the flue. I cough (yes it hurts both wounds extremely) I have a sore throat, and I am a "blow you nose with your left hand" champion.

At least the gastro stopped....  :rofl; :rofl; imagine me coughing and ..... whatever. :rofl;

Dialysis will start as soos as I can get this fistula to ripen or something. Ir wrrrs but I cannot see anything yet.

I will be going back to work on the 1 March..... 
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Please note: I am no expert. Advise given is not medical advise but from my own experience or research. Or just a feeling...

South Africa
PKD
Jan 2010 Nephrectomy (left kidney)
Jan 2010 Fistula
Started April 2010 Hemo Dialysis(hate every second of it)
Nov 2012 Placed on disalibity (loving it)
HubbysPartner
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« Reply #52 on: February 02, 2010, 03:53:30 AM »

Oh, Des, what a time!  I'm glad you're home at least.  Sorry about your fistula placement.  I hope you get over your cold soon, that sounds like no fun at all.  Take care.   :grouphug;
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Caregiver to husband, Lou, diagnosed 2/2008
4/2009 - Fistula
10/2009 - Started NxStage training
112009 - Finished training; at home with nxstage

Our family - husband, Lou; me, Marge; sons, Marc & Keith; daughter, Liz
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YLGuy
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« Reply #53 on: February 02, 2010, 06:46:56 AM »

DES! We missed you.  :grouphug;
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cariad
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« Reply #54 on: February 02, 2010, 10:16:49 AM »

Des, I was thinking about you this morning. How great to log on and hear from you.

Your doctor should probably explain himself with regards to your fistula placement. Was that the only place he could find decent veins? Sounds :urcrazy; to me.

Welcome back!  :cuddle;
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My two beautifull granddaughters

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« Reply #55 on: February 02, 2010, 10:44:00 AM »

Oh, Des,
Although it is WONDERFUL to hear from you, I'm sad about everything you have been through.  :thumbdown;

I wish you could have gotten a better fistula. That's a bummer!

 :grouphug; :grouphug; :grouphug;

I hope from here on you just feel better an better!

 :cuddle; Aleta
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Wife to Carl, who has PKD.
Mother to Meagan, who has PKD.
Partner for NxStage HD August 2008 - February 2011.
Carl transplanted with cadaveric kidney, February 3, 2011. :)
billybags
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« Reply #56 on: February 02, 2010, 11:16:00 AM »

Des, lovely to hear from you, and so glad you are home. You sound like you have been through the mill, what the hell have they been doing to you? So it is upwards and onwards now. You take care and don't go back to work too soon.
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fc2821
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Just another hamster on the dialysis W.O.F.

« Reply #57 on: February 02, 2010, 12:48:06 PM »

       Des it is great to have you back.   :yahoo; :yahoo;

       You sure have had a tough time.   :grouphug;   :bestwishes;

        That sure is a syrange place for the fistula.  Any explinatipn why there, only place they could find?  ???

        I have a silly question, but has the new fistula affected how you type?
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In center hemo dialysis since Feb 14, 2007. 

If I could type properly, I'd be dangerous!

You may be only one person in the universe but you may mean the the universe to someone else.
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Hadija, Athol, Me and Molly at Havelock North 09

« Reply #58 on: February 02, 2010, 10:07:53 PM »

Oh Des, thank God that's over!  At least it IS over.  Dunno about the fistula - I am a fistula virgin (oh my word that sounds ...um...odd).  Sorry - don't want to make you laugh - that'll hurt!!  Just think though - any day now you'll suddenly reallise you are in way less pain, but you won't have noticed for a bit.  Such a good feeling.  Thinking of you always.
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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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« Reply #59 on: February 07, 2010, 12:06:58 PM »

God be on your side.
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« Reply #60 on: February 18, 2010, 10:31:08 PM »


Just thinking of you, all you've been through. I hope you are feeling stronger. Can you start back at work with less hours if you need to rest? I hope your fistula works just fine, if it's buzzing that's a good sign. Take care!  :cuddle;
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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
Des
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« Reply #61 on: February 19, 2010, 08:20:04 AM »

Thanks Karol,

Going through a tough time. I will be starting D in 4-6weeks ( as soon as the fistula is ready) I prepared for this but somehow reality is sinking in... my life as I know it is now gone forever and a new one is going to start soon. I hope I am ready for it.

I hope Jenna is doing better. I have been thinking about your family too amongst all my troubles.
 
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Please note: I am no expert. Advise given is not medical advise but from my own experience or research. Or just a feeling...

South Africa
PKD
Jan 2010 Nephrectomy (left kidney)
Jan 2010 Fistula
Started April 2010 Hemo Dialysis(hate every second of it)
Nov 2012 Placed on disalibity (loving it)
tyefly
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This will be me...... Next spring.... I earned it.

« Reply #62 on: February 19, 2010, 08:29:24 AM »

Des.....   You have watch many of us start D and we were scared...  I am not sure if scared is the right word.... you will do fine  just like I did.... and after you start....   you will look back and say......  yup I did it too....
   Seems like the first time for everything  is life is that hardest.....at least for me.....   I am past the starting of D....  and  the next chapter for me will be transplant....  I keep reading other people stories about transplant and I often say.... can I do this....   YES  I can.....  I am glad that you are here and I do want to support you during your journey with D...... Glad you are feeling better......
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IgA Nephropathy   April 2009
CKD    May 2009
AV Fistula  June 2009
In-Center Dialysis   Sept 2009
Nxstage    Feb 2010
Extended Nxstage March 2011

Transplant Sept 2, 2011

  Hello from the Oregon Coast.....

I am learning to live close to the lives of my friends without ever seeing them. No miles of any measurement can separate your soul from mine.
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The clearest way into the Universe is through a forest wilderness.
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monrein
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« Reply #63 on: February 19, 2010, 09:44:16 AM »

It is scary Des, I think we've all felt that way.  Please know that we're here to help make the transition as least threatening as possible.  Big hugs to you.  :grouphug;
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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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