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Author Topic: Wearing wedding rings  (Read 1918 times)
MooseMom
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« on: April 21, 2010, 09:19:34 AM »

When I went to see the surgeon to get my stitches out of my fistula, he told me to just use my (left) arm as usual but to be sure to have blood drawn and bp taken with my right arm, all of which I already knew.  Then he said in passing that I should move my wedding ring from my left hand to my right because of swelling.  I don't have problems with swelling right now, although I realize that as I get closer to needing dialysis, that may become an issue.  Have any of you had to change where you wear your wedding ring?  I just don't recall anyone ever mentioning this.  Thanks.
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"Eggs are so inadequate, don't you think?  I mean, they ought to be able to become anything, but instead you always get a chicken.  Or a duck.  Or whatever they're programmed to be.  You never get anything interesting, like regret, or the middle of last week."
cloud393
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« Reply #1 on: April 21, 2010, 11:12:35 AM »

I have not been told to switch fingers for my wedding ring.  I would think if you had swelling in your left had you would also have it in your right too.  I know my ring will stay on my left hand as long as I can stand it.
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May you live as long as you want and never want as long as you live.
monrein
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Might as well smile

« Reply #2 on: April 21, 2010, 02:24:40 PM »

I gave up wearing all rings while on dialysis (except on the odd occasion).  They were either uncomfortably tight as I swelled or too loose and about to fall off when I was at my dry weight.
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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
Sunny
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Sunny

« Reply #3 on: April 21, 2010, 03:29:42 PM »

I take my wedding ring off every night because by morning it's way too tight.
Put it back on during the day. Sometimes I forget to put it on.
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Sunny, 49 year old female
 pre-dialysis with GoodPastures
galvo
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« Reply #4 on: April 21, 2010, 04:48:21 PM »

Don't have one!
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Galvo
tyefly
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This will be me...... Next spring.... I earned it.

« Reply #5 on: April 21, 2010, 06:19:11 PM »

I could not wear rings when I was in center D....but now I wear them with no problems..... everyone is different...... 
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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.....

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jbeany
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« Reply #6 on: April 21, 2010, 08:17:45 PM »

I had rings I wore through dialysis.  It helps if they aren't very thick bands, though- thin ones handle swelling better.  And yes, they did "change size" on a daily basis, and some days when I was really bad with fluids, I did have to take them off.  As long as you are still comfortable with it, I wouldn't worry about changing it around. 
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"Asbestos Gelos"  (As-bes-tos yay-lohs) Greek. Literally, "fireproof laughter".  A term used by Homer for invincible laughter in the face of death and mortality.

MooseMom
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« Reply #7 on: April 22, 2010, 08:32:12 AM »

It's funny...you know how hard it is to get family/friends to really understand the impact that kidney disease has on your life?  Sure, they are sympathetic, but they don't see the little things that are affected.  Last night I was telling my husband about the wedding ring thing, and that really bugged him.  I think it all hit home.
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"Eggs are so inadequate, don't you think?  I mean, they ought to be able to become anything, but instead you always get a chicken.  Or a duck.  Or whatever they're programmed to be.  You never get anything interesting, like regret, or the middle of last week."
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