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Author Topic: Ears ringing after dialysis  (Read 2896 times)
carol1987
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« on: December 11, 2010, 08:09:39 AM »
I just got home from hd and my ears are ringing.... Anyone experience this after treaments???
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Diagnosed with  PKD July 2002 (no family history)
Fistula placed April 2009
Placed on Transplant list April 2009
Started HD 10/6/10
Transplanted 1/6/11 (Chain Transplant My altruistic donor was  "Becky from Chicago" , and DH Mike donated on my behalf and the chain continued...)
thegrammalady
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« Reply #1 on: December 11, 2010, 08:51:19 AM »
my ears have been ringing recently, but i never associated it with dialysis. i'll have to pay a bit more attention and see what i can figure out.
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brandi1leigh
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« Reply #2 on: December 11, 2010, 11:36:18 AM »
My ears ring after dialysis frequently. It's at its worst when my blood pressure has dropped, even when they get my bp back up, my ears ring for awhile.
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casper2636
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« Reply #3 on: December 11, 2010, 01:33:20 PM »
My ears ring all the time after hd. I've been told that it's the change in blood pressure in you body and in your head.
Knowing that doesn't help, but at least you know why. I've always had a problem with significant loss of blood pressure (down to 68/48) and boy, can my ears play the bells! Has anyone else gotten any other reasons for the symphony?
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iketchum
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« Reply #4 on: December 11, 2010, 05:05:27 PM »
My ears started to ring after starting on a new medicine, One in a hundred got ringing ears from it. It may be the med and dialysis combined, but I no longer need the radio on to get to sleep now.
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Phil
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« Reply #5 on: December 11, 2010, 06:53:45 PM »
I have Alports Sydrome....and my ears ALWAYs ring!
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1993 - Diagnosed with Alport Sindrome
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May 2010 - Started HD
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Rerun
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« Reply #6 on: December 11, 2010, 07:33:13 PM »
Yes, my ears ring when I get home and it is quiet.  Turn on the tv or something.
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« Reply #7 on: December 12, 2010, 03:54:46 AM »
Yeah its BP , when mine gets way high i get a whooshing in them !
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OH NO!!! I have Furniture Disease as well ! My chest has dropped into my drawers !
carol1987
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« Reply #8 on: December 12, 2010, 05:19:18 AM »
Thanks Everyone...  good to know others have this association too.... 
Have not had it before so  I will have to see what happens on Tuesday....
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Diagnosed with  PKD July 2002 (no family history)
Fistula placed April 2009
Placed on Transplant list April 2009
Started HD 10/6/10
Transplanted 1/6/11 (Chain Transplant My altruistic donor was  "Becky from Chicago" , and DH Mike donated on my behalf and the chain continued...)
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