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Sugarlump
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10 years on and off dialysis

« on: July 28, 2014, 05:30:20 AM »

Just lately I've noticed my ears become affected towards the end of dialysis and for an hour or two afterwards.
They feel blocked, my hearing is reduced and they are generally uncomfortable until it clears?

Why would dialysis cause this? Is there a medical explanation for it?
How do I stop it???
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10 years of half a life
3 years HD 1st transplant Feb 08 failed after 3 months
Back to HD 2nd transplant Dec 10 failed after 11 months
Difficult times with a femoral line and catching MSSA (Thank you Plymouth Hospital)
Back on HD (not easy to do that third time around)
Fighting hard (two years on) to do home HD ... watch this space!
Oh and I am am getting married 1/08/15 to my wonderful partner Drew!!!
The power of optimism over common sense :)
Dman73
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« Reply #1 on: July 28, 2014, 08:44:30 AM »

If I get below my dry weight my ears don't seem to function properly even after I equalize them and only correct after going home and having dinner along with some fluid replacement.
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hd 73
tx  87
hd 01

by the yard life is hard by the inch it's a cinch...
cdwbrooklyn
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Positive Thoughts equal Positive Energy

« Reply #2 on: July 28, 2014, 12:13:23 PM »

When I was in center my ears use to get stopped up as well.   I noticed it when I use to take off too much water.  Also, it would take a while before it cleared.   I guess it’s a part of dialysis, however, I don’t really experience it now on NxStage not that I can recall. 
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Dailysis patient for since 1999 and still kicking it strong.  I was called for a transplant but could not get it due to damage veins from extremely high blood pressure.  Have it under control now, on NxStage System but will receive dailysis for the rest of my life.  Does life sucks because of this.  ABOLUTELY NOT!  Life is what you make it good, bad, sick, or healthy.  Praise God I'm still functioning as a normal person just have to take extra steps.
PrimeTimer
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« Reply #3 on: July 28, 2014, 07:00:00 PM »

My mother did not have kidney disease (she had congestive heart failure) and was on Coumadin and 2 "water pills" to keep fluid from building up and she use to complain about her ears always being stopped up. Makes you wonder if fluid build up and/or removal has anything to do with it. Will be interesting if anyone can answer your question. 
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Husband had ESRD with Type I Diabetes -Insulin Dependent.
I was his care-partner for home hemodialysis using Nxstage December 2013-July 2016.
He went back to doing in-center July 2016.
After more than 150 days of being hospitalized with complications from Diabetes, my beloved husband's heart stopped and he passed away 06-08-21. He was only 63.
raidym
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« Reply #4 on: September 08, 2014, 04:13:48 PM »

I had this all through the time I did dialysis. After my sessions I had a loud buzzing in my ears and couldn't hear a thing. I asked what could be causing it and never got an answer from the staff at my dialysis unit. One man said he had the same trouble and had been told we have tiny blood vessels around our temples and ears and that the blood flowing through so fast would maybe cause the buzzing or blocked feeling. I done the twilight shift so wasn't home till late after my treatment that feeling didn't go away till I had a good night sleep and sometimes not even then. My hearing was terrible while I was on dialysis. The explanation I got from this man was the one I stuck with as it was one I felt comfortable with. Since I had my transplant it has gone completely but I still find it hard with very low sound especially men with a low rumbly voice I find hard to hear. Sometimes I don't even realise their talking to me  :oops;
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