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Author Topic: Proteinuria  (Read 2312 times)
Jean
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« on: October 19, 2015, 01:09:37 PM »
My kidneys are blowing bubbles all of a sudden. So, it has not been diagnosed yet, but all signs point to proteiinurea. My question for you Pros is " Does proteinurea hurt?"
Thanks for your input.
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One day at a time, thats all I can do.
Deanne
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« Reply #1 on: October 19, 2015, 02:06:45 PM »
No, it doesn't hurt. I had proteinurea from age 9 until my transplant at age 51. I didn't know what urine was supposed to look like until after my transplant. It took a while to get used to not seeing foam. I never felt any pain from it.
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Deanne

1972: Diagnosed with "chronic kidney disease" (no specific diagnosis)
1994: Diagnosed with FSGS
September 2011: On transplant list with 15 - 20% function
September 2013: ~7% function. Started PD dialysis
February 11, 2014: Transplant from deceased donor. Creatinine 0.57 on 2/13/2014
kristina
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« Reply #2 on: October 20, 2015, 02:00:58 AM »
... In all my medical-doctor-hospital-letters (for over 43 years)
it was always clearly mentioned that I suffered from Chronic Proliferative Glomerulonephriits plus hypertension and proteinurea...
... Over the years I also regularly suffered from bouts of kidney-pain,
but I don't know whether or not it was connected to proteinurea or to my chronic kidney disease
or whether it was due to my suffering from regular flare-ups of SLE/MCTD which affected my frail kidney-function ...
Best wishes from Kristina. :grouphug;
« Last Edit: October 20, 2015, 02:02:14 AM by kristina » Logged
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Jean
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« Reply #3 on: October 20, 2015, 05:03:59 PM »
Thanks ladies for your input.
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kitkatz
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« Reply #4 on: October 26, 2015, 05:16:35 PM »
If you are hurting, go see your doctor and tell them what is going on honestly.
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Angiepkd
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« Reply #5 on: October 26, 2015, 08:12:46 PM »
I still have foamy urine after transplant, but no proteinuria.  Very odd.  Does not hurt at all as far as I can tell.  I think lots of us with ESRD have so many other things going on, it would be hard to pinpoint what hurts and why. Pick a spot and I can find some pain there lol.   :rofl;
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PKD diagnosis at 17
Cancer May 2011, surgery and no further treatment but placed on 2 year wait for transplant
October 2011 first fistula in left wrist
April 2012 second fistula in upper arm, disconnect of wrist
January 2013, stage 5 ESRD
March 2013 training with NxStage home hemo
April 2013 at home with NxStage
April 2013 fistula revision to reduce flow
May 2013 advised to have double nephrectomy, liver cyst ablation and hernia repair. Awaiting insurance approval to begin transplant testing. Surgery in June.
June 2013 bilateral nephrectomy.
August 2013 finishing testing for transplant, 4 potential donors being tissue typed.
January 2014 husband approved to donate kidney for me
March 4th 2014 received transplant from awesome hubby. Named the new bean FK (fat kidney) lol!  So far we are doing great!
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