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Over the past few years I have started to show protein and blood in

my urine. The loss of protein seemed to start after the birth of my

first son 3 years ago when I had severe pre-eclampsia and Hellp

syndrome, although I have always had traces of blood in my urine

since I was a child (always unexplained). My mother has polycystic

kidney disease so I always assumed it was related to this. However,

recent ultrasounds have indicated that I have only 1 cyst on one

kidney (at the age of 32) which my nephrologist says is not typical

of polycystic kidneys. The ultrasound shows " increased cortical

echogenicity consistent with medical renal disease " . My nephrologist

says he thinks I have IgA and I am waiting for the blood tests to

confirm. He said we would then discuss a biopsy. I am not very

familiar with this disease and I was wondering if any of you have had

similar ultrasound results or symptoms?

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Before, I had my biopsy...I had an ultrasound. And I had one cyst but

that was it and I was told by the internist that that was fairly common.

Actually, the internist never mentioned IgA, but did recommend I see a

nephrologist. She ordered the biopsy due to my reduced kidney function

at the time and to rule out lupus. The internist thought the issues I

was having were my heart...when I had a 24 hour blood pressure monitor,

my heart rate didn't go much higher than 54bpm...even when walking...no

wonder I was suffering dizziness and nausea. My pacemaker was set to

50bpm at the time, I have since had it elevated to 60bpm and now my

heart seems to constantly be around 60-64bpm. Weird thing was, well not

too weird, it actually makes sense...but when they increased my heart

rate with the pacer...my blood pressure went down slightly. It turned

out too that my heart muscle had grown slightly due to the extra work it

was doing. I still need the ramipril though to really control the blood

pressure.

Anyway...they first noticed the protein and blood in my urine with my

first pregnancy and I had mild hypertension that went away after she was

born and again with each of my two boys. We have no family history of

HPB or kidney disease, but all kinds of other issues. Good luck with

your tests. I am new to this too and learning more everyday. But I am

so relieved to know I am not alone and there are others I can talk to

about the tests, treatments, support etc.

S

________________________________

From: bkoehler12

Sent: Thursday, August 19, 2004 12:58 PM

To: iga-nephropathy

Subject: not formally diagnosed

Over the past few years I have started to show protein and blood in

my urine. The loss of protein seemed to start after the birth of my

first son 3 years ago when I had severe pre-eclampsia and Hellp

syndrome, although I have always had traces of blood in my urine

since I was a child (always unexplained). My mother has polycystic

kidney disease so I always assumed it was related to this. However,

recent ultrasounds have indicated that I have only 1 cyst on one

kidney (at the age of 32) which my nephrologist says is not typical

of polycystic kidneys. The ultrasound shows " increased cortical

echogenicity consistent with medical renal disease " . My nephrologist

says he thinks I have IgA and I am waiting for the blood tests to

confirm. He said we would then discuss a biopsy. I am not very

familiar with this disease and I was wondering if any of you have had

similar ultrasound results or symptoms?

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supported by donations. If you would like to help, go to:

http://www.igan.ca/id62.htm

Thank you

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I don't know of any ultrasound test for IgAN at all. Protein loss is common

with kidney disease though, regardless of the type of kidney disease.

In a message dated 8/19/2004 1:49:17 PM Pacific Daylight Time,

BKoehler@... writes:

> I am not very

> familiar with this disease and I was wondering if any of you have had

> similar ultrasound results or symptoms?

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Well, I had a few kidney ultrasounds in my time.

" increased echogenicity of upper cortex of both kidneys correlate with

chronic glomerulonephritis " .. is what the man said.

Pierre

Re: not formally diagnosed

>

> I don't know of any ultrasound test for IgAN at all. Protein loss is

common

> with kidney disease though, regardless of the type of kidney disease.

>

>

>

> In a message dated 8/19/2004 1:49:17 PM Pacific Daylight Time,

> BKoehler@... writes:

>

> > I am not very

> > familiar with this disease and I was wondering if any of you have had

> > similar ultrasound results or symptoms?

>

>

>

>

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