Does anyone get blood in their urine?

Every time I get my urine tested, it shows I have blood. The urologist has checked and I have no kidney stones, he thinks it is something to do with lupus but rheumatologist doesn't seem worried by the blood and doesn't see a connection. Who do I believe?

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14 replies

    tatty
    tatty

    hmmm i have know that one i keep leaking potassium from my kidneys Rheumalologist doesnt seem worrried GP and another consultant do think its the sle again who do i believe but more to the point who is going to check it out. so know the feeling. by the way yols is your lovely dog a shnowzer ( i know i will have spelt that wrong.) ;-(

    Yols
    Yols

    Hiya, yes he is a giant schnauzer called Hugo - am impressed you knew what he was!!
    Its worrying for us, but I guess the rheumys think there are other symptoms that need sorting with priority. Who knows eh?

    lellielesley
    lellielesley

    awww giant schnauz! I love them. :) We have a Russian Black Terrier and no one ever knows what she is - the closest we get occasionally is "is it a fat giant schnauzer?". Usually people think she's a labradoodle or ask if she's a newfoundland or something - none of which are even close!

    marypw
    marypw

    Hello, I have just been investigated for this - all my urine tests showed some blood - but it was never visible and I didn't have any symptoms. All my kidney tests and an ultrasound didn't show anything. I had a cystoscopy last week which did show some inflammation - so I am on trimethoprim for a week.

    The doctors like to find a reason for blood in urine, but protein in urine is more serious as are worsening blood tests for kidney function. I am not sure if the bladder inflammation is lupus-related but I'm seeing the rheumatologist in a couple of weeks so I will add that to my list of questions. Hope that helps to reassure you. xx

    Binkey
    Binkey

    Do please add this to you list of questions,as will I.I have been there with this problem,but was not under reumatology at the time when I had my high protein urine problems and kidney stones,or perhaps I was because I am sure I asked the surgeon who operated on me if it was related to lupus.He did not seem to think so but was vague about the lupus syndrome.

    MaryMcculloch
    MaryMcculloch

    Yes I have always had Blood and protein in Urine. Even years ago when I was pregnant I had Blood in my urine. Just makes you wonder if the lupus was there then.

    Paula1968
    Paula1968

    I have blood in my unrine and protein I have been told I have renal failure caused by the Lupus.
    I have had a number of kidney biopsy's as this is the only way you can really tell the kidney's true function.
    I'm medicated now but using blood pressure tablets and fingers crossed this keeps me on the straight and narrow and as far away from dialasis as I can be.
    If the blood and protein increase they should send you to a kidney specialsit to check your function.

    lovebird
    lovebird

    Paula - What meds on you on please?
    I have blood and protein in urine too and the function reading was 26 back in September.. The results of the kidney biopsy are being given tomorrow by the nephrologist and then I am seeing a lupus specialist too. Any information gratefully received.

    Yols
    Yols

    Thanks for all your feedback - it is a comfort to know we are not alone and others have similar probs too. Best wishes to you all. x

    lucyloo023
    lucyloo023

    Hi Yols, I have blood and protein in my urine and my rheumatologist referred me to a renal specialist. I had a kidney biopsy and it turns out I have kidney nephritist stage 4 but because I was referred so quickly it has been caught before it gets any worse. I'm on immunesuppresents, steroids, blood pressure tablets, water tablets and as yet there has been no improvement but its early days. I would ask to be referred to see a renal doc just to get everything checked out as lupus can affect any organ and its better to be safe than sorry.
    I think its so scary as there is so much unknown about lupus and I love this sight as there is support and you know there is always someone else who is going through similar things
    Hope you get it all sorted soon.

    lellielesley
    lellielesley

    I'm undiagnosed but yes, I always have blood and protein showing on dipstick tests. I've been treated for a UTI when I had no other symptoms purely because in a routine health check they noticed I had blood and thought it might be that. The UTI treatment unsurprisingly didn't make the blood or protein go away and nothing grew when they sent the sample off. No one bothered to investigate further because my renal bloods have been fine, but I have recently been wondering if those past dipstick tests were an early sign something autoimmune may be going on.

    bluebell99
    bluebell99

    Please do not be worried about this but I feel I must tell you just so that you are aware.
    I had blood in my urine for years, the rheumy clinic didn't really bother except sometimes to prescribe antibiotics.
    Three years ago when I had more than the usual pain and discomfort my GP sent me for an ultrasound and it was discovered I had a 2 inch tumour on my right kidney.
    I am fortunately in remission after 2 ops but I do implore anyone with blood that has no right to be anywhere on or from their body to speak up.
    Yols, if you have had an ultrasound and your urologist is happy there is no evidence of stones, (or tumours!) than I would think you need to bring this to the attention of the rheumatologist. Do not be fobbed off!

    Bonnie39
    Bonnie39

    Got an appointment for a cystoscopy yesterday. For the last three weeks I have had visible and non visible blood in my urine. At the start of this episode until last week I was literally peeing blood. Toilet was a blood bath. Am now on my 3rd course of antibiotics and it is painful and my GP is conceened because of the SLE and APS. I was referred for the cystoscopy under the two week oncology rule but GP thinks its probably the SLE. Iam curious why this investigation rather than a kidney scan but will follow this thread with interest.

    overnighthearingloss
    overnighthearingloss

    If you are treated at a hospital where they have no real knowledge of lupus, they are attempting to find answers from text books at best. Its incredibly difficult when you are feeling torn apart to stay abreast of things. But try at least to note the names of the various individuals you are dealing with. Best if you have a notebook to jog your memory later. I have had so many doctors come up to me without even introducing themselves.

    The good doctors are not usually afraid of announcing themselves.

    A notebook also allows you to note down things the minute after they disappear, because you have remembered something else. And make a point of asking them the next they they appear.

    It can also help you to make sense later of the train of thought followed.

    • Last edited by overnighthearingloss

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