Welcome guest, is this your first visit? Click the "Create Account" button now to join.

To disable ads, please log-in.

Shop at TeamEstrogen.com for women's cycling apparel.

Page 1 of 2 12 LastLast
Results 1 to 15 of 23
  1. #1
    Join Date
    May 2007
    Location
    Perpetual Confusion and Indecision
    Posts
    488

    Blood in my urine - am I okay?

    To disable ads, please log-in.

    Well, every year when I have my annual exam, I have a little blood in my urine - usually have to get 3 little cytology cups from the hospital, pee in them, return to the hospital, and don't hear any more about it. This time (back in May), there was more blood. I did the cup-peeing thing, and they called to say that 2 of the 3 samples had "mildly atypical cells", and my GP wanted me to see a urologist, who comes here for a day every couple of weeks. I still wasn't concerned, as my doctor is an alarmist, and after 17 years I no longer freak out when she tells me stuff - at least I get tests whenever there is a question, so things will get caught in time if there is ever anything really wrong.

    Two weeks ago, I saw the urologist, peed in a cup, and they said I had "2+ blood". He said that was too much, and he ordered a CT scan and a cytoscopy. He said he didn't know where it was coming from, but he'd figure it out. There was no protein present, so that was a good sign. I explained that I bike & run and am generally pretty active (and I was thinking maybe it was related to my saddle issues). He said that could be it, but he would test me and see.

    Had the CT scan last week, and the cytoscopy this morning. He said I have a small cyst on one kidney, but nothing to worry about (and not the source of the blood), and he saw nothing wrong inside my bladder (not a fun test, but not awful - would have been better if they had told me more what was going on while they did it).

    Here is my concern: Dr Urologist says he doesn't see anything wrong, and "we're done". Yay. However, what happened to "we'll figure it out"? If the issue isn't with my bladder, etc, then what is it? It sounds like the trail ends here, and that is that.

    I felt pretty uneasy/worried/emotional going in there this morning, more because of what he might have to say than apprehension over the test itself. When I left I felt like crying - no closure I guess. I thought he'd say:

    1.) There is nothing wrong, you are fine. Probably your saddle.
    2.) There is something minor wrong, and we will fix it.
    3.) There is a serious problem, and we don't know if we can fix it, but we know what to do (not my favorite option, obviously).
    I never expected Door #4.

    I did ask if I should just not worry about it, and he said yes. He said "I can't promise you a clean bill of health for the rest of your life, but for the next 2 years, yes". I'd really like to just go along as I have, assuming nothing is wrong. Which I plan to do.

    Anybody ever had this problem?

  2. #2
    Join Date
    Oct 2005
    Posts
    2,309
    Well I've never had THAT problem, BUT I do know what you are going through.
    My ovarian cancer tests came back "inconclusive", so they have put me on a wait and see kinda thing. Not very reassuring.
    Just keep a dialogue with your doctor. That is what they are paid to do! And remember that we have to be our own advocate as far as our health is concerned. Tell your doctor that you want at least some sort of answer. Hopefully he/she will catch on that this is stressing you out and will act.

    Sorry I'm not much help, but I do feel for you. Yes indeed I do!

  3. #3
    Join Date
    Apr 2006
    Posts
    2,059
    Don't have much, except to say that what Running Mommy said sounds right to me. I just wanted to let you know I understand. I had some ovarian cysts last year. All benign, but painful at the time, and I think I had to call the doc about 3 times and keep asking very pointed questions until I was really OK with it all.
    "The best rides are the ones where you bite off much more than you can chew, and live through it." ~ Doug Bradbury

  4. #4
    Join Date
    Apr 2007
    Location
    Limbo
    Posts
    8,769
    You are probably okay
    2008 Trek FX 7.2/Terry Cite X
    2009 Jamis Aurora/Brooks B-68
    2010 Trek FX 7.6 WSD/stock bontrager

  5. #5
    Join Date
    Jun 2005
    Location
    steuben county new york
    Posts
    626
    Skierchick..You said you run and bike. How much do you do this, and in duration? I read your story and thought of rhabdomyolsis..the break down of muscle and is filtered thru the kidneys, and can read a positive blood. Usually it occurs with muscle damage from injuries, falls with remaining in one position for a long time, and that triatheletes/marathon runners are at risk for this. I am not a dr, nor do I play one so don't take my word for it..just a suggestion.

  6. #6
    Join Date
    Feb 2006
    Location
    San Antonio, TX
    Posts
    2,024
    From what you have written, it sounds like your urologist thinks you are OK. But if you have doubts, ask a second urologist, not a bunch of cyclists. I don't mean to sound harsh, but if you are not comforatble with what your urologist has told you, then get a second MEDICAL opinion.

  7. #7
    Join Date
    Oct 2005
    Location
    Shelbyville, KY
    Posts
    1,472
    I too always have blood in my urine - sometime a trace other times 1+, etc. It was a major concern several years ago so my doctor sent me to a urologist who ordered a kidney screening (had to clean my intestines out, have dye injected, pictures taken on a set schedule). The test results showed all was well - no stones, no masses, etc. My mom also has the same problem and my urologist told me after the test it can be genetic and he felt all was well - he simply labeled it idopathic. I continue to have blood in my urine and no one questions it now unless the RBC count is high or I'm showing signs of an infection.
    Marcie

  8. #8
    Join Date
    May 2007
    Location
    Perpetual Confusion and Indecision
    Posts
    488

    Thanks

    Thanks, you guys. I think I really just needed to vent a little. I wondered if anyone here had ever dealt with similar symptoms (no - not looking for a diagnosis, just similarities - sorry if I was unclear ). I'll probably talk to my regular doctor, and see if she can clarify things a bit. We don't have a urologist of our own here - this guy travels 100 miles a couple of times a month.

    Running Mommy - I can't imagine being in your shoes. That has to be really tough. I hope everything turns out okay for you.

    Shellyj - I'll read up on rhabdomyolsis - I haven't heard of that.

    Boy, I really want to ride to work tomorrow, but I'm so uncomfortable from my exam, I don't know if I'll be able to sit on a bike saddle by morning.

    Jan

  9. #9
    Join Date
    May 2007
    Location
    Perpetual Confusion and Indecision
    Posts
    488
    Makbike,

    Yeah, I had the IVP test 10 years ago. Saw this same urologist then, and he practically laughed at me - said I was too young (31 at the time) and there was nothing wrong with me. I think it was the "mildly atypical cells" thing that got the ball rolling this time.

    It's interesting that your mom has the same thing.

  10. #10
    Join Date
    Feb 2007
    Location
    Temecula, CA
    Posts
    45
    I vote for the "we'll figure it out" and as someone else said, maybe you should see someone else or at least talk to your regular Dr. like you're planning on doing. Interesting that I haven't been on here in awhile and saw this post-my hubby was just diagnosed w/prostate cancer today from-blood in the urine-only trace amounts under a microscope but that's after 18 months and now we're wondering if it's caught early enough. Follow your gut and most likely it's nothing, but follow your gut. Hope this isn't a scare for you but I hear we have to be our own advocates . Good luck.

  11. #11
    Join Date
    Apr 2006
    Posts
    3,867
    Well, prostate cancer is not a concern for a woman. Shouldn't scare her.

    Karen

  12. #12
    Join Date
    Feb 2007
    Location
    Temecula, CA
    Posts
    45
    I realize that but my point was that after 18 months for us, it's not always "nothing." I'm sorry I said anything.
    Last edited by JanB; 08-22-2007 at 07:53 PM.

  13. #13
    Join Date
    Apr 2006
    Posts
    2,059
    Quote Originally Posted by JanB View Post
    I realize that but my point was that after 18 months for us, it's not always "nothing." I'm sorry I said anything.
    A valid point, definitely.

    Quote Originally Posted by Triskeliongirl
    From what you have written, it sounds like your urologist thinks you are OK. But if you have doubts, ask a second urologist, not a bunch of cyclists. I don't mean to sound harsh, but if you are not comforatble with what your urologist has told you, then get a second MEDICAL opinion.
    Which is why I agree with this!
    "The best rides are the ones where you bite off much more than you can chew, and live through it." ~ Doug Bradbury

  14. #14
    Join Date
    Apr 2006
    Location
    I'm the only one allowed to whine
    Posts
    10,557
    Newly minted women's pelvic health practioner here.

    I know nothing. (please bear that in mind)

    If it were me:
    1st thing I'd do: call doc back and check for urine culture lab results. any cooties? (bacteria) any white blood cells?
    2nd thing I'd do: get copies of all medical records related to this event. (they are yours, you can have them) Get a hold of another urologist. Head south if you have to. Grand Rapids. Lansing. Ann Arbor. Ask around to find a good one.

    Peace of mind is worth a 3 or 4 hour drive.

    Saddle issues shouldn't cause atypical cells. Saddle issues shouldn't cause excess blood markers in urine (that's why you take the sample mid-stream; external blood sources are "washed away" before the sample is taken)

    BTW: saddles shouldn't be causing ANYthing like this. If your saddle is this bad a fit for you, please let TE'ers know! We have a ton of saddle recommendations among us!
    Last edited by KnottedYet; 08-22-2007 at 08:34 PM.
    "If Americans want to live the American Dream, they should go to Denmark." - Richard Wilkinson

  15. #15
    Join Date
    Apr 2006
    Location
    I'm the only one allowed to whine
    Posts
    10,557
    JanB - my warmest thoughts for your husband. I'm sorry to hear he has prostate cancer, but very grateful it was found!

    There are many support groups for both men and their wives/husbands. It's nice to be around folks who know what you're both going through, also nice to be around folks who have so much information about the same situation. I've found cancer support groups to be very valuable, maybe you could try one or two and see if they are something you are interested in? (not that I'm pushing it, just that I "breathed a sigh of relief" when I found one)

    Best wishes to both of you!
    "If Americans want to live the American Dream, they should go to Denmark." - Richard Wilkinson

 

 

Posting Permissions

  • You may not post new threads
  • You may not post replies
  • You may not post attachments
  • You may not edit your posts
  •