Announcement

Collapse
No announcement yet.

Blood in urine please discuss.

Collapse
X
 
  • Filter
  • Time
  • Show
Clear All
new posts

  • Blood in urine please discuss.

    So when they (My regular uro not my specialist uro) culture my urine they find no bacteria but there's blood in my urine and white cell activity and the little sticks keep turning purple. AZO test strips too. So I test positive for infection in the office but not in the lab cultures. We've tried cipro and macrobid with no results and I'm confused and worried. Anyone have experience with this? (Personal, I know you're not doctors giving medical advice, etc. Unless you are. Lol.)

    I need feedback on this badly, it's been going on 3 months. I see moldwin in a few weeks and no they can't make it sooner.

    Help?

    Love, H.

  • #2
    Originally posted by Hannah13 View Post
    So when they (My regular uro not my specialist uro) culture my urine they find no bacteria but there's blood in my urine and white cell activity and the little sticks keep turning purple. AZO test strips too. So I test positive for infection in the office but not in the lab cultures. We've tried cipro and macrobid with no results and I'm confused and worried. Anyone have experience with this? (Personal, I know you're not doctors giving medical advice, etc. Unless you are. Lol.)

    I need feedback on this badly, it's been going on 3 months. I see moldwin in a few weeks and no they can't make it sooner.

    Help?

    Love, H.
    I'm a little disappointed no one bothered to respond to this. You guys are my only source of other ic information and even a kind word would have helped.

    Love, H.

    Comment


    • #3
      Hi Hannah,
      I just saw your post. Sorry you didn't get a response, I am sure it wasn't intentional. Anyway about your topic. I always have hematuria (blood in urine) but mine isn't visible. I have also done the at home test and it will say I have lukesytes (I know that is mispelled, sorry) but when I go to the Dr and they do a culture mine comes up negative. As I understand it, my Dr goes by the culture and not the dip stick test. Therefore, he doesn't give me an antibiotic. I thought that what showed in the culture was the definitive answer. I don't know what to tell you. I don't usually have many infections though. Hopefully someone else will see this and tell you their experience.

      I assume you are in pain from the infection? I hope they are giving you something for that.

      Sandra
      Link to the patient information, everything from What is IC? to Disability
      http://www.ic-network.com/patientlinks.html

      American Urological Association Clinical Guideline
      Diagnosis and Treatment of Intersitial Cysitis/Painful Bladder Syndrom
      http://www.auanet.org/content/guidel...ent_ic-bps.pdf

      Comment


      • #4
        Hi

        Blood in urine has been discussed many times on the boards,

        Just search it and you will lots of posts about it.

        MG
        My are with you all. May you all find a way to peace and joy in your lives.

        Comment


        • #5
          Hannah,

          I always have microscopic hematuria when I have to give a urine sample. I have never had visible blood in my urine. I was curious about this as well so I looked through some old posts on this board and found that it seems to be pretty common amongst most of us.
          I also see Dr. Moldwin. Are you in NYC? I've only seen him once, recently, and I liked him and felt like he listened. My main issue is the feeling of always needing to pee when I know I don't.
          Has Dr. Moldwin helped you out a great deal? What are your symptoms and what has helped the most?
          Don't worry about the blood. I know it would be nice if it really were an infection that could be fixed but I think it's just normal IC stuff. Ugh, this disease is ridiculous and it's even more ridiculous that through reading this board it seems like very little people figure this puzzle out. It freaks me out!

          Rachael

          Comment


          • #6
            Me too

            I've always (for years) had blood in my urine. Sometimes visible, sometimes not. I don't know if it's an IC "symptom" but I've seen that lots of people here that have it.
            Katie-46 yr old female dx'd with IC after 15 years of symptoms off and on long term antibiotic use, GERD,IBS and now IC diet, gallbladder removed, endometrial ablation w/tubes tied
            Lexapro-20 mg
            Aciphex
            Ambien-as needed
            Percocet-7.5 up to 3 per day as needed
            Valium-10 mg x2 per day
            Phenergan-1 at night
            Prelief w/everything
            Now recovering from acute pancreatitis

            Currents treatments that help somewhat:
            Heating pad
            Hot baths
            Ice
            Being VERY still while lying down with legs elevated

            Comment


            • #7
              I often have leukocytes in my urine too though not the red blood cells. When they are there my urine is cloudy and I think maybe I'm getting yet another infection....my pcp always treats me when there are white blood cells because it could be the start of an infection.
              Cindi


              Gelnique for frequency/urgency - works great
              Macrobid after sex
              Prilosec, continuous birth control pills
              synthroid .088mg, mucinex-d, restasis

              Supplements: Desert Harvest Aloe vera, Cysta-q, prelief, magnesium and calcium, Vit D, flaxseed oil

              Diag Mild IC Jan 11 but have had symptoms for 25 years. Also have GERD, TMJ, IBS-C, chronic dry eye syndrome, hashimotos thyroiditis, non-allergic rhinitis.

              IC Diet Link: http://www.ic-network.com/diet/2009icdietlist.pdf
              AUA 2011 Guidelines to diagnosing and treating IC overview- http://www.ic-network.com/forum/showthread.php?p=571592
              AUA 2011 Guidelines to diagnosing and treating IC PDF: http://www.auanet.org/content/guidel...ent_ic-bps.pdf
              Great treatment flowchart on page 19 of the pdf

              Comment


              • #8
                Originally posted by sailawaygrl View Post
                Hi Hannah,
                I just saw your post. Sorry you didn't get a response, I am sure it wasn't intentional. Anyway about your topic. I always have hematuria (blood in urine) but mine isn't visible. I have also done the at home test and it will say I have lukesytes (I know that is mispelled, sorry) but when I go to the Dr and they do a culture mine comes up negative. As I understand it, my Dr goes by the culture and not the dip stick test. Therefore, he doesn't give me an antibiotic. I thought that what showed in the culture was the definitive answer. I don't know what to tell you. I don't usually have many infections though. Hopefully someone else will see this and tell you their experience.

                I assume you are in pain from the infection? I hope they are giving you something for that.

                Sandra
                I'm so used to the pain I didn't even ask. Lol. I just use heat. That your situation even sounds like mine makes me feel a bit of relief, thanks for your response.

                Comment


                • #9
                  Originally posted by cmclien View Post
                  I often have leukocytes in my urine too though not the red blood cells. When they are there my urine is cloudy and I think maybe I'm getting yet another infection....my pcp always treats me when there are white blood cells because it could be the start of an infection.
                  Mine has a similar approach but I'm only going on a steady diet of antibiotics if Dr. moldwin says I should. Lol.

                  Love, H. (TY for your response! It helps!)

                  Comment


                  • #10
                    Originally posted by marar76 View Post
                    Hannah,

                    I always have microscopic hematuria when I have to give a urine sample. I have never had visible blood in my urine. I was curious about this as well so I looked through some old posts on this board and found that it seems to be pretty common amongst most of us.
                    I also see Dr. Moldwin. Are you in NYC? I've only seen him once, recently, and I liked him and felt like he listened. My main issue is the feeling of always needing to pee when I know I don't.
                    Has Dr. Moldwin helped you out a great deal? What are your symptoms and what has helped the most?
                    Don't worry about the blood. I know it would be nice if it really were an infection that could be fixed but I think it's just normal IC stuff. Ugh, this disease is ridiculous and it's even more ridiculous that through reading this board it seems like very little people figure this puzzle out. It freaks me out!

                    Rachael
                    Dr. Moldwin and Dr. Kohan are the 2 best IC doctors in our area (ok Long Island, close enough) IMHO. I prefer Moldwin but Kohan is great and very nice as well. My primary symptoms are frequency, pain and the ever popular periodic super bad flares. I'm in Queens. Thanks for reaching out.

                    Love, H.

                    Comment


                    • #11
                      I also have blood in my urine when they do tests. But I'm always negative for an infection.
                      Update! Feeling much better these days and no longer on any meds!

                      Pelvic pain began July 2008. Urinary frequency began in November of 2008. IC Doctor says I'm one of the worst frequency patients he has had.

                      Things that helped me the most: IC Diet, Elavil (30mg), Elmiron since June '09 (500mg/day).

                      Previously tried and quit: one series of six instillations, Neurontin, Ditropan, Oxytrol, electric stimulation to the pelvic floor, Desert Harvest Aloe, Cystoprotek and Flomax, Hydroxyzine (50mg), Alesse Birth control (this helped my period flares when my symptoms used to be bad), PTNS (I think this helped).

                      [/COLOR][/SIZE][/FONT]

                      Comment


                      • #12
                        No infection for Bob either, but he recently had blood work done and is anemic. Doc is pretty sure it is the IC bladder just weeping (crying). Baby that bladder is the only thing that works for him. Antibiotics are discussed here all over. Never had to use them, but know more women than men tend to get infections. (Could be wrong about that, we just have not had to deal with it YET). Think a lot of ICers have traces of blood in their urine??? Can't see it, and if you take pyridium, you would never be able to see it anyway.

                        Comment


                        • #13
                          We started on the path of an IC diagnosis for me, just because of what you described.

                          I had off and on abdominal pain, lower back pain, visible blood in my urine (very dark), in office test said infection, but lab culture said no infection. Then we started talking about food triggers and other tests, etc. Eventually had cystoscopy with hydrodistention in November and got official diagnosis.

                          I was getting used to the IC diagnosis and paying attention to things that made me flare when I found out that I had multiple kidney stone blockages that were causing some of my more severe pain. After I finish up my stone treatment, I will go back to tracking things that cause me flares because there won't be any confusion about if it if kidney stone or IC pain.

                          Good luck.
                          Colleen

                          * ITP - autoimmune blood disorder - spleen removed 1978 and in remission since
                          * MS- diagnosed Jan-2010
                          * IC - confirmed by cysto and hydro Nov-2010 - currently taking no medication
                          * possible adenomyosis - suspected by urogyno May-2010
                          * low Vitamin D levels - taking 2000 IU daily
                          * sleep issues - 1/2 alprazolam

                          Comment


                          • #14
                            I have visible blood in urine almost daily

                            First it was pinkish and now it's more dark. It's only visible on my panties...can't see any blood when I pee. Doctor did urinanalysis several times and it always shows blood.

                            He doesn't know what's going on - I passed two small kidney stones 4 weeks ago, had a bladder infection before then, but cultures now are clean.
                            Dg. with IC 2/15/10

                            Other conditions: depression, ADHD, lactose intolerance, celiac disease, chronic fatigue syndrome, IBS-C.

                            Medications I'm on: Vyvanse 70mg, Xanax 1 mg as needed, Wellbutrin XL 150 mg, Vicodin 5/500 as needed for pain, Microgestin 1/20 continuously.

                            Supplements I'm taking: Chondroitin Sulfate, N-acetyl-glucosamine, MSM 3gr/day, Pancreatin, B-5, Ester-C, and marshmallow root tea

                            Comment

                            Working...
                            X