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My 1st visit to see uro doc and I'm pain free!

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  • My 1st visit to see uro doc and I'm pain free!

    I feel like a fake. Last week I was in so much pain I could hardly function, took Vicodin etc. but after eliminating all the offensive foods/drinks and taking Cystoprotek I feel fine, except for minor burning.

    I almost feel like I should drink some diet Coke or take some ascorbic acid (vit.C) to be in pain again so he would believe me today.
    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

  • #2
    first visit and no pain

    Originally posted by 425runner View Post
    I feel like a fake. Last week I was in so much pain I could hardly function, took Vicodin etc. but after eliminating all the offensive foods/drinks and taking Cystoprotek I feel fine, except for minor burning.

    I almost feel like I should drink some diet Coke or take some ascorbic acid (vit.C) to be in pain again so he would believe me today.

    It never fails! It's like taking your car to the mechanic because it's making the most horrendous noise, and when you get it there, nothing!

    I'm so glad you found ways to make your bladder feel better. Now, don't do anything to make it mad again. Just tell the doctor what happened and let him take it from there.

    Good luck. Let us know what happens.
    Laurie

    Comment


    • #3
      Laurie is right. Please don't do anything that will cause you pain. IC symptoms can vary so much that your doctor will understand.


      Donna
      Stay safe


      Elmiron Eye Disease Information Center - https://www.ic-network.com/elmiron-p...mation-center/
      Elmiron Eye Disease Fact Sheet (Downloadable) - https://www.ic-network.com/wp-conten...nFactSheet.pdf

      Have you checked the ICN Shop?
      Click on ICN Shop at the top of this page. You'll find Bladder Builder and Bladder Rest, both of which we are finding have excellent results.

      Patient Help: http://www.ic-network.com/patientlinks.html

      Sub-types https://www.ic-network.com/five-pote...markably-well/

      Diet list: https://www.ic-network.com/interstitial-cystitis-diet/

      AUA Guidelines: https://www.ic-network.com/aua-guide...tial-cystitis/

      I am not a medical authority nor do I offer medical advice. In all cases, I strongly encourage you to discuss your medical treatment with your personal medical care provider. Only they can, and should, give medical recommendations to you.
      [3MG]

      Anyone who says something is foolproof hasn't met a determined fool

      Comment


      • #4
        Thats pretty funny but I wouldn't tempt fate! Clearly diet effects you and you might be able to totally manage where you are at by being "good" and following it most of the time. I'm happy for you that things are better.
        You could just be in the beginning phases of the condition where Dr. Parsons says you could have a bout or two a year and then be perfectly fine the rest of the time. If thats the case, I hope you stay that way.
        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


        • #5
          Well, I was officialy dg. with interstitial cystitis based on my symptoms and ruling out other conditions, I've had all kinds of tests done before - all negative. The doc is worried about the blood in my urine, suggesting that it might be bladder cancer. I sure hope not...but it would explain why I've been so unexplainably tired for the last few months. Anyway, he put me on Elmiron and suggested Bladder-Q as an alternative. I already take Cystoprotek and it seems to help a lot!

          He also said to call the office next time I get a flare and they'll do a rescue instillation. What do they instill? Lidocaine?? Also, he scheduled me for an in-office cystoscopy next month. That plus following the IC diet which I already do.

          Weird how things can happen to the human body. I was always healthy, energetic, and cheerfull up until last October. Ever since then it's been a downward spiral. But we're taking care of it now, so that's good.
          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


          • #6
            Originally posted by 425runner View Post
            Well, I was officialy dg. with interstitial cystitis based on my symptoms and ruling out other conditions, I've had all kinds of tests done before - all negative. The doc is worried about the blood in my urine, suggesting that it might be bladder cancer. I sure hope not...but it would explain why I've been so unexplainably tired for the last few months. Anyway, he put me on Elmiron and suggested Bladder-Q as an alternative. I already take Cystoprotek and it seems to help a lot!

            He also said to call the office next time I get a flare and they'll do a rescue instillation. What do they instill? Lidocaine?? Also, he scheduled me for an in-office cystoscopy next month.
            Lots of people with IC have blood in their urine, I'm surprised he didn't mention that. Most likely because of the inflammation and possibly pinpoint bleeding in the bladder lining. Try and not worry too much about bladder cancer, from my understanding it is rare but they like to rule it out.

            The cystoscopy will rule out the cancer. I had one done in office about 6 weeks ago myself. Luckily it wasn't a big deal. My doctor put a catheter in, put sterile saline into the bladder, looked on screen with a camera and I could see it on a tv screen etc. Emptied it out to look for blood. Filled me back up and had me pee it out. Mine didn't hurt at all, the worst part for me is always the discomfort of simply being cathed. Some doctors will numb the urethra.

            Rescue instillations -I haven't had one done yet but there are a variety of things they use. Usually something that contains an anesthetic, sometimes a steroid, sometimes something like elmiron or heparin that re-coat the gag layer. There are others people here who know lots more then me about it!
            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


            • #7
              first visit to uro and no pain

              Originally posted by 425runner View Post
              Well, I was officialy dg. with interstitial cystitis based on my symptoms and ruling out other conditions, I've had all kinds of tests done before - all negative. The doc is worried about the blood in my urine, suggesting that it might be bladder cancer. I sure hope not...but it would explain why I've been so unexplainably tired for the last few months. Anyway, he put me on Elmiron and suggested Bladder-Q as an alternative. I already take Cystoprotek and it seems to help a lot!

              He also said to call the office next time I get a flare and they'll do a rescue instillation. What do they instill? Lidocaine?? Also, he scheduled me for an in-office cystoscopy next month. That plus following the IC diet which I already do.

              Weird how things can happen to the human body. I was always healthy, energetic, and cheerfull up until last October. Ever since then it's been a downward spiral. But we're taking care of it now, so that's good.
              Hi,
              I'm glad that the doctor took you seriously and you will be working on treatments.
              I know what you mean about feeling fine and all of a sudden not feeling fine, but it does get better.
              You sound like you have a good attitude which can make a huge difference, I think.
              Keep us up to date, and good luck!
              Laurie

              Comment


              • #8
                Don't go hurting yourself girl! Anyone who lives with pain will tell you there are good days and bad, and docs understand (hopefully). And look up bladder cancer, my dad had it, it was not painful for him anyway. A lot of things can affect your pain levels, from a diet boo-boo, the weather (low pressure systems), stressing, too strenuous physical movements, and on and on. The pain can come and go, we only hope day to day that it goes. You are not nuts and it sounds as though your doc is on top of things, so he knows that too. Good luck and hope your pain free days continue for a long, long time, that is the goal after all! Jill, wife of Bob

                Comment


                • #9
                  what is it?

                  i have had burning since i was a todler im 17 now and have found that sex can make it worse, it was never bothersome till i was about 12 or 13 and then it started to become crippling i do have pressure and unable to hold it fro a long time especially if im sitting down but the burning is what gets me its teh worst part im afraid to pee because i think it will burn and it always does, ive been from dlc to doc ive seen urologists, nephrologists even gynos and everyone just shrugs thier sholders and sends me home with vicodine and pyridium, my pediatritian even suggested to my mothe that im faking it because they can never find an infection, i keep telling them its not an infection and my mother too but now ive had to drop out of school because of pain pyridium is slowly losing effect on me and everyday becomes harder, iv been to the hospital for caths and dehydration because im afraid to drink anything but sprite cuz i kno il have to pee if i drink, sprite seems to help, i cant live my life like this anylonger what should i do what could this be

                  Comment

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