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  • discomfort/pressure after voiding..?

    I came off my Ditropan XL last week after discussing TTC with my doctor; she wants me to be med free if possible, so far it's been ok! however, my biggest 'problem' with the IC is never feeling done after I void; and that has been a problem the last few days, not enough to make me jump back on the Ditropan, but it's a pain and takes me forever to get comfortable after a trip to the bathroom...

    I go back to work tomorrow and I'm worried about the length of time it takes me to do this comfortably...anyone else have this problem and if so, what helps you (medication free)? i've found heat and rest do wonders...i can't always lie down though!


  • #2
    I have the same problem, what I do is lean forward just a little bit, and then sit back, when I do this, I find that I'm able to finish without having any problems. (a Friend who has one kidney told me to do this and it works - so you might try it and see if it does for you.)

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    • #3
      I always sit until those extra couple of drops come out Kathi
      One Day At A Time
      Kathi

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      • #4
        i have the same problem...i have serious retention issues . i can spend 1/2 hr on the toilet and finally get 14-20 oz out. then once i get up, it takes awhile to get "over" going to the bathroom!
        (Added by ICNMgrJill on 5/19/08. I am sad to share that Verdicries (aka Tracy) lost her life in a tragic accident just a few days ago. We will miss her support, her encouragement, her sense of humor and, of course, the joy that she found as a mother and wife).

        Tracy ~ 29 years old with Toxoplasmosis (from birth), Fibro/CFS (since age 13...ouch), severe IC, IBS-D, severe PFD (surgery made it even worse), vulvodynia, hiatal hernia, GERD, ulcers, severe gastritis, numbness/tingling in extremeties, pelvic nerve damage--mainly urethral, urinary retention, pelvic reconstruction 7.10.07 (fixed rectocele, rectal prolapse, lifted bladder, urethra, uterus, and repaired vaginal walls), Raynaud's, 2 severely herniated discs in neck and one in low back, anemia, PCOS, anxiety/depression/panic attacks (since forever). Still having major bowel problems (inability to empty rectum...any ideas?? ).

        I'd like to be on House, MD as a medical mystery.

        Married to Craig, a saint amongst men...who puts up with me and my eccentricities...

        Connor & Mommy by the tree:


        Connor with Santa...so happy!


        I take: LIQUID Atarax, Flomax, Soma (yet again), acidophilus, Glucosamine/Chondroitin with MSM & collagen, d-mannose. MAJOR flare from Cystoprotek! Re-trying freeze dried aloe vera w/some decent results!

        Tried and failed: Elavil, Ultram, Prosed DS, Benadryl, Bentyl, Valium, Ativan, Zanaflex, Librax, Sanctura (all caused retention among other things), bladder instills (owwwwww!), Elmiron (allergic-throat tightening). Failed Interstim-no feeling in sacral nerves...

        I'm allergic to penicillan, sulfa, reglan, quinolones, clindamycin, and now LATEX!

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        • #5
          Hey,

          I have the same problem, I never feel done. I even do the lean over thing and I even leak anyway and I never ever feel done. If its really really bad, pyridium helps me, as I think sometimes the feeling is actually bladder spasms w/o anything there FOR me to go. If its just annoying and not really really bad, I use a heat pack and RECLINE my seat a little bit. It relieves the pressure a little w/o fully lying down. I always drive slightly reclined, I work slightly reclined.... if I'm sitting at all, I'm slightly reclined.

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          • #6
            If you have to be at work, those stick-on or wrap around heat packs can work wonders (some people respond better to ice), and so can the IC cushion. It's specially designed so you can sit in a chair with no pressure on your bladder. You can get one in the ICN shop. I promise I get no kickback for this , but I use mine a lot and it really, really helps me.
            Je vous souhaite de la joie, de la bonne santée, et tout ce qu'il y a de bon dans la vie.
            Wishing you happiness and good health, and all the best out of life.

            Peace, Carolyn
            ___________________________________________________

            Laura (11), Susannah (12 1/2) and Maman (that's me!), North Wildwood NJ, September 2007


            On the Beach with IC

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            • #7
              i'm so glad it's not just me!

              i do the 'leaning' and mild straining, perhaps i need bladder re-training!

              i used to take pyridium, but we are totally med free for 2.5 days now, not one IC med in me and doing alright so far! so i can't take the pyridium anymore, we're on the road to TTC...

              if there's any other suggestions, i always welcome them! i work at a spa so i'm on my feet all day; the heat wrap things are intriguing though, i should look into them - i have a body wrap you heat up in the microwave but you can't stick it on your body easily while standing!

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              • #8
                It took me a while to learn not to strain at all, but it was well worth it. Straining does make it worse. What I do now is to stand up part way, then sit back down. And when I'm finished, I hold the toilet tissue where it will catch any drips after I stand up just for a few seconds, before I toss the tissue in the toilet and flush.

                If I'm flaring, it always hurts worse immediately after I urinate and eases in about ten or fifteen minutes.

                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

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                • #9
                  ICN Donna's post

                  ICN Donna-
                  you're so very right, it causes me great discomfort to strain but sometimes it takes me forever otherwise...it's such a catch 22 for me!

                  i will continue to try that as i really want to stay med free...it's not so bad but it's not great yet either...i think it may take me some time (more than 3 days!) to figure out how i'll really feel after coming off these and re-training my body to deal without the meds to control things...

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                  • #10
                    Count me in to ladies. This drives me nuts particullaly at night when I wake up to pee, then get up agian and again until I fall asleep. Mary and Donna thanks for those tips tonight.

                    Erika
                    IC diagnosed officially via cysto/urodynamics 1/26/07

                    Grade II Endometriosis diagnosed via lap 12/11/07

                    "Fall down seven times, Stand up eight."

                    "Life is a tragedy for those who feel and a comedy for those who think."

                    Current Treatments:
                    Interstim Since 5/25/07!
                    Birth Control

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                    • #11
                      One of my signals that it is time for a treatment is what I call a backward UTI pain. There is no pain as I start to pee it is uncomfortable when I stop peeing. Another sign is the feeling of fullness even after I pee. Detrol didn't help me. All it did was slow my unrine stream to a dribble.
                      TREATMENT: PRN lidocaine/heparin Home Instillations since 2004
                      My Helpful Hints for Home Instillation: http://www.ic-network.com/forum/show...985#post309985

                      Institute of Female Pelvic Medicine (J. Dell, My MD) http://www.mypelvicmedicine.com/index.asp
                      Thank you for allowing me to share my experiences and offer support. Your physician is the only one to give you medical advice. I hope sharing the information from this site will help you and your physician develop successful management of your IC.
                      I post to encourage and offer total support for rescue instillations.
                      Find me on facebook: L. Clark Thomas
                      Louann

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                      • #12
                        I have been having the same problem lately. It seems more often than not I have 2 or 3 drops come out as soon as I get off of the toilet. I used to not have much burning afterward but over the last couple of months I have begun to have burning for 3-5 minutes after I pee. Of coruse when I am in a flare I often have burning 24/7. I have also been having more of that full feeling in my bladder afterwards than I used to. What bugs me is even when I am not in pain I continue to a have a major freqeuncy problem. I get sooooo tired of having to pee at least twice an hour. During flares it's often 4-5 times an hour. I tried Detrol before I was diagnosed with IC (when my first uro thought I had OAB) and did not do a thing for the frequency. It is so frustrating to have to spend so much time going to the little girls room especially at work. I somtimes feel like I need to move desk in the bathroom so I wouldn't be intreruppted by stupid bladder so often. I sure wish I could have my old bladder back. I feels so envious these days of people that have normal bladders. Another thing that bothers me is that this disease is sooooo misunderstood. When people here the word cystitis they think of it only being a bladder infection and wonder why I can't get rid of the infection. It really gets old telling them it's an infection but instead a chronic disease. I sure wish somone could come up with a cure for this crappy disease so we could all be nomal again.
                        TexasHoney

                        Let's keep praying for a cure.
                        IC Symptoms began in early 2001
                        Divorced : Sept 2002 (Partly due to IC)
                        Diagnosed with IC in April 2004
                        Most recent injury - Rupurtured Left Achilles Tendon
                        Wed Jan 28 2009
                        (Ice Storm Accident)
                        2nd Achilles Tendon Surgery - May 28, 2009 after re-injury on May 17
                        Other Injuries
                        Broken Left Ankle - July 2004 ( fell off ladder)
                        Broken Left Ankle (Again) - May 2005 (car accident)
                        Sprained Left Ankle - November 2006 ( fell off my aunts porch on Thanksgiving Day)

                        CURRENT MEDS
                        Elmiron, Pyridium

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                        • #13
                          I have it too...my bladder feels worse AFTER going to the bathroom, and more so with straining or a bowel movement. Strangely, when my bladder starts to "fill" up again, it seems to ease the pain a bit.

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                          • #14
                            i know how you feel - when my bladder begins to hold more urine it's much more comfortable - it's the time when i void it or when it's getting pretty full that i have the problems...it's annoying to say the least!

                            i started Amitryptaline Thursday instead of no meds as I was having too many problems and many times ending up in tears in the bathroom...it helps me relax which is nice but i need to push the fluids like w/the Ditropan (parched constantly)...when i'm full it's ok...when i void it's spasm city...no relief, enough pressure to detain me way too long!



                            i am glad i don't have a desk job b/c i'd be soooo uncomfortable all day...i stand all day instead (work at a spa) but my bus trip to and from is an hour each way...that kills!

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