Have a diagnosis with IC?

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Hi I was diagnosed almost a year ago and I was not about to take it lying down. You?

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  • GwenaLW
    GwenaLW Posts: 13 Member
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    Hi, I was diagnosed with IC in 1991. I was 21 years old. I am now approaching 43. I manage with diet, but it does cause issues at work. I was home for 10 years so it was not that big of an issue until I re-entered the workplace after my divorce and putting my kids in school (I homeschooled them until high school - could have easily homeschooled them longer but divorce prevented me). Anyway what's your story?

    Gwena
  • kunibob
    kunibob Posts: 608 Member
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    Hi Everyone! I was diagnosed in 2003 after a few years of debilitating pain and symptoms. Never thought I'd get my life back, but I'm in "near-remission" thanks to diet (though lately I've been remission-y enough to be very loose with it!), antihistamines, Elmiron, stress management and a good deal of intervention if things start to get out of control again. Rescue instillations are usually a godsend for me if things are flaring up; otherwise, hydrodistentions seem to work pretty well for me, and a day or two of heavy painkillers seems to interrupt that awful feedback loop of pain and get everything under control again. I am grateful every day for how manageable my illness has become, and how far I have come in spite of it...I was a moderate-to-severe case at diagnosis and am a mild case now! :heart: My heart breaks for folks still struggling to find that magic combination of treatments that will work for them, and I recognize every single day that I am very lucky. It may get worse again one day, so I'm going to take FULL advantage of this time and never take a moment for granted!

    Wishing everyone a flare-free day! <3
  • mthannink
    mthannink Posts: 2
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    Hi! I was diagnosed with IC (finally) just a couple of weeks ago - though have likely been struggling with it for years. This whole IC diet thing seems pretty challenging. I'd love to get some low cal IC friendly recipes/suggestions. . .Shelly
  • rjsnead
    rjsnead Posts: 4
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    Hi, Everyone.

    I just joined this site yesterday. I was diagnosed with IC in 1999. We move around a lot because of my husbands job. Have seem many doctors over the years and have tried many treatment. The last was laser surgery in October 2011. I can not take medications at all it would appear. The only thing that has helped is diet. But the food that seem to be okay for me are making me fat. Among other things, like a job where I sit at a computer 10-12 hours a day. I just finished taking a nutrition class through University of Phoenix. Now I know I must do something about my weight problem. So here I am and I need a lot of help. I have no will power.
  • katnb1124
    katnb1124 Posts: 5 Member
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    Hello there!

    I see that this is a small group and no new posts for a few months. Please respond if you are still using my fitness pal. I have had the IC diagnosis for only a short time (almost a year). I did instillations, physical therapy, Elmiron, Amitriptyline, and Tizanadine. I tend to play with my medications quite a bit to see what will work/not work. I have found that I need to keep taking the Amitriptyline and Tizanadine to keep virtually symptom free. I have periodic back pain and occasional frequency, but the horrendous pain is kept at bay with the ami. My doctor (Charles Butrick--highly recommend if you are in the Kansas City area) has been a godsend and he feels most of my major pain is from pelvic muscles rather than the mild inflammation he found in my bladder.

    Unfortunately, I am gaining weight from the amitriptyline. I have tried cutting my does from 25 mg to half, but the pain came back in both my pelvic muscles and bladder. I found this site and am hoping that if I start to monitor what I eat more and exercise more, then the weight will come back off. Before this site, I have found that I can stop the gain, but having trouble actually losing.

    Anyone else on amitriptyline? Thoughts? Alternatives to amitriptyline to control the pain?
  • sprinkels29
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    I have been loosely diagnosed in June and have been dealing with insurance change and new doctors but I see a uro gyno specialist this week which I am very excited about, more answers! Although limiting my intake to the IC diet has eliminated most of my problems (still pain, urgency etc sometimes...just not like my old bladder if that makes sense?) The IC diet has kicked my bottom into gear though, and I get very sick when eating outside of clean foods (which has helped.) I'm trying to tone up and loose body fat %. Can be hard when there are stresses which trigger...etc. Very cautious balance, I hope we can get this group going again....hard to explain what we go through to someone who doesn't have IC.
  • LouiseH238
    LouiseH238 Posts: 199 Member
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    I was diagnosed quite recently, a couple of months back. I find that amytriptiline and cimetidine combined with the IC diet help keep my flare-ups at bay most of the time, but sometimes I will have a massive bladder flare for no reason at all that I can tell, and mild pelvic flare-ups are a fairly common thing. I had a cystoscopy this week that revealed no cysts in my bladder so now being referred for pressure tests...but I am lucky, my case is controllable most of the time. I do feel so much better since I started the diet, not only in terms of my bladder and pain but my whole body feels healthier.
  • cktb4him
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    I was diagnosed with IC 10 years ago and after trying Elmiron, amitriptyline, DMSO instills, and heparin and Elmiron instills along with an elimination diet I was still having tremendous amount of pain and frequency. So I found a new OB/GYN and he said I don't have IC but endometriosis. Well, during surgery he confirmed severe IC, endo, and I had appendicitis! Have you all seen a high tolerance for pain that even amazes your docs? Anyway, after several surgeries and finally a hysterectomy (adenomyosis), following my IC diet, and using the low FODMAP diet for my IBS, my pain is finally under control.

    Now I still have issues with exercise. I started Physique 57 and started flaring due to the ab work. I realized I went from 2x's per night back up 10-12x's/night. Ughh! As a homeschool mom to 3 that cannot happen! That's when I crave coffee, chocolate, and of course sugar!

    So what exercises work for you all? And any of you with multiple conditions you have to treat?
  • cktb4him
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    If elavil is working for you then why try something else? It's so difficult to get IC pain under control because of hormones, diet, stress, and just plain driving too long in the car. If it helps I say stay on it! It worked minimally for me but I had other issues otherwise I would have stayed on it as well.

    I think we ICers need to give ourselves a break and realize we are more complex than people just wanting to lose weight with no other conditions. We want to lose weight but also be able to live somewhat painfree lives like everyone else. If that means we are not our former IC weight but we are comfortable I think that is a blessing.

    Ok now I need to read what I wrote and keep pounding it into my thick skull and believe it too! :wink:
  • PaganDream1025
    PaganDream1025 Posts: 3 Member
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    I was told last week I most likely have IC and have an appointment with a urologist in early-mid June... sucks cause I also have endometriosis (affects the uterus) and EGE (affects the bowels) and food allergies/intolerances (affects the stomach mostly)... on top of things like arthritis and asthma and a laundry list of mental health issues I just feel my whole body is shutting down...