Is it a urinary tract infection or interstitial cystitis?
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I was on elmiron 4 years after it came out....for chronic cystitis..ha dhad my bladder stretched two times bfore that for the same reason....stayed on elmiron for 3 or 4 years and then ended up on something else with it because my bladder was going int ospasms...not a night went by that I did not get up numerous times to pee. ...btu the elmiron fixed he chronic infection and brought the infmammation down. Then I went to my natruopath who put me on some chinese medicine and grapefruit seed oil and 2 months later....no more spasms...no more medication....no more infection....she also boosted my adrenal glands at the same time...made a big difference.
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Wow, such a great thread with fantastic info. Thank you Weesa for getting this started and all your great info. Sandeeonherown, where do you buy grapefruit seed oil????? I think it would definitley compliment my cranberry extract that I take. I never want a kidney stone or UTI again if I can help it. Thanks again for all the great info. Kathy
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weesa - the only thing I did that I think helped me get through the last 20 years was the following: Cannot drink anything with caffeine in it, I cannot eat rasperries, tomatoes, oranges or drink orange, cranberry, or tomatoe drinks. I think most cannot eat strawberries but I can. I also did the bladder retraining which was very hard but is still helping all these years later. Since I used to feel like I had to go even right after I went, I slowly extended the time between each time I went, starting at every hour, to every 2 hours, and so on. I also think that amitriptyline one 25 mg before bed has helped, though I hate the dry mouth it gives me.
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Thanks, blondie, you give me hope and optimism. Yes, I think avoiding those foods you mention is important. I adore tomatoes in season but they are pretty hard on the bladder. I do indulge a bit, and then take plenty of Prelief and water. The bladder retraining sounds interesting--had never heard of that.The thing that bothered me the most was doing a nuclear bone scan. I did not drink enough water or pee enough apparently between the time they injected me with the radioactive dye and the bone scan 3 hours later. My bladder lit up on the bone scan because it was full of dye. That episode gave me a bad four months.
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weesa - have you checked out the IC Network. It was my home years ago until I had to move to this new home if ya know what I mean.
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Here is what I know based on my experience--a few important things to add and a different perspective from different docs. IC is now reserved in a good portion of the medical community for a bladder condition with ulceration of the lining, called glomerulations. A generalized pain disorder with no bacterial or other bladder disease present is part of what is often being called PBS, or painful bladder syndrome. It is believed by many doctors to be a hypersensitivity issue, often triggered by an initial insult. Vaginal atrophy and lack of estrogen can be that insult, so can a UTI.
The "IC diet" works for some, and not others. Everyone is different in terms of what diet modifications are needed. Generally, clean, moderate pH water like Evian is best. Stress triggers some people, food others. It usually goes in and out of remission.
Foul urine is not necessarily a sign of IC. IC, or PBS is a very mysterious disease with sadly very little understood about it. No one medication or intervention seems to help a majority of patients. Some are on tricyclics, others opioids.
There is no definitive test, hydrodistention is considered by many docs to be an inaccurate diagnostic. The potassium test is also up for a lot of debate. Some doctors have called it "barbaric", as well as inaccurate. Many non-IC patients have pinpoint bleeding on hydrodistention. As some doctors consider the available tests inaccurate, it is diagnosed by symptom elimination (you can find this test online, though I forget what it is called--it has an acronym).
The good news is, it is not considered a degenerative disease in the PBS state. Many doctors do not speak in terms of "mild" or "moderate" in this context, as it is not understood to be progressive. The concern in the medical community, as with many pain disorders, is that chronic pain is believed to cause changes in the dorsal horn, thus creating an endless pain cycle.
IC Network is wonderful, but it is important to understand one size does not fit all with this issue. It's important to work with a doctor who is willing to experiment with medications and support you with the latest research on this disease.
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LtotheK, wow what a great post--thank you. I have not been back to my urologist in quite a while; it seems like progress has been made in understanding dicey bladders.Guess I have IC since I have glomerulations, but I wonder about so many of the women with funky bladders--that they might well have PBS, especially if they have had chemo.You have showed me --and everyone who visits here-- the complexity of this subject and the need for individual treatment.
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Weesa,it is my job, in some way, to make my experience educational for others! I went through so much, and I still do. But I am under control generally speaking.
Just wanted to clarify a bit further. My doctors in NYC felt that only in ulcerative glomerulations could the diagnosis of IC be made. My specialists didn't do hydrodistention. They did to cystoscopy to rule out cancers. But their diagnosis was made more than 10 years ago, and I realize my doctor was actually on the cutting edge (if their is one in this game). She told me I had "hypersensitive bladder" spurred by a UTI. Flash forward 10+ years, and that is known as PBS.
As many people have gloms on hydro, you do not need to feel like you have a bladder dysfunction per se (a mental state I believe leads to anxiety and worsens the condition). Many non-ICers have gloms on hydrodistention. It can be as simple as lower bladder capacity, not necessarily a faulty lining (by the way, the concept of a faulty mucosa is also seriously up for debate, many docs no longer subscribe to this idea).
What you need is good pain management. I ended up at a wonderful pain clinic, and after years of experimentations and instillations,found some relief.
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I had my bladder 'stretched' 2x was then told it only lasts about 11 months...did not want the invasive procedure done every 11 months!!! Went on Elmiron about 5 years after it had been on the American Market. Thankfully, at the time, my blue cross insurance covered it as it was new in Canada. It worked for many years and I think got rid of the infection in the bladder lining that had become chronic for me...and then I started having spasms in my bladder...would sit on the couch at night and be clenching (if you know what I mean) and racing for th etoilet for a few drops. Not cool...so I went to the naturopath..said I wanted this stuff out of my system..she put my on some chinese medicine, grapeseed tincture and there you go....no more bladder issues.
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I'm nervous about a naturopath as I have kidney issues already from medications and don't want to exacerbate the with anything. What to do? What to do????
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Good info here, thanks
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Barbe, my naturopath would take all my health issues into account, I trust her to work with medications that only fit with my profile. She has done a beautiful job so far.
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