Cystoscopy symptoms and conditions

Oh my God, where to start. The past few months I have gone through some crazy things from prostitis to having 2 cystoscopy's performed. This past weekend the scab came off the biopsy location in my bladder and blad pretty badly. It caused a large clot to block off my bladder and I could not urinate. In the ER they found a lot of bacteria in my urine and prescribed Bactrim.

Let me just say the past few months have been NOTHING last the past few days on Bactrim. First it was the crazy dreaming. Dreams that were so outlandish, yet so real it was quite frightening.

On day 2 of taking Bactrim I started to itch. It has been quite cold here in Jersey so I chalked it up to the usual dry winter skin. On day 3 I woke up (after minimal sleep) with a sore throat and chest congestion. I then found that the itching grew immensely in intensity and now was adorned with red bumps.

This rash was mainly on my upper arms and lower legs. I scratched at it so badly I drew blood, I have never felt itchy like this. This is ITCHY....EVIL ITCHY!

I woke up on day 4 the same, took another dose of Bactrim (dose #8). As I swallowed the pill something told me "Hey, I bet this pill is causing all your problems." After some research, viola! I found information online that pretty much assured me I was correct.

I went to the doc today and he advised me to take 1 Zyrtec a day and prescribed me Prednisone. I just hope this itching stops soon because I am making a mess of myself with all this scratching.

How could a pill like this be on the market and be utilized as much as it is. The testaments on this site are amazing and stunningly all similar.

Bactrim is undoubtedly the worst prescription I have ever taken or have read up on. To whoever reads this, if you are prescribed Bactrim use one of the rubber test gloves in your doctors office and slap him/her across the face with it. Dealing with the pending lawsuit would be better on you than dealing with the side effects of this drug.

EVERYONE PLEASE READ!!!! GARDASIL HAS DESTROYED MY LIFE! I am 24 years old and a year and a half ago I was graduating college and planning to be a professional dancer and go to law school...I was perfectly healthy and energetic! In February of 2007 I received my first Gardasil shot. After a few days I started to feel as though I had a Urinary Tract Infection and was also feeling more tired than usual. The doctor gave me an antibiotic and sent me on my way.

In May of 2007 I received my second Gardasil shot and yet again, a few days later I started to feel like I was getting another Urinary Tract Infection. I went to the doctor numerous times between the second and third shot...all for bladder and urinary tract pain. For months I was on different antibiotics and they were not making the pain go away. After visiting a number of urologists, I found out that the urine cultures had all been coming back negative - showing no sign of an infection, so the antibiotics were pointless. All tests that I had run, both blood and urine came back normal. It is not standard procedure for a doctor to call you if your test results come back normal, but there was clearly something wrong, so I searched for a urologist who would believe me that I wasn't making up the pain I was in.

In August 2007, I had a cystoscopy done (they took a scope and went into the bladder to look in the bladder wall) and they concluded that I have an incurable bladder disease called Interstitial Cystitis. This is a condition where there becomes a defect in the bladder wall causing it not to have the protective mucus layer inside of it. The pictures of inside my bladder show red, raw skin, obviously showing the severity of my case of it.

There is no evidence as to what causes Interstitial Cystitis, and there is no proven successful way of treating it. The initial signs are exactly the same as a Urinary Tract Infection (painful bladder spasms, painful urination, body aches and back pain). The main difference is the fact that it is not an infection. There are thousands of people with Interstitial Cystitis who are misdiagnosed as having chronic Urinary Tract Infections.

I received my third Gardasil shot in October of 2007 and that is when EVERYTHING fell apart. The bladder pain became constant and there has not been one minute in a day since that shot I have not been in unbearable pain. This is when everything else in my body began to crash down as well. The other health problems and side effects from the Gardasil that I am having are constant sore throat, vicious migraines, vision changes, back pain, body aches, joint pain, sinus problems, vomiting, constipation, dizziness...I could keep going on forever!

I have tried all of the conventional treatment for Interstitial Cystitis and have gotten NO relief from the pain and other side effects. The doctors didn't know what to do, so they put me on OxyContin and a diet consisting of no acidic foods. That has now posed its own set of problems seeing as now my body is addicted to the narcotic, and I have gone from 5'6'' 125lbs to 100lbs over the course of a year due to the diet. I am extremely malnourished and have to take B12 vitamin shots once a week due to the severe anemia. I am 24 years old, and feel like I am 100. I can not live a normal life, I am going to lose my job from numerous absences, I lost my fiancé and am not able to have an intimate relationship anymore, I am extremely depressed, I have to have my family clean my apartment because I am too sick to do it, I can not do social activities because I am too tired and in pain. This vaccine has DESTROYED my life! I am desperately seeking out someone else who is having bladder problems due to the Gardasil so that I can contact an attorney. This needs to be OFF the market a soon as possible so that it does not run any other lives! Gardasil has caused some deaths, but in my mind, I'd rather die than live with the pain I am having. I did notice there are some posts regarding girls getting urinary tract infections... PLEASE PLEASE PLEASE have your urine cultured because there is a good chance it may be Interstitial Cystitis!

I am desperately looking for someone who is having some of these symptoms so that I can go to a lawyer and get something going before things like this happen: Numerous states are pushing to make it mandatory that girls receive the vaccine before they enter the 6th grade. We can not let this happen! We all need to stick together and somehow fight this and get out lives back!

Let me know if you are IN - and also what you thought about my post!

You can email me at ******

Bless All of You!

*~Amber~*

I used NuvaRing in March of 2004 for 2.3 days and I've been paying for it ever since. My doctor's say it's just a coincidence, but I believe it was all triggered by the NuvaRing.

By the second day I had it in, I had the symptoms of a UTI and it was hurting to even walk. I pulled it out, called my OBGYN, and told them I had a UTI. They put me on the patch instead and prescribed me some antibiotics for my UTI.

After finishing the prescription, my UTI symptoms had not decreased, so I went in and gave a urine sample. They put me on a different antibiotic and after finishing that, my UTI symptoms still had not decreased.

They referred me to go see a Urologist at this point. I went in and they said my urine was fine, however I still did not feel ANY improvement. A week or so later I went back to the Urologist, and then a UTI did show up, so they treated me. Once again, I did not feel any improvement, but I went back and my urine test came out negative.

I had a done to look for possible Interstitial Cystitis, but the results were normal. Basically the Dr. told me I am fine and gave me Pyridium to use as needed to numb the bladder.

Ever since then, I've been to doctor after doctor, trying to find answers. Luckily the pain now is a lot less intense but still happens on average about 2-3 times a week, randomly.

None of the doctor's I've seen know what I have. The last dr. I saw said it's probably Chronic Urethral Pain Syndrome, but he is not sure. He'd want to do several tests, which don't sound fun. I've done so many already and to this day now I've had 3 cystoscopys, DSMO treatments that didn't help, PST tests, and so on.

My suggestion: DON"T EVER EVEN TRY THE NUVARING! Also, I was on the pill (many different brands over ten years), and don't recommend that. After getting off birth control, it took just about 3 years to get my cycles back to normal. The change in hormones also made me break out like a teenager, and I'm 34. Talk about no fun.

I started taking Levaquin for UTI on June 25th. I've had recurring UTIs since 1998 and since then have been on macrobid, bactrim, and cipro. I still had some macrobid and bactrim left, so I took a dose before I went to the ER on June 25th. I waited four hours before they saw me, and when I told the doctor about the antibiotics I've been on, he concluded that they probably weren't working for me anymore. So he prescribed a 7-day round of Levaquin, once a day. It's now the 29th, and just yesterday I woke up with my feet aching and today I woke up with aching hands. I've also experienced the frequent urination, but assumed it was due to the UTI until I saw this site. I have three more pills left, and am having a hard time deciding whether I should finish them or not. I'm frustrated and desperate to end my recurring UTIs, as I've had issues with them for MANY years, but at the same time, I don't want to have more health problems added by taking Levaquin. It's like being a cancer patient, suffering the consequences of chemo/radiation. Sure, it'll kill some cancer cells, but it'll also damage your other organs. I lost my father that way. I don't want to go through the same thing with this UTI issue and the antibiotics I've been taking for years. Sometimes I just want to stop them altogether, and look for natural cures instead. I feel like it's done a lot of damage to me already. And every doctor I see (and I've seen about 12 by now) tells me the same thing, and just gives me a bottle of pills to "shut me up." I wish they would actually do tests that look internally (ultrasounds, cystoscopy) to determine what the actual problem is instead of stuffing me full of antibiotics. No one should be getting recurring UTIs this often.

I was at the end of my rope when I looked for Levquin side effects tonight. I have been on Levaquin 500 q.d. for a UTI that I've had for months. I had a cystoscopy nearly a month ago and my urologist put me on Levaquin 500 for 30 more days. I did not have any of the common side effects listed but started having horrible joint pains right after starting on it but thought it was something else - I also have cardiomyopathy and insulin dependent diabetes and thyroid, etc. etc. Finally saw my internist yesterday who did rheumatoid panel and sed rate and called today saying my sed rate was high but rheumatoid panel was fine and offered nothing further. Thank goodness for this web site! I'm not taking another Levaquin EVER! Thanks. Jody

I took Levaquin for precautionary measure after cystoscopy and flowmeter tests for BPH, felt ok until I took the third one, then all "PAIN" has broke loose, I have flu like symptoms, every joint and muscle in my body hurts can't hardly walk a straight line,ringing in ears, the whole nine yards,I am not allergic to any medications at all but this will be the last time I take this medication.

I went to my urologist to have a cystoscopy, and they gave me levaquin right afterwards to avoid future infection. I had taken it before,, many times. This time my face swoll up and I turned beet red. The scariest thing was that my throat began to shut. My blood pressure shot up higher than I had ever seen it. After mega doses of benadryl through an IV. The symptoms slowed.. I still don't understand why I had taken it many time before, and this time it reacted funny.