Flexible Cystoscopy? Any Experience?
Jan 29, 2016
I am 39 years old and since 10 months cystitis is been part of my life. I took many antibiotic and resulted positive to 2 urine test with the “Escherichia Coli” bacterium. I went to the specialist and had an ultrasound, which was normal but now he is insisting on having the flexible cystoscopy which consist in inserting a small tube with a camera inside the bladder to make sure that nothing is obstructing the urine tract such a stones, small extra tissues etc.
Wouldn’t the ultrasound identify these if any? Has any of you done this test (Flexible Cystoscopy)?
Does any of you managed to have an Antibiogram test (or ABG) which allow to identify what antibiotic is right for that type of bacteria?
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Today I had a Flexible Cystoscopy .i have to say I was really worried about this .i to had read lots of horror stories and got myself worried .well I need not have done ,the procedure lasted bout 5 mins and was completely painless.they did use some gel and I could feel the tube but no pain and very little discomfort. My consultant told me everything was fine and after a cup of tea I came home.i have had very slight stinging when passing urine first time but even that is ok now.
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I had a flexible cystoscopy for the first time yesterday as my GP keeps finding a trace of blood showing on urine tests & I have frequency of urination. I was nervous beforehand - not helped by a wait of over 2 hours - and could find little information as to what the procedure is like for a female. I want to say to all ladies about to undergo this procedure please don't worry. It is no worse than a smear test and a trip to the dentist is far worse in my opinion!
I had no sensation of the scope being inserted due to the numbing gel, no pain whatsoever, and only a momentary twinge of discomfort as the scope was rotated. I've had no bleeding or discomfort urinating afterwards and feel fine. I think this procedure may be worse for the men!
It was interesting to see the inside of my bladder & to be reassured that there was nothing wrong. The trace of blood is normal for some people and the frequency is possibly hormonal.
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I had a Cystoscopy yesterday afternoon. I've known for about a month that I would have to have one and I have been worried sick about it. Found some awful posts on the net about it, and then fortunately found many reassuring posts on this forum! Trust me that when the ladies on here say "Don't worry"....DON'T! I've been so anxious, that I've lost sleep and my appetite over it. I was in and out of Theatre in 7 minutes! I asked my husband to time it as I knew I wanted to do a review on here to help others, as it has been this forum that got me through it yesterday!
You are in the position for a smear test for the procedure. Knees bent and apart and feet flat and together on the couch. So no stirrups (which I was glad about, as I hate that restriction, and I had expected that!) First they swab the area down, then insert the local anaesthetic. That just feels slightly cold, but not uncomfortable or painful. Then the camera is inserted, and again, that didn't hurt either. The nurse holding my hand told me it was in and then let me watch on the monitor. Whilst the camera is in, the surgeon fills your bladder with water so that he can see it all clearly. Within a couple of minutes, it's all done! I honestly wouldn't even say it was uncomfortable. You are aware something is going on, but certainly no pain. And if the surgeon told me he was going to do another Cystoscopy on me, I wouldn't lose a moments sleep over it! I was given a cup of tea after the procedure, and sat and rested for a while, and once I had passed urine the nurses discharged me from the ward. I've been passing urine normally and it hasn't even stung, so I guess I've been lucky. I had no pain until a couple of hours after the procedure, when I guess my anaesthetic had worn off. It was just like Period Pain. I took a couple of Paracetamol and it eased off, and today I am fine.
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To start with, my pain tolerance is zero. I'm such a wuss that even with simple dental filling or cleaning I have to get anesthetic. I had a flex sig done 5 hours ago and in all honesty it doesn't hurt at all. I read a lot of negative reviews about it and decided to write my own to maybe help people like me who gets scared easily. Two weeks before the flex sig I always go online to research, read forum (which made me more scared). The worst part for me is the preparation. Clear liquid diet and the laxative. Which is two days before my sig test. Once in the examination room, I was so nervous to the point that I almost passed out, I anticipated the worst (probably because I read somewhere in this forum that it is worse than childbirth) and I was surprised that it doesn't hurt at all. Little background, I have internal and external hems, and reason for this test is because I had experience rectal bleeding (bright red blood) about a week ago. Going back to the topic, as the doctor begun to insert that camera tube that was the worst part. If I would rate the pain 1-10 and 10 being the most painful I would say this is easily a 2 just because of the pressure and 2 because I have external hems which is sore (because of the laxative last night). If I don't have external hem I would easily say this is a 1, walk in the park. Then came the camera inside and the air start blowing to expand my colon. This is another discomfort that I felt because it gave me a weird feeling in my abdomen. If I were to describe it, it feels like you're about to take a massive poop. Then again tolerable. It really is just uncomfortable. As the minute passes by I was just watching the monitor and taking a good look at my own colon which is pretty amazing. Then the first corner, they have to turn to the first corner and the nurse gave me a mothers tap like everything is going to be okay and it is. I didn't feel a thing. Honestly just the air and the weird sensation of trying to stop a poop of coming out and the abdomen cramp. Then they found two polyps which they needed to remove (biopsy). Removal of the poly, I didn't feel any pain. I'm not exaggerating this. I'm honestly telling the truth. Then it was all done. If I timed it correctly it took about 12 minutes. Now I know everyone's experience is different and again I decided to write this because two weeks ago I've made the mistake of going into so much forum and read the horror stories, and thought that this review might help balance the reviews. So if you're like me who's super scared, please don't worry too much. Go with the test, the peace of mind that you'll get after is priceless. I'm 28 years old by the way, male. As for the result, just the two polyps and the internal hem is the abnormality that was found. The biopsy they took (polyp) was sent to the pathology dept for further examination. The doctor said that he can almost guarantee me that the polyps are the innocent ones (not the pre cancerous ones). I wasn't recommended further testing like colonoscopy. One last thing, if I were to do this again, for peace of mind, I will certainly do it in a heartbeat as I already know that it is not that bad versus what I've read so far. And p.s I respect everyone's opinion and I understand that everyone's different. I'm just a guy who gets hurt easily with everything and can get easily scared with anything. But I did it, and I aced it.
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Can a Cystoscopy exam in the Penis Damage the Penis in anyway?
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After reading all the posts on here, it made me postpone my flexible sigmoidoscopy 3 times as i was so scared on how painful it will be..Today i went kicking and screaming to have it done, I nearly walked out the hospital on more than one occasion. To say i was petrified is an understatement..
The nurse came and spoke to me asking if i wanted gas and air or sedation, this made me hysterical and i said no i don't want any of it..they took my blood pressure etc ..this was starting to look scary to me.. I went into the room to have it done, stiff with fright..They started doing the flexible sigmoidoscopy and by the time they had reached the top of my left bowel, i didn't feel any pain whatsoever, they pumped the air and still no pain, they took biopsies and still no pain.. I would just like to say that those of you who are posting that it's like torture are either very pathetic or just plain attention seekers.. saying the things you are saying could affect people's lives with frightening them to death with these comments, And will cause people not to have it done..
I am glad to say nothing was found sinister and im so glad ive had it done..To all of those who are worried about having a flexible sigmoidoscopy, please don't worry it really honestly doesn't hurt., you have nothing to worry about i promise..and if you have it done please do comment on here to back up what im saying.
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This evening I went for my flexible sigmoidoscopy & to say I was terrified was an understatement. I did not eat all day just in case I opted for sedation. On arrival the nurse showed me to my room & could see how nervous I was & she was so lovely & talked me through the procedure & said she really didn't think I would need sedation. I decided to go ahead without sedation & can honestly say this was the right decision. I could feel the air being put into my colon & the did have some slight pain very near the end of the procedure but it was bearable & I am quite a wimp. The worst part for me was when it was all over & I had wind but this only lasted for approx an hour. I am extremely lucky as there was nothing wrong which I am very happy about & the peace of mind is such a huge relief. I would certainly recommend having this procedure if you have any concerns. The whole thing lasted approx 15 mins.
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Had the much dreaded Flexible Sigmoidoscopy today. I was determined that I would be sedated after reading the posts on here.
As it turned out, sedation didn't happen and I can honestly say that it wasn't as bad as I had feared. Yes, it was uncomfortable and it was weird seeing my insides on the screen.
I even watched the consultant remove a polyps from my rectum - no pain felt at all.
Probably the worst part of it all was the wind pains afterwards, which fortunately didn't last too long. I have no idea just how much air they pumped in, but it felt like a lot came out!
I guess I just want to give some reassurance to anyone having to go through this procedure. It probably won't be as bad as you fear.
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After the usual IV insertion, walking to OR and walking up rather groggy, I must say the first few hours were strange. Having limited hearing in my right for the past 7 years ( and getting worse) I decided to go for the operation.
My mouth and throat were very dry (11am operation with no food or drink in 12 hours) and deep breathing was challenging. I was encouraged to take deep breaths to clear anything from my lungs. My OP ear was full of cotton and gauze so hearing from that side was nada. My good ear was very amplified like I had a microphone inside my mouth, I would scratch my head and it was LOUD. I was discharged after I could stand without aid and at home crashing on the couch.
I had a protein shake and a bowl of hot soup and felt very stable with no dizzy spells or balance issues, but still the amplification inside my head. I had ringing tones on my OP ear on and off but no pain. If I plugged my good ear I could hear nothing but the ringing.
Five hours now and I feel good but I can hear everything around me, the talking , the tv, things very far away are very clear. My dog barked right beside me and I nearly jumped off my chair, scared me. It was loud. I used to watch tv on 65 volume now it's at 40 volume.
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I am a 29-year-old male of Asian decent (Taiwanese) living in the United States. My first episode happened last November and has continued ever since. It was diagnosed by a dermatologist this April. The worst that I've suffered was when all my fingers and palms, toes and soles were covered with small itchy blisters. Currently my hands are 90% pompholyx-free (yay!).
I think there are three major factors that contribute to the outbreak (environmental, mental, and diet), and I'll explain each in more detail:
Environmental: During dry winter seasons, I develop skin rashes all around my body (guys hate lotion), I think if dry skin can contribute to skin rashes, it probably can contribute to pompholyx outbreak as well.
Solution: Make sure your body is well moisturized, I really don't enjoy the oily sensation, but it sure beats waking up to the itch in the middle of the night! Cetaphil cream (not lotion) work very well for me. Stock up when they're on sale!
Mental+Sleep: I was unemployed when the first episode occurred, and I think stress has a lot to do with it. Also, make sure you sleep at least 7 hours a day, and try to relax and think positive thoughts as much as you can.
Solution: I just try to be grateful of what I have... there are people out there who are suffering diseases 1000x worse than pompholyx or being unemployed....
Diet: The dermatologist told me to cut out chocolate and nuts (especially peanuts) completely. It was HARD. But I started about 2 weeks ago, and it's been working so far. There was a scientific study about the possibility of chromium in chocolate that induced a flare up (from breast milk)
http://www.ncbi.nlm.nih.gov/pubmed/17671414
For nerds like me, you can check it out (be aware though, it's just a sample size of 1!)
solution: see above, you can cut out coffee too, but that will be too hard for me.
Medication:
As a prophylaxis, I take a 180mg fexofenadine every night. In addition, when you see (or feel) small blisters starting to accumulate, there are two topical steroids that I use.
0.05% clobetasol propionate (GSK markets it as Dermovate), ointment form
0.5mg/gm fluocinonide, cream form
http://img.medscape.com/fullsize/migrated/551/352/dn551352.tab4.gif
clobetasol is listed as class 1, very high potency steroid, and fluocinonide is listed as class2, high potency steroid. My dermatologist assured me that applications to the extremities (fingers, toes) will not cause a lot of absorption to the body, so you can be very generous in your application.
I also take multi-vitamins. My dad (who's an MD) told me Asians do not absorb B-vitamins very well, so it's important to supplement with either B-complex or B-12 vitamins.
This is a pesky condition to have...
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I was wondering if anyone had any experience with seizures with their lupus. I had one seizure last see summer before I was diagnosed with RA. I have been told by rheumatologist that I have RA with overlapping lupus symptoms, no positive lupus labs. My question is about the seizure, it was not a grand mal type, no convulsing but I did lose consciousness for almost 5 minutes. Is this a lupus sign. They found NO medical reason at the time for this.
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it's not as bad you people think. I must admit I was fearing it a lot and this might be one of the reasons why I overreacted to the discomfort felt by the pumping of air to distend the bowels. There are no nerves in the bowels so you cannot feel any pain. Proof of this was when they did a random biopsy on me and ripped out samples of tissue from my bowels (as I watched on the screen). There was no pain at all apart from the odd sensation which felt like someone flicking a rubber band inside my gut.
It's always fear of the unknown which scares of most. After the procedure the only pain I really experienced was wind as they had probably pumped the world's gas supply into me (ok so I might have exaggerated a bit) but seriously, it's not all that bad and you'll feel ok right after one big release.
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I have had the implanon since I was 17 (now 24) and it has served me well...most of the time. I am actually considering having it removed because I have headaches five out of seven days a week; have gained about four kilos, which I cannot lose despite a healthy lifestyle and diet; I am moody; and I have trouble sleeping.
Most of these things I thought were just normal women's behaviour, but after speaking with many other women who have since gone off various other contraception, it has been brought to my attention, this all might be a side effect.
I have not had a period since having it inserted -except when it was removed after the three years while waiting to have it inserted again- which has been great. Despite this my main concern are the constant headaches, so I am having it removed and staying off contraception like this for a while to see what changes may occur.
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Anyone have experience with SI joint injections?
I have been dealing with pain (from nagging to disabling) for almost a year. A year ago, the pain slowly progressed to the point that any position was uncomfortable...sitting, standing, walking, sleeping was impossible (for some reason the pain seems worst at night). At that point, I called my spine surgeon (had a lumbar burst fracture 5 years ago so already had a doctor ), but the first available appointment was a month out...I scheduled the appointment and went to the ER after not sleeping any more than an hour or two for several weeks in a row due to pain. They gave me a Toradol injection, muscle relaxers, and Vicodin. I went home thinking that I would finally sleep...WRONG! All those drugs did nothing to stop the pain! I struggled through the next few weeks until my appointment. My doctor's first guess was a disc problem due to my history; however, MRI showed healthy discs and fracture site looking as good as a burst fracture can After a few more tests, he diagnosed me with an SI joint problem and put me on Relafen for 6 weeks to control inflammation. After 3 weeks, I did see improvement...The pain returned to the "annoying" level. Since that time, the pain has been up and down...Always there, not always awful, but sometimes miserable for weeks at a time. I had a foot/ankle reconstruction in November and had a HUGE flair up after that...I realized that I really had an issue when my back pain was keeping me awake at night, not the heel bone that had been sawed into three chunks! I was hoping this problem would just disappear as mysteriously as it began; but, unfortunately, it looks like it's here to stay. My doctor has recommended an SI joint injection as the next step.
Has anyone had success with SI joint injections? My typical symptoms are left side lower back, hip, and thigh pain from just annoying to feeling like my bones are disintegrating...that's the best description I can come up with I also have a lot of muscle soreness in those areas.
How was the "injection experience?" I've had cortisone injections in my foot before, and they were not pleasant...So, I'm definitely not excited about this. I have a high pain tolerance and have dealt with a lot of medical procedures, but something about someone sticking a big needle in my back doesn't give me a warm, fuzzy feeling.
Did you have increased pain for a few days following the injection? After the ones in my foot, I had fairly severe pain for several days...I think they called it a cortisone flair.
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Just saw this product a couple days ago, trying to search for hemorrhoids treatment for myself. Anyone try this before? Is it good? Any other suggestions which product is better for hemorrhoids treatment?
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Day 0.
Scheduled to go to the hospital at 7:30am. Booked in no problem, just thirsty from lack of water. Was no.3 on the list so went into theatre at 11:30 ish. Nice anaesthetists, no issue with the general being put in. Drifted away quickly it seems. Only bad thing was th surgical stockings they made me wear, clashed with my gown.
Woke up at 1:30 with a really sore throat and blocked nose and ears. Side effects of the general it seems. Bum was a little painful at this time. 2:00 moved to recovery room, still feeling a little sleepy. Had some water and he a nice cuppa. Had some bread and butter (they wouldn't let me leave if I didn't eat). No problems with the waterworks but did feel the need for a poo or pump. Nothing came though, no straining!!
Had an ibuprofen with the tea as felt pain. 30 minutes later it must have kicked in, as it was a dull throb then. Tried to do some puzzles in my book but kept dozing off. Nice nurse kept coming in to the my BP every so often and changed. Dressing when a bit fell out. Had a wander round the ward and got dressed. No problem walking, through balance was a bit wonky at times. Wife collected me at about 5 ready to go home.
Got in, had another pee. Opened get well box of presents, had a drink of tea, snarled some of the kids scampi and had a weetabix laced with flax seeds. Drinking lots of water,ergo peeing a lot and sitting on a hot wat bottle to relieve urge to poop. Took a codeine at 5 as well as a paracetamol and antibiotic, next set of Meds is about 10ish.
pain rating 3/10. No worse than a bad day of haemorrhoids at the moment.
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My name is Gary. I am 57 and have had problems with hemorrhoids for years. It was getting to where I was spending two weeks out of the month basically ok due to constipation from opiate medication I have to take. Then one week where I use the prep H to push the roids back into place. Then often a week of just pain, stool softeners vs pain killers, and out of service.
I got referred to a surgeon recently and he said I had a bad case and set me up for surgery. They decided to do a colonistmy (colon probe. where I guess they pump you full of air and put a tube all the way up). I did not know that it was that extensive or I might of gone without it..at least not with this surgery.
I was told afterwards that I had some of the largest they had seen. Also the colon test showed some polyps they had to burn out. They did not look cancerous.
I had trouble getting cleaned out prior to surgery due to the pain and the opiates. As required I took 250 grams of miralax stool softener, 4 laxatives, and waited. I took them at 4 pm, had surgery lined up for 8:00 am with a 6:00am arrival. The drugs did not take effect until 1:00am so I was up until we had to leave for the hospital still on the toilet..and in severe pain.
I was still eliminating when we arrived. I was given a couple of ememas to use on myself. I couldn't hold them but they came out clear so they started the surgery, colon probe, and prostate exam.
I awoke after 2 hours of surgery. I was still under the anesthesia (I was put out) and not in terrible pain. I got up and was able to urinate. I had packing in me and was told to go home, take a bath, and they would come out. I had terrible cramps and gut pain, prostate pain, and severe anus pain. I have lots of stitches down there.
I went home and ate a small bowl of cereal and some oatmeal...and waited. I drank a bunch of juice and water but could not urinate. I was leaking blood everywhere. I took several baths and finally the packing came out. I took stool softeners and drank a lot. Finally the first meal, or what was left over from before, came out in the bath. I didn't have a full bowel push because of the pain but a bunch of crap, in small strings, some packing, and a huge amount of blood came out. I would say a pint.
I ate some more: a bacon and cheese bagel, some oatmeal, and stool softeners. I drank a bunch. I also had to take a bunch of painkillers. One the third day I had an involuntary bowel push but came up empty. I couldn't take the pain. Blood was still coming out in drips all the time with a small amount of feces. I called the doctor and got more pain killers. I set up a plan last night to have a bowel movement this morning. I ate some more oatmeal after one day without food. I took several sleeping pills and some painkillers to stop the urge to have a bowel movement. I had to get up at 12:00am and take more pain killers to stop an early bowel urge which would come up with nothing as is my experience. I awoke at 7:00am, as planned, and held the pain killers aside. I forced a bowel movement and produced a large pile of soft serve sh*t which was full of blood. There was more to come but, now 6 days out, I was in too much pain to push again.
It becomes a real fight to live. I am addicted to painkillers from years of degenerative disk disease and arthritis due to an 80 foot fall in 89. I don't get my refill until the 13th which is 3 more days. I have enough for today. I have stayed away from the long acting painkillers unless I run out. I hope to pass more later today. I will probably try the same procedure.
Again, it is the sixth day, and I still cannot walk without using the furniture. I try and move around as much as possible. I have some blood a fecal leakage which I clean up each time with a bath or a soaking wet warm wash cloth. Then I fold a washcloth in half and put in between my swollen cheeks until dry. They shave you down there and the stubble that grows back is very painful to the opposite side. I have never felt such pain. Each day has been a little better except for the third in which I was worse.
I would've still done the surgery if this all turns out ok. I will eat better, drink more, and do whatever I have to do to keep this from recurring.
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i had vasectomy on nhs and it is well worth it. Very little pain during the operation which took about forty minutes,and the following two weeks were uncomfortable but bearable. I considered going private but braved it on nhs and they were brilliant.No regrets at all and dont listen to your so called friends who fill you with horror stories. It's been ten weeks now and feels no different to before.
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I had my vasectomy done and I wanted to add my experience to a balanced discussion as usually only people who have problems complain. The doctor told me the risks and I went for the snip after consideration. Met a fellow patient whose grandfather and father had it done too and recommended it. We were nervous of course....who won't be? Now the love life is great no hormones or reduced sensation, no worries, no more expensive little ones, no nappy changes! All the wives waiting at the vasectomy clinic thoroughly supports it and I realised lots of colleagues had it done without problems...be warned they will take the mic out of you before you go for it. Thoroughly recommend it. No problems. Do consider the risks but life is risky. I took it and won.
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I wanted to know if anyone here had a vasectomy reversal. If so, what was your experience like? I am thinking of getting a reversal. I got a vasectomy as a young man and today regret it deeply.
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