Prostate :: Second TURP - Symptoms Returned


Apr 28, 2016

Had TURP many years ago but old problems have returned.

Urologist has said I need TURP doing again and has placed me on waiting list. I have great difficulty peeing, doesn't completely void and dribbles when I put it away. Surgeon has offered to put a Foley Catheter in while I am awaiting surgery but as far as I can remember the Foley was only used following surgery. Should I agree to having this catheter inserted to relieve symptoms while I'm waiting?

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I just had a cystoscopy and it seems like I am headed for a TURP. My local urologist seems quite competent but I am wondering if I would do better with a large medical center perhaps equipped with robotic surgery like Da Vinci.

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Prostate :: TURP Experience

JUst wanted to share my experience with my turp surgery. I'm 45yrs old, too young some say for me to having prostate issues but I put it down to my father side of the family (my father and uncles all currently suffer from enlarged prostates) 

For the last couple of years been suffering from weak urine stream, having a full night sleep and waking up in the morning with the urge to go wee just to wee a small trickle. I also suffered from time to time having blood in the urine.

Went to see the Urologist, he did some testing, test on the strength on my urine flow (very weak the doc said) he put a camera up my penis to see inside and we could see clearly that my prostate was enlarge and was putting pressure on my bladder which probably explained why sometimes I could see blood on my urine. I have a benign enlarged prostate, no cancer worries which is good.

While I decided if I wanted to have surgery, doctor put me on Avodart. It did help but I wasn't sure if I wanted to take antibiotics for the rest of my life. Avodart temporary reduces the size of the prostate but if you stop taking it, you will still have the same problem again and it will only get worse.

Decided to have the surgery, I had it three weeks ago. spinal block, stayed in hospital one full day with a catheter inserted. Catheter was removed the following day in the morning, had to urine a few times into a container, followed by a scan machine pressed to my belly to see how much urine was left in the bladder. Passed the test and  was allowed to go home that day at midday.

I can see the immediate benefit of the surgery where my urine stream is very strong. When I get up in the morning with a full bladder, no more urine trickle, just a strong urine flow. On the other side, I'm still suffering from post surgery effects, for example, frequent urges to go to the toilet and pee ( I probably go every 40 to 60 minutes) blood on the urine and pain (burning/stinging) every time I have to take a piss. The doctor says is normal for this symptoms to happen and it will take weeks before everything is back to normal. how long?  it depends on the individual. I can get an erection, it feels a bit different and I will suffer from retro ejaculation ( I was warned about this)

Anyone that had Turp done, how long it took until you were pain free? (no blood and pain)  Did you take any medicine to stop the pain or the bleeding?

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Prostate :: TURP - Any Experiences?

I am told that I need TURP for my enlarged prostate problem . could anyone recommend a good Urologist in Dallas Metroplex area who has good experience in this procedure

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I had my TURP operation 8 weeks ago, the bleeding stopped after about 10 days and along with a few scabs. At the moment I find when I go to pass urine, although it comes out fast, there does not seem to be a great amount. Has anyone else come across this.

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Had a Turp almost 6 years ago. It's a feeling of being raped and you don't know it's happening until after it happens. It happens so fast to you and then it's done. How do men cope with it that have had it done in their late 50's or early 60's? Also can Prostatitis issues bring men into having turps done even though they have urinary issue? In my case I had bladder stones, a prominent middle lobe was discovered during the Turp and my urine flow rate was only 3.2 cc/ sec. Still I had feeling of a" golf ball " which brought me to a decision to have the Turp done. Anyone with similar experiences?

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Large Prostate - TURP Surgery? Feedback / Reviews - Penile Implant

I'm 48 and would like feedback on the TURP surgery...

I've had issues with my prostate over the past 2 years. Last October it was 3.9 cm x 4.9 cm. An now its measured at 5.9 cm x 5.7 cm during the past year I've noticed I was getting 5-8 times a night and during the having to rush to the restroom with no time spare, in the past 4 months I've had to force my urine out. Called doc he ordered urodynamics test, it showed that my bladder has no reaction when I'm full of urine. Doc said MY prostate is so large it's shutting off my urethra tube. So he said I need the TURP surgery. .

I'm so unsure about this because I've had penile implant surgery this past Jan. and if I have the TURP I'll lose my ejaculation...

I also would like to know how to do all with not being able to cum?

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Endometriosis :: Symptoms Returned After 2 Years

After years of pain, heavy periods, aches and really bad PMT I was finally diagnosed with endo about five years ago after scans and internal examinations.  I was operated on and was ok for a couple of years. Then the symptoms returned and only after breaking down in the GPs room did they do the same again.

Just less than two years ago I started a new job but have had time off sick as my symptoms haven't improved. I'm tired, run down, back ache, stomach ache, pick up every could/bug going etc etc. Now I don't know what to do. My boss has called me in for a meeting about my sickness next week.

The Dr hasn't prescribed me anything but I feel all these symptoms are linked to endo and to the cyst I also had removed during my first op.  I struggle almost daily. I'm sick of going to the doctor and begging, telling them I feel like rubbish.

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Has this happened to anyone else. I had my op 18 months ago and they have returned with a vengeance !!

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I have this bacteria called IMPETIGO. To be honest it's the worst thing I had in my life. I'm 18 years old and having this kind of bacteria is simply awful. It all started when I returned from the sea side, I was there on holiday with my best friend. During the trip I had nothing, everything was fine, but the last day a juicy wound appeared on my knee. It was itching a bit. The next day when I arrived home another one appeared on my FACE! I was traumatized! I stood like this for 2-3 days, after I told my mom she took me to a specialist. The doctor gave me antibiotics and Fucidin cream. I started the treatment about 3 days ago, the wounds are looking better now. The major problem is that in 6 days from now I'm leaving to London to visit some relatives and they have a daughter, she's 10. I'm so scared that I could give this bacteria to her, I feel so embarrassed. Please help me, could someone tell me if there is any possibility that I can avoid this ?

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Anxiety :: Just Have Physical Symptoms, No Mental Symptoms?

I admit I have had multiple Anxiety attacks, I am a cashier at Walmart, I usually get them if I had rude customer like after I had a nasty customer who came down from self-check to customer service towards me, I was in tears before that, then my manager told me to hide behind the Customer Service desk. My worst anxiety attack I had a lady who's coupons would not work, I took the coupon price off the items she could not understand that and told me to take the items off period and demanded I give the coupons back to her, I already did. My brain got foggy so I asked her if she wanted me to take the items off, she said yes so I kept doing it, suddenly I wasn't feeling to well, I went to go see my manager to ask for help when I started hyperventilating, my manager had me sit down right there at the empty register. Another cashier was able to take over and finish it for me. My manager helped me over to the bench at customer service, where I suddenly lost feeling in my hands, they ended up curling up from the pinky in. I tried prying them apart using the metal bench but that didn't even work. That scared me, the same manager asked if I was okay I told her that I couldn't feel my hands, staring down at my fists. They finally unfroze after 10 minutes. The lady was so upset with me she left all of her items.

Anyway I will get dizzy, like it ranges from feeling as though I am spinning, I have to clutch on to something to keep from falling over, to the world tipping around me with every step, to not being able to see, not sure if that's exactly dizziness, but it started with dizziness. I'll get flushed randomly. I'll have PAC's. There have been a few times I have almost fainted, one time it was from not breathing, like I noticed that I wasn't breathing, my body was just like woah what's the matter you aren't breathing, I had to have a manager finish while I sat down. I was up and doing my job before I was supposed to so I did not feel well the rest of the day. My arms will also get exhausted suddenly if I have to lift them to head level, like I can barely do a pony tail without them being exhausted, the kinda feeling you get after a hard work out.

I've had the flushing and dizziness when I was talking to my mom and hanging out with my friends. My friends all know and are really accepting if they need to stop doing whatever so I can sit down.

My doctor originally thought it was POTS if anyone knows what that is, I'm getting a tilt table test in 2 weeks, now he seems to think it's anxiety. I'm sitting down while working just in case, it does seem to help slightly. It's just annoying, this has been going on for 3 months and I'm sitting down because of the time I have almost fainted also. Anyway people will say you're lucky you get to sit down, I don't consider everything and almost fainting lucky.

I'm not sure if it is anxiety since it is just physical symptoms, I've had no mental or emotional ones. Just feels like mental ones from fear of my physical ones.

I've done a stress echo and a holter monitor and blood work done.

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Prostate :: Why Biopsy? When We Have MRI And PSA

Having agonised about what to do for over a year now I have finally decided. Nothing. Well, not quite nothing but what is termed ‘watchful waiting’. My PSA has steadily increased over the past two years from 5.4 to 7.4 and in September my GP referred me to a urologist. The urologist, who arrived very late to the surgery, did a quick DRE then said that he would refer me for a biopsy. I wanted to discuss the options, including MRI as I didn’t want to undergo an invasive procedure without proper discussion. Also, I had read that in a test conducted on 223 biopsy-naïve men that biopsy was no better at detecting PCa than MRI. The link to the study is here - [URL....]

We found that mpMRI/MRGB reduces the detection of low-risk PCa and reduces the number of men requiring biopsy while improving the overall rate of detection of intermediate/high-risk PCa.

Unsure how to proceed I asked my GP to refer me to a private urologist with the hope of being able to discuss the alternatives.

In the meantime I did some extensive research and discovered two further studies which concluded that for low grade PCa (PSA<10) the outcome for watchful waiting was no worse in terms of morbidity that invasive treatment and the outcome in terms of quality of life was much better. Both studies were conducted over at least 10 years by reputable agencies. One, conducted by the New England Journal of medicine is here [URL] ... . The other can be found by searching 'PIVOT'. Also, a number of well-known doctors have published articles in favour of doing nothing – Dr Mark Porter in The Times and Dr Sarah Jarvis in this very website, not to mention other articles in The Daily Mail, Telegraph and Independent. I got to thinking that if invasive treatments did not improve my outcome, what was the point of a biopsy?

I finally got to see a private urologist who discussed the options and, although he was marginally in favour of a biopsy, did not object to my proposal. So now I am going to monitor my PSA and I will reassess the situation if/when my PSA goes into double digits. I have since gone on a no-dairy and low red meat diet and my latest PSA (Dec14) was down marginally to 7.2 – still high but moving in the right direction. I appreciate that this course of (in)action is not for everyone and not knowing is frustrating at times, but for me at least, I feel it is the best current option.

I am 56 years of age and my father, who is still very well had an RP for PCa about 15 years ago. All DREs have reported ‘enlarged but benign-feeling’.

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Facing Prostate Shaving

After initially being diagnosed with stage 4 terminal bladder cancer and told I only had weeks to live, plus there was nothing they could do for me, I became a pro-active patient (doctors advise, I decide). All that was nearly 7 years ago.

I have been on Tamsulosin on and off (definitely on in the last year) to help peeing.

In the last year, my blood pressure has risen to dangerous levels. Hypertension pills have helped somewhat, and by experimenting I've got to a good combination with little swelling and other side-effects. But then my remaining kidney started failing.

Investigating this a couple of weeks ago, it was found that my retention (no-one mentioned PVR) had worsened from an earlier 'normal' of 500-600mL to 1.2L and this was thought to have caused the kidney problems. 

I'm now catheterised for 4 weeks (half-way through now), and both my blood pressure and kidney function tests are showing an improvement.

The last thing the urologist said was that they'd probably be considering prostate shaving. Hence my coming to this forum and reading up on the alternatives (Urolift sounds an attractive option if I'm suitable). Whilst I understand that TURP is both the gold-standard and generally OK, the stories here have underlined the serious risk of bad side-effects. So I'll see if I'm eligible for some of the alternatives (not just Urolift, but PAE and WHY).

I'll update when I've seen the urologist next.

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