Prostate :: Urolift Procedure Didn't Work
Sep 1, 2015
I am healthy non smoking 65 year old, very active physically and overall healthy. I had the urolift procedure done May 23 2015 at which time the surgeon installed 5 clips. Prior to surgery I was on 8 mg of flomax which made it possible for me to urinate.I did wear a catheter bag for awhile then. After surgery I was on 4mg of flomax for approx. 1 month. I was able to urinate adequately for about 8 weeks. Never but once what you would consider a flow. At about the 9th week I started slowing down again until it got to the point (about 11 weeks) where it took me 8 minutes to start peeing and then it took two more times in the next half hour to finally eliminate somewhat completely. Now in the 14th week of post op I'm on 8mg of flomax right back where I was before surgery.I am now considering what options are available to me now.
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During the night I have to go to the loo 5 or 6 times this is despite not having anything to drink after 7pm. does anyone else have similar problem and have they successfully been able to do anything about it. Has anyone heard of urology surgeon Neil Barber and the "urolift" procedure and would be most grateful to hear from anyone who has undergone this procedure
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I had a Prostatic Arterial Embolization (PAE) procedure done at the University of Miami on June 2, 2015 by Dr. Shivank Bhatia. Prior to the procedure I had completely lost my urinary function and was wearing an in dwelling Foley Catheter. I had been told by a prominent Urologist at UM that I would never urinate on my own again, I needed to learn how to self catheterize and that if I chose to have the PAE procedure I should expect it would not be successful. My prostate was over 100 grams, I was not a candidate for the TURP and I should go home and have a nice weekend.
My attitude was I had nothing to lose. If the PAE did not work I was no worse off than if I did not try. Dr. Bhatia was an expert in this procedure so I took a shot. My results have been nothing short of miraculous. The procedure was done on 6/2/15. I never had one ounce of pain, either during or after the PAE. I continued to wear the Foley, but it was horrible. I went for my first follow-up 10 days after the PAE. I still could not pee on my own. Dr. Bhatia wanted me to continue wearing the Foley for another week, but I just could not. He was understanding of my discomfort and I was shown how to self catheterize and went home without the Foley, thank God!
I used the catheters approx. every 6 hours or 4 times per day. Each time I used them, I would try to urinate on my own. On June 25th at around midnight I attempted to pee on my own and 6 drops came out. It was a revelation. I then used the catheter and went to bed, arising at 6 am. This time when I went to use the catheter 12 drops came out. Each time I went to use the catheter things would improve. From a weak stream to ultimately a regular pee. I reduced using the catheter from 4 times per day to 3, then 2, then I was comfortable knowing I did not need them at all. On July 1, 2015 I stopped using catheters. I never have looked back.
Three months post procedure I had an MRI. My prostate had shrunk from 0ver 100 grams to 72 grams. My PSA had gone from 8.7 to 2.5. I no longer had any symptoms that would indicate prostate or urinary issues. I sleep through the night. I pee when I have to go, but can go 6-8 hours in between bathroom breaks. I have no discomfort, no pain, my sex life is outstanding and I am 66 years old! Dr. Bhatia has given me my life back.
My suggestion to anyone who is having symptoms: Explore ALL OF YOUR OPTIONS!! I am certain the PAE will become Standard of Care in the future. Try and understand what the potential side effects are of the "traditional" surgical procedures. They may be acceptable for some, but they were not acceptable for me. I take no drugs or medications. The PAE had no side effects. There was no possibility of becoming incontinent or impotent or having an orgasm without an external ejaculation. Find a facility that is doing clinical trials with the PAE and a Dr. who is experienced. Peeing through a straw for the rest of my life was a real possibility. Now I function like I was 40 years old, not 66 years old. I highly recommend Dr. Shivank Bhatia of the University of Miami. He learned this procedure from the man who invented it and he trained with him in South America to perfect it. You have very little, if anything to lose, and you have getting the rest of your life back to normal to gain. Happy to answer any questions or inquiries. Good Luck to all.
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Basically in april 2015 i went to consultant for pile treatment, he advised me to have them treated by injection, i went ahead with this procedure, for a week i was fine then i noticed the itching and pile/pain had returned went back to my consultant he told me he thinks it was a fissure and to take creams and come back to him in 3 weeks time for further consultation.
alas 2 weeks later i was in severe pain and discomfort and phoned the consultants office that i was in bad pain and was told the consultant was on holidays and would not be back for a further week!
at this stage i was told by my doctor to attend hospital a+e for emergency
treatment ,this i did and was told to present myself at the hospital fasting from night before to see a new consultant---Phew it gets worse!
arrived at the hospital new consultant in fairness said he would put me under a full GA and see what is going on there
the following morning he told me yes indeed the piles were back there was one internal and one external and that i was better off going for the laser treatment called THD, which i booked in for the following week this was at this stage mid may had the procedure and for 2 weeks felt great
however on the third week i was in severe pain in the anal area and knew something was wrong (bearing in mind i was told the THD procedure has a 90%success rate..presented myself back to the consultant in hospital had to go under a full ga again he told me afterwards that the procedure had not worked for me for fu..s sake i was one of the 10% that it did not work for so i was booked in for the following week to have the piles which i was now told one of them was thrombosed removed by surgery so have had this done in mid june and have been in terrible pain since, especially after bm to the point where all i could do is sit/lie in the house all day taking pain killers stool softeners and baths every day. every time i phoned the consultant i was told it takes time to heal so after 7 weeks of severe pain id had enough, i went to my doctor got a letter of him to see the consultant urgently as i was in severe pain meet with the consultant am now booked in again for early next week this is what he said the wound is healing however it is a time thing, he will have a further look at me to see if there is something else causing this awful pain he said there is no fissure but wants to give me a botox injection in the anal area to help with the healing, can anyone please advise with this as i do not want to get any worse pain than i am in presently sorry for the long rant but this is actually what happened to me it has changed my life whereby in the last 6 months being in terrible pain and discomfort and am now wary about this botox injection
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I've had worms since last September which is almost 7 months. The worms are white and small. I've take ovex about 10-15 times in the past 6 months. I've taken pripsen about 4 times. Neither have worked.
My nose has been itching and really bad itching anus which is depressing me. Could this be anything other than threadworms(which I've sent a stool sample and sticky tape test off and all come back negative).
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I'm 17 years old I've played volleyball basketball and track my whole high school career and I've always had problems with my knees and ankles but I've been going to the doctor for my knees for like 2 years now and I've had like 3 MRIs they never tell me anything I've tried braces but they don't work. My left knee is way worse than my right but they both hurt. It started out feeling like I just had to crack my knee like if you straighten your elbow and it cracks but then it progressed and know it hurts extremely bad when I start running and I can't stand up after sitting like straightening them hurts horribly bad. Sometimes while I'm sitting they ache and I feel like it's on the inner side of my knee and on my left knee it's on the left side inside and if I go on my tip toe it hurts really bad like a shooting pain kind of it's like a line kinda. And it's also worse when they're cold like I have to drive with the heat on them even when it's 80 degrees outside.
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Degenerative discs and spondylolisthesis,had injections worked well for 5 days now all back ...
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After meeting someone on a dating site (getting along very well) a month later I started to itch and little lumps with a white centre started to appear. I thought I had been bitten by mosquitoes and treated them as such. Another few weeks past and they were getting worse not better. That's when I realised what they were. I told the person who I had met and they would do nothing about it so I discontinued the relationship. However I was left with this mess. So far i have used 20 tubes of lyclear and a bottle of tea tree oil. All to no avail. I am at my wits end now especially after reading a lot of the stories. This is horrific. I desperately need help in getting rid of this curse.
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Is there any natural medicine to cure fibroids?
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I opened a heavy window at work in April this year 2014 (twice in a matter of a few days) I've had 11 sessions of physio to which this didn't respond to. I've had horrendous pain over the months and now had a scan to show a prolapse disk. On Thurs 27 November I had an epidural injection which doesn't seem to have made any difference and I am currently off work this is my 5th week off. Prior to this had four weeks off intermittently. I am due to see the Neurosurgeon again on 17 Dec to discuss surgery that he said he can offer me. I keep as active as possible but to walk sometimes if really painful and I can't work with this. This has gone on for so long, any advice on how to treat this? Should this have gone off for this long? The L5 S1 disk is prolapsed.
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I was diagnosed with SVT from an early age, and spent most of my childhood going to and from appointments at the children's hospital. Eventually, after many many episodes (and of increasing length!) I was suitable for an ablation. I had the ablation at aged 17, however, unfortunately it did not work and I had an episode 6 weeks later - frustrating! However, it has somewhat modified it and my episodes are less frequent and the length of episodes has decreased substantially from 3 hours to just 5 minutes! So I would definitely recommend the ablation surgery, although it didn't quite have the desired effect for me it has improved the condition and the effect on my life. I now control my episodes through the various maneuvers suggested (and with success thankfully.
My question is, how do people with SVT get on with exercise? I have always been keen to compete in sports, especially during school - however the severity and frequency of my episodes before the operation meant that this tailed off a little. I am now 22 and I am keen to get back into running, moreover, running distances for charity etc.! I am just a bit apprehensive about overexertion and effects on my heart! I would thoroughly appreciate any help/advice about how much exercise people tend to do! especially those who have been diagnosed with SVT from birth or a young age.
I am due to run the race for life in a few weeks, and have been running a little in preparation for that. But I am keen to get back into running longer distances with a view to doing half-marathons/marathons. Has anyone run these kind of distances with SVT?
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I'm not sure if anyone else experiences this? I tend to find something will work for me down there, then it does not. For example: coconut oil has been quite soothing in the past, lately it just irritates me no end.
I tried Olive Oil but it wasn't that great. The Doctor prescribed Sylk vaginal moisturizer and that can either be Okay or not.
Has anyone else got other 'comforters' for LS? Mine gets sore and stingy as opposed to itchy.
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I have got lichen planus on arms very bad, legs, vulva, oral and now starting on my chest. I have used cetraben, dermovate, dermal, doublebase cream, hydrocortisone, calamine lotion, aqueous cream..my GP been excellent.
Also Tramalgin, betnovate for below and am now tearing my hair out with sleepless nights with itching.
I go to work like a zombie and it's so embarrassing having to scratch, they say the monkeys here as a joke.
This has gone on for 6months nearly...am waiting to see the dermatologist. I had a vulvar flare 4 years ago and was ok up until early this year.
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I have diagnosed with IBS for nearly 2 years now and have tried a number of medicines (including Fybogel Mebeverine, Colpermin, Wind Eze, Buscopan hyoscine butylbromide, and VSL#3). This has been complimented by cutting out gluten and following the Fodmap diet. Nothing has changed and I’m an in constant discomfort i.e. every day, with peaks of pain (stomach pains, wind, need for toilet etc.) and troughs of just simple discomfort in the stomach. I have lost count of the amount of times I have gone to the doctors and I’m now being broadly told: “you have IBS, deal with it”. Does anyone have any similar experience of this and has anyone got any suggestions as to what I can try next? I feel that I am stuck.
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My pee smells like asparagus but didn't eat any, can something you eat cause this besides asparagus?
About two weeks ago, I noticed a pain in my back together with the asparagus smell, I took an antibiotic for a few days, the pain cleared within a day but the asparagus smell did not clear.
Two years ago my pee smelled like asparagus too and since I was convalescent from a physical injury and had antibiotics I took them and the smell cleared. Am a celibate person with clean health habits so it could not be an std, and I don't have any of the symptoms of a uti. Can something you eat besides asparagus cause this?
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I was diagnosed with low B12 levels and further tests revealed that I had intrinsic factor.
I was given the 6 injection course and was told I would have another in 12 weeks then again and then blood tested again. 6 weeks since my last injection and my symptoms are back. Feeling vague, tired, lethargic, irritated etc. How can it be that I have intrinsic factor but obviously have low B12?
is it likely something else is going on? - any ideas/suggestions?
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I've had a brown fairly flat mole on my left cheek since as far back as I can remember. It started to annoy me so I decided to get it removed. I saw a dermatologist who said a shave excision might not work but he would give it a go.
Everything has healed now but I am left with a small 'crater' where the cut was made but the coloring of the mole is still there. If anything, it looks worse than before. I'd really like to get rid of this.. what are my options?
I've attached 2 images of how it looks from the side and also front-on (which shows how it caves in now). I know it's not a huge thing and is purely cosmetic.
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I started taking birth control pills two months ago. I completed one pack of the pills. I had a menstrual cycle last month but I didn't have one this month. Is it possible that I might be pregnant?
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I have been suffering from some internal Hemorrhoids that prolapse after a bowel movement for almost a decade. After they prolapse i gently insert them back into where they belong and it has been ok and hasn't affected my life much.
However the past a few days ago after making a bowl movement i noticed when they prolapsed they were very inflamed and large and painful, i couldn't put them back inside me. I waited until the next morning but unfortunately the couldn't go in so i had to go to a hospital. The doctors managed to insert them back in when they applied some gel but it was painful and not easy.
Then 2 days after same problem but they kept on bleeding, had to go back to the Hospital and same thing.
I hope they get better more manageable soon but i doubt it.
Anyway i really want to avoid the traditional Hemorrhoid surgery as i have read the horror stories on here about being in pain for 4-8 weeks, complications and also i can't afford to take so much time off work.
Hence why i am considering the HAL/RAR Procedure, from my research it is less painful and hypothetically you can be off work for only 48 hours.
has anyone experienced this procedure? What was the pain like?
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I had THD (sometimes known as HALO) procedure 9 days ago, the last couple of days it feels like i have external haemorrhoids back, my husband says they look like them, large and inflamed!... I'm so upset and frustrated, had been feeling ok as was recovering quite well. Very uncomfortable and painful after bms but i was expecting this and had prepared for it mentally and physically. I've not had to strain when going to toilet, in fact going regularly since 2nd day, so no constipation. I've also had a stitch come out today after bm (surgeon said all my stitches were internally) Has anyone else had any similar experiences??...
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As much as I have read about this procedure, I feel somewhat prepared going into my consult visit with the Dr.
I am wondering if there were any questions/discussions anyone feels they should have asked BEFORE the procedure?
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