Total Robotic Hysterectomy :: Can't Have Sex
May 5, 2015
I had a total robotic hysterectomy on 11/17/14. after my 6wk ok for sex, it was very painful, bleeding,watery dishcharge, felt something inside my vag. I went to dr. an he said I had scar tissue and possibly didn't get all my cervix(how is that poss)so he put silver nitrate on it and I went back 4wks. said I still had some so put more silver nitrate on.. went back 2 wks later, said it was all gone and didn't see cervix & I didn't feel anything either (was ok for sex)we had sex 1x and very easy. was painful but not horrible. haven't since until 4/28/15. it was horrible, bleeding, cramps, excruciating pain. deep thrusts especially. since ive had watery yellow discharge (some odor)again -so much its like I pee myself-not pee, and feel a hard, thin something inside vag. (tongue shaped)when i touch it or move it, I instantly cramp bad. I need to know what is going on, y I cant have sex (never had prob presurgery)could it be torn cuff? is that my cervix still left?
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I had a total robotic hysterectomy 5 weeks ago. Sunday night had unplanned sex. It was not painful, I'd say uncomfortable. When my husband ejaculated, it burned!
Today, Wed. Still burning, uncomfortable and frequent urination.
Does this sound like an infection? Or irritation because it was too soon.
I even resorted to using hydrocortisone last night because it was driving me crazy and I could not sleep.
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I had a robotic hysterectomy Jan. 2010. I have had pain ever since. I have recently been diagnosed with nerve damage. Has anyone else had any kind of problems after the robotic surgery?
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I had a month ago, a robotic assisted partial hysto, I have only my left ovary. I chose to keep in, being 39, I was not ready for hormone replacement therapy. So, I feel pain so bad, and a warm burning sensation in my pelvic area. I was feeling better a week ago, Now, back to the pain before, I had Endometriosis removed during my hysterectomy, and two loose staples (internal) from my surgery in 12-14-15 (appendicitis/Fallopian right tube removal). I was wondering is there anyone else having pain? I was told Oh you'll feel so good in a month after the surgery.....
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24 year old and yesterday my hysterectomy has been agreed by two gynecology professionals one of them being the surgeon
And I have also had my pre-op assessment and am now just waiting for a date however the surgeon has said he will perform the surgery by robotic assisted key hole surgery.
And I was wondering if anyone else has had this type of hysterectomy and any I formation....
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I just saw a Urogynecologist yesterday who says I need a total vaginal hysterectomy. Of course, I am scared! They did Urodynamics study and my bladder is OK. I originally thought when I went in that my bladder was falling. That's what my GYN at home told me. Not true according to this St. Louis doc. His name is Dr. Veronikis at Mercy hospital. Would love to hear from anyone who has info on him. I haven't scheduled the surgery yet. Still thinking, praying, researching, etc. until I decide. My prob is that my uterus is falling down and pushing out my vagina. Quite an ugly sight!! lol He will do a TVH and repair the vagina. Let me hear from anyone who has stories to tell or similar experiences.
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I had a total hysterectomy due to endometriosis. i was put on climaval hrt patches after which caused headaches and pains and i was then changed to livial approx a year ago but for the last 2 to 3 months i have started to experience the abdomen pains, back pains, leg aches, exhaustion, joint pains and bloating etc that i had before my hysterectomy. its not as bad but its still bad enough to cause problems to my everyday life and routine especially with my 4 year old daughter here. please could anyone recommend any other hrt or treatment for hysterectomy after endometrial? i am now taking my co codamol and voltaren tablets for the pain that i was on before my op!
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I was given a sick note for 6 weeks but my husband is wanting me to return after 4 weeks.
Said I won't need 6 weeks as i am different now to when I had op 10 days ago so won't need 6 weeks.
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I am in a bit of a quandary is there anyone out there that has had their prostrate removed with the use of a robotic arm,I need to find out as much information as possible as I am thinking this may be the lesser of the two evils that they say I need. I would like to find out everything about the op and how it impacts on your life after, how long does it take to heal, how long do you wear a bag, how long before you can have sex or is that part of your life just a memory
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I am having a da vinci robotic laparoscopic myomectomy on Tuesday and I am really scared. I am scared of the general anesthesia, I am scared of the pain meds and recovery. I am scared of not being able to do things. I am even scared of being scared. Anybody else go through this surgery that could ease my mind...only positive stories please I can't take anything negative.
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Just got Gleason score 4+3
PSA risen from 17.8 to 20
plan for robotic radical prostatectomy in 3 weeks - has anyone else had this surgery?
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I have been diagnosed with Perthes when I was 15 and have had pain since then. I had limited mobility but was able to live my life till now. 2 weeks back there was a severe pain in my right hip and i have been given strong painkillers and steroid. It helps but the pain is still there. I have been told to look at total hip replacement as an option.
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I had total jaw joint replacement a year ago. This was a last resort that resulted from trauma that happened 40 years ago. I am not doing as well as I hoped and suffer from chronic pain. Is there anyone who has had this surgery who could share their post surgery results?
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i am a 74 year old male and had my THR one week ago. There is no pain, a little discomfort, and I am walking with two sticks. The only problem is having to get up 5 or 6 times in the night to go to the bathroom. I never had this before. I am OK during the day. Could it be because of the catheter I had for 2 days, or medication? Has anyone had anything similar?
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I got my surgery on the 19th and since yesterday im experiencing bloating and has but I can't go. I'm on a Okinawan hospital and language barrier is huge and completely frustrating, plus pain management meds here are completely different. This happened to any of you? Should I take something natural?
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I'm a 22 y/o female. I have always had an irregular period, but it's now been almost 4.5 months without one. I had an LH of 25 and an Fsh of 6.6. My doctor at student health says this is normal, but after doing some research that appears so only if I'm about to have my period. It has been 7 days and no period. I also had low fasting insulin serum and a total testosterone of 103 (normal 8-60) my free testosterone was normal though at 1.1. My prolactin was 13.3 and my TSH was low normal.
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I am ten years post a Perthes-related total hip replacement! It really has been a godsend for me.
Briefly- I had Perthes diagnosed aged 8, but they caught it late so hip ball was pretty badly misshapen- cue osteotomy, hip spica etc- followed by 2 more osteotomies before the age of 13. By 15 I'd developed secondary osteoarthritis and the joint deteriorated rapidly (v v painful) and pretty much as soon as I stopped growing my consultant opted for a full hip replacement (I was 19). I had a custom made joint designed after a number of scans, partly due to thickening of the femur from my previous ops, and it is a ceramic plastic composite (ceramic ball onto plastic cup I think).
The initial 3 months post op were fairly hard going, you are not able to move beyond 90 degrees abduction so can only sit of high seats- and need a special raised loo seat! I was in a student house at the time so it was a bit embarrassing but I was kitted out by the Red Cross who lent me all the stuff needed for those 3 months- my housemates got so used to the special loo they said they missed it once it was gone! :oops: But after lots of physio I can honestly say that it made the world of difference...within days of the op my pain levels were far below what they'd been, I was off crutches within 6 weeks, and cycling a bike again at 3 months (after not being able to cycle since 13!!)- and 6 months later I spent 3 months SCUBA diving in Malaysia!
At first I had yearly check-ups (x-rays), then every 2 years, until 2 years ago when I was discharged (at least temporarily) from my consultants care! The hip is still not showing any sign of wear- and I am active- walk a lot, have had 2 children with the new hip etc.- so although the initial prospect had been of it lasting only 10-15 years we're now hoping for 20. Anyway crossing each bridge as we come to it. The pain in my hip is 99% gone, but I do suffer a touch with my back and my "good" leg's knee- but both have had to bear the brunt of a lot as I grew up so it's inevitable really... And I see a good (private admittedly) physio fairly regularly to keep on to of things, and try to swim whenever possible...(but not breast-stroke- that's a big no-no for those with hip replacements!). I do still have a leg length discrepancy (2cm) which is partly what causes my back/knee issues.
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I'm preparing my home for post op recovery, and wondering if I need to buy a recliner?
Some of the hippies on this site seem to swear by them, others don't mention them.
a recliner is pretty expensive, and I don't want to go OTT unless it's likely to be a good help in recovery.
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I just wondered if anyone else just feels so tired.. I am 6 weeks today post op .the op went well and I am progressing well. But I am just so tired. How is everyone else feeling ?
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I had both hips replaced in Feb and Sept 2011. Prior to this I had many years of pain and a great deal of difficulty with medical fields trying to determine what was causing my pain. Anyway once it was decided to replace both hips I was happy they had at last found a cause and what I thought was a solution. My first his replaced was my right and this seemed to go okay, it was a total different story with my left. I have been in excruciating back and leg pain since, I cannot walk any distance or stand for any more than five minutes. I need to use a wheelchair if I go out and crutches also, I am stuck at home all day while my family go out to work - I am frustrated and feel useless.
My pain is across my lower back and generates down my legs, my last three toes on my right foot go numb constantly. The pain is tingling, numbness, sharp, deep pulsating pain and electric shock type pain. The more I try to do the worse the pain gets. I spend most of my time with my legs raised as this helps, the pain never goes away but does ease when resting. I have painkillers and muscle relaxants but they do not really help. My hip surgeon like most of the forums I have read told me my hips are fine according to the MRI scan. He then referred me to the Spinal consultant, after nearly a year of seeing the spinal people they have now turned round and said the pain is not coming from my back and there is nothing they can do to help. I asked them what I was supposed to do and they said they had no answers!! I have attended all the physio appointments and even did a three week intensive course along with hydrotherapy - nothing has made a difference.
I lost my job due to all this pain and I am now registered disabled. I had more mobility (although painful) prior to my surgery than I do now. It was nice to read that other people are going through what I am experiencing (although I would not wish this on anyone) it somehow makes me feel better.
I have had numerous cortisone injections in the hips, nerve block of the L4/5 nothing has worked for me post surgery. I had cortisone injection prior to my surgery and guess what it helped - work that one out. I am now being referred to the Pain Clinic (again) and Rheumatology as it was noticed on one visit to the hospital that I had a butterfly like redness on my face and they queried Lupus (still waiting for those appointments - surprise, surprise).
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I wonder if anyone out there has experienced anything like this. Briefly I started off almost 2 years ago with what the Docs thought was Vaginal Atrophy but after taking HRT for a year or so and no change, I came off the HRT. Some months later I self diagnosed with Interstitial Cystitis. Most irritating whatever the collection of symptoms are known as. Thankfully though I don't get all the symptoms at once, although there is no set pattern to them. One of the worst symptoms is urgency to wee. In ordinary circumstances, I would get this strong urge and easily get to the bathroom in time.
However last Sunday I came home from hospital following a total hip replacement! In the early hours of Monday morning I got that severe urge to wee and struggled to get out of bed. I half fell at the side of the bed in sheer panic and ended up with my right leg with the new hip holding me up as my other leg had gone out behind me. Such pain and to make it worse I was wetting myself! So shocked. Anyway I managed to sort myself out but since then I've not been able to wee properly during the day, almost like I am retaining urine. Then I have to get up twice in the night to empty my bladder. I get no normal urge to wee during the day either.
I read up about Fowler's Syndrome the other day and it pretty much describes me. It's about your sphincter not being able to relax properly. I'm wondering if the shock in the early morning last Monday has resulted in my sphincter tightening or something and it relaxes at night when I'm in bed, so I'm able to wee normally again? Anyone else experienced anything like this? I just want my waterworks to come back to normal. At least I can get out of bed easier and quicker now so that's better if nothing else.
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