Bigger Or Narrower Vagina ? After Cystocele / Rectocele Repair
Mar 10, 2016
I am worried that after my repair I will be left with a bigger vagina. When I push my front wall to where it should be I have a gap below my fingers. This really concerns me as I don't want to be bigger than I am now! I know Rectocele repairs can make the vagina narrower but the front wall of the vagina is attached to the pubic bone so is very different. Can anyone tell me how it was after your Cystocele repair?
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I'm due to have Rectocele and cystocele repair. I had my last consultation with my surgeon back in August 2015 had my pre op assessment in September. I was told I would be in for surgery around December and I'm still waiting, I spoke to someone at the gynae waiting list team today and they said I'm not even on the list yet as they are so far behind. I completely understand that they are busy and their are woman out there a lot worse then me it's just that walking and lifting is becoming a real pain and I'm sick of taking co dydramol which blocks me up when I already struggle to go to the toilet for a bm.
Sorry for ranting I just wondered if anybody had any advice as I'm starting feel like I'm moaning all the time to my husband.
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I had a cystocele and rectocele repair on the 21st (so 4 days ago). The doctor used a tape sling for the cystocele and stitching for the rectocele. I honestly had no idea what to expect and didn't even know that he would be cutting 2 slits on my outer labia. What's actually hurting me now are the interior stitches which I assume are from the rectocele repair. I wanted to check out what was going on down there and there is a lump, almost like 1/2 of a finder, bulging out of my vaginal canal. Is this normal? Am I just swollen?
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I'm wondering if anyone has had this in the past year. What can I expect? Any words of wisdom?
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I have rectal & vagina vault prolapse - Rectocele & Cystocele( lower 1/3rd) and sex is quite painful and difficult. I have 3 choices at the moment ;
1/ do nothing until the prolapse gets much worst but this means having uncomfortable & sometimes painful sex ..I am coping with bladder & bowel problems with kegal exercises but hate the look and feeling of it down there.
2nd... try a pressery? If I pressary works my Gyna would preform a much simple perinuem repair to fix the tight skin problem. This still involves stiches so I wonder if pressary is the way to go and I have heard that can affect sex too? or have the surgery. I had huge cuts to deliver my first child as she was stuck in my birth channel and then they figure I didn't had the width to deliver here???!!!. So many stiches and at least 2 further opreations to try and correct the terrible job the first surgeon had done on me. I have literally a thin area of skin in my perinium that is only about a 1 cm wide which is treched so tightly it hurts when touched. Sex has been uncomfortable for the past 30 years and several positions are out of the question. As I have grown older 58 now and the symptoms of menopause have raised their ugly heads. This area has lost its elasticity and has become hard and very taut.
3/ Do the surgery for the rectocelle & cystocele .. I really worry especially after reading this forum that it won't fix the problem and could make it heaps worst.
Does anyone have any stats on % of successful operations? This site is full of bad experiences.
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I am a 53 year old and had this surger y 8 days ago. I had a cystocele before and recovery was only a couple of days but unfortunately i had to have it redone. I and am very surprised at how sore my bottom is and my legs just feel tired. I am normally very active and find it hard to not be able to do much. I havent drove yet just don't feel I could even walk from parked car into a store. Just wanted to know how long before it started to feel better and back to somewhat normal.
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I have a rectocele and I am getting it repaired next month. When I saw the surgeon she said I also had some stress incontinence based on the urodynamics study that she did. I know I do, but it isn't bad. Sometimes a drop when I sneeze but it's not awful. She said it might get worse after the rectocele repair and suggested a mid-urethral sling. It is made of a synthetic mesh.
Any suggestions on resources for information about this procedure? Right now I don't feel like the symptoms are bad enough to risk side effects but I don't have enough information to decide.
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Need answers for reason for the swelling sensation. Feels like vagina and rectum being pushed out as before. Went to doctor 1 week post op because of this, bladder still in place. Doctor had no explanation. Scheduled to go for check up in 3 weeks. This will be the 6th week since surgery. Can't rest or sleep well because of the constant swelling.
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I have had a breathing for about two years now, and every year it gets worst. My nasal passage is gradually getting narrower (i think) because i have realised that my fitness is getting affected this. I used to be able to run all game (soccer) but now after about 30 mins, i'm out of breath. i have not changed my diet or anything else. Most of the time i'm picking my nose just to try and open it and it very uncomfortable especially when i'm going to sleep. I can not breath at all. I don't know what kind of problem i have but in need answers really quick before it ruins my future!
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I had cystocele and hysterocele surgery 5 months ago and after surgery I have developed a rectocele. It is mild but I have problems in the bathroom and feel like a ball in my rectum constantly.
I went to my check last week and my gyn confirmed that I have a rectocele. He saw also some stitches inside my vagina. He told me to have surgery for the rectocele and he would remove the stitches in the op also. He told me not to worry, he would use stitches for the rectocele repair (not mesh). He scheduled the op for June.
Well... the following day I had an app with my physio who said "DO NOT OPERATE THE RECTOCELE!!!". He explained that my rectocele is mild, he is sure that I can fix it with rehabilitation. Rectocele surgery has bad results, he said, and many problems afterwards with sex. Is that true?
It is the same situation I lived two years ago, when I began to feel the cysto and hysterocele, the physio said not to operate, but after 1 year physio treatment, finally I had to operate.
What do I do? . I do believe in physiotherapy, but as a complement of surgery. For my experience, I don't believe in it as a substitute of surgery. Should I postpone the op, do the physio treatment and see what it happens? Or should I operate now? It would be very stressful for me to have like a year of treatment just to have the surgery finally. What do you think?
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I have rectal prolapse, enterocele, & rectocele ,plus chronic pain disease & other issues. I have to manually remove my bowels, which is very painful and getting worse. I have seen rectal colon docs and urogynae. Some want to do a colostomy, and some want to do a robotic rectopexy on me. Ism in my 70's, and need help I don't know what to do.
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I am a 65 year old female with a grade 3 or 4 cystocele. In the past few days I am having extreme difficulty emptying my bladder. I am freaking out because the issue of surgery rears its ugly head. I do not want surgery in as much as the failure rate if as high as 50% and I would never have mesh because of the ugly hideous complications of using it. Does anybody with this problem have any other ideas? I may try a pessary. I was wondering if there are ways of emptying ones bladder by utilizing certain positions to facilitate urination ( like standing for example). I have had this cystocele for 10 years but not it has obviously gotten worse.
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Anyone have a cystocele (prolapsed bladder) and still have intercourse? My husband passed away two years ago and I have been attracted to someone. My husband and I had no problems, but I am concerned about the size of the penis perhaps causing problems. I have had the cystocele repaired once but it occurred again. Has not caused any problems so far, however I have not had sex since my husband passed away.
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I had a cystocele 3 1/2 weeks ago. It seemed I was healing well with some mild tenderness in the lower abdomen. Which I felt was normal. But a little over a week ago I suddenly began to experience excruciating (level 8-10) pain in my right hip area. The surgeon said it is the tendon/ligament (?) where the sling was attached to that is hurting so bad. Has anyone else experienced this after cystocele surgery? And if so, how long did it last?
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I went to the doctor as i am constantly running to the toilet. I also feel a lot of pressure. I am 46 years old. I am trying to loose weight but can't walk far as i then need to pee. I pee approx 15-20 times a day. Blood tests show no diabetes etc. My doctor examined me and says i have a cystocele, he said it wasn't as bad as he expected going by my symptoms. He did say tho that everything is crammed in there (whatever exactly that means i am not sure) He is referring me to get a pelvic ultrasound and then consult with gynecologist. He thinks i may benefit more from surgery as he thinks the other treatments don't work as well for me.
Anyone had similar symptoms with a mild cystocele?
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It's now been 27 days since my cystocele repair, i had a wee feel the other day and felt like a lump , im sure its where my stitches are/were , is this normal ? , i did have an infection 2 weeks ago and saw my doctor and she said everything looked fine but now i'm worried sick my operation has failed, anyone else felt this, could it just be swelling ?
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Three months ago I had a Cystocele and hysterocele surgery, It was done by a good dr here in Spain, he promised everything was going to be fine and the sick leave was of 40 days. The surgery was through the vagina, he removed the uterus, left the ovaries and lifted the bladder with a "net". I was happy the following day: no pain, no feeling something was dropping out from my vagina... I had repose for one month and a half, then I Started to have stings inside, I came back to dr and told me I refused the stitches, he had to cauterize. Now the stings have gone but for one month I have felt the same sensations I had before the surgery! It's like someone were pulling from my top of the deep vagina, I feel again something dropping and feel as if I had something inside the vagina. My dr said everything is ok, nothing out of normal. Then I started to visit a pelvic floor physiotherapist last week and said that everything is ok the net is being absorbed by my vaginal tissues, but I'm still healing, the scars inside are tight and my pelvic floor is too weak. Besides she has found out that I have a little rectocele! And my gyne didn't tell me anything about that! I am so sad, I can't stop crying, too worried... I have not tried sex yet... I feel sad about my kid and my husband cos I am all day obsessed with this and I don't feel like going out... I used to be a sportive person but I am not anymore... By the way, I began work three weeks ago and feel too weak and depressed, Very hard for me get up in the morning, I went yesterday to the social security dr who is the dr that gives you the sick leaves and she prescribed tranquilizer and told me I can work. I feel I can't go on with my life... I feel that I'm starting depression, I know that if I felt a bit better I would cheer up but I feel worse. Please anyone can help me with any piece of advice? Will I ever be happy?
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About 4 years ago I got this small lump by my ear it does not hurt or anything but I notice this year it got a little bigger can you give me some advice or maybe someone has heard of this it alarmed me a bit when it got bigger this year
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i was never told not to squat, and so I bent my knees when picking up something from the floor...because I was told not to bend. Do you think that is why my bladder is coming down? I had a Colpocleisis and MiniArc Sling Placement. The only instruction I was given was not to lift over 5 pounds, no bending, no baths, no pulling or pushing for 3 months. That was all! I wonder if bending my knees when picking up items I dropped on the floor was considered squatting...and that's why my bladder fell.
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I have just been diagnosed with having a large lipoma at the top of my leg i had it for about 18months it has grown gradually bigger and has recently become painful especially in bed at night. My gp has referred me for a scan to assess the size and says it may need removing.
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do some races have bigger clitorises than others?
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