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Pt 7 (Feb13) Any old prolapse! Uterus/womb prolapse, rectocele, cystocele, enterocele, urethrocele, incontinence, pelvic floor, anterior and posterior repair, TVT etc(993 Posts)
This is thread 7 (again - see below) of a long-running series of posts from ladies suffering from pelvic prolapses to support each other through the process of diagnosis, repair and recovery.
With apologies for confusion in thread numbers - the previous thread was called part 7 but it was actually the 6th thread.
Here are the previous threads:
Info from BBC Health
What is a pelvic prolapse?
As the muscles, ligaments and supporting tissues in the pelvis become weaker, they are less able to hold in the organs of the pelvis such as the womb (uterus) or bladder.
Gravity pulls these organs down and, in the more severe cases, may appear through the entrance to the vagina.
A variety of problems can occur, depending on where the weakness lies and which organs are able to descend, but in every case there is some degree of prolapse of the vaginal wall, which begins to invert (rather like a sock turning inside out).
Prolapse of the womb or uterus is the most common prolapse, affecting as many as one in eight older women to some degree
Prolapse of the bladder, known as a cystocele, is less common.
Prolapse of the urethra (the tube that carries urine out of the bladder) is known as a urethrocele.
Prolapse of the intestines is quite rare, and known as an enterocele or rectocele.
Symptoms depend on which tissues descend, and how severe the prolapse is.
They may include:
A sense of heaviness or pressure in the pelvis.
The appearance of a bulge of tissue in the genital area, which can be quite alarming, and is often red and sore.
Urinary problems, such as having to urinate more frequently, feeling the need urgently, being incontinent (losing control of the bladder) or, conversely, being unable to pass urine when you need to.
Pain in the pelvis or lower back.
Sexual problems, including pain and decreased libido.
Vaginal discharge or bleeding.
Treatment and recovery
Once a prolapse has developed, surgery to fix the affected organs is usually the only way to cure it effectively.
However, another option is to use a device known as a vaginal ring pessary. This is rather like a contraceptive diaphragm or cervical cap. It's made of silicone or latex, and placed in the vagina to push back the prolapsed organs and hold them in place. Many women happily manage their prolapse this way.
Homebird, OH how I envy you! Good luck!
Message withdrawn at poster's request.
Message withdrawn at poster's request.
Homebird - I've found drinking one of those Actimel a day after surgery has helped - especially as they pump you full of antibiotics at hospital - seem to really help re-balance my system. Easy to drink and lots of nutrients too.
Not sure if you're prone to cystitis - I am and thought as they'd fiddled with all my bits this may be a time it would make an entrance. I've stocked up on Cranberry juice and been drinking a couple of glasses a day since surgery. I've also stocked up on cycstocalm sachets but not needed them at all yet.
Good luck - when is your surgery?
Message withdrawn at poster's request.
I know what you mean - it felt surreal when I was at hospital, couldn't quite believe they were going to 'fix' me after all those years. I was weeping with relief in the anaesthetic room.
Hope it all goes well for you.
nanna although I see that there is some kind of get out clause regarding "monitoring your condition " I woder if there is anything in these links that might help ?
Maybe you could contact the Clinical Commissioning Group mentioned here ?
^You can contact the hospital or clinic providing your
treatment, or the organisation arranging your treatment
(this is usually your Clinical Commissioning Group).
Clinical Commissioning Groups must provide advice or
assistance to patients who have waited or will wait
longer than 18 weeks, or two weeks if your GP thinks it
is possible you have cancer.^
I have my op in the morning. Feeling a bit nervous. Can't sleep. What might I have forgotten?
Good luck musttidy, nerves completely natural. I was like a zombie beforehand. Be thinking of you. Hope it all goes well, x
Hi, I feel a bit like crying! I have been back to the GP today who is lovely, I went in about my kidney scan but ended up telling him I am still feeling uncomfortable so he examined me and said my vagina is open at the bottom?? He asked me to cough and said it looks like the muscle tissue isn't supporting my pelvic organs properly. I am seeing the consultant again on the 18th, do you think I should push to have another operation to tighten me up? My GP said he thinks I could do with it being tightened a bit more but there is the risk of them tightening it up too much. I don't know what to do now, I am only 32 so don't want to never have sex again but I also just want it to be properly fixed.
What was the op you had?
Hopefully the consultant can give you the pros and cons of an op when you go there.
TBH, I had a perineum repair with my op, and was told it would make things tighter and to use lube. It seemed so at first, and the geography is slightly different, but does not feel any tighter in a bad way, and I have to use lube anyway (meno), so I wouldn't let that put you off.
They just have to give you a standard list of downsides and you need to understand it, so that you know what can 'go wrong'
nana as you have an intussusception could you ask your GP to refer you for biofeedback? My posterior and anterior repairs have sadly not fixed my need to splint, and post surgery I have more problems going to the loo than I did before. I was sent for a defecating proctogram (my 3rd) and they found an intussusception. This along with a few other rectal problems cause me more problems than my rectocele ever did However I have started to see a physio specifically for biofeedback and it is helping, even after just a few sessions. Certainly worth a try for you, even if its just as a short term aid prior to surgery.
Thanks summertime, I am disappointed it didn't work 100% first time but I'm hoping it is something that can still be fixed, things have improved since the op but my GP said today I have got some scar tissue and I'm a bit worried that I will get more if I have another op. But hopefully it will not be such a big op next time? I guess I need to stop worrying about it until I talk to the consultant as he is the only one that can give me any answers.
Oh by the way the op I had was a posterior and anterior repair.
Sadly I didn't get to see the surgeon who did my op , my pain got worse and worse and I ended up at A&E in agony , after a week in hosptial it has been decided I have nerve damage , I'm on all kind of narcotic painkillers and nobody seems to have any answers, I'm devastated and in pain every day , I'm told to wait and see if the nerve gets better . I didn't know that this surgery could leave me like this , don't know if ill be able to work and as sex is not possible due to pain I don't know how my marriage will go ... I wish I never had the op I the first place it was the worst decision of my life . Today I'm seeing a nerve pain specialist to help with my quality of life and see if he has any suggestions for how to proceed , I first thought that there must be a way to fix it if surgery caused it , but it's not that simple . Has anyone heard of this happening before ?
Gingeroots - thanks, I've looked at both links, however no-one seems to display the indicators for surgical intervention. I've read, on other sites, that pain, digital evacuation, and difficulties with vaginal intercourse are considered to indicate the need for surgery, but I can't prove that the NHS should be obliged to intervene surgically. Anyone know where I could find this? I can't give up! I've also contacted the surgeon's secretary, and asked for a report of their findings/reasons for their decision, to be sent to my GP (I saw him this morning), and to see them sooner than 3 mths. She was so helpful, and understanding, and said she will try to bring the next appointment closer. By-the-way, does anyone know if Estrogen? creams/pessaries help with any of this (I was asked, in the hospital, if I currently take any HRT)? Has anyone tried the Aquaflex pessaries for improving muscle tone? I've even ordered those, to make sure my muscles are in tip-top working order (maybe get a 5 out of 5 score lol!) and maybe they can hold things back a little?
Hugs and thanks to all!
Troubled - I was hoping that hoisting everything back up might stretch the intussusception out, or would this not be the case if they did that sling surgery? I tend to think that if it's stretched taller (ie - back to whence it came), it's going to take up the width (rather like a pair of tights on the right-sized legs.
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