Any experience with rectocele? No one EVER talks about this!
My situation: Self-diagnosed rectocele. Have appointment in 4 days to hopefully confirm or R/O. After 20 years on anti-depressants my constipation was so bad that I developed a rectocele. I hope to find out soon how large it is and how to treat it... Have been doing Kegels. Have had no other pelvic issues of any kind - ever (lucky, I know). Am post-menopausal, age 62. After ~4 months I successfully tapered off Venlafaxine down to zero (was NOT easy and that Mayo group was VERY helpful to me). One of the first things I noticed in tapering/ending AD's was being able to poop again! Hallelujah! But 20 years of constipation had taken its toll. Caution The Following is not for the faint of heart/squeamish (but this is a topic no one is talking about and I KNOW I can't be "the only one"...): I am getting too old for the physical contortionism necessary to extract poop from my rectum, not to mention sick of it. I go for annual gyno exam EVERY YEAR. Every visit I have complained about severe constipation. Lately I have even described how difficult it is to completely eliminate and having to use my fingers to get the poop out. Why has NO ONE ever said "rectocele"????? It took me several hours of sleuthing online to even find a word for it. And when I did it seemed like a fairly common physical ailment for women - and yet - there is very little out there about this condition. Most of the sites that mention rectocele do so 'in passing' while discussing pelvic prolapses. I in no way mean to belittle THAT horrible state of affairs... it's just not my personal issue and I want to know more about my personal issue. But everytime I try to find more info I end up reading stories about OTHER pelvic issues because if rectocele is mentioned at all it is in conjunction with these others. Please... has anyone else had this as their main or single issue who would be willing to share diagnosis, procedures, outcomes, what to expect/avoid? If so I would be truly grateful!
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I would definitely ask your gastro doc to order one.
Malabsorption
Update. My specialist at U Of M ordered eight tests! Two x-rays of my bowel, two stool test, a pelvic MRI, gastric emptying study, colonoscopy, and possibly another endoscopy. I will keep you updated.
I have had three prolapse surgeries, uterine prolapse in 2011, vaginal prolapse in 2018 and rectocele repair 5 weeks ago. The rectocele repair was due to urinary incontinence/pelvic floor prolapse.I have also had chronic constipation issues but that was not part of my discussion with urogynocologist who did my rectocele repair. Three weeks into recovery I developed a UTI caused by gardnerella vaginalis and am currently on my third antibiotic…Leviflaxen. I’ve have the “ urgency to pee” 24/7 and have had to cancel pretty much everything on my calendar for the past two weeks and am up and down all night long. Has anyone else had experience with this type of UTI after surgery? Seems like I should’ve been put on some type of antibiotic for this just prior to surgery to prevent this from happening.
bile salts needed? bile is needed for digestive system to work--if low on it, there is taurine and enzymes with ox bile. see dr Berg on you tube. (liver specialist).
I had rectocele repair surgery 6 weeks ago for UTI issues due to my bladder not being able to completely empty. Three weeks after surgery I got a UTI and haven’t been able to get rid of it…have taken Cephlex, Flagyl and Leviflaxen, still have symptom…vey difficult to sleep at night with burning and pee urgency. It gets worse starting early afternoon and I am constantly making trip to the bathroom. I also ache and have to use a heating pad starting in the afternoon. I am starting to wonder if something is amiss with the surgery but the urogynecologist who did my surgery seems to have washed her hands of me…she did ask me to come back in a week after being off antibiotics to get another urine sample. In the meantime I have an appt with a Urolgy PA next week. I am scared I have some type of chronic issue now!
Have you had a pancreatic enzyme insufficiency PEI done?
I have not yet, Susan. I did just get a MRCP which is an MRI of my pancreas and other organs. I haven't heard back from the doctor yet however they did find some issues. I also had two x-rays and I'm having a Stool analysis done. I'll keep you updated. Thanks for checking in on me. I really appreciate it.
Please let us know the results of your fecal elastase test. That is what doctors use to diagnose EPI, which I suspect you have.
Thank you for mentioning this…I thought the same as well, but hesitated to say anything. As someone with severe EPI I have been told that this is rare, However I suspect that many have been misdiagnosed with IBS-D as I was for 30 years.
EPI is no joke and the medication is very costly.
Anyone that has the symptoms mentioned above should request testing for EPI, it could save them years of suffering. There is hope with medication and working with registered dietitian with experience concerning EPI.