Minimal Pain, but CRS recommends LIS

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Minimal Pain, but CRS recommends LIS

Postby vdb324 » 18 Feb 2014, 22:18

Hi all,

I am a bit torn about what to do about my LIS surgery at the beginning of March. I have tried two rounds of Botox, as well as more conservative treatments like nifedipine lidocaine. The CRS says things haven't improved. I had a setback after some recovery on the second round. And, it was really noticeable when I went in for my appointment, and the CRS applied some light pressure to see if it caused me pain, and it most definitely did.

However, since my last appointment about a month ago, I haven't had very much pain. There is still some light bleeding, but not very often.

The CRS highly recommend surgery seeing the first two rounds of Botox didn't work. Should I go ahead with my surgery, or should I wait a little to see if I continue without pain? My concerns with the surgery are the risks, but at the same time, there are risks to leaving a fissure - like fistulas and other issues.

Could a fissure get well on its own after not responding to Botox and conservative treatments, or am I just delaying the inevitable?

EDIT: As a side note, it has been over a year. My pain seems to come and go, but overall, it was a lot worse last year.
My last round of botox was in December.
Feb. 2013 - Developed AF
July 2013 - Diagnosed AF;nifidepine lidocaine treatment
Oct. 2013 - 1st round of Botox & skin tag removal
Dec. 2013 - 2nd Botox
March 2014 - Spinchterotomy
June 2015 - Diagnosed with Pelvic Floor Dysfunction/Vulvodynia
vdb324
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Re: Minimal Pain, but CRS recommends LIS

Postby owmybum » 19 Feb 2014, 13:22

I would trust in your surgeon. You are probably feeling less pain because you still have the full effects of the Botox at the moment. If you have doubts though, you could just put it off for another couple of months and see how you go?

OMB x
fissure after hem banding and tag removal feb 11
Pelvic floor therapy
Diltiazem
Botox June 13
Nitro
Internal flap July 14
EUA and polyps removed Nov 14
Diagnosed with neuropathy Jan 15
Diagnosed with HS EDS type 3 (causes poor wound healing )
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Re: Minimal Pain, but CRS recommends LIS

Postby vdb324 » 19 Feb 2014, 17:43

Thanks, OMB. I've asked the advice of loved ones, and my mother told me to delay, but my husband said to go ahead. Seeing he's been around me most during this, I think he notices how much it was/is affecting me. Chances are, I'll just go ahead and get it done. I did notice some slight pain today, but again, nothing that's that noticeable. I think part of it is that we live with the pain so long, and at some times the pain is so bad, that when it isn't terrible, we don't really react to it.

It's been over a year. That's long enough. I've gone up and down on recovery/pain that I don't really trust the weeks where I feel okay as an indicator that I am healing. Three good weeks, and like two bad days, and I had a terrible setback after Botox.
Feb. 2013 - Developed AF
July 2013 - Diagnosed AF;nifidepine lidocaine treatment
Oct. 2013 - 1st round of Botox & skin tag removal
Dec. 2013 - 2nd Botox
March 2014 - Spinchterotomy
June 2015 - Diagnosed with Pelvic Floor Dysfunction/Vulvodynia
vdb324
Proctosphincteranalogist
 
Posts: 281
Topics: 52
Joined: 05 Oct 2013, 22:07
Has thanked: 2 times
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