What a long, strange trip it's been. First let me say thanks to those of you who have been so supportive. It's made a HUGE difference.
I'm a week post-op and I can already happily say "why didn't I do this sooner". I'm just now starting to realize how much my fissures were having a negative impact on my quality of life. The anxiety and mild depression are just now becoming clear to me. Why did I put up with these fissures for years?
So what about the LIS experience? Well the surgery itself went well. My pain meds (I didn't use much) made me slightly constipated. That sucked. I got a thrombosed hemmy the day after surgery. That REALLY, REALLY sucked. Had to revisit the CRS after 5 days to have it excised. The pain from the hemmy was 5x worse than the pain from LIS recovery. My CRS said sometimes the hemmies just happen after surgery down there (but not too often). Lucky me. My first and all BM's after LIS were MUCH less painful (even being slightly constipated and having the thrombosed hemmy) than the weeks leading up to surgery. My pre-op BM's were a 6-8 on the pain scale (1-10) and now they are a 1-2. I'm having no problem "leaking" or with gas issues. Not to say I won't but I haven't yet.
My advice for those of you thinking about LIS:
1. If your fissure is chronic and really painful...do it sooner rather than later.
2. Find a CRS with a lot of experience. Shop around until you find somebody you feel good about. Not a general surgeon, a CRS.
3. Avoid pain meds if at all possible. Stick with OTC stuff if you can take it.
4. Keep your post-op diet really healthy, drink lots of water, and take the stool softener that works for you.
5. Don't be in too much of a hurry to get back to work/life. Let your body heal. But do move around some...blood flow is good.
6. Share your experience here. It's cheaper than therapy and can help others.
So that's my story. But don't worry, I'll be around to share my next few weeks and help those dealing with their own PITA!