Hi
Has anyone had sacral nerve stimulation to help deal with slow transit constipation? If so did it work / does it help to produce ‘normal’ BMs?
Hi
Has anyone had sacral nerve stimulation to help deal with slow transit constipation? If so did it work / does it help to produce ‘normal’ BMs?
It’s very hard to deal with
I always wonder if pelvic exercises would help
We are lucky to get a diagnosis to be honest
I had the surgery 2 years ago but my surgeon warned me it might not help so I had ace malone surgery first and sns a year later. In my case sns would not have worked without the ace malone surgery.
HI Amanda how long did it take to work properly and where did you have it done
It took about a year for things to settle down and establish a routine that worked for me. However, I'm still getting problems 4 years after the ops. I'm in Ireland and had the ops at Cork University Hospital.
I’m in Dublin did you have to get gastro to diagnose you first or how did you go about it
I was with my gastro for 4 years before he sent me to a surgeon. I was given every new drug available, everytime he went to a conference he came back with something new. It became obvious I needed surgery when I had 6 hospital admissions in 10 months, my longest stay being 5 weeks, where I was experiment on, I was basically a guinea pig for them. At that point my gastro could see that I had had enough and he could do no more. Initially I was angry that I had been left to suffer for 4 years and not been given surgery earlier but I now realise it was a last resort because it completely changes your life as regards work, travel, socialising etc.
Interesting topic. I have had slow transit constipation since infancy. I also had Spina bifida at birth. That is when you have a slight whole at the base of your spine at birth. It needs to finish closing. I found out today that can severe pain with any pressure. Constipation is a real culprit for increased pain. I HAVE PAIN!