1 month after surgery
Posted: Thu Dec 13, 2018 5:16 pm
In July 2018 I posted on here asking the question surgery or no surgery?
Well I decided to go and get tested with Dr Bautrant in France
As even though I was being treated for PNE I had never been tested and everything I was trying was just making me worse.
So I went in August and I had the Doppler test and Dr Bautrant assessed me and you could definitely see on the test results that I had pudendal nerve entrapment on the left.
He said if nothing has give you any relief then the only thing left is surgery. Even though my pain specialist here had me booked in for the caudal effect epidural because the ganglion blocks and pudendal vaginal nerve block left me in agony for weeks after and gave me no relief whatsoever!!!!
Dr Bautrant was really nice and spoke excellent English and he doesn't have the usual god like complex. So I booked in for the 9th November and I must say I was scared to death even though I am a tough cookie but my husband actually made me realise could I get any worse.
Not being dramatic but when I was being put to sleep I did have a moment when I thought I hope I don't wake up because I didn't know what pain I would be in when I woke up as anyone with this will know that feeling.
I had the trans ischio rectal approach which isn't as bad as the decompression surgery as it's more about freeing the nerve. What should have been an hour surgery took just under 2 hours, he said once he had freed the nerve he cleaned up all the tissues around it as well.
Had it done on the Friday afternoon, Saturday morning they took the catheter out and had me walking small paces to the bathroom etc. Then on the Sunday morning they took the drain out and I was doing well and had the only medicine I had been on was paracetamol on the Saturday and Sunday so I asked could I go home a day earlier as I was feeling like I would be more comfortable back at the hotel so they let me out a day early.
I had to stay a week in France and had to go back to get checked over by Dr Bautrant make sure I had no infection. It was nice to recuperate at the hotel and I went for a few strolls around the hotel courtyard and around the street as the doctor told me to do that.
It really wasn't as bad as I thought it was going to be and the flight home wasn't either although I did double up on the lycra and we booked the back aisle seat and I was able to stand up when I needed to and a cheeky vodka helped as well.
I have been home 3 weeks and I am still taking it easy but pottering round the house and walking around the block a couple of times a day and I am trying to sit down for really short periods.
I know it is early days yet but I can now stand up straight which I couldn't for the last 12 months without stooping in pain especially stood in one spot. I can also lie in bed with my legs straight because I got to a point where I could only lie with my left leg bent and a cushion underneath it. I also don't have to lie on a special memory foam mattress anymore either.
He said I should be back at work in 6 Weeks and hopefully back to normal in 4 to 6 months but I know everyone us different and I am not going to put too much pressure on myself.
I am just so glad I went because no amount of physio or injections could have fixed the entrapment I had. So I am not coming on here to post a success story YET but hopefully I will be soon. I would just advise people to find out if you have got it because for years I was unsure and didn't know if the doctors and physio here were making me worse because I am usually fit and healthy. I went from walking 6 miles a day and working lots of hours to working part-time and then coming home lying in bed having no life. I am not one to come on forums but i just hope that my story will help someone else to get answers especially anyone suffering in the UK. If it helps just one person because sometimes you just need answers and I felt like I had to prove to my family and husband that I haven't been a hypochondriac for the last 2 years. It doesn't sound a long time but trust me I felt like I had it forever.
If anyone would like any information about what I had done I will help in anyway I can.
Well I decided to go and get tested with Dr Bautrant in France
As even though I was being treated for PNE I had never been tested and everything I was trying was just making me worse.
So I went in August and I had the Doppler test and Dr Bautrant assessed me and you could definitely see on the test results that I had pudendal nerve entrapment on the left.
He said if nothing has give you any relief then the only thing left is surgery. Even though my pain specialist here had me booked in for the caudal effect epidural because the ganglion blocks and pudendal vaginal nerve block left me in agony for weeks after and gave me no relief whatsoever!!!!
Dr Bautrant was really nice and spoke excellent English and he doesn't have the usual god like complex. So I booked in for the 9th November and I must say I was scared to death even though I am a tough cookie but my husband actually made me realise could I get any worse.
Not being dramatic but when I was being put to sleep I did have a moment when I thought I hope I don't wake up because I didn't know what pain I would be in when I woke up as anyone with this will know that feeling.
I had the trans ischio rectal approach which isn't as bad as the decompression surgery as it's more about freeing the nerve. What should have been an hour surgery took just under 2 hours, he said once he had freed the nerve he cleaned up all the tissues around it as well.
Had it done on the Friday afternoon, Saturday morning they took the catheter out and had me walking small paces to the bathroom etc. Then on the Sunday morning they took the drain out and I was doing well and had the only medicine I had been on was paracetamol on the Saturday and Sunday so I asked could I go home a day earlier as I was feeling like I would be more comfortable back at the hotel so they let me out a day early.
I had to stay a week in France and had to go back to get checked over by Dr Bautrant make sure I had no infection. It was nice to recuperate at the hotel and I went for a few strolls around the hotel courtyard and around the street as the doctor told me to do that.
It really wasn't as bad as I thought it was going to be and the flight home wasn't either although I did double up on the lycra and we booked the back aisle seat and I was able to stand up when I needed to and a cheeky vodka helped as well.
I have been home 3 weeks and I am still taking it easy but pottering round the house and walking around the block a couple of times a day and I am trying to sit down for really short periods.
I know it is early days yet but I can now stand up straight which I couldn't for the last 12 months without stooping in pain especially stood in one spot. I can also lie in bed with my legs straight because I got to a point where I could only lie with my left leg bent and a cushion underneath it. I also don't have to lie on a special memory foam mattress anymore either.
He said I should be back at work in 6 Weeks and hopefully back to normal in 4 to 6 months but I know everyone us different and I am not going to put too much pressure on myself.
I am just so glad I went because no amount of physio or injections could have fixed the entrapment I had. So I am not coming on here to post a success story YET but hopefully I will be soon. I would just advise people to find out if you have got it because for years I was unsure and didn't know if the doctors and physio here were making me worse because I am usually fit and healthy. I went from walking 6 miles a day and working lots of hours to working part-time and then coming home lying in bed having no life. I am not one to come on forums but i just hope that my story will help someone else to get answers especially anyone suffering in the UK. If it helps just one person because sometimes you just need answers and I felt like I had to prove to my family and husband that I haven't been a hypochondriac for the last 2 years. It doesn't sound a long time but trust me I felt like I had it forever.
If anyone would like any information about what I had done I will help in anyway I can.