What is recovery from cryablation like?
Posted: Thu Dec 05, 2024 5:55 pm
Hi all,
When I was first diagnosed I spent a lot of time on this website. Thank you for creating it! It has been helpful to me.
I have cryoablation of the PN scheduled for tomorrow. My question is, how has recovery been for anyone else? Is it painful? Has it been successful for anyone else? I couldn't find any posts discussing this.
I have had PN for 5-6 years now and it continues to get worse and more entrenched. My first 2 sets nerve blocks gave some temporary relief. Since then I have had maybe 10 RFAs and sometimes they worked and the disorder went away for a while but for the last 2+ years they haven't done much so we agreed this is the next step. My PN affects the penis and scrotum but not the anus. I have heard incontinence is an issue.
I am almost resigned that this PN will never go away. What is scary is that it keeps getting worse and my world is becoming even smaller and more painful.
Ross
When I was first diagnosed I spent a lot of time on this website. Thank you for creating it! It has been helpful to me.
I have cryoablation of the PN scheduled for tomorrow. My question is, how has recovery been for anyone else? Is it painful? Has it been successful for anyone else? I couldn't find any posts discussing this.
I have had PN for 5-6 years now and it continues to get worse and more entrenched. My first 2 sets nerve blocks gave some temporary relief. Since then I have had maybe 10 RFAs and sometimes they worked and the disorder went away for a while but for the last 2+ years they haven't done much so we agreed this is the next step. My PN affects the penis and scrotum but not the anus. I have heard incontinence is an issue.
I am almost resigned that this PN will never go away. What is scary is that it keeps getting worse and my world is becoming even smaller and more painful.
Ross