Guest guest Posted February 21, 2008 Report Share Posted February 21, 2008 --Hila, Welcome! I would say, even if you do nerve blocks, give PT a really good try. I never did bio-feedback - you need to see someone who does skin rolling and trigger point release. I had to go weekly for 8 months before I was able to have intercourse again, and I was doing a lot of work at home in between appointments too! So don't give up on it yet. You will learn a lot here! Melinda Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 25, 2008 Report Share Posted February 25, 2008 Hila, welcome to the group. I've had two rounds of Pudendal Nerve blocks and most recently a Caudal Epidural. I have Pudendal Neuralgia, IC, & v.pain. I can tell the blocks have reduced inflammation for me, though they've not helped completely (the worst for me right now is the pain with sitting). If you will go to the home page of the group, you can use the search box and find really good info from past posts. Some of the ladies in CA are finding good help from a couple of PT's ....here is the link to their site: http://www.pelvicpainrehab.com You could contact them and ask if there is a PT closer to you that might could help you. Hugs, Chelle Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 25, 2008 Report Share Posted February 25, 2008 Hila, welcome to the group. I've had two rounds of Pudendal Nerve blocks and most recently a Caudal Epidural. I have Pudendal Neuralgia, IC, & v.pain. I can tell the blocks have reduced inflammation for me, though they've not helped completely (the worst for me right now is the pain with sitting). If you will go to the home page of the group, you can use the search box and find really good info from past posts. Some of the ladies in CA are finding good help from a couple of PT's ....here is the link to their site: http://www.pelvicpainrehab.com You could contact them and ask if there is a PT closer to you that might could help you. Hugs, Chelle Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 25, 2008 Report Share Posted February 25, 2008 Hila, welcome to the group. I've had two rounds of Pudendal Nerve blocks and most recently a Caudal Epidural. I have Pudendal Neuralgia, IC, & v.pain. I can tell the blocks have reduced inflammation for me, though they've not helped completely (the worst for me right now is the pain with sitting). If you will go to the home page of the group, you can use the search box and find really good info from past posts. Some of the ladies in CA are finding good help from a couple of PT's ....here is the link to their site: http://www.pelvicpainrehab.com You could contact them and ask if there is a PT closer to you that might could help you. Hugs, Chelle Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 25, 2008 Report Share Posted February 25, 2008 Hila, welcome to the group. I've had two rounds of Pudendal Nerve blocks and most recently a Caudal Epidural. I have Pudendal Neuralgia, IC, & v.pain. I can tell the blocks have reduced inflammation for me, though they've not helped completely (the worst for me right now is the pain with sitting). If you will go to the home page of the group, you can use the search box and find really good info from past posts. Some of the ladies in CA are finding good help from a couple of PT's ....here is the link to their site: http://www.pelvicpainrehab.com You could contact them and ask if there is a PT closer to you that might could help you. Hugs, Chelle Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 25, 2008 Report Share Posted February 25, 2008 Hila, welcome to the group. I've had two rounds of Pudendal Nerve blocks and most recently a Caudal Epidural. I have Pudendal Neuralgia, IC, & v.pain. I can tell the blocks have reduced inflammation for me, though they've not helped completely (the worst for me right now is the pain with sitting). If you will go to the home page of the group, you can use the search box and find really good info from past posts. Some of the ladies in CA are finding good help from a couple of PT's ....here is the link to their site: http://www.pelvicpainrehab.com You could contact them and ask if there is a PT closer to you that might could help you. Hugs, Chelle Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 25, 2008 Report Share Posted February 25, 2008 Hila, welcome to the group. I've had two rounds of Pudendal Nerve blocks and most recently a Caudal Epidural. I have Pudendal Neuralgia, IC, & v.pain. I can tell the blocks have reduced inflammation for me, though they've not helped completely (the worst for me right now is the pain with sitting). If you will go to the home page of the group, you can use the search box and find really good info from past posts. Some of the ladies in CA are finding good help from a couple of PT's ....here is the link to their site: http://www.pelvicpainrehab.com You could contact them and ask if there is a PT closer to you that might could help you. Hugs, Chelle Quote Link to comment Share on other sites More sharing options...
Recommended Posts
Join the conversation
You are posting as a guest. If you have an account, sign in now to post with your account.
Note: Your post will require moderator approval before it will be visible.