As the time goes on...
As the time goes on, I continue to have procedures, try new medications, and participate in pelvic floor therapy (which has now totaled several years) I have not made much progress, the insurance is not wanting to approve any more sessions. I do participate in Myofascial release which is a type of massage technique used to break up the scar tissue in the fascia. This is in hopes of helping my Cerebral Spinal Fluid to continue to flow without obstruction throughout my spine and to my brain. I have monthly membership at a local massage place. Not many masseuse are trained in this technique, I am very lucky I have found one close to my home. I continue to be wheelchair bound when going outside of the home shopping etc. The spasms from the Pudendal nerve and injury to my spine is much to great to withstand walking/standing for longer than just a couple minutes. My Dr has ordered an electric scooter for me, although I have not yet received it. I was recently able to take a trip to