I saw my neuro this morning and explained about the pelvic pain and the external feeling in the nether region.

My neuro believes it's the MS, sensory in nature.....geez, at least I no longer feel like I'm crazy. He said since I have spinal lesions it's not uncommon to have pelvic pain due to those lesions. He said what they like to see with MS patients are other things ruled out, which I had, then the comfort level is there to say yes it's the MS.

We talked about different meds that might help and the decision was made for me to go back on Cymbalta.....it's the only one that won't add to my fatigue.

I told him my PCP wanted me on an AD for depression and I told him no, I'm not depressed. My neuro smiled and said he would mention in his report to my PCP that the Cymbalta is to help with nerve pain and not depression

I don't like being told I'm depressed when I'm not.....been there, know how it feels and ask for help when I need an AD.

Now I'm just waiting to hear from my sister. She sees the neuro for the first time today.