Thanks for your reply and concern. I had been aware of FND prior to my diagnosis and on many levels, it did sound like the closest "explanation" for the vastness of my symptoms. So yes, during the past 6-8 months I have posted many times on FND Hope and I've read quite a bit on neurosymptoms.org. These are the 2 most reputable sites relative to FND.
I had a c6 c7 fusion to alleviate spinal cord compression (on imaging) which they thought was casuing my symptoms. In hindsight, I'm not sure it was. I've learned that it isn't rare for people to have spinal surgeries, only to find out their neuro issues aren't due to structural issues. Sad.
And regarding physiotherapy, I am / was a high level athlete (hockey) who still stays very active/strong(..as much as I can with what I've been through). I dont say this in a snarky manner, but I think it's safe to say that my own routines would trump any sort of physiotherapy I would be prescribed. My Dr's have echoed that sentiment so they have directed me more towards the psychiatry/psychology routes. As mentioned, I have my own spiritual/meditative practice which I have leaned on, but from a physical symptom standpoint, to not much avail.