Over the last four years I’ve been up and down on whether or not I had developed MS.  Back in 2014 when my feet got tingly and went numb we suspected MS but then it turned out to probably be antibiotic induced peripheral neuropathy.  In 2015 when we ran an extensive autoimmune panel and found I had myelin antibodies plus some new weird neurological symptoms we went back and did an MRI and, no sign of MS.  I thought I’d put it to rest when in 2017 I started getting burning pain in my lower left leg.  At first it was sporadic and chiropractic seemed to help so I thought it was structural.   By the start of 2018 the pain was daily and interfering more with life.  My ND at the time thought it was compression related so back to running an MRI to see what was going on with my discs.

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