Plantars Fasciitis Anyone?

Dr. Google has once more helped me slay a demon. The onset of weak painful joints was just one of the gifts at the time of my living with no diagnosis.

Life is now regulated with Neurontin, Flexaril, Cymbalta and THC. But these ankles are weak and these heels hurt so bad some evenings that I fantasize calling the Texas Chainsaw Massacre tool of terror and beg him to chop my feet off above the ankle. Painful!

Out of the air… “heel spurs”. I google and BOOM: Plantars Fasciitis. PERFECT! I have narrowed down something. It has a name. A treatment. A destiny. I sigh.

My next Dr appointment is 3/12, so I’ll go on til then and print out some wikipedia to take along. Sure, they tend to scoff and show their pride when I do this, but my instincts about my dwelling have always been more accurate and timely than their suppositions from memories past.

Anyone else have PF with Lyme? Anyone else heard 70% of Lymies get Fibromyalgia? Think that’s a confused statistic that they don’t have enough information to be claiming at this time.

Have a super weekend!