I have had EM for 8 1/2 yrs. Burning feet almost sent me over the edge. Tried everything imaginable and a year ago last July I had a neuro-stimulator implanted in my back with a probe running along my spine. It has been a God-send. It masks the pain and I encourage you all to discuss it with your pain doctors. I have a Medtronic stimulator but St Jude makes one and I am sure there are others out there. Good luck to you all. PATTY
Dear Patty, how wonderful that after more than 8 years you have finally found what works for you, Your courage is inspirational and your share brings hope to us all. Personally, i know little of said methods use in EM. I would very much like to hear more of your journey. More and more it is clear that EM 'ers must never give up fighting for a diagnosis or the chance to trial/test the vast array of medications, and treatment options out there. I hope 2014 continues to be a happy and healthy one for you.
God bless
mads x