Before I write I want to say I respect this forum and hope I am not out of question, I dont trust the neurologists I see because I know they wont even think of saying Lyme in the early stage. I have been through hell with lyme treatment two years,
I had an EMG because I'm left with calf twitching over 9 months.. the EMG NCS study showed mild polyneurapthy with axonal and demyelinating features one leg worse. I have no weakness but twitching and muscle loss. Lyme doctor says maybe Mononueritis Multiplex and the other says just mild that can be reversed. She wants me to continue treating lyme, both doctors got very angry when I brought up my concerns.
I have a dear friend who had twicthing long time before ALS , I would just like to know if anyone had this early on. I am in the middle of the LYME drama and I am going nuts.
god bless you
I had an EMG because I'm left with calf twitching over 9 months.. the EMG NCS study showed mild polyneurapthy with axonal and demyelinating features one leg worse. I have no weakness but twitching and muscle loss. Lyme doctor says maybe Mononueritis Multiplex and the other says just mild that can be reversed. She wants me to continue treating lyme, both doctors got very angry when I brought up my concerns.
I have a dear friend who had twicthing long time before ALS , I would just like to know if anyone had this early on. I am in the middle of the LYME drama and I am going nuts.
god bless you