https://www.sapiens.org/body/chronic...ase-treatment/

This can easily be seen to be pertinent to many of us with SPS or MS> I sure can relate to his experience of self and of docs.

I learned , painfully, to ditch docs like these right off the bat. My most recent was the doc at Mayo and his staff who implied perhaps stress caused my symptoms.

Skim through the info on Lyme to get the personal experience of the writer. The similarities of experience in patients with SPS are striking.