Certainly! It’s the same in the Lyme & Co-infection communities. Except we are used to being treated as second class patients, it’s all in our heads, tests and treatments not reimbursable or don’t work, misinformation and cover-ups, research to benefit the shareholders, and so on.

Sorry, probably not the place to share. I hear you sister. This whole thing is a drag. I hope you get through without more troubles.

❤️