Cardiologist tried to pitch Lyme disease based on inconclusive tests and worried about whether I should see someone new

Honestly, from someone who went with a gp who was probably a little too open-minded, it didn’t go great.

Turns out I just have POTS. Have probably always just had POTS. My POTS is idiopathic. But I’m otherwise healthy.

When I caught a virus (most likely mono) early last year and started having significant issues that were worse than my normal, I sought help from the first source I could get. (At that point, the pandemic had just started so it was hard to find an appointment.)

The gp i went to immediately realised I had POTS and was determined to find the reason. She was convinced there HAD to be one. And I was very appreciative of that determination.

But,

/r/dysautonomia Thread