I've had severe GI problems for the past 20 months. I've seen several conventional GI doctors aand they're useless--tests that don't yield a diagnosis and prescriptions that only make symptoms worse.
An LLMD thought I may have Bell's Palsy of the Gut. She prescribed bicillin injections because my stomach can't handle oral meds. But I had no improvement at all from 3x/week injections for 4 months. She said GI doctors can't help because they don't acknowledge the existence of Bell's Palsy of the Gut.
Maybe if I could find a Lyme-literate GI doctor, they could figure it out. At least they wouldn't be antagonistic to the idea that I might have Bell's Palsy of the Gut.
If I could get this problem solved, then maybe I could handle the Mepron or Malarone needed for the babesia that was diagnosed almost a year ago. I haven't been able to take either med because they severely worsen the GI problem.