u/SpecialMaple

What was your process for identifying what triggered your Menieres? How long after coming into contact with your triggers would you have an episode?
I was diagnosed with Menieres Cochlear Hydrops last year, started on diuretics and had steroid injection in my affected ear. For about a year I didn’t have any more symptoms or significant changes in hearing. Now, I can’t seem to feel normal again no matter what I do and I’m not sure what is triggering it.
I just joined Reddit and I have found it helpful reading about everyone’s individual experiences. So, what was your experience in figuring out what worked for you?