If you have had testing indicating that your Meniere's is of the Autoimmune origin, you should definitely give Low Dose Natrexone a try. It's helped me a ton! ldndirect.com
Definitely want to put a pin in this for investigation. I think what would be most helpful (and we should really have separate posts dedicated to this): Can we assemble a list of markers that could indicate for someone that their Meniere's is of an auto-immune origin?
Would be very interesting! In my case, the doctors say it might be something autoimmune , but no tests. Greetings from Bremen Lilja
Looking into an integrative medicine specialist as the next step on my journey. One of the therapies they offer is Low Dose Naltrexone. Are you still finding favorable results with it? If so, any effect on fullness, pressure, hearing loss, or progression of your MD? Can you share anything about the dosing/protocol you used. Very interested.