I wrote the MdDS organization and got a brochure to share with my PCP and ENT doctor.

Thanks for this very helpful info, Holley. After reading, it seems that my symptoms more closely match MdDS rather than vertigo. I’ve sent the link to my doctor and will follow through with her. 💚

Yes, and when I’m on a bike. I guess in those situations I am somehow oriented in space. It’s wonderful to have that.

Kuna Yala is a functioning matriarchal society ❤️

I don’t think I have MdDS, but I do have full time vertigo, seemingly caused by ear damage. For me it’s like walking on a swaying boat while carrying a 20 pound sack of potatoes.