After my third cruise, I never got my land legs back. I saw my family doctor and explained my symptoms to him and he referred me to two neurologists; one said it was an ongoing migraine and the other said vertigo.
As a result of the challenges in learning about and adjusting to life with MdDS, Roger and I began a crusade to increase awareness about the disorder.
WARNING: this is a long post. If you have MdDS and are bothered by scrolling, we recommend printing to read offline. To print Mickie’s story, press Command+P on a Mac or Control+P on a PC. Then don’t forget to share it! Rocking and Swaying After a Cruise My name is Mickie Agee and I live in Nashville, […]