The reason I first decided to write and share my Mal de Debarquement Syndrome experience was because I was curious about how other people’s symptoms changed over time. I figured other people with MdDS might be interested in that same thing. It is hard not knowing what to expect. My post about my symptoms andContinue reading “Land, Ho?”
Here are some things that seem to help me, listed in order of helpfulness, from somewhat helpful to definitely helpful. (Please note that I am not a doctor and these are not recommendations. However, I do hope readers can find something on this list that could help them, too! I am so grateful to theContinue reading “Staying Afloat: Things That Help”
Mal de Debarquement Syndrome is truly an invisible illness. If you didn’t know me well, you wouldn’t know anything was wrong with me. My symptoms are all in my brain, so they aren’t outwardly noticeable. In the past 4 months, I’ve recovered enough that I can do most of my usual daily activities. It isContinue reading “Landlubber: My Symptoms”
The vacation where it all began.
What does it feel like to have Mal de Debarquement Syndrome?