This is a time-sensitive announcement. The 2018 Giving Season launches on November 27 with two matching challenges. Challenge #1: $7 Million Match on Facebook Starting at 5am PST/8am EST donations to nonprofits on Facebook, like the MdDS Foundation, will be matched until $7 million in Facebook matching funds are dispersed. Just donate through our special Matching […]
Mal de Débarquement Syndrome (MdDS).is a neurological disorder that leaves patients feeling as if they are rocking and swaying. Imagine always feeling in motion.
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Living with MdDS
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The Faces of MdDS
Picture Perfect
I believe that pictures are the most beautiful things that exist. You are capturing a moment in time that lasts forever. Everything stops for that moment and is still. Little did I know that this picture would be my last ‘still’ moment. I wanted to capture the moment of the wanderlust girl I am, well […]
The Facts of MdDS
It is typically triggered by motion: cars, trains, airplanes, ships, boats, and even fast elevators.
The average person sees 20+ doctors before getting a diagnosis.
Many people are suffering from MdDS and don’t know that they have it. They are undiagnosed.
The scale of the problem is not matched by research dollars.
The MdDS phenomenon is the natural result of the human brain adapting to environmental motion and is thus the quintessential neurological disorder.
Yoon-Hee Cha, MD
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Make the Matches 🙌 Announcing Two Matching Challenges!
Rare Diseases Are Not Rare!
This is a test of the MdDS broadcasting system. 1 in 10 Americans has a rare disease or disorder. Globally, the figure is 350 million. Rare diseases are not rare! Here are a few submissions by MdDS warriors to the National Center for Advancing Translational Sciences (NCATS) “Rare Diseases Are Not Rare!” competition, which challenged individuals […]