The MdDS Foundation is an all-volunteer 501(c)(3) organization that seeks to promote awareness of, and to support bio-medical research into a cause, treatment, and a cure for MdDS. In addition, the Foundation assists medical professionals and patients suffering with MdDS through its website, which contains a list of related bio-medical research, and social media based support groups. Mal de Debarquement syndrome (MdDS) or disembarkment syndrome is a rare disorder of perceived motion that most often develops after a motion event including, but not limited to. ocean cruises, plane, train, automobile or other type of travel.
Although there are more cases reported in females, there are many men diagnosed with MdDS. MdDS symptoms include persistent and long-lasting sensations of motion (rocking, swaying, or bobbing); this perceived motion is associated with fatigue, imbalance, and impaired cognitive function. MdDS is frequently misdiagnosed or goes undiagnosed because many in the health care community are unaware. Unfortunately, effective MdDS treatments/therapies are lacking and the cause of MdDS remains unknown.
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Patient Worthy Posts on MdDS
According to a story from abc.net.au, an unusual and poorly known rare disease has been making its presence known in the country of Australia. This
A team of great researchers need your help! While the researchers who devised this survey (see below for the link) have had a great response
Kimberly Warner Kimberly Warner was diagnosed with mal de débarquement syndrome (MdDS) after enduring a traumatic biking accident in May of 2014. The accident caused