he MdDS Foundation promotes education and research on Mal de Débarquement Syndrome (MdDS), a chronic neurological disorder causing sensations of rocking and swaying. We advocate for and seek treatments to end suffering caused by MdDS.
Mission goals
provide support and education for patients and families of those with MdDS
facilitate clinical studies designed to improve the diagnosis and treatment of MdDS
promote basic and clinical research to better understand the cause of this unique syndrome
collect, collate, and distribute demographic and other information from those with MdDS to further knowledge of the condition
update professionals who provide medical care and treatment of MdDS patients
The MdDS Foundation is an all-volunteer 501(c)(3) nonprofit foundation. The Foundation promotes international awareness of Mal de Débarquement Syndrome (MdDS), while advocating for those living with MdDS, seeking treatments and a cure for people suffering from this rare neurological disorder.
With this Patient Insights Network (PIN), we seek to establish consistent patient information to provide more accurate data to medical professionals and researchers.
he MdDS Foundation promotes education and research on Mal de Débarquement Syndrome (MdDS), a chronic neurological disorder causing sensations of rocking and swaying. We advocate for and seek treatments to end suffering caused by MdDS.
Mission goals
provide support and education for patients and families of those with MdDS
facilitate clinical studies designed to improve the diagnosis and treatment of MdDS
promote basic and clinical research to better understand the cause of this unique syndrome
collect, collate, and distribute demographic and other information from those with MdDS to further knowledge of the condition
update professionals who provide medical care and treatment of MdDS patients