Mal de Débarquement, Disembarkment or Debarkation Syndrome is a disorder that leaves patients with a constant feeling of movement, as if on a boat. The MdDS Foundation advocates for and seeks treatments to end the suffering from MdDS. Learn more!| MdDS Foundation
Get our educational brochure in English, German, French and Spanish. Easy to download, print and share! Find them & more resources here.| MdDS Foundation
Tracking may reveal patterns that enable you to adjust your management tactics, take control of your MdDS, and maybe even achieve remission.| MdDS Foundation
This story from an older male is unusual. Bill writes about the feeling of constant movement in the "rather weird world" we live in and offers a message of hope. The post MdDS Insights from a Male Senior Citizen appeared first on MdDS Foundation.| MdDS Foundation
My name is Lynn. I'm sharing my story to help others, and let them know… You are not alone. And there is hope!| MdDS Foundation
Cayman Charter Boat—>Motion Sickness Forever| MdDS Foundation
Presently, there are no tests that can provide a definitive diagnosis of MdDS. However, your doctor will probably want to rule out other disorders that may have similar symptoms. MdDS is primarily diagnosed using patient history (such as a recent boat, air or train travel or other motion experience) and the elimination of other disorders which may have similar symptoms.| MdDS Foundation
Like any chronic disorder, living with MdDS can be a daily challenge. The best advice for managing persistent symptoms? Reduce stress, be well rested and pay attention to symptom triggers. MdDS Foundation is here to help!| MdDS Foundation
MdDS is a neurological disorder that leaves patients feeling as if they are rocking and swaying, constantly moving. The MdDS Foundation can help! Learn how.| MdDS Foundation
Award aims to recognize the importance of good clinical research and encourage early career investigators in clinical studies in MdDS| MdDS Foundation
This poem expresses both the disorientation and emotional toll of MdDS and the strength, resilience, and grace required to navigate it.| MdDS Foundation
Win your very own zebra to take everywhere you go. Snap photos. And tell everyone your MdDS Zebra Tale. Learn how!| MdDS Foundation
Remarkably simple to use and available as a book mark. 🖨️ Or download and print to start using today. Bridge the communication gap between doctors and patients! The post NEW Severity Scale Simplifies MdDS Symptom Tracking appeared first on MdDS Foundation.| MdDS Foundation
The MdDS Foundation is proud to have a distinguished group of volunteers dedicated to supporting the MdDS Patient Registry. In the coming weeks, we'll be highlighting other members and the important work they do. The post Advisory Board Member Spotlight: Dr. Jennifer Stoskus, PT appeared first on MdDS Foundation.| MdDS Foundation
It’s silly, but sometimes it's a bit of comic relief that pulls me from despair. My superpower is a special ability, and why I feel the way I do. The post Disability or Superpower? appeared first on MdDS Foundation.| MdDS Foundation
Summit Recap: Over the course of the three-day event, I met many other Patient Advocacy Organizations with shared challenges and successes. The post Part 2: The 2024 Breakthrough Summit, Tote & PAOs appeared first on MdDS Foundation.| MdDS Foundation
"I hope to help people understand how debilitating MdDS is and how frustrating it is to look fine on the outside but silently suffer." ~Dawn #thestruggleisreal| MdDS Foundation
MdDS is a disorder that leaves patients feeling as if they are rocking and bobbing, as if on a boat. Learn more about the syndrome's symptoms and diagnosis.| MdDS Foundation
