June 1, 2022 – In collaboration with the American Academy of Neurology (AAN), the MdDS Foundation and American Brain Foundation (ABF) are funding a Clinical Research Training Scholarship focused on MdDS. The award aims to recognize the importance of good clinical research and to encourage early career investigators in clinical studies in Mal de Débarquement Syndrome and Central Vestibular Neurological Disorders. The application for the research program scholarship is available on the AAN website.
I was diagnosed with MdDS in 2017. I live in Houston, TX. Would love to find support groups!
Hi, LeClaire! I was diagnosed with MdDS in 2020. I’m in the Los Angeles area. Facebook has an amazing group that you can join where you can receive support, information and encouragement from others who suffer from this horrible condition. The group’s name is Mal de Debarquement Syndrome-MdDS Friends. Everyone is kind and understanding and it has helped me through some anxious times in dealing with the symptoms. Best of luck!
This is wonderful news – thank you for letting us know
The URL link doesn’t work for me, unfortunately. Please can you let me/us know if there’s another one so that I can help to spread the news 
You are welcome, Polly. The link has been tested and works, but here is another one for you to use. Thank you for helping spread the news. https://bit.ly/mddscrts