2026 | MdDS Foundation

Faces of MdDS 09/19/2026

Finding Hope and Empathy: “My Poem For MdDS Sufferers” by Debbie Whitmer

“If people only knew what this pain feels like…” Living with MdDS for eight years, Debbie Whitmer shares a moving poem on empathy, understanding, and hope within the MdDS community. Read her story and share your thoughts.

Announcements, Research 08/12/2026

Supporting the Next Generation of MdDS Research

Next Generation Research Grant (NGRG) The MdDS Foundation has partnered with the American Brain Foundation (ABF) to offer the Next Generation Research Grant in Mal de Débarquement Syndrome (MdDS). This two-year, $150,000 award is designed to support and encourage early-career researchers: who are studying MdDS disease mechanisms or translational research specifically designed to develop treatments for […]

PROspective, Research 08/11/2026

Bridging Gaps: Connecting Data and Clinical Outcomes

Turning insights into answers: Read how evidence-based research is accelerating targeted treatment solutions.

Faces of MdDS 06/30/2026

Finding My Footing: How I Regained Control After an MdDS Diagnosis

A deeply personal story of resilience and recovery, this a powerful reminder of the strength within our community. Dakota shares what helped him the most and offers hope. Read his story on the blog!

I Am Empowered, Patient Registry 03/17/2026

MdDS Patient Registry

Living with MdDS is hard enough—contributing to research shouldn’t be. The upcoming MdDS Patient Registry is being designed with you in mind! • Simple multiple choice surveys • Point-and-click ease • Start and stop at your convenience! See how your journey can fuel new treatments and connect you with community insights.

I Am Empowered, Raising Awareness 02/27/2026