Cayman Charter Boat—>Motion Sickness Forever | MdDS Foundation Blog
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
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
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
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
"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
