My Nonprofit Reviews

In my mid-20s I first experienced MdDS. I went to several doctors and none had an idea of what was wrong. It cleared up after a few weeks but since then I’ve had more episodes, each getting longer and longer. This last episode has gone on for over a year and still is ongoing. I found the MdDS Foundation during my last episode and they are doing such an amazing job of connecting people to information. This condition is not well understood by the medical community and the MdDS Foundation has developed pamphlets to allow education to individuals. They keep tabs on research that is ongoing and provide it to its community, and allow it’s community members to discuss their experiences with each other to allow them to feel not alone with this deviating condition.