My Nonprofit Reviews

The MdDS Foundation is made up of extremely hard-working, and dedicated volunteers, most of whom suffer from this incredibly debilitating disorder themselves.

I was lucky to get a MdDS diagnosis from a doctor 10 days after my symptoms began - the ENT who diagnosed me referenced the MdDS Foundation website in order to help diagnose me.

MdDS is so much of a rare disorder that it hardly even categorizes as one, so the need to spread awareness is crucial. The MdDS Foundation works tirelessly to help achieve that goal.