JACKSONVILLE, Fla. — About 70 million people worldwide live with a condition called dysautonomia, but too often it goes undiagnosed. "It's the most common condition you've never heard of," Lauren ...
Dysautonomia International is working to raise awareness for people living with autonomic nervous system disorders. The non-profit organization is working to identify causes and cures for all forms of ...
Natacha T. Pires of Astoria has joined Dysautonomia International in East Moriches as director of medical and public affairs. She held a similar position at The Neuropathy Association in Manhattan.
Like a lot of those struck by the indistinct symptoms of dysautonomia, St. George resident Cyndee Jacobson lived for years undiagnosed, unable to find an adequate explanation for her condition but ...
KNOXVILLE, Tenn. (WATE) — They’re often called “invisible illnesses.” Forms of Dysautonomia can impact the entire body causing a wide array of symptoms and different levels of disability. Oftentimes, ...
An error has occurred. Please try again. With a The Portland Press Herald subscription, you can gift 5 articles each month. It looks like you do not have any active ...
The 2016 race to raise awareness for postural orthostatic tachycardia syndrome will be held at 10 a.m. on Saturday, May 7 at the Mystic River Bend Park, near Hormel Stadium, Locust Street, Medford.
NPR's Scott Simon talks to Lauren Stiles, president of Dysautonomia International, about a new diagnosis that could answer why some people still suffer symptoms months after contracting COVID-19.
In 2013 Lee Wiltshire (27) from Mandeni KwaZulu-Natal was diagnosed with Dysautonomia. She’d had symptoms since she was a child, but only started getting really sick a few years ago. Because of this ...
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