After months of collaborative development with community members and researchers, we opened the You + ME Registry for enrollment in June 2020. You + ME is driven by a big vision — building a community of thousands contributing health information to create the largest dataset ever for ME/CFS research. Many research projects have come to a stop due to COVID-19 stay-at-home orders and lab closures, but You + ME is completely online, turning each individual and their data into a research project incubator from the comfort and safety of home.
In this webinar, Solve M.E. Chief Scientific Officer Dr. Sadie Whittaker and CEO Oved Amitay take a closer look at what the registry has to offer, and how to make the most of your You + ME experience!
When: Wednesday, December 16 at 10 am PT/1 pm ET
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Did you get helpful info from a Solve M.E. webinar? You’re not alone. Nearly 30,000 people have registered for or viewed one of our informational videos about ME/CFS in the last two years. Your gift makes all the difference in providing this open resource to the ME/CFS community.
We create as many as 10 webinars every year, each with timely research updates or targeted educational content valuable to patients, researchers, and health care providers.
You can watch all of our webinars here.
Producing them requires funding and resources. Please consider making a donation to Solve M.E. today to help us continue to provide the most accurate and up-to-date information about ME/CFS to the world at large!