The CFIDS Association has announced a couple of upcoming webinars you all might be interested in for September. The first one is on Wednesday, September 1st, with Dr. Peter Rowe from Johns Hopkins University. His webinar … [Read more...] about CFIDS Association September Webinars
The CFIDS Association has joined forces with the Genetic Alliance BioBank to create the SolveCFS BioBank. The CFIDS Association says about their new venture: The SolveCFS BioBank will collect and store a bank of biological … [Read more...] about Enrollment for SolveCFS BioBank
I wanted to make everyone aware of two upcoming CFIDS Association webinars that will be held on May 4th and May 5th. The CFIDS Association has expanded their webinars to two programs per month and you can register by … [Read more...] about Upcoming CFIDS Association Webinars – May 4 & May 5
On Wednesday, April 14th, (2:00 p.m. EST) the CFIDS Association will host their next webinar on Defining CFS: Diagnostic Criteria & Case Definition. Here is info. on the upcoming webinar from the registration page: In … [Read more...] about Webinar: Defining CFS: Diagnostic Criteria & Case Definition
I previously took a survey by the CFIDS Association regarding ME/CFS symptoms and which ones were worse. The CFIDS Association has revealed the results of that survey and I thought readers might find it interesting. Here is … [Read more...] about Results of CFIDS Association ME/CFS Symptoms Survey
The CFIDS Association has an anonymous survey that you can take that closes tomorrow at midnight on August 31st. What is the survey about? According to the CFIDS Association: This profile survey will help us get a better … [Read more...] about CFIDS Association Anonymous Survey – Take It Today!
Post-Mono CFS in Teen Girls Ben Z. Katz, M.D., of Northwestern University has just published results from a study of teens who were followed for two years after the onset of acute infection with Epstein-Barr virus … [Read more...] about August News from the CFIDS Association
From the Desk of Kim McCleary Summer is often a time to “go with the flow.” But CFS patients, perhaps as many as 70% of them, who experience forms of orthostatic intolerance (OI) generally find that summer is a better time … [Read more...] about July News from the CFIDS Association
I received an email the other day from the CFIDS Association regarding their hard work in trying to get more research efforts from the CDC on ME/CFS. Show your support by leaving your comments to the CDC no later than June … [Read more...] about Tell CDC To Change Their Research Plans for ME/CFS!