CFSAC is Wednesday (12/13) and Thursday (12/14) of this week! Please stand with us as we continue to urge the U.S. government to fund ME fairly and equally.
View the calendar event here.
This Chronic Fatigue Syndrome Advisory Committee (CFSAC) meeting will take place at the Hubert H. Humphrey Building, 200 Independence Avenue, S.W., Washington, D.C. 20201.
Those planning to attend CFSAC in person must submit their name(s) via email –[email protected] to register for in-person attendance. The meeting will also be livestreamed and recorded.
Livestream: www.hhs.gov/live
Call in number: (888) 469-1760
Participant passcode: 4510479
https://www.hhs.gov/ash/advisory-committees/cfsac/meetings/2017-12-13/index.html
#MEAction is a non-voting liaison organization member with CFSAC. Have questions, concerns or comments for us? Email [email protected].
SOS: Save our Science
April 11, 2025
1 Comment
People disabled by ME and Long Covid across the UK send out an SOS. It’s time to send out our SOS signal, if we want to have funded research. May 12th, is Myalgic Encephalomyelitis Awareness Day. On this day, the #MillionsMissing of people with myalgic encephalomyelitis (ME) gather to demand an increase in research and
1 thought on “Don't Miss the CFS Advisory Committee Meeting This Wednesday & Thursday”
WE NEED THE GOVERNMENT TO STAND UP AND LISTEN TO US WHO HAVE FALLEN SEVERELY ILL TO CHRONIC FATIGUE IMMUNE DYSFUNCTION …I HAVE BEEN ADVOCATING ENDLESSLY WITH NO PREVAIL…THIS HAS TO STOP…WE NEED AMPLIGEN APPROVED, SO WE CAN LIVE AND NOT SUFFER BEYOND REASON….WE ARE THE LIVING DEAD….IT’S OUTRAGEOUS THAT WE ARE SUFFERING SO IMMENSELY…THE GOVERNMENT HAS FAILED US…WE WILL NOT TOLERATE THIS ANYMORE….WASHINGTON WAKE UP AND GET BUSY….
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