Advocacy Week is a nationwide advocacy effort to connect people with ME/CFS, Long Covid, and other chronic illnesses; scientists; clinicians and caregivers to share their unique stories with Congress. Our ultimate goal is to make ME/CFS and other post-infection diseases widely understood, diagnosable, and treatable.
Social media is a powerful tool to engage your elected representatives and online community. Download and share the images below to help #StopTheLongHaul, and #CareForLongCovid.
SAMPLE LANGUAGE FOR SOCIAL
Twitter:
I hope [@TwitterHandle] will join me in supporting the #CAREforLongCOVID Act 2023. Help us fund research, education, and support services for people with infection-associated chronic illnesses like #LongCOVID and #MECFS #StopTheLongHaul
Facebook:
I hope [@FacebookHandle] will join me in supporting the #CAREforLongCOVID Act 2023. Help us fund research, education, and support services for people with infection-associated chronic illnesses like #LongCOVID and #MECFS #StopTheLongHaul
Even if you didn’t register for Advocacy Week meetings, you can still get involved! Our Advocacy Week Remote Action Kit has everything you need to make the most of your advocacy experience. This one-stop-advo-shop provides tools and templates to post to social media, send customized tweets, and engage with your members of Congress.
350 N Glendale Ave.
Suite B #368
Glendale, CA 91206
SolveCFS@SolveCFS.org
704-364-0016
EIN: 56-1683450
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