3 Ways You Can Join in a #TimeforUnrest

Update: View a recording of the call here – https://www.youtube.com/watch?v=LQWgvK1UsdQ
—————————
The September kickoff of the #TimeforUnrest campaign is just around the corner, and we at #MEAction couldn’t be more excited! Last week we recorded our first community call where we got to know the Unrest team, hear about the film’s release plan and got a sneak peek into the impact campaign and its potential to add fuel and visibility to our ME movement.
This Saturday, August 19, at 2pm ET (New York), 7pm BST (London) we will host a second community call with the Impact Campaign Team to talk in detail about 3 ways you can participate in a #TimeforUnrest.
Don’t forget to RSVP!

 
P.S. We love connecting with you live to be able to answer your questions, but if you can’t make the time, don’t worry! We’ll upload all #TimeforUnrest Community Calls to this youtube video playlist. You can also get a quick overview of ways to get involved from this handout. Still have questions? Join the #TimeforUnrest Facebook Group to get answers and support!

Facebook
Twitter
WhatsApp
Email

1 thought on “3 Ways You Can Join in a #TimeforUnrest”

  1. Hi
    My names Carol im from Cardiff an have gad severe M.E. for 24years most of which ive been bedbound. Id like to be part of #timeforunrest campaign in uk particularly in Cardiff & rest of Wales.id like to take part an help promote unrest in Wales. Id love to have been part of the film but didnt know how to so i want to be part of unrest now. Ive suffered much neglect & abuse from med profession. I want to be heard an raise awareness of the beast that is M.E.!!

Comments are closed.

Latest News

Facets of ME: Temperature Dysregulation

Welcome to June’s #FacetsOfME! Facets of ME is an educational feature where we dive into a particular aspect (or facet) of ME and explore it more in depth. This month we are focusing on temperature dysregulation- heat and cold intolerance. It is surprising how difficult this symptom can be to manage until you experience it.

Read More »

Dept. of Labor Updates Information on ME/CFS for Workers, Employers

The U.S. Department of Labor’s Office of Disability Employment Policy (ODEP) has updated the information on ME/CFS provided at its Job Accommodation Network website to align with the most current CDC guidance. This action will help workers and employers find accurate information on ME/CFS and combat stigma and improve workplace outcomes. At #MEAction’s recent meeting

Read More »

#MillionsMissing: 7 Days in Self Portraits with ME/CFS

After taking #MEAction’s photography workshop with photographer Lucia Doynel for #MillionsMissing, Terra Dumont produced these stunning photos as a glimpse into her life as someone living with ME/CFS. Terra spread this experience over 7 days, focusing on a different theme each day. See her wonderful work and accompanying commentary below. Click on any of the

Read More »

Help keep our work going

We rely on donations from people like you to keep fighting for equality for people with ME.

Donate

Get actions alerts and news direct to your inbox

You can choose what you want to be kept up to date on.

Subscribe
Scroll to Top