Join the MILLIONSMISSING Chicago Protest/Day of Action

Share on facebook
Share on twitter
Share on email

The Chicago protest #MillionsMissing will feature talks by Dr. Leonard Jason, Dr. Marcie Zinn, well-known epidemiologists; Carol Head, of Solve ME/CFS; Barbara Morrison; ME/CFS patients; and families and friends.
It will take place at the James Thompson Center, 100 W. Randolph St, Chicago between 11:30am-12:30pm.
Please click below to attend, learn more and donate to your local protest cities. RSVPs are also available on my.meaction.net/events/MILLIONSMISSING-Chicago. We have 60 people attending so far.
Please join us, we need your voices!


[button_color url=”https://www.crowdrise.com/millionsmissing-round-2″ content=”Ensure a budget for your local protests!” target=”https://www.crowdrise.com/millionsmissing-round-2″]
[button_color url=”http://meaction.net” content=”RSVP for Chicago” target=”https://my.meaction.net/events/millionsmissing-chicago”]
[button_color url=”http://millionsmissing.org/” content=”Learn more about #MillionsMissing” target=”http://millionsmissing.org/”]
Share on facebook
Facebook
Share on twitter
Twitter
Share on whatsapp
WhatsApp
Share on email
Email

Leave a Comment

Your email address will not be published. Required fields are marked *

Latest News

In Memory of Dr. Ronald G. Tompkins MD, ScD

Mourning the loss of Dr. Ron Tompkins

Today #MEAction joins the community in mourning the loss of Dr. Ronald G. Tompkins, MD, ScD, who passed away this week. Ron Tompkins was a clinician, clinical researcher, and friend and ally to people with ME. He was the Sumner M. Redstone Professor of Surgery at Harvard Medical School, Founding Director of the Center for

Read More »
National Institutes of Health campus buildings from above

NIH Long COVID research lacks clear plan to identify and track ME/CFS

MEAction has written to the National Institutes of Health (NIH) expressing our deep concern that the RECOVER Initiative research agenda lacks a clear plan for how to accurately identify or consistently track the onset of myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) cases among patients with Long COVID. This is of particular importance because a sizable fraction

Read More »

The Last Two Years Changed the World…

What a year 2021 was! People with ME have always faced formidable challenges: every day combatting stigma, lack of understanding from clinicians, NIH’s and CDC’s low budgetary commitments, and a world of challenges navigating disability on top of symptoms.  It’s no exaggeration to say that 2020 and 2021 changed the world – and the world of chronic,

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