millions missing

#MEAction has started planning for Millions Missing campaign (May 12) in the USA. Why We’re Sending out an SOS this #MillionsMissing If you go to that link you'll see there's a lot of information including this US toolkit (separate plans are in the works for the UK and other locations --...

Reminder for anyone who wants to help out with the 2022 Millions Missing protest scheduled for Monday, September 19. There's an online training session tomorrow - Sunday, September 11, 12 pm Pacific Time, 3 pm Eastern Time - for people who will be taking action from home. I believe that...

full blog here http://www.broadagenda.com.au/home/millionsmissing-gender-bias-adds-to-the-burden-of-disease/

From last year but don't think it was posted. From the South China Morning post. https://www.scmp.com/lifestyle/health-wellness/article/2157439/why-me-or-yuppie-flu-aids-was-once-misunderstood-or also covers #MillionsMissing, Ron Davis, OMF shame we don't get coverage like this in UK. eta:

Starts around 2.11.00 John Darvall. Interview with ME sufferer (ME for 20 years) Liz, who participated in pre PACE Frenchay trial in 2002. Mentions PACE trial and GET being discredited, #MillionsMissing campaign. Also talks to her husband re NICE guidelines and debate in HofC. good stuff...

https://www.shropshirestar.com/news/voices/readers-letters/2018/05/18/more-cash-and-understanding-needed-to-help-me-sufferers/

https://www.thecanary.co/opinion/2018/05/13/i-was-humbled-by-the-millions-missing-yesterday-now-its-time-for-unrest/

Bustle: "You may have noticed the hashtag #MillionsMissing trending on social media, or may have seen some landmarks lighting up blue over the past few days. That's because May 12 is International Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) Awareness Day, and the folks posting in...

Thought it would be good to have a thread to help people follow what's happening today, worldwide. If you go here and click 'Latest' (just below the blue #MillionsMissing bar), there's tons of tweets: https://twitter.com/search?q=#millionsmissing&lang=en Anybody got links to video coverage...

http://www.marieclaire.co.uk/reports/millionsmissing-campaign-me-595261

https://www.sundaypost.com/fp/belle-and-sebastians-stuart-murdoch-to-join-campaigners-marking-me-awareness-day/

https://www.meaction.net/virtual-protest-2018/

https://thebristolcable.org/2018/05/from-bed-and-the-streets-campaign-for-me-equality/

" THIS week marks ME Awareness Week, culminating in a campaign day called ‘Millions Missing’ in cities across the world. Leamington and Stratford Observer deputy editor Laura Kearns is using this as a chance to speak out about her battle with the illness and talk to others with the condition...

https://themighty.com/2018/05/millions-missing-chronic-fatigue-syndrome-myalgic-encephalomyelitis-events/

http://www.insidesources.com/congress-hear-army-sick-petitioners/

The MEAction website has info on how to set up or participate in #MillionsMissing protests on May 12, 2018. https://millionsmissing.meaction.net/get-started/

This CNN article profiles several people who were unable to march (for many different reasons) in Saturday's "March for Our Lives" protest but who supported the movement in other ways. The second profile in the article is about someone with ME/CFS. I'm thrilled that this CNN article...

Info here:

#MillionsMissing 2018 Kick-off Call Wednesday, February 21, 4 PM PST #MillionsMissing global day of action will be May 12, 2018. Join this kick-off call to learn more about the plans for this year and how you can participate. RSVP...