From an e-mail from #MEAction: It’s already time to start thinking and planning for #MillionsMissing 2020! This year #MillionsMissing global...
Australia: International Awareness Day for Chronic Immunological and Neurological Diseases (CIND) including myalgic encephalomyelitis (ME) /...
My husband and I are planning a small #MillionsMissing event at our local library in Beaverton, Oregon. We plan to set up a small table in front...
There is lots of information on the web. If you know someone with ME listen to them and believe what they say – they are not lazy – they want to...
BELLE and Sebastian frontman Stuart Murdoch will call on people to “make a noise” to help improve the lives of at least 20,000 Scots living with...
BEFORE May 12: Ask Congress to support people with ME. Using our one-click software, it’ll only take a few seconds. Contact Congress now....
Sufferers of ME/CFS are taking to Queen Square this weekend. The Cable spoke to an organiser about why the government needs to take action on the...
The “millions missing” from life due to myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) are coming together worldwide to fight for...
Dear Free Psychotherapy Network, I was very interested in the article on your website calling on therapists not to collude with harmful...
http://www.insidesources.com/congress-hear-army-sick-petitioners/ A different voice will be heard on Capitol Hill on May 12 to 15: a gentle, sad...
Info here: [MEDIA]
#MillionsMissing 2018 Kick-off Call Wednesday, February 21, 4 PM PST #MillionsMissing global day of action will be May 12, 2018. Join this...
Hi, I guess you've all seen the other thread (or got the email) that the planning for the Millions Missing protests have started:...
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