Meet virtually to train for our in-person #MillionsMissing September 2022 Protest with an experienced lawyer and activist on the purpose of protest, how to do both civil disobedience and lawful protest. This training for protesting in-person, will only focus on the US based #MillionsMissing Protest.We will be using BlueJeans for this virtual call. You can …
Update: Please note that this is the new date for #MillionsMissing Scotland, following its postponement. Address: The Scottish Parliament, Holyrood, Edinburgh, EH99 1SP Join #MEAction Scotland outside the Scottish Parliament to demand more for people with ME. This will be a smaller, more focussed demonstration than some of our previous #MillionsMissing events, as our aim …
#MILLIONSMISSING SCOTLAND SEPTEMBER 2022- NEW DATE Read More »
Please join us for the monthly California #MEAction support and informational meeting every last Thursday of the month at 6:00 pm (PDT). The purpose of the meeting is to bring together Californians who have ME, along with their family and friends, to discuss their concerns, let out their feelings, exchange information, and develop advocacy strategy. …
#MEAction California State Chapter Monthly Meetings Read More »
Please join us for our new monthly #MEAction Maryland Advocacy meeting! All people with ME/CFS, caregivers and allies are welcome. We meet on the first Tuesday of the month at 7:00 pm Eastern time. The agenda will change from month-to-month but open discussion is always encouraged and new-comers are welcome. The purpose of the meeting is …
#MEAction UK is excited to announce a new date for #MillionsMissing London 2022. Join us at Parliament Square on 18th October from 1-3pm to demand the millions of pounds missing from ME research in the UK! Mark your calendars now! While we are asking for those that can attend to join us in person on Tuesday …
#MEAction is excited to partner with Shannon Williams-Bramburger of Nourish Therapeutic Yoga to provide a 30 minute, virtual yoga class on Friday, Oct 28th at 12pm PT/3pm ET/8pm BST that has been crafted specifically for people with ME. The whole class will be lying down and can be done from bed.What to expect in this …
Please join us for the monthly California #MEAction support and informational meeting every 2nd Thursday of the month at 6:00 pm (PDT). The purpose of the meeting is to bring together Californians who have ME, along with their family and friends, to discuss their concerns, let out their feelings, exchange information, and develop advocacy strategy. …
#MEAction California State Chapter Monthly Meetings Read More »
Join #MEAction Scotland volunteers for an informal chat about ME activism in Scotland. These community calls take place quarterly and give us a chance to connect with more of you, tell you about what we’re up to, and get your input too. We know there are lots of people with ME in Scotland who aren’t …
#MEAction is thrilled to announce, we will be hosting a virtual #MEAction x The Long COVID Survival Guide Panel featuring editor Fiona Lowenstein and contributors Rachel Robles, Chimére L. Smith, and Terri L. Wilder from the recently released book on Tuesday, Jan 17th at 4pm PST/6pm CST/7pm EST.This panel will be led by Ben HsuBorger …
Please join the #MEAction Minnesota State Chapter for this month's chapter meeting! All people with ME/CFS, caregivers and allies are welcome. Our agenda will change from meeting to meeting. Open discussion is always encouraged and new-comers are welcome. The purpose of this chapter is to focus on advocacy and policy and to form a Minnesota …
Join #MEAction for our exciting “Writing From Our ME Lives” Writers’ Salon on Wed, January 25th at 11am PST/2pm EST/7pm UK, held virtually via Zoom. This live Salon will feature readings by the authors of both comic and serious, stories, scenes and poems, that were created for the weekly virtual meetings, commonly called “Pillow Writers”, …
#MEAction’s “Writing From Our Lives” Writers’ Salon Read More »
Please join the #MEAction Minnesota State Chapter for this month’s chapter meeting! All people with ME/CFS, caregivers and allies are welcome. Our agenda will change from meeting to meeting. Open discussion is always encouraged and new-comers are welcome. The purpose of this chapter is to focus on advocacy and policy and to form a Minnesota …
