As a way to celebrate and highlight the amazing artists within our community, please join us for a live event on Wednesday, December 15th at 12pm PST/3pm EST for our Winter Virtual Artist Salon featuring artists and their work. This will be a fun gathering where artists will share their work and the inspiration for …
Please join us for the monthly California #MEAction support and informational meeting. 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. Especially in these times, many of us are at loose …
Everyone is welcome to join us for our monthly planning meeting and contribute or just listen in! We meet on the 4th Friday of the month from 10 -11:30 am MT. Click the website link below to join by computer. Or, join by phone: Dial +1.408.317.9253 if you’re in the US +44.203.608.5256 for UK +61.2.8103.4256 …
A People with ME and Long COVID writing group! Come, Try it out!! #MEAction is excited to partner with longtime ME advocate and mother of a pwME, Bobbi Ausubel, to host a writing group for people with ME and Long COVID, Pillow Writers. The group will be offered every week on Thursdays from 11am PST/2pm …
Join #MEAction for our first exciting “Writing From Our ME Lives” Salon on Friday, January 21st at 12pm PST/3pm EST, held virtually via BlueJeans. 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", over …
#MEAction Presents: Writing From Our ME Lives Salon Read More »
It’s time to PARTY at the #MillionMissing Castle!Join the #MEAction community for the final celebration of last year’s Giving Adventure–a virtual party at the #MillionsMissing Castle. This will be a chance to gather as a community to celebrate the wins from last year and build strength for the battles ahead! As you gather in the …
Giving Adventure Virtual Party @ The #MillionsMissing Castle Read More »
Everyone is welcome to join us for our monthly planning meeting and contribute or just listen in! We meet on the 3rd Friday of the month from 10 -11:30 am MT. Click the website link below to join by computer. Or, join by phone: Dial +1.408.317.9253 if you’re in the US +44.203.608.5256 for UK +61.2.8103.4256 …
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 »
Join #MEAction Scotland volunteers for an informal chat about ME activism in Scotland. We know there are lots of people with ME in Scotland who aren’t able to volunteer with us but are interested in activism and have thoughts and ideas about campaigning. This will be the first of the quarterly community calls we are …
Sign up to a free online workshop inspired by nature and supported by #MEAction UK to mark ME Awareness Week. No experience necessary, everyone welcome.Information about the Moving Mountains Workshop:Creative Writing WorkshopWith Nic Wilson and Louise Kenward Do you enjoy watching nature out of the window, in the garden or in the local landscape? Perhaps …
Join your Minnesota friends for virtual #MillionsMissing on May 11th at 7:00 p.m. - Dr. Ruby Tam from Northwest Family Clinics will share her experiences treating Minnesota patients with ME/CFS and Long-Covid. We will have time for personal sharing and an update from the Minnesota ME/CFS Alliance.The event will be held on Zoom and you …
Minnesota ME/CFS Alliance’s #MILLIONSMISSING VIRTUAL EVENT Read More »
#MEAction’s #MillionsMissing Global Virtual Event on May 12th at 10am PT/1pm ET/6pm UK! Join ME community members and change makers for this amazing event. The event will be an opportunity for our community to gather to experience the stories of those with ME, gain insight from doctors and researchers, connect with those living with Long …
