Chat to NICE ME/CFS guideline committee members
On Tuesday 30th November at 5pm, we’re holding a community Q&A, and will be joined by two of the NICE committee members, who have spent almost 3 years working on the new ME/CFS guideline.
On Tuesday 30th November at 5pm, we’re holding a community Q&A, and will be joined by two of the NICE committee members, who have spent almost 3 years working on the new ME/CFS guideline.
As part of our end-of-year Giving Adventure, #MEAction is excited to announce our Holiday D&D Event! We have an exciting line-up of guests who will be joining us for a one-hour session of Dungeons & Dragons live-streamed on Twitch right at this link: https://www.twitch.tv/meactionnetworkDo you need an account to watch? No, you don’t! Simply click …
For crossing the $50,000 mark in our end-of-year Giving Adventure, we are pleased to offer an exciting AMA with our Press and Public Relations Manager, Adriane Tillman, and our Director of Scientific and Medical Outreach, Jaime Seltzer! The AMA will last for an hour on Monday, December 6th at 11am PST. Join us at the …
Ask me Anything: with Adriane Tillman and Jaime Seltzer Read More »
#MEAction hosted a live Q&A and reading with Peter Staley, famous HIV activist. Peter gives a reading from his new book, Never Silent: ACT UP and My Life in Activism. The event was moderated by #MEAction NY co-leader and long-time activist, Terri Wilder.#MEAction co-founder Jennifer Brea's interview with Peter Staley in 2014 can be viewed …
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 »