Community Symposium Summaries Now Published

Community Symposium Summaries Now Published

As you have probably heard by now, our recent Community Symposium on the Molecular Basis of ME/CFS at Stanford University was a huge hit! You can now read about the details in two pieces published by Raeka Aiyar, who emceed the symposium:

  • A high-level summary article, originally published on the Stanford School of Medicine Scope blog.
  • A detailed Storify post telling the story of the symposium, in an illustrative, easy-to-read format that combines photos, social media highlights, links, and useful resources for those who want to dig deeper.

If you’re still hungry for more, check out the full YouTube video of the symposium. Also, please read Dr. Davis’ heartfelt welcome message to attendees.  Thank you once again to all those who participated, either at Stanford or virtually, to make this an event to remember!
The video will be released on the OMF YouTube Channel soon. The event DVD’s can be ordered here.

Facebook
Twitter
WhatsApp
Email

Latest News

a multi-water colored image with the words, Severe ME Artists Project 2024 in white font outlined in black. the meaction action logo in the bottom right hand corner.

Severe ME Artists Project 2024

Quick Overview: Submit one piece of artwork – image, writing, or video Label your artwork with your name as you want it to appear, an underscore, and the number of years with severe ME Example: Lastname_FirstName_14 FirstNameOnly_ No copyrighted material If you are submitting a video, it must be under two minutes. Submission due by

Read More »
Light blue square with rainbows in the top left and bottom right corner. In the middle are the words, -Pride is Valid- No Matter How One Celebrates or Experiences It. #MEAction Board Member, Jennifer England, shares her views on Pride. The #MEAction logo in the top right corner.

Pride Is Valid No Matter How One Celebrates or Experiences It

In honor of Pride Month, #MEAction is sharing a heartfelt message from our board member, Jennifer England, about what Pride means to her and her wife who lives with severe ME. My wife and I have both been queer our whole lives, but in the 70s that was the quiet part you didn’t say out

Read More »

Questions to Ask Prospective MPs About ME/CFS

In the next few weeks, candidates will be knocking on doors seeking votes for the upcoming UK Election. It’s important that candidates from all parties are made aware of the challenges facing people with ME and Long Covid. It can be a little daunting to be unprepared so here are some questions you might want

Read More »
Scroll to Top