Check out the Updated, Expanded, Revamped MEpedia!

Great news! About six months ago, we began a project to updateexpand, and revamp MEpedia. Due to a generous grant, we were able to create a project scope, hire respected experts in accessibility and MediaWiki development, and make several important changes to MEpedia!

Screen shot of the new home page of #MEpedia.

MEpedia is a vital resource

MEpedia is one of the most utilized resources for researchers, clinicians, and people living with ME/CFS, with over 36 million page views.  However, the software running MEpedia, MediaWiki, was out of date. We hired an expert to upgrade our software to a version of MediaWiki that will be supported until 2025. We also hired an accessibility expert to suggest fixes and made changes to our site layout based on their recommendations. Finally, we fixed some bugs, and updated the site’s graphics to be more consistent.

Now our MEpedia content has a safe and stable long-term home!

What we’ve accomplished so far

Over the past six months, we:

  • Upgraded MediaWiki in stages
  • Moved to a new hosting platform
  • Enacted version control, so that we can see and keep track of what changes are made to MEpedia code over time
  • Integrated MEpedia with Slack so that our staff and volunteers can monitor changes to MEpedia and enact changes immediately
  • Engaged an accessibility expert to audit the new MEpedia and enacted vital changes including updating our color contrast standards, and making MEpedia friendlier for screen readers, keyboard navigation, browser zoom, and text spacing
  • Designed new graphics for MEpedia including logos, banners, and body system-based portal images

What’s Next

Our next major goal is to reach new people with information about ME/CFS, Long COVID, and other infection-associated chronic illnesses. 

MEpedia is an important source of information on ME/CFS, and its value is growing every day! 

In order to provide researchers, clinicians, and people with infection-associated chronic illnesses with up-to-date resources, we will also expand the Long COVID content covered on MEpedia by:

  • Adding new Long COVID topic pages
  • Updating existing pages that need Long COVID content

Finally, we will be translating some of our most popular pages into several other languages.  We’ve identified these high-priority pages and determined which languages will be prioritized based on the current users of MEpedia, and which languages are most spoken worldwide.

This monumental project provides a service to researchers, clinicians, and people who live with infection-associated chronic illnesses!  If you value projects like this, I hope you will continue to support #MEAction.

Facebook
Twitter
WhatsApp
Email

1 thought on “Check out the Updated, Expanded, Revamped MEpedia!”

  1. Once again many thanks for posting this news on your website and not just on social media.

    To give one example, those who don’t have a twitter account can see a single tweet, if someone sends them a link, but they can’t see a full thread.

    News items posted here are very helpful if I want to spread the word to my friends, my family, or even doctors and researchers. I can send them a link to this website without worrying about which social media accounts they have.

Comments are closed.

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