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We’re delighted to announce the launch of our new website and ME Friends Online forum! 🎉
Our previous website was outdated & wasn’t as accessible as it could be, making it harder to find resources, raise awareness & support more people affected by #MECFS
We’re delighted to announce the launch of our new website and ME Friends Online forum! 🎉
Our previous website was outdated & wasn’t as accessible as it could be, making it harder to find resources, raise awareness & support more people affected by #MECFS
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Comments
With 250k visits in the past year & reported in finding info & resources, alongside our ME Friends Online forum not meeting users’ needs, an upgrade was essential.
Over the past year, we've been working alongside our key stakeholders, including #pwME, to redevelop our website.
We've produced both a summary & long read version of the announcement, which is also available on our new site 👇
https://www.actionforme.org.uk/news/our-new-website/
If you notice or experience any issues after this point, please report them to us directly and we will look to fix them.
Thank you 🧡
#pwME #MECFS #MyalgicE #MyalgicEncephalomyelitis
https://www.actionforme.org.uk/news/foi-report-highlights-shocking-lack-of-specialist-care