Blogger

Help us write news and opinion content for #MEAction and join a vibrant community of patient activists.

Description: #MEAction’s volunteer bloggers develop their own stories and write content ideas suggested by the MEAction team.

We are looking for folks who can write on any topics but are especially interested in covering science and policy.

We are committed to developing a deep bench of bloggers from diverse countries. Currently we have capacity for English only but would love to talk to anyone interested in writing in their native language or in translating existing content into their native language.

We prefer that bloggers write under their own names but it is possible to write anonymously for those who need to protect their anonymity.

Skills: Strong writing skills.

Hours: Bloggers can contribute as much or as little as they are able. Plus: able to commit to one article a week.

Pay: Volunteer basis.

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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

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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

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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

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