Send your ME/CFS story on a 240-km journey

On Saturday, 7 May 2016, Mike Sutton will begin a 240-km (150-mi) journey along the Camino del Norte to raise awareness and generate more funding for ME/CFS.
Mike is dedicating each day of the ten-day walk to an ME/CFS sufferer, using the hike as a platform to tell their story, share a picture of them during the walk that day, and help show the world that just because governments aren’t taking this illness seriously doesn’t mean it isn’t serious.  Sutton hopes that the hike will raise awareness and generate funding for ME/CFS.
If you are interested in making your story part of Mike’s journey:

  • Contact Mike and answer a few questions about your ME/CFS experience
  • On the day dedicated to you, he will share a picture of you ‘with’ him on the walk; you’ll need to download a special app for this on an Android phone
  • He will put up a page with the image and a description of your ME/CFS experience; you are invited to make any changes you want

Mike hopes through his efforts, he can ensure that this very human illness has a human face.
Contact Mike by visiting his blog entry I’m Going for a Walk and leaving him a comment to let him know you are interested.  Act fast to ensure your story is heard; Sutton starts his walk in just one week!
 

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