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

greyish rectangle image with the words: #MEAction is Excited to Announce: Pillow Writers Anthology Issue 1: Near-Life Experiences. In a small grey square the words Get Your Copy Today! with a black line underneath. On the right hand side of the square is the image of the book cover that has a water color of flowers. the #meaction logo is at the bottom of the image.

Pillow Writers Anthology, Issue 1: Near-Life Experiences Available Now!

The Pillow Writers Anthology, Issue 1: Near- Life Experiences is a new literary magazine in the disability community. This inaugural issue features poems, stories, and essays by 17 writers who call themselves the Pillow Writers. The Pillow Writers are an international group of writers living with the neuro-immune diseases of myalgic encephalomyelitis (ME) and Long

Read More »

#MEAction UK’s email/letter to Andrew Gwynne MP

To: Andrew Gwynne, Under Secretary of State for Public Health and Prevention Subject: Treatment of Very Severe ME  email [email protected] Dear Andrew Gwynne,  Thank you for being an ally to people with ME  (myalgic encephalomyelitis) and Long Covid and committing to ensuring publication of the DHSC ME/CFS Delivery Plan without more delay.  We trust your

Read More »
Scroll to Top