Skip to content
ME and Me

ME and Me

  • About
  • Contact
  • Articles
  • Press
  • Resources
  • Personal Stories
    • ME & Me Series
    • My Story
    • Podcast: My Story
  • Leeds Millions Missing
    • Leeds Millions Missing 2019
    • Leeds Millions Missing 2021
    • Leeds Millions Missing 2020
    • Leeds Millions Missing 2022
  • Facebook
  • Twitter
  • YouTube

Tag Archives: MECFS

Plans underway for Leeds Millions Missing 2021 – get involved by sending a selfie!

Posted byME and MeApril 28, 2021May 2, 2021Posted in#MEAction UK, Millions MissingTags:#MEActionUK, MECFS, MillionsMissing, MyalgicE, MyalgicEncephalompyelitis1 Comment on Plans underway for Leeds Millions Missing 2021 – get involved by sending a selfie!

ME & Me Series: Jonathan’s story

Posted byME and MeApril 21, 2021April 21, 2021Posted inME & Me series, Personal StoryTags:EarlyRetirement, Leeds, LifeStory, MECFS, MyalgicEncephalompyelitis, MyStory1 Comment on ME & Me Series: Jonathan’s story

York ME Community reports of increased support needed during COVID-19 pandemic

Posted byME and MeApril 14, 2021April 23, 2021Posted inActivism, Local ME NewsTags:COVID19, LocalNews, MECFS, MyalgicEncephalompyelitis, Pandemic, SupportGroupLeave a comment on York ME Community reports of increased support needed during COVID-19 pandemic

The Yorkshire Evening Post features ME & Me website launch

Posted byME and MeApril 13, 2021Posted inActivism, Local ME NewsTags:Local, MECFS, MyalgicEncephalompyelitis, NewsLeave a comment on The Yorkshire Evening Post features ME & Me website launch

‘Blue Sunday’ fundrasier wants more people than ever to host their own tea parties

Posted byME and MeMarch 31, 2021March 31, 2021Posted inActivism, FundraisingTags:Fundraising, MECFS, MyalgicEncephalompyelitis, Spoonie1 Comment on ‘Blue Sunday’ fundrasier wants more people than ever to host their own tea parties

ME & Me Series: Lucy’s story

Posted byME and MeMarch 24, 2021March 24, 2021Posted inME & Me series, Personal StoryTags:Chronic Fatigue Syndrome, MECFS, MyalgicEncephalompyelitis, PersonalStory, StoryLeave a comment on ME & Me Series: Lucy’s story

Spoonie Survival Kits: the small Yorkshire project that made a huge difference

Posted byME and MeMarch 17, 2021March 20, 2021Posted inActivismTags:Activism, Charity, Fundraising, MECFS, MyalgicEncephalompyelitis, Spoonie, SpoonieSurvivalKitLeave a comment on Spoonie Survival Kits: the small Yorkshire project that made a huge difference

Book review: Waiting for Superman

Posted byME and MeMarch 6, 2021March 6, 2021Posted in#MEAction UK, ReviewsTags:Book Review, MECFS, MyalgicEncephalompyelitis, ReviewLeave a comment on Book review: Waiting for Superman

REVIEW: Moving Short Film “This Is ME”

Posted byME and MeFebruary 20, 2021February 21, 2021Posted in#MEAction UK, ReviewsTags:Film Review, MECFS, MyalgicEncephalompyelitis, ReviewLeave a comment on REVIEW: Moving Short Film “This Is ME”

Open letter: UK Government Should Add ME To Vaccine Priority List

Posted byME and MeFebruary 20, 2021February 20, 2021Posted in#MEAction UK, ActivismTags:#MEActionUK, Activism, MECFS, MyalgicEncephalompyelitisLeave a comment on Open letter: UK Government Should Add ME To Vaccine Priority List

Posts navigation

Newer posts 1 2 3
ME and Me, Website Powered by WordPress.com.
  • Follow Following
    • ME and Me
    • Join 318 other followers
    • Already have a WordPress.com account? Log in now.
    • ME and Me
    • Customize
    • Follow Following
    • Sign up
    • Log in
    • Report this content
    • View site in Reader
    • Manage subscriptions
    • Collapse this bar