advocacy

  1. Andy

    Walk a mile in my shoes: trying on CWTCH's chronic illness symptom suit

    https://www.westerntelegraph.co.uk/news/17284361.walk-a-mile-in-my-shoes-trying-on-cwtchs-chronic-illness-symptom-suit/
  2. Andy

    MEAction: " All I want for Christmas is #ScienceNotStigma"

    https://www.meaction.net/2018/12/05/all-i-want-for-christmas-is-sciencenotstigma/
  3. Andy

    Blog: Super Pooped: "Cause and Effect piece" [comic illustrating life with ME/CFS]

    Read more, and see the comic, at https://superpooped.blogspot.com/2018/12/cause-and-effect-piece.html
  4. Snowdrop

    Canadian Medical Assoc -- Patient Voice

    I'm posting this in case there are Cdn advocates here who are not aware of this group and who might find connecting with this group of possible use for ME advocacy: https://www.cma.ca/En/Pages/patient-voice.aspx The CMA Patient Voice is our patient liaison group and is made up of 14...
  5. JaimeS

    #MEAction ideas for Giving Tuesday

    A few things have begun to aggregate, so I figured I would start a new thread and post them here. First, #MEAction's general article on how to donate on #GivingTuesday: https://www.meaction.net/2018/11/16/givingtuesday/ Right now, Facebook is matching donations, so consider clicking on the...
  6. Sly Saint

    Nov 29th #YoungHeartsDay - for #KidswithME

    just wondering if we could do something to show our support?
  7. Kalliope

    #MEAction: Fall advocacy round-up - A season of protest and petition

    #MEAction: Fall advocacy round-up - a season of protest and petition An extensive summary of this autumn's advocacy work around the world. Quite impressive list! :) Includes petitions, introduction of new staff members, news from different parts of the world, protests, and updates on among...
  8. ahimsa

    US action: Ask your health care professional (doctor, nurse, therapist, etc) to watch Unrest online for credit

    Here's a relatively easy advocacy action for patients in the USA: Ask your health care professional to watch Unrest online and get continuing education credit. What I did was print out some flyers (found here https://www.meaction.net/wp-content/uploads/2018/10/Doctor-flyer.pdf ) and then gave...
  9. Andy

    Dialogues for a neglected illness - videos on experiences of people with ME (funded by Wellcome Foundation)

    http://voicesfromtheshadowsfilm.co.uk/2018/dialogues-for-a-neglected-illness-a-new-mecfs-project-awarded-wellcome-funding/
  10. A

    Merryn Crofts - our last family statement

    Hi, I apologise if this is the wrong area to post this but this is our last formal statement as a family. I’m unsure how to get it to come up on here so I have included a link to the Facebook post we have written. I’m a bit useless with technology so I do apologise! Many thanks and sending...
  11. JaimeS

    A masterlist of ME facts & the citations that support them

    We have a bunch of facts we use both for advocacy and for scientific research that we cite often. I spend a good amount of time at #MEAction providing citations to other advocates, and I know that advocates spend hours... and hours... and hours searching for the right citation to support a fact...
  12. JaimeS

    Who was it that said being in support groups leads to poor outcome?

    Halp. Looking for a resource on this? I'll start the hunt through Phoenix Rising, but if someone has it handy, I'd really appreciate it.
  13. T

    ME advocates you can endorse (=vote for) in the WegoHealth awards 2018

    I thought I would open a thread on this as I'm aware of a number of people who have been nominated. Also votes numbered in the hundreds seem to have been enough to get into the final so it's not unachievable for people to become a finalist. For example, some people I recall who were finalists...
  14. Joh

    Great interview: "From Fit Nurse To ME Warrior"

    Great video interview "From Fit Nurse To ME Warrior With Ashanti Daniel" by Valentine Ewudo: https://thinkalpha.net/fit-nurse-to-me-warrior-ashanti-daniel/
  15. Daisymay

    The Biopolitics of CFS/ME

    https://www.sciencedirect.com/science/article/pii/S1369848617300705 The Biopolitics of CFS/ME Author Nikos Karfakis Highlights •The diagnosis of CFS/ME is not only a scientific issue nor only contested within the confines of the clinic, but a much broader, biopolitical problem. •Attempts...
  16. Samuel

    Strategic framework for activism with practical advice

    /Movement Action Plan/, by Bill Moyer. http://www.indybay.org/uploads/movement_action_plan.pdf excerpt: === STAGE TWO: PROVE THE FAILURE OF INSTITUTIONS The intensity of public feeling, opinion, and upset required for social movements to occur can happen only when the public realizes that...
  17. Andy

    Opinion piece: If only Brexit had been run like Ireland’s referendum [not posted for the politics]

    https://www.theguardian.com/commentisfree/2018/may/29/brexit-ireland-referendum-experiment-trusting-people Not posted for the Brexit or abortion topics but for the last section of the article that I have included in the quote above. I believe that this is something really important that we can...
  18. RuthT

    #MEAction - UK Organiser

    #ME Action Network have just announced a fundraiser for a U.K. organiser. “to support another year of mass awareness, medical and scientific outreach, advocacy, and community for impact like #MillionsMissing and our parliamentary actions” Edit: Link will be added when can work out how to do...
  19. Andy

    Advocacy Alert: What’s Up TV Wants Your Voice for ME - Deadline is Friday 1st June

    http://ldifme.org/2018/05/18/whats-up-tv-wants-your-voice-for-me/
  20. Andy

    #MEAction: Four things you can do to advance the fight for health equality

    https://www.meaction.net/take-action/
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