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    USA: News from the Bateman Horne Center

    Post about the discussion is here: Is Long Covid a type of ME/CFS? Discussion thread
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    The Atlantic - Long COVID Has Forced a Reckoning for One of Medicine's Most Neglected Diseases - by Ed Yong

    Senator Markey is my senator and while I appreciate this because it’s better than nothing (Stockholm Syndrome), I would have also liked to see tweets pushing for ME/CFS funding commensurate with disease burden, homecare/paid carers, and for members of congress to do something to get us out of...
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    USA - 2022 Millions Missing protest: Online training session for those taking action from home

    Good find, @ahimsa :thumbup:. What a heartbreaking story. This jumped out at me. I don't think I've come across this information before.
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    USA - 2022 Millions Missing protest: Online training session for those taking action from home

    Laurie Jones at ME Action sent me an email today saying, "Thanks, Laurie! We love Rebecca Vallas and work with her closely. I will see if she could give a quote specifically." Yay! :)
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    USA - 2022 Millions Missing protest: Online training session for those taking action from home

    I sent one more letter to ME Action: Dear Laurie Jones, Please send this to your press team too so they can have these talking points along with the ones I already sent you from the Time article, “Democrats Want to Reform This Program That Helps Poor Elderly and Disabled Americans.” There are...
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    USA - 2022 Millions Missing protest: Online training session for those taking action from home

    I received this email tonight regarding the information I sent to ME Action that is in post #9 above. It would have been nice if she told me what the line was edited to.
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    USA - 2022 Millions Missing protest: Online training session for those taking action from home

    This is the email I got from ME Action today. I sent them the 2 things I posted above in posts #8 and #9. I’ve been sick since 1983 and I’m severe/very severe. I’ve left my home once since 2008 and it was to go to the ER by ambulance. I don’t have homecare or an abled caregiver. I often have...
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    USA - 2022 Millions Missing protest: Online training session for those taking action from home

    Biden needs to be held to his promise to expand SSI benefits! Democrats Want to Reform This Program That Helps Poor Elderly and Disabled Americans https://time.com/6082787/democrats-sherrod-brown-ssi/ Edited to add article title.
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    USA - 2022 Millions Missing protest: Online training session for those taking action from home

    Direct link to #MillionsMissing 2022 Activism From Home Toolkit https://docs.google.com/document/d/11vr3VLii0j6Jq8Kvk0eTG11M940u6Nk6v1iKx4v0WYg/edit# I just sent this letter to ME Action using the "contact us" link on the bottom of their website.
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    Dr Ron Davis - Updates on ME/CFS research - September 2019 onwards

    But we don’t say “negative physical stress” or “negative cognitive stress” so I see no reason why we should be saying “negative emotional stress” instead of just “emotional exertion” which can happen across the spectrum of emotions.
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    Dr Ron Davis - Updates on ME/CFS research - September 2019 onwards

    I didn't mean open talks for patients instead of their closed meeting. I meant it would have been nice if they created some presentations for us to watch in addition to their closed meeting to keep us updated and make us part of things.
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    Dr Ron Davis - Updates on ME/CFS research - September 2019 onwards

    Janet gave us context about "Type A personality" in her tweet: "This is exactly why these meetings are not public. There is absolutely nothing unscientific about hypothesizing that people who are high achievers and work hard and over exert themselves may be at risk for something." We also...
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    Dr Ron Davis - Updates on ME/CFS research - September 2019 onwards

    I can’t comprehend how people don’t see how things like “Type A personality” and “Negative Emotional Stress” stigmatize and harm us further. Not only can most of us not get medical care, it’s hard to even find safe documents to share with a doctor should we be fortunate enough to find one who...
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    Dr Ron Davis - Updates on ME/CFS research - September 2019 onwards

    WTF? We deserve so much better. :banghead:
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    USA: NIH National Institutes of Health news - latest ME/CFS webinar 14 Jan 2025

    NIH Extends Funding for ME/CFS Research Centers https://www.meaction.net/2022/09/07/nih-extends-funding-for-mecfs-research-centers/
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    Long Covid in the media and social media 2022

    How long covid studies could help scientists solve the long-unsolved mystery of post-viral illnesses Increased awareness, funding and research participants could spark progress and new treatments...
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    Long Covid in the media and social media 2022

    Doctors are taking it on themselves to figure out long Covid Absent more guidance from the government, physicians are sharing ideas for treating the mysterious condition. https://www.politico.com/news/2022/09/07/doctors-are-taking-it-on-themselves-to-figure-out-long-covid-00054748
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    Long Covid in the media and social media 2022

    Unbelievable, the experimental treatment for "brain fog" is a video game! :banghead:
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    Dr Ron Davis - Updates on ME/CFS research - September 2019 onwards

    Unfortunately, it's not going to be recorded for us to be able to watch. Edited to add: Later in the video Janet said that an individual researcher may request that their presentation be recorded and that the recording will be given to that researcher to do what they want with. Edited to add...
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    News from the USA, United States of America

    “How Long?” For People with Long COVID, asks Powerful National Public Service Announcement https://www.healthrising.org/blog/2022/08/10/how-long-long-covid-psa/ How Long Until We Solve Long Covid? https://solvecfs.org/solve-long-covid/ Edited to add link. "How Long?" PSA starts with...
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