Join me and demand congress create a Federal ME/CFS Advisory Committee. #MECFS may be invisible but we are not! #SolveMECFS@PlzSolveCFS@MEActNet https://t.co/ckhxzIV230
“Time doesn’t exist...it’s simply impossible to go anywhere.
You will always be alive.
At death, we finally reach the imagined borders of ourselves.” -Robert Lanza @secondfirsts https://t.co/2ZBHsjGPTN
Land's End, a residential community in Yantis, Texas, recently began trapping deer in nets & then transporting them to be SLAUGHTERED. Urge this community to stop killing deer via @PETA! https://t.co/4fxnMoJRLM
Major clothing company @Coach just joined the ever-growing list of fur-free brands & retailers. Tell them to take the next step & ban the horrific abuse of goats & rabbits used for mohair and angora wool too! via @PETA https://t.co/80QPrMHyAy
@voluptuouswitch Thx for your thoughtful post. I’ve been bed bound for 3 years now and I still can’t ask for help w/o shame, intense mental struggle and scraping the inside of the same pb jar for 4 days.
On #WorldMentalHealthDay I want to say how grateful I am for the wonderful women of @inviscabaret who give me the gift of an open, honest and safe space to express experiences with mental illness - something I wish for everyone and will strive to provide for all of my patients.
Thrilled to announce thanks to our friends at @AMWADoctors@IUMedSchool@MEActNet that doctors, nurses, and other medical providers across the US can now watch @unrestfilm and receive Continuing Education credit! Register here to get started: https://t.co/JXGLpll1tU
So after medical providers watch Unrest, they'll watch this ten minute video on the diagnosis and management of #mecfs by Dr. David Kaufman. https://t.co/7E37Il3enu
Print out this flyer: https://t.co/Cm9gztkRgd and bring it to your next doctor's appointment. Hell, make a few copies and ask your doctor to share with his friends and colleagues. Tell them they get to watch a movie. That's actually kind of good. For credit! How awesome is that?
Thank you for protesting on my behalf and for countless others who can’t be there in person. Decades of stigma and gaslighting; the marginalization and silencing of our voices; billions not spent on research or invested in medical education & care have left us greviously ill.
We will wear the badge of pro-science, pro-patient, pro-disability rights ACTIVIST loud and proud. This wonderful article by @exceedhergrasp1 explains why: https://t.co/Q15iAgU4jJ #ScienceNotStigma
Selma Blair on her MS diagnosis: “I have had symptoms for years but was never taken seriously...I am relieved to at least know.” We need new systems to protect patients from being dismissed and support fast and accurate diagnosis. The bespoke, human model is failing us.
I emailed my congressman today asking them to support the SAVE Right Whales Act of 2018. We need as much support as we can to pass this law and give right whales a fighting chance. Please consider joining me and contacting your congressman! https://t.co/E6RDUE9E5T
@netflix's #afflicted docuseries perpetuates harmful and wrong stigma against people w/ chronic illness. Sign petition to remove now! Support people w/ disabilities telling their own stories & create compelling, ethical, authentic cinema. https://t.co/7uwAk4kTSb
Don't let @CDCgov repeat a terrible mistake. Demand #pwme and expert input for ME treatment guidelines! Sign and share the petition today. #mecfs#NoMoreShoddyWork https://t.co/JpptLMaOQE
URGENT: Terrified pigs are going to be forced to "race" in Ford Model Ts at @TillamookFair in #Oregon! Act now via @PETA to tell them not to use live animals! https://t.co/NATFlWaTBP