Top Tweets for #ScienceforME
"We now have 77 organisations, including most national ME/CFS charities, calling for the Larun et al review to be removed", heißt es im jüngsten Update der Cochrane-Petition, die der Fatigatio e.V. - Bundesverband ME/CFS selbstverständlich unterstützt.
#ScienceForME #MECFS
PETITION: @s4me_info Cochrane: Withdraw the harmful 2019 Exercise therapy for CFS review - 10,091 signatures so far......
Please consider signing and sharing:
https://t.co/bEoREzGlOB
#pwME #MECFS #MyalgicE #MyalgicEncephalomyelitis #NICEGuideline #ScienceforME #CochraneReview
PETITION: @sci4me_info Cochrane: Withdraw the harmful 2019 Exercise therapy for CFS review - 8,674 signatures so far......
Please consider signing and sharing:
https://t.co/bEoREzGlOB
#pwME #MECFS #MyalgicE #MyalgicEncephalomyelitis #NICEGuideline #ScienceforME #CochraneReview
@meganranney Did you make it to DC? Couldn’t help but notice you took this picture down. Any chance it’s because you have scolded folks for any social activity these last 10 months? Probably just felt bad you are vaccinated while there are more at risk folks who have to wait! #scienceforme
#ScienceForMe is asking questions and challenging the status quo with logic and evidence
#NationalScienceDay🇮🇳 #ScienceMatters
Have kids around? This #NationalScienceDay, ask what #science means to them! Use placard ⏬ and tell us with #ScienceForMe
Also, we begin our festivities in the #ScienceFest and #OpenDay @THSTIFaridabad tomorrow 👥
If around, come see us for all things fun and science-y!🤹🏽♀
Happy #NationalScienceDay2020 🦠🧬🔬#ScienceForMe is driven by #Curiosity ❓💡#Enthusiasm - to do more👩🏻🔬& #ScienceForAll @IndiaBioscience @India_Alliance @SarahHyder @ShreyaScilens
Thank you @India_Alliance for this initiative! Here's our team and our wishlist for #WomeninScience (and some thoughts on #ScienceForMe) #MyWish4WiS @SarahHyder
#ScienceForMe is admitting that we don't know all the answers but answers EXIST & can be found - and #MyWish4WiS is that little girls who want to find answers to burning questions don't get told that maths and science are too difficult for them @India_Alliance #NationalScienceDay
Thank you @India_Alliance for this initiative! Here's our team and our wishlist for #WomeninScience (and some thoughts on #ScienceForMe) #MyWish4WiS @SarahHyder
Thank you @India_Alliance for this initiative! Here's our team and our wishlist for #WomeninScience (and some thoughts on #ScienceForMe) #MyWish4WiS @SarahHyder
And don't forget to do this 👇 #ScienceForMe
Have kids around? This #NationalScienceDay, ask what #science means to them! Use placard ⏬ and tell us with #ScienceForMe
Also, we begin our festivities in the #ScienceFest and #OpenDay @THSTIFaridabad tomorrow 👥
If around, come see us for all things fun and science-y!🤹🏽♀
Catch my fabulous colleagues @HinaLateef @yukti_7 @India_Alliance booth tomorrow @THSTIFaridabad for some science-y fun & games
#NationalScienceDay #ScieEd #publicengagement #MyWish4Wis #ScienceForMe
Have kids around? This #NationalScienceDay, ask what #science means to them! Use placard ⏬ and tell us with #ScienceForMe
Also, we begin our festivities in the #ScienceFest and #OpenDay @THSTIFaridabad tomorrow 👥
If around, come see us for all things fun and science-y!🤹🏽♀
Have kids around? This #NationalScienceDay, ask what #science means to them! Use placard ⏬ and tell us with #ScienceForMe
Also, we begin our festivities in the #ScienceFest and #OpenDay @THSTIFaridabad tomorrow 👥
If around, come see us for all things fun and science-y!🤹🏽♀
Een eerste uitgebreid onderzoek onder jeugd in Chicago toont aan dat 1% ME/cvs heeft. Dat betekent een groter aantal jonge patiënten dan ooit geschat. Check het artikel (engels) hier en doe mee aan de poll. #pwme #scienceforME #pediatricME
https://t.co/hymwrojeM4
On a happy note, we are on a perfect path for identifying potential transferable factors in ME/CFS blood that can cause mito dysfunction. Today was a great day for us in the lab. We might have our first factor in hand and as an icing on cake we have two potential diagnostic tests
Thank you for your support. We are grateful for your time, your dollars, your Data and your generosity. Together, we will lead the fight to cure ME/CFS. #ThankyouWednesday #MECFS #pwME #spoonies #mygivingstory #scienceforME #investinME #chronicillnesswarrior #invisibleillness #ME
Dr Ron Davis' talk at Einstein College of medicine can be seen on You Tube now.
#scienceforME #sciencenotstigma #educateME
https://t.co/05zqBvd68v
Zeer goed artikel om te delen met je arts, fysio, familie... Dit is waarom bewegen/inspanning schadelijk is bij #pwme! Dank @ME_gids voor deze goede vertaling.
#scienceforME #sciencenotstigma #educateME
OMF Scientific Advisory Board Director Ron Davis, PhD, will be speaking at the Albert Einstein College of Medicine at @Columbia University in New York on the progress and challenges of developing a diagnostic test for ME/CFS. (Continued in thread)
A must read for #pwme! This is really interesting research!
#sciencenotstigma #scienceforME #educateME
Powerful Models Accurately Predict Response to Exercise and Treatments in #MECFS
https://t.co/fwubiT1LnI
We congratulate Dr Younger on this funding and are glad this important research can continue. #pwme #scienceforME
This is fabulous! I love it so much 😍 not just the florals but all the amazing research work you do for #pwME. We appreciate it! 👏👏👏🙌🙌🙌😍😍😍🥰🥰🥰
#scienceheroes #myalgicE #MEcfs #scienceForME
Today the @CardingLab celebrate their very first #worldfloralshirtday raising money for @Invest_in_ME who support research at the
@TheQuadram Institute
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