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People suffering from
#MECFS are so ill that they are no longer able to fight on the streets for medical care, research into and recognition of their disease. But we desperately want our lives back! For this aim we do whatever we still can: Welcome to another#MEawarenesshour.pic.twitter.com/B0H1r2PKH8
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»We could have our first transferable factor in
#MECFS blood« Big news from Prusty Lab at University of Würzburg! But they need financial resources to continue their great work. Now we all can help them out together! Retweets appreciated!#GOfundMECFS https://bit.ly/gofundmecfs pic.twitter.com/G7Gq6QMg4P
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Hello
@jenbrea, would you like to help us raising funds for#MECFS research by Prusty Lab at@Uni_WUE through spreading the news about our campaign?https://twitter.com/loy_daniel_de/status/1224694096457076736 …
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Cell-Based Blood Biomarkers for Myalgic Encephalomyelitis/Chronic Fatigue Syndrome. The authors say that a combination of three tests yields a biomarker with close to 100% sensitivity and specificity.
#MECFS https://www.preprints.org/manuscript/202002.0029/v1 …Prikaži ovu nit -
"Left Out" - an ME/CFS Movie of Commitment, Hope and Despair Pal Schaathun evocatively portrays the hopes and dreams of an ME/CFS community in dramatic fashion as two oncologist mount the largest drug trial ever in
#MECFS. https://www.healthrising.org/blog/2020/02/03/left-out-rituximab-chronic-fatigue-me-cfs/ … -
#MECFS has ruined my life! How pointless spending 8 years training and 15 years teaching. I had to leave my job. Sell our house. Get rid of my car. Use all of my savings to live. And no one is listening ! Where do we go from rock bottom?#MyalgicEncephalomyelitis#seeME -
Every Wednesday, worldwide (8pm UK time) on Twitter is
#MEAwarenessHour. It's a weekly online protest to raise awareness of the illness Myalgic Encephalomyelitis#MECFS I have created the following post as a guide on how to get involved#StrongerTogetherhttps://www.ajourneythroughthefog.co.uk/2020/02/please-join-us-for-me-awareness-hour/ … -
checkout our solution for
#MECFS tested & its free -
#Howitworks#MECFS solution Metformine generate energy & HuperzineA use that energy to repair ANS, Huperzine stay 10-14hrs in body produce oxygen to brain & cross blood brain barrier create/repair neurons too Metformine(1000)+HuperzineA(400mcg) dosage once/day testing https://twitter.com/TheSimpleMuscle/status/1224699308324331520 …
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We are testing metformine+huperzineA (both cheap to source) from past 2months for
#MECFS it targets ANS & fix every thing ANS connected to -so far results are amazing, its total independent energy solution, we r overwhelmed with results & now in 3rd month will share updates pic.twitter.com/bT9ogWoXdv
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»We might have our first transferable factor in
#MECFS blood«
But nevertheless there are no grants. So it is up to us. Help Prusty Lab finish the job by donating for their groundbreaking #MECFS research now!#GOfundMECFS PLEASE SHARE & DONATE
http://bit.ly/gofundmecfs https://twitter.com/BhupeshPrusty/status/1223242526188089344 …pic.twitter.com/3fMpyT2l56
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Twas fun while it lasted. Last-minute physio booked for this Friday morning, for pain management. Was hoping to last until next week but alas!
#chroniclife#MEcfs#sickdayshttps://twitter.com/1987clairebear/status/1224232671037001728 … -
Millions of people still die of cancer each year. We had some great successes (2.5 million lives saved past 25 years) but we need drastically more funding & research for all cancers & also debilitating diseases like
#MECFS &#aging & others. This is#warondisease!#WorldCancerDay
pic.twitter.com/1Eytb87ECf
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To everybody interested in
#MECFS: Stay tuned, we have a big announcement to make in exactly 90 minutes from now.
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Spent a 1 hr appointment with a medical specialist today explaining all about
#MECFS and then got slugged $220 for the privilege. That was the extent of my appt. Shouldn’t it work the other way round and#PWME get paid for educating the ‘experts’..???#WhyDoIBother -
#AbleismInFourWords is trending... All in your head You don't look sick Come on, try harder I get tired too Have you tried yoga? Sleeping all day? Lovely!#MECFS#pwME -
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Oh Happy Day! Thank you
@BhupeshPrusty for your continued research into#MECFS#letscureME!
https://twitter.com/BhupeshPrusty/status/1223242526188089344 … -
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@NINDSdirector what can you tell us about the brains in people w/#MEcfs? YOU are preventing research progress by persistently underfunding biomed research on#MECFS. $12 million in FY 2019 with no set-aside funds? Millions suffer in this living death because of YOUR apathy. pic.twitter.com/gUVuNuihfR
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