RT @TomKindlon: The study it discusses is "Differentiating Multiple Sclerosis from #MyalgicEncephalomyelitis and #ChronicFatigueSyndrome" (…
The study it discusses is "Differentiating Multiple Sclerosis from #MyalgicEncephalomyelitis and #ChronicFatigueSyndrome" (2017) https://t.co/DmalVfLJEl A subsequent study with similar results is https://t.co/QKPfknEEv8 #MEcfs #CFS #MyalgicE https://t.co
RT @3tweetiebirds: Functional Status and Well-Being in People with Myalgic Encephalomyelitis/Chronic Fatigue Syndrome Compared with People…
RT @3tweetiebirds: Functional Status and Well-Being in People with Myalgic Encephalomyelitis/Chronic Fatigue Syndrome Compared with People…
Functional Status and Well-Being in People with Myalgic Encephalomyelitis/Chronic Fatigue Syndrome Compared with People with Multiple Sclerosis and Healthy Controls. https://t.co/JYysW2YFbg https://t.co/JYysW2YFbg
@MrsNickyClark Please read these papers on the quality of life and levels of disability of people with ME: https://t.co/RHzhtLVuCm https://t.co/6rvY1i7KQW Thank you.
RT @sfcmadrid: #SFCem y calidad de vida https://t.co/qiBvPJPDAw
RT @sfcmadrid: #SFCem y calidad de vida https://t.co/qiBvPJPDAw
#SFCem y calidad de vida https://t.co/qiBvPJPDAw
No toda la discapacidad es visible. En el siguiente enlace puedes ver el último estudio, realizado en Gran Bretaña, que compara la calidad de vida entre enfermos de esclerosis múltiple y enfermos de EM/SFC: https://t.co/ZB8KVLf4K1
RT @me_perspective: #MyalgicE Patienten sind laut Studien stärker behindert als MS Patienten, sind aber ohne medizische Versorgung! Schwers…
RT @julierehmeyer: People with ME/CFS are more disabled, poorer, and less able to work than people with MS. Given that, their mental health…
RT @sonya_lala_: @richardvallee Actually, #MEcfs is not as disabling on average as MS. ME/CFS is much, much worse. I know people with MS wh…
RT @sonya_lala_: @richardvallee Actually, #MEcfs is not as disabling on average as MS. ME/CFS is much, much worse. I know people with MS wh…
RT @sonya_lala_: @richardvallee Actually, #MEcfs is not as disabling on average as MS. ME/CFS is much, much worse. I know people with MS wh…
RT @ValeBodi: @johnthejack @PaulWhiteleyPhD Here's the correct link to the Kingdon's paper https://t.co/q1yQENJXo4
RT @ValeBodi: @johnthejack @PaulWhiteleyPhD Here's the correct link to the Kingdon's paper https://t.co/q1yQENJXo4
@johnthejack @PaulWhiteleyPhD Here's the correct link to the Kingdon's paper https://t.co/q1yQENJXo4
On recognizing "the disabling effects of #ME/CFS" @PaulWhiteleyPhD reflects on the recently Kingdon published paper - Functional Status and Well-being in #pwME/Cfs compared to #pwMS and #HC - https://t.co/q1yQENJXo4 #mecfs #pwME #disability #SF36v2 https:
@profmsharpe @PeterTatchell @NHScampaigners @saveournhs This statement by Michael relates to patients with ME which a recent study has shown "are measurably more disabled, work fewer hours and have lower incomes than people with Multiple Sclerosis. https:/
@richardvallee Actually, #MEcfs is not as disabling on average as MS. ME/CFS is much, much worse. I know people with MS who can run marathons. As a #pwme, I can’t even walk 2 houses down, let alone prepare my own food or bathe regularly. https://t.co/6UWyV
@maxdavie @wilshica @CoyneoftheRealm @dcweisman @simaspeciura @davecurtis314 I'd even doubt the correlation. It's weaker than for exemple in MS. https://t.co/P8Bvp9pWKA Also psychological dxs are simply attributed to you if you see a MP with ME. At least i
RT @ConneelyD: The latest research on how debilitating #ChronicFatigueSyndrome #MECFS is. https://t.co/HdDKD2TnGP Functional Status and We…
Functional Status and Well-Being in People with Myalgic Encephalomyeli - Springer https://t.co/AS8yrMH7oj via @nuzzel thanks @justask
RT @PatientJournal: Wow! This article has now been downloaded 19,000 times since it was published on 13 March. @ApplHealthEcon https://t.co…
Wow! This article has now been downloaded 19,000 times since it was published on 13 March. @ApplHealthEcon https://t.co/WxZ3d65ZY9
RT @ConneelyD: The latest research on how debilitating #ChronicFatigueSyndrome #MECFS is. https://t.co/HdDKD2TnGP Functional Status and We…
RT @TomKindlon: This open access paper has been downloaded a huge number of times (18,000!) since it was published on March 13. https://t.…
RT @keithgeraghty: Neat observation in recent @mecfsbiobank paper - UK cohort same as US cohort which confirms Unger's table that its physi…
RT @ssppeerroo: New from Nacul: "Functional Status and Well-Being in People with ME/CFS Compared with People with Multiple Sclerosis and He…
RT @sonya_lala_: Hey, @NIHDirector @NINDSdirector, any idea why #pwME don’t do more advocacy or fund more research? Here’s a clue: "More pe…
RT @Hervorrager: Are you still thinking #MECFS is only a little bit #fatigue? Are you still thinking MECFS is a #psychosomatic #disease? Ar…
RT @sonya_lala_: Hey, @NIHDirector @NINDSdirector, any idea why #pwME don’t do more advocacy or fund more research? Here’s a clue: "More pe…
RT @Dr_M_Guthridge: New UK study suggests that in almost all areas measured, people with #MECFS experience greater impact of their disease…
RT @Dr_M_Guthridge: New UK study suggests that in almost all areas measured, people with #MECFS experience greater impact of their disease…
RT @sonya_lala_: Hey, @NIHDirector @NINDSdirector, any idea why #pwME don’t do more advocacy or fund more research? Here’s a clue: "More pe…
RT @ConneelyD: The latest research on how debilitating #ChronicFatigueSyndrome #MECFS is. https://t.co/HdDKD2TnGP Functional Status and We…
RT @ConneelyD: The latest research on how debilitating #ChronicFatigueSyndrome #MECFS is. https://t.co/HdDKD2TnGP Functional Status and We…
RT @ConneelyD: The latest research on how debilitating #ChronicFatigueSyndrome #MECFS is. https://t.co/HdDKD2TnGP Functional Status and We…
RT @ConneelyD: The latest research on how debilitating #ChronicFatigueSyndrome #MECFS is. https://t.co/HdDKD2TnGP Functional Status and We…
RT @TomKindlon: This open access paper has been downloaded a huge number of times (18,000!) since it was published on March 13. https://t.…
RT @omega_oxon: "These findings should encourage the health community to recognise the disabling effects of ME/CFS, to advocate for the nee…
RT @ConneelyD: The latest research on how debilitating #ChronicFatigueSyndrome #MECFS is. https://t.co/HdDKD2TnGP Functional Status and We…
RT @Hervorrager: Are you still thinking #MECFS is only a little bit #fatigue? Are you still thinking MECFS is a #psychosomatic #disease? Ar…
RT @omega_oxon: "These findings should encourage the health community to recognise the disabling effects of ME/CFS, to advocate for the nee…
RT @ChronicallyTina: @FrancisCollins @NIHDIRECTOR @NINDSdirector @Washingtonpost Its time you help us... Decades of malfeasance is enough!…
@BBCWomansHour @janegarvey1 The diagram tells the story. https://t.co/v8743cU2Wc
RT @omega_oxon: "These findings should encourage the health community to recognise the disabling effects of ME/CFS, to advocate for the nee…
RT @ConneelyD: The latest research on how debilitating #ChronicFatigueSyndrome #MECFS is. https://t.co/HdDKD2TnGP Functional Status and We…
RT @ConneelyD: The latest research on how debilitating #ChronicFatigueSyndrome #MECFS is. https://t.co/HdDKD2TnGP Functional Status and We…
RT @ConneelyD: The latest research on how debilitating #ChronicFatigueSyndrome #MECFS is. https://t.co/HdDKD2TnGP Functional Status and We…
RT @ConneelyD: The latest research on how debilitating #ChronicFatigueSyndrome #MECFS is. https://t.co/HdDKD2TnGP Functional Status and We…
RT @sonya_lala_: Hey, @NIHDirector @NINDSdirector, any idea why #pwME don’t do more advocacy or fund more research? Here’s a clue: "More pe…
RT @sonya_lala_: Hey, @NIHDirector @NINDSdirector, any idea why #pwME don’t do more advocacy or fund more research? Here’s a clue: "More pe…
RT @omega_oxon: "These findings should encourage the health community to recognise the disabling effects of ME/CFS, to advocate for the nee…
RT @ConneelyD: The latest research on how debilitating #ChronicFatigueSyndrome #MECFS is. https://t.co/HdDKD2TnGP Functional Status and We…
RT @ConneelyD: The latest research on how debilitating #ChronicFatigueSyndrome #MECFS is. https://t.co/HdDKD2TnGP Functional Status and We…
Are you still thinking #MECFS is only a little bit #fatigue? Are you still thinking MECFS is a #psychosomatic #disease? Are you still thinking patients only have to pull themselves together? Are you able to read English scientific papers? Then read! #Gover
RT @ChronicallyTina: @FrancisCollins @NIHDIRECTOR @NINDSdirector @Washingtonpost Its time you help us... Decades of malfeasance is enough!…
RT @ChronicallyTina: @FrancisCollins @NIHDIRECTOR @NINDSdirector @Washingtonpost Its time you help us... Decades of malfeasance is enough!…
RT @sonya_lala_: Hey, @NIHDirector @NINDSdirector, any idea why #pwME don’t do more advocacy or fund more research? Here’s a clue: "More pe…
@FrancisCollins @NIHDIRECTOR @NINDSdirector @Washingtonpost Its time you help us... Decades of malfeasance is enough! #MECFS #timeforunrest #millionsmissing #chronicillness #womenshealth #PRAYERTOSTFRANCISCOLLINS https://t.co/8r4oD95b5O
RT @sonya_lala_: Hey, @NIHDirector @NINDSdirector, any idea why #pwME don’t do more advocacy or fund more research? Here’s a clue: "More pe…
RT @sonya_lala_: Hey, @NIHDirector @NINDSdirector, any idea why #pwME don’t do more advocacy or fund more research? Here’s a clue: "More pe…
RT @sonya_lala_: Hey, @NIHDirector @NINDSdirector, any idea why #pwME don’t do more advocacy or fund more research? Here’s a clue: "More pe…
RT @sonya_lala_: Hey, @NIHDirector @NINDSdirector, any idea why #pwME don’t do more advocacy or fund more research? Here’s a clue: "More pe…
RT @sonya_lala_: Hey, @NIHDirector @NINDSdirector, any idea why #pwME don’t do more advocacy or fund more research? Here’s a clue: "More pe…
RT @sonya_lala_: Hey, @NIHDirector @NINDSdirector, any idea why #pwME don’t do more advocacy or fund more research? Here’s a clue: "More pe…
Hey, @NIHDirector @NINDSdirector, any idea why #pwME don’t do more advocacy or fund more research? Here’s a clue: "More people w #MEcfs than people w MS lost their jobs, and the income of people w ME decreased markedly more than for people w MS." https://t
RT @TomKindlon: This open access paper has been downloaded a huge number of times (18,000!) since it was published on March 13. https://t.…
RT @omega_oxon: "These findings should encourage the health community to recognise the disabling effects of ME/CFS, to advocate for the nee…
RT @omega_oxon: "These findings should encourage the health community to recognise the disabling effects of ME/CFS, to advocate for the nee…
RT @omega_oxon: "These findings should encourage the health community to recognise the disabling effects of ME/CFS, to advocate for the nee…
RT @TomKindlon: This open access paper has been downloaded a huge number of times (18,000!) since it was published on March 13. https://t.…
RT @omega_oxon: "These findings should encourage the health community to recognise the disabling effects of ME/CFS, to advocate for the nee…
RT @omega_oxon: "These findings should encourage the health community to recognise the disabling effects of ME/CFS, to advocate for the nee…
Funktioneller Status_im Vergleich_März 2018 ⌛️ME<MS ...🔋 https://t.co/gvynwQCHg8
RT @omega_oxon: "These findings should encourage the health community to recognise the disabling effects of ME/CFS, to advocate for the nee…
The latest research on how debilitating #ChronicFatigueSyndrome #MECFS is. https://t.co/HdDKD2TnGP Functional Status and Well-Being in People with Myalgic Encephalomyelitis/Chronic Fatigue Syndrome Compared with People with Multiple Sclerosis and Healthy
RT @omega_oxon: "These findings should encourage the health community to recognise the disabling effects of ME/CFS, to advocate for the nee…
RT @omega_oxon: "These findings should encourage the health community to recognise the disabling effects of ME/CFS, to advocate for the nee…
RT @TomKindlon: This open access paper has been downloaded a huge number of times (18,000!) since it was published on March 13. https://t.…
RT @TomKindlon: This open access paper has been downloaded a huge number of times (18,000!) since it was published on March 13. https://t.…
RT @TomKindlon: This open access paper has been downloaded a huge number of times (18,000!) since it was published on March 13. https://t.…
RT @TomKindlon: This open access paper has been downloaded a huge number of times (18,000!) since it was published on March 13. https://t.…
Wow! Validation! Hoorah! https://t.co/cEeJsDThGa
RT @TomKindlon: This open access paper has been downloaded a huge number of times (18,000!) since it was published on March 13. https://t.…
RT @TomKindlon: This open access paper has been downloaded a huge number of times (18,000!) since it was published on March 13. https://t.…
RT @TomKindlon: This open access paper has been downloaded a huge number of times (18,000!) since it was published on March 13. https://t.…
RT @TomKindlon: This open access paper has been downloaded a huge number of times (18,000!) since it was published on March 13. https://t.…
RT @TomKindlon: This open access paper has been downloaded a huge number of times (18,000!) since it was published on March 13. https://t.…
This open access paper has been downloaded a huge number of times (18,000!) since it was published on March 13. https://t.co/xsqM1Xvtai #MEcfs #CFS #MyalgicE #MyalgicEncephalomyelitis #ChronicFatigueSyndrome https://t.co/AeGonKGf53
People with #mecfs were measurably more disabled than PWMS or HCs. #cfs https://t.co/brrTpeIk29
RT @me_perspective: #MyalgicE Patienten sind laut Studien stärker behindert als MS Patienten, sind aber ohne medizische Versorgung! Schwers…
RT @sonya_lala_: This fantastic MS breakthrough may also have applications for #mecfs, a disease that disables 1-2.5 million Americans “mea…
This fantastic MS breakthrough may also have applications for #mecfs, a disease that disables 1-2.5 million Americans “measurably more than MS” per recent study https://t.co/ZI293txvnh and costs the U.S. $17-24B/yr. @JanetDafoe @NIHDirector @NINDSdirector
RT @MEAssociation: These findings should encourage the health community to: - recognise the disabling effects of #MECFS, - advocate for th…
RT @ssppeerroo: New from Nacul: "Functional Status and Well-Being in People with ME/CFS Compared with People with Multiple Sclerosis and He…
RT @sfcmadrid: Un estudio científico revela un severo nivel de discapacidad causado por #SFCem... https://t.co/IUeD9yOBRs