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
RT @numeratrix: Measurably more than disabled than people with MS & yet my #MECFS is totally untreated due to no access to health coverage.…
RT @sfcmadrid: Un estudio científico revela un severo nivel de discapacidad causado por #SFCem... https://t.co/IUeD9yOBRs
RT @sfcmadrid: Un estudio científico revela un severo nivel de discapacidad causado por #SFCem... https://t.co/IUeD9yOBRs
Un estudio científico revela un severo nivel de discapacidad causado por #SFCem... https://t.co/IUeD9yOBRs
RT @Dr_M_Guthridge: @mecfsbiobank Yes, the Kingdon study (different to th 1988 Meg Porter study I quoted above) clearly document the severe…
RT @Dr_M_Guthridge: New UK study suggests that in almost all areas measured, people with #MECFS experience greater impact of their disease…
RT @me_perspective: #MyalgicE Patienten sind laut Studien stärker behindert als MS Patienten, sind aber ohne medizische Versorgung! Schwers…
RT @me_perspective: #MyalgicE Patienten sind laut Studien stärker behindert als MS Patienten, sind aber ohne medizische Versorgung! Schwers…
RT @jenbrea: A new study, but same finding has been made in several other countries (sorry MS folk, don't know why you guys are always the…
RT @me_perspective: #MyalgicE Patienten sind laut Studien stärker behindert als MS Patienten, sind aber ohne medizische Versorgung! Schwers…
RT @keithgeraghty: Neat observation in recent @mecfsbiobank paper - UK cohort same as US cohort which confirms Unger's table that its physi…
RT @mecfsbiobank: -- NEW PAPER PUBLISHED -- Kingdon et al., "Functional Status and Well-Being in People with Myalgic Encephalomyelitis/Chr…
RT @ME_Suffolk: The ME/CFS Biobank has just published research demonstrating that people with#MEcfs are "measurably more disabled " than pe…
RT @me_perspective: #MyalgicE Patienten sind laut Studien stärker behindert als MS Patienten, sind aber ohne medizische Versorgung! Schwers…
RT @me_perspective: #MyalgicE Patienten sind laut Studien stärker behindert als MS Patienten, sind aber ohne medizische Versorgung! Schwers…
RT @me_perspective: #MyalgicE Patienten sind laut Studien stärker behindert als MS Patienten, sind aber ohne medizische Versorgung! Schwers…
RT @me_perspective: #MyalgicE Patienten sind laut Studien stärker behindert als MS Patienten, sind aber ohne medizische Versorgung! Schwers…
RT @me_perspective: #MyalgicE Patienten sind laut Studien stärker behindert als MS Patienten, sind aber ohne medizische Versorgung! Schwers…
RT @me_perspective: #MyalgicE Patienten sind laut Studien stärker behindert als MS Patienten, sind aber ohne medizische Versorgung! Schwers…
RT @me_perspective: #MyalgicE Patienten sind laut Studien stärker behindert als MS Patienten, sind aber ohne medizische Versorgung! Schwers…
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 @me_perspective: #MyalgicE Patienten sind laut Studien stärker behindert als MS Patienten, sind aber ohne medizische Versorgung! Schwers…
RT @me_perspective: #MyalgicE Patienten sind laut Studien stärker behindert als MS Patienten, sind aber ohne medizische Versorgung! Schwers…
RT @me_perspective: #MyalgicE Patienten sind laut Studien stärker behindert als MS Patienten, sind aber ohne medizische Versorgung! Schwers…
#MyalgicE Patienten sind laut Studien stärker behindert als MS Patienten, sind aber ohne medizische Versorgung! Schwerst krank kämpfen viele seit Jahren um ihr Überleben. Es muss dringendst gehandelt werden! @jensspahn @AnjaKarliczek #MEdizinischerSkandal
Using SF-36v2™ scores as a proxy, people with ME/CFS were measurably more disabled than PWMS or HCs in this study population. https://t.co/xpf60cx7JV
RT @hankalapotilas: Uuden tutkimuksen mukaan CFS/ME:tä sairastavilla on selvästi huonompi fyysinen vointi ja toimintakyky kuin MS:ää sairas…
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 @julierehmeyer: People with ME/CFS are more disabled, poorer, and less able to work than people with MS. Given that, their mental health…
RT @ME_Suffolk: The ME/CFS Biobank has just published research demonstrating that people with#MEcfs are "measurably more disabled " than 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 @marydimmock: Kingdon et al... "These findings should encourage the health community to recognise the disabling effects of ME/CFS, to ad…
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…
@mecfsbiobank Yes, the Kingdon study (different to th 1988 Meg Porter study I quoted above) clearly document the severe impact on Health-Related Quality of Life (HRQoL) experienced by ME/CFS patients https://t.co/16BZwDaEe6 https://t.co/dqovmda9bX
RT @Dr_M_Guthridge: New UK study suggests that in almost all areas measured, people with #MECFS experience greater impact of their disease…
RT @jenbrea: A new study, but same finding has been made in several other countries (sorry MS folk, don't know why you guys are always the…
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 @Dr_M_Guthridge: New UK study suggests that in almost all areas measured, people with #MECFS experience greater impact of their disease…
Measurably more than disabled than people with MS & yet my #MECFS is totally untreated due to no access to health coverage. Hey @MinnesotaDHS & #mnleg your discriminatory MA rules & exclusions are killing people! https://t.co/cBjBdg1ipz
RT @jenbrea: A new study, but same finding has been made in several other countries (sorry MS folk, don't know why you guys are always the…
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 @Dr_M_Guthridge: New UK study suggests that in almost all areas measured, people with #MECFS experience greater impact of their disease…
RT @jenbrea: A new study, but same finding has been made in several other countries (sorry MS folk, don't know why you guys are always the…
RT @ME_Suffolk: The ME/CFS Biobank has just published research demonstrating that people with#MEcfs are "measurably more disabled " than 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 @julierehmeyer: People with ME/CFS are more disabled, poorer, and less able to work than people with MS. Given that, their mental health…
RT @Dr_M_Guthridge: New UK study suggests that in almost all areas measured, people with #MECFS experience greater impact of their disease…
RT @MEawareness: Evident & worrying that many medical institutions & practitioners have trouble accepting why ME (G93.3) & MS (G35) are cla…
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 @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 @Dr_M_Guthridge: New UK study suggests that in almost all areas measured, people with #MECFS experience greater impact of their disease…
RT @MEawareness: Evident & worrying that many medical institutions & practitioners have trouble accepting why ME (G93.3) & MS (G35) are cla…
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…
The ME/CFS Biobank has just published research demonstrating that people with#MEcfs are "measurably more disabled " than people with MS, yet @EastCoastCH have withdrawn support for benefit claims for #PwME https://t.co/3A8JLpSAGg https://t.co/ANvMdzmB3g
RT @jenbrea: A new study, but same finding has been made in several other countries (sorry MS folk, don't know why you guys are always the…
RT @Dr_M_Guthridge: New UK study suggests that in almost all areas measured, people with #MECFS experience greater impact of their disease…
RT @jenbrea: A new study, but same finding has been made in several other countries (sorry MS folk, don't know why you guys are always the…
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 @jenbrea: A new study, but same finding has been made in several other countries (sorry MS folk, don't know why you guys are always the…
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 @MEawareness: Evident & worrying that many medical institutions & practitioners have trouble accepting why ME (G93.3) & MS (G35) are cla…
RT @jenbrea: A new study, but same finding has been made in several other countries (sorry MS folk, don't know why you guys are always the…
RT @MEawareness: Evident & worrying that many medical institutions & practitioners have trouble accepting why ME (G93.3) & MS (G35) are cla…
RT @jenbrea: A new study, but same finding has been made in several other countries (sorry MS folk, don't know why you guys are always the…
RT @TinaRodwell1: And yet for decades our Dr are taught the opposite. Cherry picking research, hiding facts, covering the truth as a politi…
RT @jenbrea: A new study, but same finding has been made in several other countries (sorry MS folk, don't know why you guys are always the…
RT @Dr_M_Guthridge: New UK study suggests that in almost all areas measured, people with #MECFS experience greater impact of their disease…
RT @mecfsbiobank: -- NEW PAPER PUBLISHED -- Kingdon et al., "Functional Status and Well-Being in People with Myalgic Encephalomyelitis/Chr…
RT @jenbrea: A new study, but same finding has been made in several other countries (sorry MS folk, don't know why you guys are always the…
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 @jenbrea: A new study, but same finding has been made in several other countries (sorry MS folk, don't know why you guys are always the…
RT @jenbrea: A new study, but same finding has been made in several other countries (sorry MS folk, don't know why you guys are always the…
RT @jenbrea: A new study, but same finding has been made in several other countries (sorry MS folk, don't know why you guys are always the…
RT @jenbrea: A new study, but same finding has been made in several other countries (sorry MS folk, don't know why you guys are always the…
RT @MEAssociation: Latest study from the UK @MECFSBiobank team: 'This study suggests that at a group level people with ME/CFS are more disa…
RT @jenbrea: A new study, but same finding has been made in several other countries (sorry MS folk, don't know why you guys are always the…
RT @mecfsbiobank: -- NEW PAPER PUBLISHED -- Kingdon et al., "Functional Status and Well-Being in People with Myalgic Encephalomyelitis/Chr…
RT @MEAssociation: These findings should encourage the health community to: - recognise the disabling effects of #MECFS, - advocate for th…
RT @jenbrea: A new study, but same finding has been made in several other countries (sorry MS folk, don't know why you guys are always the…
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 @Dr_M_Guthridge: New UK study suggests that in almost all areas measured, people with #MECFS experience greater impact of their disease…