How freakin scary is that???? https://t.co/r8TWGxzw2e
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…
Evident & worrying that many medical institutions & practitioners have trouble accepting why ME (G93.3) & MS (G35) are classified by .@WHO under the same ICD chapter: Diseases of the nervous system. And causes of BOTH remain a mystery. https://
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 @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 @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…
‘People with myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) continue to struggle to have their condition recognised as disabling in the face of public and professional prejudice and discrimination.’ read on @CMA_Docs @IRSC_CIHR @PHAC_GC https
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 @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 @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 @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 @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 @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 @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…
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 comparison set!) My guess a lot of the difference is due to the fact that most people's ME is 100% untreated. https://t.co/nAsoLmD
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 @julierehmeyer: People with ME/CFS are more disabled, poorer, and less able to work than people with MS. Given that, their mental health…
New UK study suggests that in almost all areas measured, people with #MECFS experience greater impact of their disease on life functioning/employment than people with Multiple Sclerosis. https://t.co/nPB0JqKnOj https://t.co/pPb7DMJKMa
RT @mecfsbiobank: -- NEW PAPER PUBLISHED -- Kingdon et al., "Functional Status and Well-Being in People with Myalgic Encephalomyelitis/Chr…
RT @keithgeraghty: Neat observation in recent @mecfsbiobank paper - UK cohort same as US cohort which confirms Unger's table that its physi…
RT @keithgeraghty: Neat observation in recent @mecfsbiobank paper - UK cohort same as US cohort which confirms Unger's table that its physi…
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 @julierehmeyer: People with ME/CFS are more disabled, poorer, and less able to work than people with MS. Given that, their mental health…
RT @mecfsbiobank: -- NEW PAPER PUBLISHED -- Kingdon et al., "Functional Status and Well-Being in People with Myalgic Encephalomyelitis/Chr…
RT @marydimmock: Kingdon et al... "These findings should encourage the health community to recognise the disabling effects of ME/CFS, to ad…
RT @marydimmock: Kingdon et al... "These findings should encourage the health community to recognise the disabling effects of ME/CFS, to ad…
RT @TinaRodwell1: And yet for decades our Dr are taught the opposite. Cherry picking research, hiding facts, covering the truth as a politi…
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 @julierehmeyer: People with ME/CFS are more disabled, poorer, and less able to work than people with MS. Given that, their mental health…
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 @mecfsbiobank: -- NEW PAPER PUBLISHED -- Kingdon et al., "Functional Status and Well-Being in People with Myalgic Encephalomyelitis/Chr…
RT @mecfsbiobank: -- NEW PAPER PUBLISHED -- Kingdon et al., "Functional Status and Well-Being in People with Myalgic Encephalomyelitis/Chr…
RT @TinaRodwell1: And yet for decades our Dr are taught the opposite. Cherry picking research, hiding facts, covering the truth as a politi…
RT @mecfsbiobank: -- NEW PAPER PUBLISHED -- Kingdon et al., "Functional Status and Well-Being in People with Myalgic Encephalomyelitis/Chr…
RT @mecfsbiobank: -- NEW PAPER PUBLISHED -- Kingdon et al., "Functional Status and Well-Being in People with Myalgic Encephalomyelitis/Chr…
Oh, VERY interesting. https://t.co/LijsX9xewJ
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 @mecfsbiobank: -- NEW PAPER PUBLISHED -- Kingdon et al., "Functional Status and Well-Being in People with Myalgic Encephalomyelitis/Chr…
RT @TinaRodwell1: And yet for decades our Dr are taught the opposite. Cherry picking research, hiding facts, covering the truth as a politi…
RT @mecfsbiobank: -- NEW PAPER PUBLISHED -- Kingdon et al., "Functional Status and Well-Being in People with Myalgic Encephalomyelitis/Chr…
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 @TinaRodwell1: And yet for decades our Dr are taught the opposite. Cherry picking research, hiding facts, covering the truth as a politi…
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 @julierehmeyer: People with ME/CFS are more disabled, poorer, and less able to work than people with MS. Given that, their mental health…
RT @ValeBodi: https://t.co/1sf9c4UrDa #pwME #SF36 score vs. #pwMS https://t.co/Blnqfyosda
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 @julierehmeyer: People with ME/CFS are more disabled, poorer, and less able to work than people with MS. Given that, their mental health…
RT @keithgeraghty: Neat observation in recent @mecfsbiobank paper - UK cohort same as US cohort which confirms Unger's table that its physi…
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 @julierehmeyer: People with ME/CFS are more disabled, poorer, and less able to work than people with MS. Given that, their mental health…
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 @julierehmeyer: People with ME/CFS are more disabled, poorer, and less able to work than people with MS. Given that, their mental health…
RT @TinaRodwell1: And yet for decades our Dr are taught the opposite. Cherry picking research, hiding facts, covering the truth as a politi…
RT @mecfsbiobank: -- NEW PAPER PUBLISHED -- Kingdon et al., "Functional Status and Well-Being in People with Myalgic Encephalomyelitis/Chr…
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 @julierehmeyer: People with ME/CFS are more disabled, poorer, and less able to work than people with MS. Given that, their mental health…
So grateful that my disability status application was accepted in Canada and that I have a supportive husband with a good job and doctors that have believed me from day one. I hear way too many #MECFS horror stories to not be grateful. https://t.co/rJkK9vw
Given that, the #NIH severely underfunds #MECFS vs #MultipleSclerosis despite more than double, triple, quadruple the people affected. https://t.co/RCkGSG928E
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 @keithgeraghty: Neat observation in recent @mecfsbiobank paper - UK cohort same as US cohort which confirms Unger's table that its physi…
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 @mecfsbiobank: -- NEW PAPER PUBLISHED -- Kingdon et al., "Functional Status and Well-Being in People with Myalgic Encephalomyelitis/Chr…
RT @julierehmeyer: People with ME/CFS are more disabled, poorer, and less able to work than people with MS. Given that, their mental health…
And yet for decades our Dr are taught the opposite. Cherry picking research, hiding facts, covering the truth as a political gain and empire building against public health is scandalous who gains #PACEtrialMafia https://t.co/EBz0RN33gX
RT @julierehmeyer: People with ME/CFS are more disabled, poorer, and less able to work than people with MS. Given that, their mental health…
People with ME/CFS are more disabled, poorer, and less able to work than people with MS. Given that, their mental health isn't bad. https://t.co/LDtOewev57
RT @mecfsbiobank: -- NEW PAPER PUBLISHED -- Kingdon et al., "Functional Status and Well-Being in People with Myalgic Encephalomyelitis/Chr…
RT @mecfsbiobank: -- NEW PAPER PUBLISHED -- Kingdon et al., "Functional Status and Well-Being in People with Myalgic Encephalomyelitis/Chr…
RT @keithgeraghty: Neat observation in recent @mecfsbiobank paper - UK cohort same as US cohort which confirms Unger's table that its physi…
RT @dxrevisionwatch: Functional Status and Well-Being in People with Myalgic Encephalomyelitis/ Chronic Fatigue Syndrome Compared with Peop…