RT @Dr_M_Guthridge: 4/ Many ME/CFS patients are too sick to work #MECFS is so disabling that only ~13% of patients are able to maintain fu…
RT @Dr_M_Guthridge: 4/ Many ME/CFS patients are too sick to work #MECFS is so disabling that only ~13% of patients are able to maintain fu…
RT @Dr_M_Guthridge: 4/ Many ME/CFS patients are too sick to work #MECFS is so disabling that only ~13% of patients are able to maintain fu…
RT @Dr_M_Guthridge: 4/ Many ME/CFS patients are too sick to work #MECFS is so disabling that only ~13% of patients are able to maintain fu…
RT @Dr_M_Guthridge: 4/ Many ME/CFS patients are too sick to work #MECFS is so disabling that only ~13% of patients are able to maintain fu…
RT @Dr_M_Guthridge: 4/ Many ME/CFS patients are too sick to work #MECFS is so disabling that only ~13% of patients are able to maintain fu…
RT @Dr_M_Guthridge: 4/ Many ME/CFS patients are too sick to work #MECFS is so disabling that only ~13% of patients are able to maintain fu…
RT @Dr_M_Guthridge: 4/ Many ME/CFS patients are too sick to work #MECFS is so disabling that only ~13% of patients are able to maintain fu…
RT @Dr_M_Guthridge: 4/ Many ME/CFS patients are too sick to work #MECFS is so disabling that only ~13% of patients are able to maintain fu…
RT @Dr_M_Guthridge: 4/ Many ME/CFS patients are too sick to work #MECFS is so disabling that only ~13% of patients are able to maintain fu…
RT @Dr_M_Guthridge: 4/ Many ME/CFS patients are too sick to work #MECFS is so disabling that only ~13% of patients are able to maintain fu…
Only 13% able to maintain full time employment. #MEawarenesshour #MEAwarenessHour https://t.co/vwX5pmZF9Y
4/ Beaucoup de malades d’EM/SFC sont trop souffrants pour travailler L’#EMSFC est tellement invalidant que seuls ~13% des malades peuvent travailler à temps plein contre 70% avant de tomber malade #EncephalomyeliteMyalgique #MEAwarenessHour https://t.co
RT @Dr_M_Guthridge: 4/ Many ME/CFS patients are too sick to work #MECFS is so disabling that only ~13% of patients are able to maintain fu…
RT @Dr_M_Guthridge: 4/ Many ME/CFS patients are too sick to work #MECFS is so disabling that only ~13% of patients are able to maintain fu…
RT @Dr_M_Guthridge: 4/ Many ME/CFS patients are too sick to work #MECFS is so disabling that only ~13% of patients are able to maintain fu…
RT @Dr_M_Guthridge: 4/ Many ME/CFS patients are too sick to work #MECFS is so disabling that only ~13% of patients are able to maintain fu…
RT @Dr_M_Guthridge: 4/ Many ME/CFS patients are too sick to work #MECFS is so disabling that only ~13% of patients are able to maintain fu…
RT @Dr_M_Guthridge: 4/ Many ME/CFS patients are too sick to work #MECFS is so disabling that only ~13% of patients are able to maintain fu…
RT @Dr_M_Guthridge: 4/ Many ME/CFS patients are too sick to work #MECFS is so disabling that only ~13% of patients are able to maintain fu…
RT @Dr_M_Guthridge: 4/ Many ME/CFS patients are too sick to work #MECFS is so disabling that only ~13% of patients are able to maintain fu…
RT @Dr_M_Guthridge: 4/ Many ME/CFS patients are too sick to work #MECFS is so disabling that only ~13% of patients are able to maintain fu…
4/ Many ME/CFS patients are too sick to work #MECFS is so disabling that only ~13% of patients are able to maintain full-time employment (FTE) compared to 70% FTE prior to disease #SickNotWeak #pwME #MyalgicEncephalomyelitis #ChronicIllness https://t.co
RT @MTackCVS: @TomKindlon @jennywren_10 @Huisarts_Vink @LouCorsius Kingdon CC, Bowman EW, Curran H, Nacul L, Lacerda EM. Functional Status…
@TomKindlon @jennywren_10 @Huisarts_Vink @LouCorsius Kingdon CC, Bowman EW, Curran H, Nacul L, Lacerda EM. Functional Status and Well-Being in People with Myalgic Encephalomyelitis/Chronic Fatigue Syndrome Compared with People with Multiple Sclerosis and H
We were very pleased to have Dr Eliana Lacerda from @mecfsbiobank to speak at our AGM last week. She spoke about several areas of research including "Functional Status and Well-Being in People with ME/CFS Compared with People with MS and Healthy Controls:
RT @Dr_M_Guthridge: Of these 13 diseases, Myalgic Encephalomyelitis/Chronic Fatigue Syndrome #MECFS patients have the lowest Quality of Lif…
As @Dr_M_Guthridge states - #mecfs patients have the lowest quality of life of all of the patients with of the illnesses included in this graph. Most, if not all, of the others have some form of effective treatment. M.E./C.F.S does not. #education
@StripyLightCIC
RT @Dr_M_Guthridge: Of these 13 diseases, Myalgic Encephalomyelitis/Chronic Fatigue Syndrome #MECFS patients have the lowest Quality of Lif…
RT @Dr_M_Guthridge: Of these 13 diseases, Myalgic Encephalomyelitis/Chronic Fatigue Syndrome #MECFS patients have the lowest Quality of Lif…
RT @Dr_M_Guthridge: 5. Yet #pwME have a worse quality of life than these 13 diseases @OfficialNIHR @NIH @NIHDirector #MECFS #chronicillnes…
RT @Dr_M_Guthridge: 5. Yet #pwME have a worse quality of life than these 13 diseases @OfficialNIHR @NIH @NIHDirector #MECFS #chronicillnes…
😞
RT @Dr_M_Guthridge: Of these 13 diseases, Myalgic Encephalomyelitis/Chronic Fatigue Syndrome #MECFS patients have the lowest Quality of Lif…
RT @Dr_M_Guthridge: 5. Yet #pwME have a worse quality of life than these 13 diseases @OfficialNIHR @NIH @NIHDirector #MECFS #chronicillnes…
RT @Dr_M_Guthridge: 5. Yet #pwME have a worse quality of life than these 13 diseases @OfficialNIHR @NIH @NIHDirector #MECFS #chronicillnes…
RT @Dr_M_Guthridge: 5. Yet #pwME have a worse quality of life than these 13 diseases @OfficialNIHR @NIH @NIHDirector #MECFS #chronicillnes…
RT @Dr_M_Guthridge: 5. Yet #pwME have a worse quality of life than these 13 diseases @OfficialNIHR @NIH @NIHDirector #MECFS #chronicillnes…
RT @Dr_M_Guthridge: 5. Yet #pwME have a worse quality of life than these 13 diseases @OfficialNIHR @NIH @NIHDirector #MECFS #chronicillnes…
RT @Dr_M_Guthridge: 5. Yet #pwME have a worse quality of life than these 13 diseases @OfficialNIHR @NIH @NIHDirector #MECFS #chronicillnes…
RT @Dr_M_Guthridge: 5. Yet #pwME have a worse quality of life than these 13 diseases @OfficialNIHR @NIH @NIHDirector #MECFS #chronicillnes…
RT @Dr_M_Guthridge: 5. Yet #pwME have a worse quality of life than these 13 diseases @OfficialNIHR @NIH @NIHDirector #MECFS #chronicillnes…
RT @Dr_M_Guthridge: 5. Yet #pwME have a worse quality of life than these 13 diseases @OfficialNIHR @NIH @NIHDirector #MECFS #chronicillnes…
RT @Dr_M_Guthridge: Of these 13 diseases, Myalgic Encephalomyelitis/Chronic Fatigue Syndrome #MECFS patients have the lowest Quality of Lif…
RT @Dr_M_Guthridge: 5. Yet #pwME have a worse quality of life than these 13 diseases @OfficialNIHR @NIH @NIHDirector #MECFS #chronicillnes…
RT @Dr_M_Guthridge: 5. Yet #pwME have a worse quality of life than these 13 diseases @OfficialNIHR @NIH @NIHDirector #MECFS #chronicillnes…
RT @Dr_M_Guthridge: 5. Yet #pwME have a worse quality of life than these 13 diseases @OfficialNIHR @NIH @NIHDirector #MECFS #chronicillnes…
5. Yet #pwME have a worse quality of life than these 13 diseases @OfficialNIHR @NIH @NIHDirector #MECFS #chronicillness https://t.co/uG0FJO8Krp
RT @Dr_M_Guthridge: 4. Patients with Myalgic Encephalomyelitis #MyalgicE are more disabled than those with #MultipleSclerosis https://t.co/…
RT @Dr_M_Guthridge: 4. Patients with Myalgic Encephalomyelitis #MyalgicE are more disabled than those with #MultipleSclerosis https://t.co/…
RT @Dr_M_Guthridge: 4. Patients with Myalgic Encephalomyelitis #MyalgicE are more disabled than those with #MultipleSclerosis https://t.co/…
RT @Dr_M_Guthridge: 4. Patients with Myalgic Encephalomyelitis #MyalgicE are more disabled than those with #MultipleSclerosis https://t.co/…
RT @Dr_M_Guthridge: 4. Patients with Myalgic Encephalomyelitis #MyalgicE are more disabled than those with #MultipleSclerosis https://t.co/…
@PaulaLorgelly @ruth_howells @RitaINdeFaria @NICEcomms @ApplHealthEcon Ha Ha - now i don't want to disappoint you but he had an article with 28K downloads last year https://t.co/NNkuLpxetD
RT @Dr_M_Guthridge: 4. Patients with Myalgic Encephalomyelitis #MyalgicE are more disabled than those with #MultipleSclerosis https://t.co/…
RT @Dr_M_Guthridge: 4. Patients with Myalgic Encephalomyelitis #MyalgicE are more disabled than those with #MultipleSclerosis https://t.co/…
RT @Dr_M_Guthridge: 4. Patients with Myalgic Encephalomyelitis #MyalgicE are more disabled than those with #MultipleSclerosis https://t.co/…
RT @Dr_M_Guthridge: 4. Patients with Myalgic Encephalomyelitis #MyalgicE are more disabled than those with #MultipleSclerosis https://t.co/…
4. Patients with Myalgic Encephalomyelitis #MyalgicE are more disabled than those with #MultipleSclerosis https://t.co/16BZwDaEe6 Yet #MECFS was not included in this @TheLancetNeuro study on neurological disease burden #millionsmissing #pwME https://t.co
RT @Dr_M_Guthridge: @MMissingGermany @Berlijntje I selected the diseases in the graph (above) to compare with #MECFS for 2 reasons: 1. the…
RT @Dr_M_Guthridge: @MMissingGermany @Berlijntje I selected the diseases in the graph (above) to compare with #MECFS for 2 reasons: 1. the…
@AnjaLenaerts @MMissingGermany Also Anja, I didnt include #Dementia in the above pie chart because I couldnt include all diseases. The rationale for selecting the diseases for the pie chart is outlined in the tweets below: https://t.co/w2atbQxFWB
@MMissingGermany @Berlijntje I selected the diseases in the graph (above) to compare with #MECFS for 2 reasons: 1. the diseases have been compared to #MECFS (2 pubs linked below) and ALL have a quality of life measurably worse than ME/CFS https://t.co/16
RT @Dr_M_Guthridge: By 2021, only 19% will remain in full-time employment. The debilitating symptoms of #MECFS make full-time work imposs…
RT @Dr_M_Guthridge: By 2021, most of the ~9,900 #MECFS patients will struggle with financial insecurity with an average lost earnings of £2…
@ChrisCoons @SenatorCarper @LisaBRochester yet #myalgicE has one of the lowest Funds 4 NIH research. our researchers need $ for bigger studies. Still facing years of neglect. Minimal care. No fda treatment . few docs diagnosed/ treat. R we worthless?👇
The least studied diseases are, ironically, the ones one has almost zero influence on by making lifestyle changes. In other words: prevention is impossible. So the most biomedical research goes to diseases which would be much less common if people adopt he
RT @Dr_M_Guthridge: Of these 13 diseases, Myalgic Encephalomyelitis/Chronic Fatigue Syndrome #MECFS patients have the lowest Quality of Lif…
RT @Dr_M_Guthridge: Of these 13 diseases, Myalgic Encephalomyelitis/Chronic Fatigue Syndrome #MECFS patients have the lowest Quality of Lif…
RT @Dr_M_Guthridge: Of these 13 diseases, Myalgic Encephalomyelitis/Chronic Fatigue Syndrome #MECFS patients have the lowest Quality of Lif…
@RepSwalwell for years your constituents have been begging for your leadership in stopping the medical abuse of constituents w/ devastating #MyalgicEncephalomyelitis #MEcfs in CA-15 and across the nation. Not one FDA-approved medication! Where are you?
RT @Dr_M_Guthridge: By 2021, most of the ~9,900 #MECFS patients will struggle with financial insecurity with an average lost earnings of £2…
RT @Hervorrager: Functional Status & Well-Being in People with #MECFS @dg_mecfs @VdK_Deutschland @Paritaet @Caritas_web @CaritasEuropa @je…
Functional Status & Well-Being in People with #MECFS @dg_mecfs @VdK_Deutschland @Paritaet @Caritas_web @CaritasEuropa @jensspahn @AnjaKarliczek @RobertHabeck @ABaerbock @jusos @gruene_jugend @MariaKlSchmeink @BayernSPD @CSU @LudwigHartmann @KathaSchul
Stigma loses to facts #MECFS
RT @Dr_M_Guthridge: By 2021, most of the ~9,900 #MECFS patients will struggle with financial insecurity with an average lost earnings of £2…
RT @Dr_M_Guthridge: By 2021, only 19% will remain in full-time employment. The debilitating symptoms of #MECFS make full-time work imposs…
Functional Status & Well-Being in People with #MECFS Patients more disabled than people affected by multiple sclerosis (#MS)! ME associated with reduction in time spent at work & lower income! @BMG_Bund @BMBF_Bund @MelanieHuml @cducsubt @spdbt @Die
RT @Dr_M_Guthridge: By 2021, only 19% will remain in full-time employment. The debilitating symptoms of #MECFS make full-time work imposs…
RT @Dr_M_Guthridge: By 2021, most of the ~9,900 #MECFS patients will struggle with financial insecurity with an average lost earnings of £2…
RT @Dr_M_Guthridge: By 2021, only 19% will remain in full-time employment. The debilitating symptoms of #MECFS make full-time work imposs…
RT @Dr_M_Guthridge: By 2021, most of the ~9,900 #MECFS patients will struggle with financial insecurity with an average lost earnings of £2…
RT @Dr_M_Guthridge: By 2021, only 19% will remain in full-time employment. The debilitating symptoms of #MECFS make full-time work imposs…
RT @Dr_M_Guthridge: By 2021, most of the ~9,900 #MECFS patients will struggle with financial insecurity with an average lost earnings of £2…
RT @Dr_M_Guthridge: Of these 13 diseases, Myalgic Encephalomyelitis/Chronic Fatigue Syndrome #MECFS patients have the lowest Quality of Lif…
RT @Dr_M_Guthridge: By 2021, most of the ~9,900 #MECFS patients will struggle with financial insecurity with an average lost earnings of £2…
RT @Dr_M_Guthridge: By 2021, only 19% will remain in full-time employment. The debilitating symptoms of #MECFS make full-time work imposs…
RT @Dr_M_Guthridge: By 2021, only 19% will remain in full-time employment. The debilitating symptoms of #MECFS make full-time work imposs…
RT @Dr_M_Guthridge: By 2021, most of the ~9,900 #MECFS patients will struggle with financial insecurity with an average lost earnings of £2…
RT @Dr_M_Guthridge: Of these 13 diseases, Myalgic Encephalomyelitis/Chronic Fatigue Syndrome #MECFS patients have the lowest Quality of Lif…
RT @Dr_M_Guthridge: By 2021, most of the ~9,900 #MECFS patients will struggle with financial insecurity with an average lost earnings of £2…
RT @Dr_M_Guthridge: By 2021, only 19% will remain in full-time employment. The debilitating symptoms of #MECFS make full-time work imposs…
RT @Dr_M_Guthridge: By 2021, most of the ~9,900 #MECFS patients will struggle with financial insecurity with an average lost earnings of £2…
RT @Dr_M_Guthridge: By 2021, most of the ~9,900 #MECFS patients will struggle with financial insecurity with an average lost earnings of £2…
RT @Dr_M_Guthridge: By 2021, most of the ~9,900 #MECFS patients will struggle with financial insecurity with an average lost earnings of £2…
RT @Dr_M_Guthridge: By 2021, only 19% will remain in full-time employment. The debilitating symptoms of #MECFS make full-time work imposs…
By 2021, most of the ~9,900 #MECFS patients will struggle with financial insecurity with an average lost earnings of £20,000pa @FamHealthGuide @gmcuk @mjauk @RCPLondon @RoySocMed @TheBMA #medtwitter https://t.co/6Jh0jknLnq