I hope to hear from as many people as possible around the world! Your thoughts will help me shape my annual letter.
Please share my call! It will be open for the next 24h.
Use #ShareWithTedros.
Together, for a healthier, fairer, safer w
rld!
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Thank you all for sharing your health hopes for 2020 with me! I will try to address as many as possible in my annual letter. Stay tuned! Together, for a healthier, safer, fairer w
rld! #HealthForAllpic.twitter.com/9lQIUCzQ8VDiesen Thread anzeigen
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Can you help us patients with ME/CFS? The challenge we face is that this devastating illness has been severely neglected. Doctors don't learn about it and/or are taught false information about it, for example that it's related to deconditioning and reversible with exercise.
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There is hardly any research and no treatment, patients usually go undiagnosed or are only diagnosed after many years. That needs to change.
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@DrTedros, this is the story of Myalgic Encephalomyelitis as I told it last year. Sufferers, whose lives are passing them by whilst lying in darkened rooms, unseen by the rest of the world, are desperate for biomedical research & treatments. Many have diedhttps://artzstudios1.wixsite.com/globaladvocatesmeicc/single-post/2018/05/17/Thank-you-Carol-Binks … -
@DrTedros this from Dr@JanetDafoe, Psychologist, Whitney’s Mum (pictured) & Ron Davis’ wife https://en.wikipedia.org/wiki/Ronald_W._Davis …. Dr Davis & team in race to save Whitney’s life & those of countless others with#ME. Complacent Health Authorities worldwide. Please help!https://twitter.com/janetdafoe/status/1201263264396496896?s=21 …
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That the millions of
#veterans,#chronicpain,#cancer and#sicklecell patients suffering in pain will be allowed their medication again, at whatever dose works best for them.#painpatientsvote#opioidhysteria -
Also that the DEA will be reigned in and no longer allowed to raid clinics & doctor's offices, destroying the physicians livelihood and leaving thousands of patients without a doctor. Why aren't they going after
#illicitfentanyl and#heroin?? Too hard?
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Dear Dr. Tedros, I wish in 2020 there will funding to research Myalgic Encephalomyelitis / Chronic Fatigue Syndrome
#mecfs Approx 30 Million people worldwide are terribly suffering, yet they do not receive any medical care. Greetings from Germany
pic.twitter.com/F0KV9fO9CLDiese Medien könnten sensibles Material enthalten. Mehr erfahren
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I hope that funding for M.E. increases to what it should be for the 30 million people who have it worldwide, that all doctors are taught to recognise it as the serious, neurological disease that it is, and that the harmful treatment of M.E. with GET and CBT is withdrawn.
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