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International Alliance for M.E.
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== Projects == === 9 November 2016: protesting the Edward Shorter lecture === On 9 November 2016 the ME/CFS International Alliance, a predecessor of IAFME, published a protest letter against the planned lecture of historian [[Edward Shorter]] at the [[National Institutes of Health]].<ref>{{Cite web | url = https://www.actionforme.org.uk/news/me/cfs-international-alliance-protests-shorter-lecture/ | title = ME/CFS International Alliance protests Shorter lecture | last = | first = |website=Action for ME|access-date=2018-12-06 | date = | authorlink = |archive-url=|archive-date=|url-status=}}</ref> The letter listed ME/CFS advocates such as Carol Head and Jennifer Brea as "current members of the International Alliance", even though these persons did not gave formal consent to joining or supporting a new organisation.<ref>{{Cite web | url = https://forums.phoenixrising.me/index.php?threads/new-org-me-cfs-international-alliance.47920/ | title = New Org!: ME/CFS International Alliance | website = Phoenix Rising ME / CFS Forums|language=en|access-date=2018-12-06 | date = | last = | first = | authorlink = |archive-url=|archive-date=|url-status=}}</ref> ME patients were suspicious of the International Alliance as very little information was given about the organisation except for what appeared on the website of Action for ME, the UK charity that was behind the initiative. Nothing was heard about International Alliance until the existence of IAFME was announced one and a half years later.<ref>{{Cite web | url = https://www.s4me.info/threads/iame-international-alliance-for-me-anyone-know-about-them.4108/ | title = IAME -International Alliance For ME - anyone know about them?|website=Science for ME|language=en-US|access-date=2018-12-06 | date = | last = | first = | authorlink = |archive-url=|archive-date=|url-status=}}</ref> === 12 May 2018: MillionsMissing at Geneva === On 12 May 2018, IAFME organized a [[Millions Missing protests|MillionsMissing]] event in front of WHO headquarters, Geneva, Switzerland. A letter was send to Dr Tedros Ghebreyesus of the [[World Health Organization|WHO]] calling for urgent action action to address M.E. globally. IAFME asked the WHO to recognize ME as a chronic multisystem disease and to “support accelerated biomedical research to develop better diagnostic methods and treatments for M.E.”<ref name=":1" /> === 4 December 2018: the trans-national consensus document === On 4 December, 2018 IAFME produced a trans-national consensus document called “Recognition, research and respect: An agenda for change in ME”. It was supported by over 60 clinicians, researchers, and non-governmental organisations from 28 different countries. The signees include [[BACME]], the [[UK CFS/ME Research Collaborative]] and [[EUROMENE]]. The consensus document had three aims: 1) To provide an overview of M.E. and the disease burden, 2) To highlight barriers to progressing research in the M.E. field, 3) To propose an agenda for change.<ref>{{Cite web | url = https://twitter.com/IAforME/status/1069953598099021825 | title = We have produced a trans-national consensus document covering M.E. which has the support of over 60 clinicians, researchers and NGOs from 28 different countries | last = | first = | date = 2018-12-04 | website = IAforME|language=en|access-date=2018-12-06 | authorlink = |archive-url=|archive-date=|url-status=}}</ref> The document demands that definitions of ME include the hallmark symptom of the disease, post-exertional malaise, and to retire the broad Oxford and Fukuda criteria. The text reads: “Treatments, such as [[Cognitive behavioral therapy|CBT]] and [[Graded exercise therapy|GET]], tested using the criteria which does not require post-exertional malaise, should not be recommended for people with ME.” The document states that disease experts do not recommend GET or CBT but instead that patients manage their activities to stay within their “energy envelope” to prevent crashes. The IAFME also highlights another problem in ME-research, namely the lack of sick controls to show that changes are unique to ME rather than generic ill-health markers. The IAFME document has been applauded by ME advocates such as [[Mary Dimmock]]<ref>{{Cite web | url = https://twitter.com/marydimmock/status/1070355984617496584 | title = Excellent letter calling on WHO to provide leadership for people living with ME | last = Dimmock | first = Mary | date = 2018-12-05 | website = Twitter|language=en|access-date=2018-12-06 | authorlink = |archive-url=|archive-date=|url-status=}}</ref> but criticized by others. [[Ellen Goudsmit]] argued that it is too focused on the literature of proponents of cognitive behavioral therapy and doesn’t include adequate information about pacing.<ref>{{Cite web | url = https://www.facebook.com/IAforME/ | title = IAFME - International Alliance for ME|website=facebook|language=en|access-date=2018-12-06 | date = | last = | first = | authorlink = |archive-url=|archive-date=|url-status=}}</ref> Referencing the multiple ME outbreaks, [[Jerrold Spinhirne]] argued that it is incorrect for the document to call ME a non-communicable disease.<ref>https://www.facebook.com/groups/IAforME/</ref>
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