Scott Simpson, Patient Advocate, Millions Missing Canada Mr. Scott Simpson is Co-founder of the ME advocacy group Millions Missing Canada. A three-time member of the national triathlon team, Scott first became sick with ME in August 2012. It would take another five years to get an official diagnosis. Scott worked with the medical humanitarian organization Dignitas International as an advocate to bring HIV medications to sub-Saharan Africa. Now, in an ironic twist of fate, he’s been forced to become an advocate to bring ME medications to Canada.
M. Scott Simpson est cofondateur de Millions Missing Canada, un groupe de défense des patients atteints d’EM. Ancien triathlonien sélectionné à trois reprises dans l’équipe nationale, M. Simpson est atteint d’EM depuis août 2012, mais a dû attendre cinq ans avant d’avoir un diagnostic officiel. M. Simpson a milité auprès de Dignitas International, une organisation humanitaire médicale, pour permettre à l’Afrique subsaharienne d’avoir accès à des médicaments contre le VIH. Aujourd’hui, il se bat pour que les Canadiens aient accès à des médicaments pour l’EM.
Montréal, du 3 au 5 mai 2018 Conférence collaborative canadienne sur l’EM/SFC Faire progresser un programme de recherche international en identifiant les priorités de recherche sur l’EM/SFC
9 mars 2018 - Dignitas International as an advocate to bring HIV medications to sub-Saharan Africa. Now, in an ironic twist of fate, he's been forced to become an advocate to bring ME medications to. Canada. M. Scott Simpson est cofondateur de Millio
20 avr. 2018 - Ms. Barbara Fifield, patient advocate and co- founder of Millions Missing Canada, has been profoundly affected with myalgic encephalomyelitis.
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