tag:blogger.com,1999:blog-5704399741044225276.post2383874395666801435..comments2023-05-17T13:30:54.725-07:00Comments on X-treme denial: Leona Aglukkaq thinks 5 cents per patient for ME research is okAnonymoushttp://www.blogger.com/profile/12281551619335996831noreply@blogger.comBlogger1125tag:blogger.com,1999:blog-5704399741044225276.post-62049962076681622632013-02-04T13:20:01.411-08:002013-02-04T13:20:01.411-08:00That's excellent, Kati. You might be intereste...That's excellent, Kati. You might be interested in an article in today's Toronto Star. It's entitled "Side-effects reporting bolstered". It's interesting because, in this case, Leona Aglukkaq is promising federal action on that issue which includes Health Canada placing notices in 22 journals for health professionals about the issue AND commissioning Accreditation Canada to develop a new standard for reporting to be used by certified health-care centres. So, if Health Canada can do outreach like that for adverse effects reporting, then why not for educating health professionals on ME?Anonymousnoreply@blogger.com