I called the Province of Ontario to ask if there would be a Center (U.S. spelling) of Excellence in Ontario in the future and they said the only resources for my daughter would be the Nightingale Foundation and the ME association of Ontario (http://www.meao.ca/) in the Province. Isn't the Nightingale Foundation Dr. Byron Hyde costing quite a few thousands $? I then sent an email to the Premier's Office asking when a Centre would be available. I encourage everyone in Ontario to write the Premier's Office or your local MP to move this along. Given that there will be an International Conference in the Province in September, I think the Provincial Government should take respectable steps to offer hope - an announceable so people can be diagnosed rather than float around to multi-doctors who have no understanding of cfs/me. You can post a message with Premier Dalton McGuinty's Office at https://correspondence.premier.gov.on.ca/en/feedback/feedback.aspx There is no need to leave address information or anything - just send a message so they understand the benefits or needs.