Numb. That\u2019s how Lois Miller describes having MS. \u201cI\u2019m not just talking about the physical side of the disease. I\u2019m talking about the mental side, too,\u201d she says. \u201cI often experience the sensation of my body going numb, from head to toe. But I\u2019m numb every time that I stop and think: I have MS.\u201d<\/p>\n
Lois was referred to Dr. Micheal Levin, the Saskatchewan MS Clinical Research Chair, who sees patients one day a week as part of his research and clinical work. Through Dr. Levin she met Dr. Valerie Verge, director of the Cameco MS Neuroscience Research Centre (CMSNRC).<\/p>\n
Her experience made her realize how important it is to fund MS Research. \u201cWe know more about what we don\u2019t know than we do know. We don\u2019t understand fully how to treat it or stop it from getting worse.\u201d<\/p>\n
As a result, Lois became an honourary ambassador for Golfun, the annual tournament organized to raise funds for the Cameco MS Neuroscience Research Centre (CMSNRC).<\/p>\n","protected":false},"excerpt":{"rendered":"
Numb. That\u2019s how Lois Miller describes having MS. \u201cI\u2019m not just talking about the physical side of the disease. I\u2019m talking about the mental side, too,\u201d she says. \u201cI often…<\/p>\n","protected":false},"author":1,"featured_media":201,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"_acf_changed":false,"_monsterinsights_skip_tracking":false,"_monsterinsights_sitenote_active":false,"_monsterinsights_sitenote_note":"","_monsterinsights_sitenote_category":0,"footnotes":""},"categories":[4],"tags":[],"acf":[],"yoast_head":"\n