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X-WR-CALNAME:International Alliance of ALS/MND Associations
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DTSTART:20250309T070000
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DTSTART;TZID=America/Toronto:20250516T130000
DTEND;TZID=America/Toronto:20250516T140000
DTSTAMP:20261011T163008
CREATED:20250505T133224Z
LAST-MODIFIED:20250505T133245Z
UID:18477-1747400400-1747404000@www.als-mnd.org
SUMMARY:Webinar from Les Turner ALS Foundation: Breaking Barriers: Building a Health Equity Approach to Make ALS Livable for All
DESCRIPTION:About the Program \nUnderstanding our gaps in knowledge about the social and structural determinants of health inequities in ALS is integral to making sure ALS becomes a livable disease. In this session\, Dr. Chelsey R. Carter highlights several determinants and offers approaches to improve ALS epidemiology\, patient outcomes\, and disparities. By building a health equity approach for ALS\, she describes various research initiatives and inclusive care models to improve ALS care and research for individuals\, caregivers\, and families. \nThe Les Turner ALS Foundation is proud to offer this webinar at no cost to the ALS community. Thank you to the Gilbert & Jacqueline Fern Foundation & Mitsubishi Tanabe Pharma America for sponsoring this webinar. \nAbout the Speaker \nChelsey R. Carter is an Assistant Professor of Public Health in the Department of Social and Behavioral Sciences at Yale University\, with a secondary affiliation in the Department of Anthropology. Her research program examines how scientific knowledge production\, clinical care\, and systemic marginalization impact historically underrepresented communities affected by rare and neurodegenerative diseases like ALS. Dr. Carter is also undertaking a book project tentatively titled\, Finding the Forgotten: Race\, Bias\, and Care in the World of ALS\, which includes an ethnographic study of the diverse experiences of living with ALS\, and draws on over 15 years of experience with Black communities affected by ALS. She is Founder & Director of The LEITH (Lived Experiences Igniting Transformations in Health) Lab.
URL:https://www.als-mnd.org/event/webinar-from-les-turner-als-foundation-breaking-barriers-building-a-health-equity-approach-to-make-als-livable-for-all/
LOCATION:Newcastle United Football Club
ORGANIZER;CN="Les Turner ALS Foundation":MAILTO:info@lesturnerals.org
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DTSTART;TZID=America/Toronto:20250522T130000
DTEND;TZID=America/Toronto:20250522T170000
DTSTAMP:20261011T163008
CREATED:20250505T133432Z
LAST-MODIFIED:20250505T133432Z
UID:18480-1747918800-1747933200@www.als-mnd.org
SUMMARY:Webinar from Les Turner ALS Foundation: Tackling the Delay to ALS Diagnosis: How Can We Do Better?
DESCRIPTION:About the Program  \nJoin us for our May ALS Learning Series with Dr. Kelly Gwathmey from Virginia Commonwealth University. She will explore the causes and consequences of ALS diagnostic delay\, along with potential solutions to address this problem. A Q&A will follow. \nThe Les Turner ALS Foundation is proud to offer this webinar at no cost to the ALS community. Thank you to the Gilbert & Jacqueline Fern Foundation & Mitsubishi Tanabe Pharma America for sponsoring this webinar. \nAbout the Speaker  \nKelly Gwathmey is an Associate Professor of Neurology at Virginia Commonwealth University in Richmond\, Virginia. She studied Neuroscience and Behavioral Biology at Emory University in Atlanta\, Georgia. She then attended Eastern Virginia Medical School in Norfolk\, Virginia. Her Neurology and Clinical Neurophysiology training was completed at the University of Virginia. Following this\, she completed a Neuromuscular Medicine fellowship at both Brigham and Women’s Hospital and Massachusetts General Hospital in Boston. At the University of Virginia\, she started the multidisciplinary MDA clinic\, was co-director of the ALS clinic\, and was the fellowship director for both the Neuromuscular and Clinical Neurophysiology fellowships. She joined VCU in January 2019 and currently serves in the capacity of Neuromuscular Division Chair\, Neuromuscular Medicine Program Director and EMG Laboratory Director. Dr. Gwathmey sees a wide spectrum of neuromuscular patients and performs electrodiagnostic studies (nerve conduction studies and electromyography). Her research interests include environmental risk factors in ALS\, diagnostic delay in ALS\, and racial disparities in healthcare.
URL:https://www.als-mnd.org/event/webinar-from-les-turner-als-foundation-tackling-the-delay-to-als-diagnosis-how-can-we-do-better/
LOCATION:Online
CATEGORIES:Webinar
ORGANIZER;CN="Les Turner ALS Foundation":MAILTO:info@lesturnerals.org
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