BEGIN:VCALENDAR
VERSION:2.0
PRODID:-//International Alliance of ALS/MND Associations - ECPv6.8.3//NONSGML v1.0//EN
CALSCALE:GREGORIAN
METHOD:PUBLISH
X-WR-CALNAME:International Alliance of ALS/MND Associations
X-ORIGINAL-URL:https://www.als-mnd.org
X-WR-CALDESC:Events for International Alliance of ALS/MND Associations
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BEGIN:VTIMEZONE
TZID:America/New_York
BEGIN:DAYLIGHT
TZOFFSETFROM:-0500
TZOFFSETTO:-0400
TZNAME:EDT
DTSTART:20260308T070000
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BEGIN:STANDARD
TZOFFSETFROM:-0400
TZOFFSETTO:-0500
TZNAME:EST
DTSTART:20261101T060000
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BEGIN:VEVENT
DTSTART;TZID=America/New_York:20261021T070000
DTEND;TZID=America/New_York:20261021T083000
DTSTAMP:20261021T010412
CREATED:20260417T182222Z
LAST-MODIFIED:20260807T113704Z
UID:19429-1792566000-1792571400@www.als-mnd.org
SUMMARY:Member Roundtable: Defining Rights in the Genetics Era of ALS/MND
DESCRIPTION:As genetics becomes increasingly relevant in ALS/MND care and research\, important questions are emerging around access\, consent\, privacy\, equity\, and support. This member roundtable will examine what rights should guide policy and practice in the genetics era\, and how the global community can respond.\n \nGroup discussion (two options to accommodate time zones):\n\nGroup 1: 9:00–10:30 AM ET\nGroup 2: 6:00–7:30 PM ET\n\nRegistration Note: Members only. To register or request more information\, email alliance@als-mnd.org.
URL:https://www.als-mnd.org/event/member-roundtable-defining-rights-in-the-genetics-era-of-als-mnd/
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