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Register todayAsk Questions Do you have a question about the latest research that you would like to ask our panel of MS experts? Submit them, and they’ll do their best to address them. Send in your question Invite Others to Join with #ECTRIMS4me Help us spread the word about Patient Community Day using the #ECTRIMS4me campaign. Visit the socialize and share webpage to invite others to participate. Post your support Why This Event Matters ECTRIMS understands the impact of MS and related neurological conditions on your lives. This event is a result of its commitment to share the groundbreaking research unveiled during its annual congress with the community that matters the most – YOU! Proudly Supported by the National MS Society The National MS Society is supporting this event because we passionately believe that such collaborations provide us with an invaluable opportunity to push the boundaries of our knowledge and forge a stronger, more resilient path of collective support and well-being. " c-nmssatomrichtext_nmssatomrichtext-host="">Patient Community Day – an online and onsite event hosted by the European Committee for Treatment and Research in Multiple Sclerosis (ECTRIMS) and supported by the National MS Society – is your opportunity to join a global gathering of education and support and learn about the latest advancements directly impacting your ongoing care and treatment options. Here are some things you can expect: Empowering Insights: A roundtable panel of international experts will simplify complex research and share knowledge that matters most to you.Engaging Q&A: Pose your questions to leading neurological experts and receive insightful answers about the latest research shaping your condition's landscape.Multilingual Experience: The event will be held in English, with AI-powered simultaneous translations in 50+ languages.Patient Community Day Event Details Friday, September 26 9 a.m. – 12 p.m. EDT Online or in-person at Barcelona International Convention Center This event is FREE to attend. Pre-registration is required so be sure to secure your spot in advance. Register today Ask Questions Do you have a question about the latest research that you would like to ask our panel of MS experts? Submit them, and they’ll do their best to address them. Send in your question Invite Others to Join with #ECTRIMS4me Help us spread the word about Patient Community Day using the #ECTRIMS4me campaign. Visit the socialize and share webpage to invite others to participate. Post your support Why This Event Matters ECTRIMS understands the impact of MS and related neurological conditions on your lives. This event is a result of its commitment to share the groundbreaking research unveiled during its annual congress with the community that matters the most – YOU! Proudly Supported by the National MS Society The National MS Society is supporting this event because we passionately believe that such collaborations provide us with an invaluable opportunity to push the boundaries of our knowledge and forge a stronger, more resilient path of collective support and well-being. Register todayAsk Questions Do you have a question about the latest research that you would like to ask our panel of MS experts? Submit them, and they’ll do their best to address them. Send in your question Invite Others to Join with #ECTRIMS4me Help us spread the word about Patient Community Day using the #ECTRIMS4me campaign. Visit the socialize and share webpage to invite others to participate. Post your support Why This Event Matters ECTRIMS understands the impact of MS and related neurological conditions on your lives. This event is a result of its commitment to share the groundbreaking research unveiled during its annual congress with the community that matters the most – YOU! Proudly Supported by the National MS Society The National MS Society is supporting this event because we passionately believe that such collaborations provide us with an invaluable opportunity to push the boundaries of our knowledge and forge a stronger, more resilient path of collective support and well-being. " c-nmssatomrichtext_nmssatomrichtext-host="">Patient Community Day – an online and onsite event hosted by the European Committee for Treatment and Research in Multiple Sclerosis (ECTRIMS) and supported by the National MS Society – is your opportunity to join a global gathering of education and support and learn about the latest advancements directly impacting your ongoing care and treatment options. Here are some things you can expect: Empowering Insights: A roundtable panel of international experts will simplify complex research and share knowledge that matters most to you.Engaging Q&A: Pose your questions to leading neurological experts and receive insightful answers about the latest research shaping your condition's landscape.Multilingual Experience: The event will be held in English, with AI-powered simultaneous translations in 50+ languages.Patient Community Day Event Details Friday, September 26 9 a.m. – 12 p.m. EDT Online or in-person at Barcelona International Convention Center This event is FREE to attend. Pre-registration is required so be sure to secure your spot in advance. Register today Ask Questions Do you have a question about the latest research that you would like to ask our panel of MS experts? Submit them, and they’ll do their best to address them. Send in your question Invite Others to Join with #ECTRIMS4me Help us spread the word about Patient Community Day using the #ECTRIMS4me campaign. Visit the socialize and share webpage to invite others to participate. Post your support Why This Event Matters ECTRIMS understands the impact of MS and related neurological conditions on your lives. This event is a result of its commitment to share the groundbreaking research unveiled during its annual congress with the community that matters the most – YOU! Proudly Supported by the National MS Society The National MS Society is supporting this event because we passionately believe that such collaborations provide us with an invaluable opportunity to push the boundaries of our knowledge and forge a stronger, more resilient path of collective support and well-being. nationalmssociety.org, Facebook , X (formerly known as Twitter), Instagram , YouTube or 1-800-344-4867 . " c-nmssatomrichtext_nmssatomrichtext-host="">About Multiple Sclerosis Multiple sclerosis is an unpredictable disease of the central nervous system. Currently there is no cure. Symptoms vary from person to person and may include disabling fatigue, mobility challenges, cognitive changes, and vision issues. An estimated 1 million people live with MS in the United States. Early diagnosis and treatment are critical to minimize disability. Significant progress is being made to achieve a world free of MS. About the National Multiple Sclerosis Society The National MS Society, founded in 1946, is the global leader of a growing movement dedicated to creating a world free of MS. The Society funds cutting-edge research for a cure, drives change through advocacy and provides programs and services to help people affected by MS live their best lives. Connect to learn more and get involved: nationalmssociety.org , Facebook , X (formerly known as Twitter), Instagram , YouTube or 1-800-344-4867 . nationalmssociety.org, Facebook , X (formerly known as Twitter), Instagram , YouTube or 1-800-344-4867 . " c-nmssatomrichtext_nmssatomrichtext-host="">About Multiple Sclerosis Multiple sclerosis is an unpredictable disease of the central nervous system. Currently there is no cure. Symptoms vary from person to person and may include disabling fatigue, mobility challenges, cognitive changes, and vision issues. An estimated 1 million people live with MS in the United States. Early diagnosis and treatment are critical to minimize disability. Significant progress is being made to achieve a world free of MS. About the National Multiple Sclerosis Society The National MS Society, founded in 1946, is the global leader of a growing movement dedicated to creating a world free of MS. The Society funds cutting-edge research for a cure, drives change through advocacy and provides programs and services to help people affected by MS live their best lives. Connect to learn more and get involved: nationalmssociety.org , Facebook , X (formerly known as Twitter), Instagram , YouTube or 1-800-344-4867 .
ECTRIMS Patient Community Day