National nonprofit org & leading resource for the #MScommunity, #ImprovingLivesToday through vital services & support. Get texts from MSAA: go.txting.io/wna4sm

Joined August 2009
3,086 Photos and videos
On August 8, 1988, Patrick Kiernan was diagnosed with #multiplesclerosis. In 2025, Jessica and her brother Joseph ran as #TeamMSAA participants in #runDisney® in honor of their dad, with the support of their entire family. Read more about their journey: mymsaa.org/publications/moti…
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🎙️Listen now to the newest episode of MSAA’s Podcast with MS specialist and #MSassociation's Chief Medical Officer Dr. Barry Hendin and Tina Brown, a patient advocate living with #multiplesclerosis. 🎧 Available wherever you listen to podcasts, or at MyMSAA.org/Podcasts
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Have you or a loved one been recently diagnosed with #multiplesclerosis? @MSassociation created this checklist to offer step by step guidance, emotional support, and trusted #MSresources to help you feel organized and empowered from the start. 🔗 mymsaa.org/publications/newl…
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"I was diagnosed with #multiplesclerosis in 2007, and art has become both refuge from MS and my resistance to MS." This June, #MSassociation's Artist of the Month is Chris Pero with her work “Ocean's Ember” #MSawareness #MSartshowcase
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"Living with #multiplesclerosis has taught me a lot... One of the biggest things I’ve learned is the importance of protecting my peace. I actually live by my motto: ‘I keep my peace by any means necessary.’” - Nicole Robinson Read now! blog.mymsaa.org/protecting-m…?
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MSAA offers a toll-free Helpline and Chat for individuals with #multiplesclerosis to connect with experienced specialists who can provide information, support, and offer a variety of MS-related resources. Learn more today! #MSsupport #MSresources #MSassociation
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On this Memorial Day, MSAA honors and remembers those who have lost their lives in military service. Please note that our offices are closed in recognition of Memorial Day and will reopen Tuesday, May 26th.
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Read the latest edition of MSAA’s “What’s New in #MSResearch.” 🔬 This article features a wide variety of new insights from data presented at the annual meeting of the American Academy of Neurology (AAN) in April. 🔎 Read about the latest research! mymsaa.org/news/whats-new-in…
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MSAA is very pleased to announce the appointment of Amanda Montague, EdM, to the position of President & CEO. Amanda has been a dedicated member of MSAA’s senior management team and an integral part of MSAA for more than 20 years...
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...leading innovative programs and providing strategic direction for our organization. Amanda is a steadfast advocate for individuals living with multiple sclerosis and will continue to lead our organization with a focus on improving lives today for the MS community!
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“What causes the pain and tight pressure around the body known as an 'MS hug,' how is it treated, and can it be avoided?” Read MSAA’s latest Ask the Expert article with Chief Medical Officer Dr. Barry A. Hendin by visiting: blog.mymsaa.org/ask-the-expe… #MSsymptoms
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May is Mental Health Awareness Month. Many individuals with #multiplesclerosis may experience anxiety, depression, and cognitive changes. Support is available. Learn more about the various resources #MSassociation offers by visiting MyMSAA.org
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To everyone who helped us make MSAA’s 12th Improving Lives Benefit such an amazing event, THANK YOU! Congratulations once again to our very special honorees Tyler Campbell (@tcspeaks32) and @icometrix!
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Thank you to our Presenting Sponsor: @Novartis Pharmaceuticals Corporation
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✨Couldn’t make the event but still want to show your support? Visit: bit.ly/3QUfj0l Pre-set donation amounts cover the cost of assistive equipment & cooling vests for individuals living with MS – or you can choose to make a donation of any size.
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📢The newest online edition of the #MSassociation's magazine, The Motivator, is now available! This issue’s cover story, “Enhanced Wellness,” focuses on creating personalized health strategies for people living with #multiplesclerosis 🔗 mymsaa.org/publications/moti…
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