Missed last Wednesday's webinar on 'Neuroimaging in Multiple System Atrophy'? No worries! You can catch up on the enlightening session now in our Resource Library.

To view the webinar, click here: missionmsa.org/resource-libra…

Reflecting on an inspiring experience at #AANAM in Denver, Colorado last week! Thank you for hosting such a wonderful event, American Academy of Neurology. Here's to advancing neurology and spreading awareness! 🧠

Tomorrow's the day! Join our webinar on the breakthroughs in neuroimaging for MSA with Dr. Paula Trujillo. Discover diagnostic advances & future tech. Don’t miss out! Register now: bit.ly/3UaSdl7 #MSA #Neuroimaging

Spread awareness with style! Wearing our merch helps raise visibility for our mission in the fight against Multiple System Atrophy. Wear your support and help us lead the charge toward a cure today!

Visit our storefront: bonfire.com/store/missionm…

Kicking off our first day at American Academy of Neurology's #AAN 2024 in Denver, Colorado and we couldn't be more excited! 🧠🧠Meeting incredible minds, sharing insights, diving deep into the latest in neurology.

#MSA #multiplesystematrophy #neurology #AAN AM #AAN #AmericanAcademyofNeurology

Are you passionate about building community and supporting others? We need volunteers like YOU to help sustain a welcoming and engaging online environment for those affected by Multiple System Atrophy. Learn more and apply today: bit.ly/MSA-Connect-Am…

Don't miss our upcoming webinar with Dr. Paula Trujillo, PhD who will spotlight the evolution of neuroimaging over the past 2 decades, its critical role in enhancing diagnostic accuracy, and how it's shaping the future of MSA management. Register today: bit.ly/3UaSdl7

We understand that navigating the journey of living with multiple system atrophy can be daunting. That's why we're thrilled to introduce a feature on our new website: an easier way to find MSA Support Groups! Discover support that meets your needs today: MissionMSA.org/finding-support

We were beyond proud to honor Hadley Ferguson for her extraordinary dedication to the MSA community with our Patient Advocate Award in 2023. Congratulations, Hadley, your light continues to shine bright for all affected by MSA.

Learn more: missionmsa.org/patient-advoca…

Introducing Mission MSA's new palette of purpose! As you navigate through our freshly launched website and become familiar with our new branding, you'll encounter a spectrum of colors carefully chosen to reflect the core pillars that make up Mission MSA.

Big news! We're thrilled to unveil our brand-new website! From our fresh look to enriched content, it's all designed with YOU in mind. Swipe to peek at some of the amazing features waiting for you. Dive in and explore today: missionmsa.org

Mission MSA is more than a name change—it's a reflection of our collective purpose and spirit. We're a community of champions, standing together in strength, compassion, and unwavering support for those affected by Multiple System Atrophy. Read more: bit.ly/49dd0ZA

Swipe through to explore the versatile versions of our new logo that can be found in all our digital and printed resources, videos, emails, social media, and more. Tell us what you think in the comments!

Our CEO, Joe Lindahl, shares his excitement for the rebrand and what it means for our organization moving forward! It's more than just a new name—it's a bold statement of our mission and urgency. Join us as we lead the charge towards finding a cure for MSA.

Starting today, the MSA Coalition is now Mission MSA. This rebrand signifies our enduring dedication to combatting multiple system atrophy and marks a fresh chapter. Click to explore our evolution: bit.ly/49dd0ZA

Stay tuned for our new website launch next week!

Join us for our final MSA Awareness Month event: the Clinical Trial Round Up!

Register now to secure your spot: msa.tradewing.com/events/YFa6oM4…

Week Four of MSA Awareness Month starts tomorrow and our focus is on MSA Research!🌟 For more information about MSA Awareness Month and Week Four's events, click here: multiplesystematrophy.org/msa-awareness/…

#MSA #MSA wareness #MSA AwarenessMonth #multiplesystematrophy #raredisease

Support MSA Awareness & Enter Our Raffle! 🎟️Show your support and win a cozy sweatshirt & mug! Donate $15.24 for one entry, $25.24 for two, or $103.24 for twelve entries: support.multiplesystematrophy.org/give/310191/#!…

Welcome to the final day of the MSA Myth vs. Fact challenge!

Myth or Fact? Some individuals with MSA may experience visual disturbances.

Take part in our MSA Myth vs. Challenge by clicking the link below and join us in debunking myths and learning facts: surveymonkey.com/r/Friday-MSAMy…

As we continue to raise awareness for MSA, we wanted to remind you of the crucial advocacy efforts of or Letter Campaign Challenge for the National Plan to End Parkinson’s Act. We need your help to make a lasting impact, take action now: multiplesystematrophy.org/advocacy/#/