Mission MSA

MSA Spark's opening session features Sarah Mitchell Chen, LCSW, APHSW-C, and David A. Gonzalez, PhD, ABPP, who will provide expert insights on improving mental health and well-being for individuals living with MSA and their care partners. Learn more & reserve your spot today: https://lnkd.in/gShMNvJd #MSASpark #MSA #webinar #energizingcare #care #rarediseasecare #rarediseaseawareness #education #support #msaawareness #mutliplesystematrophy #parkinsons #parkinsonism #lbd #nutrition #exercise #health #webinarseries #rarediseaseevent #rarediseasecommunity #MissionMSA Parkinson's disease #parkinsonsdisease rare disease #patient #carepartner patient

🎉 Happy New Year’s Eve! We’re in the final hours to make an impact in 2024, and with your help, we can finish this year stronger than ever. Your donation today will provide crucial support to families living with MSA and fund critical research for better treatments—and one day, a cure. Your generosity can change lives. Before the clock strikes midnight, will you donate $20.25 to celebrate the new year? 💜Donate Today: bit.ly/MissionMSADonation Don’t let this final opportunity slip by. Together, we can create a brighter future for the MSA community and start 2025 with renewed hope. Thank you for supporting our mission! #MSA #multiplesystematrophy #msaawareness #raredisease #rarediseaseawareness #donate #getinvolved #rarediseasefundraiser #community #rarediseasecommunity #rarediseasestory #communitystory #parkinsons #parkinsonism #parkinsonsdisease #patient #caregiver #awareness #giving #donate #donation #contribute #contribution #missionmsa #nonprofit #msacommunity

⏳ The final 30 hours of 2024 are here! As the year comes to a close, your support can make a lasting impact—providing critical resources for families facing MSA and funding vital research for better treatments and a cure. A donation of $20.25 symbolizes hope and a fresh start for the New Year. Will you help us close out 2024 and set the stage for Mission MSA’s most impactful year to come? Donate Here: bit.ly/MissionMSADonation #MSA #multiplesystematrophy #msaawareness #raredisease #rarediseaseawareness #donate #getinvolved #rarediseasefundraiser #community #rarediseasecommunity #rarediseasestory #communitystory #parkinsons #parkinsonism #parkinsonsdisease #patient #caregiver #awareness #giving #donate #donation #contribute #contribution #missionmsa #nonprofit #msacommunity

Share your research with the global MSA community! There’s still time to submit your abstract for the 2025 International MSA Congress—deadline: January 13, 2025. Join world-renowned experts, researchers, and clinicians in advancing the future of multiple system atrophy (MSA) care and research. “At the 2025 International MSA Congress, we’re bringing together groundbreaking researchers to catalyze innovation and discovery in our field.” – Vik Khurana, MD, PhD Explore the Schedule at a Glance and see our list of speakers, panelists, and moderators: https://lnkd.in/gHyURrvV Learn more and submit your abstract today: https://lnkd.in/gh69CkmV #MSA #multiplesystematrophy #raredisease #rarediseaseevent #liveevent #rarediseaseinsights #msainsights #internationalmsacongress #2025internationalmsacongress #parkinsonism #rarediseaseawareness #rarediseaseeducation #rarediseaseresearch #msaresearch #clinicians #researchers #patients #carepartners #BostonMA #Boston #research

Together, we can accelerate research and provide support for those facing this rare disease. Let’s make these final 5 days count! ✨ Donate Today: bit.ly/MissionMSADonation #MSA #multiplesystematrophy #msaawareness #raredisease #rarediseaseawareness #donate #getinvolved #rarediseasefundraiser #community #rarediseasecommunity #rarediseasestory #communitystory #parkinsons #parkinsonism #parkinsonsdisease #patient #caregiver #awareness #giving #donate #donation #contribute #contribution #missionmsa #nonprofit #msacommunity

Thank you for believing in our mission and helping us achieve so much this year. In 2024, Mission MSA brought our community together—both in person and virtually—for the first time since 2020! What we’ve accomplished, thanks to you: 🌟 Raised $70,000 through Path to a Cure events in Dallas, Chicago, and virtually on World MSA Day. 🌟 Announced MSA Spark to educate and support patients and families. Register today: https://lnkd.in/gShMNvJd 🌟 Planned the 2025 International MSA Congress to unite researchers, clinicians, and the MSA community. Learn more: https://lnkd.in/gF-S2aTn Your generosity makes all of this possible. Every donation helps us bring people together and make a difference for those impacted by MSA. Donate today: bit.ly/MissionMSADonation #MSA #multiplesystematrophy #msaawareness #raredisease #rarediseaseawareness #donate #getinvolved #rarediseasefundraiser #community #rarediseasecommunity #rarediseasestory #communitystory #parkinsons #parkinsonism #parkinsonsdisease #patient #caregiver #awareness #giving #donate #donation #contribute #contribution #missionmsa #nonprofit #msacommunity

⏳ The countdown is on: only 10 DAYS remain to make your mark in 2024! Thanks to your support, Mission MSA has made incredible strides this year—funding research, connecting families, and providing vital resources. With just 10 days left, your gift can strengthen our community. Give the gift of hope today and help us finish the year strong! 💪 Donate: bit.ly/MissionMSADonation #MSA #multiplesystematrophy #msaawareness #raredisease #rarediseaseawareness #donate #getinvolved #rarediseasefundraiser #community #rarediseasecommunity #rarediseasestory #communitystory #parkinsons #parkinsonism #parkinsonsdisease #patient #caregiver #awareness #giving #donate #donation #contribute #contribution #missionmsa #nonprofit #msacommunity

As we reflect on this past year, we are filled with gratitude for the incredible MSA community and your unwavering support.   Our office will be closed from Tuesday, December 24, through Wednesday, January 1, reopening on Thursday, January 2. During this time, our Support Hotline will not be staffed. Messages will be returned when we reopen.   Thank you for making a meaningful difference for those affected by MSA. Wishing you a joyful holiday season and a bright new year! 💜

Your support brings resources like this to life! We’re excited to share a new resource in our Resource Library: 🎥 Skin Testing for Early Diagnosis of Rare Autonomic Diseases, presented by Dr. Junie Koay, MBBS, MRCP, PhD. Learn how skin testing for alpha-synuclein can enable earlier diagnosis of MSA, Parkinson’s disease, and PAF, and help distinguish between these conditions. This is a valuable tool for patients, caregivers, and clinicians alike. Watch now: https://lnkd.in/ghzr2Jrw A donation to Mission MSA makes our ability to share resources like this with our community possible, and our ability to help extend further. Your support is grateful appreciated as we seek to promote our educational webinars and share new research updates. Donate today: https://lnkd.in/gCXMcPnq #multiplesystematrophy #raredisease #research #msa #skintesting #rareautonomicdisease #autonomicdisease #resource #rarediseaseresource #msaresource #donate #giveagift #resourcelibrary #education #rarediseaseeducation #rarediseaseresearch

After decades of dedication to the MSA community, Mission MSA Board Chair Pam Bower will conclude her tenure on December 31, 2024. Pam’s leadership has helped secure $3.5 million for MSA research and shaped Mission MSA into the impactful organization it is today. In her words: “Something terrible brought me to and to help so many good people.” Honor Pam’s incredible contributions with a donation to Mission MSA and help continue the progress she’s championed. Make a contribution today: https://lnkd.in/gCXMcPnq #MSA #multiplesystematrophy #msaawareness #raredisease #rarediseaseawareness #donate #getinvolved #rarediseasefundraiser #community #rarediseasecommunity #rarediseasestory #communitystory #parkinsons #parkinsonism #parkinsonsdisease #patient #caregiver #awareness #giving #donate #donation #contribute #contribution #missionmsa #nonprofit #msacommunity