In this episode, host Ken Vinacco interviews Mission MSA CEO Joe Lindahl, and DD SIG liaison physical therapist Lindsay Beatty to share how the organization champions connection, education and research related to Multiple System Atrophy. Join us to learn more about this rare neurodegenerative disease and discover resources to help empower your patients. For more information on Mission MSA, visit www.missionmsa.org For questions about this podcast, please contact [email protected]. Guest Information Joe Lindahl, MA, CAE Chief Executive Officer Mission MSA Related Resources Mission MSA www.missionmsa.org Centers of Excellence: https://missionmsa.org/centers-of-excellence/ Patient Support Line: 866-737-5999; https://calendly.com/mission-msa/mission-msa-patient-support-scheduler MSA Connect (patient community): https://missionmsaconnect.org/ Support Groups: https://missionmsa.org/finding-support/ MSA Essential Guidebook: https://missionmsa.org/resource-library/your-essential-msa-guidebook/ Resource Library (brochures, webinars): https://missionmsa.org/resource-library/ Care Grant (Respite Care): https://missionmsa.org/missionmsacares/ International MSA Congress: https://missionmsa.org/internationalmsacongress/ Webinar: Physical Therapy and Exercise for People with MSA: https://www.youtube.com/watch?v=yFTpfN7aMPQ Show notes available here

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“What did the council decide on item 42?” — answered with the speaker and the moment.