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In this episode, host Kevin Vinnaco is joined by Anushka Shiell, National Director of Programs and Services of the American Parkinson Disease Association (APDA). Anushka discusses the APDA’s programs and services that support patients, families, caregivers, and professionals. They discuss valuable resources developed by APDA such as the Let’s Keep Moving Webinar Series, and Good Start.  This episode is ideal for anyone seeking for resources and programs to support people living with Parkinson’s Disease.   For more information on the APDA, visit https://www.apdaparkinson.org/  For questions about this podcast, please contact [email protected].  Show notes available here

In this episode, host Ken Vinacco is joined by CSM 2026 DD SIG Platform Award winner Franchino Porciuncula. They discuss this study on use of RAS for improving gait automaticity in people with PD. In this study, Dr. Porciuncula explored the possible mechanisms by which RAS works. We also learn more about FNIRS technology for mobile brain imaging. Ever wondered what’s going on in the brain when you turn on your metronome in the clinic? This one’s for you!  For questions about this podcast, please contact [email protected].  Show notes available here

In this episode, we’re sharing an edited audio recording of our DD SIG educational session from March 2026, during which we talked to 3 experts about fatigue in neurodegenerative diseases. Our panel includes Vanina Dal Bello-Haas who focuses on fatigue in ALS, Herb Karpatkin discussing fatigue in MS, and Maggie Abbott who covers fatigue in PD. The panelists share specifics on fatigue in each diagnosis and also come together to answer audience questions. If you missed the meeting, be sure to catch up here to learn more about this very common symptom across neurodegenerative conditions.   For questions about this podcast, please contact [email protected].  Show notes available

In this episode, host Ken Vinacco is joined by CSM 2026 DD SIG Poster Award winner Paria Darbandsari. They discuss her study on the effects of telerehabilitation on Parkinson’s Disease including what telerehabilitation methods have been studied, and what potential benefits it may have. If you are interested in expanding access to care, especially for those with Parkinson’s, this episode may be for you!  For questions about this podcast, please contact [email protected].  Show notes available: https://app.box.com/s/szjm5tofml6oxssu3teik8jddp8yysr8

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

In this episode, created in collaboration with ANPT’s Assistive Technology and Wheeled Mobility (ATSWM) SIG, host Chris Buke is joined by AT/SWM SIG Chair Wendy Koesters and special guest Pam Glazener to discuss wheeled seating considerations for people living with ALS. Drawing from their experience in specialized wheelchair clinics, Wendy and Pam share practical insights on key wheelchair components, drive control considerations, and essential documentation strategies.  Whether you’re new to seating and mobility and looking to better support your patients, or a seasoned seating specialist seeking deeper clinical insight, this episode offers valuable takeaways to enhance your practice when working with individuals with ALS.  For questions about this podcast, please contact [email protected].   Show notes available here: https://app.box.com/s/szj3bis39kg8k0vcj4wexihk8tvq6eps

Get ready for a slam dunk! Join our podcast team members Madison Catalano, Ken Vinacco, and Sara Zoeller as they discuss the degenerative diseases programming at this year’s CSM in Anaheim, CA. This podcast highlights talks to help you plan your best "February Madness" experience. The DD SIG committee and members of the 4D podcast team will be visible at the Myelin Melter on Friday evening and at the poster session on Saturday from 12-2 pm and. Please come find us and introduce yourself, we'd love to hear your ideas for our podcast (comments, future topics, etc). Happy CSM!  The Degenerative Diseases Special Interest Group is part of the Academy of  Neurologic Physical Therapy – www.neuroPT.org  For more information about Combined Sections Meeting, visit https://csm.apta.org/   For questions about this podcast, please contact [email protected].

In this episode, host Ken Vinacco interviews Jessica Shurer, CurePSP’s Director of Clinical Affairs and Advocacy, to share how the organization is leading initiatives to expand support, outreach, and education for individuals with PSP, MSA and CBS/CBD. The conversation highlights current advocacy efforts, the importance of early recognition, and the need for interdisciplinary collaboration. If you’re interested in  elevating care for patients with atypical Parkinsonism, this episode is for you!  For questions about this podcast, please contact [email protected].  Show notes available here: https://app.box.com/s/o8b2u47sgoqnj133ky3d93cpo70ge7ab

In this episode, host Ken Vinacco talks with guest Brooke Smith to learn more about the resources and role of the Muscular Dystrophy Association.  The Degenerative Diseases Special Interest Group is part of the Academy of  Neurologic Physical Therapy – www.neuroPT.org. For questions about this podcast, please contact [email protected].  Show notes available: https://app.box.com/s/lg8ac18l51pcf98maa0pcyua9iauhrsy

In this episode, host Parm Padgett interviews Dr. Daniel Peterson about how to conceptualize and begin to intervene in the area of reactive balance. He discusses his work with people with Parkinson’s Disease and Multiple Sclerosis and other emerging areas of work in the field. If you are curious about making balance training functional and impactful for your patients, this is for you!  For questions about this podcast, please contact [email protected].   Show notes available at: https://app.box.com/s/7nyf8q4ic6dow6vdm9ulil91nvy5ur1z

In this episode, we bring together a panel of guests to discuss neurologic physical therapy residencies. Host Chris Burke talks to ANPT RF SIG chair Christina Platko, along with DD SIG volunteers Madison Catalano, a residency graduate, and our very own podcast intern, Ayesha Sawnani, a PT student interested in residency. From logistics of applying to tips on knowing what to look for in a residency, this is the perfect listen for prospective residents as you start your search!  If you are listening around our publishing date in 2025 and are interested in the Virtual Residency Fair on November 12th, click here to sign up!  For questions about this podcast, please contact [email protected] or [email protected]   Show notes available here

In this episode, we tune into the audio from a special webinar from the Myotonic Dystrophy Foundation (MDF) about exercise for people with Myotonic Dystrophy (DM). Join Dr. Andy Rohrwasser- MDF Chief Scientific Officer, Dr. Donovan Lott- a PT and PhD at University of Florida and specialist in muscular dystrophy, and cardiologist Dr. Matt Wheeler as they explore the latest research on movement and exercise in this population. Stay tuned for a Q&A at the end as the experts answer questions from the DM community.   A special thank you to the Myotonic Dystrophy for sharing this content with our special interest group! For questions about this podcast, please contact [email protected].  See the full webinar video here: https://www.myotonic.org/digital-academy/stump-doctor-exercise-dm-2025-myotonic-dystrophy-motion-awareness-month  Access the MDF Exercise Guide here:  https://www.myotonic.org/sites/default/files/pages/files/MDF_Exercise-Guide-for-the-Community_1_21.pdf  For a quick look, check out the MDF’s Infographic on Exercise: https://www.myotonic.org/sites/default/files/2024-07/MDF_Exercising-with-Myotonic-Dystrophy_Infographic.pdf  Show notes available: https://app.box.com/s/yhuzygfl6ekyv7trw832f89w37g6izxs

In this episode, host Parm Padgett interviews Dr. Sarah Milne about different rehabilitation strategies for physical therapists working with people with degenerative cerebellar ataxias. Dr. Milne shares results from her clinical trials, as well as tips and treatment approaches from her time in Friedreich Ataxia Clinic.  If you’re curious about components of effective rehabilitation for degenerative ataxias, this episode is for you!  For questions about this podcast, please contact [email protected].  Show notes available at: https://app.box.com/s/1c3b6g4jgih64skasv1kxrwg3gji9nko

In this episode, host Ken Vinacco talks with guests Andrew Rosen and Ashley Durando to discuss the National Ataxia Foundation mission and resources.The Degenerative Diseases Special Interest Group is part of the Academy ofNeurologic Physical Therapy – www.neuroPT.orgFor questions about this podcast, please contact [email protected] InformationAndrew Rosen, CEO of the National Ataxia FoundationAshley Dorundo, PT, DPT, DD SIG Liaison to the National Ataxia FoundationResources from the NAFhttps://www.ataxia.org/[email protected] of Excellence: https://www.ataxia.org/ace/No-cost genetic testing program: https://www.ataxia.org/genetics/Support Groups: https://www.ataxia.org/support-groups/NAF Events: https://www.ataxia.org/events/Health Care Provider Resources: https://www.ataxia.org/provider-resources/Fact sheets: https://www.ataxia.org/fact-sheets/Exercise videos: https://www.ataxia.org/exercise/General references: https://www.ataxia.org/general-references/Citation: Rosen A, Dorundo A, Vinacco K. DD SIG Navigating the Path Episode 5: The National Ataxia Foundation. 4D: Deep Dive Into Degenerative Diseases, a podcast of the ANPTDegenerative Diseases Special Interest Group. Published 07/31/2025.https://podcasts.neuropt.org/?p=1985This is for informational and educational purposes only. It should not be used as a substitute forclinical decision making. The Academy of Neurologic Physical Therapy and its collaborators disclaim any liability to any party for any loss or damage by errors or omissions in this publication. The views or opinions expressed are those of the individual creators and do not necessarily represent the position of the Academy of Neurologic Physical Therapy.

In this episode, host Ken Vinacco talks with guest Gia Mannone to discuss the resources that the Huntington’s Disease Society of America (HDSA www.hdsa.org ) offers for people with HD. Gia discusses events, ways to find specialized medical care, and education for people with HD in all stages of the disease. If you treat people with HD, you’ll likely find something new to share after a listen!   The Degenerative Diseases Special Interest Group is part of the Academy of Neurologic Physical Therapy – www.neuroPT.org  For questions about this podcast, please contact [email protected]. Show notes available: https://app.box.com/s/87w9nzdiaqqyo937ibcgc392hifagq8m