Forsidebilde av showet Parkinson’s Looks Like Me Podcast

Parkinson’s Looks Like Me Podcast

Podkast av YOPN

engelsk

Teknologi og vitenskap

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Les mer Parkinson’s Looks Like Me Podcast

Real, in-depth conversations about living with Young Onset Parkinson's Disease (YOPD). Join cohosts Esther, Mel, and Chris as they talk with care partners, healthcare experts, and treatment developers to better understand this neurodegenerative disease and those living with it. Brought to you by the Young Onset Parkinson's Network of PMD Alliance

Alle episoder

70 Episoder

episode Coping with the Financial Cost to Your Family: Part One cover

Coping with the Financial Cost to Your Family: Part One

Tune in for part one of a frank discussion on the financial and bureaucratic hurdles you may have to overcome while living with Young Onset Parkinson's. Co-hosts Esther, Mel, and Chris open up about the juggling they've done, the hard choices they've had to make, and the guilt that they manage.   ~~~ HOSTS ~~~ Melissa Livingston | @missmliv [https://www.instagram.com/missmliv/] Esther Labib-Kiyarash | @shakinginmyboots1 [https://www.instagram.com/shakinginmyboots1/] Chris Sutphin | @cesutphin [https://www.instagram.com/cesutphin/] with support from hosting organization, Parkinson & Movement Disorder Alliance [https://www.pmdalliance.org/] ~~~ LEARN MORE ~~~   FIND FINANCIAL ASSISTANCE | PMD Alliance's Quick-start Guide to Assistance Programs [https://www.pmdalliance.org/treatments/financial-assistance/] * PMD Alliance's Free Membership Program for People with YOPD & Care Partners [https://yopnetwork.org/] * Members can join the monthly community gathering held live on Zoom every 4th Tuesday/month, and you'll likely see our co-hosts there!  MORE ON PD COST | What Does Parkinson's Actually Cost You? by Beatrice Zatorska, Founder and CEO of PD Buddy App [https://www.pmdalliance.org/2025/08/07/what-does-parkinsons-actually-cost-you-a-frank-look-at-the-financial-toll-of-living-with-young-onset-pd-by-beatrice-zatorska-founder-and-ceo-of-pd-buddy-app/] GET IN-PERSON SUPPORT | PMD Alliance's Directory for Groups, Providers, & Events [https://www.pmdalliance.org/directory/] Don't forget to follow, subscribe, and share! Because the conversation continues in the comments on Podbean [https://yopn.podbean.com/e/thetruthaboutacure/?token=e3869bd027118a8bbbe9ac8361fa92f8], across social media, and in YOPN's Monthly Community Gatherings. Tell us what you think!

19. juni 2026 - 33 min
episode Hope We See You at the 2026 World Parkinson's Congress! cover

Hope We See You at the 2026 World Parkinson's Congress!

In this special mini-episode, Mel and Chris talk Parkinson's travel and the importance of gathering with community members in anticipation of the upcoming World Parkinson's Congress in Phoenix, AZ. ~~~ HOSTS ~~~ Melissa Livingston | @missmliv [https://www.instagram.com/missmliv/] Chris Sutphin | @cesutphin [https://www.instagram.com/cesutphin/] with support from hosting organization, Parkinson & Movement Disorder Alliance [https://www.pmdalliance.org/] ~~~ LEARN MORE ~~~ JOIN YOPN | PMD Alliance's Free Membership Program for People with YOPD [https://yopnetwork.org/] GET IN-PERSON SUPPORT | PMD Alliance's Directory for Groups, Providers, & Events [https://www.pmdalliance.org/directory/] Don't forget to follow, subscribe, and share! Because the conversation continues in the comments on Podbean [https://yopn.podbean.com/e/thetruthaboutacure/?token=e3869bd027118a8bbbe9ac8361fa92f8], across social media, and in YOPN's Monthly Community Gatherings. Tell us what you think!

22. mai 2026 - 13 min
episode The Truth About Finding a Cure with Alberto Espay, MD cover

The Truth About Finding a Cure with Alberto Espay, MD

"We need to start moving away from the idea that there will be 'a cure.' There will be many cures, and all cures are not going to come in an equal way..." In this deep-diving episode, we sit down with Alberto Espay, MD to dig into what's really stalling the research community, how bad actors take advantage of the placebo effect, and what people with Parkinson's can do to push for change. ~~~ HOSTS ~~~ Melissa Livingston | @missmliv [https://www.instagram.com/missmliv/] Esther Labib-Kiyarash | @shakinginmyboots1 [https://www.instagram.com/shakinginmyboots1/] Chris Sutphin | @cesutphin [https://www.instagram.com/cesutphin/] with support from hosting organization, Parkinson & Movement Disorder Alliance [https://www.pmdalliance.org/] ~~~ GUEST ~~~ Alberto Espay, MD Professor and Endowed Chair of the James J. and Joan A. Gardner Center for Parkinson’s Disease at the University of Cincinnati Explore his work > [https://www.vjneurology.com/speaker/alberto-espay/] ~~~ LEARN MORE ~~~ READ | The Science Behind Parkinson's from Cure Parkinson's UK [https://cureparkinsons.org.uk/about-parkinsons/the-science-behind-parkinsons/] WATCH | Parkinson's Research YouTube Playlist from PMD Alliance [https://youtube.com/playlist?list=PL2HoMK6NmADjdfVOjIKpA2dbkch-ui5Z0&si=71FHqCWuWmZ0DyEZ] JOIN YOPN | PMD Alliance's Free Membership Program for People with YOPD [https://yopnetwork.org/] Don't forget to follow, subscribe, and share! Because the conversation continues in the comments on Podbean [https://yopn.podbean.com/e/thetruthaboutacure/?token=e3869bd027118a8bbbe9ac8361fa92f8], across social media, and in YOPN's Monthly Community Gatherings. Tell us what you think!

24. april 2026 - 29 min
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