Parkinson’s Looks Like Me Podcast

Alternative Therapies for Parkinson's disease

41 min · 12 de dic de 2025
Portada del episodio Alternative Therapies for Parkinson's disease

Descripción

Join us as we explore alternative therapies for Parkinson's disease and share our experiences researching and trying various approaches and also fads. It's time to debunk the junk and separate fact from fiction.

Comentarios

0

Sé la primera persona en comentar

¡Regístrate ahora y únete a la comunidad de Parkinson’s Looks Like Me Podcast!

Prueba gratis

Empieza 7 días de prueba

$99 / mes después de la prueba. · Cancela cuando quieras.

  • Podcasts solo en Podimo
  • 20 horas de audiolibros al mes
  • Podcast gratuitos

Todos los episodios

70 episodios

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

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 de jun de 202633 min
episode Hope We See You at the 2026 World Parkinson's Congress! artwork

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 de may de 202613 min
episode The Truth About Finding a Cure with Alberto Espay, MD artwork

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 de abr de 202629 min