Podcasts about michael j fox foundation

Elizabeth Barnes is an author and Professor of philosophy at the University of Virginia in Charlottesville, she reflects on her unconventional journey into philosophy, and her experience living with disabilities. Elizabeth questions conventional views on disability, advocating for a more nuanced understanding of wellbeing, and shares how philosophy helps her find comfort and meaning in life's challenges.Learn more about Elizabeth and read her books!Donate to The Michael J. Fox Foundation for Parkinson's ResearchDonate to The Davis Phinney Foundation for Parkinson'sKeep up to date with Peter on SubstackKeep up to date with Kasia!If you would like to support the podcast please consider our PatreonExecutive Producer: Rachel BarrettThanks to our volunteer researchers Hendrik Dahlmeier and Mihika Chechi, and Chris van Ryn!And special thanks to Suzi Jamil! Hosted on Acast. See acast.com/privacy for more information.

In the P2P fundraising world, we often look to the spark of organic, supporter-led moments like the Ice Bucket Challenge as examples of what's possible when passion meets purpose. But when lightning strikes, are you ready to catch it?This episode dives into one such moment: when four friends, Pat Morissey, Brendan Cusick, Peter Durso, and Scott Forman, decided to row 2,800 miles across the Pacific Ocean to raise funds for The Michael J. Fox Foundation For Parkinson's Research. With the right support, strategic partnership and a community rallying behind them, their effort transformed into a powerful campaign that inspired the Parkinson's community worldwide.Pat Morrissey, the first person with Parkinson's to complete this journey, and Liz Deemer, Vice President of Community Fundraising at MJFF, join P2PPF's Marcie Maxwell to share the behind-the-scenes story of Team Human Powered Potential—recipients of the 2025 Cash, Sweat & Tears Award—and the incredible impact of this campaign.In this episode, we'll also explore:How to recognize and respond to bold, supporter-led fundraising opportunitiesWhat makes staff–fundraiser relationships thrive under high-stakes pressurePractical takeaways for activating your community in powerful and unexpected waysMentioned Linkswww.michaeljfox.orgwww.teamfox.org www.humanpoweredpotential.orgOn Instagram: @humanpoweredpotentialStay Connected on LinkedInConnect with LizConnect with MarcieConnect with the Peer-to-Peer Professional Forum (00:00) - Welcome to The P2P Soap Box (02:22) - Introducingt the Team (03:42) - Pat's Journey (10:53) - Liz's Journey (15:46) - The Story of the Numbers (28:30) - On the Water (33:57) - Organizational Challenges (37:28) - Advice for Professionals (42:14) - Learn More about MJFF

In this episode of The Extra Mile Podcast, we're joined by Pat Morrissey and Brendan Cusick of Human Powered Potential—a four-person team that rowed across the Pacific Ocean to raise over $43 million for the Michael J. Fox Foundation. Pat, who lives with early onset Parkinson's, shares his powerful journey from diagnosis to joining this life-changing mission. Brendan, the team's skipper, walks us through the inspiration behind the row, the mental and physical preparation, and what it was like to face 30-foot waves and total isolation in the middle of the ocean. Together, they talk about the strength of community, the power of purpose, and how the support they received from thousands kept them moving through even the hardest days. This is a story of resilience, teamwork, and pushing beyond limits for something bigger than yourself. Don't miss this incredible conversation. Every mile matters.

$41M, 41 days, 2800 miles. Those are the stats for Team Human Potential who competed in the World's Toughest Row. The boat race happens annually and showcases teams of four, rowing across the Pacific Ocean from California to Hawaii. Patrick Morrisey with Team Human Potential became the first person with Parkinson's to finish the race. They raised over $41M for the Michael J Fox Foundation for Parkinson's research. Amazing. We spoke with Patrick and his skipper, Brendan Cusick about their experiences, challenges, commitment, and learnings on the trip. What did it reveal about working together and becoming close brothers in the end? How did Patrick manage his symptoms while rowing and living on a small boat for 41 days? What did they learn about their mental and physicial limitations? What's next? Listen on to enjoy some time with this engaging, generous and courageous team. https://humanpoweredpotential.org/ https://www.dbsandme.com/en.html 

I am running the New York City marathon after running it 12 years ago on the Michael J. Fox Foundation team. This Foundation is raising money for Parkinson's disease research. I'm so proud to be back with them and slightly terrified to be dragging my old ass over 26 + miles around the 5 Boroughs. This ep I tell a lot of stories of how Running was a severe punishment for me as a kid and how I changed my mind about it. I cross some funny roads and am not giving any words of encouragement or motivation don't worry- zero jive. Thanks -GFIf you want to support my race please do here:https://give.michaeljfox.org/fundraiser/6151559 The Full Blast Podcast on Instagram:https://instagram.com/thefullblastpodcast?igshid=YmMyMTA2M2Y=If you want to support Full Blast Support  Feder Knives - ( go buy a shirt )https://www.federknives.com/Take a class: https://centerformetalarts.org/Follow CMA on Instagram https://www.instagram.com/centerformetalarts/?hl=enJoin us in Barcelona for the 2025 weekend Workshops!https://florentinekitchenknives.com/pages/workshopsPlease subscribe, leave a review and tell your friends about the show. it helps me out a lot! Welcome back! Nordic Edge:@nordic_edge on IG Nordicedge.com.auNordic Edge is about the joy of making something with your own hands. our one stop shop for tools, supplies and help when it comes to knife making, blacksmithing, leatherworking, spoon carving and other crafts where you get to take some time out for yourself and turn an idea into something tangible. Nordic Edge also holds hands-on workshops in the “lost arts” of blacksmithing, knife making and spoon carving. Come spend a day with us and go home with new skills and something you made with your own hands. They have the  guidance to help accelerate your creativity and the  Tools, products, supplies to help you manifest your ideas. NordicEdge.com.auThank you Baker Forge & Tool for your beautiful Steel. Go to Bakerforge.com to see all the incredible steels they offer. ‘FullBlast' gets you 10% off your orderWelcome to our new Sponsor- EVENHEAT- Manufacturers of the best heat treating ovens available.  To find your next oven go to Evenheat-kiln.comFollow them on Instagram: Welcome aboard Texas Farrier Supply! For all your forging and knife making supplies go to www.texasfarriersupply.com   and get 10% off your order with PROMOCODE Knifetalk10Brodbeck Ironworks Makers of an Incredibly versatile grinder, with Many different attachmentsLeather sewing equipment and even abrasives Check out Brodbeck Ironworks for yourself:https://brodbeckironworks.com/“Knifetalk10” gets you 10% off Follow Brodbeck Ironworks on Instagramhttps://www.instagram.com/brodbeck_ironworks/Trojan Horse Forge Get your THF Stabile Rail knife finishing vise at https://www.trojanhorseforge.com/And when you use the promo code “FULLBLAST10 you get 10%off everything on the site.Follow them on instagram:https://www.instagram.com/trojan_horse_forge/ TotalBoatAdhesives, paints, primers and polishing compounds.Go to http://totalboat.com/FULLBLASTTo support the podcastG.L. Hansen & Sons On Instagramhttps://instagram.com/g.l._hansenandsons?igshid=MzRlODBiNWFlZA== Gcarta.bigcartel.comG-Carta is unique composite of natural fibers and fabrics mixed with epoxy under pressure and heat Boofa, ripple cut, Tuxini, by Mikie, Mahi Mahi, Radio worm g-cartaPheasant by MikieColorama by MikieHoopla by MikeAmazing colors and razzle dazzle for your project. MARITIME KNIFE SUPPLIESMaritimeknifesupply.CAAll your knifemaking needs, belts abrasive, steals, kilns forges presses, heat treating ovens anvils and everything you need to get started or resupply. Including Dr. Thomas's book:“Knife Engineering”They're in Canada but ship to the US with ease and you can take advantage of the exchange rate The steel selection is always growing and Lawrence just got 3900 lbs. of steel in.10% off on abrasive belt packs of 10 get a hold of https://www.instagram.com/maritimeknifesupply/ and see what the fuss is about.Welcome Tormek as a sponsor to the show. Take your sharpening to a new level. I love these sharpening machines. Waterfed, easy to use. Jigs included. Definitely check out what they have to offer. If you need it sharpened, Tormek is definitely something for you:https://tormek.com/en/inspiration/woodworking--craftsVisit Tormek's website: https://tormek.com/enFollow Tormek on Instagram:https://www.instagram.com/tormek_sharpening/?hl=enFollow Tormek on TikTokhttps://www.tiktok.com/@tormek_sharpening?lang=enGo look at the course curriculum at CMA:https://centerformetalarts.org/workshops/** Taking classes from some of the best in forging at one of the best facilities in the country is an excellent opportunity to propel yourself as a blacksmith. Not to be missed. And with housing on the campus it's a great way to get yourself to the next level. Advertising Inquiries: https://redcircle.com/brandsPrivacy & Opt-Out: https://redcircle.com/privacy

You could take any two humans on earth and their genetic code will be roughly 99 percent the same — it's the small differences in code that lead to different experiences and outcomes, including the risk of developing diseases like Parkinson's. Scientists are learning more about which genetic changes are linked to Parkinson's disease, revealing important insights into disease biology and progression. Tune into this episode of our award-winning “Parkinson's Science POV” series to learn how researchers are using genetics to better understand the disease and work toward better treatments for all.Like our podcasts? Please consider leaving a rating or review and sharing the series with your community. https://apple.co/3p02Jw0 The Foundation's landmark study, the Parkinson's Progression Marker's Initiative, also known as PPMI, is recruiting volunteers. Join the study that's changing everything at michaeljfox.org/podcast-ppmi. This episode was made possible by Prevail Therapeutics. Partner support allows us to furnish high-quality educational content to the Parkinson's community while maintaining our commitment to allocate donor dollars to high-impact research. Editorial control of all Michael J. Fox Foundation-published content rests solely with the Foundation. Mentioned in this episode:The Foundation's landmark research study is exploring the connection between sense of smell and brain disease. People with and without Parkinson's can help by taking a free scratch-and-sniff test. Get yours at mysmelltest.org/request.

Emmy award-winning actor Michael J. Fox shocked the world when he announced over 25 years ago that he had been diagnosed with Parkinson's disease. Since then, he's devoted his talents to eliminating Parkinson's in our lifetime. Researchers with The Michael J. Fox Foundation now have impressive progress to report. They've developed a biomarker test to measure the protein alpha synuclein that's helping to diagnose Parkinson's with more than 90% accuracy, even proving effective at identifying people who may later develop... Read More Read More The post Michael J. Fox's Foundation Makes Parkinson's Breakthrough appeared first on Healthy Communities Online.

Emmy award-winning actor Michael J. Fox shocked the world when he announced over 25 years ago that he had been diagnosed with Parkinson's disease. Since then, he's devoted his talents to eliminating Parkinson's in our lifetime. Researchers with The Michael J. Fox Foundation now have impressive progress to report. They've developed a biomarker test to measure the protein alpha synuclein that's helping to diagnose Parkinson's with more than 90% accuracy, even proving effective at identifying people who may later develop the disease. “I think this is going to be a game changer for clinical trials and for patient care in the future,” says Samantha Hutten, Ph.D., a neuroscientist and vice president of translational research at the foundation. “But right now it is really a research tool that can be used to inform research and also how we design clinical trials.” A positive test, for example, may not be able to tell patients which type of alpha synuclein disease they have, whether it's Parkinson's, Lewy body dementia or multiple systems atrophy. “I think there's huge excitement around it, particularly about the impact on clinical trials,” says Rebecca Miller, Ph.D., an associate professor at Yale University's School of Medicine who was diagnosed with Parkinson's in 2013 at age 38. “We're all looking for a drug that will really be disease-modifying.” Hutten tells hosts Mark Masselli and Margaret Flinter that the biomarker test is an “all-comers” study, meaning patients can participate if they've been diagnosed or have family with Parkinson's, or have risk factors like loss of sense of smell or REM sleep behavior disorder. The test comes at a crucial time: the global rate of Parkinson's has doubled since Fox first revealed his condition. Learn more about your ad choices. Visit podcastchoices.com/adchoices

Emmy award-winning actor Michael J. Fox shocked the world when he announced over 25 years ago that he had been diagnosed with Parkinson's disease. Since then, he's devoted his talents to eliminating Parkinson's in our lifetime.Researchers with The Michael J. Fox Foundation now have impressive progress to report. They've developed a biomarker test to measure the protein alpha synuclein that's helping to diagnose Parkinson's with more than 90% accuracy, even proving effective at identifying people who may later develop the disease.“I think this is going to be a game changer for clinical trials and for patient care in the future,” says Samantha Hutten, Ph.D., a neuroscientist and vice president of translational research at the foundation. “But right now it is really a research tool that can be used to inform research and also how we design clinical trials.”A positive test, for example, may not be able to tell patients which type of alpha synuclein disease they have, whether it's Parkinson's, Lewy body dementia or multiple systems atrophy.“I think there's huge excitement around it, particularly about the impact on clinical trials,” says Rebecca Miller, Ph.D., an associate professor at Yale University's School of Medicine who was diagnosed with Parkinson's in 2013 at age 38. “We're all looking for a drug that will really be disease-modifying.”Hutten tells hosts Mark Masselli and Margaret Flinter that the biomarker test is an “all-comers” study, meaning patients can participate if they've been diagnosed or have family with Parkinson's, or have risk factors like loss of sense of smell or REM sleep behavior disorder.The test comes at a crucial time: the global rate of Parkinson's has doubled since Fox first revealed his condition. Learn more about your ad choices. Visit podcastchoices.com/adchoicesSee Privacy Policy at https://art19.com/privacy and California Privacy Notice at https://art19.com/privacy#do-not-sell-my-info.

How can startups and academic institutions successfully collaborate with a global biopharmaceutical company? In this episode, host James Zanewicz, JD, LLM, RTTP, sits down with Key Opinion Leader Lidia Sobków, PhD, Senior Manager of Technology Licensing & Collaborations at AbbVie, to discuss how her team identifies cutting-edge research and partners with academic institutions and biotech startups to drive innovation. From securing collaborations to leveraging industry consortia, Lidia shares invaluable insights on how to position your research for success with major pharmaceutical companies. In this episode, you'll discover: What AbbVie looks for in potential partners and how universities and startups can stand out. The role of consortia in fostering industry-academic collaboration for groundbreaking research. Real-world examples of successful partnerships that have advanced neuroscience and imaging technologies. Tune in to learn how to navigate industry partnerships and make an impact in the biotech ecosystem! Links: Connect with Lidia Sobków, PhD, and learn more about AbbVie. Connect with James Zanewicz, JD, LLM, RTTP and learn about Tulane Medicine Business Development and the School of Medicine. Check out The Michael J. Fox Foundation and Critical Path Institute. Check out Gedeon Richter and Enigma Biomedical Group. Check out BIO on the BAYOU and make plans to attend October 28 & 29, 2025. Learn more about BIO from the BAYOU - the podcast. Bio from the Bayou is a podcast that explores biotech innovation, business development, and healthcare outcomes in New Orleans & The Gulf South, connecting biotech companies, investors, and key opinion leaders to advance medicine, technology, and startup opportunities in the region.

On this week's episode of The 1 Girl Revolution Podcast, we welcome Dr. Karen Jaffe, a powerhouse advocate, retired OB-GYN, and co-founder of InMotion—a nonprofit organization dedicated to empowering people with Parkinson's disease through exercise, education, and support. After being diagnosed with Parkinson's disease in 2007, Dr. Jaffe refused to let her diagnosis define her. Instead, she turned her personal challenge into a mission to help others. Through InMotion, Dr. Jaffe and her team are transforming the way people live with Parkinson's—offering a supportive community and innovative resources, all at no cost. In this episode, you'll hear: Dr. Jaffe's personal journey with Parkinson's disease and how it led her to advocacy; The story behind InMotion and the life-changing impact it's making; The importance of exercise, education, and community in living well with Parkinson's; How Dr. Jaffe continues to challenge the stigma around Parkinson's and empower others; Powerful stories of resilience, hope, and transformation; And so much more! For more information on InMotion, visit: www.1GirlRevolution.com/drkarenjaffe 

In this episode of Stimulating Brains, we're thrilled to have Jim McNasby join us. Jim is a deep brain stimulation (DBS) patient and the Chief Counsel at the Michael J. Fox Foundation. Jim has an inspiring story, not just as a DBS patient but also as a legal professional working at the forefront of Parkinson's research advocacy. We'll dive into his personal experience with DBS—how it has shaped his life since his diagnosis in 2000 and his surgery in 2019—and explore his crucial role at the Michael J. Fox Foundation, where he helps drive forward their mission to find a cure for Parkinson's disease. I had the pleasure of hearing Jim speak at the Neuromodec Conference, where he shared a powerful story of how DBS transformed his life, even showing a video that vividly captured its positive effects. We'll talk about that, his DBS wishlist, and the work he's doing to advocate for patients and drive research. In this episode, we explore his personal experiences, the impact of DBS, and his role in advancing Parkinson's research and advocacy at the foundation. Jim also reflects on the transformative moment when his DBS was first activated and discusses his vision for the future of patient care and innovation in the field.

Parkinson's disease significantly impacts various aspects of communication, and this can make it challenging for people with the disease to communicate effectively, be understood by others, and engage in social situations. Dr. Gemma Moya-Galé joins this episode to talk about her work on voice and communication in people with Parkinson's disease. In particular, she discusses a novel app she and her team are developing, with funding from The Michael J. Fox Foundation, to help people with Parkinson's improve how well their speech is understood. The app uses evidence-based principles from speech therapy and noise-augmented automatic speech recognition to provide speech training and feedback. She also shares her recent research on linguistically and culturally responsive methods for addressing communication challenges in both English- and Spanish-speaking individuals with Parkinson's disease, and how this approach has the potential to improve clinical care. Gemma is an Assistant Professor of Communication Sciences and Disorders, as well as the Director of the Communication, Technology, and Language Diversity Lab at Teachers College, Columbia University.This podcast is geared toward researchers and clinicians. If you live with Parkinson's or have a friend or family member with PD, listen to The Michael J. Fox Foundation Parkinson's Podcast at michaeljfox.org/podcasts. We're excited to announce that we will be merging our two podcasts in 2025, and we invite you to subscribe to our Michael J. Fox Foundation Parkinson's Podcast on Apple Podcasts or wherever you get your podcasts for future episodes featuring scientists, doctors and people with Parkinson's talking about different aspects of life with the disease as well as new research toward treatment breakthroughs.

Parkinson's disease significantly impacts various aspects of communication, and this can make it challenging for people with the disease to communicate effectively, be understood by others, and engage in social situations. Dr. Gemma Moya-Galé joins this episode to talk about her work on voice and communication in people with Parkinson's disease. In particular, she discusses a novel app she and her team are developing, with funding from The Michael J. Fox Foundation, to help people with Parkinson's improve how well their speech is understood. The app uses evidence-based principles from speech therapy and noise-augmented automatic speech recognition to provide speech training and feedback. She also shares her recent research on linguistically and culturally responsive methods for addressing communication challenges in both English- and Spanish-speaking individuals with Parkinson's disease, and how this approach has the potential to improve clinical care. Gemma is an Assistant Professor of Communication Sciences and Disorders, as well as the Director of the Communication, Technology, and Language Diversity Lab at Teachers College, Columbia University.This podcast is geared toward researchers and clinicians. If you live with Parkinson's or have a friend or family member with PD, listen to The Michael J. Fox Foundation Parkinson's Podcast at michaeljfox.org/podcasts. We're excited to announce that we will be merging our two podcasts in 2025, and we invite you to subscribe to our Michael J. Fox Foundation Parkinson's Podcast on Apple Podcasts or wherever you get your podcasts for future episodes featuring scientists, doctors and people with Parkinson's talking about different aspects of life with the disease as well as new research toward treatment breakthroughs.

Send us a textIt's time for our last Foxvember movie. To close things out, Shawn and Colin are watching the 90s buddy cop team up 'The Hard Way'. We discuss all those important topics such as tiptoeing that line between action and comedy, enormous Times Square billboards, questionable definitions of what a sex symbol is, a villain that may or may not belong in the real world, societal face blindness and so much more. Is this the team up we've all been sleeping on? What did we think? Tune in to find out!And also a shoutout to the Michael J. Fox Foundation at https://www.michaeljfox.org/5 Star reviews help drive us up the charts. Please take a minute and review us.If you would like to contact or donate to us: iusedtolikethisone@gmail.comwww.patreon.com/iusedtolikethisoneWebsite: www.iusedtolikethisone.comInstagram: @iusedtolikethisoneTwitter: @iused2likethis1Facebook: I Used To Like This OneBluesky: @iusedtolikethisone.bsky.socialSnapchat: @iused2likethis1Created/Produced/Hosted by: Shawn Wells and Colin StewartOfficial Substitute Co-host: Aaron Knowles @betteractions @oblivionbarpod @shredthestress Edited by: Shawn WellsOriginal Music by: Lindon Carter (look for his band 'Carter & the Capitals' on all music streaming platforms)Website design: David SonSponsorship Corner sponsored by movieposters.com *****With over 100,000 titles to choose from, movieposters.com is the #1 destination for posters from your favorite films + stars. Use LIKETHISONE at checkout for 15% off your purchase. *****Special Thanks To: Tracy Sheremeta, Lindon Carter, Kris Wells and Graham Wells for their contributions to the show.Hear more content from Shawn with his other podcast 'In Front Of The Yellow Line'.Support the mental health of Military Veterans with Aaron Knowles's non-profit www.shredthestress.org©️2024 And Sometimes Why? Productions.

To help meet the growing global need for more movement disorders specialists, The Michael J. Fox Foundation created the Edmond J. Safra Fellowship in Movement Disorders in collaboration with longtime partner the Edmond J. Safra Foundation. This program supports the training of movement disorders specialists who will provide expert care and drive advances in Parkinson's research. The program is positively impacting early-career clinician-researchers, as well as the centers where they train. These impacts will continue to grow over the years as more fellows are trained. In this episode, Dr. Marcelo Merello and Dr. Sergio Castillo-Torres share their insights and perspectives as a Fellowship Director and a Fellow in the program, respectively. Marcelo is Director of the Department of Neurosciences and Chief of the Movement Disorders Clinic at the Institute for Neurological Research or Fleni Hospital. He is fellowship Director at Fleni and the University of Buenos Aires. In addition, Marcelo is Principal Investigator with the National Council for Scientific and Technical Research and Professor of Neurodegenerative Diseases at the Pontifical Catholic University of Argentina. Sergio is an Associate Professor in Neurology and Internal Medicine at the Dr. Jose E. Gonzales University Hospital of the Autonomous University of Nuevo Leon. He was an Edmond J. Safra Fellow in Movement Disorders at Fleni Hospital. Visit michaeljfox.org/fellowship to learn more about the Edmond J. Safra Fellowship in Movement Disorders.This podcast is geared toward researchers and clinicians. If you live with Parkinson's or have a friend or family member with PD, listen to The Michael J. Fox Foundation Parkinson's Podcast. Hear from scientists, doctors and people with Parkinson's on different aspects of life with the disease as well as research toward treatment breakthroughs at https://www.michaeljfox.org/podcasts.

To help meet the growing global need for more movement disorders specialists, The Michael J. Fox Foundation created the Edmond J. Safra Fellowship in Movement Disorders in collaboration with longtime partner the Edmond J. Safra Foundation. This program supports the training of movement disorders specialists who will provide expert care and drive advances in Parkinson's research. The program is positively impacting early-career clinician-researchers, as well as the centers where they train. These impacts will continue to grow over the years as more fellows are trained. In this episode, Dr. Marcelo Merello and Dr. Sergio Castillo-Torres share their insights and perspectives as a Fellowship Director and a Fellow in the program, respectively. Marcelo is Director of the Department of Neurosciences and Chief of the Movement Disorders Clinic at the Institute for Neurological Research or Fleni Hospital. He is fellowship Director at Fleni and the University of Buenos Aires. In addition, Marcelo is Principal Investigator with the National Council for Scientific and Technical Research and Professor of Neurodegenerative Diseases at the Pontifical Catholic University of Argentina. Sergio is an Associate Professor in Neurology and Internal Medicine at the Dr. Jose E. Gonzales University Hospital of the Autonomous University of Nuevo Leon. He was an Edmond J. Safra Fellow in Movement Disorders at Fleni Hospital. Visit michaeljfox.org/fellowship to learn more about the Edmond J. Safra Fellowship in Movement Disorders.This podcast is geared toward researchers and clinicians. If you live with Parkinson's or have a friend or family member with PD, listen to The Michael J. Fox Foundation Parkinson's Podcast. Hear from scientists, doctors and people with Parkinson's on different aspects of life with the disease as well as research toward treatment breakthroughs at https://www.michaeljfox.org/podcasts.

Oct. 25, 2024 - We explore the potential benefits of a state Parkinson's disease registry with Zach Hardy, state government relations manager for the Michael J. Fox Foundation for Parkinson's Research.

I'd love to hear from you! Send me a text message here and let me know what you thought about the episode. :)Do you know about Donor-Advised Funds (DAFs)? This 3-letter word has been on a LOT of people's minds, which is why I'm joined by Mitch Stein, Head of Strategy at Chariot, to learn how these tax-advantaged accounts are reshaping charitable giving. Mitch introduces us to the revolutionary DAF Pay, an innovation that simplifies the donation process to feel just like using a credit card, making it easier for nonprofits to connect with donors. We also talk about the democratization of DAFs, driven by major players like Fidelity and Schwab, which has opened the door for everyday donors to make a difference without the hurdles of high minimums and grant sizes.Even leading nonprofits like the Michael J. Fox Foundation are capitalizing on DAFs to inspire increased generosity!From creating engaging content to educating donors on viewing DAFs as active charitable wallets, Mitch generously shares how organizations can maintain top-of-mind awareness and encourage frequent use of DAFs. P.S. Applications are now open for the next round of my Monthly Giving Mastermind. Visit positiveequation.com/mastermind to apply.P.P.S. Are you a nonprofit leader running an established monthly giving program with 10,000 or more recurring donors? DM me @positivequation to learn more about my Monthly Giving Leaders Mastermind (with an in-person retreat!)Resources & LinksConnect with Mitch on LinkedIn and check out Chariot's first ever DAF Fundraising Report and their blog for more education on Donor-Advised Funds.Want to make Missions to Movements even better? Take a screenshot of this episode and share it on Instagram. Be sure to tag @positivequation so I can connect with you. Giving season is just around the corner and DonorPerfect has your back. Jumpstart your end-of-year content in seconds with DonorPerfect's FREE fundraising AI bot at donorperfect.com/bot.The Nonprofit Podcast by Donorbox has over 100 episodes to help you take your nonprofit to the next level. Check out my appearance on Episode 130: Master Monthly Giving.My book, The Monthly Giving Mastermind, is here! Grab a copy here and learn my framework to build, grow, and sustain subscriptions for good.Let's Connect! Send a DM on Instagram or LinkedIn and let us know what you think of the show! Head to YouTube for digital marketing how-to videos and podcast teasers Want to book Dana as a speaker for your event? Click here!

Stem cell models derived from patients with Parkinson's disease are valuable tools that are helping researchers around the world to better understand the underlying causes of neurodegeneration and to develop biomarkers and new therapies. To maximize the potential impacts of these tools, it is critical that they are developed and shared according to the principles of open science. In her interview, Dr. Birgitt Schüle discusses her work developing alpha-synuclein cell lines, challenges and opportunities in the field, and important considerations surrounding open science. She goes in-depth on how the cell lines were developed, characterized, and deposited with the American Tissue and Cell Collection (ATCC) with funding support from The Michael J. Fox Foundation, as well as how these cells can be used to fuel future discoveries. Birgitt is an Associate Professor in the Department of Pathology at Stanford University School of Medicine and Co-Director of the Alzheimer's Disease Research Center, Neuropathology, and Induced Pluripotent Stem Cell (iPSC) Core. This podcast is geared toward researchers and clinicians. If you live with Parkinson's or have a friend or family member with PD, listen to The Michael J. Fox Foundation Parkinson's Podcast. Hear from scientists, doctors and people with Parkinson's on different aspects of life with the disease as well as research toward treatment breakthroughs at https://www.michaeljfox.org/podcasts.

Stem cell models derived from patients with Parkinson's disease are valuable tools that are helping researchers around the world to better understand the underlying causes of neurodegeneration and to develop biomarkers and new therapies. To maximize the potential impacts of these tools, it is critical that they are developed and shared according to the principles of open science. In her interview, Dr. Birgitt Schüle discusses her work developing alpha-synuclein cell lines, challenges and opportunities in the field, and important considerations surrounding open science. She goes in-depth on how the cell lines were developed, characterized, and deposited with the American Tissue and Cell Collection (ATCC) with funding support from The Michael J. Fox Foundation, as well as how these cells can be used to fuel future discoveries. Birgitt is an Associate Professor in the Department of Pathology at Stanford University School of Medicine and Co-Director of the Alzheimer's Disease Research Center, Neuropathology, and Induced Pluripotent Stem Cell (iPSC) Core. This podcast is geared toward researchers and clinicians. If you live with Parkinson's or have a friend or family member with PD, listen to The Michael J. Fox Foundation Parkinson's Podcast. Hear from scientists, doctors and people with Parkinson's on different aspects of life with the disease as well as research toward treatment breakthroughs at https://www.michaeljfox.org/podcasts.

The Chicago Marathon is one of six World Major Marathons, and this year will host around 50,000 runners from around the world, not to mention the spectators, vendors, and volunteers. So, is it possible for an event of this magnitude to be sustainable? On this episode, Casey and Sara chat with Cat Morris, the Sustainability Manager at Chicago Event Management, overseeing the Chicago Marathon. Hear about how the Chicago Marathon became certified as an Evergreen Inspire event through the Council for Responsible Sport, how waste, from water cups to gel packets, is being diverted from landfills, and how runners and spectators can get involved!   Sara will be running the 2024 Chicago Marathon as part of Team Fox, raising funds for the Michael J Fox Foundation for Parkinson's Research. If you'd like to donate to support the Foundation's work to find a cure for Parkinson's, you can donate through Sara's fundraising page here: https://give.michaeljfox.org/fundraiser/5270913   Resources for this episode:  Chicago Marathon Sustainability Community Impact through Compost: Chicago Distance Series Instagram: Tina Muir, Chicago Marathon Sustainability Ambassador Instagram: Chicago Marathon Know Before You Go: Sustainability  

New qualitative and quantitative tools are being developed to measure and track changes in proteins relevant for neurodegenerative disease, and these tools have the potential to accelerate drug discovery and clinical trials. In this episode, Dr. Judith Steen discusses her work creating novel qualitative and quantitative tools and workflows at the interface of proteomics and transcriptomics, including their novel FLEXI platform. This platform uses targeted, high- throughput quantitative mass spectrometry to isolate, quantify, and identify molecular changes in proteins. She describes her ongoing project, funded by The Michael J. Fox Foundation, to develop FLEXISyn, which aims to track post-translational changes in alpha-synuclein to better understand how the protein becomes dysfunctional and begins misfolding and forming toxic aggregations in Parkinson's disease. Judith is Associate Professor of Neurology at Harvard Medical School, a member of the Harvard Stem Cell Institute, and Director of the Neuroproteomics Laboratory in the F.M. Kirby Neurobiology Center at Boston Children's Hospital.This podcast is geared toward researchers and clinicians. If you live with Parkinson's or have a friend or family member with PD, listen to The Michael J. Fox Foundation Parkinson's Podcast. Hear from scientists, doctors and people with Parkinson's on different aspects of life with the disease as well as research toward treatment breakthroughs at https://www.michaeljfox.org/podcasts.

New qualitative and quantitative tools are being developed to measure and track changes in proteins relevant for neurodegenerative disease, and these tools have the potential to accelerate drug discovery and clinical trials. In this episode, Dr. Judith Steen discusses her work creating novel qualitative and quantitative tools and workflows at the interface of proteomics and transcriptomics, including their novel FLEXI platform. This platform uses targeted, high- throughput quantitative mass spectrometry to isolate, quantify, and identify molecular changes in proteins. She describes her ongoing project, funded by The Michael J. Fox Foundation, to develop FLEXISyn, which aims to track post-translational changes in alpha-synuclein to better understand how the protein becomes dysfunctional and begins misfolding and forming toxic aggregations in Parkinson's disease. Judith is Associate Professor of Neurology at Harvard Medical School, a member of the Harvard Stem Cell Institute, and Director of the Neuroproteomics Laboratory in the F.M. Kirby Neurobiology Center at Boston Children's Hospital.This podcast is geared toward researchers and clinicians. If you live with Parkinson's or have a friend or family member with PD, listen to The Michael J. Fox Foundation Parkinson's Podcast. Hear from scientists, doctors and people with Parkinson's on different aspects of life with the disease as well as research toward treatment breakthroughs at https://www.michaeljfox.org/podcasts.

In this episode of the Life Science Success Podcast, my guest is Dr. Russ Lebovitz. Dr. Lebovitz is a seasoned expert in the life sciences, with over 15 years of experience as a senior scientist and research physician. He has served on the faculties of Baylor College of Medicine and The Fox Chase Cancer Center. Transitioning from academia to industry, he has led biotech companies in the diagnostics field, focusing on early detection of neurodegenerative diseases. As the CEO of Amprion, Dr. Lebovitz is pioneering innovative technologies to revolutionize brain health. He collaborates with organizations like the Alzheimer's Drug Discovery Foundation and the Michael J. Fox Foundation to advance research and awareness. Join us as we delve into his remarkable journey and the groundbreaking work he's doing to transform the future of diagnostics. Dr. Lebovitz shares his extensive experience in life sciences, discussing the journey and development of Amprion from its early days to the present. He explains the science behind prion-like particles, misfolded proteins, and how they relate to neurodegenerative diseases such as Alzheimer's and Parkinson's. He also talks about the company's groundbreaking technology, its FDA recognition, and the critical role of collaborations with organizations like the Michael J. Fox Foundation and the Alzheimer's Drug Discovery Foundation. Tune in to learn about the innovations in diagnostics and the impactful strides being made in the field.   00:00 Introduction to Life Science Success Podcast 00:36 Sponsor Message: D3 Digital Media Marketing 01:27 Meet Dr. Russ Lebovitz 01:53 Dr. Lebovitz's Journey in Life Sciences 02:33 Founding Amprion: The Early Days 04:22 Breakthroughs in Neurodegenerative Disease Research 14:27 The Science Behind Amprion's Technology 19:41 Collaborations and FDA Support 24:52 Amprion's Unique Approach and Availability 32:05 Personal Insights and Reflections 37:20 Conclusion and Farewell

On this week's episode of You Are What You Read, we are joined by award-winning television and film actor, bestselling author, and champion of Parkinson's Research, Michael J. Fox. You know Michael from his notable roles as Alex P. Keaton on the sitcom Family Ties, Marty McFly in Back to the Future, and more… The Secret of My Success, Doc Hollywood, Casualties of War, and The American President. Michael returned to television in his award-winning lead role in Spin City, and also appeared in Rescue Me, Curb Your Enthusiasm, and The Good Wife. His many awards include five Emmys, four Golden Globes, one Grammy, two Screen Actors Guild awards, the People's Choice award, and GQ Man of the Year. In 2000, Michael launched the Michael J. Fox Foundation for Parkinson's Research, which is now the leading Parkinson's organization in the world. He is the author of four New York Times bestselling books: Lucky Man, Always Looking Up, A Funny Thing Happened on the Way to the Future, and No Time Like the Future: An Optimist Considers Mortality. Our dear friend Nelle Fortenberry also joins the conversation to talk about her longtime work with Michael as his producer and creative partner. Nelle is on the board of directors for the Michael J. Fox Foundation and won an Emmy as the Executive Producer of Still: A Michael J. Fox Movie. Learn more about your ad choices. Visit megaphone.fm/adchoices

From 18th century London to the promise of a global cure: the 200-year history of Parkinson's disease. Parkinson's, a neurodegenerative disorder most commonly characterized by tremors and other motor symptoms, is so complex, many medical professionals are starting to classify it as a group of diseases, rather than a single disease. In this episode, we explain those complexities, including: • The motor symptoms (e.g. cogwheel rigidity, bradykinesia) and non-motor symptoms (e.g. depression, sleep disorders) • How the industrial revolution may have brought about environmental factors which contribute to Parkinson's • The differences and similarities between Parkinson's and other neurodegenerative diseases, like Alzheimer's • How Parkinson's manifests in our brains • Why one nurse was able to detect Parkinson's through smell • The neurogenetics of Parkinson's, and the ethical quandaries of evolving genetic technology • Why lifestyle — nutrition, exercise, etc. — is so key to preventing and managing Parkinson's Joining us for this extensive conversation are three incredible guests: • Dr. Rachel Dolhun, Senior Vice President of Medical Communications at The Michael J. Fox Foundation for Parkinson's Research • Dr. Michael Okun, evolutionary biologist, movement disorders specialist, and Director of the Norman Fixel Institute for Neurological Diseases • Dr. Matthew Farrer, neurogenetics expert and Professor Of Neurology at the University of Florida ‘Your Brain On' is hosted by neurologists, scientists and public health advocates Ayesha and Dean Sherzai. Drs. Ayesha and Dean are now welcoming patients via the Brain Health Institute: https://brainhealthinstitute.com/ ‘Your Brain On... Parkinson's' • SEASON 3 • EPISODE 1 (SEASON 3 DEBUT) ————— LINKS   Dr. Rachel Dolhun: At the Michael J. Fox Foundation: https://www.michaeljfox.org/bio/rachel-dolhun-md-dipablm  ‘Ask the MD' series: https://www.michaeljfox.org/ask-md  The Michael J. Fox Foundation on YouTube: https://www.youtube.com/@michaeljfoxfoundation/videos  Dr. Michael Okun: At the University of Florida: https://neurology.ufl.edu/profile/okun-michael/  The book ‘Ending Parkinson's Disease': https://endingpd.org/  The Norman Fixel Institute: https://fixel.ufhealth.org/   Dr. Matthew Farrer: At the University of Florida: https://neurology.ufl.edu/profile/farrer-matthew/ ————— References: Bloem, B. R., Okun, M. S., & Klein, C. (2021). Parkinson's disease. The Lancet, 397(10291), 2284-2303. Morris, H. R., Spillantini, M. G., Sue, C. M., & Williams-Gray, C. H. (2024). The pathogenesis of Parkinson's disease. The Lancet, 403(10423), 293-304. Dorsey, E., Sherer, T., Okun, M. S., & Bloem, B. R. (2018). The emerging evidence of the Parkinson pandemic. Journal of Parkinson's disease, 8(s1), S3-S8. Dorsey, E. R., Okun, M. S., & Tanner, C. M. (2021). Bad Air and Parkinson Disease—The Fog May Be Lifting. JAMA neurology, 78(7), 793-795. Tsalenchuk, M., Gentleman, S. M., & Marzi, S. J. (2023). Linking environmental risk factors with epigenetic mechanisms in Parkinson's disease. npj Parkinson's Disease, 9(1), 123. Reynoso, A., Torricelli, R., Jacobs, B. M., Shi, J., Aslibekyan, S., Norcliffe‐Kaufmann, L., ... & Heilbron, K. (2024). Gene–Environment Interactions for Parkinson's Disease. Annals of Neurology, 95(4), 677-687. Golsorkhi, M., Sherzai, A., & Dashtipour, K. The Influence of Lifestyle on Parkinson's Disease Management. In Lifestyle Medicine, Fourth Edition (pp. 919-924). CRC Press. Sherzai, A. Z., Tagliati, M., Park, K., Pezeshkian, S., & Sherzai, D. (2016). Micronutrients and risk of Parkinson's disease: a systematic review. Gerontology and geriatric medicine, 2, 2333721416644286. ————— FOLLOW US  Join the NEURO Academy: NEUROacademy.com  Instagram: @thebraindocs Website: TheBrainDocs.com More info and episodes: TheBrainDocs.com/Podcast

I'd love to hear from you! Send me a text message here and let me know what you thought about the episode. :)Could leveraging Facebook Messenger transform your nonprofit's fundraising strategy? In this episode, we sit down with Becca Lockhart and Ty Hyacinth from the Michael J. Fox Foundation to uncover the digital strategies that have catapulted their annual giving. Discover how their innovative use of Facebook Messenger campaigns, combined with integrated donor engagement tactics, has revolutionized their approach to funding Parkinson's research, leading to remarkable growth in revenue and donor interaction.The Michael J. Fox Foundation's shift to Facebook fundraising, in partnership with Good United, offers a masterclass in authentic community-building. Join us as Becca and Ty reveal the power of personalized interactions and the critical role of staff members stepping into the spotlight with a conversational tone. Hear how ongoing engagement and expressing gratitude have been pivotal in fostering trust, belonging, and sustained support through various campaigns and challenges.We celebrate the foundation's impressive achievements in 2023, particularly through their "Year in Review" report. Listen to how they've leveraged Facebook Messenger for transparency and impactful communication, creating an engaged community where members share personal stories and support each other. As we look forward to April's Parkinson's Awareness Month, Becca and Ty share their excitement for upcoming community efforts and advocacy. Don't miss this episode packed with valuable insights and heartfelt stories from the front lines of nonprofit fundraising.Can we meet in Nashville? The 8th annual Raise fundraising conference, hosted by OneCause, will be held at the Country Music Hall of Fame & Museum in Nashville, TN September 9-10, 2024. Use code MISSIONS200 to receive $200 off: https://bit.ly/4bNqihi Let's Connect! Send a DM on Instagram or LinkedIn and let us know what you think of the show! Head to YouTube for digital marketing how-to videos and podcast teasers Want to book Dana as a speaker for your event? Click here!

Health Questions Or Comments?  Text Tammy Directly - (720) 303-8868   Contact Tammy Here - ❤️  https://bit.ly/44FeoDE  ❤️   Need Help With your Health? -

How realistic is the science of time travel as depicted in Back to the Future?Back to the Future just celebrated its 40th anniversary. Let's put that in perspective for you: Back to the Future is now older than the period of time that Marty McFly traveled in that first film, where he rocketed at 88mph from 1985 back to 1955. And while the concept of using a weird, well, concept car as a time machine might seem a little quirky, it certainly didn't hamper this flick, which is generally considered a pretty timeless classic, despite its ‘80s trappings. For the record, we consider it one of those classics, too!And while we generally believe that you probably shouldn't spend too much time thinking about the logistics of time travel (although we already covered a little of that in our episode about the TARDIS from Doctor Who), the specific mechanisms of time travel in Back to the Future are just too cool and appealing (not to mention iconic) to ignore. So in this episode, Hakeem and Tamara tackle it all! What are the specific rules of time travel in the Back to the Future trilogy? What's the significance of hitting 88mph in order to go back in time? Is there a real world equivalent to the flux capacitor? And, of course, the age old question… “what the hell is a gigawatt?!?”All this and more in the latest episode of…Does it Fly?SUGGESTED VIEWING At this point it's hard to imagine any of you haven't at least seen the original Back to the Future, one of the most beloved movies of the 1980s. But we suppose it's possible that a few of you might not have watched the entire trilogy. Well, guess what? Those movies rule pretty hard, too and Hakeem and Tamara went through all three films to make sense of the time travel science and story rules. Get going!There's also Expedition: Back to the Future which is a fun capstone to the film's legacy, the DeLorean, and more. Check it out on Max!FURTHER READING Do you want to delve a little deeper into the facts, concepts, and stories Hakeem and Tamara referenced in today's episode? Here are a few recommendations!“It ain't so much the things we don't know that get us into trouble. It's the things we know for sure that just ain't so.”Hakeem's quoting Mark Twain via his friend, Professor Edward W. Kolb, has some additional scientific context in the link above!The scientific case for time travel.“It turns out that our speed through space squared plus our speed through time squared is equal to the speed of light squared. So all things in the universe that exist are always moving at the speed of light through spacetime. So if you move more quickly through space, you'll move more slowly through time…so the higher the energy situation, the more slow the time travel is.”Tachyons“These are hypothetical particles that can only travel greater than the speed of light.”(Look, we know Hakeem was pretty harsh on these hypothetical particles, but they're pretty darn cool anyway.)(1.21) gigawatts!“What the hell is a gigawatt?” (Marty McFly…not Hakeem or Tamara. They're much more articulate and thoughtful). (flux) Capacitors“A capacitor is something that stores energy. They come in different geometrical configurations…”The Many Worlds Interpretation“But when you make a measurement, you can only ever actually see one state at a time. So the ‘many worlds interpretation' basically just says that when you make an observation, the only thing you've discovered is what world you're in. Every possible outcome actually occurred.”ScirensCertainly by now you've checked out Tamara's incredible other project dealing with the intersection of science and storytelling, right? And if not, what are you waiting for? Go now!And while you're here, might we suggest making a donation to the Michael J. Fox Foundation?WANT MORE FROM DOES IT FLY?Twisters is in theaters now and we took a look at the science of the film, via the lens of the original 1996 movie!Star Wars: The Acolyte just completed its inaugural season on Disney+. Time to learn how lightsabers work…and why none of you should have them!FOLLOW US!Stay in the loop! Follow DoesItFly? on YouTube and TikTok and let us know what you think! And don't forget to follow Roddenberry Entertainment:Instagram: @RoddenberryOfficial Facebook: RoddenberryTwitter: @Roddenberry  For Advertising Inquiries: doesitfly@roddenberry.com

Marc Price, famously known as "Skippy" from the beloved TV show Family Ties takes us on a journey through his illustrious career, sharing hilarious anecdotes from his time on Family Ties, his adventures in the world of stand-up comedy, and his roles in cult classics like "Killer Tomatoes Eat France" and "Trick or Treat" alongside legends like Ozzy Osbourne and Gene Simmons.     Highlights: Early Career and Family Ties: Marc's entry into show business through his father's influence. His journey to becoming a beloved character on Family Ties. Memorable moments from the set and working with Michael J. Fox. Cult Classics: Stories from the sets of "Killer Tomatoes Eat France" and "Trick or Treat." Marc's reflections on his co-stars and the films' lasting impact. Stand-Up Comedy: Marc's experiences on the road as a stand-up comedian. Insight into his comedy style and influences. Tales from his touring adventures and interactions with other comedians. Current Projects: Marc's efforts in raising money for the Michael J. Fox Foundation. His upcoming horror film "Witchy Ways," where he plays the antagonist. Reflections on the evolving entertainment industry and future aspirations. Personal Anecdotes: Hilarious and heartwarming stories about Marc's personal life and career. His unique perspective on the changes in Hollywood over the years. Marc's humorous take on life, fame, and his beloved pet dog, Casper.   You're going to love my conversation with Marc Price Facebook Website Merch IMDB Michaell J Fox Foundation   Follow Jeff Dwoskin (host): Jeff Dwoskin on Twitter The Jeff Dwoskin Show podcast on Twitter Podcast website Podcast on Instagram Join my mailing list Subscribe to my Youtube channel (watch Crossing the Streams!) Yes, the show used to be called Live from Detroit: The Jeff Dwoskin Show   Ways to support the show: Buy me a coffee (support the show) TeePublic Store: Classic Conversations merch and more! Love the books I talk about on the show? Here is my Amazon store to shop.  

Over one million people in the United States are living with Parkinson's Disease. This is a chronic, progressive neurologic disorder that can affect people in their 20's to their 90's, however, most are diagnosed in their 60's. Of course, given the progressive nature of the disabilities associated with PD, the disease affects thousands more spouses, children, and other caregivers. There is some good news in that a renaissance is taking place in Parkinson's research and therapeutic development. The Michael J. Fox Foundation is leading the charge toward a world without Parkinson's disease. Joining Cheri Hill today is Dr. Mindy Lokshin of The Parkinson Support Center of Northern Nevada founded in 2021 so that no one has to face Parkinson's disease alone. pscnn.org Sageintl.com

Demand for movement disorder specialists continues to grow, but not enough neurologists are receiving focused training in Parkinson's and related conditions in order to meet the current and projected needs in the U.S. and around the world. In collaboration with longtime partner the Edmond J. Safra Foundation, The Michael J. Fox Foundation created the Edmond J. Safra Fellowship in Movement Disorders with the goal of growing the global base of movement disorders specialists. In this episode Dr. Rachel Dolhun shares more about this fellowship program, the application process, and how the program supports the training of movement disorders clinician-researchers who will become leaders in Parkinson's care and advance science in the field. Rachel is Senior Vice President of Medical Communications at The Michael J. Fox Foundation for Parkinson's Research. Visit michaeljfox.org/funding to learn more about the Edmond J. Safra Fellowship in Movement Disorders. This podcast is geared toward researchers and clinicians. If you live with Parkinson's or have a friend or family member with PD, listen to The Michael J. Fox Foundation Parkinson's Podcast. Hear from scientists, doctors and people with Parkinson's on different aspects of life with the disease as well as research toward treatment breakthroughs at https://www.michaeljfox.org/podcasts.

Demand for movement disorder specialists continues to grow, but not enough neurologists are receiving focused training in Parkinson's and related conditions in order to meet the current and projected needs in the U.S. and around the world. In collaboration with longtime partner the Edmond J. Safra Foundation, The Michael J. Fox Foundation created the Edmond J. Safra Fellowship in Movement Disorders with the goal of growing the global base of movement disorders specialists. In this episode Dr. Rachel Dolhun shares more about this fellowship program, the application process, and how the program supports the training of movement disorders clinician-researchers who will become leaders in Parkinson's care and advance science in the field. Rachel is Senior Vice President of Medical Communications at The Michael J. Fox Foundation for Parkinson's Research. Visit michaeljfox.org/funding to learn more about the Edmond J. Safra Fellowship in Movement Disorders. This podcast is geared toward researchers and clinicians. If you live with Parkinson's or have a friend or family member with PD, listen to The Michael J. Fox Foundation Parkinson's Podcast. Hear from scientists, doctors and people with Parkinson's on different aspects of life with the disease as well as research toward treatment breakthroughs at https://www.michaeljfox.org/podcasts.

Meelya Gordon Memorial Lecture In conversation with Tamala Edwards, anchor, 6abc Action News morning edition. ABC News' Chief Anchor, the host of This Week with George Stephanopoulos, and co-anchor of Good Morning America, George Stephanopoulos joined the network in 1997 as an analyst for This Week. He previously served in the Clinton administration as the senior advisor to the president for policy and strategy. His book All Too Human, a political memoir about his time on the campaign trail and in the White House, was a no. 1 New York Times bestseller. A member of the board of directors at the Michael J. Fox Foundation and former Rhodes Scholar, Stephanopoulos' many honors include three Emmy Awards, a DuPont Award, three Murrow Awards, and two Cronkite Awards. In The Situation Room, he offers an insider's perspective on the highly restricted space in which 12 presidents have made their most critical, history-changing decisions. Because you love Author Events, please make a donation to keep our podcasts free for everyone. THANK YOU! (recorded 5/17/2024)

In this episode, hosted by Larry and Rebecca Gifford, members of The Michael J. Fox Foundation's Patient Council and their care partners share their honest reactions to their diagnosis — from panic and denial to sadness and loneliness. This group of men and women of different ages and backgrounds offers words of wisdom about what to consider, what they've lost and what they've gained – and you'll be surprised to hear how, for some, what they've gained is more than what they lost. Like our podcasts? Please consider leaving a rating or review and sharing the series with your network. https://apple.co/3p02Jw0    If you or a loved one was recently diagnosed and you're wondering where to start, visit https://www.michaeljfox.org/newlydiagnosed to find helpful resources, including an educational guide, support groups and videos. Whether you've been newly diagnosed or have been living with Parkinson's for many years, The Michael J. Fox Foundation's Parkinson's Buddy Network is a free, online platform that helps you find new connections, access educational resources and engage in important dialogue. Join our community today at parkinsonsbuddynetwork.org.  The Foundation's landmark study, the Parkinson's Progression Markers Initiative, also known as PPMI, is recruiting volunteers. Join the study that's changing everything at michaeljfox.org/podcast-ppmi.

In this raw and emotional conversation, four women with Parkinson's living in four different countries discuss the challenges faced because of delayed diagnosis, hormonal changes, lack of information and treatment, research inequity and gender biases. They share how they live better with the disease by advocating for themselves with their health care team and how they empower other women through awareness and activism. Like our podcasts? Please consider leaving a rating or review and sharing the series with your network. https://apple.co/3p02Jw0    Connect with other women who share your experiences with Parkinson's. The Michael J. Fox Foundation's Parkinson's Buddy Network is a free, online platform that helps you find new connections, access educational resources and engage in important dialogue. Join our community today at parkinsonsbuddynetwork.org. The Foundation's landmark study, the Parkinson's Progression Markers Initiative, also known as PPMI, is recruiting volunteers. Join the study that's changing everything at michaeljfox.org/podcast-ppmi.

  A Son's Journey From Parkinson's Disease Caregiver to Advocate Geoge talks about his mother memory and finding a cure for parkinson's Disease.   “One person CAN make a difference. One person CAN bring positive change". Hardcover at  

Living with Parkinson's comes with a variety of symptoms, some of which can be unexpected, and frankly, embarrassing. Drooling, bladder issues and sexual dysfunction are hard to talk about, even with loved ones or your doctor – and can affect your self-image, your intimate relationships or the way you move through the world. In audio from this Third Thursdays webinar, listen to our expert panel of people living with Parkinson's, a care partner and a movement disorder specialist discuss Parkinson's taboo topics and ways that you can navigate hard conversations and embarrassment. Like our podcasts? Please consider leaving a rating or review and sharing the series with your network. https://apple.co/3p02Jw0 Whether you've been newly diagnosed or have been living with Parkinson's for many years, The Michael J. Fox Foundation's Parkinson's Buddy Network is a free, online platform that helps you find new connections, access educational resources and engage in important dialogue. Join our community today at parkinsonsbuddynetwork.org.  The Foundation's landmark study, the Parkinson's Progression Markers Initiative, also known as PPMI, is recruiting volunteers. Join the study that's changing everything at michaeljfox.org/podcast-ppmi.

A 13-year-old girl witnesses an upright wolf on Old 2 Road in Watersmeet, Michigan in 1999. Special thanks to Casey for sharing her experience. Picture of Booker our new dog mascot. Alec found him, and Keith (from episode 2 of Matchbook Flashback) adopted him. Thank you Keith!   Link to “The Legend” Song by Steve Cook https://www.youtube.com/watch?v=5uwFZYCwnS0 Link to Coast to Coast AM episode 10/21/2011 https://www.coasttocoastam.com/show/2011-10-21-show/ Link to Linda Godfrey's Book: https://a.co/d/3QUnkhx Link to donate to the Michael J. Fox Foundation for Parkinson's Research: https://give.michaeljfox.org/give/421686/#!/donation/checkout If you have an unusual story you'd like to share on the show, please email alec@parasaur.co   Created by Alec Ogg Parasaur Studios © 2024

The Michael J. Fox Foundation for Parkinson's Research established its Research Tools Program to address gaps in the field and common challenges surrounding the development of reagents and models that slowed the initial stages of promising research projects. In collaboration with many partners and stakeholders, the Research Tools Program helps ensure that scientists around the world have access to high-quality reagents, models, and more. These tools have been instrumental in launching novel research projects to better understand Parkinson's disease and to develop promising new treatment strategies. This episode features Dr. Nicole K. Polinski, Director of Research Resources at The Michael J. Fox Foundation for Parkinson's Research. In our conversation, she discusses her role in the organization, the wide variety of tools available through the Research Tools Program, and how academic and industry researchers can share their insights and feedback on current tools and future directions for tool development.This podcast is geared toward researchers and clinicians. If you live with Parkinson's or have a friend or family member with PD, listen to The Michael J. Fox Foundation Parkinson's Podcast. Hear from scientists, doctors and people with Parkinson's on different aspects of life with the disease as well as research toward treatment breakthroughs at https://www.michaeljfox.org/podcasts.

Meet Becca and Ty. These annual giving pros have mastered the art of 'stoking' to spark movements and create campaigns that resonate deeply with their audience

Whether it's serving as Race Director of the Front Runners New York LGBT Pride Run, leading the Global Parkinson's Genetic Program at the Michael J. Fox Foundation for Parkinson's Research, or advocating for non-binary inclusion in races, J Solle supports and raises up others.  For complete show notes and links, visit our website at runningforreal.com/episode390. Photo credit (podcast player inset): Da Ping Luo/NYRR   Thank you to AG1, HydraPak, and Tracksmith for sponsoring this episode.    AG1 is the daily Foundational Nutrition supplement that delivers comprehensive nutrients to support whole-body health.  With its science-driven formulation of vitamins, probiotics, and whole-food sourced nutrients, AG1 replaces your multivitamin, probiotic, and more in one simple, drinkable habit. And just as importantly, it actually tastes good! If a comprehensive solution is what you need from your supplemental routine, go to http://drinkag1.com/TINA and get a FREE 1-year supply of Vitamin D AND five free AG1 Travel Packs with your first order!   HydraPak is the number one original equipment manufacturer of reservoirs and soft flasks in the world. They are continually looking for ways to help runners and their communities lessen their environmental footprint, and consequently their reusable hydration products are aimed not only at supporting athletes in pursuit of their personal goals, but at reducing single-use waste. Most recently, they unveiled their Cupless Racing Partnership Program, designed to support trail and road races across the country in eliminating race day waste by offering their collapsible and reusable SpeedCup as an alternative to single-use cups at running events. Find out more at https://hydrapak.com/pages/tina.   Tracksmith is an independent running brand inspired by a deep love of the sport. They're so committed to their mission of getting runners to do their best that they are offering a $100 gift card to any runner who runs a PR before April 30th. You can find all of the details under the “It's PR Season” section at tracksmith.com/tina. If you're a new customer, go to tracksmith.com/tina and use the code TINANEW at checkout to get $15 off your order of $75 or more. Returning customers can use the code TINAGIVE, and Tracksmith will give you free shipping and donate 5% of your order to TrackGirlz.   Thanks for listening! If you haven't already, be sure to subscribe wherever you're listening to this podcast. And if you enjoy “Running for Real,” please leave us a review! Keep up with what's going on at Running for Real by signing up for our weekly newsletter on our website, https://runningforreal.com/. Follow Tina on Instagram, Facebook, and X (Twitter). You'll find Running for Real on Instagram too! Want to be a member of the Running for Real community? Join #Running4Real Superstars on Facebook!  Subscribe to our YouTube channel (https://www.youtube.com/@TinaMuir) for additional content, including our “RED-S: Realize. Reflect. Recover” series of 50+ videos. Thank you for your support - we appreciate each and every one of you!

The drug development pipeline is key to bringing new therapies to people with Parkinson's disease (PD). With major breakthroughs in research in the past year, including a new biomarker for PD, The Michael J. Fox Foundation's Parkinson's Progression Markers Initiative (PPMI) study and other initiatives can be leveraged to create better designed trials. This audio from our Third Thursdays Webinar features a conversation about all the ways clinical trial design is changing, and why leaders in the space believe those changes will lead to better treatments. The webinar includes contributions from a person with PD, a researcher and an industry leader. Like our podcasts? Please consider leaving a rating or review and sharing the series with your network. https://apple.co/3p02Jw0 Whether you have Parkinson's or not, you can help move research forward. Join the study that's changing everything. Find out more at michaeljfox.org/podcast-ppmi.

The Movers and Shakers are back in the pub to kickstart series 3! And what better way to mark this new beginning than by picking up where the last series left off: with the attempt to write a charter for Parkinson's care in the UK. The gang have been speaking to international Parkinson's groups and collating your thoughts and recommendations, and they're here to announce the BIG FIVE charter commitments that they'll be taking to Downing Street. They're also joined in the pub by Caroline Rassell, CEO of Parkinson's UK, and down-the-line by Ted Thompson of the Michael J. Fox Foundation.Presented by Rory Cellan-Jones, Gillian Lacey-Solymar, Mark Mardell, Paul Mayhew-Archer, Sir Nicholas Mostyn and Jeremy Paxman.Produced and edited by Nick Hilton for Podot.Music by Alex Stobbs.Artwork by Till Lukat.PR by Sally Jones.Movers and Shakers is generously sponsored by the Judge's old chambers, and by the contributions of private donors. Hosted on Acast. See acast.com/privacy for more information.

Fiona Davis: Side Car (2 ounces cognac, 1 ounce Cointreau, lemon juice, garnish with orange rind)Fiona talks about her earlier careers in theater and journalism, the rigorous research she does for her historical novels and some of the joyous moments that have happened during her research, bringing Radio City and the history of the Rockettes to life on the page in the latest novel THE SPECTACULAR, her revelation of Parkinson's disease and her work with the Michael J. Fox Foundation, and her favorite hidden bar in NYC that feels like walking through a time machine.

Donate to the Michael J. Fox Foundation here and let's help find a cure for Parkinson's: https://give.michaeljfox.org/fundraiser/4638040 Today's word of the day is ‘storied' as in historic as in past time as in historic as in the Chicago Bears. What is happening with this team? Did Justin Fields call out his coaches did he not? Are the Bears leaving downtown or are they not? Did the defensive coordinator resign or did he not? What is happening!? (24:45) Something happened at the Patriots game over the weekend and a fan died. It could be from a fight with a rival fan. It may have been caused by health reasons. (36:15) Review: Virgin River Season 5. (37:40) James Dolan doesn't like being an owner. Hates it. Despises it. His words! (44:40) NPPOD Learn more about your ad choices. Visit megaphone.fm/adchoices

Donate to the Michael J. Fox Foundation here and let's help find a cure for Parkinson's: https://give.michaeljfox.org/fundraiser/4638040 Today's word of the day is ‘storied' as in historic as in past time as in historic as in the Chicago Bears. What is happening with this team? Did Justin Fields call out his coaches did he not? Are the Bears leaving downtown or are they not? Did the defensive coordinator resign or did he not? What is happening!? (24:45) Something happened at the Patriots game over the weekend and a fan died. It could be from a fight with a rival fan. It may have been caused by health reasons. (36:15) Review: Virgin River Season 5. (37:40) James Dolan doesn't like being an owner. Hates it. Despises it. His words! (44:40) NPPOD Learn more about your ad choices. Visit megaphone.fm/adchoices

Michael J. Fox: When Your Hero Comes on Your Podcast(Recorded May 2022) Mike welcomes one of his all time heroes, Michael J. Fox. Not only is Michael a five time Emmy award winning actor who has starred in ‘Family Ties' and ‘Back to The Future,' but his foundation has raised over 1 billion dollars to help fund Parkinson's research programs. This week Mike and Michael work out material about not getting the Hugh Jackman treatment at the airport and Michael offers profound wisdom like: “You have to accept the truth of the situation before you address it.”For a transcript of this episode, click here.Please consider donating to: The Michael J. Fox Foundation