Podcasts about parkinson canada

The Parkinson's Shaker Cabaret is in Regina this year on March 29th in support of Parkinson Canada. JoAnne Leigh, lead chair for the Parkinson's Shaker Cabaret and Hali Ludwik, bilingual events coordinator with Parkinson Canada, join Evan to discuss the event and the importance of Parkinson's awareness.

This week, host Lisa Laronde interviews Julie Cafley, a leader in Diversity, Equity & Inclusion (DEI). They discuss the importance of inclusive leadership in advancing gender equity, emphasizing the need for both men and women to be involved in the conversation to effect meaningful change. They highlight the value of allies in the fight for gender equality and share their personal experiences on advocating for gender equity and inclusivity in leadership roles. Julie emphasizes the need for organizations to create inclusive systems and policies, support women as their careers grow, and promote empathic leadership. She also reflects on Catalyst Canada's research on women on the front line and the barriers they face. Julie believes that ongoing discussions and pragmatic DEI efforts are crucial for creating positive change. More about Dr. Julie Cafley: Dr. Julie Cafley is the Executive Director of Catalyst Canada, an organization that drives inclusive workplaces. She is a creative, strategic leader and an accomplished academic with expertise in equity and inclusion, public policy and higher-education leadership. In 2023, she was chosen as a member of the Canadian delegation to the United Nations for the Commission on the Status of Women (CSW67). She is a frequent writer and speaker on higher education, leadership and gender equity. Julie holds a PhD in education leadership from the University of Ottawa with sought-after expertise in university presidential mandates. Her thesis focused on higher education leadership and governance through the lens of unfinished terms of Canadian university presidents. Julie is an active community builder and a collaborative change maker. Whether it is serving coffee and muffins to the region's unhoused people, serving on the board of Parkinson Canada, mentoring young policy wonks, or supporting her alma mater on its Campaign Cabinet and Dean's advisory council, giving back is integral to who she is and a part of her every day. Julie is a committed advocate for women and leadership, a constant ally for First Nations, Inuit, and Metis peoples and an indefatigable champion for diversity initiatives. Connect with Julie: X: @Jcafley Instagram: @Jcafley and @Catalystinc Linked In: Julie Cafley, PhD | LinkedIn, Catalyst Inc.: My Company | LinkedIn

Parkinson's is a neuro-degenerative disease, for which there is no cure. Jon Denman is a certified Zoom facilitator with Parkinson Canada, who is helping people connect who live with the disease. He has also been diagnosed with Parkinson's for five years.

In this bittersweet finale of "When Life Gives You Parkinson's," we reflect on the incredible journey we've shared over 124 episodes. From the very first episode to this one, we've laughed, cried, and learned together. Countless guests have graced our show, sharing their stories, insights, and expertise, making each episode a treasure trove of knowledge and connection. Hosts Larry and Rebecca take a moment to express gratitude to everyone who has contributed to the success of the podcast. Whether you've been a guest, a listener, or a supporter, your presence has made a difference. Through the highs and lows, the triumphs and challenges, we've built a community bound by a shared mission: to raise awareness, offer support, and ultimately find a cure for Parkinson's disease. As we bid farewell to "When Life Gives You Parkinson's," we carry with us the memories, the laughter, and the friendships forged along the way. Thank you, everyone, for being part of this incredible journey. Though this may be the final episode, the impact of our collective efforts will continue to resonate far beyond the confines of this podcast. From all of us at "When Life Gives You Parkinson's," thank you, and be well. EMAIL US: Larry@PDAvengers.com JOIN PD AVENGERS: www.pdavengers.com Thanks to Rebecca Gifford, Niki Reitmayer, Chris Duncombe, Dila Velazquez, Rob Johnson, Greg Schott, and Corus Entertain. Special thanks to Parkinson Canada who has been there supporting the podcast since the beginning.

In this episode of "When Life Gives You Parkinson's," Larry and Rebecca dive into Larry's recent Deep Brain Stimulation (DBS) surgery. It's the culmination of their DBS series, showcasing moments before and after the procedure. (Episode six of our 2023 DBS series) Larry shares his experiences, from the anticipation of the surgery to post-surgery reflections. He describes the fears he had about the head frame and the surgical process itself, emphasizing the involvement of Nurse Nancy and Dr. Honey. The detailed account covers the electrode installation, the testing of potential targets for relief, and the moments of consciousness during the surgery. Post-surgery, Larry discusses the "Honeymoon" period, a phase of initial relief and remarkable changes. He talks about the reduction in medication intake, improved bodily functions, and sensory experiences like regaining his sense of smell. Despite these positive changes, he notes signs of needing to gradually reintroduce medication as he experiences disorientation and fatigue. Larry and Rebecca conclude with observations of minor personality changes and a heartfelt conversation about what comes next. It's a personal, insightful episode that offers a firsthand account of the realities and changes that come with DBS surgery for Parkinson's Disease.   MAIL Larry and Rebecca: ParkinsonsPod@curiouscast.ca Have a topic or questions that you would like Larry & Rebecca to address on a future episode? We would love you to click here and leave a message  https://www.speakpipe.com/WhenLifeGivesYouParkinsons Follow us, Larry & Rebecca Gifford  Facebook: Facebook.com/ParkinsonsPod Instagram: @parkinsonspod Twitter: @ParkinsonsPod Thanks to Curiouscast Our Presenting Partner is Parkinson Canada. Diagnosed with Parkinson's? You are not alone. Contact presenting partner Parkinson Canada http://www.parkinson.ca/, call the toll free hotline 1-800-565-3000 or on Twitter you can message @ParkinsonCanada. Additional thanks to...  PD Avengers – We are building a global alliance to end Parkinson's. Join us. 

Season 6, Episode 6 SHOW NOTES                                                                                                           Oct 17, 2023 TITLE:  DBS Pre-Op Talks: Love and Transition  Podcast Notes: In the latest episode of the When Life Gives You Parkinson's podcast, hosts Larry and Rebecca Gifford discuss the upcoming Deep Brain Stimulation (DBS) surgery. The surgery is scheduled for October 24th, 2023, at UBC Hospital in Vancouver, British Columbia, Canada. Larry and Rebecca take the audience through their preparations, discussions, and feelings as the surgery date approaches. They touch on a wide range of topics, including their emotional and practical preparations, managing their son Henry's needs, and the changes in household responsibilities. They also discuss the potential outcomes of the surgery and what they hope to achieve. They emphasize the importance of quality-of-life improvements and share their gratitude and love for each other. MAIL Larry and Rebecca: ParkinsonsPod@curiouscast.ca Have a topic or questions that you would like Larry & Rebecca to address on a future episode? We would love you to click here and leave a message  https://www.speakpipe.com/WhenLifeGivesYouParkinsons Follow us, Larry & Rebecca Gifford  Facebook: Facebook.com/ParkinsonsPod Instagram: @parkinsonspod Twitter: @ParkinsonsPod Thanks to Curiouscast Dila Velazquez – Story Producer Greg Schott – Sound Design Our Presenting Partner is Parkinson Canada. Diagnosed with Parkinson's? You are not alone. Contact presenting partner Parkinson Canada http://www.parkinson.ca/, call the toll free hotline 1-800-565-3000 or on Twitter you can message @ParkinsonCanada. Thanks also to    PD Avengers – We are building a global alliance to end Parkinson's. Join us. 

In this episode of "When Life Gives You Parkinson's," Larry Gifford and Rebecca Gifford delve into the world of Deep Brain Stimulation (DBS), continuing their 2023 series on this treatment option. While sharing their optimism about Larry's upcoming DBS surgery, they also address the importance of discussing the risks associated with it. They present real stories from individuals who've undergone DBS, shedding light on the complexities and varied experiences associated with this treatment. Kim Cornelis shares her personal journey, highlighting both the potential benefits and challenges of DBS. The episode also explores alternative treatments, like light therapy, and emphasizes the significance of open communication about the emotional and psychological impact of DBS, including discussions about suicidal ideation. Join Larry and Rebecca as they provide valuable insights and a balanced perspective on the choices facing individuals with Parkinson's disease. They emphasize the importance of well-informed decisions, emotional support, and understanding within the Parkinson's community. The podcast aims to raise awareness about the mental health aspects of living with Parkinson's and undergoing treatment. If you have no one to talk to about your suicidal thoughts, call your country's suicide hotline. INTERNATIONAL SUICIDE HOTLINES In Canada, it's 1-833-456-4566. In the U.S. Dial 988. In Australia, 131-114. And in the UK dial 0800 689 5652. KEY LINKS Thank You to: Kim Cornelis, PwP, Portland, Oregon Becca Miller, PhD, PwP Parkinson's Resources of Oregon Dr. Wayne Markman, founder & CEO of Symbyx Biome If you have no one to talk to about your suicidal thoughts, call your country's suicide hotline. INTERNATIONAL SUICIDE HOTLINES In Canada, it's 1-833-456-4566. In the U.S. Dial 988. In Australia, 131-114. And in the UK dial 0800 689 5652. MAIL Larry and Rebecca: ParkinsonsPod@curiouscast.ca Have a topic or questions that you would like Larry & Rebecca to address on a future episode? We would love you to click here and leave a message  https://www.speakpipe.com/WhenLifeGivesYouParkinsons Follow us, Larry & Rebecca Gifford  Twitter: @ParkinsonsPod Facebook: Facebook.com/ParkinsonsPod Instagram: @parkinsonspod Thanks to Curiouscast Dila Velazquez – Story Producer Greg Schott – Sound Design Our Presenting Partner is Parkinson Canada. Diagnosed with Parkinson's? You are not alone. Contact presenting partner Parkinson Canada http://www.parkinson.ca/, call the toll free hotline 1-800-565-3000 or on Twitter you can message @ParkinsonCanada. Thanks also to   PD Avengers – We are building a global alliance to end Parkinson's. Join us.    

In this episode of "When Life Gives You Parkinson's," Larry and Rebecca dive into Larry's upcoming Deep Brain Stimulation (DBS) surgery. They introduce Dr. Chris Honey, the neurosurgeon who will perform the procedure the brain surgeon. Dr. Honey breaks down what to expect and the possible risks of DBS, stressing the importance of picking the right surgeon and keeping a positive mindset. After the surgery, the plan is to use the DBS device to replicate Larry's best moments on medication, with the hope of eventually cutting down or even ditching the meds. The episode also brings in Tim Hague Sr., who shares his experience with the medication challenge, underlining just how much Levodopa (medication) can make a world of difference for folks dealing with Parkinson's. The podcast wraps up with a chat about making essential medications accessible worldwide and some cool facts about DBS. Check out these videos of Larry's OFF CHALLENGE My Eye Opening DBS "Off Challenge" https://youtu.be/GrlCmrHbtb0?si=PGRaESoYWMt4L5Uc The Power of Levodopa https://youtu.be/Mg91r2hT6p4?si=xFgVhnCSiRX8haLZ Thank You to: Neurosurgeon Dr. Christopher Honey www.DrHoney.com Nurse Nancy at the Vancouver Coastal Health DBS Clinic   Tim Hauge Sr. www.TimSr.ca founder of www.uturnparkinsons.org www.pdavengers.com TV Show House Heel & Toe Films Shore Z Productions Bad Hat Harry Productions Moratim Produktions NBC Universal Television (2004-2007) Universal Media Studios (UMS) (2007) The Brain Surgeon - That Mitchell & Webb Look , Series 3 - BBC Two MAIL Larry and Rebecca: ParkinsonsPod@curiouscast.ca Have a topic or questions that you would like Larry & Rebecca to address on a future episode? We would love you to click here and leave a message https://www.speakpipe.com/WhenLifeGivesYouParkinsons Follow us, Larry & Rebecca Gifford  Facebook: Facebook.com/ParkinsonsPod Instagram: @parkinsonspod Twitter: @ParkinsonsPod Thanks to Curiouscast Dila Velazquez – Story Producer Greg Schott – Sound Design Our Presenting Partner is Parkinson Canada. Diagnosed with Parkinson's? You are not alone. Contact presenting partner Parkinson Canada http://www.parkinson.ca/, call the toll free hotline 1-800-565-3000 or on Twitter you can message @ParkinsonCanada. Thanks also to    PD Avengers – We are building a global alliance to end Parkinson's. Join us.    

Hosts Larry and Rebecca Gifford are preparing for Larry's DBS surgery scheduled for October 24, 2023. During the evaluation for DBS surgery. Larry needed to completely go off meds for at least 12 hours. The medical team tests motor symptoms while OFF levodopa and then after taking a dosage and waiting forty minutes repeat the tests. Evaluators were looking for a 40% or more difference in my motor symptoms from OFF to ON. It was truly revelatory to see just how much levodopa, the medication commonly used for Parkinson's, impacts daily life. MAIL Larry and Rebecca: ParkinsonsPod@curiouscast.ca LEAVE US A MESSAGE: Have a topic or questions that you would like Larry & Rebecca to address on a future episode? We would love you to click here and leave a message  https://www.speakpipe.com/WhenLifeGivesYouParkinsons WATCH: Here is a link to see a comparison of Larry ON Levodopa and OFF levodopa Follow us, Larry & Rebecca Gifford  Twitter: @ParkinsonsPod Facebook: Facebook.com/ParkinsonsPod Instagram: @parkinsonspod Thanks to Curiouscast Dila Velazquez – Story Producer Greg Schott – Sound Design Our Presenting Partner is Parkinson Canada. Diagnosed with Parkinson's? You are not alone. Contact presenting partner Parkinson Canada http://www.parkinson.ca/, call the toll free hotline 1-800-565-3000 or on Twitter you can message @ParkinsonCanada. Thanks also to    PD Avengers – We are building a global alliance to end Parkinson's. Join us. www.pdavengers.com

Norm Murray speaks with Scott McMillan, Director of Events for Parkinson Canada about this weekend's "Mississauga SuperWalk" The 2KM walk is happening at J.C. Saddington Park in Port Credit from 11:00 am-2:30 pm. Opening ceremonies with Norm Murray as emcee begin at 12pm with the walk starting at 12:30 pm. http://www.mississaugawalk.ca

Donate to the World Parkinson Coalition to support this and future World Parkinson Congresses. World Parkinson Congress 2023 (WPC2023) was a true testament to unity and shared vision. It saw the participation of more than 2,600 people, drawn from 73 countries, all converging under one roof with one common objective: unraveling the mysteries of Parkinson's. This assembly comprised nearly a thousand medical doctors and researchers, 450 registered nurses, therapists, and other clinicians, 685 brave individuals living with Parkinson's, and 260 dedicated care partners and family members. In this episode, Larry and Rebecca share their experiences and discuss some of the most poignant lessons, enlightening stories, and groundbreaking revelations from the congress. They will introduce you people making a difference in their local communities and the world stage. KEY LINKS Our Presenting Partner is Parkinson Canada. Diagnosed with Parkinson's? You are not alone. Contact presenting partner Parkinson Canada http://www.parkinson.ca/, call the toll free hotline 1-800-565-3000 or on Twitter you can message @ParkinsonCanada. Tight Rope Theatre Improv for Parkinson's – Sign up NOW for fall classes “Improv for Parkinson's” – no experience necessary. The PwP Improv Players Arne Johansen Clara Kluge Larry Gifford Miriam Bram Peter Jarvis Shabbir Latif Dan Dumsha, Director -- Improv for Work & Wellness Rosemary Morrison – Improv for Wellness Coordinator Donate to help support the Amazing Rosemary who organized the Improv for Parkinson's troupe and found a theatre for us to perform in while in Barcelona. PD Avengers – We are building a global alliance to end Parkinson's. Join us. World Parkinson Congress WHO iSupport Thanks to: Julie Worden, Brooklyn, NY Dance for PD Jane Williams London, KY Parkinson's in Motion Amy Lavalle, Brian Grant Foundation www.briangrant.org Geoff Constable, Melbourne, Australia www.fightparkinsons.org.au WLGYP: What's your superpower? Tina Gillespie, South Australia, Australia Parkinson's South Australia Craig Gillespie, South Australia, Australia Parkinson's South Australia Sheena Botrill – South Australia, Australia Parkinson's South Australia  Eric Aquino, Eastern Pennsylvania Gray Strong Foundation – Trembling EMT Podcast  Dr. Tash (Natasha) Fothergill-Misbah Newcastle University Joy Milne, Ted X Manchester This Nurse Can Smell Parkinson's Disease WLGYP: A 3-minute test for a Parkinson's diagnosis WLGYP: World Parkinson Congress – Day 2 (Kyoto) Paul Mayhew Archer Incurable Optimist WLGYP: They say laughter is the best medicine Donate to the World Parkinson Coalition to support this and future World Parkinson Congresses. MAIL Larry and Rebecca: ParkinsonsPod@curiouscast.ca Have a topic or questions that you would like Larry & Rebecca to address on a future episode? We would love you to click here and leave a message  https://www.speakpipe.com/WhenLifeGivesYouParkinsons Follow us, Larry & Rebecca Gifford  Twitter: @ParkinsonsPod Facebook: Facebook.com/ParkinsonsPod Instagram: @parkinsonspod Thanks to Curiouscast Dila Velazquez – Story Producer Greg Schott – Sound Design

Larry & Rebecca Gifford dive into the growing interest and research being conducted around red light and infrared light laser therapy for Parkinson's disease. In Hamilton, Ontario PD Avenger and care partner Lorna Dueck, a retired radio and TV host, visits Gaitway Physical Therapy. She interviews physiotherapist Orla Hares and research assistant Jenna Sykes. Intrigued, Larry tracks down the CEO of Symbyx Biome, Dr. Wayne Markman of Australia, to discuss the handheld laser being used on the gut and vagus nerve and the infrared helmet – both designed to reactivate the mitochondria inside the dopamine cells.  and learns more about the research, science and tradition of therapy of light which dates back to Florence Nightingale in the 1850s. KEY LINKS Symbyx Biome https://symbyxbiome.com/en-ca CEO Wayne Markman featured in Forbes Australia ·        Find out how this Australian med-tech company is tackling Parkinson's disease Gaitway Physical Therapy https://gaitwayneurophysio.com/research/ Lorna Dueck https://lornadueckcreative.com/ ·        Context Beyond the Headlines: Lorna Dueck's journey through Parkinson's with her beloved Vern. Her final appearance as host of the TV Show featuring PD Avengers founders Soania Mathur, Tim Hague Sr, and Larry Gifford. APDA Light Therapy for Parkinson's Disease MAIL Larry and Rebecca: ParkinsonsPod@curiouscast.ca Have questions, comments, or a story idea? We would love you to click here and leave a message  https://www.speakpipe.com/WhenLifeGivesYouParkinsons Follow us, Larry & Rebecca Gifford  Twitter: @ParkinsonsPod Facebook: Facebook.com/ParkinsonsPod Instagram: @parkinsonspod Thanks to Curiouscast Dila Velazquez – Story Producer Greg Schott – Sound Design Our Presenting Partner is Parkinson Canada. Diagnosed with Parkinson's? You are not alone. Contact presenting partner Parkinson Canada http://www.parkinson.ca/, call the toll free hotline 1-800-565-3000 or on Twitter you can message @ParkinsonCanada. Thanks also to our content and promotional partners The Michael J. Fox Foundation's landmark study Parkinson's Progression Markers Initiative (PPMI)    PD Avengers – We are building a global alliance to end Parkinson's. Join us. World Parkinson Congress 2023 – It's time to make your congress and hotel registrations. Details on the website.  Spotlight YOPD – One of the only Parkinson's organizations dedicated to raising awareness for Young Onset Parkinson's disease and funds for the Cure Parkinson's Trust.  

The banner headline on the homepage of the Michael J. Fox Foundation's website reads “Breaking News: Parkinson's Disease Biomarker Found.” It sounds exciting, but what does it really mean? Debi Brooks, CEO and cofounder of The Michael J. Fox Foundation, joins Larry Gifford for a chat about what she says is the most important finding the Foundation has discovered in its history. It is already changing the way researchers recruit for some studies. It will lead to faster diagnosis, more customized and personalized treatment, faster, cheaper, more targeted pharmaceuticals, and ultimately it is another step closer to stopping Parkinson's in its tracks. Important Links The Lancet Neurology Article The Michael J. Fox Foundation Coverage of the Biomarker PPMI: The Study That's Changing Everything STAT Article featuring Michael J. Fox's reaction Michael J. Fox Op-Ed for STAT The Presenting Partner is Parkinson Canada... where people with Parkinson's are at the centre of everything they do. Parkinson Canada funds critical research, provides information and support, increases awareness and advocates for improved healthcare outcomes for people with Parkinson's across Canada. Learn more at Parkinson.ca Thank you to our promotional partners Spotlight YOPD PD Avengers World Parkinson Congress 2023 in Barcelona

In the first hour of NOW with Dave Brown: Karen Lee from Parkinson Canada explains what you need to know for Parkinson's Awareness Month (14:22). Milena Khazanavicius explains how Haligonians can voice their concerns about e-scooters in the city (24:06). And Anu Pala continues the conversation on accessible travel (41:54).

Trichloroethylene (TCE). You cannot see it or smell it. It could be in the air you breath, the water you drink, and the food you eat. It is a carcinogen and is linked to clusters of cancer and Parkinson's. In Journal of Parkinson's Disease, Dr. Ray Dorsey at the University of Rochester and eleven colleagues have published a research article asking the question “Is Trichlorethylene an invisible cause of Parkinson's?” The authors go on to make a convincing case. Dr. Dorsey joins the podcast to explain the dangers of TCE, how it seeps into ground water, your home, schools, and office buildings, how to protect yourself, and where you can look to see if a TCE Superfund site is near where you live.  KEY LINKS BOOK: ENDING PARKINSON'S DISEASE; A PRESCRIPTION FOR ACTION JOURNAL OF PARKINSON'S DISEASE (SCIENTIFIC JOURNAL)  Trichloroethylene: An Invisible Cause of Parkinson's Disease? THE GUARDIAN (UK) Rates of Parkinson's disease are exploding. A common chemical may be to blame (TCE) Secret files suggest chemical giant feared weedkiller's link to Parkinson's disease (Paraquat) NEW YORK NEWSDAY (NY/USA) A NEWSDAY INVESTIGATION: The Grumman Plume; Decades of Deceit CBS MORNING (USA) Service members and families affected by toxic water at Camp Lejeune Marine base still seeking justice decades later LOS ANGELES TIMES (CA/USA) Is a common industrial chemical fueling the spread of Parkinson's disease? THE TORONTO STAR (ON/CAN) Dry cleaning chemical linked to Parkinson's in international study (2011/Canada) DAYTON DAILY NEWS (OH/USA) VOICES: How toxic industrial spills have contaminated our groundwater EPA FACT SHEET | TRICHLOROETHYLENE EPA SUPERFUND HOME PAGE  WIKIPEDIA CANADIAN FEDERAL CONTAMINATED SITES INVENTORY (FCSI) CONTAMINATED SITES HOMEPAGE Much gratitude for your content A Civil Action: Touchstone Pictures, Paramount Pictures, and Wildwood Enterprises, Inc  SaferChemicals on YouTube WATCH “TOXIC CHEMICAL LOBBY: EXCLUSIVE LEAKED FOOTAGE” EMAIL Larry and Rebecca: ParkinsonsPod@curiouscast.ca Have questions, comments, or a story idea?  We would love you to click here and leave a message https://www.speakpipe.com/WhenLifeGivesYouParkinsons Follow us, Larry & Rebecca Gifford  Twitter: @ParkinsonsPod Facebook: Facebook.com/ParkinsonsPod Instagram: @parkinsonspod Thanks to Curiouscast Dila Velazquez – Story Producer Greg Schott – Sound Design Our Presenting Partner is Parkinson Canada. Diagnosed with Parkinson's? You are not alone. Contact presenting partner Parkinson Canada http://www.parkinson.ca/, call the toll free hotline 1-800-565-3000 or on Twitter you can message @ParkinsonCanada. Thanks also to our content and promotional partners  The Michael J. Fox Foundation's landmark study Parkinson's Progression Markers Initiative (PPMI)   PD Avengers – We are building a global alliance to end Parkinson's. Join us.  World Parkinson Congress 2023 – It's time to make your congress and hotel registrations. Details on the website.  Spotlight YOPD – One of the only Parkinson's organizations dedicated to raising awareness for Young Onset Parkinson's disease and funds for the Cure Parkinson's Trust. 

Lithium is more than a drug, it's the third element on the Periodic Table of Elements. Symbol is LI. It's lightest metal known to mankind. Lithium-ion batters are used in electric cars. Lithium is also present in vaping devices, many personal electronics such as cell phones, tablets, and laptops, E-Bikes, electric toothbrushes, tools, hoverboards, scooters, and for solar power backup storage. Its origins can be traced back to the Big Bang.  For 70 years it's successfully been used to treat bi-polar disease. Now there's hope it could be game changing for Parkinson's disease. Tom Guttuso Jr., MD is a professor of Neurology at the University of Buffalo and Co Director of the Movement Disorder. His new book, titled the Promise of Lithium: How an Over-The-Counter Supplement May Prevent and Slow Alzheimer's and Parkinson's disease.” Dr. Guttuso joins the pod to discuss the potential of Lithium and stopping Parkinson's.  Much Gratitude for your music: Nirvana Lithium Evanescence Lithium Pink We've Got Scurvy from the album Sponge Bob's Greatest Hits The Steve Miller Band Fly Like an Eagle EMAIL Larry and Rebecca: ParkinsonsPod@curiouscast.ca Have questions, comments, or a story idea?  We would love you to click here and leave a message https://www.speakpipe.com/WhenLifeGivesYouParkinsons Follow us, Larry & Rebecca Gifford  Twitter: @ParkinsonsPod Facebook: Facebook.com/ParkinsonsPod Instagram: @parkinsonspod KEY LINKS  BOOK: The Promise of Lithium: How an Over-the-Counter Supplement May Prevent and Slow Alzheimer's and Parkinson's disease Thanks to Curiouscast Dila Velazquez – Story Producer Our Presenting Partner is Parkinson Canada. Diagnosed with Parkinson's? You are not alone. Contact presenting partner Parkinson Canada http://www.parkinson.ca/, call the toll free hotline 1-800-565-3000 or on Twitter you can message @ParkinsonCanada. Thanks also to our content and promotional partners  The Michael J. Fox Foundation's Parkinson's IQ + You Events PD Avengers – We are building a global alliance to end Parkinson's. Join us.  World Parkinson Congress 2023 – It's time to make your congress and hotel registrations. Details on the website.  Spotlight YOPD – One of the only Parkinson's organizations dedicated to raising awareness for Young Onset Parkinson's disease and funds for the Cure Parkinson's Trust. 

January 17 marks the 81st anniversary of the birth of one of the greatest Parkinson's advocates of all time, Muhammad Ali. In this episode, we learn more about the champ's journey from his eldest daughter Maryum “May May” Ali – the stigma her father dealt with after his diagnosis, when she first noticed changes in her dad, struggles with speaking and medication, and how he improved his quality of life.  In addition to exploring Ali's Parkinson's legacy, Dr. Michael S. Okun, the head of neurology for the University of Florida Norman Fixel Institute for Neurological Diseases, sheds light on Ali's PD diagnosis. Okun and two other neurologists, the final three neurologists to treat Ali over the course of many years, published an article in October 2022 to clear up misinformation about his diagnosis. Ali was a young onset Parkinson's disease patient that responds to Levodopa which is different if his Parkinson's onset due to his boxing career and punches to the head.   EMAIL Larry and Rebecca: ParkinsonsPod@curiouscast.ca Have questions, comments, or a story idea?  We would love you to click here and leave a message https://www.speakpipe.com/WhenLifeGivesYouParkinsons Follow us, Larry & Rebecca Gifford  Twitter: @ParkinsonsPod Facebook: Facebook.com/ParkinsonsPod Instagram: @parkinsonspod KEY LINKS  Maryum “May May” Ali - website RESOURCES Muhammad Ali and Young-Onset Idiopathic Parkinson Disease—The Missing Evidence Thanks to Curiouscast Dila Velazquez – Story Producer Our Presenting Partner is Parkinson Canada. Diagnosed with Parkinson's? You are not alone. Contact presenting partner Parkinson Canada http://www.parkinson.ca/, call the toll free hotline 1-800-565-3000 or on Twitter you can message @ParkinsonCanada. Thanks also to our content and promotional partners  The Michael J. Fox Foundation's Parkinson's IQ + You Events PD Avengers – We are building a global alliance to end Parkinson's. Join us.  World Parkinson Congress 2023 – It's time to make your congress and hotel registrations. Details on the website.  Spotlight YOPD – One of the only Parkinson's organizations dedicated to raising awareness for Young Onset Parkinson's disease and funds for the Cure Parkinson's Trust. 

One of the dark symptoms of Parkinson's is apathy. Describing apathy is a bit like describing what it feels like when a dementor in the Harry Potter books kisses a character – the ability to drain happiness and hope from its victims. When a person with Parkinson's spirals into a an apathetic state they lack motivation and lose interest in activities they used to enjoy. To experience apathy is like being in a bubble of indifference. You stop caring about yourself or other people in your life with a total void of emotion. In this episode we hear firsthand from Jeff and Kristin Krantz what it's like as a person with Parkinson's living in a apathetic state and how it impacts the care partner and others in the family. Dr. Bradley McDaniel offers advice on how to escape apathy through pursuit of your meaning in life.  EMAIL Larry and Rebecca: ParkinsonsPod@curiouscast.ca Have questions, comments, or a story idea?  We would love you to click here and leave a message https://www.speakpipe.com/WhenLifeGivesYouParkinsons Follow us, Larry & Rebecca Gifford  Twitter: @ParkinsonsPod Facebook: Facebook.com/ParkinsonsPod Instagram: @parkinsonspod KEY LINKS  Dr. Bradley McDaniels https://hps.unt.edu/bradley-mcdaniels-phd-crc  Resources Mentioned Ending Parkinson's Disease book by Ray Dorsey MD, Michael Okun MD, Todd Sherer PhD and Bas Bloem MD, PhD Man's Search for Meaning by Victor Frankl The Spirituality of Imperfection Storytelling and the Search for Meaning by Ernest Kurtz and Katherine Ketchum  Jeff & Kristen Krantz Thanks to Curiouscast Dila Velazquez – Story Producer Our Presenting Partner is Parkinson Canada. Diagnosed with Parkinson's? You are not alone. Contact presenting partner Parkinson Canada http://www.parkinson.ca/, call the toll free hotline 1-800-565-3000 or on Twitter you can message @ParkinsonCanada. Thanks also to our content and promotional partners  The Michael J. Fox Foundation's Parkinson's IQ + You Events PD Avengers – We are building a global alliance to end Parkinson's. Join us.  World Parkinson Congress 2023 – It's time to make your congress and hotel registrations. Details on the website.  Spotlight YOPD – One of the only Parkinson's organizations dedicated to raising awareness for Young Onset Parkinson's disease and funds for the Cure Parkinson's Trust. 

When John O'Leary was a nine-year-old boy, he was burned on 100% of his body. He was in his garage playing with matches and gasoline—just like he'd had seen the older boys on his block do. A fire exploded, consuming the garage, sending him flying back against the wall and turning his whole world upside down. He talks with Larry & Rebecca about how he was given 1% chance to live. Now, 36-years later, John is living an inspired life. He has two national best-selling books “On Fire” and “In Awe.” he's a podcast host, an in-demand international speaker and is someone who intimately understands the impact that Parkinson's can have on a family. Email Larry and Rebecca: ParkinsonsPod@curiouscast.ca Have questions, comments, or a story idea? We would love you to click here and leave a message  https://www.speakpipe.com/WhenLifeGivesYouParkinsons Follow us, Larry & Rebecca Gifford  Twitter: @ParkinsonsPod Facebook: Facebook.com/ParkinsonsPod Instagram: @parkinsonspod KEY LINKS John O'Leary Website www.JohnOLearyInspires.com Live Inspired Podcast https://johnolearyinspires.com/podcast/ ·        Episode featuring Larry & Rebecca Gifford and When Life Gives You Parkinson's Books ·        On Fire: The 7 Choices to Ignite a Radically Inspired Life ·        In Awe: Rediscover our childlike wonder + unleash inspiration, meaning and joy. Facebook @JohnOLearyRisingAbove Instagram @joholeary.inspires Linked In @John-O-Leary-08b2805 Twitter @JOLearyInspires Thanks to Curiouscast Dila Velazquez – Story Producer Greg Schott – Sound Design Our Presenting Partner is Parkinson Canada. Diagnosed with Parkinson's? You are not alone. Contact presenting partner Parkinson Canada http://www.parkinson.ca/, call the toll free hotline 1-800-565-3000 or on Twitter you can message @ParkinsonCanada. Thanks also to our content and promotional partners The Michael J. Fox Foundation's Parkinson's IQ + You Events PD Avengers – We are building a global alliance to end Parkinson's. Join us. World Parkinson Congress 2023 – It's time to make your congress and hotel registrations. Details on the website.  Spotlight YOPD – One of the only Parkinson's organizations dedicated to raising awareness for Young Onset Parkinson's disease and funds for the Cure Parkinson's Trust.  

Kat Hill and Nancy Peate are the authors of Being Well with a Chronic Illness: A Guide to Joy and Resilience with Your Diagnosis. In their book they offer wisdom, language, research-supported guidance and personal stories to help people with Parkinson's and other chronic conditions navigate their wellness journey. In this episode, Rebecca talks with the authors — who also happen to be good friends — about their own experiences with Parkinson's and how they have cultivated tools to find joy and resilience. Larry and Rebecca also discuss and offer their reactions to the book. EMAIL Larry and Rebecca: ParkinsonsPod@curiouscast.ca Have questions, comments, or a story idea? We would love you to click here and leave a message https://www.speakpipe.com/WhenLifeGivesYouParkinsons Follow us, Larry & Rebecca Gifford  Twitter: @ParkinsonsPod Facebook: Facebook.com/ParkinsonsPod Instagram: @parkinsonspod KEY LINKS  Being Well with Chronic Illness: A Guide to Joy & Resilience with Your Diagnosis by Kat Kill and Nancy Peate (Paperback and e-Book) Penguin Random House United States US$18.00 Canada C$23.00 Australia A$32.99 WHSmith (UK) United Kingdom £15.63 PD Lemonade – Kat Hill's podcast VIDEO: Advocacy Pyramid ARTICLE: Tom Isaac's Advocacy Pyramid explained from Grand Challenges 2014 Women's Parkinson's Project Thanks to  Dila Velazquez – Story Producer Greg Schott – Sound Design Our Presenting Partner is Parkinson Canada. Diagnosed with Parkinson's? You are not alone. Contact presenting partner Parkinson Canada http://www.parkinson.ca/, call the toll free hotline 1-800-565-3000 or on Twitter you can message @ParkinsonCanada. Thanks also to our content and promotional partners  The Michael J. Fox Foundation Parkinson's Podcast hosted by Larry Gifford  PD Avengers – We are building a global alliance to end Parkinson's. Join us.  World Parkinson Congress 2023 – It's time to make your congress and hotel registrations. Details on the website.  Spotlight YOPD – One of the only Parkinson's organizations dedicated to raising awareness for Young Onset Parkinson's disease and funds for the Cure Parkinson's Trust. 

Geoff Constable is a PD Avenger and an Ambassador for the World Parkinson Congress 2023 in Barcelona. We met at the last WPC2019 in Kyoto. Like many of us with YOPD, Geoff's diagnosis was delayed six years as doctors tried to figure out root issue of his symptoms. In 2008, at the age of 50, he finally was able to put a name to the issues he had, Parkinson's disease. Geoff spent his teen years sleeping on friends couches and sometimes living on the street. He earned a degree in Naval Architecture and designed 16 Ships for the Royal Australian Navy and spent countless hours battle testing the ships in extreme conditions.  At 44-years old he talked to his doctor about onsetting symptoms. It took six years to diagnose him with Young Onset Parkinson's. He was happy to have a name for it, but bummed because there was no cause, no cure, and no standard disease path.  Listen to how Geoff took his diagnosis of Parkinson's and discovered his own superpowers on how to incorporate and accept it. Using his own body as vessel, he put himself through battle testing and discovered he was capable of far more than he or his doctors believed possible.  EMAIL Larry and Rebecca: ParkinsonsPod@curiouscast.ca Have questions, comments, or a story idea? We would love you to click here and leave a message https://www.speakpipe.com/WhenLifeGivesYouParkinsons Follow us, Larry & Rebecca Gifford  Twitter: @ParkinsonsPod Facebook: Facebook.com/ParkinsonsPod Instagram: @parkinsonspod KEY LINKS  WPC2023 Registration and Hotel Geoff Constable's blog VIDEO: Geoff Constable's 2022 Moomba performance Thanks to  Dila Velazquez – Story Producer Greg Schott – Sound Design   Our Promotional Partners include:  Diagnosed with Parkinson's? You are not alone. Contact presenting partner Parkinson Canada http://www.parkinson.ca/, call the toll free hotline 1-800-565-3000 or on Twitter you can message @ParkinsonCanada. Thanks also to our content and promotional partners  The Michael J. Fox Foundation Parkinson's Podcast hosted by Larry Gifford as featured in the MJFF2021 Year in Review.  PD Avengers – We are building a global alliance to end Parkinson's. Join us.  World Parkinson Congress 2023 – It's time to make your congress and hotel registrations. Details on the website.  Spotlight YOPD – One of the only Parkinson's organizations dedicated to raising awareness for Young Onset Parkinson's disease and funds for the Cure Parkinson's Trust. 

Updates on several stories we've shared on the podcast. Reactions to the three-minute test to diagnose Parkinson's. The final 30km on a cross-country bike tour for Parkinson's leaves bikers spinning their wheels. * We catch up with the Rigid Riders. Plus, Ozzy Osbourne on stage for the first time since his Parkinson's diagnosis. *Don't forget to push the donut button.  EMAIL Larry and Rebecca: ParkinsonsPod@curiouscast.ca Have questions, comments, or a story idea? We would love you to click here and leave a message https://www.speakpipe.com/WhenLifeGivesYouParkinsons Follow us, Larry & Rebecca Gifford  Twitter: @ParkinsonsPod Facebook: Facebook.com/ParkinsonsPod Instagram: @parkinsonspod KEY LINKS  Spinning Wheels - www.spinningwheelstour.ca  Spinning Wheels – YouTube: https://www.youtube.com/channel/UCR1_sRarZ_nt6neUqAXNMPw  Thanks to  Dila Velazquez – Story Producer Greg Schott – Sound Design University of Manchester Jim Redmond Steve Iseman Mike Loghrin Darlene Richards-Loghrin BBC Sport “The Talk” on Talk TV Network And YOU! Our Promotional Partners include:  Diagnosed with Parkinson's? You are not alone. Contact presenting partner Parkinson Canada http://www.parkinson.ca/, call the toll free hotline 1-800-565-3000 or on Twitter you can message @ParkinsonCanada. Thanks also to our content and promotional partners  The Michael J. Fox Foundation Parkinson's Podcast hosted by Larry Gifford as featured in the MJFF2021 Year in Review.  PD Avengers – We are building a global alliance to end Parkinson's. Join us.  World Parkinson Congress 2023 – It's time to start thinking about making your plans to join us for #WPC2023 in Barcelona, Spain for the sixth triennial congress.  Spotlight YOPD – One of the only Parkinson's organizations dedicated to raising awareness for Young Onset Parkinson's disease and funds for the Cure Parkinson's Trust. 

This is a breakthrough, breaking news episode featuring Professor Perdita Barren, University of Manchester and Joy Milne, the woman who can smell Parkinson's. Today. their latest research paper was published at 12:01am (BST) September 7, 2022. This research has led to a three-minute non-invasive test to determine a positive or negative Parkinson's diagnosis. Clinical Research will begin within two years at University of Manchester and has the potential to be approved as a diagnostic tool for neurologists before the end of the decade. LISTEN TO JOY MILNE in previous episodes June 05, 2019                The Woman Who Can Smell Parkinson's | World Parkinson Congress | Kyoto October 20, 2019           The Smell of Parkinson's EMAIL Larry and Rebecca: ParkinsonsPod@curiouscast.ca Have questions, comments, or a story idea? We would love you to click here and leave a message  https://www.speakpipe.com/WhenLifeGivesYouParkinsons Follow us, Larry & Rebecca Gifford  Twitter: @ParkinsonsPod Facebook: Facebook.com/ParkinsonsPod Instagram: @parkinsonspod Thanks to Dila Velazquez – Story Producer Greg Schott – Sound Design Our Promotional Partners include:  Diagnosed with Parkinson's? You are not alone. Contact presenting partner Parkinson Canada http://www.parkinson.ca/, call the toll free hotline 1-800-565-3000 or on Twitter you can message @ParkinsonCanada. Thanks also to our content and promotional partners The Michael J. Fox Foundation Parkinson's Podcast hosted by Larry Gifford as featured in the MJFF2021 Year in Review. PD Avengers – We are building a global alliance to end Parkinson's. Join us. World Parkinson Congress 2023 – It's time to start thinking about making your plans to join us for #WPC2023 in Barcelona, Spain for the sixth triennial congress. Spotlight YOPD – The only Parkinson's organization dedicated to raising awareness for Young Onset Parkinson's disease and funds for the Cure Parkinson's Trust.  

Dave Iverson was diagnosed with Parkinson's in 2004. He is a founding member of The Michael J Fox Foundation (MJFF) Patient Council and was the first host of the MJFF Parkinson's Podcast. We caught up at a patient council meeting in New York City to chat about his new book “Winter Stars.”  Parkinson's runs deep in Dave's family, but this book is not strictly about Parkinson's. It's about family, life choices and a bone between a mother and son.  At the age of 59, having spent nearly forty years in public broadcasting, Dave paused his career. His 95-year old mother had a rough bout with pneumonia and couldn't care for herself anymore. So, he paused his career, moved in with her and became her caregiving.   That decision resulted in a decade of self-discovery, an odyssey that forced Dave to come face to face with his personal weaknesses and uncharacteristic anger, while strengthening the bond to his mother and learning to live with, learn from and love dementia.  Winter Stars by Dave Iverson is available wherever you buy your books.  EMAIL Larry and Rebecca: ParkinsonsPod@curiouscast.ca Have questions, comments, or a story idea? We would love you to click here and leave a message https://www.speakpipe.com/WhenLifeGivesYouParkinsons Follow us, Larry & Rebecca Gifford  Twitter: @ParkinsonsPod Facebook: Facebook.com/ParkinsonsPod Instagram: @parkinsonspod KEY LINKS  “Winter Stars” by Dave Iverson – Sample Chapters, Listen to an Excerpt, Read Reviews, and Purchase  My Father, My Brother and Me – Watch Dave Iverson's FRONTLINE documentary online.  Capturing Grace – Homepage for Dave Iverson's film about Parkinson's and Dance. Care Partner Resources PARKINSON CANADA Care Partnering Home Page – Access the free care partner book, self-assessment guide, care partner burden calculator, home safety evaluation, activities of daily living, daily needs and routine tracker, Parkinson's disease daily diary, and a “What-if” planning tool.  MICHAEL J FOX FOUNDATION  Care Partner Guide – “You, Your Loved One and Parkinson's Disease” FREE DOWNLOAD from The Michael J Fox Foundation  Caregiving and Parkinson's “Ask the MD” – The Michael J Fox Foundation's Dr. Rachel Dolhun offers insight and advice to Care Partners in this four-minute video.  PARKINSON'S FOUNDATION Care Partner Resources – Early in the Journey to Advanced Parkinson's, getting outside help, Hotlines, government agency contacts, medication and financial assistance, and end of life planning.  AMERICAN PARKINSON'S DISEASE ASSOCIATION (APDA) Care Partner Resources PARKINSON'S UK Care Partner Resources  European Parkinson's Disease Association (EPDA) Caring and Parkinson's Resource Page WRITING WORKSHOP Tightrope Theatre - Rebecca Gifford's online virtual writing workshop “Express Yourself” is open to everyone from anywhere. The six-week course begins in September 2022 and is open for registration through Tightrope Theatre.  Thanks to  Dila Velazquez – Story Producer Greg Schott – Sound Design Our Promotional Partners include:  Diagnosed with Parkinson's? You are not alone. Contact presenting partner Parkinson Canada http://www.parkinson.ca/, call the toll free hotline 1-800-565-3000 or on Twitter you can message @ParkinsonCanada. Thanks also to our content and promotional partners  The Michael J. Fox Foundation Parkinson's Podcast hosted by Larry Gifford as featured in the MJFF2021 Year in Review.  PD Avengers – We are building a global alliance to end Parkinson's. Join us.  World Parkinson Congress 2023 – It's time to start thinking about making your plans to join us for #WPC2023 in Barcelona, Spain for the sixth triennial congress.  Spotlight YOPD – The only Parkinson's organization dedicated to raising awareness for Young Onset Parkinson's disease and funds for the Cure Parkinson's Trust. 

SUMMARY: In the book, “Mary & Me,” author Robyn Cotton draws upon her own experiences with Parkinson's in a fictional novel based in contemporary times and early 1800's London, England when Dr. James Parkinson was roaming the streets and noticing a condition, he called shaky palsy. Not often does Parkinson's play such a key role in a fictional piece of work, Robyn's journey grounds the book in near-real experiences as she and her characters struggle with the degenerative brain disease.  EMAIL Larry and Rebecca: ParkinsonsPod@curiouscast.ca Have questions, comments, or a story idea? We would love you to click here and leave a message https://www.speakpipe.com/WhenLifeGivesYouParkinsons Follow us, Larry & Rebecca Gifford  Twitter: @ParkinsonsPod Facebook: Facebook.com/ParkinsonsPod Instagram: @parkinsonspod KEY LINKS  “Mary & Me” by Robyn Cotton – Buy it on Amazon The BC Brain Wellness Program Tightrope Theatre – “Playing with Words” workshops and the more intense “Express Yourself” six-week course with Rebecca Gifford are open for registration.  Thanks to  Dila Velazquez – Story Producer Our Promotional Partners include:  Diagnosed with Parkinson's? You are not alone. Contact presenting partner Parkinson Canada http://www.parkinson.ca/, call the toll free hotline 1-800-565-3000 or on Twitter you can message @ParkinsonCanada. Thanks also to our content and promotional partners  The Michael J. Fox Foundation Parkinson's Podcast hosted by Larry Gifford as featured in the MJFF2021 Year in Review.  PD Avengers – We are building a global alliance to end Parkinson's. Join us.  World Parkinson Congress 2023 – It's time to start thinking about making your plans to join us for #WPC2023 in Barcelona, Spain for the sixth triennial congress.  Spotlight YOPD – The only Parkinson's organization dedicated to raising awareness for Young Onset Parkinson's disease and funds for the Cure Parkinson's Trust. 

Larry & Rebecca Gifford highlight two Canadians with Parkinson's who are sparking awareness, raising money and building community by riding their bicycles across every Canadian Province over the next three months.  Jim Redmond and Steve Iseman take a break from pedaling to sit down with Larry at picnic table outside their RV on Day two of the journey when they stopped at the Capilano River RV Park in West Vancouver.  Thank you for listening. Add your voice to the show and leave a message for us here; https://www.speakpipe.com/WhenLifeGivesYouParkinsons Follow us, Larry & Rebecca Gifford  Twitter: @ParkinsonsPod Facebook: Facebook.com/ParkinsonsPod Instagram: @parkinsonspod Thank you to the following people and organizations featured in this episode: Jim Redmond  - LISTEN to Jim's episodes from Season One  Parkinson's Doesn't Have to Be a Career Killer. Hope, Fear, Frustration and Levadopa Steve Iseman    Mike Loghrin Darlene Richards-Loghrin WANDA (The RV) Diagnosed with Parkinson's? You are not alone. Contact presenting partner Parkinson Canada http://www.parkinson.ca/, call the toll free hotline 1-800-565-3000 or on Twitter you can message @ParkinsonCanada. Here is a link to Parkinson Canada's “Together: No Matter What” campaign Thanks also to our content and promotional partners The Michael J. Fox Foundation Parkinson's Podcast hosted by Larry Gifford Spotlight YOPD – The only Parkinson's organization dedicated to raising awareness for Young Onset Parkinson's disease and funds for the Cure Parkinson's Trust.   PD Avengers –  We are building a global alliance to end Parkinson's. Join us. World Parkinson Congress 2023 –Make plans to join us for #WPC2023 in Barcelona, Spain. Credits Dila Velazquez – Story Producer Greg Schott – Sound Design See omnystudio.com/listener for privacy information.

For this episode, in honour of Parkinson's Awareness Month, my guests are Barbara Salsberg Mathews - a multi-disciplinary visual and performance artist, retired teacher, and Board member of the Guelph Arts Council, and Tristan O'Malley - a Grade 1 teacher with a myriad of passions and interests including athletics, and playing music. Both were diagnosed with Parkinson's Disease in 2020, and they got together for Parkinson's Awareness Month to discuss life since their diagnosis': how it has impacted their outlook on their futures, where they have found support and helpful information, and how they have managed to find silver-linings or ways to adapt or manage symptoms to continue exploring their projects and interests while navigating their changing bodies and abilities.We really appreciate them making the time to connect and opening up about their experiences!Helpful links/resources for Parkinson's Disease:Guelph Wellington Parkinson's Support Group: https://psso.ca/support.../guelph-parkinsons-support-group/Parkinson Canada: https://www.parkinson.ca/Michael J Fox - https://www.michaeljfox.org/Davis Phinney Foundation - "Every victory counts" - https://davisphinneyfoundation.org/every-victory-counts.../"My Degeneration: A Journey Through Parkinson's" by Peter Dunlap-Shohlhttps://bookshelf.ca/product/view/9780271071022“Diagnosed with Parkinson’s Now What?” Edited by Liz Voogjarv (Available through the editor - diagnosedwithparkinsonsnowwhat@gmail.com)And listen to our previous episode with "Theresa Daly" - Volunteer Administrator for the Guelph Wellington Parkinson's Support Group: https://bridgingthesocialdistance.substack.com/.../202...This interview was originally recorded on April 9th, 2022 This is a public episode. If you would like to discuss this with other subscribers or get access to bonus episodes, visit bridgingthesocialdistance.substack.com

April is "Parkinson's Awareness Month", and I will be sharing two new episodes this month aimed to raise awareness about this disease. For this episode, I interview Theresa Daly - the Volunteer Administrator of the "Guelph Wellington Parkinson's Support Group".Theresa has had a 40+ career in health care, starting as a registered nurse. While working in the "Family Life" area of hospitals, working with new parents, caregivers, and people facing long medical journeys ahead, her nursing practice expanded, and she added a masters degree in Social Work - she recognized the emotional, family, financial, and social impact of illness on people, and that there are a myriad of factors that affect how a person can cope with a long-term diagnosis. She started a private practice devoted to older adults and their families facing medical challenges to help them navigate and increasingly complex healthcare system, and provided public education and consultation for Health Care Professionals.In 2014, when she tried to retire, she was giving a talk at the local chapter of a Parkinson's Support Group. The group had 14 members at that time, and no professional support, which was when she volunteered to be their Administrator. In the eight years since the group has expanded to 70+ people with Parkinson's and closer to 140 including their caregivers who she also supports. This group caught her spark - it felt like her whole career pointed her towards this work. Theresa has been incredible at walking with people on their journeys with long-term illnesses.The Guelph Wellington Parkinsons Support Group is part of a network of support, including the national organization Parkinson Canada (parkinson.ca) and the regional Parkinson Society Southwestern Ontario (psso.ca). Every single day in Canada 25 people are diagnosed with Parkinson's.Theresa does all her work as a volunteer (also volunteering at the Guelph Humane Society, fostering cats and kittens :) ) and she could use our support! Theresa is looking for volunteers to help with this group, including someone to help co-facilitate the group with her - People with skills in hospitality, social work, computer skills and social media skills, someone to learn how to facilitate meetings, and help the members with Parkinson's get in and out of meetings. So if you are interested in supporting, please connect with Theresa at dalycounselling@rogers.comThank you so much to Theresa for sharing with us, and for the incredible work you do supporting our community.This interview was originally recorded on March 11th 2022 This is a public episode. If you would like to discuss this with other subscribers or get access to bonus episodes, visit bridgingthesocialdistance.substack.com

This is part one of three of a mini-series of episodes we are calling “Down Under.” Host Larry Gifford gets you ready for World Parkinson's Day. Learn about the new international symbol for Parkinson's disease named “THE SPARK” and how you can use it.  Where to watch the world premiere of the new documentary “The Long Road to Hope: Ending Parkinson's Disease.” The Parkinson Unity Walk in Central Park in New York City is going to take place April 23. IF you can't make it, you can still participate, we'll tell you how.   The featured guest is Founder of PD Warrior and the Insight into Parkinson's virtual conference Melissa McConaghy, FACP. Melissa takes us behind the curtains of PD Warrior and gets us ready for Insight into Parkinson's Conference. We discuss stigma, self care, and neuro plasticity. Thank you for listening. EMAIL US: ParkinsonsPod@CuriousCast.ca   Have questions for Larry & Rebecca?  Want to share how your conversations go with your partner? We would love you to click and call us here.   https://www.speakpipe.com/WhenLifeGivesYouParkinsons Follow us, Larry & Rebecca Gifford  Twitter: @ParkinsonsPod Facebook: Facebook.com/ParkinsonsPod Instagram: @parkinsonspod KEY LINKS FOR THIS EPISODE Documentary: The Long Road to Hope | Ending Parkinson's Disease The Spark     www.WorldParkinsonsDay.com PD Warrior   www.PDWarrior.com Insight into Parkinson's www.PDWarrior.com/insight-into-PD Unity Walk – www.unitywalk.com Mediflix – www.mediflix.com Thanks to Dila Velazquez – Story Producer Greg Schott – Sound Design Our Promotional Partners include:   Diagnosed with Parkinson's? You are not alone. Contact presenting partner Parkinson Canada http://www.parkinson.ca/, call the toll free hotline 1-800-565-3000 or on Twitter you can message @ParkinsonCanada. Thanks also to our content and promotional partners The Michael J. Fox Foundation Parkinson's Podcast hosted by Larry Gifford as featured in the MJFF2021 Year in Review. PD Avengers –  We are building a global alliance to end Parkinson's. Join us. World Parkinson Congress 2023 – It's time to start thinking about making your plans to join us for #WPC2023 in Barcelona, Spain for the sixth triennial congress. Spotlight YOPD – The only Parkinson's organization dedicated to raising awareness for Young Onset Parkinson's disease and funds for the Cure Parkinson's Trust.       See omnystudio.com/listener for privacy information.

This is the final instalment of our three episode mini-series we are calling “The Talk.” Hosts Larry and Rebecca Gifford talk about how Parkinson's can send them into a hopeless spiral – at times it feeling as if they aren't both committed to the marriage. And then there are times when Parkinson's brings them closer together than ever.   A difficult, intimate, deeply personal conversation about keeping connected and the importance of communication for people with Parkinson's and care partners.  This episode is dedicated to our dog Nina. We mention her a couple times in here. After this recording, her health turned and she's no longer of this earth, but is someone where she can run free, where bully sticks are unlimited and she is free of pain.  Thank you for listening.  EMAIL US: ParkinsonsPod@CuriousCast.ca   Have questions for Larry & Rebecca?  Want to share how your conversations go with your partner? We would love you to click and call us here.   https://www.speakpipe.com/WhenLifeGivesYouParkinsons   Follow us, Larry & Rebecca Gifford  Twitter: @ParkinsonsPod Facebook: Facebook.com/ParkinsonsPod Instagram: @parkinsonspod Thanks to  Dila Velazquez – Story Producer Greg Schott – Sound Design   Our Promotional Partners include:   Diagnosed with Parkinson's? You are not alone. Contact presenting partner Parkinson Canada http://www.parkinson.ca/, call the toll free hotline 1-800-565-3000 or on Twitter you can message @ParkinsonCanada.   Thanks also to our content and promotional partners  The Michael J. Fox Foundation Parkinson's Podcast hosted by Larry Gifford. The latest podcast, released on February 16th, 2022 features Larry & Rebecca and Kat & Ken Hill about intimacy and Parkinson's. Happy Valentine's Day. PD Avengers –  We are building a global alliance to end Parkinson's. Sign up today and check out the events calendar at www.PDAvengers.com  World Parkinson Congress 2023 – It's time to start thinking about making your plans to join us for #WPC2023 in Barcelona, Spain for July 2023… It'll be here before you know it.   Spotlight YOPD – The only Parkinson's organization dedicated to raising awareness for Young Onset Parkinson's disease and funds for the Cure Parkinson's Trust.   See omnystudio.com/listener for privacy information.

This is part two of three for a mini-series of episodes we are calling “The Talk.” Hosts Larry and Rebecca Gifford are also the guests this week. In this episode, they check share the emotional toll Parkinson's takes on each of them. How to maintain agency of your life while dealing with Parkinson's, how apathy impacts everything and where hope is found when you feel hopeless.   Thank you for listening.  EMAIL US: ParkinsonsPod@CuriousCast.ca   Have questions for Larry & Rebecca?  Want to share how your conversations go with your partner? We would love you to click and call us here.   https://www.speakpipe.com/WhenLifeGivesYouParkinsons   Follow us, Larry & Rebecca Gifford  Twitter: @ParkinsonsPod Facebook: Facebook.com/ParkinsonsPod Instagram: @parkinsonspod   Thanks to  Dila Velazquez – Story Producer Greg Schott – Sound Design   Our Promotional Partners include:   Diagnosed with Parkinson's? You are not alone. Contact presenting partner Parkinson Canada http://www.parkinson.ca/, call the toll free hotline 1-800-565-3000 or on Twitter you can message @ParkinsonCanada.   Thanks also to our content and promotional partners  The Michael J. Fox Foundation Parkinson's Podcast hosted by Larry Gifford as featured in the MJFF2021 Year in Review. Also noted in the 34 page booklet was… PD Avengers –  We are building a global alliance to end Parkinson's. The next Assemble meeting is Tuesday, Jan 25th at 11a PT. Join us. Details under “meetings” at PD Avengers dot com.  World Parkinson Congress 2023 – It's time to start thinking about making your plans to join us for #WPC2023 in Barcelona, Spain for t he sixth triennial congress.  Spotlight YOPD – The only Parkinson's organization dedicated to raising awareness for Young Onset Parkinson's disease and funds for the Cure Parkinson's Trust.   See omnystudio.com/listener for privacy information.

This is part one of three for a mini-series of episodes we are calling “The Talk.” Hosts Larry and Rebecca Gifford are also the guests this week. They will check on how each other is doing physically and emotionally.  They will talk about personal priorities, advocacy, and how chronic disease changes and challenges the dynamics of a family. We will also get into what gives us hope. In part one, that you are about to hear – we are talking about where our life sits from a practical perspective, the joys and pressures.  Also, what we are discovering about what we need as people and a family to maintain balance and productivity in our relatively new life where Parkinson's is a main character. We are figuring out how to take true breaks, a concept and practice that changes its meaning constantly and looks different as Parkinson's progresses. And we're relearning how energy conservation and awareness affects our wellbeing and ability to be present and as healthy as possible.  Thank you for listening.  EMAIL US: ParkinsonsPod@CuriousCast.ca   Have questions for Larry & Rebecca?  Want to share how your conversations go with your partner? We would love you to click and call us here.   https://www.speakpipe.com/WhenLifeGivesYouParkinsons Follow us, Larry & Rebecca Gifford  Twitter: @ParkinsonsPod Facebook: Facebook.com/ParkinsonsPod Instagram: @parkinsonspod   Thanks to  Dila Velazquez – Story Producer Greg Schott – Sound Design This episode is dedicated in memory of my friend and fellow improve performer Sukhi. Thanks for the laughs pal. Godspeed.   Our Promotional Partners include:   Diagnosed with Parkinson's? You are not alone. Contact presenting partner Parkinson Canada http://www.parkinson.ca/, call the toll free hotline 1-800-565-3000 or on Twitter you can message @ParkinsonCanada.   Thanks also to our content and promotional partners  The Michael J. Fox Foundation Parkinson's Podcast hosted by Larry Gifford as featured in the MJFF2021 Year in Review. Also noted in the 34 page booklet was… PD Avengers –  We are building a global alliance to end Parkinson's. The next Assemble meeting is Tuesday, Jan 25th at 11a PT. Join us. Details under “meetings” at PD Avengers dot com.  World Parkinson Congress 2023 – It's time to start thinking about making your plans to join us for #WPC2023 in Barcelona, Spain for t he sixth triennial congress.  Spotlight YOPD – The only Parkinson's organization dedicated to raising awareness for Young Onset Parkinson's disease and funds for the Cure Parkinson's Trust.   See omnystudio.com/listener for privacy information.

Larry & Rebecca Gifford dive deep in to deep brain stimulation (DBS). We learn about the innovative technology used for DBS from Dr. Alfonso Fasano, the chair of Neuromodulation and multi-disciplinary care at the University of Toronto and University Health Network. Sonia Soriano-Espert from Valencia, Spain, through translator and friend Sabela Avion, shares her experience of having DBS surgery conducted by a robot. This interview first aired on ODNA PK radio in Spain. The hosts are PD Avengers and members of Con P de Parkinson, a growing group of women who speak Spanish and have PD. In part-one of this two-part arc, Heather Kennedy and Becca Miller were preparing for DBS Surgery. In part two, both women share their surgery experience. The share how their children responded and how they feel about DBS, now that they have had it.  Thank you for listening.  Send us songs you would want to listen to while undergoing DBS.   EMAIL US: ParkinsonsPod@CuriousCast.ca  Or add the songs you'd want to listen to during DBS to the WLGYP DBS PLAYLIST on Spotify Have questions for Larry & Rebecca? Do you want to share your DBS story or have an idea for an upcoming podcast? Want to share how the podcast has helped you? Click the link on your laptop or desktop and leave us a voice message.https://www.speakpipe.com/WhenLifeGivesYouParkinsons Follow us, Larry & Rebecca Gifford  Twitter: @ParkinsonsPod Facebook: Facebook.com/ParkinsonsPod Instagram: @parkinsonspod Thank you to the following people and organizations featured in this episode: Alfonso Fasano, MD, PhD, Chair in Neuromodulation and Multi-Disciplinary Care, Neurologist, Co-Director of the Surgical Program, Movement Disorders Centre, Toronto Western Hospital.   Heather Kennedy, PwP, WPC2023 Ambassador a.k.a. Kathleen Kiddo Becca Miller, PhD, PwP, Michael J. Fox Foundation Patient Council, Assistant Professor of Psychiatry at Yale University.  Michael S. Okun, MDUniversity of Florida Kelly D. Foote, MD University of Florida Ted X Talk about DBS from Michael Okun, MD and Kelly Foote, MD (2012) Sonia Soriano-Espert, PwP, Valencia, Spain. Con P de Parkinson Sabela Avion, PwP, NYC & Spain. Founder of Parkinsonic. Con P de Parkinson Special music acknowledgements. Thank you to Justin Timberlake. We played 12 seconds of “Cant Stop The Feeling!” Credit goes to the song writers Timberlake, Max Martin, and Johan Schuster. Timberlake and Martin are also credited as producers along with Shellback.   Thank you to Taylor Swift. We played :17 of “Shake it Off.” The song was written by Swift, Max Martin and Shellback. It was released on Big Machine records in 2014. A special thanks to Dorothy and Scarecrow. “If I Only Had a Brain,” is heard for 31 seconds. The song is featured in the 1938 film The Wizard of Oz. It is written by Harold Arlen and Yip Harburg. Ray Bolger and Judy Garland sang it when their characters first met along the yellow brick road. The film is still under copyright by Warner Pictures. Our Promotional Partners include:   Diagnosed with Parkinson's? You are not alone. Contact presenting partner Parkinson Canada http://www.parkinson.ca/, call the toll free hotline 1-800-565-3000 or on Twitter you can message @ParkinsonCanada. Here is a link to Parkinson Canada's “Together: No Matter What” campaign Thanks also to our content and promotional partners The Michael J. Fox Foundation Parkinson's Podcast hosted by Larry Gifford Spotlight YOPD – The only Parkinson's organization dedicated to raising awareness for Young Onset Parkinson's disease and funds for the Cure Parkinson's Trust.   PD Avengers –  We are building a global alliance to end Parkinson's. Join us. World Parkinson Congress 2023 –Make plans to join us for #WPC2023 in Barcelona, Spain. Credits Dila Velazquez – Story Producer Greg Schott – Sound Design See omnystudio.com/listener for privacy information.

Larry & Rebecca Gifford dive deep in to deep brain stimulation (DBS). We challenge the Neuroscience perception that the brain is everything we know and do, and everything we are. We believe, more than just a brain that makes us human, empathetic, and real.  This first part prepares you for the surgery. We call it DBS 101. We will explain terminology detail the lead up to the surgery, and tell you why it matters where the lead wires are placed in your brain. We explore our personal hesitations surrounding DBS. And we revisit friends of the podcast, Heather Kennedy and Becca Miller, both of whom are recovering from recent DBS surgeries.  Thank you for listening. Add your voice to the show and leave a message for us here; https://www.speakpipe.com/WhenLifeGivesYouParkinsons   Follow us, Larry & Rebecca Gifford  Twitter: @ParkinsonsPod Facebook: Facebook.com/ParkinsonsPod Instagram: @parkinsonspod   Thank you to the following people and organizations featured in this episode: Heather Kennedy, PwP, WPC2023 Ambassador a.k.a. Kathleen Kiddo Becca Miller, PhD, PwP, Michael J. Fox Foundation Patient Council, Assistant Professor of Psychiatry at Yale University.  Michael S. Okun, MD University of Florida Kelly D. Foote, MD University of Florida Ted X Talk about DBS from Michael Okun, MD and Kelly Foote, MD (2012) Diagnosed with Parkinson's? You are not alone. Contact presenting partner Parkinson Canada http://www.parkinson.ca/, call the toll free hotline 1-800-565-3000 or on Twitter you can message @ParkinsonCanada. Here is a link to Parkinson Canada's “Together: No Matter What” campaign Thanks also to our content and promotional partners The Michael J. Fox Foundation Parkinson's Podcast hosted by Larry Gifford Spotlight YOPD – The only Parkinson's organization dedicated to raising awareness for Young Onset Parkinson's disease and funds for the Cure Parkinson's Trust.   PD Avengers –  We are building a global alliance to end Parkinson's. Join us. World Parkinson Congress 2023 –Make plans to join us for #WPC2023 in Barcelona, Spain. Credits Dila Velazquez – Story Producer Greg Schott – Sound Design See omnystudio.com/listener for privacy information.

The first three episodes of Season 4 of When Life Gives You Parkinson's go deep inside the brain. It has been five years since the United Nations recognized one BILLION people or one in six person's alive today on the planet suffers from a neurological disorder, from Alzheimer and Parkinson disease, strokes, multiple sclerosis, and epilepsy to migraine, brain injuries and neuro-infections. Each year, nearly 7 million dying from neurological issues each year. Every two-and-half minutes, another person dies from Parkinson's disease. What's happening to us? The Brain is Under Siege. In the kickoff episode of Season 4, Howard Weiner MD, a Harvard professor and Co-Director of the Ann Romney Center at Brigham and Women's hospital shares his theories. Weiner released a book in October 2021 called, “The Brain Under Siege; Solving the Mystery of Brain Disease, and How Scientists are Following the Clues to a Cure.”  He suggests the key to solving this diseases is to treat them like crime scenes. Learn along with Larry as Dr. Weiner details Alpha Synuclean, Microbiome, the Brain Gut Connection, and the importance of volunteering for research. He also explains how many of these brain issues have more in common that we first thought.   Thank you for listening. Add your voice to the show and leave a message for us here; https://www.speakpipe.com/WhenLifeGivesYouParkinsons   Follow us, Larry & Rebecca Gifford  Twitter: @ParkinsonsPod Facebook: Facebook.com/ParkinsonsPod Instagram: @parkinsonspod   Thank you to the following people and organizations featured in this episode: Dr. Howard Weiner, Harvard professor, Co-Director of The Ann Romney Center at Brigham and Women's Hospital and author of “The Brain Under Siege.” Dr. Ray Dorsey, co-author “Ending Parkinson's Disease.” Dr. Gregory Petsko – Ted Talk Dr. Silke Cresswell – Studies role of Gut Biome Ted Talks Djavad Mowafaghian Centre for Brain Health Diagnosed with Parkinson's? You are not alone. Contact presenting partner Parkinson Canada http://www.parkinson.ca/, call the toll free hotline 1-800-565-3000 or on Twitter you can message @ParkinsonCanada.   Here is a link to Parkinson Canada's “Together: No Matter What” campaign   Thanks also to our content and promotional partners The Michael J. Fox Foundation Parkinson's Podcast hosted by Larry Gifford Spotlight YOPD – The only Parkinson's organization dedicated to raising awareness for Young Onset Parkinson's disease and funds for the Cure Parkinson's Trust.   PD Avengers –  We are building a global alliance to end Parkinson's. Join us. World Parkinson Congress 2023 –Make plans to join us for #WPC2023 in Barcelona, Spain.   Credits Dila Velazquez – Story Producer Greg Schott – Sound Design See omnystudio.com/listener for privacy information.

This episode of When Life Gives You Parkinson’s features former NBA star Brian Grant who was diagnosed with Parkinson’s disease (PD) in 2008. He spent 12 years battling for rebounds and putting points on the board playing professional basketball and the last 13 years battling Parkinson’s and putting points on the board as a PD advocate.   “You know, when I go onto court and go up against somebody who was a big name, I’d grit my teeth to try to be an animal out there,” Grant shared. But he admits, YOPD is a different beast than pro basketball, “You can do that at Parkinson's, but it's just going to sit there and say, keep gritting your teeth and when you get done gritting your teeth…  I'm going to have your cheekbone.” From denial and depression to acupuncture and advocacy, Brian Grant’s PD story is a unique but relatable journey for many suffering and living with the disease. His honesty and vulnerability are on display as he, like many of us, try to come to terms with a disease determined to do whatever it pleases, whenever it wants to.  You can find out more about the Brian Grant Foundation at BrianGrant.org. His book Rebound: Soaring in the NBA, Battling Parkinson’s, and Finding What Really Matters is available everywhere you buy books… Thank you for listening. Add your voice to the show and leave a message for us here; https://www.speakpipe.com/WhenLifeGivesYouParkinsons Follow us, Larry & Rebecca Gifford  Twitter: @ParkinsonsPod Facebook: Facebook.com/ParkinsonsPod Instagram: @parkinsonspod Thank you to the following people featured in this episode:  Diagnosed with Parkinson’s? You are not alone. Contact presenting partner Parkinson Canada http://www.parkinson.ca/, call the toll free hotline 1-800-565-3000 or on Twitter you can message @ParkinsonCanada. Here is a link to Parkinson Canada’s “Together: No Matter What” campaign Thanks also to our content and promotional partners The Michael J. Fox Foundation Parkinson’s Podcast hosted by Larry Gifford Spotlight YOPD – The only Parkinson’s organization dedicated to raising awareness for Young Onset Parkinson’s disease and funds for the Cure Parkinson’s Trust.   PD Avengers - United to end Parkinson’s. Join us. World Parkinson Congress 2022 –Make plans to join us for #WPC2022 in Barcelona, Spain. See omnystudio.com/listener for privacy information.

This episode of When Life Gives You Parkinson’s is all about care partners and caregivers advocating for themselves. We take our jobs very seriously and often put caring for ourselves last on our lists. Our lives and well-beings are affected on nearly every level by our Person with Parkinson’s condition, and we have our own needs, yet we still are often considered predominantly in relationship to them. How do we as care partners, caregivers and Partners in Parkinson’s advocate for equal consideration in and out of our relationships? How do we make sure we have what we need to take care of ourselves, not to mention the time and space to do it? How do we learn to consistently consider our own well-being first? Rebecca takes the lead this episode and talks to three wise and wonderful care partners. First, she speaks frankly about the challenges and lessons that Cherryl Choi and Sheryl Hague have learned as they navigate their life as care partners, mothers and humans. Then she speaks to Leslie Davidson, an award-winning writer and Person with Parkinson’s who also was a care partner and caregiver to her late husband Lincoln, who had Lewy Body Dementia. She tells us what she’s learned by being on both sides of the experience and the role her writing plays in her own advocacy. And, of course, Rebecca and Larry talk about how they move through these waters in their relationship. U-Turn Parkinson’s is Sheryl and Tim Hague’s wellness center in Winnipeg. Find out more about all that Cherryl and Jimmy Choi do at a TheFoxNinja.com. Writer Leslie Davidson’s website. Thank you for listening. Add your voice to the show and leave a message for us here; https://www.speakpipe.com/WhenLifeGivesYouParkinsons   Follow us, Larry & Rebecca Gifford  Twitter: @ParkinsonsPod Facebook: Facebook.com/ParkinsonsPod Instagram: @parkinsonspod Thank you to the following people featured in this episode:   Diagnosed with Parkinson’s? You are not alone. Contact presenting partner Parkinson Canada http://www.parkinson.ca/, call the toll free hotline 1-800-565-3000 or on Twitter you can message @ParkinsonCanada. Here is a link to Parkinson Canada’s “Together: No Matter What” campaign Thanks also to our content and promotional partners The Michael J. Fox Foundation Parkinson’s Podcast hosted by Larry Gifford Spotlight YOPD – The only Parkinson’s organization dedicated to raising awareness for Young Onset Parkinson’s disease and funds for the Cure Parkinson’s Trust.   PD Avengers - United to end Parkinson’s. Join us. World Parkinson Congress 2022 –Make plans to join us for #WPC2022 in Barcelona, Spain. See omnystudio.com/listener for privacy information.

April is Parkinson’s Awareness Month! This episode of When Life Gives You Parkinson’s addresses stigma of Parkinson is in Uganda. You will meet Hannington Kabugo and learn how the passion and resourcefulness of a single advocate can help drive change in the world. Hannington and his two sisters moved with their father out of their home after the village determined his Mom was a witch. They were never to return. He tells us the stories of what happened when he sneaked back to see her. Years later, Hannington realized she was exhibiting all the signs of Parkinson’s. He has established Parkinson’s Si Buko, which means Parkinson’s is not witchcraft or a curse.  Thank you for listening. Add your voice to the show and leave a message for us here; https://www.speakpipe.com/WhenLifeGivesYouParkinsons Follow us, Larry & Rebecca Gifford  Twitter: @ParkinsonsPod Facebook: Facebook.com/ParkinsonsPod Instagram: @parkinsonspod Thank you to the following people featured in this episode: Kabugo Hannington – is the Director of Operations of Parkinson’s Si Buko Uganda Gavin Mogan – is a PwP, living in Texas, and is Executive Director of Parkinson’s Si Buko Uganda  Diagnosed with Parkinson’s? You are not alone. Contact presenting partner Parkinson Canada http://www.parkinson.ca/, call the toll free hotline 1-800-565-3000 or on Twitter you can message @ParkinsonCanada. Here is a link to Parkinson Canada’s “Together: No Matter What” campaign Thanks also to our content and promotional partners The Michael J. Fox Foundation Parkinson’s Podcast hosted by Larry Gifford Spotlight YOPD – The only Parkinson’s organization dedicated to raising awareness for Young Onset Parkinson’s disease and funds for the Cure Parkinson’s Trust.   PD Avengers - United to end Parkinson’s. Join us. World Parkinson Congress 2022 –Make plans to join us for #WPC2022 in Barcelona, Spain. See omnystudio.com/listener for privacy information.

April is Parkinson’s Awareness Month! This episode of When Life Gives You Parkinson’s Larry interviews Allan Cole from the PD Wise blog and the author of a new book Counseling Persons with Parkinson’s Disease. Allan, 53, received his diagnosis nearly five years ago. In addition to his advocacy work, he is a father of two teenaged girls, he is coming up on his 30th wedding anniversary and he is a professor and academic dean in Steve Hicks School of Social Work at the University of Texas at Austin. Halfway through this episode, the host becomes the guest as Allan interviews Larry. The discussions wind their way through work life with PD, family, advocacy, leadership and what gives them hope. Thank you for listening. Add your voice to the show and leave a message for us here; https://www.speakpipe.com/WhenLifeGivesYouParkinsons Follow us, Larry & Rebecca Gifford  Twitter: @ParkinsonsPod Facebook: Facebook.com/ParkinsonsPod Instagram: @parkinsonspod Thank you to the following people featured in this episode: Allan Hugh Cole Blog: PD Wise, Book: Counseling Persons with Parkinson’s Disease Follow Allan on Twitter: @PDWise Allan mentioned an episode of When Life Gives You Parkinson’s when I spoke with colleagues. Here’s a link to “Parkinson’s doesn’t have to be a career killer.” Diagnosed with Parkinson’s? You are not alone. Contact presenting partner Parkinson Canada http://www.parkinson.ca/, call the toll free hotline 1-800-565-3000 or on Twitter you can message @ParkinsonCanada. Here is a link to Parkinson Canada’s “Together: No Matter What” campaign Thanks also to our content and promotional partners The Michael J. Fox Foundation Parkinson’s Podcast hosted by Larry Gifford Spotlight YOPD – The only Parkinson’s organization dedicated to raising awareness for Young Onset Parkinson’s disease and funds for the Cure Parkinson’s Trust.  PD Avengers - United to end Parkinson’s. Join us. World Parkinson Congress 2022 –Make plans to join us for #WPC2022 in Barcelona, Spain. See omnystudio.com/listener for privacy information.

April is Parkinson’s Awareness Month! This episode of When Life Gives You Parkinson’s is about women with Parkinson’s who are diagnosed less often, less accurately and offered treatments that are less effective often because hormonal cycles play a role and it’s a rather unexplored area of the disease. We will hear from three women with Parkinson’s who also experienced pregnancy, giving birth and parenting with PD. All of their experiences were different, but certainly complicated by their Parkinson’s disease. And all three are now advocates for women like them. Thank you for listening. Add your voice to the show and leave a message for us here; https://www.speakpipe.com/WhenLifeGivesYouParkinsons Follow us, Larry & Rebecca Gifford  Twitter: @ParkinsonsPod Facebook: Facebook.com/ParkinsonsPod Instagram: @parkinsonspod Thank you to the following people featured in this episode: Soania Mathur, MD - Sonia was a family physician and pregnant with her first child when she was diagnosed at 27. She is co-founder of PD Avengers, co-chair of The Michael J Fox Patient Council,  on the Board of Directors for the Davis Phinney Foundation, and the medical boards of the Brian Grant Foundation and Parkinson Canada. She and her two daughters have also written two Children’s books on Parkinson’s; My Grandpa’s Shaky Hand and Shaky Hands – A Kids Guide to Parkinson’s Disease. Caitlin Nagy – After denying and hiding her diagnosis for seven years, Caitlin, a 38-year-old mother, is sharing her story of Parkinson’s in Parkinson Canada’s April Awareness Campaign “Together: No Matter What.” Paola Celli - Paola was born in Ecuador and diagnosed at the age of 12. She was married and then moved to Texas where she gave birth to two children.   Diagnosed with Parkinson’s? You are not alone. Contact presenting partner Parkinson Canada http://www.parkinson.ca/, call the toll free hotline 1-800-565-3000 or on Twitter you can message @ParkinsonCanada. Here is a link to Parkinson Canada’s “Together: No Matter What” campaign    Thanks also to our content and promotional partners The Michael J. Fox Foundation Parkinson’s Podcast hosted by Larry Gifford Spotlight YOPD – The only Parkinson’s organization dedicated to raising awareness for Young Onset Parkinson’s disease and funds for the Cure Parkinson’s Trust.  PD Avengers - United to end Parkinson’s. Join us. World Parkinson Congress 2022 –Make plans to join us for #WPC2022 in Barcelona, Spain. Credits Dila Velazquez – Story Producer Rob Johnson  – Sound Design   See omnystudio.com/listener for privacy information.

In this episode of When Life Gives You Parkinson’s, I am the host of a live event with four leading experts in the Parkinson’s world. Together they wrote a book called “Ending Parkinson’s Disease” and launched a red letter campaign to the White House. It’s been one year since the book was released and it has helped to inspired the movement PD Avengers, which I co-founded. What’s new in Parkinson’s? What have they learned? What’s standing in our way of success? Listen as Dr. Ray Dorsey, Dr. Bas Bloem, Dr. Michael Okun, and Dr. Todd Sherer sit down for one on one interviews with me and learn how, no matter where you are in the world, you can help make a difference.   Thank you for listening. Add your voice to the show and leave a message for us here; https://www.speakpipe.com/WhenLifeGivesYouParkinsons Follow us, Larry & Rebecca Gifford  Twitter: @ParkinsonsPod Facebook: Facebook.com/ParkinsonsPod Instagram: @parkinsonspod Thank you to the following people featured in this episode: Dr. Todd Sherer, CEO Michael J Fox Foundation Dr. Michael Okun, Chair and professor of Neurology, University of Florida Dr. Bas Bloem, Prof. Bas Bloem is the medical director of the Department of Neurology at Radboud University Medical Center. Dr. Ray Dorsey, Prof. Department of Neurology , Director of Center for Health and Technology (SMD)     at the University of Rochester   Buy the Ending Parkinson’s Book or Join the Red Letter Campaign www.endingpd.org Diagnosed with Parkinson’s? You are not alone. Contact presenting partner Parkinson Canada http://www.parkinson.ca/, call the toll free hotline 1-800-565-3000 or on Twitter you can message @ParkinsonCanada. Here is a link to the Parkinson’s Canada Preventing Falls Guide.   Thanks also to our content and promotional partners The Michael J. Fox Foundation Parkinson’s Podcast hosted by Larry Gifford Spotlight YOPD – The only Parkinson’s organization dedicated to raising awareness for Young Onset Parkinson’s disease and funds for the Cure Parkinson’s Trust.  PD Avengers - United to end Parkinson’s. Join us. World Parkinson Congress 2022 –Make plans to join us for #WPC2022 in Barcelona, Spain.   Credits Dila Velazquez – Story Producer Greg Schott – Sound Design   See omnystudio.com/listener for privacy information.

This episode of When Life Gives You Parkinson’s is about exploring Eastern holistic healing modalities as a complement to the pharmaceuticals relied upon by Western Medicine. Parkinson’s touches a global community, so we might as well use all the global tools to address our health and wellness. Sometimes it is a matter of having the courage to try something new. For me, last year, that was acupuncture. I am afraid of needles, but quite enjoyed the pain relief it provide and calming, centering sensation it provided. Practitioners of traditional Eastern medicine stress the importance of finding an energetic balance and energetic awareness. I have never had Reiki. Rebecca experienced it at World Parkinson Congress in Kyoto. We talk to the two Reiki masters who were in the “renewal room” and the impact that they observed Reiki had on people with Parkinson’s and care partners. We also chat with Karl and Angela Robb. Karl has had PD for thirty years. After discovering the benefits of Reiki, they both became Reiki masters and use it to manage life’s challenges. Thank you for listening. Add your voice to the show and leave a message for us here; https://www.speakpipe.com/WhenLifeGivesYouParkinsons Follow us, Larry & Rebecca Gifford  Twitter: @ParkinsonsPod Facebook: Facebook.com/ParkinsonsPod Instagram: @parkinsonspod Thank you to the following people featured in this episode: Muniqui Muhammad and Lena Takahashi www.healinglandreiki.com Karl and Angela Robb www.KarlRobb.com and check out their book A Soft Voice in a Noisy World: A Guide to Dealing and Healing with Parkinson’s Disease Book Diagnosed with Parkinson’s? You are not alone. Contact presenting partner Parkinson Canada http://www.parkinson.ca/, call the toll free hotline 1-800-565-3000 or on Twitter you can message @ParkinsonCanada. Here is a link to the Parkinson’s Canada Preventing Falls Guide.  Thanks also to our content and promotional partners The Michael J. Fox Foundation Parkinson’s Podcast hosted by Larry Gifford Spotlight YOPD – The only Parkinson’s organization dedicated to raising awareness for Young Onset Parkinson’s disease and funds for the Cure Parkinson’s Trust.  PD Avengers - United to end Parkinson’s. Join us. World Parkinson Congress 2022 –Make plans to join us for #WPC2022 in Barcelona, Spain. See omnystudio.com/listener for privacy information.

Hi, it’s Larry. I’m 49 and I have Parkinson’s disease. This episode of When Life Gives You Parkinson’s is about managing falls. It is winter and where we live snow and ice and black ice and freezing rain are all hazards, which increase everyone’s chances of falling. People with Parkinson’s are more prone to slipping and stumbling, skidding and tumbling to the ground. So, we should talk about it. I didn’t consider it a topic I’d need to know much about until I get much older. I was wrong. One reason we're doing this episode is because over the holidays I had four falls.   I am on the mend with help from NeuroFit BC’s Naomi Casiro. Rebecca and I talk with Physiotherapist Nicole Ascera, PhD. She’s a clinical specialist in neurosciences and wrote the Parkinson Canada Guide on Preventing Falls. I also meet the creator of the ACTIVATOR Poles by Urban Poling, Mandy Shintani. These are great tools especially for gait, balance and confidence issues. Through the episode, Rebecca and I realize we have a lot to do to prepare mentally, physically, emotionally and spiritually for the next fall. And the fall after that one. And the one after that one. Thank you for listening. Add your voice to the show and leave a message for us here; https://www.speakpipe.com/WhenLifeGivesYouParkinsons Follow us, Larry & Rebecca Gifford  Twitter: @ParkinsonsPod Facebook: Facebook.com/ParkinsonsPod Instagram: @parkinsonspod Thank you to the following people featured in this episode: Naomi Casiro (Founder/ Registered Physiotherapist) BSc. (Kin), MPT, Certified PWR! https://www.neurofitbc.com/ Nicole Acerra, PhD Nicole Acerra, PhD, is a physiotherapist with a passion for neurological and vestibular rehabilitation. She is one of the authors of the Parkinson Canada’s Preventing Falls Guide Mandy Shintani OT & Gerontologist, Developer ACTIVATOR Poles & Founder Urban Poling Inc. Diagnosed with Parkinson’s? You are not alone. Contact presenting partner Parkinson Canada http://www.parkinson.ca/, call the toll free hotline 1-800-565-3000 or on Twitter you can message @ParkinsonCanada. Here is a link to the Parkinson’s Canada Preventing Falls Guide. Thanks also to our content and promotional partners The Michael J. Fox Foundation Parkinson’s Podcast hosted by Larry Gifford Spotlight YOPD – The only Parkinson’s organization dedicated to raising awareness for Young Onset Parkinson’s disease and funds for the Cure Parkinson’s Trust.  PD Avengers - United to end Parkinson’s. Join us.World Parkinson Congress 2022 –Make plans to join us for #WPC2022 in Barcelona, Spain See omnystudio.com/listener for privacy information.

In this episode of When Life Gives You Parkinson’s, my wife Rebecca and I discover and discuss integrated medicine with Dr. Indu Subramanian. Integrated medicine is where Western and Eastern medicines meet. Activities we all are aware of like yoga, mindfulness, acupuncture and massage are among the activities that fall into integrated medicine. I first met Indu when she interviewed me on a webinar for PMD Alliance in September 2020. Indu is Canadian, having been born and raised in Ontario, she now lives in LA. She runs the Center of Excellence for Parkinson’s at the West Los Angeles Veteran’s Hospital and is a neurologist on staff at UCLA hospital. She’s also certified in Integrated Medicine, has more than 200 hours of yoga training and loves to explore unconventional and non-pharma treatments to improve life for people with PD. Her study on loneliness during the pandemic causing an increase of PD symptoms was widely reported on in medical journals, newspapers and popular magazines alike. She is approachable, positive, curious, and empowering. We talk about her love of the brain, the PD Avengers, the power of storytelling, and why integrated medicine does come with some warning labels. We hope you will enjoy this conversation as much as we do. Thank you for listening. Add your voice to the show and leave a message for us here; https://www.speakpipe.com/WhenLifeGivesYouParkinsons Follow us, Larry & Rebecca Gifford  Twitter: @ParkinsonsPod Facebook: Facebook.com/ParkinsonsPod Instagram: @parkinsonspod Thank you to the following people featured in this episode: Dr. Indu Subramanian, Movement Neurologist over seeing Parkinson’s Center of Excellence at the West Los Angeles Veteran’s Hospital and a neurologist at UCLA Hospital. Follow her on twitter at @drisubramanian  Diagnosed with Parkinson’s? You are not alone. Contact presenting partner Parkinson Canada http://www.parkinson.ca/, call the toll free hotline 1-800-565-3000 or on Twitter you can message @ParkinsonCanada Thanks also to our content and promotional partners The Michael J. Fox Foundation Parkinson’s Podcast hosted by Larry Gifford Spotlight YOPD – The only Parkinson’s organization dedicated to raising awareness for Young Onset Parkinson’s disease and funds for the Cure Parkinson’s Trust.  PD Avengers - United to end Parkinson’s. Join us. World Parkinson Congress 2022 –Make plans to join us for #WPC2022 in Barcelona, Spain. Credits Dila Velazquez – Story Producer Greg Schott – Sound Design See omnystudio.com/listener for privacy information.

In the first episode of our third season, Peter Brenders, CEO of the New Brunswick Health Research Foundation, talks with Dr. Karen Lee, President and CEO of Parkinson Canada, about the impact of Covid-19 on the health charitable sector and research funding. Get on the email list at healthbiz.substack.com

In this episode of When Life Gives You Parkinson’s, my wife Rebecca and I are talking with two leaders of Parkinson's organizations about the impact coronavirus has had on advocacy, collaboration, new programs. Karen Lee and Elizabeth “Eli” Pollard are true leaders with serious minds and senses of humor, and both are visionary when it comes to bringing the Parkinson community together with a purpose.  Dr. Karen Lee took on the role of President and CEO of Parkinson’s Canada in the middle of the Coronavirus pandemic. She’s taking the work-at-home mandate as a chance to meet and get to know her staff, advocates, and leaders of other organizations virtually, “We talk with all the various groups, look for opportunities, synergies, it's not about trying to compete and were not looking to duplicate efforts, but really looking for efficiencies and opportunities.” Parkinson Canada is also establishing a Parkinson Advisory Council to help inform decisions and make recommendations to the charity. Eli Pollard, Executive Director of World Parkinson Coalition, would typically make 12 to 15 trips to various destinations as she plans for the World Parkinson Congress 2022 in Barcelona. With travel restricted by COVID-19, she has been busy creating new programs including a dual language webinar series where the same presenters host a webinar first in English and then thirty minutes later in Spanish.  She’s also just announced that May 17-21, 2021 is the inaugural VIRTUAL World Parkinson Congress, “We've been chewing on this idea for a long time and COVID sort of pushed our hand, which is great. So it would be sort of “year one” is the in-person Congress, “year two” and “year three” would be a virtual Congress. And so we're calling it WPC Virtual.” This year’s theme is advancing science care and living with Parkinson's. Their will be around 80 presenter's, with 5 tracks, but all the content for each day will be release at once for virtual attendees to watch it at their convenience. There will be live Q&A sessions 24 hours after each scheduled session. The WPC Virtual admission is $25.00, all inclusive.                                      Thank you for listening. Add your voice to the show and leave a message for us here; https://www.speakpipe.com/WhenLifeGivesYouParkinsons Follow us, Larry & Rebecca Gifford  Twitter: @ParkinsonsPod Facebook: Facebook.com/ParkinsonsPod Instagram: @parkinsonspod Thank you to the following people featured in this episode: Dr. Karen Lee – President and CEO of Parkinson Canada@Dr_KarenLee To learn more about the Parkinson Advisory Council https://www.parkinson.ca/listing/parkinson-advisory-council-member/ Eli Pollard – Executive Director, World Parkinson Coalition #WPC2022 For more information on Dual Language webinars https://www.worldpdcoalition.org/page/webinarseries For more information on 2021’s VIRTUAL World Parkinson Congress https://www.worldpdcoalition.org/page/WPCVirtual For more information on the WPC Research Spotlight https://www.worldpdcoalition.org/events/EventDetails.aspx?id=1470125 For more information on 2022’s World Parkinson Congress in Barcelona https://www.worldpdcoalition.org/events/EventDetails.aspx?id=1470125 Diagnosed with Parkinson’s? You are not alone. Contact presenting partner Parkinson Canada http://www.parkinson.ca/, call the toll free hotline 1-800-565-3000 or on Twitter you can message @ParkinsonCanada Thanks also to our content and promotional partners The Michael J. Fox Foundation Parkinson’s Podcast hosted by Larry Gifford Spotlight YOPD – The only Parkinson’s organization dedicated to raising awareness for Young Onset Parkinson’s disease and funds for the Cure Parkinson’s Trust.  PD Avengers - United to end Parkinson’s. Join us. World Parkinson Congress 2022 –Make plans to join us for #WPC2022 in Barcelona, Spain. See omnystudio.com/listener for privacy information.

In this episode of When Life Gives You Parkinson’s, Larry and Rebecca Gifford welcome 2021 by digging through a sack full of hope. Each week there seems to be another headline that signals major breakthroughs – as in bio-markers and disease altering treatments – are just around the corner for Parkinson’s. We talk to two people who confirm we are on the precipice of major changes in how we view and treat the disease.  However, it is not just about the diagnosis and treatments. PD advocates come in all shapes and sizes – from 80 year old driveway walkers, to middle aged soccer players, to geeks and nerds sitting behind a computer screen. Each are unleashing their super powers on the PD community and owning it. Get ready for lasers in your head, a race with the moon and the inaugural Parkython. Plus, there’s a tomato… a laser… a magic ring…  Uma Thurman….Barcelona, and a serious discussion of wearables for non-invasive measuring of dopamine levels. If you are a half-glass empty person, this episode will either be so packed with hope is shooting out your ears or you will have 17 more great, positive, groundbreaking, even life changing, “wow” moment things to find flaw with. Thank you for listening. Add your voice to the show and leave a message for us here; https://www.speakpipe.com/WhenLifeGivesYouParkinsons Follow us, Larry & Rebecca Gifford  Twitter: @ParkinsonsPod Facebook: Facebook.com/ParkinsonsPod Instagram: @parkinsonspod Thank you to the following people featured in this episode: David Vocadlo, Canada Research Chair in Chemical Biology, Simon Fraser University. His research website is here. Debi Brooks, Co-Founder and Executive Vice Chairman of the Michael J. Fox Foundation. Listen to Episode One of the podcast series “Milestones and Momentum in Parkinson’s Research” Charlie Appleyard –  Learn about Sport Parkinsons here. The “Race the Moon” announcement will be on Monday, January 11, 2021. Rui Cuoto – Read about Parkython (Parkinsons + Hackathon) and register to be a part of it! Kevin Krejci – Learn more about the Oura Ring we discussed.  John Dean – For details on the EPDA’s Keep on Moving and ExerciseCast click the links.  Ralph & Berys Richardson – Check out Team Ralph on the SuperWalk website Greg Hicks – Greg documents Ralph’s campaign on Facebook Special thanks to Pulp Fiction and Uma Thurman’s tomato joke, Dave Clark (Happy 10th-Parkyversary), the generic voice guy for Vie Light, and Babe Ruth for calling his shot. Here’s a link to the photo of the Levodopa Tomato. Diagnosed with Parkinson’s? You are not alone. Contact presenting partner Parkinson Canada http://www.parkinson.ca/, call toll free hotline 1-800-565-3000, on Twitter @ParkinsonCanada Thanks also to our content and promotional partners The Michael J. Fox Foundation Parkinson’s Podcast hosted by Larry Gifford Spotlight YOPD – The only Parkinson’s organization dedicated to raising awareness for Young Onset Parkinson’s disease and funds for the Cure Parkinson’s Trust.  PD Avengers - United to end Parkinson’s. Join us. World Parkinson Congress 2022 –Make plans to join us for #WPC2022 in Barcelona, Spain. See omnystudio.com/listener for privacy information.

In this episode of When Life Gives You Parkinson’s, you will meet Ralph and Berys Richardson who have been married 52 years. Five years ago, doctors diagnosed Ralph with Lewy Body Dementia and then Parkinson’s disease a few years later. When COVID-19 hit, Ralph’s usual exercise programs were cancelled. So, with the help of Berys and his caretaker Greg Hicks, he decided to walk up and down his driveway everyday. He set his mind to doing 30 laps. He reach his goal in 17 days. Then he set his sights a bit higher, walk 100 days to raise $10,000. More than 200 days later, he’s still walking and he’s raised more than $30,000 for Parkinson Canada. Also, this episode is the final episode for contributor Niki Reitmayer. We say farewell and good luck. Thank you for listening. Add your voice to the show and leave a message for us here; https://www.speakpipe.com/WhenLifeGivesYouParkinsons Follow us, Larry & Rebecca Gifford  Twitter: @ParkinsonsPod Facebook: Facebook.com/ParkinsonsPod Instagram: @parkinsonspod A fond farewell to Co-host and Producer Niki Reitmeyer. We love you, will miss you and wish all the best. Thanks for going on this journey with us. Thank you to the following people featured in this episode: Ralph & Berys Richardson – Check out Team Ralph on the SuperWalk website Greg Hicks – Greg documents Ralph’s campaign on Facebook Diagnosed with Parkinson’s? You are not alone. Contact presenting partner Parkinson Canada http://www.parkinson.ca/, call toll free hotline 1-800-565-3000, on Twitter @ParkinsonCanada Thanks also to our content and promotional partners Parkinson’s IQ + You– A free, series of Parkinson’s events from the Michael J. Fox Foundation Spotlight YOPD – The only Parkinson’s organization dedicated to raising awareness for Young Onset Parkinson’s disease and funds for the Cure Parkinson’s Trust. PD Avengers - We want to help end Parkinson’s disease. Join us. World Parkinson Congress 2022 –Make plans to join us for #WPC2022 in Barcelona, Spain.   Credits Dila Velazquez – Story Producer Greg Schott – Sound Design See omnystudio.com/listener for privacy information.

In this episode of When Life Gives You Parkinson’s, what happens when the side effects of your medication are causing more harm than the disease itself? Many people with Parkinson’s are treated with dopamine agonists, which work perfectly for thousands of people, but can cause uncontrollable, destructive behaviors for others. Among the issues are compulsive shopping, hyper-sexuality, binge eating, internet addictions, and excessive gambling. Larry, Rebecca and Niki will introduce you to two people with Parkinson’s who experienced impulse control disorder while on agonists. One of them gained 60 pounds and the other went deep in debt, lost her inhibitions, her job and nearly everything else. Thank you for listening. Add your voice to the show and leave a message for us here; https://www.speakpipe.com/WhenLifeGivesYouParkinsons Follow us, Larry & Rebecca Gifford  Twitter: @ParkinsonsPod Facebook: Facebook.com/ParkinsonsPod Instagram: @parkinsonspod Follow Co-host and Producer Niki Reitmeyer Twitter: @Niki_Reitmayer Thank you to the following people featured in this Vicki Dillon – PwP, follow Vicki on Twitter and her website Ken Robinson – Vicki’s Partner                                                                                                          Susan O’Rourke – PwP, President of Artfront Galleries in Newark, NJ Dr. Elana Clar – Neurologist, Movement Disorder Specialist, New Jersey Brain and Spine Dave Andrews – PwP, Follow Dave on Twitter Gil Thelon – PwP, Gil writes about Parkinson’s at www.shufflingeditor.com Dr. Jonathon Squires – Neurologist, Movement Disorder Specialist at Djavad Mowafaghian Centre for Brain Health Special thanks to Niki Reitmayer for sharing her findings from her UBC Psych 301 Final: Impulse Control Disorders: The Strange Side Effect of Dopamine Agonists When Used to Treat Parkinson’s Disease. CREDIT: Sex, Lies and Parkinson’s Documentary 2011, Channel 4 production. Directed by Oliver Cheetham, Produced by Oliver Cheetham and James Rogan Diagnosed with Parkinson’s? You are not alone. Contact presenting partner Parkinson Canada http://www.parkinson.ca/, call toll free hotline 1-800-565-3000, on Twitter @ParkinsonCanada Thanks also to our content and promotional partners Parkinson’s IQ + You– A free, series of Parkinson’s events from the Michael J. Fox Foundation Spotlight YOPD – The only Parkinson’s organization dedicated to raising awareness for Young Onset Parkinson’s disease and funds for the Cure Parkinson’s Trust.  PD Avengers - We want to help end Parkinson’s disease. Join us. World Parkinson Congress 2022 –Make plans to join us for #WPC2022 in Barcelona, Spain. See omnystudio.com/listener for privacy information.

The Bay Downtown has closed its doors early (0:05); Parkinson Canada on Giving Tuesday (9:45); Preparing for vaccine scams (14:00) & Are Church restrictions legal? (17:01) See omnystudio.com/listener for privacy information.