Too Young For This Sh*t with Allie Signorelli
Allie Signorelli
0
This is a podcast about fighting back and finding joy in the face of the difficult things life throws our way...no matter what age we are! Here we laugh, we cry, and sometimes we employ a few explicit battlecries, but most of all, we share authentic stories about how to survive this thing we call life.
Episodes
-
Rachel Reid, Author of Heated Rivalry Talks About Having Parkinson's 09.06.2026 35mMy guest this week is New York Times best selling author of Heated Rivalry, the incredible Rachel Reid! Heated Rivalry took the world by storm earlier this year and is now a global phenomenon with millions of passionate fans. But what many people may not have known is that Rachel was diagnosed with Parkinson’s disease the exact same week that she was approached to turn her beloved book series into a television show. We talk about navigating the whirlwind media and events tours she’s been on while being a working mom with writing deadlines AND a chronic disease. Phew!
-
Tom Dumont, No Doubt Guitarist & Living with Young Onset Parkinson's 02.06.2026 45mIt would be safe to say I don’t have many memories of college that don’t include a song from No Doubt. They are the soundtrack of my generation and guitarist Tom Dumont is a true legend. What an honor it was to chat with him about navigating his young onset Parkinson’s diagnosis and how he’s been able to continue creating music for us his fans. Tom is thoughtful and insightful and an all around bad ass and I am so glad we got to chat.
-
Ryan Reynolds, Actor, Entrepreneur, and Parkinson's Advocate 19.05.2026 33mIf I’ve learned one thing in the last few years about Parkinson’s, it’s that this disease doesn’t care who you are – and often, the only thing connecting people living with it is the disease itself. Imagine my surprise then, to form a common bond with someone I never thought I’d even meet, let alone become friends with. (Ok friends is a strong word here…ha! but let’s go with it). I’m so happy to share my conversation with Ryan Reynolds about our shared experiences with this disease, but also our collective commitment to raising awareness about it and specifically some of the more challenging aspects and symptoms. Ending stigma about Parkinson’s is vitally important to improving the lives of those of us facing it every day. I am grateful to Ryan for using his platform to help do this and look forward to continuing to chat and hopefully do our part to change the course of Parkinson’s as best as two Canadian kids from the 80s can. Well, I guess three if you count that other guy. ;)
-
Rebecca King Crews, Singer, Actress, Designer, Producer & Living with Young Onset Parkinson's 05.05.2026 40mRebecca King-Crews is a singer, actress, producer, and author, and the wife of actor Terry Crews. She recently announced that she has been living with Parkinson’s disease and she shares more about her decision to go public, her recent procedure and how she is living well with the disease.
-
Connie Carpenter-Phinney, Olympic Gold Medalist & Parkinson's Care Partner 28.04.2026 51mConnie Carpenter-Phinney is well known in the Parkinson’s world for the incredible organization and she her husband, fellow Olympian, Davis Phinney, created. But well before that, Connie was the first woman to ever win the Olympic Gold Medal in cycling. She is a legend in the sport, and now a hero to so many others as an advocate not only for people living with Parkinson’s, but for their care partners as well.
-
Greg Schaefer, 19 Time Ironman Competitor Living With Parkinson's 14.04.2026 41mGreg Schaefer is an 19-time IRONMAN who is living with Young Onset Parkinson’s disease. For nearly a year, the disease robbed him of movement and left him questioning whether the athlete he had been his entire life was gone forever. This year, Greg will compete in the Ironman World Championships in Kona. Greg and I talk about finding out he had Parkinson’s, how it has affected his family, and how he’s come back to racing with resilience.
-
Dan Feehan, Chief Policy Officer, Michael J. Fox Foundation 31.03.2026 51mJoining me this week on the podcast is Dan Feehan, Chief Policy Officer for The Michael J. Fox Foundation. After witnessing the September 11 attacks while a student at Georgetown University, Dan joined the Army, completed Ranger School, and served two combat tours in Iraq. His service was recognized with the Bronze Star and Army Commendation Medal with Valor. Following his military career, Daniel dedicated himself to education, teaching middle school math in underserved communities in Chicago, Illinois and Gary, Indiana. His commitment to public service led him to the White House Fellowship program, after which he went on to serve as Principal Deputy Assistant Secretary of Defense for Readiness at the Pentagon. Dan received his master’s in public policy from Harvard’s Kennedy School of Government and joined the Fox Foundation last summer where he now leads the government relations team. We talk about his incredible career, the state of Parkinson’s policy, the importance of advocacy and how listeners can get involved.
-
Esther Labib-Kiyarash aka "Shaking In My Boots" 24.03.2026 50mEsther Labib-Kiyarash, aka “Shaking In My Boots” is my funny, brilliant, blunt young onset Parkinson’s bestie who understands the highs and lows of living our lives online. It’s a role we take seriously despite being totally giggly 99% of the time we talk. In this episode we pull back the curtain on the role of social media in advocacy, how we try to bridge the gap between patients and providers, our families, our futures and so much more.
-
Molly R. Stern, MakeUp Artist To The Stars with Special Guest Mandy Moore 10.03.2026 48mMolly R. Stern is an incredibly successful and in-demand celebrity make-up artist, a mom and an advocate. At the height of her career, Molly was diagnosed with Parkinson’s disease and on this episode, we talk about resilience and what it takes to keep working and doing the things you love in the face of a shocking diagnosis. I invited one of Molly’s clients and friends, actress and brain health advocate Mandy Moore to join us as a special surprise. Enjoy!!!
-
Toby The Neuroscientist 03.03.2026 40mJoin me in a great chat with neuroscientist Toby Curless for a chat about neurodegenerative diseases, fashion, social media and more!
-
Sue Monk Kidd 24.02.2026 43mJoin me and celebrated author of The Secret Life of Bees, Sue Monk Kidd as we talk about her incredible career and her life with Parkinson's. Too Young is a podcast about fighting back and finding joy in the face of the difficult things that life throws our way...no matter what age we are. Here we laugh, we cry, and sometimes we employ a few explicit battle cries, but most of all, we share authentic stories about how to survive this thing we call life. More to Parkinson’s is an educational campaign, sponsored by Acadia Pharmaceuticals Inc., to increase awareness among caregivers and patients of the existence of hallucinations and delusions as possible parts of Parkinson’s disease. Acadia Pharmaceuticals is a sponsor of this podcast. Ryan Reynolds is a spokesperson for Acadia. Views expressed are those of the hosts. Visit moretoparkinsons.com to learn more and for additional resources.
-
Michael J. Fox & Nelle Fortenberry 17.02.2026 28mFor the official inaugural episode of the Too Young for this Sh*t podcast, Allie welcomes the one and only Michael J. Fox. Michael joins Allie to talk about his newest book Future Boy and they are joined by his co-author and longtime friend and collaborator Nelle Fortenberry. The book shares the incredible story of the time in Michael’s career when he was filming Family Ties during the day, and Back to the Future at night. They also talk about creating the Fox Foundation 25 years ago and his return to acting on the hit show Shrinking opposite Harrison Ford. I hope you enjoy my conversation with Michael and Nelle! The Too Young For This Sh*t Podcast is sponsored in part by Acadia Pharmaceuticals. Visit www.moretoparkinsons.com
-
Katie Couric 14.12.2025 31mI mean...do we even need a description here? My sit down with the legendary news icon Katie Couric. We talked all about Parkinson's and a million other things that I can't even really remember because I am pretty sure I blacked out for most of this conversation. What I do know is that she is hysterical and generous and I am lucky to know her.
-
Dr. Dorsey & Dr. Okun - The Parkinson's Plan 14.08.2025 44mAn episode about the New York Times bestselling book The Parkinson’s Plan written by two neurologists on the cutting edge of Parkinson’s research, Dr. Ray Dorsey and Dr. Michael Okun.
-
Ai-jen Poo 25.11.2024 43mJoin me as I chat with the amazing Ai-jen Poo who has been recognized among Fortune’s 50 World’s Greatest Leaders and Time’s 100 Most Influential People in the World, and she has been the recipient of countless awards, including a 2014 MacArthur "Genius" Award. Ai-jen has been a featured speaker at TEDWomen, Aspen Ideas Festival, Cannes Lions Festival of Creativity, Skoll World Forum, and the Obama Foundation Inaugural Summit.
-
Lauren Miller Rogen 16.10.2024 26mA conversation with producer, actress, writer, director and nonprofit founder Lauren Miller Rogen who started Hilarity for Charity (HFC) with her husband Seth Rogen. Lauren lost her mom to early onset Alzheimer's and created HFC to bring light to the disease and to support caregivers. Lauren shares her mom's story and the incredible work HFC is doing today to educate the next generation about the importance of brain health.
-
Dr. Rachel Dolhun 27.08.2024 13mDr. Rachel Dolhun is a double-board-certified neurology and lifestyle medicine physician and fellowship-trained movement disorder specialist, who joined The Michael J. Fox Foundation in 2014 to lead medical communication. This conversation is about being a woman with Parkinson's and all that that entails. Spoiler alert: PD is not the same experience for women as it is for men. Join us as we talk all things gals, brains and more!
-
Dr. Michael Okun 26.06.2024 57mJoin me and Dr. Michael Okun, New York Times bestselling author of The Parkinson's Plan and He is a leading national spokesperson for Parkinson's disease, and has been extensively quoted in The New York Times, Wall St. Journal, USA Today, CNN and other media. He is the former Chair of Neurology at the University of Florida. He is the co-founder and Executive Director of the Norman Fixel Institute for Neurological Diseases at the University of Florida Health. The Institute is unique in that it is comprised of more than 150 interdisciplinary faculty members from diverse areas of campus, all of whom are dedicated to care, outreach, education and research. The Institute is well known for its science and service hub model of care and research as well as for its international think tanks. Dr. Okun holds the Adelaide Lackner Professorship in Neurology and has published more than 600 peer-reviewed articles and trained over 80 MD fellows in Parkinson’s disease. His research is funded by the National Institutes of Health, he is a published poet (Lessons From the Bedside, 1995) and author of 15 books including most recently The Parkinson’s Plan (2025). His research is highly cited and has appeared in the New England Journal of Medicine, JAMA, Lancet and many other peer-reviewed venues. He has been invited to speak about Parkinson's disease and movement disorders all over the world and was honored at the White House in 2015 as a champion for change in Parkinson’s disease. His book Parkinson’s Treatment: 10 Secrets to a Happier Life has been translated into more than 20 languages.
-
Congressman Gus Bilirakis 25.06.2024 15mJoin me and Congressman Gus Bilirakis (R-FL) as we talk about the historic passing of the National Plan to End Parkinson's act which was named in honor of his brother Dr. Emmanuel Bilirakis who lived with Parkinson's disease. This was recorded shortly after President Biden signed the law to create the National Parkinson's Project in July 2024.
-
Dr. Ray Dorsey 15.04.2024 42mDr. Ray Dorsey is a leading voice in Parkinson’s disease research and care, and a tireless advocate for rethinking how we approach chronic illness. A neurologist by training, he combines deep clinical experience with a passion for how technology can fuel health care innovation and change. “I knew I wanted to be a doctor in first grade,” says Dr. Dorsey, whose parents were both psychiatrists. “I’ve always loved learning and I still do.” Dr. Dorsey holds a Bachelor of Science in biological sciences from Stanford University, and a joint MD/MBA degree from the University of Pennsylvania Perelman School of Medicine and the Wharton School
Popular in
The podcast also appears in the podcast charts of these countries.