Best fibrosis podcasts we could find (Updated February 2018)
Related podcasts: Cystic Cf Health and Well-Being Jerry Esiason Cahill Boomer Bef Foundation Science Medicine Cftr Therapies Cme Education Society Pediatrics Mutation US Government Conversations  
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Breathe In: A Cystic Fibrosis Podcast
 
A dynamic podcast exploring the different experiences people with cystic fibrosis may face during their lives. Gunnar Esiason joins Tiffany Rich and Lea Faraone, otherwise known as the Salty Cysters, to talk about the in's and out's of cystic fibrosis from some of the anxieties and stresses that patients face to some of the lighter sides of the disease. Breathe In: A Cystic Fibrosis Podcast aims to characterize the disease in a positive way while showcasing the challenges that people with cy ...
 
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Cystic Fibrosis in Focus
Daily+
 
Cystic fibrosis (CF) is one of the most prevalent global congenital disorders, affecting some 70,000 individuals worldwide and 30,000 children and adults in the United States. While clinical efforts are expanding worldwide to improve diagnostic testing and treatment approaches for this progressive lung disease, targeted therapies for CF against any specific mutation remain elusive.The Cystic Fibrosis in Focus series gathers the latest information from leading medical experts devoted to advan ...
 
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Jerry Cahill's Cystic Fibrosis Podcast
 
54 Years Old and Living-Breathing Succeeding With Cystic Fibrosis
 
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Cystic Fibrosis Review
Rare
 
Timely commentary on current research, best practices and clinical management issues, provided by an expert panel of Cystic Fibrosis Specialists
 
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Cystic Fibrosis Podcast
Rare
 
Jerry Cahill's Cystic Fibrosis Podcast is presented by the Boomer Esiason Foundation. A non-profit organization dedicated to funding research for CF and improving the quality of life of those affected by cystic fibrosis. Jerry Cahill is a 57 year old male with CF who has been able to thrive with a disease that has a average lifespan of 31 years. In this podcast Jerry gives his views on living with CF.
 
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My Journey With Cystic Fibrosis
Monthly+
 
This Podcast was created using www.talkshoe.com
 
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Jerry Cahill's Cystic Fibrosis Podcast
 
54 Years Old and Living-Breathing Succeeding With Cystic Fibrosis
 
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Jerry Cahill's Cystic Fibrosis Podcast
 
54 Years Old and Living-Breathing Succeeding With Cystic Fibrosis
 
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AHEAD OF THE CURVE: Cystic Fibrosis
 
Stay Ahead of the Curve with these valuable continuing education resources for the Cystic Fibrosis Care Team.
 
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CF Pioneers
Rare
 
Welcome to the CF Pioneers Podcast! I am your host, Eric Marten. The purpose of this podcast is to highlight Pioneers in the Cystic Fibrosis community. Advances in medicine and awareness, have increased the median life expectancy, which has allowed people living with CF, to pursue their dreams, and reach goals, that were unheard of just a few generations ago. There is still a long ways to go, and many obstacles to overcome, but as we move forward, together we will make it another day.
 
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Lung Story Short
Weekly
 
Each week tune in to hear about different subjects spanning from Cystic Fibrosis, transplant, outdoors, sisterhood, friendships and more.
 
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Joshland Unfiltered
Rare
 
An original podcast that gets inside the heads of the Cystic Fibrosis Community to talk about all kinds of topics with respect and honesty.
 
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Jerry Cahill's CF Wind Sprints
 
The Boomer Esiason Foundation has launced a series of brief videos - "Jerry Cahill's CF Wind Sprints"-answering the cystic fibrosis community's questions about living with CF.
 
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Listen to The Lancet Respiratory Medicine
 
The Lancet Respiratory Medicine publishes a range of article types in respiratory medicine and critical care. These include Original Research, Reviews, Personal Views, Comments, and News articles. Topics include but are not limited to asthma, COPD, tobacco control, critical care, lung cancer, cystic fibrosis, pneumonia, sarcoidosis, mesothelioma, sleep medicine, and respiratory infections.
 
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CF Podcast
Daily+
 
I talk about life with Cystic Fibrosis
 
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Making it Matter with Gunnar Esiason and Julia Rae
 
Highlighting the the challenges people with cystic fibrosis face, and the people who face them. Join Gunnar Esiason and Julia Rae as they discuss the highs and lows of a life with cystic fibrosis through their eyes as people fighting back against the disease. This is not medical advice, this is their real life experiences.
 
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Simon J Green's Storytelling
Rare
 
Simon J Green is a Melbourne writer telling stories steeped in the joy of genre. Working in science fiction, horror and comedy, he uses tropes of the fantastic to blow up our social anxieties. Living with cystic fibrosis, Simon is driven by telling dangerously fun stories readers love.
 
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Ahead of the Curve: Genetics Revolution for the CF Care Team
 
This 90-minutes symposium was presented at NACFC Anaheim 2011, offering information on the current treatment options for patients with cystic fibrosis, as well as information on emerging therapies. The topics include:- CFTR gene modifiers: what are they & how they work- The importance of the CFTR genotype/phenotype interaction- The role of gene modifiers in determining CF presentations- Using gene-targeted therapies to implement individualized treatment
 
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Making it Matter with Gunnar Esiason and Julia Rae
 
Highlighting the the challenges people with cystic fibrosis face, and the people who face them. Join Gunnar Esiason and Julia Rae as they discuss the highs and lows of a life with cystic fibrosis through their eyes as people fighting back against the disease. This is not medical advice, this is their real life experiences.
 
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Broken Boner Radio with Daniel Canfield, the Voice of Erectile Dysfunction
 
Laugh and learn about a delicate subject! Known as The Voice of Erectile Dysfunction, Daniel was diagnosed with a very common degenerative condition called Corporal Erectile Tissue Fibrosis. He knows all to well the anxieties, frustrations and embarrassment of living with erectile dysfunction. After exploring all the medically approved treatments including vacuum pumps, various E.D. pills and injections to his penis, Daniel ultimately underwent a life changing penile implant surgery in 2012. ...
 
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CF Matters Podcast
Rare
 
CF Matters is a podcast about improving health and care in the CF community. CF Matters is hosted by Erin and Breck, two mothers of children with the life-shortening disease, cystic fibrosis, who share our experiences, thoughts and insights of living with a chronic condition.
 
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Francis Collins
Rare
 
At age 15, Francis Collins "...had no interest in biology, or medicine, or any of those aspects of science that dealt with this messy thing called life. It just wasn't organized, and I wanted to stick with the nice pristine sciences of chemistry and physics, where everything made sense." A few years later, this farm boy from Virginia's Shenandoah Valley discovered the emerging field of DNA research and changed his whole life direction in life. Already a graduate student with a wife and child ...
 
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show series
 
More than 100 Cochrane Reviews of interventions for people with cystic fibrosis are now underway, with nearly ninety published in full. In October 2017, this list was added to with a review of the effects of a breathing technique called autogenic drainage. We asked the lead author, Pamela McCormack from Alder Hey Children's Hospital in Liverpoo ...…
 
This weeks podcast we talk about a not so fun subject. Being catfished in the Cystic Fibrosis community. Yes, ladies and gentlemen, it's a thing. No one seems to be addressing it publicly so of course Rima and I am. We do so because we have just gone through one of the craziest experiences I've ever encountered or heard of. Anytime we tell peop ...…
 
This week’s episode is a special one. My guest is Jen Sabin Sattley, an incredible woman who has lived her whole life with Cystic Fibrosis. Not only that, but she’s lived through a lung transplant from two living donors, a kidney transplant, and has created a wildly popular recipe blog. There is something so special about Jen and her perspectiv ...…
 
Our final show of the year! WOW – it went by super fast it seems. Tonight, it’s once again round-the-globe to Christchurch, New Zealand this time to speak with Evelin Bourne. Evelin and I “met” on FaceBook and as I followed some of the things she was doing and saying, I wanted to know more about her. American born and raised, Evelin and her wif ...…
 
Merry Xmas! In order to get in the proper seasonal mood we went through a lot of Snow and Ice levels through the Mario Kart series. Tracks:Rosalina's Ice World, Mario Kart 7, Special Cup, Race 2Mount Wario, Mario Kart 8, Star Cup, Race 4Ice Ice Outpost, Mario Kart 8, Triforce Cup, Race 3Animal Crossing, Mario Kart 8, Crossing Cup, Race 4 (to in ...…
 
Gunnar, Tiff and Lea talk about finding positivity in illness. Cystic fibrosis is a constant uphill battle, and the stress of constant adversity certainly is taxing, but the trio discussing points of motivation throughout their paths with chronic illness. Tiffany talks about her "weekly events" that she planned for herself when she was in end-s ...…
 
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Awesome Spaceship
 
Merry Xmas! Tori and Andrew enjoy each other's company by chatting about Xmas music via a new game "Xmas Joys or Xmas Noise?". We get into another festive Name Game and Tres Preguntas sets us up for some apt Xmas music conversation. Thanks to Michaela for the special Xmas moment email. Very touching. Thanks to Moses J Bird for singing loud and ...…
 
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Breathe In: A Cystic Fibrosis Podcast
 
The trio talks about the evolution of cystic fibrosis nutrition. The podcast starts with the group talking about the "old days" of CF nutrition when any and all high calorie diets were pushed on patients. Tiffany talks about daily trips to In-N-Out burger, while Gunnar and Lea talk about after school milkshakes. The trio then discusses how CF n ...…
 
In this podcast, we interviewed Dr. Paul Wotton, CEO, about Sigilon Therapeutics’ discovery platform. The platform combines cell engineering and biocompatible Afibromer™ technology to enable cell therapies that do not trigger fibrosis
 
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Kick This!
 
Anthony Simonetti from Just Breathe Foundation joins SoccerSam with news of this year's Cystic Fibrosis Christmas Ball.
 
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Five Things I Read This Week
 
Christianity has always been countercultural, and that's what we're going to talk about on the show today. We hold a lot of positions that are rapidly falling out of favor in American culture, and as a result, we have to be prepared for the reality that our life is going to look a little bit different than that of our neighbor. Maybe in the pas ...…
 
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Peds in a Pod: A Pediatric Board Review
 
Have fun learning about Cystic Fibrosis with Drs. Ashley Grigsby & Heather Munston
 
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Breathe In: A Cystic Fibrosis Podcast
 
The trio takes a question from a CF mom who asks, "how can I convince my kid of the importance of staying compliant with his treatments?" The episode starts off with the big topic, "were we compliant as kids?" Ultimately the group determines that CF treatments have evolved so much since the early 90's that it's tough to compare the one or two n ...…
 
Claire Wineland is an activist, entrepreneur, YouTube personality and author. Through her non-profit organization, Claire’s Place Foundation, she works to support people with terminal and chronic illness and their families She is also the author of the book Every Breath I Take, Surviving and Thriving with Cystic Fibrosis and a TEDx speaker.———— ...…
 
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Speeches by President of Ireland, Michael D. Higgins
 
See http://www.president.ie/en/diary/details/president-receives-members-of-cystic-fibrosis-ireland
 
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Breathe In: A Cystic Fibrosis Podcast
 
Tiffany celebrates the first anniversary of the double lung transplant, or her "Lungiversary" as she calls it. She takes us through the day she received "the call," which was actually her first call for transplant after several years of waiting on the transplant list, from waking up around 2am to her hospital discharge - about a month. Tiffany ...…
 
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Michelle Corr Media
 
TBA
 
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I'm Aware That I'm Rare: the phaware® podcast
 
Dr. Stephen Mathai is an Associate Professor of medicine at the Johns Hopkins University School of Medicine. His areas of clinical expertise include pulmonary disease and critical care medicine. His research interests include scleroderma-associated pulmonary hypertension, idiopathic pulmonary fibrosis and pulmonary complications of connective t ...…
 
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I'm Aware That I'm Rare: the phaware® podcast
 
Dr. Stephen Mathai is an Associate Professor of medicine at the Johns Hopkins University School of Medicine. His areas of clinical expertise include pulmonary disease and critical care medicine. His research interests include scleroderma-associated pulmonary hypertension, idiopathic pulmonary fibrosis and pulmonary complications of connective t ...…
 
Patients with non-cystic fibrosis bronchiectasis (NCFBE), a progressive pulmonary disease, currently have no treatment options in the US. Nancy Pecota, CFO of Aradigm Corporation, discusses NCFBE and what Aradigm is doing to help these patients and possibly others who have an un-diagnosed condition . Their inhalable drug Linhaliq™ is currently ...…
 
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ASAPodKarting: the Mario Kart Show
 
New Participant Mike hops on to this edition of ASAPodKarting and joins Cara and Andrew for some hot Mario Kart 8 Deluxe action on Nintendo Switch. We punish ourselves with a little 200cc, Hard Com, All Items settings and tackle Baby Park and Cheep Cheep Beach and so much more!Amazon Link to Help Fight Cystic Fibrosis: https://tinyurl.com/ASAPo ...…
 
Tori and Andrew enjoy each other's company by chatting about their recent vacation, Shameless, previous Audio Quality, Birthdays and our engagement story.The Dude stops by for this edition of the Name Game and Tres Preguntas gets into Halloween Specials, Embarrassment and Religious ghosts.Be sure to support us on November 11th for our podcastin ...…
 
Dr. Ben Weitz interviews Dr. Isaac Eliaz, who discusses Galectin-3, an inflammatory protein measured in the blood, that increases risk of nearly every chronic disease, including heart disease, diabetes, arthritis, cancer, chronic kidney disease, and heart failure. [If you enjoy this podcast, please give us a positive review on Itunes, so more p ...…
 
Listen in as Vicky Ro and Andrew start shaping up for the Halloween season. Tori tells us about a third UFO encounter and warns Andrew about Fire in the Sky. We get into Tres Preguntas Brick by Brick and take a walk down memory lane about our preferred pickle presentation. Name Game 7 was chest bursting piece of cake, but Andrew thought Tori mi ...…
 
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ASAPodKarting: the Mario Kart Show
 
We just love chatting so much we forgot to race this episode. But much wisdom was exchanged. Join Shaline, Cara and Andrew for an all talking ep of ASAPodKarting!Amazon Link to Help Fight Cystic Fibrosis: https://tinyurl.com/ASAPodcastingAmazonFB: https://www.facebook.com/groups/askyrimaddictpodcast/Twitter: https://twitter.com/ASAPodKartingEma ...…
 
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Bill is Boring (But His Friends Aren't)
 
This week, Bill meets up with old pal Hilary Becker, tune is as they talk about fast food, slow food and cystic fibrosis. Tune in. Follow Hilary @hmjbLearn more or donate
 
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Awesome Spaceship
 
Tori and Andrew have a downer episode. Call your senators, tell them to fund the CHIP program NOW!On the lighter side we get into Clothing, Unpopular opinions and pizza chains for Tres Preguntas, with a Quatro thrown in to boot. "And I will strike down upon thee with great vengeance and furious anger..." on this week's Name Game! (with an added ...…
 
Managing Idiopathic Pulmonary Fibrosis: Comprehensive Approaches Across the Disease Continuum
 
These are the stories that I love to tell. Meet Deryl & Meredith Sweeney, a couple, along with 3 other families, who are working to cure Cystic Fibrosis. CF, as it's referred to, affects tens of thousands of people and reduces the ability to breathe over time. Their son was diagnosed shortly after birth. Instead of accepting things as they were ...…
 
On the Vox Markets Podcast Today - 20th September 2017 Stephen Hughes, Vice President, Exploration at Asiamet Resources #ARS discusses the multiple high potential targets identified for drilling in the BK District in Kalimantan, Indonesia.(Interview starts at 1 minute 27 seconds) Graham Lumsden, CEO of Motif Bio #MTFB discusses why their lead d ...…
 
In honor of Rock CF Foundation's 10-year anniversary as an IRS-approved 501c3 nonprofit corporation, here is the re-release of the premier episode of Get After It with Emily Schaller, Rock CF's indomitable founder and CEO. The Rock CF Foundation is dedicated to increasing the quality of life for people with Cystic Fibrosis. With the help of a c ...…
 
Life on the Other Side of a Double Lung Transplant with Lizz Kaup Originally on the cystic fibrosis podcast series around three years ago, Lizz returns to discuss her life after her double lung transplant in March 2016. Lizz is 37 years old and was diagnosed at age 3. She is from a small town in Oklahoma. She loves the outdoors and traveling. L ...…
 
In today’s episode, I am joined by Jan Kern as my co-host for a powerful conversation with a remarkable woman—Kim Fredrickson. Kim is a sought-after speaker, writer, and counselor with expertise in cultivating self-compassion in our lives. She is the author of Give Yourself a Break: How to Turn Your Inner Critic into a Compassionate Friend and ...…
 
00:00 - WINNIPEG TRAFFIC CURIOSITIES Round 2, with Luis Escobar, Transportation Manager for the City of Winnipeg 37:57 - Luis has left the building, but the traffic discussion continues! 56:01 - Carolyn Klassen, therapist with Conexus Counselling, www.conexuscounselling.ca -- "Live like you're dying", that's what Claire Wineland says. She's an ...…
 
Tunnelers and deathclaws and marked men, oh my! **** Character art by Caitlin Hoyt! **** T-Shirts! https://www.etsy.com/shop/ASAPodcasting **** Do us a solid and use our Amazon link. Amazon proceeds defray hosting costs, and excess proceeds benefit the Cystic Fibrosis Foundation, a cause near and dear to the hearts of all of us at ASAPodcasting ...…
 
Continuing on with my conversation with Riggs, this is the episode where we talk about what it's like for him to be a stay-at-home dad with his daughter who has cystic fibrosis. We talk about what he does to level up his dad skills as well as how this experience of being a stay-at-home dad … Continue reading "004: Part 2 – Trophy Husbanding wit ...…
 
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Making it Matter with Gunnar Esiason and Julia Rae
 
http://www.gunnaresiason.com/wp-content/uploads/2017/07/MiM-47-audio.mp3
 
There are now more than 80 Cochrane Reviews of a wide variety of interventions for people with cystic fibrosis. In May 2017, one of these was updated by Lisa Morrison and Stephanie Milroy from the Queen Elizabeth Hospital in Glasgow in Scotland to bring together the latest evidence on the effects of oscillating devices. Lisa tells us what they ...…
 
Incorporating New Advances and the Latest Science to Improve Recognition and Treatment of Idiopathic Pulmonary Fibrosis
 
Welcome to the 28th edition of the Fallout Feed Roundtable! Its the 10th episode of season three. We are the show who compares and contrasts Fallout experiences through a lively Roundtable discussion by playing through the same quests with characters who have been randomly assigned drastically different attributes. Welcome Everyone!Please join ...…
 
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