Best cystic podcasts we could find (Updated April 2018)
Related podcasts: Fibrosis Cf Health and Well-Being Science Cftr Therapies Cme Medicine Society Pediatrics Jerry Esiason Cahill Boomer Bef Mutation Foundation Conversations Education Aotc  
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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 ...
 
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 ...
 
54 Years Old and Living-Breathing Succeeding With Cystic Fibrosis
 
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.
 
Timely commentary on current research, best practices and clinical management issues, provided by an expert panel of Cystic Fibrosis Specialists
 
This Podcast was created using www.talkshoe.com
 
Stay Ahead of the Curve with these valuable continuing education resources for the Cystic Fibrosis Care Team.
 
Podcast by JustinLivinLife
 
C
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.
 
L
Lung Story Short
Monthly+
 
Each week tune in to hear about different subjects spanning from Cystic Fibrosis, transplant, outdoors, sisterhood, friendships and more.
 
An original podcast that gets inside the heads of the Cystic Fibrosis Community to talk about all kinds of topics with respect and honesty.
 
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.
 
C
CF Podcast
Daily+
 
I talk about life with Cystic Fibrosis
 
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.
 
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.
 
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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show series
 
Join the Fallout Feed Crew as we check in with the Play-Along community Season 5 Character Creation feedback. We listen to audio from Jeremy and Leon, while Cara digs into the mail bag for correspondence from Wendy, Chris and Craig. Patreon: https://www.patreon.com/asapodcastingRoll a random character to Play-Along with the Fallout Roundtable:F ...…
 
Vitamin D might be key to syndrome affecting half of women aged 50 and over. The benefit of olive oil in the Mediterranean diet for osteoporosis. I'm a 56-year-old female with several cystic and fibroid conditions, how can I get rid of them? My 11-year-old son has seasonal allergies and now a chronic cough, is this related to his nasal spray?…
 
Cystic Fibrosis, an inherited disease that damages the lungs and digestive system, fewer than 200,000 diagnosed cases each year, this is what we’ll be addressing in this inspiring episode. Meet my name twin, a fellow Lauren Marie, a woman who’s life changed dramatically after receiving a diagnosis of cystic fibrosis in her early 20’s. This girl ...…
 
Today we sit down and discuss the buzz surrounding the documentary "Six Feet of Separation". This documentary follows three WHS students with Cystic Fibrosis and takes a deeper look into their everyday routines, along with the meticulous planning needed to make attending school possible. Six Feet of Separation will premiere at the 16th Annual W ...…
 
In this episode of Humans of Chelmsford we are joined by personal trainer, speaker and blogger Sophie Holmes. After being born 10 weeks premature, Sophie was diagnosed with cystic fibrosis at four months old. Her parents were told that she might not make the age of 30, let alone her teens, and she has to take up to 80 tablets a day to stay aliv ...…
 
Listen to this audiobook free with a 30-day trial. Go to http://audiobookspace.com/free Title: The Brand New CatastropheSubtitle: A MemoirAuthor: Mike ScaliseNarrator: Mike ScaliseFormat: UnabridgedLength: 7 hrs and 22 minsLanguage: EnglishRelease date: 01-31-17Publisher: Audible StudiosRatings: 4 of 5 out of 81 votesGenres: Bios & Memoirs, Per ...…
 
Listen to audiobook in full for free on hotaudiobook.com/free Title: SnowboundAuthor: Blake CrouchNarrator: Jeffrey KaferFormat: UnabridgedLength: 7 hrs and 6 minsLanguage: EnglishRelease date: 05-20-14Publisher: Mountainside Books, LLCRatings: 4 of 5 out of 699 votesGenres: Mysteries & Thrillers, SuspensePublisher's Summary:For Will Innis and ...…
 
It's Cara and Shaline, what more could you need?Patreon: https://www.patreon.com/asapodcastingAmazon Link to Help Fight Cystic Fibrosis: https://tinyurl.com/ASAPodcastingAmazonFB: https://www.facebook.com/groups/askyrimaddictpodcast/Twitter: https://twitter.com/ASAPodKartingEmail: asapodkarting@gmail.comForum: ASAPodcasting.Proboards.com…
 
Michael McDonnell has Cystic Fibrosis and Diabetes, this has not stopped him running a successful mindset coaching business. Mike shares with us the challenges of health issues and mindset issues and how he keeps going, knowing that every small incremental progress he makes goes towards to where he wants to be. He believes that the questions yo ...…
 
Shaline and Cara join Andrew for some exciting kart action but more chat about Nintendo lore than anything. Start your engines!Patreon: https://www.patreon.com/asapodcastingAmazon Link to Help Fight Cystic Fibrosis: https://tinyurl.com/ASAPodcastingAmazonFB: https://www.facebook.com/groups/askyrimaddictpodcast/Twitter: https://twitter.com/ASAPo ...…
 
On today's show..... A fixture of the radio and television business for the past 17 years, David Shimkus Host is best known for his sales on the Home Shopping Network as both a host and a guest. With over 7000 hours of on-air sales experience and years behind the microphone in voice over work and sports radio in Chicago, Dave is like an old fri ...…
 
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 ...…
 
Amber Shewfelt is the definition of toughness. She is living a triumphant life with Cystic Fibrosis, setting and achieving goals regardless of the daily adversity. Her main goal is to make life better for others dealing with CF in a selfless and remarkable way. We discuss life, death, and how to share your message in a way that can change a lif ...…
 
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 ...…
 
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 ...…
 
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 ...…
 
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 ...…
 
Anthony Simonetti from Just Breathe Foundation joins SoccerSam with news of this year's Cystic Fibrosis Christmas Ball.
 
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 ...…
 
Have fun learning about Cystic Fibrosis with Drs. Ashley Grigsby & Heather Munston
 
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 ...…
 
See http://www.president.ie/en/diary/details/president-receives-members-of-cystic-fibrosis-ireland
 
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 ...…
 
CRISPR technology could change the world. Essentially, CRISPR is a technique that allows scientists to make precision edits to any DNA, whether bacterial or human. The potential for this technology is huge: if scientists have the accuracy to replace just a few faulty genes, it might be possible to cure genetic disorders as serious as cystic fib ...…
 
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 ...…
 
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 ...…
 
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 ...…
 
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 ...…
 
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
 
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 ...…
 
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 ...…
 
Listen to this audiobook free with a 30-day trial. Go to http://audiobookspace.com/free Title: Caleb and KitAuthor: Beth VrabelNarrator: Adam McArthurFormat: UnabridgedLength: 5 hrs and 50 minsLanguage: EnglishRelease date: 09-18-17Publisher: Hachette AudioGenres: Teens, Ages 11-13Publisher's Summary:From award-winning author Beth Vrabel comes ...…
 
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 ...…
 
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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