Journeys through pulmonary fibrosis artwork

Journeys through pulmonary fibrosis

25 episodes - English - Latest episode: 10 months ago - ★★★★★ - 5 ratings

Being diagnosed with a rare disease can often leave people with more questions than answers. This is especially true for those living with the rare lung condition, Pulmonary Fibrosis. In an effort to build and give a voice to this courageous community, we bring you ‘Journeys through Pulmonary Fibrosis’ – a podcast series aimed at bringing together the inspirational people living with this condition, their carers, and the researchers and doctors working tirelessly to support them. Join us as we travel through their journeys, we hear heart-warming stories of determination, resilience and the importance of using these experiences to truly live life to the full.

Medicine Health & Fitness pulmonary fibrosis ild interstitial lung disease lung fibrosis patient journey rare disease scleroderma sarcoidosis ipf
Homepage Apple Podcasts Google Podcasts Overcast Castro Pocket Casts RSS feed

Episodes

Reality of living with RA-ILD

July 14, 2023 13:50 - 22 minutes - 18.1 MB

In this special episode Liz tells us about her experience of living with RA-ILD, which is short for rheumatoid arthritis-associated interstitial lung disease. We explore the profound impact of this life-changing diagnosis on Liz and her loved ones as well as the need for increased awareness of the condition. Throughout Liz provides advice and strategies for maintaining a positive outlook despite the challenges RA-ILD presents.

Innovating today for patients of tomorrow

May 16, 2023 12:58 - 14 minutes - 12.2 MB

In this episode, we explore how innovating today could have a positive impact on those diagnosed with pulmonary fibrosis. We are joined by extraordinary guests, including researchers, healthcare providers, innovators, and a patient impacted by this rare disease. Keeping patients’ lived experiences front and center can help lead to new ideas and progress, all while inspiring us to remain hopeful for the future.

Relationships

January 03, 2023 14:02 - 20 minutes - 16.6 MB

In the fifth and final episode of season 3, we learn about the impact that pulmonary fibrosis can have on relationships with family and friends, and even on the more intimate aspects of partner relationships. Our contributors also take time to emphasize the value that they derive from healthy and supportive relationships when living with this challenging condition.

Shared decision making

November 30, 2022 14:16 - 21 minutes - 17.4 MB

In our fourth episode, we examine the importance of shared decision making, which helps empower patients to make choices about their disease management in collaboration with their medical teams. We hear from people who are living with pulmonary fibrosis, a wife and care partner and from medical specialists, each underlining the value of shared decision making and providing some examples of this best practice in action.

Multidisciplinary teams and the importance of communication

November 22, 2022 13:50 - 19 minutes - 15.8 MB

In the third episode of Season 3 of our ‘Journeys Through Pulmonary Fibrosis’ podcast series, we explore the role multidisciplinary teams (MDTs) play in providing care for people living with pulmonary fibrosis. Our guests first help us to understand what an MDT is, who participates and how the team functions. We then examine the benefits and improvements in care that the approach can deliver for people with pulmonary fibrosis. We also hear about some of the challenges that an MDT approach can...

Diet and nutrition

November 14, 2022 15:31 - 18 minutes - 15.1 MB

In the second episode of Season 3 of our Journey Through Pulmonary Fibrosis podcast, we are once again joined by several people who live with the condition, including a wife and care partner, and by a group of specialists. Hear about some of the challenges that people with pulmonary fibrosis face in terms of meeting their dietary and nutritional needs and learn about how these challenges are best managed through tools and techniques like keeping a food diary and managing portion sizes.

Mental Health

November 02, 2022 13:20 - 19 minutes - 16.4 MB

In the first episode of Season 3, we are joined by a courageous group of guests that includes people living with pulmonary fibrosis, a care partner, and specialized healthcare providers to explore the mental health impact of the disease. The discussion explores the impact of receiving a pulmonary fibrosis diagnosis and the ongoing challenges of living with the disease. Our guests share the mental and emotional challenges they face, as well as helpful tips on how to cope, where to find support...

Special episode: Childhood interstitial lung disease (chILD)

October 18, 2022 07:50 - 36 minutes - 29.3 MB

Childhood interstitial lung disease (chILD) includes more than 200 rare disorders with debilitating symptoms that can include cough, difficulty breathing and rapid breathing. With no established diagnostic criteria, few management guidelines, and no approved therapies, chILD can have a devastating impact on patients and their loved ones. In this episode Dr. Robin Deterding, Director of the Breathing Institute, Children’s Hospital Colorado, speaks to Carlee Gilbert, mother of Finn, who is now ...

Special episode: The scleroderma conversation

June 28, 2022 09:09 - 44 minutes - 36.3 MB

In this special episode of Journeys through Pulmonary Fibrosis we a proud to collaborate with FESCA. Sue Farrington, President of the Federation of European Scleroderma Associations (FESCA) and Chief Executive of Scleroderma and Raynaud’s UK, speaks with Ilaria, who lives with Scleroderma and is Vice Chair of FESCA, and her husband Sergio. Ilaria was diagnosed with Scleroderma in 1996, and lung involvement in 1997, just three months after her relationship with Sergio began. They discuss the...

Taking control of the path ahead

March 17, 2022 22:21 - 22 minutes - 18.6 MB

In the seventh and final episode of season two, we are joined by our courageous group of guests made up of those living with various pulmonary fibrosis conditions, their care partners and specialized doctors. In this episode, we explore the benefits pulmonary rehabilitation can have on those living with the condition in helping them understand their new limits. While these adjustments can be frustrating, we’ll hear how our guests have not only adapted their new exercise routines but also thei...

Journey into the unknown

January 14, 2022 15:50 - 16 minutes - 13.9 MB

In the sixth episode of season two, we are joined by our courageous group of guests made up of those living with various pulmonary fibrosis conditions, their care partners and specialized doctors. In this episode, we explore the different and unpredictable ways pulmonary fibrosis can progress and the various approaches our guests have taken to confront the condition head-on. While the unpredictability can make planning for the future a challenge, we’ll hear how it has taught our guests resili...

Rare, but not alone

December 09, 2021 20:45 - 16 minutes - 14.3 MB

In the fifth episode of season two, we are joined again by our exceptional group of guests made up of those living with various pulmonary fibrosis conditions, their care partners and specialized doctors. In this episode, we discuss the key role support groups play in not only finding accurate information, but also a like-minded community of individuals on a similar path. While seeing those at a later stage in their condition can be challenging, all our guests agree that support groups have gi...

The unsung heroes

December 01, 2021 21:55 - 20 minutes - 17 MB

In the fourth episode of season two, we are joined again by our exceptional group of guests made up of those living with various pulmonary fibrosis conditions, their care partners and specialized doctors. In this episode, we discuss the crucial role of care partners, from helping the patients better understand the initial diagnosis to taking on more of the household jobs. This shift in dynamic can be a hard adjustment, but talking to fellow carers going through a similar experience can really...

Finding the answer

November 11, 2021 14:15 - 19 minutes - 16.5 MB

In the third episode of season two, we are joined again by our new, exceptional group of guests made up of people living with various pulmonary fibrosis conditions, care partners and specialized doctors. In this episode we explore the moment of diagnosis and the different ways in which patients react to this life-altering news. Getting a diagnosis for a rare condition can leave them with more questions than answers however finding accurate information is often a challenge in itself. So join u...

The Journey Ahead

November 02, 2021 10:50 - 20 minutes - 17.7 MB

In the second episode of season two, we are joined again by our new, exceptional group of guests made up of people living with various pulmonary fibrosis conditions, care partners and specialized doctors. In this episode we explore the journey to diagnosis. Getting a diagnosis for a rare condition such as pulmonary fibrosis can be difficult and patients can often go undiagnosed for years. In this episode, we hear about the emotions that patients felt when meeting with various specialists, and...

Special episode - 'shedding light on pulmonary fibrosis'

October 14, 2021 08:40 - 57 minutes - 46.7 MB

This special episode features a recording of a one hour conversation of the twitter spaces event 'shedding light on pulmonary fibrosis' that took place on the 16th September 2021. The discussion focused on the signs and symptoms of pulmonary fibrosis, what actions can be taken when symptoms develop, and how people living with pulmonary fibrosis can find hope and community post-diagnosis. If you have any medical questions or experience any symptoms we encourage you to address those with your d...

Recognizing the signs

September 23, 2021 07:10 - 17 minutes - 15 MB

In the first episode of season two, we meet a new, exceptional group of guests made up of people living with various pulmonary fibrosis conditions, care partners and specialized doctors. In this episode we explore the first signs and symptoms of pulmonary fibrosis. These changes are often gradual and not always instantly noticeable. The symptoms can also often be confused with other conditions. Given these issues that patients face, we discuss how they can advocate for themselves.

Pushing the boundaries

August 05, 2021 13:35 - 20 minutes - 17.4 MB

In the final episode of season one, we are joined by Kristin who was a competitive swimmer until she was diagnosed with Sjogren’s syndrome and later progressive fibrosis, a rare lung condition. Listen to her explain how she adapted her routine to continue pursuing her passions and the importance of taking each day as it comes.

Creating a dream team

April 09, 2021 08:45 - 23 minutes - 19.6 MB

We are joined by John who spent a decade seeking a correct diagnosis of the rare lung disease, Idiopathic Pulmonary Fibrosis. Listen to him explain the importance of sharing symptoms with your doctor and how he considers his eventual diagnosis to be the beginning of a new journey.

Support and empowerment

March 25, 2021 16:10 - 27 minutes - 22.5 MB

In this episode we are joined by Andrew, who was diagnosed with scleroderma with interstitial lung disease. Listen to him speak about the importance of support throughout the patient journey and how he has been able to empower others within this unique community.

Stronger together

March 11, 2021 16:40 - 30 minutes - 24.9 MB

In the third episode of the series, we are joined by Cheryl, who was diagnosed with a rare lung condition called sarcoidosis-associated interstitial lung disease. Listen to her speak about rediscovering many of her previous passions, and how, with the right attitude, her journey became one of growth and revival.

An optimistic approach

February 24, 2021 13:00 - 33 minutes - 27.3 MB

We are joined by Jim, who spent nearly three years seeking a correct diagnosis of a rare lung disease called RA-ILD (Rheumatoid Arthritis-Associated Interstitial Lung Disease). Listen to Jim discuss his father’s journey with the same condition and how Jim’s diagnosis changed his perspectives.

The effects of COVID-19 on the pulmonary fibrosis community

February 05, 2021 07:35 - 32 minutes - 26.4 MB

In a special episode on COVID-19 and the effect on the pulmonary fibrosis community, we are joined by Bill Vick, Founder of PF Warriors, and pulmonologist Dr. Leticia Kawano-Dourado. Listen to them share their experiences of the pandemic and discuss how those living with pulmonary fibrosis can best protect themselves during these uncertain times.

Trailer

January 05, 2021 15:55 - 30 seconds - 549 KB

A podcast series aimed at bringing together the inspirational people living with this condition, their carers, and the researchers and doctors working tirelessly to support them.

Creating a positive journey

December 04, 2020 09:25 - 34 minutes - 28.3 MB

In the first episode of the series we are joined by special guest Dr Craig Conoscenti, medical expert in interstitial lung disease on the clinical development and medical affairs team at Boehringer Ingelheim. Listen to him discuss his experiences as both physician and caregiver to his own father, and the importance of creating a positive patient journey.