Podcast appearances and mentions of tiffany rich

In this interview episode, Ashley welcomes back Tiffany Rich. In this, “Where Are They Now” episode, we talk about how our lives with cystic fibrosis have changed over the year. We discuss the highs and lows of our journeys, and we celebrate milestones in each other's lives. We also go on a slight tangent about Taylor Swift. - Links Mentioned - Tiffany Rich Instagram: https://www.instagram.com/tiffrich22/ Twitter: https://mobile.twitter.com/tiffrich22/ Foundation Instagram: https://instagram.com/lovebreathelive_/ - Follow Ashley - Podcast Instagram: https://www.instagram.com/bloomingrosespodcast/ Personal Instagram: https://www.instagram.com/ashleys.roses/ YouTube: https://www.youtube.com/c/ashleysroses

In this interview episode, Ashley interviews Tiffany Rich, friend, cystic fibrosis advocate and CF Warrior, herself. Tiffany talks about the journey of living with cystic fibrosis, hardships she has overcome, and the importance of the CF community. She also shares the importance of asking questions and bringing awareness to cystic fibrosis. - Links Mentioned - Tiffany Rich https://www.instagram.com/tiffrich22/ https://twitter.com/tiffrich22 https://www.youtube.com/channel/UCr27CNqLqiyfbkj-5H36Evg https://www.facebook.com/tiffany.rich.56 - Follow Ashley - Instagram: @bloomingrosespodcast https://www.instagram.com/bloomingrosespodcast/ Instagram: @ashleys.roses https://www.instagram.com/ashleys.roses/ YouTube: Ashley's Roses https://www.youtube.com/c/ashleysroses

KCBS Radio afternoon anchor and A2A founder Jeff Bell spotlights Tiffany Rich, who has lived with Cystic Fibrosis since birth. In 2016 she underwent a double lung transplant after being on the donor list for 973 days. Tiffany is the co-founder of Salty Cysters, an organization that creates awareness of CF and unites the CF Community. She also co hosts a weekly CF podcast called Breathe In.

KCBS Radio afternoon anchor and A2A founder Jeff Bell spotlights Tiffany Rich, who has lived with Cystic Fibrosis since birth. In 2016 she underwent a double lung transplant after being on the donor list for 973 days. Tiffany is the co-founder of Salty Cysters, an organization that creates awareness of CF and unites the CF Community. She also co hosts a weekly CF podcast called Breathe In.

Buck Tail Johnnys creators Johnny Richie & Sammy Cruz give us a look at the Company & what they are all about & Tiffany Rich talks with us about the 2018 Cast for kids event. What an awesome show

Buck Tail Johnnys creators Johnny Richie & Sammy Cruz give us a look at the Company & what they are all about & Tiffany Rich talks with us about the 2018 Cast for kids event. What an awesome show

On this weeks podcast we have the pleasure of interviewing one of Rima’s amazing salty cysters. What may you ask is a salty cyster, well, these special nicknames are used between friends in the Cystic Fibrosis community, referring to another person who has CF. Rima and Tiffany are not just friends, or salty cysters but also have experienced very similar journeys recently. Receiving a double lung transplant and moving through the motions of post transplant life. Tiff get’s real about her journey with Cystic Fibrosis and getting a transplant. We discuss organ donation, which is very close to Tiffany’s heart. Check out this episode and learn more about this amazing woman who is so full of life and passion. You can find her on YouTube at Tiffany Rich. IG @tiffrich22 @Saltycysters and listen to her own podcast at @breathe_in_pod

Cystic Fibrosis advocate Tiffany Rich joins Heather in the studio to talk about her own journey with the disorder to the point of receiving a double-lung transplant, and how she turned her experience into a way of raising awareness and donations through her many online ventures.

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 cystic fibrosis face and the people who face them.