Q&A ll My Life With Cystic Fibrosis ll

**Be sure to watch in HD!

Link to "How to Get Through School With Cystic Fibrosis" *here*:    • Going To School With Cystic Fibrosis  

Hi friends! :) -- Thanks for watching! --

My name is Tiffany Rich, and I am a twenty-six year old living a life-threatning disease called Cystic Fibrosis. I am currently listed on the double-lung transplant list, and decided to document my journey while I wait for my second chance at life!

This summer, I posted a picture on social media that ended up going viral, and led me to my number 1 bucket list item: TO MEET TAYLOR SWIFT! Because of all the love and support I received from people around the world, I was able to make my dream become a reality. Through this process I found I had hundreds of people wanting to know my story, and I felt this was the perfect platform to document my life with Cystic Fibrosis, as well as getting awareness out for this disease and organ donors.

Upcoming Vlogs:
-My story of how I met TAYLOR SWIFT
-A routine visit to Stanford hospital with my transplant team
-How to cope during the hard times
-Importance of organ donation

Please be sure to like and subscribe to my channel for weekly vlogs!

Come Find Me:
Snapchat: @LUNGS4TIFF

Instagram: @tiffrich22

Twitter: @tiffrich22

E-mail: [email protected]

LOVE, Tiffany
#JustBreathe


Misc.:
https://www.cff.org/