Christie Patient,  —

In 2019 Christie Patient relocated to San Francisco to care for her mother, Holly, before and after her double-lung transplant. Holly’s idiopathic pulmonary fibrosis diagnosis came only months before an acute exacerbation that led to a four-month stay in the intensive care unit, and her eventual transplant. Years later Christie is still writing about the experience, in hopes that her family’s story will connect readers to all the beautiful and terrible parts of the transplant journey. Holly has returned to her home in the Sierra Nevada mountains, and Christie currently resides in Hawaii with her husband, Jonny, and their two four-legged friends.

Articles by Christie Patient

I Feel Most Human When My Heart Is Heavy

For all the time I’ve spent in my 31 years “sitting in the U-bend, thinking about death,” as Moaning Myrtle from the “Harry Potter” series says, facing the loss of a loved one hasn’t gotten any easier. In spite of all my pondering, reading, and writing on the subject of…

Social Media Advocacy Requires Radical Vulnerability

As a millennial, I came of age with the internet. I remember the thrill of choosing the perfect screen name for AOL Instant Messenger before going to camp. (luv4pigs31, if you were wondering.) In eighth grade, I created my first social media account. Back in the early 2000s, Myspace was…

Busting 4 Common Lung Transplant Myths

When I was growing up, I loved the show “MythBusters.” I tuned in regularly to watch Adam Savage and Jamie Hyneman bust famous myths and answer burning questions like, “Will using a cellphone near a gas pump cause an explosion?” 2003 seemed like a simpler time, didn’t it?…

Caregiving Was a Catalyst to Telling Rare Disease Stories

I have several roles here at BioNews, the parent company that publishes Pulmonary Fibrosis News and other rare disease websites. I started with this humble column and eventually joined the forums team as a co-moderator. My most recently acquired title is “columns lead,” in which I manage and mentor…