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

Start Journaling, Write Away!

Earlier this month, I wrote a column about mental health and therapy options available during the pandemic. Hopefully, I made a strong case for giving therapy a try if you have been hesitant. I will always encourage people to try it out, but I…

Embracing Caregiving: Learning to Accept a Diagnosis

Receiving a pulmonary fibrosis diagnosis is a life-changing event. Accepting this new reality may initially seem impossible. There are so many new things to consider that never were on the radar before they suddenly became important. In addition to finding your footing in the present, you must…

Lung Transplant Memories: Greatest Hits

I’ve been going through a second (Third? Fourth?) wave of grief for all things pre-pandemic. I am still mourning things that once brought me joy but are currently off-limits — rugby, concerts, being a wedding photographer, and date night out, to name a few things. I’m still hurting…

My Hardest Days as My Mom’s Caregiver

Two weeks after my mom, Holly’s, double-lung transplant, she was discharged from the hospital. Although she was weak, she was walking, talking, eating, and, best of all, breathing on her own. After three months on a ventilator, the transplant brought her back to life.