Have you ever tried to explain to someone who has never experienced a rare disease how patients can develop lasting…
Samuel Kirton
Sam Kirton started his column in November 2021 and writes from his home at Lake Anna, Virginia, where he lives with his wife Susan. His diagnosis at age 59 with idiopathic pulmonary fibrosis in January 2017 began a journey of awareness and advocacy. Sam was listed for a lung transplant on March 19, 2021 and received a bilateral lung transplant on July 10, 2021. This was quite the change from his career as a special agent for the Office of Special Investigations and as a corporate security executive. Sam plans to share his journey so you, too, can make every breath count. You can follow Sam’s thoughts on LinkedIn.
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Articles by Samuel Kirton
A pulmonary fibrosis journey is marked by many firsts, especially in relation to medical tests. Prior to my…
What do you do with information you didn’t necessarily ask for or expect? While attending support group meetings or scanning…
Michel de Notredame, more commonly known as Nostradamus, was a French astrologer, physician, and to many, seer. He…
I regularly pick up and read my journal from the early days after my diagnosis of idiopathic pulmonary fibrosis…
American comedian Bill Engvall is known for his punchline “Here’s your sign,” which he’d often say in response to an…
A recurring topic of discussion among the rare disease community is whether people would consider donating an organ. I’ve heard…
On Tuesday, Sept. 15, 2020, I received an email asking if I would participate in an exercise on how deceased…
When I was diagnosed with idiopathic pulmonary fibrosis (IPF) on Jan. 31, 2017, I quickly understood three things…
One of the most certain parts of our lives is the order of the calendar. “Thirty days has September,/ April,…