What an interesting month August has been. Regular readers of my column may recall that the month started with…
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
The end of life is a period fraught with emotion. Losing someone who touched our lives creates a sudden void.
Writing “Make Every Breath Count” for you each week is an opportunity for me to share my journey, which…
Some of the most important interactions in our professional lives do not occur at work, at the boardroom table, or…
The idiopathic pulmonary fibrosis (IPF) journey is, if nothing else, full of surprises. Some of those surprises come in…
When is a larger number the better choice? It depends. Recently, I’ve noticed some people in the pulmonary fibrosis…
How much of a powerhouse in the world of rare disease medicine do you have to be to effect change?…
Have you ever experienced a period in your life when nothing seemed to go right? While that may seem an…
July is a month of celebration at our house. Though it begins with the Fourth of July, my personal “Independence…
Adversity is something rare disease patients face on a regular basis. It can take many forms, but it often involves…