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Family DNA disease connection: How my breast cancer diagnosis saved my father from pancreatic cancer

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Dr. Pamela Munster and her father. Image credit: NBC News
This article or excerpt is included in the GLP’s daily curated selection of ideologically diverse news, opinion and analysis of biotechnology innovation.

In April 2012, as I prepared to undergo a double mastectomy, it was [my grandma] Gertrud’s face that flashed before me. I’d just endured weeks of worry, testing and decisions following an unlikely breast cancer diagnosis at the age of 48.

By the following summer, I was back in control—past the diagnosis and multiple surgeries. In November 2012, we had discovered that I carried the BRCA2 gene.

Life had barely returned to normal when, during one of our weekly calls, my father mentioned that he was having a bit of stomach trouble. Healthy all his life and with no reason to worry about what seemed to be indigestion, he did not think much of it.

But I did not think of ulcers or constipation. My mind went directly to pancreatic cancer.

For someone with a BRCA2 mutation, the risk for pancreatic cancer is up to 10 times higher than for those without the mutation.

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Knowing that Papa was a BRCA2 carrier drastically raised my concern that this could be pancreatic cancer, but in 2013, at the time of his diagnosis, there were no recommendations to regularly screen someone with a BRCA2 mutation for pancreatic cancer. My own circumstances and my knowledge of the mutation were undoubtedly part of what saved him.

[This essay is adapted from Dr Pamela Munster’s new book, “Twisting Fate: My Journey with BRCA—From Breast Cancer Doctor to Patient, and Back,” published by The Experiment. She is a professor of medicine at the University of California, San Francisco.]

Editor’s note: Full article is behind paywall

Read full, original post: My Father’s Fight Against the Breast-Cancer Gene

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