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Rob Weker’s story is remarkable for many reasons.
First and foremost, he has beaten cancer.
Not once. Not twice. But three times.
Getting the third diagnosis, this time it was pancreatic cancer, really got his attention. Only 7% of pancreatic patients live beyond 5-years.
I met Rob at last year’s Patients as Partners conference and really enjoyed his perspective. His plea was for the conference attendees to walk in his boots. And yes, he had those boots on stage.
You see, Rob is also a veteran of pharmaceutical R&D. He had a deeper message for his professional colleagues. In his professional life, he turned his propensity for asking questions into a career looking at the process improvement and quality.
Rob is very methodical in how he analyzes problems – whether at work or as a patient. His experience has taught him that it is very important to keep asking questions until there are none. In this episode, he shares a few stories of how this has worked well for him as he battled for his life.
Obviously, on the health side, he has beaten the odds. He just passed the 5-year mark since his diagnosis.
And now he is turning his energy to bridge the gap between patients, industry, and the rest of healthcare.
You can read Rob’s blog on LinkedIn (click here) It’s about being proactive and not relying on luck.
We’ve all been there. You are at a party and someone asks, “So, what do you do?” Dr. Kirsch always found it hard to explain his career as a discovery scientist. He decided to write a book about it. The Drug Hunters: An Improbable Quest to DIscover New Medicines is a colorful, fact-filled narrative history of the search for new medicines from our Neolithic forebears to the professionals of today, and from quinine and aspirin to Viagra, Prozac, and Lipitor.
We talk to Dr. Kirsch about his own experiences as a scientist, the daunting odds of finding an actual medicine, and the additional human hurdles that can make these discoveries even harder. He also talks to us about the things he learned as he wrote The Drug Hunters with his co-author Ogi Ogas, Ph.D.
Credits:
Sound Design: Jacob Tompkins ([email protected])
Music: “Origins” Per Kilstofte https://machinimasound.com/
“AS – Tribal O1” Aaron Spencer https://machinimasound.com/
Graphic Design: Heather McCullen ([email protected])
Today we hear from David Pearce, PhD, President of Innovation and Research, Sanford Health and Vice Chair, Consortium Assembly, International Rare Disease Research Consortium (IRDiRC)
Dr. Pearce’s rare disease background emanates from publishing over 100 research papers on Batten Disease. David talks to us about how he got involved in Batten Disease research and where that work has taken him since.
In his role as President of Innovation and Research at Sanford he is responsible for overseeing the development of research programs across Sanford’s nine-state footprint, including more than 450 researchers, eight research centers and more than 300 ongoing clinical trials. This includes a national registry for rare diseases, Coordination of Rare Diseases at Sanford (CoRDS).
The International Rare Disease Research Consortium comprises more than 50 international entities.
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