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By John Rosengard In November 2017, I was diagnosed with multiple myeloma, a form of blood plasma cancer. At the time, my general practitioner and diagnosis team had referred me to their peers in the oncology group and I had my first meeting with my new oncologist. In explaining this disease and the treatment plan ahead, he mentioned forthcoming developments with CAR-T cells and newer generations of current medications.
Published on January 20, 2020 Key Takeaways Broad information available about myeloma can be a blessing and a curse, because each case is different. Patients are more educated nowadays and play a strong role in making decisions with their doctors. Understanding the myeloma profile is really critical to interpreting myeloma lab results.
Published on December 20, 2019 Key Takeaways Have a partnership with your provider to explore clinical trials. Work together to define a clear plan for your treatment. Ongoing conversations between the patient and the physician can also help to understand the disease better.
Published on October 24, 2019 Multiple myeloma patient and advocate John Rosengard sits down with his own doctor, Dr. Nina Shah, a leading expert from the University of California San Francisco (UCSF) Health, to discuss tips, tools and resources for becoming an empowered patient.
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