Resource Library
Showing 31 to 40 of 217 results
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Dr. Kareem Jamani talks to us about CML treatment options and diagnosis.
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Dr. Gilles Robichaud speaks about CLL research. He shares information about his current research and how it could help inform CLL treatment in the future.
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Joanne was diagnosed with Polycythemia vera in 2012. She shares her experience with her diagnosis, the support she received from local groups and how it has changed her life.
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Just a few days before Christmas in 2010, Patrick Alexander, an LLSC First Connection volunteer from Vancouver, was diagnosed with Multiple Myeloma. He talks to us about his experience with his diagnosis, treatment and how it changed his view on life.
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Max Parrot, professional Canadian snowboarder, speaks candidly about his blood cancer experience and its impact on his life and career. Max explains why he felt like "a lion in a cage" throughout treatment, and lets listeners in on what it took to get his health and mindset back on track.
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Scott Bellerby, outpatient hematology nurse at the Tom Baker Cancer Center in Calgary, talks to us about the ways this pandemic has affected how we manage a chronic blood cancer and provides some insights on how we can continue to care for ourselves effectively.
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When Lois Lewis was diagnosed with AML in 2010, she had just retired from a career filled with music - as a music therapist, music teacher and leader of an intergenerational choir. Lois shares her cancer experience, which, not surprisingly, included the Gaelic version of the song Auld Lang Syne.
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Andy Friedman returned to Ontario from BC’s Gabriola Island with a plan to spend more time with his grandchildren. What he did not plan on was a chronic lymphocytic leukemia diagnosis. In this episode, Andy talks about the good and bad of his post-diagnosis life, including his experience with watch and wait. He also shares two important pieces of advice for…
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Gail Whiteford returned from a 2014 hiking trip in Japan and Australia, visited her doctor for her annual physical, and was shocked to, soon after, be diagnosed with myelodysplastic syndrome (MDS). In this episode, Gail shares her treatment experience and some of the important lessons she has learned, maybe the most important one being, "I learned it…
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Ever since he was diagnosed with myelofibrosis 20 years ago, Doug Chisolm has tried to live every day to the fullest, even spending all his retirement savings and having to start saving again. In this episode, Doug speaks about the ups and downs of his blood cancer experience, why he thinks it's crucial to have a strong support system and what he…