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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.
C. Elizabeth Dougherty is a Social Worker and Educator. In this podcast, she helps us understand the different types of grief, explains how we can manage the grief that the current pandemic is causing us all to experience, as well as strategies for adapting to all the changes that we are experiencing, especially as the holidays approach.
Michelle Lambert speaks with Veronica Vardy, mother of 5 year old Amelia who is an ALL survivor. Veronica discusses the impact cancer had on her daughter, her family, and what her role as caregiver was like.
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…
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.
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…
When she was diagnosed with Philadelphia positive acute ALL (PH+ ALL) in 2007, Jeanette Castillo leaned heavily on her healthcare background to cope. Having seen many people go through their own health challenges with a hopeful perspective, she adopted a similar attitude. Now 14 years post-stem cell transplant, Jeannette admits is was a long a scary road,…
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.
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.
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.