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“We’re hoping that when individuals living with illness, and their families, hear the term “palliative’ they shift their perspective from being afraid they’re coming to the end of life, and start to feel that palliative care is going to support their well-being and quality of life,” says Valerie Fiset, director of the Champlain Hospice Palliative Care…
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Chronic myeloid leukemia: a discussion with a survivor and an expert
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This webcast takes participants through today’s treatment options—from initial therapies to newer and more advanced approaches now available. The session highlights what patients can typically expect at each stage of treatment, including how decisions are made and how care is tailored to individual needs.
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Dr. Florian Kuchenbauer explains the basics of AML diagnosis, treatment, side effects, and research.
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Mrs. Linda August talks about her experience with Lymphoma and how she learned the importance of taking an active part in her care and treatments.
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Tiffany Woodworth shares her story of receiving a Hodgkin lymphoma diagnosis as a young adult, and the supports that she received during her experience.
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Mayra Husic shares her experience with Follicular Lymphoma.
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Bob Sisler has been in remission from Angioimmunoblastic T-cell lymphoma, a type of Peripheral T-cell lymphoma, since 2015. Bob shares with us his personal experience with diagnosis, treatments, and life after blood cancer. As a Peer Support Volunteer, Bob gives back to the blood cancer community through the LLSC’s First Connection program.
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Eric Pitters talks about living with chronic lymphocytic leukemia (CLL), the treatments he underwent and how he now gives his time to supporting people who are newly diagnosed with CLL.
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In this episode we talk to Elizabeth Corkum about what it was like caring for her husband when he was diagnosed with acute myeloid leukemia (AML).