"I'm an example of what can be done for someone with multiple myeloma," says David Johnson, of B.C., first diagnosed with the disease in 2012 in his early 50s. Having had 2 relapses, 2 stem cell transplants, and participated in a clinical trial for CAR T-cell therapy, David is in remission today. He helps others in the blood cancer community by volunteering for couple of programs at The Leukemia & Lymphoma Society of Canada. Also in this podcast, Dr. Anthony Reiman, a medical oncologist at St. John Regional Hospital in New Brunswick, talks about advances in recent years in treatment for and longevity of people with multiple myeloma. For more information about this form of blood cancer, please visit:https://www.bloodcancers.ca/i-have-blood-cancer/myeloma/multiple-myeloma
Graft vs Host Disease, known as GvHD, is a side effect of a life-saving procedure. People who undergo an allogeneic stem cell transplant - where a donor's stem cells are transplanted into the recipient - can experience either acute or chronic GvHD. Listen to blood cancer survivor Libby Goszer who shares her coping strategies for living with chronic GvHD, a condition she describes as "a continual rollercoaster ride that has both expected and unexpected twists and turns." The B.C. resident has lived with cGvHD for 16 years; she's learned to enjoy the 'ride' of her life as a mom, wife, professional, and volunteer. Also in this episode, a Canadian hematologist-oncologist and a specialist in GvHD, Dr. Kirk Schultz talks about chronic as well as acute GvHD, symptoms, and advances in medical treatments. Read more about GvHD from The Leukemia & Lymphoma Society of Canada (LLSC) with these easy-to-understand, short factsheets: Understanding GvHD - https://www.bloodcancers.ca/sites/default/files/2024-10/lls1768-f-fs-gvhd-understand-e03.pdf Treating GvHD - https://www.bloodcancers.ca/sites/default/files/2024-10/lls1769-c-fs-gvhd-treating-e02.pdf If you have any questions about your blood cancer experience, or that of a loved one, please reach out for personalized support from a trained LLSC community worker in your region. Find their contact information at: https://www.bloodcancers.ca/i-have-blood-cancer/how-we-can-help/access-one-one-personalized-support You are not alone.
It may be the first time you've talked about your blood cancer, since your diagnosis, with anyone outside immediate family, or it may be after years of living with cancer... Either way, the LLSC community services lead in your region is ready to listen and support you in any way you need. Geoffrey Molle, one of those leads, talks about the confidential, safe space he creates for anyone impacted by a blood cancer, in this podcast episode. Access one-on-one personalized support with the community service lead in your region; details at: https://www.bloodcancers.ca/i-have-blood-cancer/how-we-can-help/access-one-one-personalized-support
Tziona Lugasi, clinical psychologist in the hemato-oncology department at CHU Sainte-Justine, talks about the impact of cancer on children, teens and their parents, and the transition from pediatric care to adult health care. Are you a parent of a child with a blood cancer? Find more resources on the LLSC website at: https://www.bloodcancers.ca/i-care-someone-blood-cancer/blood-cancers-kids-teens-young-adults/childhood-blood-cancers#for-parents-and-caregivers
Maura C. had recently returned to work after maternity leave when her daughter, then 15 months old, was diagnosed with acute myeloid leukemia (AML) and immediately admitted to the oncology ward. “This is a nightmare I’m not waking up from,” Maura thought over the 5 months her toddler was in the hospital. She says she and her husband moved from their initial “fight-or-flight” mode, to chronic anxiety – both over the treatment period and afterwards when “we felt anxiety about the cancer coming back.” Maura acknowledges that support for mental health was important for her. "Our family doctor was an ally and a resource,” she says, “and I had an "amazing therapist" to deal with marriage strain challenges as well, and support from close friends and her parents. Are you a parent of a child with blood cancer? Find resources and support here: https://www.bloodcancers.ca/i-care-someone-blood-cancer/blood-cancers-kids-teens-young-adults/childhood-blood-cancers#for-parents-and-caregivers
The emotional cost of caregiving when a loved one has a blood cancer is no small matter – as Saskatchewan’s Lori Galbraith can attest. The mother of four was the caregiver of her husband Jim, who was diagnosed with acute myeloid leukemia (AML) and underwent a stem cell transplant. “The hardest part was providing positive emotional support [to my husband] when I was worried and wondering if I’d ever get back the husband I had prior to AML... I’m trying to support him through it all – but what do I do with my thoughts?” Lori says in this podcast. Are you caring for someone with a blood cancer? The Leukemia and Lymphoma Society of Canada has support, services, and resources for caregivers, including a peer-to-peer support program. Visit: https://www.bloodcancers.ca/i-care-someone-blood-cancer
The term, “palliative approach to care” refers to a person-centered, holistic approach including emotional, spiritual, social and psychological care, offered by a larger team of healthcare professionals (beyond doctors and nurses) and introduced earlier in a cancer experience for full integration into an individual’s care plan. Valerie Fiset, director of the Champlain Hospice Palliative Care Program at the St-Vincent Hospital in Ottawa hopes individuals and their families shift their perspective on palliative care "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."
Researchers are focused on maintaining an excellent cure rate in diffuse large B-cell lymphoma (DLBCL) and minimizing some of the treatment individuals receive – reduce the number of cycles of chemotherapy or avoid radiation, and looking at new drugs to improve the cure rate for others with DLBCL. Join us as we chat with Dr. John Kuruvilla, working as a hematologist-oncologist for 20 years (currently at the Princess Margaret Cancer Centre in Toronto) including as a researcher in DLBCL, which is the largest form on non-Hodgkin lymphoma. Learn more about DLBCL at: https://www.bloodcancers.ca/diffuse-large-b-cell-lymphoma-dlbcl
Dr. Rena Buckstein from Odette Cancer Centre in Toronto shares the basics of myelodysplastic syndromes (MDS) diagnosis, treatment, and side effects. In Canada, it is estimated that up to 5,900 new cases of MDS are diagnosed each year - most often in older adults. There are two main types of MDS: primary (de novo) and secondary MDS. The treatment for MDS varies according to the type and stage of the disease with the goal of slowing or stopping the MDS from becoming acute myeloid leukemia (AML). For more information about MDS, visit: https://www.bloodcancers.ca/i-have-blood-cancer/myelodysplastic-syndromes
Mayra Husic shares her experience with Follicular Lymphoma.
Dr. Philip Kuruvilla, hematologist-oncologist at the William Osler Health Centre at the Brampton Civic Hospital in Brampton, Ontario talks about chronic lymphocytic leukemia (CLL): Current treatment options, potential side effects and how to manage those side effects. CLL is the most common type of leukemia in adults. For more information about CLL, visit: https://www.bloodcancers.ca/I-Have-a-blood-cancer/Leukemia/chronic-lymphocytic-leukemia
Dr. Tobias Berg, an associate professor and researcher from McMaster University explains maintenance therapy as a treatment option for acute myeloid leukemia (AML) and the factors that influence the decision to start this type of treatment. Maintenance therapy is treatment given after the first (primary) therapy used to manage your cancer, or to stop it from coming back. Some people may use maintenance therapy for a long time. This type of therapy can include drugs, vaccines, antibodies, or hormones. Maintenance therapy can be used after a stem cell transplant for a blood cancer or after your first therapy if a stem cell transplant is not an option or not recommended for you. Maintenance therapy is often given at a low intensity, but over a long period of time. The goal is to help keep you in remission and to prevent relapse (also known as cancer recurrence). Maintenance therapy has a role to play in some types of blood cancers such as multiple myeloma and acute myeloid leukemia (AML). Acute means the disease progresses quickly. AML is the most common acute leukemia in adults. Learn more about AML at: https://www.bloodcancers.ca/i-have-blood-cancer/leukemia/acute-myeloid-leukemia-aml
What started as a normal trip to the cottage ended up leading Tom to take a trip to the hospital- where he was diagnosed with myelodysplastic syndrome. Tom shares his blood cancer experience and how learning about his diagnosis, staying positive, and staying active are what helped him through the difficult times of treatment.
Rachel Sutherland is an Indigenous Patient Navigator at the London Regional Cancer Program and Dr. Samantha Boshart is a Family Physician who is also the Regional Indigenous Cancer Lead for the Southwest Regional Cancer Program. In this podcast, both experts discuss the unique challenges experienced by the Indigenous Community in Cancer Care and the efforts that our hospitals are taking to ensure that they receive equitable care in their cancer experience.
Alyssa Brandone was 11 years old when she was diagnosed with Acute Myeloid Leukemia. In this podcast episode, Alyssa shares her experience with a pediatric blood cancer and how the support of her family and friends helped her overcome the challenges of integrating back into “normal” life after treatment.
In this episode of our AYA podcast series, Sukant Sharma shares his experience balancing work, side effects, and his personal life after being diagnosed with Acute Lymphoblastic Leukemia.
After being diagnosed with leukemia at 21 years old, Shae-Lynn Way shares her experience with shifting her mindset while preparing for a second stem cell transplant after her leukemia returned.
Originally thought to be a locked muscle from exercise, Michelle Burleigh shockingly discovered that she had a rare form of Acute Leukemia. In this podcast, Michelle recounts her experience being diagnosed with APL, revealing how her sudden diagnosis taught her about finding perspective, slowing down, and making the most of each day despite living with uncertainty.
Blood cancer survivor Meredith, 26, talks about her love life after stage 2 Hodgkin's lymphoma. She was diagnosed at age 18 and in university. A love life can be positively or negatively affected if one of the partners is diagnosed with cancer. Meeting a new partner following the disease could also cause several concerns. How to discuss changes in the relationship with your partner? How to deal with possible sexuality and fertility problems? Should someone tell a new date that they had cancer? If so how and when?
Eric Pesarchuk, 36, survivor of B-cell lymphoma diagnosed in 2021 who underwent 2 spinal surgeries, 11 rounds of radiation and 5 months of chemotherapy. He had to learn to walk again - and today is in remission. He lives with wife, their 5 year old daughter, in British Columbia. Being affected by cancer at the beginning of the adult life often forces to put various projects on hold. The impacts of the disease are numerous, and they sometimes affect the identity of the person. Once the remission is pronounced, how is it possible to go back to a normal life?