A Rare Purpose

Jemma Caprioli
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In rarity we unite, connect and find our way to purpose.

الحلقات

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    Having Cancer Saved My Life, Andres Varela's Story.

    "I didn't expect the cancer to fix everything." Many of us sit on cruise control through life, and it can be hard for people to find true perspective on both the fragility and the beauty of being alive until either something earth shattering happens or we are faced with our own mortality. Andres Varela spent most of his life from teen years struggling through depression, so when he was told by the doctor at only 30 years old that he had stage 3 colorectal cancer he didn't react like most others would, "If I had received the news of my cancer alone, I probably would have just let it take me."  Fortunately, Andres was not alone when he visited the doctor that day and he agreed to an aggressive chemotherapy and radiotherapy treatment plan. Three surgeries later, Andres is now free of Colorectal Cancer, but of course living with a very different digestive system in place of what most of us have.  Looking for the "little wins" as he calls it, Andres is an inspiration, although he wouldn't say that of himself. He moves through each day seeking out the moments of joy that will elevate himself and those around him. He hasn't let go of the pain he went through because it helps in driving him to live a much more fulfilled and consciously present life.

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    Finding Calm Amid The Chaos: Sandra Russell's Journey Through Cancer With Mindfulness

    In this episode, I had an incredibly moving conversation with Sandra Russell, a former psychotherapist and author of "The Feeling of Cancer". Diagnosed with multiple myeloma, Sandra faces a relentless battle with an incurable cancer, which has pushed her to reevaluate life's priorities, embrace mindfulness, and navigate the complex layers of emotional health and self-care. Her profound insights into self-compassion, the nuances of empathy versus sympathy, and the importance enjoying simple pleasures and personal indulgence over the manic pursuit of bucket-list activities make this episode a must-hear for anyone dealing with a cancer diagnosis. Sandra shares here complete story in her book "The Feeling of Cancer" which is available in paperback and on Kindle.

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    The Government Doesn't Care That Your Cancer Is Rare, With Cathy Slattery, Head of Patient Programs At Rare Cancers Australia.

    Imagine you are diagnosed with a cancer that's so uncommon that even your doctor is uncertain of the pathway you need to take. You are isolated in your illness and you turn to investigating yourself online. Is it right that because your cancer is rare, that you should receive less support? When you have a rare cancer the treatment options are often more complex, and alongside complexity comes expense.  Rare Cancers Australia is a pillar of support for more than 40,000 Australians facing their own rare cancer experience right now. Cathy Slattery from Rare Cancers Australia talks openly about the challenges and differences that people with a rare or less common cancer encounter every day - from uncertainty in their health pathway, to the inequities in government support.

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    When Cancer Affects More Than Just Your Body, with Michele Molnar, Founder of Cancer Chicks.

    A compelling and emotional episode that touches on the many challenges young women affected by Cancer go through. Joined by the founder of the not for profit Cancer Chicks, Michele Molnar. We have a candid conversation about relationships, emotional wellbeing, parenting, and grieving our body parts. Although Cancer can take a lot from you, Cancer Chicks is about finding community, your tribe, and a place of belonging so you can find meaning and friendships beyond your diagnosis.  https://www.cancerchicks.org.au/

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    A Cancer Discovery with Professor Parry Guilford: Clinical Trials, Research Funding and a Candid Chat about Hereditary Cancers

    Professor Parry Guilford is known for successfully in identifying the first known genetic mutations in the CDH1 gene, leading to the description of a new cancer syndrome Hereditary Diffuse Gastric Cancer (HDGC). This discovery has conservatively saved 27,000 people from developing a severe form of stomach cancer. Parry is determined to continue to change the course of HDGC stomach cancer patients outcomes, he is invested in the CDH1 mutation families and feels their trials as if they were his own. We discuss genetic counselling, the age at which we test our children for hereditary cancers, his work on lobular breast cancer, bowel cancer and funding research.

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    GI Cancers and Genetics with Professor Alex Boussioutas

    Professor Alex Boussioutas is one of Australia's most prominent and accomplished Gastroenterologists. We dive right into a conversation about the latest innovations in cancer surveillance and precision medicine. As a GI Cancer specialist Alex talks about the prevalence of bowel cancer in Australia and we chat about screening challenges and the need for further education in the community. Alex is also the Director of Genetics and Genomics at The Alfred, so we touch on genetics in respect of rare cancers, and finally Alex shares his perspective on patient experience.

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    Life without a stomach with endurance athlete Julian Grennell

    'What do you mean you don't have a stomach?' This is a question our very first podcast guest Julian Grennell often encounters, and a reality he shared with many other members of his family after discovering they all carry the rare genetic mutation of CDH1 Hereditary Diffuse Gastric Cancer. We dive into life post total gastrectomy and how Julian was inspired by his diagnosis to challenge himself by pursuing endurance events. Through his journey he has questioned the support available for cancer patients and their families, and as such launched himself into advocating for the Not for Profit sector, recently becoming the president of NZ Cancer Society.

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In rarity we unite, connect and find our way to purpose.

المعلومات

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    Jemma Caprioli
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    © 2025 Jemma Caprioli