Episodi

  • Ep. 4: Our Caregivers Pt. 1
    Feb 22 2026

    In this episode, Candice and Rachael invite their partners/caregivers to discuss the hurdles, pitfalls, stressors, and joys of being a partner and caregiver to a chronically ill person living with Systemic Mastocytosis. You'll hear what it has been like for our partners to be on the diagnostic journey with us, and what it's like to start dating someone knowing they have a mast cell disease and the accommodations that have to be made.

    In this episode we mention some fragrance free products that have worked for us. Here is a link to Rachael's affiliated Amazon list https://www.amazon.com/shop/hedonish We're working on making a new one for future episodes.

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    57 min
  • Ep. 3: Our Stories Pt. 2
    Dec 22 2025

    In this episode, Candice and Rachael further discuss their experiences living with SM, their coping mechanisms, things they've learned along the way, and share how they approach advocacy for themselves and others.

    If you have any questions or suggestions for the hosts, email us at podhost@mastcastpod.com. Please follow us on Instagram @mastcastpod.

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    1 ora e 20 min
  • Ep. 2: Our Stories
    Nov 20 2025

    In this episode, Candice and Rachael share a little about themselves, how they met, how the podcast came to be, their individual paths to diagnosis, their current symptoms, and call for your questions for them to answer in part 2!

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    1 ora e 16 min
  • Ep. 1: Interview with Jessica Fraser of The Mast Cell Disease Society
    Oct 20 2025
    In our very first episode, we talk to Jessica Fraser, executive director of The Mast Cell Disease Society (TMS). She shares with us her very personal connection to systemic mastocytosis and, gets deep into the many resources TMS provides for patients, caregivers and providers. We discuss the mission of TMS, the upcoming conference, support groups, advocacy, support for newly diagnosed patients, CMEs for medical providers, the nursing “hotline”, and what other disease states the TMS advocates for. You can find all of that at www.tmsforacure.org but below are some specific links to topics we discussed: ER Plan: https://tmsforacure.org/wp-content/uploads/2025/08/TMS_ER-Protocol-2022_fillable-Adults-UPDATE.pdf Conference: https://tmsforacure.org/tms-together-2025-community-care-in-mast-cell-diseases/ Virtual Support Groups: https://tmsforacure.org/find-support/ Provider CMEs: https://tmsforacure.org/echo/ Take some time to explore the TMS website. It is full of information, resources and support. Remember, we are not medical providers, and are not offering medical advice. We are sharing our personal experiences and stories. As always, talk to your doctor about an challenges you are facing. If you have any questions, comments, or would like to share your story, email us at podhost@mastcastpod.com.
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    1 ora e 6 min