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Mast Cast: An SM Podcast
Mast Cast: An SM Podcast
3 episodes
2 weeks ago

A podcast where your hosts Candice and Rachael explore the complexities of living with a rare, chronic disease through personal experience, patient guests' stories, care-giver perspectives, insights from specialists, and updates from the research and advocacy communities - with the purpose of bringing knowledge, connection, and hope to those affected by systemic mastocytosis and related conditions.

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All content for Mast Cast: An SM Podcast is the property of Mast Cast: An SM Podcast and is served directly from their servers with no modification, redirects, or rehosting. The podcast is not affiliated with or endorsed by Podjoint in any way.

A podcast where your hosts Candice and Rachael explore the complexities of living with a rare, chronic disease through personal experience, patient guests' stories, care-giver perspectives, insights from specialists, and updates from the research and advocacy communities - with the purpose of bringing knowledge, connection, and hope to those affected by systemic mastocytosis and related conditions.

Show more...
Medicine
Leisure,
Hobbies,
Health & Fitness
Episodes (3/3)
Mast Cast: An SM Podcast
Ep. 3: Our Stories Pt. 2

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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2 weeks ago
1 hour 20 minutes 15 seconds

Mast Cast: An SM Podcast
Ep. 2: Our Stories

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 month ago
1 hour 16 minutes 23 seconds

Mast Cast: An SM Podcast
Ep. 1: Interview with Jessica Fraser of The Mast Cell Disease Society
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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2 months ago
1 hour 5 minutes 53 seconds

Mast Cast: An SM Podcast

A podcast where your hosts Candice and Rachael explore the complexities of living with a rare, chronic disease through personal experience, patient guests' stories, care-giver perspectives, insights from specialists, and updates from the research and advocacy communities - with the purpose of bringing knowledge, connection, and hope to those affected by systemic mastocytosis and related conditions.