LET'S TALK MCAS

Mast Cell Action
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From the UK’s only MCAS charity — expert insight, real stories and practical tools for living with Mast Cell Activation Syndrome.

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  1. 7. Aug.

    Mould and MCAS | Lisa Malyon

    Mould is something many of us think of as little more than an inconvenience, but for some people it can have a profound impact on their health. In this episode of the Let’s Talk MCAS Podcast, Deborah Bircham is joined by Lisa Malyon, founder of Indoor Air Aware and the UK Centre for Mould Safety, to explore the growing evidence around indoor mould exposure and why it matters, particularly for people living with complex chronic illnesses such as Mast Cell Activation Syndrome. Drawing on her own family's experience of mould-related illness, Lisa shares the events that led her to establish Indoor Air Aware and create the Mums vs. Mould community, which now supports thousands of people navigating the challenges of unhealthy indoor environments. Together, Deborah and Lisa discuss the wide-ranging health effects that can be associated with mould exposure, why some people appear to be more susceptible than others, and the role that genetics may play in determining individual risk. The conversation also tackles common misconceptions about mould remediation, explaining why simply cleaning visible mould is often not enough, and offers practical guidance on assessing indoor environments, testing for mould, and reducing exposure safely and effectively. Whether you are living with MCAS, supporting someone with a chronic illness, or simply want to better understand the health implications of damp and mould, this episode provides an informative and thought-provoking discussion. It also shines a light on the urgent need for greater public awareness, more research, and improved housing standards to help protect people's health. Indoor Air Aware: https://www.indoorairaware.co.uk/  UK Centre for Mould Safety: https://training.ukcms.org/home Mums v Mould FB group: https://www.facebook.com/groups/347649538392335 WattsWatt: https://wattswatt.co.uk/

  2. 3. Juli

    How to talk to your doctor | Penny Parkes

    In this episode, Deborah is joined by author, health journalist and patient advocate Penny Parkes. They discuss Penny’s new book ‘How to Talk So Your Doctor Will Listen’, and explore the concept of advocacy in relation to chronic illness and MCAS specifically. Those of us living with MCAS often face difficulties with being heard and understood by our doctors, and Penny explores why this is, and how we can ‘work the system’ to improve our chances of getting a successful outcome from medical appointments. If you live with MCAS and you have experienced dismissal from medical professionals, or have left appointments feeling unheard and frustrated, then this episode is a ‘must-listen’. You will never look at a medical appointment in the same way again! Link to Penny’s book: https://amzn.eu/d/0blXKRUx Link to Penny’s social: https://www.instagram.com/how2talktoyourdoctor/

  3. 28. Apr.

    Preparing for Surgery and Anaesthesia with MCAS | Dr Anton Krige

    In this episode, Community Support Coordinator Deborah Bircham is joined by Dr Anton Krige, an NHS consultant anaesthetist and functional medicine practitioner specialising in MCAS. Together, they explore how to navigate surgery and anaesthesia safely when living with MCAS. Dr Krige breaks down the potential risks, explains how different types of anaesthesia may be tolerated, and shares practical strategies to help you prepare for your operation with confidence. A topic frequently raised within the Mast Cell Action community, surgery can feel particularly daunting for those with MCAS. In this conversation, Dr Krige outlines the key considerations, discusses what information to share with your clinical team, and offers expert guidance on both pre-operative planning and post-operative care. Whether you’re facing an upcoming procedure or simply want to feel more informed about future possibilities, this episode is a must-listen for anyone wanting some clear, reassuring, and clinically grounded advice about navigating surgery with MCAS.

  4. 26. März

    Welcome to Mast Cell Action!

    Mast Cell Action are launching our podcast! Join us for our first ever episode, where our Community Support Coordinator, Deborah, chats with Joy Mason, Mast Cell Action’s CEO! Find out about Joy’s own personal journey with MCAS, what keeps her going through the tough times, and also get some behind the scenes info about what’s going on at Mast Cell Action. Joy updates us on her journey from volunteer to CEO, and shares what the charity is working on and the steps we are taking to improve the lives of people living with MCAS. Listen on Apple podcast, Spotify, or wherever you get your podcasts. Join our community at Mast Cell Action, subscribe or follow for more great conversations, and why not share with someone else who might find it helpful. We’d love to know what you think of this episode – please leave us a comment below! https://www.mastcellaction.org/mast-cell-action-events https://www.mastcellaction.org/articles/resources

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From the UK’s only MCAS charity — expert insight, real stories and practical tools for living with Mast Cell Activation Syndrome.

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  • Erstellt von
    Mast Cell Action
  • Jahre aktiv
    2026
  • Folgen
    4
  • Bewertung
    Unbedenklich
  • Copyright
    © 2026 Mast Cell Action
  • Sendungswebsite
    LET'S TALK MCAS

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