In the Tall Grass

Auteur(s): Two Alpha Gals
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  • Résumé

  • Join the Two Alpha Gals as they share their experience reinventing life with alpha-gal syndrome. Listen to interviews and inspiring stories on resilience and rediscovering joy from others navigating the journey through the tall grass.
    Copyright Two Alpha Gals
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Hygiene & Healthy Living
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Épisodes
  • Heal Out Loud: A Conversation with Meghan Bradshaw about Reclaiming Your Power

    Heal Out Loud: A Conversation with Meghan Bradshaw about Reclaiming Your Power
    Feb 13 2025
    Tick-borne disease often feels like it takes everything from you. Meghan Bradshaw is no exception. As a healthy 20-something, Meghan’s health suddenly declined. Her journey led her from misdiagnosis to multiple joint replacements, fusions, and physiological and emotional devastation. Rather than sitting back and accepting her illness, Meghan instead chose to use her experience to inspire change. Check out her story and listen in to what she’s doing now!

    To learn more about the work Meghan is doing visit: https://www.meghanbradshaw.com/

    Be sure to follow Meghan on social media platforms @mcbradshaw

    To learn more about Center For Lyme Action and the 2025 Virtual Fly In visit: https://centerforlymeaction.org/events/

    The Alpha-gal Allergen Inclusion Act (HR 9382)
    In August 2024, Congressman Van Drew introduced H.R. 9382, the Alpha-gal Allergen Inclusion Act (AGAIA). This bill will amend the Federal Food, Drug, and Cosmetic Act to add alpha-gal to the definition of “major food allergen.” If enacted, the bill will require labeling of alpha-gal on packaged foods sold in the U.S. in the same way other top allergens such as milk, eggs, and peanuts are currently labeled.

    To fill out the two-minute form asking your Representative for support visit: https://alphagalaction.org/take-action-on-the-alpha-gal-allergen-inclusion-act/
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    54 min
  • Holding Hope: A Conversation on Healing Through Purpose with Ali, Founder of The Tick Chicks

    Holding Hope: A Conversation on Healing Through Purpose with Ali, Founder of The Tick Chicks
    Jan 30 2025
    Ali knew something was not right, even when she was told repeatedly, “everything is normal.” Although relentless in her pursuit to find answers, it still took more than six years for her lyme diagnosis. Ali walks us through her journey and how it began by shifting her mindset to show up each day. Her “5 Minute Mindset” inspired her work at The Tick Chicks, a platform built to help others see the light at the end of the tunnel. You won't want to miss this empowering conversation, so tune in now!

    Ali, lives in LA with her family and is the founder of the Tick Chicks, a platform where she blogs, hosts The Lyme Time podcast, and offers incredible resources for diagnosing, managing, and healing Lyme disease.

    To learn more about the work Ali is doing at the Tick Chicks visit: https://thetickchicks.com/
    Find Ali on all social media platforms @thetickchicks
    Listen to inspiring stories and interviews on the Lyme Time Podcast
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    45 min
  • Pulling the Pin: Stories of Anaphylaxis and Epinephrine

    Pulling the Pin: Stories of Anaphylaxis and Epinephrine
    Jan 16 2025
    Using your auto-injector is NOT like pulling the pin on a grenade! In this episode, we share our experiences with anaphylaxis and how we let fear cloud our understanding of the relief brought by proper treatment, including epinephrine. Anaphylaxis can be scary, but it doesn’t have to be. Preparation is key. We discuss the steps we take and the tools we have in place for when a reaction hits. Join us for an open conversation on preparing for the worst case scenario.

    To learn more about allergy & anaphylaxis emergency plans visit FAACT:
    https://www.foodallergyawareness.org/food-allergy-and-anaphylaxis/what-is-anaphylaxis/allergy-and-anaphylaxis-emergency-plans/
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    30 min

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