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Ep. 217: Exploring Alpha-Gal Syndrome
Manage episode 447453224 series 3392202
Innehåll tillhandahållet av FAACT's Roundtable Podcast. Allt poddinnehåll inklusive avsnitt, grafik och podcastbeskrivningar laddas upp och tillhandahålls direkt av FAACT's Roundtable Podcast eller deras podcastplattformspartner. Om du tror att någon använder ditt upphovsrättsskyddade verk utan din tillåtelse kan du följa processen som beskrivs här https://sv.player.fm/legal.
The US Centers for Disease Control and Prevention states, “Alpha-Gal syndrome (AGS) is a serious, potentially life-threatening allergic condition that can occur after a tick bite.” But how do you get AGS and tackle this condition? We’re exploring living with AGS with two change makers and AGS powerhouses, Candice Matthis and Debbie Nichols. They are the founders of Two Alpha-Gals and the new Alpha-Gal Foundation, which is committed to offering solutions. We’ll learn more about this growing community of support. This podcast is part 1 of a two-part series exploring life with Alpha-Gal Syndrome.
Resources to keep you in the know:
- Alpha-Gal Foundation Website
- Two Alpha-Gals Website
- Alpha-Gals Basics Free Resource Guide
- Alpha-Gal 101 Resource Guide
- In the Tall Grass Two Alpha-Gals Podcast
- The Alpha-Gal Allergen Inclusion Act
Follow Two Alpha Gals on Social Media:
FAACT's Roundtable Podcast can be found on Apple Podcast, Pandora, Spotify, iHeart Radio, or wherever you listen to podcasts.
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Thanks for listening! FAACT invites you to discover more exciting food allergy resources at FoodAllergyAwareness.org!
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